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血管紧张素II促进小鼠c-kit阳性心脏干细胞分化为起搏样细胞。

Angiotensin II promotes differentiation of mouse c-kit-positive cardiac stem cells into pacemaker-like cells.

作者信息

Xue Cheng, Zhang Jun, Lv Zhan, Liu Hui, Huang Congxin, Yang Jing, Wang Ten

机构信息

Department of Cardiology, The Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan 637000, P.R. China.

Department of Cardiology, Renmin Hospital of Wuhan University, Cardiovascular Research Institute, Wuhan University, Wuhan, Hubei 430060, P.R. China.

出版信息

Mol Med Rep. 2015 May;11(5):3249-58. doi: 10.3892/mmr.2015.3149. Epub 2015 Jan 7.

Abstract

Cardiac stem cells (CSCs) can differentiate into cardiac muscle‑like cells; however, it remains unknown whether CSCs may possess the ability to differentiate into pacemaker cells. The aim of the present study was to determine whether angiotensin II (Ang II) could promote the specialization of CSCs into pacemaker‑like cells. Mouse CSCs were treated with Ang II from day 3-5, after cell sorting. The differentiation potential of the cells was then analyzed by morphological analysis, flow cytometry, reverse transcription‑polymerase chain reaction, immunohistochemistry and patch clamp analysis. Treatment with Ang II resulted in an increased number of cardiac muscle‑like cells (32.7 ± 4.8% vs. 21.5 ± 4.8%; P<0.05), and inhibition of smooth muscle‑like cells (6.2 ± 7.3% vs. 20.5 ± 5.1%; P<0.05). Following treatment with Ang II, increased levels of the cardiac progenitor‑specific markers GATA4 and Nkx2.5 were observed in the cells. Furthermore, the transcript levels of pacemaker function‑related genes, including hyperpolarization‑activated cyclic nucleotide‑gated (HCN)2, HCN4, T‑box (Tbx)2 and Tbx3, were significantly upregulated. Immunofluorescence analysis confirmed the increased number of pacemaker‑like cells. The pacemaker current (If) was recorded in the cells derived from CSCs, treated with Ang II. In conclusion, treatment of CSCs with Ang II during the differentiation process modified cardiac‑specific gene expression and resulted in the enhanced formation of pacemaker‑like cells.

摘要

心脏干细胞(CSCs)可分化为心肌样细胞;然而,CSCs是否具有分化为起搏细胞的能力仍不清楚。本研究的目的是确定血管紧张素II(Ang II)是否能促进CSCs向起搏样细胞的特化。在细胞分选后的第3至5天,用Ang II处理小鼠CSCs。然后通过形态学分析、流式细胞术、逆转录-聚合酶链反应、免疫组织化学和膜片钳分析来分析细胞的分化潜能。用Ang II处理导致心肌样细胞数量增加(32.7±4.8%对21.5±4.8%;P<0.05),并抑制平滑肌样细胞(6.2±7.3%对20.5±5.1%;P<0.05)。用Ang II处理后,在细胞中观察到心脏祖细胞特异性标志物GATA4和Nkx2.5的水平升高。此外,包括超极化激活环核苷酸门控(HCN)2、HCN4、T盒(Tbx)2和Tbx3在内的起搏功能相关基因的转录水平显著上调。免疫荧光分析证实起搏样细胞数量增加。在经Ang II处理的CSCs来源的细胞中记录到起搏电流(If)。总之,在分化过程中用Ang II处理CSCs可改变心脏特异性基因表达,并导致起搏样细胞形成增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9def/4368082/35a7a75053f4/MMR-11-05-3249-g00.jpg

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