The relationship between endoplasmic reticulum stress and apoptosis in the process of adipose-derived stromal cells differentiating into astrocytes.

IF 3.3 3区 生物学 Q3 CELL BIOLOGY Cell Adhesion & Migration Pub Date : 2024-12-01 Epub Date: 2024-11-19 DOI:10.1080/19336918.2024.2430561
Pingshu Zhang, Wen Li, Ya Ou, Qi Yan, Qi Wu, Xiaodong Yuan
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引用次数: 0

Abstract

The potential of adult adipose-derived stromal cells (ADSCs) to differentiate into astrocytes holds promise for future cell transplantation therapies. However, the growth of differentiated astrocytes is unstable, and their survival rate is low. Endoplasmic reticulum (ER) pathway mediated apoptosis is one of the causes of cell death, but whether there is ER stress response in the differentiation of ADSCs into astrocytes is still unclear. In this study, the expression of protein factors related to endoplasmic reticulum stress (ERS) and apoptosis, including GRP78, ATF6, PERK, CHOP, Caspase12, and Caspase3, was detected in cells. It was found that the expression of ERS pro-survival factors was highest in the ADSCs group and decreased with prolonged induction time. Conversely, the expression levels of pro-apoptotic factors increased with the extension of induction time. Thus, ERS occurs during the differentiation of ADSCs into astrocytes, and ERS can mediate apoptosis of ADSC-derived astrocytes.

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脂肪基质细胞分化为星形胶质细胞过程中内质网应激与细胞凋亡之间的关系
成体脂肪源性基质细胞(ADSCs)具有分化成星形胶质细胞的潜力,这为未来的细胞移植疗法带来了希望。然而,分化后的星形胶质细胞生长不稳定,存活率低。内质网(ER)通路介导的细胞凋亡是细胞死亡的原因之一,但 ADSCs 分化为星形胶质细胞的过程中是否存在 ER 应激反应仍不清楚。本研究检测了细胞中与内质网应激(ERS)和细胞凋亡相关的蛋白因子的表达,包括GRP78、ATF6、PERK、CHOP、Caspase12和Caspase3。结果发现,ADSCs 组中 ERS 促生存因子的表达量最高,并随着诱导时间的延长而降低。相反,促凋亡因子的表达水平随着诱导时间的延长而增加。因此,ERS发生在ADSCs向星形胶质细胞分化的过程中,并且ERS可以介导ADSCs衍生的星形胶质细胞的凋亡。
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来源期刊
CiteScore
6.40
自引率
0.00%
发文量
7
审稿时长
53 weeks
期刊介绍: Cell Adhesion & Migration is a multi-disciplinary, peer reviewed open access journal that focuses on the biological or pathological implications of cell-cell and cell-microenvironment interactions. The main focus of this journal is fundamental science. The journal strives to serve a broad readership by regularly publishing review articles covering specific disciplines within the field, and by publishing focused issues that provide an overview on specific topics of interest within the field. Cell Adhesion & Migration publishes relevant and timely original research, as well as authoritative overviews, commentaries, and perspectives, providing context for the work presented in Cell Adhesion & Migration and for key results published elsewhere. Original research papers may cover all topics important in the field of cell-cell and cell-matrix interactions. Cell Adhesion & Migration also publishes articles related to cell biomechanics, biomaterial, and development of related imaging technologies.
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