COL12A1 rs970547 Polymorphism Predisposes Anterior Cruciate Ligament Injury by Inducing ER Stress and Impairing Fibroblast Function.

IF 3.2 3区 生物学 Q3 MATERIALS SCIENCE, BIOMATERIALS
Wenchuan Zhao, Hong Chen, Junwei Wang, Yixin Li, Rui Chen, Jingyi Zhou
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引用次数: 0

Abstract

COL12A1 SNPs are linked to ACL injury risk, but functional effects are unknown. We examined COL12A1 rs970547 genotype distribution in Chinese male ACL injury patients versus controls, and its impact on collagen homeostasis and fibroblast function. ACL-derived fibroblasts with rs970547(A/A) or (A/G) were obtained from patients and controls. Collagen synthesis, COL12A1 protein stability, and ER stress were assessed. The (A/A) genotype was over-represented in ACL patients. It reduced COL12A1 protein levels via destabilization, while increasing total collagen synthesis. This was associated with ER stress induction. Inhibiting ER stress rescued the functional phenotype of (A/A) fibroblasts. COL12A1 rs970547(A/A) disrupts collagen regulation and triggers ER stress, functionally impairing ACL fibroblasts and potentially elevating ACL injury risk.

COL12A1 rs970547多态性通过诱导内质网应激和损害成纤维细胞功能而易导致前交叉韧带损伤。
COL12A1 snp与ACL损伤风险有关,但功能影响尚不清楚。我们检测了COL12A1 rs970547基因型在中国男性前交叉韧带损伤患者和对照组中的分布,及其对胶原稳态和成纤维细胞功能的影响。从患者和对照组中获得含有rs970547(A/A)或(A/G)的acl源性成纤维细胞。评估胶原合成、COL12A1蛋白稳定性和内质网应激。(A/A)基因型在ACL患者中被过度代表。它通过不稳定降低COL12A1蛋白水平,同时增加总胶原合成。这与内质网应激诱导有关。抑制内质网应激恢复了(A/A)成纤维细胞的功能表型。COL12A1 rs970547(A/A)破坏胶原蛋白调节,引发内质网应激,功能损害前交叉韧带成纤维细胞,并可能增加前交叉韧带损伤的风险。
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
Advanced biology
Advanced biology Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
6.60
自引率
0.00%
发文量
130
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