Zebrafish embryo extract counteracts human stem cell senescence.

Federica Facchin, Silvia Canaider, Eva Bianconi, Margherita Maioli, Umberto Santoro, Sara Santaniello, Valentina Basoli, Pier Mario Biava, Carlo Ventura
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引用次数: 3

Abstract

Human adult stem cells hold promise for regenerative medicine. They are usually expanded for multiple passages in vitro to increase cell yield prior to transplantation. Unfortunately, prolonged culture leads to cell senescence, a major drawback from successful outcomes in cell therapy approaches. Here, we show that an extract from early Zebrafish embryo (ZF1) counteracted senescence progression in human adipose-derived stem cells (hASCs) along multiple culture passages (from the 5th to the 20th). Exposure to ZF1 strongly reduced the expression of senescence marker beta-galactosidase. Both stemness (NANOG, OCT4, and MYC) and anti-senescence (BMI1, and telomerase reverse transcriptase - TERT) related genes were overexpressed at specific experimental points, without recruitment of the cyclin-dependent kinase Inhibitor 2A (CDKN2A, ali-as p16). Increased telomerase activity was associatt-ed with TERT overexpression. Both osteogenic and adipogenic abilities were enhanced. In conclusion, hASCs exposure to ZF1 is a feasible tool to counteract and reverse human stem cell senescence in long-term culturing conditions.

斑马鱼胚胎提取物对抗人类干细胞衰老。
人类成体干细胞有望用于再生医学。它们通常在体外扩增多次传代,以增加移植前的细胞产量。不幸的是,长时间的培养会导致细胞衰老,这是细胞治疗方法成功的一个主要缺点。在这里,我们展示了早期斑马鱼胚胎(ZF1)的提取物在多个培养传代(从第5代到第20代)中抵消了人类脂肪源性干细胞(hASCs)的衰老进程。暴露于ZF1强烈降低了衰老标志β -半乳糖苷酶的表达。干细胞(NANOG, OCT4和MYC)和抗衰老(BMI1,端粒酶逆转录酶- TERT)相关基因在特定的实验点过表达,没有募集细胞周期蛋白依赖性激酶抑制剂2A (CDKN2A, ali-as p16)。端粒酶活性增加与TERT过表达有关。成骨和成脂能力均增强。综上所述,暴露于ZF1的hASCs是一种在长期培养条件下抵消和逆转人类干细胞衰老的可行工具。
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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