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通过基质金属蛋白酶-9的激动剂偏向性信号传导促进细胞外基质重塑。

Agonist-Biased Signaling via Matrix Metalloproteinase-9 Promotes Extracellular Matrix Remodeling.

作者信息

Qorri Bessi, Kalaydina Regina-Veronicka, Velickovic Aleksandra, Kaplya Yekatrina, Decarlo Alexandria, Szewczuk Myron R

机构信息

Department of Biomedical and Molecular Sciences, Queen's University, Kingston, ON K7L 3N6, Canada.

Department of Biology, Biosciences Complex, Queen's University, Kingston, ON K7L 3N6, Canada.

出版信息

Cells. 2018 Aug 26;7(9):117. doi: 10.3390/cells7090117.

Abstract

The extracellular matrix (ECM) is a highly dynamic noncellular structure that is crucial for maintaining tissue architecture and homeostasis. The dynamic nature of the ECM undergoes constant remodeling in response to stressors, tissue needs, and biochemical signals that is are mediated primarily by matrix metalloproteinases (MMPs), which work to degrade and build up the ECM. Research on MMP-9 has demonstrated that this proteinase exists on the cell surface of many cell types in complex with G protein-coupled receptors (GPCRs), and receptor tyrosine kinases (RTKs) or Toll-like receptors (TLRs). Through a novel yet ubiquitous signaling platform, MMP-9 is found to play a crucial role not only in the direct remodeling of the ECM but also in the transactivation of associated receptors to mediate and recruit additional remodeling proteins. Here, we summarize the role of MMP-9 as it exists in a tripartite complex on the cell surface and discuss how its association with each of the TrkA receptor, Toll-like receptors, epidermal growth factor receptor, and the insulin receptor contributes to various aspects of ECM remodeling.

摘要

细胞外基质(ECM)是一种高度动态的无细胞结构,对于维持组织结构和体内平衡至关重要。ECM的动态性质会响应应激源、组织需求和生化信号而不断重塑,这主要由基质金属蛋白酶(MMPs)介导,它们负责降解和构建ECM。对MMP - 9的研究表明,这种蛋白酶以与G蛋白偶联受体(GPCRs)、受体酪氨酸激酶(RTKs)或Toll样受体(TLRs)形成复合物的形式存在于许多细胞类型的细胞表面。通过一个新颖但普遍存在的信号平台,发现MMP - 9不仅在ECM的直接重塑中起关键作用,还在相关受体的反式激活中起关键作用,以介导和招募其他重塑蛋白。在这里,我们总结了MMP - 9作为其存在于细胞表面三方复合物中的作用,并讨论其与TrkA受体、Toll样受体、表皮生长因子受体和胰岛素受体中的每一种的关联如何促进ECM重塑的各个方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13d2/6162445/98f8fbb96439/cells-07-00117-g001.jpg

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