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胶原蛋白XII在皮肤稳态与修复中的作用。

Role of collagen XII in skin homeostasis and repair.

作者信息

Schönborn Katrin, Willenborg Sebastian, Schulz Jan-Niklas, Imhof Thomas, Eming Sabine A, Quondamatteo Fabio, Brinckmann Jürgen, Niehoff Anja, Paulsson Mats, Koch Manuel, Eckes Beate, Krieg Thomas

机构信息

Translational Matrix Biology, University of Cologne, Medical Faculty, Cologne, Germany.

Department of Dermatology, University Hospital Cologne, Cologne, Germany.

出版信息

Matrix Biol. 2020 Dec;94:57-76. doi: 10.1016/j.matbio.2020.08.002. Epub 2020 Sep 2.

Abstract

Skin integrity and function depends to a large extent on the composition of the extracellular matrix, which regulates tissue organization. Collagen XII is a homotrimer with short collagenous domains that confer binding to the surface of collagen I-containing fibrils and extended flexible arms, which bind to non-collagenous matrix components. Thereby, collagen XII helps to maintain collagen suprastructure and to absorb stress. Mutant or absent collagen XII leads to reduced muscle and bone strength and lax skin, whereas increased collagen XII amounts are observed in tumor stroma, scarring and fibrosis. This study aimed at uncovering in vivo mechanisms by which collagen XII may achieve these contrasting outcomes. We analyzed skin as a model tissue that contains abundant fibrils, composed of collagen I, III and V with collagen XII decorating their surface, and which is subject to mechanical stress. The impact of different collagen XII levels was investigated in collagen XII-deficient (Col12-KO) mice and in mice with collagen XII overexpression in the dermis (Col12-OE). Unchallenged skin of these mice was histologically inconspicuous, but at the ultrastructural level revealed distinct aberrations in collagen network suprastructure. Repair of excisional wounds deviated from controls in both models by delayed healing kinetics, which was, however, caused by completely different mechanisms in the two mouse lines. The disorganized matrix in Col12-KO wounds failed to properly sequester TGFβ, resulting in elevated numbers of myofibroblasts. These are, however, unable to contract and remodel the collagen XII-deficient matrix. Excess of collagen XII, in contrast, promotes persistence of M1-like macrophages in the wound bed, thereby stalling the wounds in an early inflammatory stage of the repair process and delaying healing. Taken together, we demonstrate that collagen XII is a key component that assists in orchestrating proper skin matrix structure, controls growth factor availability and regulates cellular composition and function. Together, these functions are pivotal for re-establishing homeostasis after injury.

摘要

皮肤的完整性和功能在很大程度上取决于细胞外基质的组成,细胞外基质调节组织的组织结构。胶原蛋白XII是一种同三聚体,具有短的胶原结构域,可与含I型胶原蛋白的纤维表面结合,并具有延伸的柔性臂,可与非胶原蛋白基质成分结合。因此,胶原蛋白XII有助于维持胶原蛋白超结构并吸收应力。胶原蛋白XII突变或缺失会导致肌肉和骨骼强度降低以及皮肤松弛,而在肿瘤基质、瘢痕形成和纤维化中观察到胶原蛋白XII含量增加。本研究旨在揭示胶原蛋白XII可能实现这些相反结果的体内机制。我们将皮肤作为模型组织进行分析,皮肤含有丰富的纤维,由I型、III型和V型胶原蛋白组成,胶原蛋白XII装饰在其表面,并且受到机械应力作用。在胶原蛋白XII缺陷(Col12-KO)小鼠和真皮中胶原蛋白XII过表达的小鼠(Col12-OE)中研究了不同胶原蛋白XII水平的影响。这些小鼠未受刺激的皮肤在组织学上不明显,但在超微结构水平上显示胶原蛋白网络超结构存在明显异常。在两个模型中,切除伤口的修复均与对照组不同,愈合动力学延迟,然而,这是由两种小鼠品系中完全不同的机制引起的。Col12-KO伤口中无序的基质无法正确隔离TGFβ,导致肌成纤维细胞数量增加。然而,这些细胞无法收缩和重塑缺乏胶原蛋白XII的基质。相比之下,过量的胶原蛋白XII会促进伤口床中M1样巨噬细胞的持续存在,从而使伤口停滞在修复过程的早期炎症阶段并延迟愈合。综上所述,我们证明胶原蛋白XII是协助协调适当皮肤基质结构、控制生长因子可用性以及调节细胞组成和功能的关键成分。这些功能共同对于损伤后重新建立内环境稳态至关重要。

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