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心肌细胞因子 1 样蛋白在缺血/再灌注损伤中的潜在治疗作用。

Putative therapeutic impacts of cardiac CTRP9 in ischaemia/reperfusion injury.

机构信息

Cardiovascular Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Department of General and Vascular Surgery, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

J Cell Mol Med. 2022 Jun;26(11):3120-3132. doi: 10.1111/jcmm.17355. Epub 2022 May 10.


DOI:10.1111/jcmm.17355
PMID:35535510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9170823/
Abstract

Recently, cytokines belonging to C1q/tumour necrosis factor-related proteins (CTRPs) superfamily have attracted increasing attention due to multiple metabolic functions and desirable anti-inflammatory effects. These various molecular effectors exhibit key roles upon the onset of cardiovascular diseases, making them novel adipo/cardiokines. This review article aimed to highlight recent findings correlated with therapeutic effects and additional mechanisms specific to the CTRP9, particularly in cardiac ischaemia/reperfusion injury (IRI). Besides, the network of the CTPR9 signalling pathway and its possible relationship with IRI were discussed. Together, the discovery of all involved underlying mechanisms could shed light to alleviate the pathological sequelae after the occurrence of IRI.

摘要

最近,属于 C1q/肿瘤坏死因子相关蛋白(CTRPs)超家族的细胞因子由于其多种代谢功能和理想的抗炎作用而引起了越来越多的关注。这些不同的分子效应物在心血管疾病的发生中起着关键作用,使它们成为新型的脂肪/心脏细胞因子。本文综述了与 CTRP9 的治疗效果和特定于 CTRP9 的其他机制相关的最新发现,特别是在心肌缺血/再灌注损伤(IRI)中的作用。此外,还讨论了 CTRP9 信号通路的网络及其与 IRI 的可能关系。总之,发现所有涉及的潜在机制可以减轻 IRI 发生后的病理后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04c1/9170823/a6d34a818611/JCMM-26-3120-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04c1/9170823/8d9f7a7f9d9a/JCMM-26-3120-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04c1/9170823/7ea0dcff786e/JCMM-26-3120-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04c1/9170823/a6d34a818611/JCMM-26-3120-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04c1/9170823/8d9f7a7f9d9a/JCMM-26-3120-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04c1/9170823/7ea0dcff786e/JCMM-26-3120-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04c1/9170823/a6d34a818611/JCMM-26-3120-g002.jpg

相似文献

[1]
Putative therapeutic impacts of cardiac CTRP9 in ischaemia/reperfusion injury.

J Cell Mol Med. 2022-6

[2]
Inhibition of CTRP9, a novel and cardiac-abundantly expressed cell survival molecule, by TNFα-initiated oxidative signaling contributes to exacerbated cardiac injury in diabetic mice.

Basic Res Cardiol. 2012-12-5

[3]
Cardiac-derived CTRP9 protects against myocardial ischemia/reperfusion injury via calreticulin-dependent inhibition of apoptosis.

Cell Death Dis. 2018-6-20

[4]
Detrimental effects of prolonged warm renal ischaemia-reperfusion injury are abrogated by supplemental hydrogen sulphide: an analysis using real-time intravital microscopy and polymerase chain reaction.

BJU Int. 2012-10-9

[5]
Erythropoietin pretreatment ameliorates renal ischaemia-reperfusion injury by activating PI3K/Akt signalling.

Nephrology (Carlton). 2015-4

[6]
Tim-3 exacerbates kidney ischaemia/reperfusion injury through the TLR-4/NF-κB signalling pathway and an NLR-C4 inflammasome activation.

Clin Exp Immunol. 2018-5-7

[7]
A novel interpretation of immune redundancy and duality in reperfusion injury with important implications for intervention in ischaemic disease.

Med Hypotheses. 2007

[8]
CTRP9: An emerging potential anti-aging molecule in brain.

Cell Signal. 2020-9

[9]
Molecular mechanisms of liver ischemia reperfusion injury: insights from transgenic knockout models.

World J Gastroenterol. 2013-3-21

[10]
Tumour necrosis factor-α promotes liver ischaemia-reperfusion injury through the PGC-1α/Mfn2 pathway.

J Cell Mol Med. 2014-9

引用本文的文献

[1]
CTRP9 attenuates peripheral nerve injury-induced mechanical allodynia and thermal hyperalgesia through regulating spinal microglial polarization and neuroinflammation mediated by AdipoR1 in male mice.

Cell Biol Toxicol. 2024-10-26

本文引用的文献

[1]
C1q/Tumor Necrosis Factor-Related Protein 9: Basics and Therapeutic Potentials.

Front Physiol. 2022-3-18

[2]
Novel Adipokines CTRP1, CTRP9, and FGF21 in Pediatric Type 1 and Type 2 Diabetes: A Cross-Sectional Analysis.

Horm Res Paediatr. 2022

[3]
Role of First-Trimester Serum C1q/TNF-Related Protein 9 in Gestational Diabetes Mellitus.

Clin Lab. 2020-12-1

[4]
C1q/TNF-related protein-9 attenuates palmitic acid-induced endothelial cell senescence via increasing autophagy.

Mol Cell Endocrinol. 2021-2-5

[5]
Protective Role of CTRP3 and CTRP9 in the Development of Gestational Diabetes Mellitus.

Clin Lab. 2020-11-1

[6]
C1q/TNF-related Protein 9 Inhibits High Glucose-Induced Oxidative Stress and Apoptosis in Retinal Pigment Epithelial Cells Through the Activation of AMPK/Nrf2 Signaling Pathway.

Cell Transplant. 2020

[7]
C1q/TNF-Related Protein 9 Promotes Revascularization in Response to Ischemia an eNOS-Dependent Manner.

Front Pharmacol. 2020-8-21

[8]
Adipocytokine expression, platelet-to-lymphocyte ratio and TGF-1/Smad signaling activity in diabetic patients complicated with pulmonary infection.

J Int Med Res. 2020-6

[9]
CTRP9: An emerging potential anti-aging molecule in brain.

Cell Signal. 2020-9

[10]
C1q/Tumor Necrosis Factor-Related Protein-9 Attenuates Diabetic Nephropathy and Kidney Fibrosis in db/db Mice.

DNA Cell Biol. 2020-4-13

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