Regulation of toll-like receptor (TLR) signaling pathways in atherosclerosis: from mechanisms to targeted therapeutics
Atherosclerosis, one of the life-threatening cardiovascular diseases (CVDs), has been demonstrated to be a chronic inflammatory disease, and inflammatory and immune processes are involved in the origin and development of the disease. Toll-like receptors (TLRs), a class of pattern recognition receptors that trigger innate immune responses by identifying pathogen-associated molecular patterns (PAMPs) and danger-associated molecular patterns (DAMPs), regulate numerous acute and chronic inflammatory diseases. Recent studies reveal that TLRs have a vital role in the occurrence and development of atherosclerosis, including the initiation of endothelial dysfunction, interaction of various immune cells, and activation of a number of other inflammatory pathways. We herein summarize some other inflammatory signaling pathways, protein molecules, and cellular responses associated with TLRs, such as NLRP3, Nrf2, PCSK9, autophagy, pyroptosis and necroptosis, which are also involved in the development of AS. Targeting TLRs and their regulated inflammatory events could be a promising new strategy for the treatment of atherosclerotic CVDs. Novel drugs that exert therapeutic effects on AS through TLRs and their related pathways are increasingly being developed. In this article, we comprehensively review the current knowledge of TLR signaling pathways in atherosclerosis and actively seek potential therapeutic strategies using TLRs as a breakthrough point in the prevention and therapy of atherosclerosis.
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References
- Tsao CW, Aday AW, Almarzooq ZI, Alonso A, Beaton AZ, Bittencourt MS, et al. Heart disease and stroke statistics-2022 update: a report from the American Heart Association. Circulation. 2022;145:e153–e639. ArticlePubMedGoogle Scholar
- Roy P, Orecchioni M, Ley K. How the immune system shapes atherosclerosis: roles of innate and adaptive immunity. Nat Rev Immunol. 2022;22:251–65. ArticleCASPubMedGoogle Scholar
- Libby P. Inflammation in atherosclerosis. Nature. 2002;420:868–74. ArticleCASPubMedGoogle Scholar
- Soehnlein O, Libby P. Targeting inflammation in atherosclerosis-from experimental insights to the clinic. Nat Rev Drug Discov. 2021;20:589–610. ArticleCASPubMedPubMed CentralGoogle Scholar
- Blasius AL, Beutler B. Intracellular toll-like receptors. Immunity. 2010;32:305–15. ArticleCASPubMedGoogle Scholar
- Wang Y, Song E, Bai B, Vanhoutte PM. Toll-like receptors mediating vascular malfunction: Lessons from receptor subtypes. Pharmacol Ther. 2016;158:91–100. ArticleCASPubMedGoogle Scholar
- Bayan N, Yazdanpanah N, Rezaei N. Role of toll-like receptor 4 in diabetic retinopathy. Pharmacol Res. 2022;175:105960. ArticleCASPubMedGoogle Scholar
- Shafeghat M, Kazemian S, Aminorroaya A, Aryan Z, Rezaei N. Toll-like receptor 7 regulates cardiovascular diseases. Int Immunopharmacol. 2022;113:109390. ArticleCASPubMedGoogle Scholar
- Almeida SO, Budoff M. Effect of statins on atherosclerotic plaque. Trends Cardiovasc Med. 2019;29:451–5. ArticleCASPubMedGoogle Scholar
- Kobiyama K, Ley K. Atherosclerosis. Circ Res. 2018;123:1118–20. ArticleCASPubMedPubMed CentralGoogle Scholar
- Kales SN, Soteriades ES, Christophi CA, Christiani DC. Emergency duties and deaths from heart disease among firefighters in the United States. N Engl J Med. 2007;356:1207–15. ArticleCASPubMedGoogle Scholar
- Koskinas KC, Feldman CL, Chatzizisis YS, Coskun AU, Jonas M, Maynard C, et al. Natural history of experimental coronary atherosclerosis and vascular remodeling in relation to endothelial shear stress: a serial, in vivo intravascular ultrasound study. Circulation. 2010;121:2092–101. ArticlePubMedPubMed CentralGoogle Scholar
- Allahverdian S, Pannu PS, Francis GA. Contribution of monocyte-derived macrophages and smooth muscle cells to arterial foam cell formation. Cardiovasc Res. 2012;95:165–72. ArticleCASPubMedGoogle Scholar
- Hopkins PN. Molecular biology of atherosclerosis. Physiol Rev. 2013;93:1317–542. ArticleCASPubMedGoogle Scholar
- Sun HJ, Wu ZY, Nie XW, Bian JS. Role of endothelial dysfunction in cardiovascular diseases: the link between inflammation and hydrogen sulfide. Front Pharmacol. 2019;10:1568. ArticleCASPubMedGoogle Scholar
- Mori H, Torii S, Kutyna M, Sakamoto A, Finn AV, Virmani R. Coronary artery calcification and its progression: what does it really mean? JACC Cardiovasc Imaging. 2018;11:127–42. ArticlePubMedGoogle Scholar
- Shi X, Gao J, Lv Q, Cai H, Wang F, Ye R, et al. Calcification in atherosclerotic plaque vulnerability: friend or foe? Front Physiol. 2020;11:56. ArticlePubMedPubMed CentralGoogle Scholar
- Kapustin AN, Chatrou MLL, Drozdov I, Zheng Y, Davidson SM, Soong D, et al. Vascular smooth muscle cell calcification is mediated by regulated exosome secretion. Circ Res. 2015;116:1312–23. ArticleCASPubMedGoogle Scholar
- Libby P. Molecular and cellular mechanisms of the thrombotic complications of atherosclerosis. J Lipid Res. 2009;50:S352–S7. ArticlePubMedPubMed CentralGoogle Scholar
- Vijay K. Toll-like receptors in immunity and inflammatory diseases: past, present, and future. Int Immunopharmacol. 2018;59:391–412. ArticleCASPubMedPubMed CentralGoogle Scholar
- Fitzgerald KA, Kagan JC. Toll-like receptors and the control of immunity. Cell. 2020;180:1044–66. ArticleCASPubMedPubMed CentralGoogle Scholar
- Asami J, Shimizu T. Structural and functional understanding of the toll-like receptors. Protein Sci. 2021;30:761–72. ArticleCASPubMedPubMed CentralGoogle Scholar
- Jaén RI, Val-Blasco A, Prieto P, Gil-Fernández M, Smani T, López-Sendón JL, et al. Innate immune receptors, key actors in cardiovascular diseases. JACC Basic Transl Sci. 2020;5:735–49. ArticlePubMedPubMed CentralGoogle Scholar
- Wang YC, Lin S, Yang QW. Toll-like receptors in cerebral ischemic inflammatory injury. J Neuroinflammation. 2011;8:134. ArticleCASPubMedPubMed CentralGoogle Scholar
- Salvador B, Arranz A, Francisco S, Córdoba L, Punzón C, Llamas MÁ, et al. Modulation of endothelial function by Toll like receptors. Pharmacol Res. 2016;108:46–56. ArticleCASPubMedGoogle Scholar
- Alonso-Pérez A, Franco-Trepat E, Guillán-Fresco M, Jorge-Mora A, López V, Pino J, et al. Role of toll-like receptor 4 on osteoblast metabolism and function. Front Physiol. 2018;9:504. ArticlePubMedPubMed CentralGoogle Scholar
- Vollmer S, Strickson S, Zhang T, Gray N, Lee KL, Rao VR, et al. The mechanism of activation of IRAK1 and IRAK4 by interleukin-1 and Toll-like receptor agonists. Biochem J. 2017;474:2027–38. ArticleCASPubMedGoogle Scholar
- Yamamoto M, Sato S, Hemmi H, Hoshino K, Kaisho T, Sanjo H, et al. Role of adaptor TRIF in the MyD88-independent toll-like receptor signaling pathway. Science. 2003;301:640–3. ArticleCASPubMedGoogle Scholar
- Leulier F, Lemaitre B. Toll-like receptors-taking an evolutionary approach. Nat Rev Genet. 2008;9:165–78. ArticleCASPubMedGoogle Scholar
- Cahill PA, Redmond EM. Vascular endothelium-Gatekeeper of vessel health. Atherosclerosis. 2016;248:97–109. ArticleCASPubMedPubMed CentralGoogle Scholar
- Ciesielska A, Matyjek M, Kwiatkowska K. TLR4 and CD14 trafficking and its influence on LPS-induced pro-inflammatory signaling. Cell Mol Life Sci. 2021;78:1233–61. ArticleCASPubMedGoogle Scholar
- Xu W, Zhou W, Wang H, Liang S. Roles of Porphyromonas gingivalis and its virulence factors in periodontitis. Adv Protein Chem Struct Biol. 2020;120:45–84. ArticlePubMedPubMed CentralGoogle Scholar
- Mougeot JLC, Stevens CB, Paster BJ, Brennan MT, Lockhart PB, Mougeot FKB. Porphyromonas gingivalis is the most abundant species detected in coronary and femoral arteries. J Oral Microbiol. 2017;9:1281562. ArticlePubMedPubMed CentralGoogle Scholar
- Joshi C, Bapat R, Anderson W, Dawson D, Hijazi K, Cherukara G. Detection of periodontal microorganisms in coronary atheromatous plaque specimens of myocardial infarction patients: A systematic review and meta-analysis. Trends Cardiovasc Med. 2021;31:69–82. ArticleCASPubMedGoogle Scholar
- Xie M, Tang Q, Yu S, Sun J, Mei F, Zhao J, et al. Porphyromonas gingivalis disrupts vascular endothelial homeostasis in a TLR-NF-κB axis dependent manner. Int J Oral Sci. 2020;12:28. ArticleCASPubMedPubMed CentralGoogle Scholar
- Inaba H, Yoshida S, Nomura R, Kato Y, Asai F, Nakano K, et al. Porphyromonas gulae lipopolysaccharide elicits inflammatory responses through Toll-like receptor 2 and 4 in human gingivalis epithelial cells. Cell Microbiol. 2020;22:e13254. ArticleCASPubMedGoogle Scholar
- Lin G, Chen S, Lei L, You X, Huang M, Luo L, et al. Effects of intravenous injection of porphyromonas gingivalis on rabbit inflammatory immune response and atherosclerosis. Mediators Inflamm. 2015;2015:364391. ArticlePubMedPubMed CentralGoogle Scholar
- Grelier A, Cras A, Balitrand N, Delmau C, Lecourt S, Lepelletier Y, et al. Toll-like receptor 3 regulates cord blood-derived endothelial cell function in vitro and in vivo. Angiogenesis. 2013;16:821–36. ArticleCASPubMedGoogle Scholar
- Gimbrone MA, García-Cardeña G. Endothelial cell dysfunction and the pathobiology of atherosclerosis. Circ Res. 2016;118:620–36. ArticleCASPubMedPubMed CentralGoogle Scholar
- Yeung J, Li W, Holinstat M. Platelet signaling and disease: targeted therapy for thrombosis and other related diseases. Pharmacol Rev. 2018;70:526–48. ArticleCASPubMedPubMed CentralGoogle Scholar
- Schrottmaier WC, Mussbacher M, Salzmann M, Assinger A. Platelet-leukocyte interplay during vascular disease. Atherosclerosis. 2020;307:109–20. ArticleCASPubMedGoogle Scholar
- Gremmel T, Frelinger AL 3rd, Michelson AD. Platelet physiology. Semin Thromb Hemost. 2016;42:191–204. ArticleCASPubMedGoogle Scholar
- Rondina MT, Schwertz H, Harris ES, Kraemer BF, Campbell RA, Mackman N, et al. The septic milieu triggers expression of spliced tissue factor mRNA in human platelets. J Thromb Haemost. 2011;9:748–58. ArticleCASPubMedPubMed CentralGoogle Scholar
- Libby P, Tabas I, Fredman G, Fisher EA. Inflammation and its resolution as determinants of acute coronary syndromes. Circ Res. 2014;114:1867–79. ArticleCASPubMedPubMed CentralGoogle Scholar
- D’ Atri LP, Schattner M. Platelet toll-like receptors in thromboinflammation. Front Biosci (Landmark Ed). 2017;22:1867–83. ArticlePubMedGoogle Scholar
- Holinstat M. Normal platelet function. Cancer Metastasis Rev. 2017;36:195–8. ArticleCASPubMedPubMed CentralGoogle Scholar
- Niklaus M, Klingler P, Weber K, Koessler A, Boeck M, Kobsar A, et al. The involvement of toll-like receptors 2 and 4 in human platelet signalling pathways. Cell Signal. 2020;76:109817. ArticleCASPubMedGoogle Scholar
- Koupenova M, Clancy L, Corkrey HA, Freedman JE. Circulating platelets as mediators of immunity, inflammation, and thrombosis. Circ Res. 2018;122:337–51. ArticleCASPubMedPubMed CentralGoogle Scholar
- Bakogiannis C, Sachse M, Stamatelopoulos K, Stellos K. Platelet-derived chemokines in inflammation and atherosclerosis. Cytokine. 2019;122:154157. ArticlePubMedGoogle Scholar
- Jakob A, Schachinger E, Klau S, Lehner A, Ulrich S, Stiller B, et al. Von Willebrand factor parameters as potential biomarkers for disease activity and coronary artery lesion in patients with Kawasaki disease. Eur J Pediatr. 2020;179:377–84. ArticleCASPubMedGoogle Scholar
- Rivadeneyra L, Carestia A, Etulain J, Pozner RG, Fondevila C, Negrotto S, et al. Regulation of platelet responses triggered by Toll-like receptor 2 and 4 ligands is another non-genomic role of nuclear factor-kappaB. Thromb Res. 2014;133:235–43. ArticleCASPubMedGoogle Scholar
- Damien P, Cognasse F, Payrastre B, Spinelli SL, Blumberg N, Arthaud CA, et al. NF-κB links TLR2 and PAR1 to soluble immunomodulator factor secretion in human platelets. Front Immunol. 2017;8:85. ArticlePubMedPubMed CentralGoogle Scholar
- Shi C, Pamer EG. Monocyte recruitment during infection and inflammation. Nat Rev Immunol. 2011;11:762–74. ArticleCASPubMedPubMed CentralGoogle Scholar
- Jakubzick CV, Randolph GJ, Henson PM. Monocyte differentiation and antigen-presenting functions. Nat Rev Immunol. 2017;17:349–62. ArticleCASPubMedGoogle Scholar
- Guilliams M, Mildner A, Yona S. Developmental and functional heterogeneity of monocytes. Immunity. 2018;49:595–613. ArticleCASPubMedGoogle Scholar
- Blériot C, Dupuis T, Jouvion G, Eberl G, Disson O, Lecuit M. Liver-resident macrophage necroptosis orchestrates type 1 microbicidal inflammation and type-2-mediated tissue repair during bacterial infection. Immunity. 2015;42:145–58. ArticlePubMedGoogle Scholar
- Machiels B, Dourcy M, Xiao X, Javaux J, Mesnil C, Sabatel C, et al. Author Correction: A gammaherpesvirus provides protection against allergic asthma by inducing the replacement of resident alveolar macrophages with regulatory monocytes. Nat Immunol. 2018;19:1035. ArticleCASPubMedGoogle Scholar
- Aegerter H, Kulikauskaite J, Crotta S, Patel H, Kelly G, Hessel EM, et al. Influenza-induced monocyte-derived alveolar macrophages confer prolonged antibacterial protection. Nat Immunol. 2020;21:145–57. ArticleCASPubMedPubMed CentralGoogle Scholar
- Guilliams M, Svedberg FR. Does tissue imprinting restrict macrophage plasticity? Nat Immunol. 2021;22:118–27. ArticleCASPubMedGoogle Scholar
- Honda T, Egen JG, Lämmermann T, Kastenmüller W, Torabi-Parizi P, Germain RN. Tuning of antigen sensitivity by T cell receptor-dependent negative feedback controls T cell effector function in inflamed tissues. Immunity. 2014;40:235–47. ArticleCASPubMedPubMed CentralGoogle Scholar
- Coillard A, Guyonnet L, De Juan A, Cros A, Segura E. TLR or NOD receptor signaling skews monocyte fate decision via distinct mechanisms driven by mTOR and miR-155. Proc Natl Acad Sci USA. 2021;118:1–12. ArticleGoogle Scholar
- Watanabe T, Kitani A, Murray PJ, Strober W. NOD2 is a negative regulator of Toll-like receptor 2-mediated T helper type 1 responses. Nat Immunol. 2004;5:800–8. ArticleCASPubMedGoogle Scholar
- Gamrekelashvili J, Kapanadze T, Sablotny S, Ratiu C, Dastagir K, Lochner M, et al. Notch and TLR signaling coordinate monocyte cell fate and inflammation. Elife. 2020;9:e57007. ArticleCASPubMedPubMed CentralGoogle Scholar
- Arazi A, Rao DA, Berthier CC, Davidson A, Liu Y, Hoover PJ, et al. The immune cell landscape in kidneys of patients with lupus nephritis. Nat Immunol. 2019;20:902–14. ArticleCASPubMedPubMed CentralGoogle Scholar
- Bonnardel J, Guilliams M. Developmental control of macrophage function. Curr Opin Immunol. 2018;50:64–74. ArticleCASPubMedGoogle Scholar
- Radtke F, MacDonald HR, Tacchini-Cottier F. Regulation of innate and adaptive immunity by Notch. Nat Rev Immunol. 2013;13:427–37. ArticleCASPubMedGoogle Scholar
- Akilesh HM, Buechler MB, Duggan JM, Hahn WO, Matta B, Sun X, et al. Chronic TLR7 and TLR9 signaling drives anemia via differentiation of specialized hemophagocytes. Science. 2019;363:eaao5213. ArticleCASPubMedPubMed CentralGoogle Scholar
- Song R, Gao Y, Dozmorov I, Malladi V, Saha I, McDaniel MM, et al. IRF1 governs the differential interferon-stimulated gene responses in human monocytes and macrophages by regulating chromatin accessibility. Cell Rep. 2021;34:108891. ArticleCASPubMedPubMed CentralGoogle Scholar
- Mogensen TH. IRF and STAT transcription factors - from basic biology to roles in infection, protective immunity, and primary immunodeficiencies. Front Immunol. 2018;9:3047. ArticleCASPubMedGoogle Scholar
- Negishi H, Taniguchi T, Yanai H. The interferon (IFN) class of cytokines and the IFN regulatory factor (IRF) transcription factor family. Cold Spring Harb Perspect Biol. 2018;10:a028423. ArticleCASPubMedPubMed CentralGoogle Scholar
- Platanitis E, Decker T. Regulatory networks involving STATs, IRFs, and NFκB in inflammation. Front Immunol. 2018;9:2542. ArticlePubMedPubMed CentralGoogle Scholar
- Rajagopalan S, Lee EC, DuPrie ML, Long EO. TNFR-associated factor 6 and TGF-β-activated kinase 1 control signals for a senescence response by an endosomal NK cell receptor. J Immunol. 2014;192:714–21. ArticleCASPubMedGoogle Scholar
- Sager HB, Dutta P, Dahlman JE, Hulsmans M, Courties G, Sun Y, et al. RNAi targeting multiple cell adhesion molecules reduces immune cell recruitment and vascular inflammation after myocardial infarction. Sci Transl Med. 2016;8:342ra80. ArticlePubMedPubMed CentralGoogle Scholar
- Jinnouchi H, Guo L, Sakamoto A, Torii S, Sato Y, Cornelissen A, et al. Diversity of macrophage phenotypes and responses in atherosclerosis. Cell Mol Life Sci. 2020;77:1919–32. ArticleCASPubMedGoogle Scholar
- Yan J, Horng T. Lipid metabolism in regulation of macrophage functions. Trends Cell Biol. 2020;30:979–89. ArticleCASPubMedGoogle Scholar
- Liu X, Guo JW, Lin XC, Tuo YH, Peng WL, He SY, et al. Macrophage NFATc3 prevents foam cell formation and atherosclerosis: evidence and mechanisms. Eur Heart J. 2021;42:4847–61. ArticleCASPubMedGoogle Scholar
- Tall AR, Yvan-Charvet L. Cholesterol, inflammation and innate immunity. Nat Rev Immunol. 2015;15:104–16. ArticleCASPubMedPubMed CentralGoogle Scholar
- Yang X, Yin Y, Yan X, Yu Z, Liu Y, Cao J. Flagellin attenuates experimental sepsis in a macrophage-dependent manner. Crit Care. 2019;23:106. ArticlePubMedPubMed CentralGoogle Scholar
- Ellenbroek GHJM, van Puijvelde GHM, Anas AA, Bot M, Asbach M, Schoneveld A, et al. Leukocyte TLR5 deficiency inhibits atherosclerosis by reduced macrophage recruitment and defective T-cell responsiveness. Sci Rep. 2017;7:42688. ArticleCASPubMedPubMed CentralGoogle Scholar
- Hussain S, Johnson CG, Sciurba J, Meng X, Stober VP, Liu C, et al. TLR5 participates in the TLR4 receptor complex and promotes MyD88-dependent signaling in environmental lung injury. Elife. 2020;9:e50458. ArticleCASPubMedPubMed CentralGoogle Scholar
- Hemmi H, Kaisho T, Takeuchi O, Sato S, Sanjo H, Hoshino K, et al. Small anti-viral compounds activate immune cells via the TLR7 MyD88-dependent signaling pathway. Nat Immunol. 2002;3:196–200. ArticleCASPubMedGoogle Scholar
- Salagianni M, Galani IE, Lundberg AM, Davos CH, Varela A, Gavriil A, et al. Toll-like receptor 7 protects from atherosclerosis by constraining “inflammatory” macrophage activation. Circulation. 2012;126:952–62. ArticleCASPubMedGoogle Scholar
- Ishida H, Ohto U, Shibata T, Miyake K, Shimizu T. Structural basis for species-specific activation of mouse Toll-like receptor 9. FEBS Lett. 2018;592:2636–46. ArticleCASPubMedGoogle Scholar
- Fukuda D, Nishimoto S, Aini K, Tanaka A, Nishiguchi T, Kim-Kaneyama JR, et al. Toll-like receptor 9 plays a pivotal role in angiotensin II-induced atherosclerosis. J Am Heart Assoc. 2019;8:e010860. ArticlePubMedPubMed CentralGoogle Scholar
- Behmoaras J. The versatile biochemistry of iron in macrophage effector functions. FEBS J. 2021;288:6972–89. ArticleCASPubMedGoogle Scholar
- Nonnenmacher Y, Hiller K. Biochemistry of proinflammatory macrophage activation. Cell Mol Life Sci. 2018;75:2093–109. ArticleCASPubMedPubMed CentralGoogle Scholar
- Lauterbach MA, Hanke JE, Serefidou M, Mangan MSJ, Kolbe CC, Hess T, et al. Toll-like receptor signaling rewires macrophage metabolism and promotes histone acetylation via ATP-citrate lyase. Immunity. 2019;51:997–1011.e7. ArticleCASPubMedGoogle Scholar
- Sharif O, Brunner JS, Vogel A, Schabbauer G. Macrophage rewiring by nutrient associated PI3K dependent pathways. Front Immunol. 2019;10:2002. ArticleCASPubMedPubMed CentralGoogle Scholar
- Krawczyk CM, Holowka T, Sun J, Blagih J, Amiel E, DeBerardinis RJ, et al. Toll-like receptor-induced changes in glycolytic metabolism regulate dendritic cell activation. Blood. 2010;115:4742–9. ArticleCASPubMedPubMed CentralGoogle Scholar
- Wang Y, Li N, Zhang X, Horng T. Mitochondrial metabolism regulates macrophage biology. J Biol Chem. 2021;297:100904. ArticleCASPubMedPubMed CentralGoogle Scholar
- Irizarry-Caro RA, McDaniel MM, Overcast GR, Jain VG, Troutman TD, Pasare C. TLR signaling adapter BCAP regulates inflammatory to reparatory macrophage transition by promoting histone lactylation. Proc Natl Acad Sci USA. 2020;117:30628–38. ArticleCASPubMedPubMed CentralGoogle Scholar
- Artis D, Spits H. The biology of innate lymphoid cells. Nature. 2015;517:293–301. ArticleCASPubMedGoogle Scholar
- Cybulsky MI, Cheong C, Robbins CS. Macrophages and dendritic cells: partners in atherogenesis. Circ Res. 2016;118:637–52. ArticleCASPubMedGoogle Scholar
- Gallenga C, Pandolfi F, Caraffa A, Kritas S, Ronconi G, Toniato E, et al. Interleukin-1 family cytokinesand mast cells: activation and inhibition. J Biol Regul Homeost Agents. 2019;33:1–6. CASPubMedGoogle Scholar
- Ji Q, Meng K, Yu K, Huang S, Huang Y, Min X, et al. Exogenous interleukin 37 ameliorates atherosclerosis via inducing the Treg response in ApoE-deficient mice. Sci Rep. 2017;7:3310. ArticlePubMedPubMed CentralGoogle Scholar
- Liu T, Liu J, Lin Y, Que B, Chang C, Zhang J, et al. IL-37 inhibits the maturation of dendritic cells through the IL-1R8-TLR4-NF-κB pathway. Biochim Biophys Acta Mol Cell Biol Lipids. 2019;1864:1338–49. ArticleCASPubMedGoogle Scholar
- Liebner S, Dijkhuizen RM, Reiss Y, Plate KH, Agalliu D, Constantin G. Functional morphology of the blood-brain barrier in health and disease. Acta Neuropathol. 2018;135:311–36. ArticleCASPubMedPubMed CentralGoogle Scholar
- Hutchins PM, Heinecke JW. Cholesterol efflux capacity, macrophage reverse cholesterol transport and cardioprotective HDL. Curr Opin Lipido. 2015;26:388–93. ArticleCASGoogle Scholar
- Tabas I, Bornfeldt KE. Macrophage phenotype and function in different stages of atherosclerosis. Circ Res. 2016;118:653–67. ArticleCASPubMedPubMed CentralGoogle Scholar
- Martinet W, Coornaert I, Puylaert P, De Meyer GRY. Macrophage death as a pharmacological target in atherosclerosis. Front Pharmacol. 2019;10:306. ArticleCASPubMedPubMed CentralGoogle Scholar
- Santer D, Nagel F, Gonçalves IF, Kaun C, Wojta J, Fagyas M, et al. Tenascin-C aggravates ventricular dilatation and angiotensin-converting enzyme activity after myocardial infarction in mice. ESC Heart Fail. 2020;7:2113–22. ArticlePubMedPubMed CentralGoogle Scholar
- Podesser BK, Kreibich M, Dzilic E, Santer D, Förster L, Trojanek S, et al. Tenascin-C promotes chronic pressure overload-induced cardiac dysfunction, hypertrophy and myocardial fibrosis. J Hypertens. 2018;36:847–56. ArticleCASPubMedGoogle Scholar
- Luo H, Wang J, Qiao C, Zhang X, Zhang W, Ma N. ATF3 inhibits tenascin-C-induced foam cell formation in LPS-stimulated THP-1 macrophages by suppressing TLR-4. J Atheroscler Thromb. 2015;22:1214–23. ArticleCASPubMedGoogle Scholar
- Liu Y, Hu Y, Xiong J, Zeng X. Overexpression of activating transcription factor 3 alleviates cardiac microvascular ischemia/reperfusion injury in rats. Front Pharmacol. 2021;12:598959. ArticleCASPubMedPubMed CentralGoogle Scholar
- Bennett MR, Sinha S, Owens GK. Vascular smooth muscle cells in atherosclerosis. Circ Res. 2016;118:692–702. ArticleCASPubMedPubMed CentralGoogle Scholar
- Yang K, Wang X, Liu Z, Lu L, Mao J, Meng H, et al. Oxidized low-density lipoprotein promotes macrophage lipid accumulation via the toll-like receptor 4-Src pathway. Circ J. 2015;79:2509–16. ArticleCASPubMedGoogle Scholar
- Kasahara K, Nakayama Y, Sato I, Ikeda K, Hoshino M, Endo T, et al. Role of Src-family kinases in formation and trafficking of macropinosomes. J Cell Physiol. 2007;211:220–32. ArticleCASPubMedGoogle Scholar
- Moldogazieva NT, Mokhosoev IM, Mel’nikova TI, Porozov YB, Terentiev AA. Oxidative stress and advanced lipoxidation and glycation end products (ALEs and AGEs) in aging and age-related diseases. Oxid Med Cell Longev. 2019;2019:3085756. ArticlePubMedPubMed CentralGoogle Scholar
- Chen Z, Xue Q, Cao L, Wang Y, Chen Y, Zhang X, et al. Toll-like receptor 4 mediated oxidized low-density lipoprotein-induced foam cell formation in vascular smooth muscle cells via Src and Sirt1/3 pathway. Mediators Inflamm. 2021;2021:6639252. ArticlePubMedPubMed CentralGoogle Scholar
- Vandestienne M, Zhang Y, Santos-Zas I, Al-Rifai R, Joffre J, Giraud A, et al. TREM-1 orchestrates angiotensin II-induced monocyte trafficking and promotes experimental abdominal aortic aneurysm. J Clin Invest. 2021;131:e142468. ArticleCASPubMedPubMed CentralGoogle Scholar
- Nguyen TTT, Yoon HK, Kim YT, Choi YH, Lee WK, Jin M. Tryptophanyl-tRNA synthetase 1 signals activate TREM-1 via TLR2 and TLR4. Biomolecules. 2020;10:1283. ArticleCASPubMedPubMed CentralGoogle Scholar
- Joffre J, Potteaux S, Zeboudj L, Loyer X, Boufenzer A, Laurans L, et al. Genetic and pharmacological inhibition of TREM-1 limits the development of experimental atherosclerosis. J Am Coll Cardiol. 2016;68:2776–93. ArticleCASPubMedGoogle Scholar
- Zahid A, Li B, Kombe AJK, Jin T, Tao J. Pharmacological inhibitors of the NLRP3 inflammasome. Front Immunol. 2019;10:2538. ArticlePubMedPubMed CentralGoogle Scholar
- Paik S, Kim JK, Silwal P, Sasakawa C, Jo EK. An update on the regulatory mechanisms of NLRP3 inflammasome activation. Cell Mol Immunol. 2021;18:1141–60. ArticleCASPubMedPubMed CentralGoogle Scholar
- Swanson KV, Deng M, Ting JPY. The NLRP3 inflammasome: molecular activation and regulation to therapeutics. Nat Rev Immunol. 2019;19:477–89. ArticleCASPubMedPubMed CentralGoogle Scholar
- Zhao C, Zhao W. NLRP3 inflammasome-a key player in antiviral responses. Front Immunol. 2020;11:211. ArticleCASPubMedPubMed CentralGoogle Scholar
- Freigang S, Ampenberger F, Spohn G, Heer S, Shamshiev AT, Kisielow J, et al. Nrf2 is essential for cholesterol crystal-induced inflammasome activation and exacerbation of atherosclerosis. Eur J Immunol. 2011;41:2040–51. ArticleCASPubMedGoogle Scholar
- He X, Fan X, Bai B, Lu N, Zhang S, Zhang L. Pyroptosis is a critical immune-inflammatory response involved in atherosclerosis. Pharmacol Res. 2021;165:105447. ArticleCASPubMedGoogle Scholar
- Zhang X, Ren Z, Xu W, Jiang Z. Necroptosis in atherosclerosis. Clin Chim Acta. 2022;534:22–8. ArticleCASPubMedGoogle Scholar
- Jin Y, Liu Y, Xu L, Xu J, Xiong Y, Peng Y, et al. Novel role for caspase 1 inhibitor VX765 in suppressing NLRP3 inflammasome assembly and atherosclerosis via promoting mitophagy and efferocytosis. Cell Death Dis. 2022;13:512. ArticleCASPubMedPubMed CentralGoogle Scholar
- Kobayashi EH, Suzuki T, Funayama R, Nagashima T, Hayashi M, Sekine H, et al. Nrf2 suppresses macrophage inflammatory response by blocking proinflammatory cytokine transcription. Nat Commun. 2016;7:11624. ArticleCASPubMedPubMed CentralGoogle Scholar
- Nadeem A, Siddiqui N, Al-Harbi NO, Al-Harbi MM, Ahmad SF. TLR-7 agonist attenuates airway reactivity and inflammation through Nrf2-mediated antioxidant protection in a murine model of allergic asthma. Int J Biochem Cell Biol. 2016;73:53–62. ArticleCASPubMedGoogle Scholar
- Wang Y, Zhang S, Li H, Wang H, Zhang T, Hutchinson MR, et al. Small-molecule modulators of Toll-like receptors. Acc Chem Res. 2020;53:1046–55. ArticleCASPubMedGoogle Scholar
- Lee JW, Bae CJ, Choi YJ, Kim SI, Kwon YS, Lee HJ, et al. 3,4,5-Trihydroxycinnamic acid inhibits lipopolysaccharide (LPS)-induced inflammation by Nrf2 activation in vitro and improves survival of mice in LPS-induced endotoxemia model in vivo. Mol Cell Biochem. 2014;390:143–53. ArticleCASPubMedGoogle Scholar
- Joo MS, Kim WD, Lee KY, Kim JH, Koo JH, Kim SG. AMPK facilitates nuclear accumulation of Nrf2 by phosphorylating at serine 550. Mol Cell Biol. 2016;36:1931–42. ArticlePubMedPubMed CentralGoogle Scholar
- Yin S, Cao W. Toll-like receptor signaling induces Nrf2 pathway activation through p62-triggered Keap1 degradation. Mol Cell Biol. 2015;35:2673–83. ArticleCASPubMedPubMed CentralGoogle Scholar
- Sun Q, Fan J, Billiar TR, Scott MJ. Inflammasome and autophagy regulation - a two-way street. Mol Med. 2017;23:188–95. ArticleCASPubMedGoogle Scholar
- Lei L, Chai Y, Lin H, Chen C, Zhao M, Xiong W, et al. Dihydroquercetin activates AMPK/Nrf2/HO-1 signaling in macrophages and attenuates inflammation in LPS-induced endotoxemic mice. Front Pharmacol. 2020;11:662. ArticleCASPubMedPubMed CentralGoogle Scholar
- Choudhury S, Ghosh S, Gupta P, Mukherjee S, Chattopadhyay S. Inflammation-induced ROS generation causes pancreatic cell death through modulation of Nrf2/NF-κB and SAPK/JNK pathway. Free Radic Res. 2015;49:1371–83. ArticleCASPubMedGoogle Scholar
- Sabatine MS. PCSK9 inhibitors: clinical evidence and implementation. Nat Rev Cardiol. 2019;16:155–65. ArticleCASPubMedGoogle Scholar
- Giunzioni I, Tavori H, Covarrubias R, Major AS, Ding L, Zhang Y, et al. Local effects of human PCSK9 on the atherosclerotic lesion. J Pathol. 2016;238:52–62. ArticleCASPubMedGoogle Scholar
- Roche-Molina M, Sanz-Rosa D, Cruz FM, García-Prieto J, López S, Abia R, et al. Induction of sustained hypercholesterolemia by single adeno-associated virus-mediated gene transfer of mutant hPCSK9. Arterioscler Thromb Vasc Biol. 2015;35:50–9. ArticleCASPubMedGoogle Scholar
- Ding Z, Liu S, Wang X, Theus S, Deng X, Fan Y, et al. PCSK9 regulates expression of scavenger receptors and ox-LDL uptake in macrophages. Cardiovasc Res. 2018;114:1145–53. ArticleCASPubMedGoogle Scholar
- Tang ZH, Peng J, Ren Z, Yang J, Li TT, Li TH, et al. New role of PCSK9 in atherosclerotic inflammation promotion involving the TLR4/NF-κB pathway. Atherosclerosis. 2017;262:113–22. ArticleCASPubMedGoogle Scholar
- Liu S, Deng X, Zhang P, Wang X, Fan Y, Zhou S, et al. Blood flow patterns regulate PCSK9 secretion via MyD88-mediated pro-inflammatory cytokines. Cardiovasc Res. 2020;116:1721–32. ArticleCASPubMedGoogle Scholar
- Ding Z, Liu S, Wang X, Deng X, Fan Y, Sun C, et al. Hemodynamic shear stress via ROS modulates PCSK9 expression in human vascular endothelial and smooth muscle cells and along the mouse aorta. Antioxid Redox Signal. 2015;22:760–71. ArticleCASPubMedPubMed CentralGoogle Scholar
- Tavori H, Giunzioni I, Predazzi IM, Plubell D, Shivinsky A, Miles J, et al. Human PCSK9 promotes hepatic lipogenesis and atherosclerosis development via apoE- and LDLR-mediated mechanisms. Cardiovasc Res. 2016;110:268–78. ArticleCASPubMedPubMed CentralGoogle Scholar
- Shen L, Peng HC, Nees SN, Zhao SP, Xu DY. Proprotein convertase subtilisin/kexin type 9 potentially influences cholesterol uptake in macrophages and reverse cholesterol transport. FEBS Lett. 2013;587:1271–4. ArticleCASPubMedGoogle Scholar
- Adorni MP, Cipollari E, Favari E, Zanotti I, Zimetti F, Corsini A, et al. Inhibitory effect of PCSK9 on Abca1 protein expression and cholesterol efflux in macrophages. Atherosclerosis. 2017;256:1–6. ArticleCASPubMedGoogle Scholar
- Bahrami A, Parsamanesh N, Atkin SL, Banach M, Sahebkar A. Effect of statins on Toll-like receptors: a new insight to pleiotropic effects. Pharmacol Res. 2018;135:230–8. ArticleCASPubMedGoogle Scholar
- Koushki K, Shahbaz SK, Mashayekhi K, Sadeghi M, Zayeri ZD, Taba MY, et al. Anti-inflammatory action of statins in cardiovascular disease: the role of inflammasome and Toll-like receptor pathways. Clin Rev Allergy Immunol. 2021;60:175–99. ArticleCASPubMedGoogle Scholar
- Kuzmich N, Andresyuk E, Porozov Y, Tarasov V, Samsonov M, Preferanskaya N, et al. PCSK9 as a target for development of a new generation of hypolipidemic drugs. Molecules. 2022;27:434. ArticleCASPubMedPubMed CentralGoogle Scholar
- Gao W, Xiong Y, Li Q, Yang H. Inhibition of Toll-like receptor signaling as a promising therapy for inflammatory diseases: a journey from molecular to nano therapeutics. Front Physiol. 2017;8:508. ArticlePubMedPubMed CentralGoogle Scholar
- Yu Y, Liu J, Liu C, Liu R, Liu L, Yu Z, et al. Post-translational modifications of cGAS-STING: a critical switch for immune regulation. Cells. 2022;11:3043. ArticleCASPubMedPubMed CentralGoogle Scholar
- Cui G, Ye X, Zuo T, Zhao H, Zhao Q, Chen W, et al. Chloroquine pretreatment inhibits toll-like receptor 3 signaling after stroke. Neurosci Lett. 2013;548:101–4. ArticleCASPubMedGoogle Scholar
- Liu S, Jiang Q, Zhao X, Zhao R, Wang Y, Wang Y, et al. Publisher correction: a DNA nanodevice-based vaccine for cancer immunotherapy. Nat Mater. 2021;20:431–3. ArticleCASPubMedGoogle Scholar
- Cen X, Wang B, Liang Y, Chen Y, Xiao Y, Du S, et al. Small molecule SMU-CX24 targeting toll-like receptor 3 counteracts inflammation: A novel approach to atherosclerosis therapy. Acta Pharm Sin B. 2022;12:3667–81. ArticleCASPubMedPubMed CentralGoogle Scholar
- Naqvi AR, Sarwat M. MicroRNAs and immunity. Semin Cell Developmental. Biol. 2022;124:1–2. CASGoogle Scholar
- Zhang B, Zhang YF, Li R, Zhao L, Qin SG, Pan LF, et al. MiR-217 inhibits apoptosis of atherosclerotic endothelial cells via the TLR4/PI3K/Akt/NF-κB pathway. Eur Rev Med Pharmacol Sci. 2020;24:12867–77. CASPubMedGoogle Scholar
- Chen M, Li W, Zhang Y, Yang J. MicroRNA-20a protects human aortic endothelial cells from Ox-LDL-induced inflammation through targeting TLR4 and TXNIP signaling. Biomed Pharmacother. 2018;103:191–7. ArticleCASPubMedGoogle Scholar
- Yan H, Huang W, Rao J, Yuan J. miR-21 regulates ischemic neuronal injury via the p53/Bcl-2/Bax signaling pathway. Aging. 2021;13:22242–55. ArticleCASPubMedPubMed CentralGoogle Scholar
- Pan Y, Jia T, Zhang Y, Zhang K, Zhang R, Li J, et al. MS2 VLP-based delivery of microRNA-146a inhibits autoantibody production in lupus-prone mice. Int J Nanomed. 2012;7:5957–67. ArticleCASGoogle Scholar
- Wang L, Zhang H, Sun L, Gao W, Xiong Y, Ma A, et al. Manipulation of macrophage polarization by peptide-coated gold nanoparticles and its protective effects on acute lung injury. J Nanobiotechnol. 2020;18:38. ArticleGoogle Scholar
- Yang H, Fung SY, Xu S, Sutherland DP, Kollmann TR, Liu M, et al. Amino acid-dependent attenuation of Toll-like receptor signaling by peptide-gold nanoparticle hybrids. ACS Nano. 2015;9:6774–84. ArticleCASPubMedGoogle Scholar
- Foit L, Thaxton CS. Synthetic high-density lipoprotein-like nanoparticles potently inhibit cell signaling and production of inflammatory mediators induced by lipopolysaccharide binding Toll-like receptor 4. Biomaterials. 2016;100:67–75. ArticleCASPubMedGoogle Scholar
- Yang H, Kozicky L, Saferali A, Fung SY, Afacan N, Cai B, et al. Endosomal pH modulation by peptide-gold nanoparticle hybrids enables potent anti-inflammatory activity in phagocytic immune cells. Biomaterials. 2016;111:90–102. ArticleCASPubMedGoogle Scholar
- Shinchi H, Yamaguchi T, Moroishi T, Yuki M, Wakao M, Cottam HB, et al. Gold nanoparticles coimmobilized with small molecule Toll-like receptor 7 ligand and α-mannose as adjuvants. Bioconjugate Chem. 2019;30:2811–21. ArticleCASGoogle Scholar
- Wang L, Li YL, Zhang CC, Cui W, Wang X, Xia Y, et al. Inhibition of Toll-like receptor 2 reduces cardiac fibrosis by attenuating macrophage-mediated inflammation. Cardiovasc Res. 2014;101:383–92. ArticleCASPubMedGoogle Scholar
- Reilly M, Miller RM, Thomson MH, Patris V, Ryle P, McLoughlin L, et al. Randomized, double-blind, placebo-controlled, dose-escalating phase I, healthy subjects study of intravenous OPN-305, a humanized anti-TLR2 antibody. Clin Pharmacol Ther. 2013;94:593–600. ArticleCASPubMedPubMed CentralGoogle Scholar
- Arslan F, Houtgraaf JH, Keogh B, Kazemi K, de Jong R, McCormack WJ, et al. Treatment with OPN-305, a humanized anti-Toll-Like receptor-2 antibody, reduces myocardial ischemia/reperfusion injury in pigs. Circ Cardiovasc Interv. 2012;5:279–87. ArticleCASPubMedGoogle Scholar
- Monnet E, Lapeyre G, Poelgeest EV, Jacqmin P, Graaf K, Reijers J, et al. Evidence of NI-0101 pharmacological activity, an anti-TLR4 antibody, in a randomized phase I dose escalation study in healthy volunteers receiving LPS. Clin Pharmacol Ther. 2017;101:200–8. ArticleCASPubMedGoogle Scholar
- Hatterer E, Shang L, Simonet P, Herren S, Daubeuf B, Teixeira S, et al. A specific anti-citrullinated protein antibody profile identifies a group of rheumatoid arthritis patients with a toll-like receptor 4-mediated disease. Arthritis Res Ther. 2016;18:224. ArticlePubMedPubMed CentralGoogle Scholar
- Hirota T, Fujita Y, Ieiri I. An updated review of pharmacokinetic drug interactions and pharmacogenetics of statins. Expert Opin Drug Metab Toxicol. 2020;16:809–22. ArticleCASPubMedGoogle Scholar
- Guo X, Wang L, Xia X, Wang P, Li X. Effects of atorvastatin and/or probucol on recovery of atherosclerosis in high-fat-diet-fed apolipoprotein E-deficient mice. Biomed Pharmacother. 2019;109:1445–53. ArticleCASPubMedGoogle Scholar
- Moutzouri E, Tellis CC, Rousouli K, Liberopoulos EN, Milionis HJ, Elisaf MS, et al. Effect of simvastatin or its combination with ezetimibe on Toll-like receptor expression and lipopolysaccharide - induced cytokine production in monocytes of hypercholesterolemic patients. Atherosclerosis. 2012;225:381–7. ArticleCASPubMedGoogle Scholar
- Altaf A, Qu P, Zhao Y, Wang H, Lou D, Niu N. NLRP3 inflammasome in peripheral blood monocytes of acute coronary syndrome patients and its relationship with statins. Coron Artery Dis. 2015;26:409–21. ArticlePubMedGoogle Scholar
- Wang Y, Zhang MX, Meng X, Liu FQ, Yu GS, Zhang C, et al. Atorvastatin suppresses LPS-induced rapid upregulation of Toll-like receptor 4 and its signaling pathway in endothelial cells. Am J Physiol Heart Circ Physiol. 2011;300:H1743–52. ArticleCASPubMedGoogle Scholar
- Kapelouzou A, Giaglis S, Peroulis M, Katsimpoulas M, Moustardas P, Aravanis CV, et al. Overexpression of Toll-like receptors 2, 3, 4, and 8 is correlated to the vascular atherosclerotic process in the hyperlipidemic rabbit model: the effect of statin treatment. J Vasc Res. 2017;54:156–69. ArticleCASPubMedGoogle Scholar
- Hoogeveen RM, Opstal TSJ, Kaiser Y, Stiekema LCA, Kroon J, Knol RJJ, et al. PCSK9 antibody alirocumab attenuates arterial wall inflammation without changes in circulating inflammatory markers. JACC Cardiovasc Imaging. 2019;12:2571–3. ArticlePubMedGoogle Scholar
- Bernelot Moens SJ, Neele AE, Kroon J, van der Valk FM, Van den Bossche J, Hoeksema MA, et al. PCSK9 monoclonal antibodies reverse the pro-inflammatory profile of monocytes in familial hypercholesterolaemia. Eur Heart J. 2017;38:1584–93. ArticlePubMedGoogle Scholar
- Landlinger C, Pouwer MG, Juno C, van der Hoorn JWA, Pieterman EJ, Jukema JW, et al. The AT04A vaccine against proprotein convertase subtilisin/kexin type 9 reduces total cholesterol, vascular inflammation, and atherosclerosis in APOE*3Leiden.CETP mice. Eur Heart J. 2017;38:2499–507. ArticleCASPubMedPubMed CentralGoogle Scholar
- Flannery S, Bowie AG. The interleukin-1 receptor-associated kinases: critical regulators of innate immune signalling. Biochem Pharmacol. 2010;80:1981–91. ArticleCASPubMedGoogle Scholar
- Akar-Ghibril N. Defects of the innate immune system and related immune deficiencies. Clin Rev Allergy Immunol. 2022;63:36–54. ArticlePubMedGoogle Scholar
- Alfaidi M, Acosta CH, Wang D, Traylor JG, Orr AW. Selective role of Nck1 in atherogenic inflammation and plaque formation. J Clin Invest. 2020;130:4331–47. CASPubMedPubMed CentralGoogle Scholar
- Ridker PM, Everett BM, Thuren T, MacFadyen JG, Chang WH, Ballantyne C, et al. Antiinflammatory therapy with canakinumab for atherosclerotic disease. N Engl J Med. 2017;377:1119–31. ArticleCASPubMedGoogle Scholar
- Wu X, Xu M, Liu Z, Zhang Z, Liu Y, Luo S, et al. Pharmacological inhibition of IRAK1 and IRAK4 prevents endothelial inflammation and atherosclerosis in ApoE -/- mice. Pharmacol Res. 2022;175:106043. ArticleCASPubMedGoogle Scholar
- Ye T, Li Y, Xiong D, Gong S, Zhang L, Li B, et al. Combination of Danshen and ligustrazine has dual anti-inflammatory effect on macrophages and endothelial cells. J Ethnopharmacol. 2021;266:113425. ArticleCASPubMedGoogle Scholar
- Li Z-M, Xu S-W, Liu P-Q. Salvia miltiorrhizaBurge (Danshen): a golden herbal medicine in cardiovascular therapeutics. Acta Pharmacol Sin. 2018;39:802–24. ArticleCASPubMedPubMed CentralGoogle Scholar
- Luo J, Song W, Yang G, Xu H, Chen K. Compound Danshen (Salvia miltiorrhiza) dripping pill for coronary heart disease: an overview of systematic reviews. Am J Chin Med. 2015;43:25–43. ArticleCASPubMedGoogle Scholar
- Hao DC, Ge GB, Xiao PG. Anticancer drug targets of Salvia phytometabolites: chemistry, biology and omics. Curr Drug Targets. 2018;19:1–20. ArticlePubMedGoogle Scholar
- Irmak F, Kurt Yazar S, Şirvan SS, Serin M, Özağarı A. Karasoy, et al. Beneficial effects of Salvia miltiorrhiza in the healing of burn wounds: an experimental study in rats. J Plast Surg Hand Surg. 2018;52:229–33. ArticlePubMedGoogle Scholar
- Meng Z, Si CY, Teng S, Yu XH, Li HY. Tanshinone IIA inhibits lipopolysaccharide-induced inflammatory responses through the TLR4/TAK1/NF-κB signaling pathway in vascular smooth muscle cells. Int J Mol Med. 2019;43:1847–58. CASPubMedGoogle Scholar
- Du H, Wang Y, Zeng Y, Huang X, Liu D, Ye L, et al. Tanshinone IIA suppresses proliferation and inflammatory cytokine production of synovial fibroblasts from rheumatoid arthritis patients induced by TNF-α and attenuates the inflammatory response in AIA mice. Front Pharmacol. 2020;11:568. ArticleCASPubMedPubMed CentralGoogle Scholar
- Fan G, Jiang X, Wu X, Fordjour PA, Miao L, Zhang H, et al. Anti-inflammatory activity of tanshinone IIA in LPS-stimulated RAW264.7 macrophages via miRNAs and TLR4-NF-κB pathway. Inflammation. 2016;39:375–84. ArticleCASPubMedGoogle Scholar
- Gao LN, Zhou X, Zhang Y, Cui YL, Yu CQ, Gao S. The anti-inflammatory activities of ethanol extract from Dan-Lou prescription in vivo and in vitro. BMC Complement Alter Med. 2015;15:317. ArticleGoogle Scholar
- Ichimura T, Asseldonk EJ, Humphreys BD, Gunaratnam L, Duffield JS, Bonventre JV. Kidney injury molecule-1 is a phosphatidylserine receptor that confers a phagocytic phenotype on epithelial cells. J Clin Invest. 2008;118:1657–68. ArticleCASPubMedPubMed CentralGoogle Scholar
- Gao LN, Zhou X, Lu YR, Li K, Gao S, Yu CQ, et al. Dan-Lou prescription inhibits foam cell formation induced by ox-LDL via the TLR4/NF-κB and PPARγ signaling pathways. Front Physiol. 2018;9:590. ArticlePubMedPubMed CentralGoogle Scholar
- Medeiros DL, Lima ETG, Silva JC, Medeiros MA, Pinheiro EBF. Rhamnetin: a review of its pharmacology and toxicity. J Pharm Pharmacol. 2022;74:793–9. ArticlePubMedGoogle Scholar
- Zhang W, Li B, Guo Y, Bai Y, Wang T, Fu K, et al. Rhamnetin attenuates cognitive deficit and inhibits hippocampal inflammatory response and oxidative stress in rats with traumatic brain injury. Cent Eur J Immunol. 2015;40:35–41. ArticlePubMedPubMed CentralGoogle Scholar
- Kritharides L, Nordestgaard BG, Tybjærg-Hansen A, Kamstrup PR, Afzal S. Effect of APOE ε genotype on lipoprotein(a) and the associated risk of myocardial infarction and aortic valve stenosis. J Clin Endocrinol Metab. 2017;102:3390–9. ArticlePubMedGoogle Scholar
- Wang M, Wu Y, Li W. Rhamnetin ameliorates macrophage-mediated inflammation and pro-atherosclerosis pathways in apolipoprotein E-deficient mice. J Physiol Pharmacol 2021;72. https://doi.org/10.26402/jpp.2021.2.10.
- Aquila G, Morelli MB, Vieceli Dalla Sega F, Fortini F, Nigro P, Caliceti C, et al. Heart rate reduction with ivabradine in the early phase of atherosclerosis is protective in the endothelium of ApoE-deficient mice. J Physiol Pharmacol. 2018;69:35–52. CASPubMedGoogle Scholar
- Krogmann AO, Lüsebrink E, Steinmetz M, Asdonk T, Lahrmann C, Lütjohann D, et al. Proinflammatory stimulation of Toll-like receptor 9 with high dose CpG ODN 1826 impairs endothelial regeneration and promotes atherosclerosis in mice. PLoS One. 2016;11:e0146326. ArticlePubMedPubMed CentralGoogle Scholar
- Zhuang C, Chen R, Zheng Z, Lu J, Hong C. Toll-like receptor 3 in cardiovascular diseases. Heart, Lung. Circulation. 2022;31:e93–e109. Google Scholar
- Kong F, Ye B, Lin L, Cai X, Huang W, Huang Z. Atorvastatin suppresses NLRP3 inflammasome activation via TLR4/MyD88/NF-κB signaling in PMA-stimulated THP-1 monocytes. Biomed Pharmacother. 2016;82:167–72. ArticleCASPubMedGoogle Scholar
- Koike A, Tsujinaka K, Fujimori K. Statins attenuate antiviral IFN-β and ISG expression via inhibition of IRF3 and JAK/STAT signaling in poly(I:C)-treated hyperlipidemic mice and macrophages. FEBS J. 2021;288:4249–66. ArticleCASPubMedGoogle Scholar
- Chen JY, Zhu GY, Su XH, Wang R, Liu J, Liao K, et al. 7-deacetylgedunin suppresses inflammatory responses through activation of Keap1/Nrf2/HO-1 signaling. Oncotarget. 2017;8:55051–63. ArticlePubMedPubMed CentralGoogle Scholar
- Cong ZX, Wang HD, Zhou Y, Wang JW, Pan H, Zhang DD, et al. Temozolomide and irradiation combined treatment-induced Nrf2 activation increases chemoradiation sensitivity in human glioblastoma cells. J Neuro-Oncol. 2014;116:41–8. ArticleCASGoogle Scholar
- Mohan S, Gupta D. Crosstalk of toll-like receptors signaling and Nrf2 pathway for regulation of inflammation. Biomed Pharmacother. 2018;108:1866–78. ArticleCASPubMedGoogle Scholar
- Gómez-Guzmán M, Jiménez R, Romero M, Sánchez M, Zarzuelo MJ, Gómez-Morales M, et al. Chronic hydroxychloroquine improves endothelial dysfunction and protects kidney in a mouse model of systemiclupus erythematosus. Hypertension. 2014;64:330–7. ArticlePubMedGoogle Scholar
- El-Salamouni NS, Gowayed MA, Younis SE, Abdel-Bary A, Kamel MA, Labib GS. Pentoxifylline/Valsartan co-delivery in liposomal gel alters the inflammatory HMGB-1/TLR pathway and promotes faster healing in burn wounds: A promising repurposed approach. Int J Pharm. 2022;625:122129. ArticleCASPubMedGoogle Scholar
- Atwa AM, Abd El-Ghafar OAM, Hassanein EHM, Mahdi SE, Sayed GA, Alruhaimi RS, et al. Candesartan attenuates cisplatin-induced lung injury by modulating oxidative stress, inflammation, and TLR-4/NF-κB, JAK1/STAT3, and Nrf2/HO-1 signaling. Pharmaceuticals (Basel, Switzerland). 2022;15:1222. https://doi.org/10.3390/ph15101222. ArticleCASPubMedPubMed CentralGoogle Scholar
- Guo R, Li L, Su J, Li S, Duncan SE, Liu Z, et al. Pharmacological activity and mechanism of tanshinone IIA in related diseases. Drug Des Devel Ther. 2020;14:4735–48. ArticlePubMedPubMed CentralGoogle Scholar
- Song X, Tan L, Wang M, Ren C, Guo C, Yang B, et al. Myricetin: A review of the most recent research. Biomed Pharmacother. 2021;134:111017. ArticleCASPubMedGoogle Scholar
- Liu ZW, Wang JK, Qiu C, Guan GC, Liu XH, Li SJ, et al. Matrine pretreatment improves cardiac function in rats with diabetic cardiomyopathy via suppressing ROS/TLR-4 signaling pathway. Acta Pharmacol Sin. 2015;36:323–33. ArticlePubMedPubMed CentralGoogle Scholar
- Liu K, Li M, Ren X, You QS, Wang F, Wang S, et al. Huang Qi Tong Bi Decoction attenuates myocardial ischemia-reperfusion injury via HMGB1/TLR/NF-κB pathway. Mediators Inflamm. 2019;2019:8387636. ArticlePubMedPubMed CentralGoogle Scholar
- Kim WS, Kim K, Byun EB, Song HY, Han JM, Park WY, et al. RM, a novel resveratrol derivative, attenuates inflammatory responses induced by lipopolysaccharide via selectively increasing the Tollip protein in macrophages: A partial mechanism with therapeutic potential in an inflammatory setting. Int Immunopharmacol. 2020;78:106072. ArticleCASPubMedGoogle Scholar
- Chen L, Yu J. Modulation of Toll-like receptor signaling in innate immunity by natural products. Int Immunopharmacol. 2016;37:65–70. ArticlePubMedPubMed CentralGoogle Scholar
- Zhao H, Zhang M, Zhou F, Cao W, Bi L, Xie Y, et al. Cinnamaldehyde ameliorates LPS-induced cardiac dysfunction via TLR4-NOX4 pathway: The regulation of autophagy and ROS production. J Mol Cell Cardiol. 2016;101:11–24. ArticleCASPubMedGoogle Scholar
Acknowledgements
This work is supported by National Natural Science Foundation of China (grant numbers 82270500, 81870324, 82203304, U21A20419), Science and Technology Project of Huadu District in Guangzhou (21-HDWS-007) and Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (grant numbers 2017BT01Y093, 2017BT01Y036).