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衰减的细胞周期分裂蛋白 2 和升高的 Polo 样激酶 1 的有丝分裂作用特征在于外周动脉疾病中的成肌细胞融合缺陷。

Attenuated cell-cycle division protein 2 and elevated mitotic roles of polo-like kinase 1 characterize deficient myoblast fusion in peripheral arterial disease.

机构信息

University of Pittsburgh Medical Center Department of Surgery, Division of Vascular Surgery, USA.

University of Pittsburgh Medical Center Department of Surgery, Division of Vascular Surgery, USA; Department of Cardiology, Cardiovascular Institute, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, China.

出版信息

Biochem Biophys Res Commun. 2022 Jun 18;609:163-168. doi: 10.1016/j.bbrc.2022.03.161. Epub 2022 Apr 3.

Abstract

INTRODUCTION

We propose that MuSC-derived myoblasts in PAD have transcriptomic differences that can highlight underlying causes of ischemia-induced myopathy.

METHODS

Differentiation capacity among perfused and ischemic human myoblasts was compared. Following next generation sequencing of mRNA, Ingenuity Pathway Analysis (IPA) was performed for canonical pathway enrichment. Live cell imaging and immunofluorescence were performed to determine myocyte fusion index and protein expression based on insights from IPA, specifically concerning cell cycle regulators including cell-division cycle protein 2 (CDC2) and polo-like kinase 1 (PLK1).

RESULTS

Ischemic myoblasts formed attenuated myotubes indicative of reduced fusion. Additionally, myoblasts from ischemic segments showed significant differences in canonical pathways associated with PLK1 (upregulated) and G2/M DNA damage checkpoint regulation (downregulated). PLK1 inhibition with BI2536 did not affect cell viability in any group over 24 h but deterred fusion more significantly in PAD myoblasts. Furthermore, PLK1 inhibition reduced the expression of checkpoint protein CDC2 in perfused but not ischemic cells.

CONCLUSION

Differentiating myoblasts derived from ischemic muscle have significant differences in gene expression including those essential to DNA-damage checkpoint regulation and cell cycle progress. DNA-damage checkpoint dysregulation may contribute to myopathy in PAD.

摘要

简介

我们提出,PAD 中的 MuSC 衍生的成肌细胞具有转录组差异,这些差异可以突出缺血性肌病的潜在原因。

方法

比较了灌注和缺血性人成肌细胞的分化能力。在对 mRNA 进行下一代测序后,进行了 IPA 进行了经典途径富集分析。基于 IPA 的见解(特别是关于细胞周期调节剂的见解,包括细胞分裂周期蛋白 2(CDC2)和 Polo 样激酶 1(PLK1))进行了活细胞成像和免疫荧光检测,以确定肌细胞融合指数和蛋白质表达。

结果

缺血性成肌细胞形成了减弱的肌管,表明融合减少。此外,来自缺血节段的成肌细胞在与 PLK1(上调)和 G2/M DNA 损伤检查点调节(下调)相关的经典途径中存在显着差异。在 24 小时内,BI2536 对 PLK1 的抑制对任何组的细胞活力均无影响,但在 PAD 成肌细胞中融合的抑制作用更为明显。此外,PLK1 抑制降低了灌注但不是缺血细胞中检查点蛋白 CDC2 的表达。

结论

源自缺血性肌肉的分化成肌细胞在基因表达方面存在显着差异,包括对 DNA 损伤检查点调节和细胞周期进展至关重要的基因。DNA 损伤检查点失调可能导致 PAD 中的肌病。

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