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器官纤维化中胶原蛋白的酶促交联——解决方法与评估

Enzymatic cross-linking of collagens in organ fibrosis - resolution and assessment.

作者信息

Pehrsson Martin, Mortensen Joachim Høg, Manon-Jensen Tina, Bay-Jensen Anne-Christine, Karsdal Morten Asser, Davies Michael Jonathan

机构信息

Department of Biomedical Science, University of Copenhagen, Copenhagen, Denmark.

Biomarkers & Research, Nordic Bioscience A/S, Herlev, Denmark.

出版信息

Expert Rev Mol Diagn. 2021 Oct;21(10):1049-1064. doi: 10.1080/14737159.2021.1962711. Epub 2021 Aug 24.

Abstract

: Enzymatic cross-linking of the collagens within the extracellular matrix (ECM) catalyzed by enzymes such as lysyl oxidase (LOX) and lysyl oxidase like-enzymes 1-4 (LOXL), transglutaminase 2 (TG2), and peroxidasin (PXDN) contribute to fibrosis progression through extensive collagen cross-linking. Studies in recent years have begun elucidating the important role of collagen cross-linking in perpetuating progression of organ fibrosis independently of inflammation through an increasingly stiff and noncompliant ECM. Therefore, collagen cross-linking and the cross-linking enzymes have become new targets in anti-fibrotic therapy as well as targets of novel biomarkers to properly assess resolution of the fibrotic ECM.: The enzymatic actions of enzymes catalyzing collagen cross-linking and their relevance in organ fibrosis. Potential biomarkers specifically quantifying proteolytic fragments of collagen cross-linking is discussed based on Pubmed search done in November 2020 as well as the authors knowledge.: Current methods for the assessment of fibrosis involve the use of invasive and/or cumbersome and expensive methods such as tissue biopsies. Thus, an unmet need exists for the development and validation of minimally invasive biomarkers of proteolytic fragments of cross-linked collagens. These biomarkers may aid in the development and proper assessment of fibrosis resolution in coming years.

摘要

由赖氨酰氧化酶(LOX)、赖氨酰氧化酶样酶1 - 4(LOXL)、转谷氨酰胺酶2(TG2)和过氧化物酶(PXDN)等酶催化的细胞外基质(ECM)内胶原蛋白的酶促交联,通过广泛的胶原蛋白交联促进纤维化进展。近年来的研究开始阐明胶原蛋白交联在通过日益僵硬和顺应性差的ECM使器官纤维化持续进展中所起的重要作用,且与炎症无关。因此,胶原蛋白交联和交联酶已成为抗纤维化治疗的新靶点以及用于正确评估纤维化ECM消退的新型生物标志物的靶点。

催化胶原蛋白交联的酶的酶促作用及其在器官纤维化中的相关性。基于2020年11月进行的PubMed搜索以及作者的知识,讨论了特异性定量胶原蛋白交联蛋白水解片段的潜在生物标志物。

目前评估纤维化的方法涉及使用侵入性和/或繁琐且昂贵的方法,如组织活检。因此,开发和验证交联胶原蛋白蛋白水解片段的微创生物标志物存在未满足的需求。这些生物标志物可能有助于未来几年纤维化消退的研究和正确评估。

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