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MMP-2 and 9 in Chronic Kidney Disease.

作者信息

Cheng Zhengyuan, Limbu Manoj Hang, Wang Zhi, Liu Jing, Liu Lei, Zhang Xiaoyi, Chen Pingsheng, Liu Bicheng

机构信息

Department of Pathology and Pathophysiology, Medical School, Southeast University, Dingjiaqiao 87, Gulou District, Nanjing 210009, China.

Department of Nephrology, Zhongda Hospital, Southeast University, Dingjiaqiao 87, Gulou District, Nanjing 210009, China.

出版信息

Int J Mol Sci. 2017 Apr 8;18(4):776. doi: 10.3390/ijms18040776.


DOI:10.3390/ijms18040776
PMID:28397744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5412360/
Abstract

Gelatinases are members of the matrix metalloproteinase (MMPs) family; they play an important role in the degradation of the extracellular matrix (ECM). This effect is also crucial in the development and progression of chronic kidney disease (CKD). Its expression, as well as its activity regulation are closely related to the cell signaling pathways, hypoxia and cell membrane structural change. Gelatinases also can affect the development and progression of CKD through the various interactions with tumor necrosis factors (TNFs), monocyte chemoattractant proteins (MCPs), growth factors (GFs), oxidative stress (OS), and so on. Currently, their non-proteolytic function is a hot topic of research, which may also be associated with the progression of CKD. Therefore, with the in-depth understanding about the function of gelatinases, we can have a more specific and accurate understanding of their role in the human body.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e99/5412360/5839a646f23e/ijms-18-00776-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e99/5412360/e59082f97fc6/ijms-18-00776-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e99/5412360/5839a646f23e/ijms-18-00776-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e99/5412360/e59082f97fc6/ijms-18-00776-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e99/5412360/5839a646f23e/ijms-18-00776-g002.jpg

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本文引用的文献

[1]
Characterization of Lipoprotein-associated Phospholipase A2 in Serum in Patients With Stage 3-5 Chronic Kidney Disease.

Am J Med Sci. 2016-10

[2]
Tuberculosis and chronic kidney disease: an emerging global syndemic.

Kidney Int. 2016-5-10

[3]
Role of matrix metalloproteinase-9 in chronic kidney disease: a new biomarker of resistant albuminuria.

Clin Sci (Lond). 2016-4-1

[4]
Novel Epidermal Growth Factor Receptor Inhibitor Attenuates Angiotensin II-Induced Kidney Fibrosis.

J Pharmacol Exp Ther. 2016-1

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Emergence of a metalloproteinase / phospholipase A2 axis of systemic inflammation.

Metalloproteinases Med. 2015-8-13

[6]
Adipocyte-derived monocyte chemotactic protein-1 (MCP-1) promotes prostate cancer progression through the induction of MMP-2 activity.

Prostate. 2015-7-1

[7]
Activation of toll-like receptor-2 by endogenous matrix metalloproteinase-2 modulates dendritic-cell-mediated inflammatory responses.

Cell Rep. 2014-12-11

[8]
Expression of hypoxia-inducible factor-1α and hepatocyte growth factor in development of fibrosis in the transplanted kidney.

Transpl Int. 2015-2

[9]
MCP-1 stimulates MMP-9 expression via ERK 1/2 and p38 MAPK signaling pathways in human aortic smooth muscle cells.

Cell Physiol Biochem. 2014

[10]
The effect of connective tissue growth factor on renal fibrosis and podocyte injury in hypertensive rats.

Ren Fail. 2014-10

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