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TMPRSS11a 是一种新型的与年龄相关的、组织特异性的迁移和伤口愈合调节因子。

TMPRSS11a is a novel age-altered, tissue specific regulator of migration and wound healing.

机构信息

Program of Cellular and Molecular Biology, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Santiago, Chile.

Center for Bioinformatics, Simulation and Modeling (CBSM), Faculty of Engineering, Universidad de Talca, Talca, Chile.

出版信息

FASEB J. 2021 May;35(5):e21597. doi: 10.1096/fj.202002253RRR.

DOI:10.1096/fj.202002253RRR
PMID:33908663
Abstract

Aging is a gradual biological process characterized by a decrease in cellular and organism functions. Aging-related processes involve changes in the expression and activity of several proteins. Here, we identified the transmembrane protease serine 11a (TMPRSS11a) as a new age-specific protein that plays an important role in skin wound healing. TMPRSS11a levels increased with age in rodent and human skin and gingival samples. Strikingly, overexpression of TMPRSS11a decreased cell migration and spreading, and inducing cellular senescence. Mass spectrometry, bioinformatics, and functional analyses revealed that TMPRSS11a interacts with integrin β through an RGD sequence contained within the C-terminal domain and that this motif was relevant for cell migration. Moreover, TMPRSS11a was associated with cellular senescence, as shown by overexpression and downregulation experiments. In agreement with tissue-specific expression of TMPRSS11a, shRNA-mediated downregulation of this protein improved wound healing in the skin, but not in the skeletal muscle of old mice, where TMPRSS11a is undetectable. Collectively, these findings indicate that TMPRSS11a is a tissue-specific factor relevant for wound healing, which becomes elevated with aging, promoting cellular senescence and inhibiting cell migration and skin repair.

摘要

衰老是一个渐进的生物学过程,其特征是细胞和机体功能下降。与衰老相关的过程涉及几种蛋白质的表达和活性变化。在这里,我们鉴定出跨膜丝氨酸蛋白酶 11a(TMPRSS11a)是一种新的年龄特异性蛋白,在皮肤伤口愈合中发挥重要作用。TMPRSS11a 的水平在啮齿动物和人类皮肤和牙龈样本中随年龄增长而增加。引人注目的是,TMPRSS11a 的过表达会降低细胞迁移和扩散,并诱导细胞衰老。质谱、生物信息学和功能分析表明,TMPRSS11a 通过包含在 C 末端结构域内的 RGD 序列与整合素 β 相互作用,并且该基序与细胞迁移有关。此外,TMPRSS11a 与细胞衰老有关,如过表达和下调实验所示。与 TMPRSS11a 的组织特异性表达一致,shRNA 介导的这种蛋白下调可改善老年小鼠皮肤而非骨骼肌中的伤口愈合,因为在这些组织中 TMPRSS11a 无法检测到。总的来说,这些发现表明 TMPRSS11a 是一种与伤口愈合相关的组织特异性因子,它随着年龄的增长而升高,促进细胞衰老并抑制细胞迁移和皮肤修复。

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