Decoding the MMP14 integrin link: Key player in the secretome landscape

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Stephan Niland, Johannes A. Eble
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引用次数: 0

Abstract

Rapid progress has been made in the exciting field of secretome research in health and disease. The tumor secretome, which is a significant proportion of the tumor proteome, is secreted into the extracellular space to promote intercellular communication and thus tumor progression. Among the many molecules of the secretome, integrins and matrix metalloproteinase 14 (MMP14) stand out as the interplay of adhesion and proteolysis drives invasion. Integrins serve as mechanosensors that mediate the contact of cells with the scaffold of the extracellular matrix and are significantly involved in the precise positioning and activity control of the membrane-bound collagenase MMP14. As a secretome proteinase, MMP14 influences and modifies the secretome itself. While integrins and MT-MMPs are membrane bound, but can be released and are therefore border crossers between the cell surface and the secretome, the extracellular matrix is not constitutively cell-bound, but its binding to integrins and other cell receptors is a stringently regulated process. To understand the mutual interactions in detail, we first summarize the structure and function of MMP14 and how it is regulated at the enzymatic and cellular level. In particular, the mutual interactions between integrins and MMP14 include the proteolytic cleavage of integrins themselves by MMP14. We then review the biochemical, cell biological and physiological effects of MMP14 on the composition and associated functions in the tumor secretome when either bound to the cell membrane, or located on extracellular microvesicles, or as a proteolytically shed non-membrane-bound ectodomain. Novel methods of proteomics, including the analysis of extravesicular vesicles, and new methods for the quantification of MMP14 will provide new research and diagnostic tools. The proteolytic modification of the tumor secretome, especially by MMP14, may bring an additional aspect to tumor secretome studies and will have an impact on the diagnosis and most likely also on the therapy of cancer patients.
解码MMP14整合素链接:分泌组景观的关键参与者。
分泌组在健康和疾病领域的研究进展迅速。肿瘤分泌组是肿瘤蛋白质组的重要组成部分,分泌到细胞外空间,促进细胞间的通讯,从而促进肿瘤的进展。在分泌组的许多分子中,整合素和基质金属蛋白酶14 (MMP14)作为粘附和蛋白水解的相互作用驱动入侵而脱颖而出。整合素作为机械传感器,介导细胞与细胞外基质支架的接触,并在膜结合胶原酶MMP14的精确定位和活性控制中发挥重要作用。作为一种分泌组蛋白酶,MMP14影响和修饰分泌组本身。虽然整合素和MT-MMPs是膜结合的,但可以释放,因此是细胞表面和分泌组之间的边界交叉点,但细胞外基质不是构成细胞结合的,但其与整合素和其他细胞受体的结合是一个严格调节的过程。为了更详细地了解它们之间的相互作用,我们首先总结了MMP14的结构和功能,以及它是如何在酶和细胞水平上被调节的。特别是,整合素和MMP14之间的相互作用包括MMP14对整合素本身的蛋白水解裂解。然后,我们回顾了MMP14对肿瘤分泌组的组成和相关功能的生化、细胞生物学和生理学影响,无论是结合到细胞膜上,还是位于细胞外微泡上,或者作为蛋白水解脱落的非膜结合外域。包括囊外囊泡分析在内的蛋白质组学新方法和MMP14的定量新方法将提供新的研究和诊断工具。肿瘤分泌组的蛋白水解修饰,尤其是MMP14的修饰,可能会给肿瘤分泌组的研究带来额外的方面,并将对癌症患者的诊断产生影响,很可能也会对癌症患者的治疗产生影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Matrix Biology
Matrix Biology 生物-生化与分子生物学
CiteScore
11.40
自引率
4.30%
发文量
77
审稿时长
45 days
期刊介绍: Matrix Biology (established in 1980 as Collagen and Related Research) is a cutting-edge journal that is devoted to publishing the latest results in matrix biology research. We welcome articles that reside at the nexus of understanding the cellular and molecular pathophysiology of the extracellular matrix. Matrix Biology focusses on solving elusive questions, opening new avenues of thought and discovery, and challenging longstanding biological paradigms.
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