奈比洛尔的新功能:刺激脂肪来源的干细胞增殖和抑制分化。

IF 1.1 Q4 CELL & TISSUE ENGINEERING
Journal of Stem Cells & Regenerative Medicine Pub Date : 2020-05-27 eCollection Date: 2020-01-01 DOI:10.46582/jsrm.1601003
Dong Lin, Joana E Ochoa, Zahra Barabadi, Andreas B Pfnur, Stephen E Braun, Reza Izadpanah, Eckhard Alt
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引用次数: 0

摘要

组织工程受到支架播种所需细胞培养扩增时间的限制。因此,一种加速干细胞增殖的简单方法可能代表着一项重大进展。本研究研究了奈比洛尔对脂肪源性干细胞(ASCs)复制能力的影响。本研究表明,在细胞分化前,与未处理的细胞相比,奈比洛尔处理的ASCs数量显著增加了51.5%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Novel function of Nebivolol: Stimulation of Adipose-derived Stem Cell Proliferation and Inhibition of Differentiation.

Tissue engineering is limited by the time of culture expansion of cells needed for scaffold seeding. Thus, a simple means of accelerated stem cell proliferation could represent a significant advance. Here, Nebivolol was investigated for its effect on the replicative capacity of adipose-derived stem cells (ASCs). This study indicates that the number of ASCs with Nebivolol treatment showed a significant population increase of 51.5% compared to untreated cells (p<0.01). Cell cycle analysis showed a significant decrease in the percentage of ASCs in G1 phase with Nebivolol treatment compared to untreated cells (p<0.01), suggesting that Nebivolol shortens the G1 phase of ASCs, resulting in a faster proliferative rate. Furthermore, our results showed that Nebivolol significantly increased colony-forming units of ASCs (p<0.01). Despite increasing ASC proliferative potential, we showed that Nebivolol has an inhibitory effect on adipogenic and osteogenic differentiation potential as indicated by significantly reduced expression of CCAAT Enhancer Binding Protein alpha (P<0.01) and lipoprotein lipase (P<0.01) and inhibited activity of alkaline phosphatase (P<0.01), respectively. Taken together, these results showed that Nebivolol accelerated ASC proliferation through shortening G1 phase, while inhibiting both adipogenic and osteogenic potentials of ASCs. These data identify a novel and simple approach to accelerate stem cell expansion in vitro before cell differentiation.

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来源期刊
CiteScore
3.40
自引率
0.00%
发文量
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审稿时长
14 weeks
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