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探索细胞外基质交联作为一种治疗纤维化的方法。

Exploring Extracellular Matrix Crosslinking as a Therapeutic Approach to Fibrosis.

作者信息

Lloyd Sarah M, He Yupeng

机构信息

AbbVie Inc., 1 North Waukegan Rd., North Chicago, IL 60064, USA.

出版信息

Cells. 2024 Mar 2;13(5):438. doi: 10.3390/cells13050438.

Abstract

The extracellular matrix (ECM) provides structural support for tissues and regulatory signals for resident cells. ECM requires a careful balance between protein accumulation and degradation for homeostasis. Disruption of this balance can lead to pathological processes such as fibrosis in organs across the body. Post-translational crosslinking modifications to ECM proteins such as collagens alter ECM structure and function. Dysregulation of crosslinking enzymes as well as changes in crosslinking composition are prevalent in fibrosis. Because of the crucial roles these ECM crosslinking pathways play in disease, the enzymes that govern crosslinking events are being explored as therapeutic targets for fibrosis. Here, we review in depth the molecular mechanisms underlying ECM crosslinking, how ECM crosslinking contributes to fibrosis, and the therapeutic strategies being explored to target ECM crosslinking in fibrosis to restore normal tissue structure and function.

摘要

细胞外基质(ECM)为组织提供结构支持,并为驻留细胞提供调节信号。ECM需要在蛋白质积累和降解之间保持精确平衡以维持内环境稳定。这种平衡的破坏会导致诸如全身各器官纤维化等病理过程。对ECM蛋白(如胶原蛋白)进行翻译后交联修饰会改变ECM的结构和功能。交联酶的失调以及交联成分的变化在纤维化中很常见。由于这些ECM交联途径在疾病中发挥着关键作用,因此正在探索调控交联事件的酶作为纤维化的治疗靶点。在此,我们深入综述ECM交联的分子机制、ECM交联如何导致纤维化,以及正在探索的针对纤维化中ECM交联以恢复正常组织结构和功能的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00b9/10931134/7301b06b5f4a/cells-13-00438-g001.jpg

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