NR4A1、NR4A2、IL-36 与冠状动脉性心脏病及心肌缺血再灌注损伤关系的研究进展
摘要
关键词
全文:
PDF参考
MALAKAR A K, CHOUDHURY D, HALDER B, et al. A review
on coronary artery disease, its risk factors, and therapeutics[J]. J
Cell Physiol,2019,234(10):16812-16823.
GANJALI S, GOTTO A M, JR., RUSCICA M, et al. Monocyteto-HDL-cholesterol ratio as a prognostic marker in cardiovascular
diseases[J]. J Cell Physiol,2018,233(12):9237-9246.
DENG R M, ZHOU J. The role of PI3K/AKT signaling pathway
in myocardial ischemia-reperfusion injury[J]. Int Immunopharmac
ol,2023(123):110714.
CHEN L, FAN F, WU L, ZHAO Y. The nuclear receptor 4A family
members: mediators in human disease and autophagy[J]. Cell Mol
Biol Lett,2020,25(1):48.
HAN Y, HUARD A, MORA J, et al. IL-36 family cytokines
in protective versus destructive inflammation[J]. Cell Signal,
(75):109773.
WANG Z, BENOIT G, LIU J, et al. Structure and function of
Nurr1 identifies a class of ligand-independent nuclear receptors[J].
Nature, 2003,423(6939):555-560.
MIAO L, YANG Y, LIU Y, et al. Glycerol kinase interacts with
nuclear receptor NR4A1 and regulates glucose metabolism in the
liver[J]. Faseb j,2019,33(6):6736-6747.
PEKAYVAZ K, GOLD C, HOSEINPOUR P, et al. Mural cellderived chemokines provide a protective niche to safeguard
vascular macrophages and limit chronic inflammation[J].
Immunity, 2023,56(10):2325-2341.
JIANG Y, ZENG Y, HUANG X, et al. Nur77 attenuates
endothelin-1 expression via downregulation of NF-κ B and p38
MAPK in A549 cells and in an ARDS rat model[J]. Am J Physiol
Lung Cell Mol Physiol,2016,311(6):L1023-l1035.
ZHU F, MA J, LI W, et al. The orphan receptor Nur77 binds
cytoplasmic LPS to activate the non-canonical NLRP3
inflammasome[J].Immunity, 2023,56(4):753-767.
YUAN R, ZHANG W, NIE P, et al. Nur77 Deficiency Exacerbates
Macrophage NLRP3 Inflammasome-Mediated Inflammation and
Accelerates Atherosclerosis[J]. Oxid Med Cell Longev,2022:
SHAO Q, HAN F, PENG S, HE B. Nur77 inhibits oxLDL induced
apoptosis of macrophages via the p38 MAPK signaling pathway[J].
Biochem Biophys Res Commun, 2016,471(4):633-638.
BONTA P I, VAN TIEL C M, VOS M, et al. Nuclear receptors
Nur77, Nurr1, and NOR-1 expressed in atherosclerotic lesion
macrophages reduce lipid loading and inflammatory responses[J].
Arterioscler Thromb Vasc Biol,2006,26(10):2288-2294.
SINHA R, DUFOUR S, PETERSEN K F, et al. Assessment of
skeletal muscle triglyceride content by (1)H nuclear magnetic
resonance spectroscopy in lean and obese adolescents: relationships
to insulin sensitivity, total body fat, and central adiposity[J].
Diabetes, 2002,51(4):1022-1027.
CHAO L C, WROBLEWSKI K, ZHANG Z, et al. Insulin
resistance and altered systemic glucose metabolism in mice lacking
Nur77[J]. Diabetes,2009,58(12):2788-2796.
CHAO L C, BENSINGER S J, VILLANUEVA C J, et al. Inhibition
of adipocyte differentiation by Nur77, Nurr1, and Nor1[J]. Mol En
docrinol,2008,22(12):2596-2608.
ARKENBOUT E K, DE WAARD V, VAN BRAGT M, et
al. Protective function of transcription factor TR3 orphan92
receptor in atherogenesis: decreased lesion formation in carotid
artery ligation model in TR3 transgenic mice[J]. Circulati
on,2002,106(12):1530-1535.
BONTA P I, POLS T W, VAN TIEL C M, et al. Nuclear receptor
Nurr1 is expressed in and is associated with human restenosis and
inhibits vascular lesion formation in mice involving inhibition of
smooth muscle cell proliferation and inflammation[J]. Circulation,
,121(18):2023-2032.
ZHOU M, YU Y, LUO X, et al. Myocardial Ischemia-Reperfusion
Injury: Therapeutics from a Mitochondria-Centric Perspective[J].
Cardiology,2021,146(6):781-792.
CHENG Z, VöLKERS M, DIN S, et al. Mitochondrial translocation
of Nur77 mediates cardiomyocyte apoptosis[J]. Eur Heart
J,2011,32(17):2179-2188.
XU A, LIU J, LIU P, et al. Mitochondrial translocation of
Nur77 induced by ROS contributed to cardiomyocyte apoptosis
in metabolic syndrome[J]. Biochem Biophys Res Commun,
,446(4):1184-1189.
MELTON E, QIU H. Interleukin-36 Cytokine/Receptor Signaling:
A New Target for Tissue Fibrosis[J]. Int J Mol Sci,2020,21(18).
GRESNIGT M S, VAN DE VEERDONK F L. Biology of IL-
cytokines and their role in disease[J]. Semin Immunol,
,25(6):458-465.
ZHANG M, LIU J, GAO R, et al. Interleukin-36γ aggravates
macrophage foam cell formation and atherosclerosis progression in
ApoE knockout mice[J]. Cytokine, 2021(146):155630.
TIAN Y, LING X Y, CHEN D L, et al. Interleukin-36 receptor
antagonist attenuates atherosclerosis development by inhibiting
NLRP3 inflammasome[J]. J Cell Physiol, 2020,235(12):9992-9996.
KAZEMIAN S, AHMADI R, RAFIEI A, et al. The Serum Levels of
IL-36 in Patients with Coronary Artery Disease and Their Correlation
with the Serum Levels of IL-32, IL-6, TNF-α , and Oxidative
Stress[J]. Int Arch Allergy Immunol, 2022,183(10):1137-1145.
EL-AWAISI J, KAVANAGH D P, RINK M R, et al. Targeting IL-
improves age-related coronary microcirculatory dysfunction and
attenuates myocardial ischemia/reperfusion injury in mice[J]. JCI
Insight,2022,7(5).
EL-AWAISI J, MITCHELL J L, RANASINGHE A, KALIA N.
Interleukin-36 is vasculoprotective in both sexes despite sexspecific changes in the coronary microcirculation response to IR
injury[J]. Front Cardiovasc Med, 2023(10):1227499.
DOI: http://dx.doi.org/10.12345/yzlcyxzz.v6i12.14898
Refbacks
- 当前没有refback。
此作品已接受知识共享署名-非商业性使用 4.0国际许可协议的许可。