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Tent5a 通过维持肌生成素表达来调节青少年特发性脊柱侧凸中的肌纤维形成。

Tent5a modulates muscle fiber formation in adolescent idiopathic scoliosis via maintenance of myogenin expression.

机构信息

Department of Orthopedic Surgery and Orthopedic Research Institute, West China Hospital, Sichuan University, Chengdu, China.

Department of Orthopedics, Zhongnan Hospital, Wuhan University, Wuhan, China.

出版信息

Cell Prolif. 2022 Mar;55(3):e13183. doi: 10.1111/cpr.13183. Epub 2022 Feb 9.

Abstract

OBJECTIVE

Paravertebral muscle asymmetry may be involved in the pathogenesis of adolescent idiopathic scoliosis (AIS), and the Tent5a protein was recently identified as a novel active noncanonical poly(A) polymerase. We, therefore, explored the function of the AIS susceptibility gene Tent5a in myoblasts.

MATERIALS AND METHODS

RNA-seq of AIS paravertebral muscle was performed, and the molecular differences in paravertebral muscle were investigated. Twenty-four AIS susceptibility genes were screened, and differential expression of Tent5a in paravertebral muscles was confirmed with qPCR and Western blot. After the knockdown of Tent5a, the functional effects of Tent5a on C2C12 cell proliferation, migration, and apoptosis were detected by Cell Counting Kit-8 assay, wound-healing assay, and TUNEL assay, respectively. Myogenic differentiation markers were tested with immunofluorescence and qPCR in vitro, and muscle fiber formation was compared in vivo.

RESULTS

The AIS susceptibility gene Tent5a was differentially expressed in AIS paravertebral muscles. Tent5a knockdown inhibited the proliferation and migration of C2C12 cells and inhibited the maturation of type I muscle fibers in vitro and in vivo. Mechanistically, the expression of myogenin was decreased along with the suppression of Tent5a.

CONCLUSIONS

Tent5a plays an important role in the proliferation and migration of myoblasts, and it regulates muscle fiber maturation by maintaining the stability of myogenin. Tent5a may be involved in the pathogenesis of AIS by regulating the formation of muscle fiber type I.

摘要

目的

椎旁肌不对称可能与青少年特发性脊柱侧凸(AIS)的发病机制有关,最近发现 Tent5a 蛋白是一种新型的活跃非典型多(A)聚合酶。因此,我们探讨了 AIS 易感基因 Tent5a 在成肌细胞中的功能。

材料与方法

对 AIS 椎旁肌进行 RNA-seq,研究椎旁肌的分子差异。筛选 24 个 AIS 易感基因,并用 qPCR 和 Western blot 验证 Tent5a 在椎旁肌中的差异表达。敲低 Tent5a 后,通过细胞计数试剂盒-8 检测、划痕愈合试验和 TUNEL 试验分别检测 Tent5a 对 C2C12 细胞增殖、迁移和凋亡的功能影响。体外通过免疫荧光和 qPCR 检测成肌分化标志物,体内比较肌纤维形成。

结果

AIS 易感基因 Tent5a 在 AIS 椎旁肌中差异表达。敲低 Tent5a 抑制 C2C12 细胞的增殖和迁移,并抑制体外和体内 I 型肌纤维的成熟。机制上,随着 Tent5a 的抑制,肌生成素的表达降低。

结论

Tent5a 在成肌细胞的增殖和迁移中发挥重要作用,通过维持肌生成素的稳定性调节肌纤维成熟。Tent5a 可能通过调节 I 型肌纤维的形成参与 AIS 的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/571e/8891553/849b1f3cd10f/CPR-55-e13183-g005.jpg

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