Megakaryocyte maturation involves activation of the adaptive unfolded protein response

IF 1.3 4区 生物学 Q4 CELL BIOLOGY Genes to Cells Pub Date : 2024-08-13 DOI:10.1111/gtc.13151
Mifra Faiz, Maggie L. Kalev-Zylinska, Caitlin Dunstan-Harrison, Dean C. Singleton, Michael P. Hay, Elizabeth C. Ledgerwood
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Abstract

Endoplasmic reticulum stress triggers the unfolded protein response (UPR) to promote cell survival or apoptosis. Transient endoplasmic reticulum stress activation has been reported to trigger megakaryocyte production, and UPR activation has been reported as a feature of megakaryocytic cancers. However, the role of UPR signaling in megakaryocyte biology is not fully understood. We studied the involvement of UPR in human megakaryocytic differentiation using PMA (phorbol 12-myristate 13-acetate)-induced maturation of megakaryoblastic cell lines and thrombopoietin-induced differentiation of human peripheral blood-derived progenitors. Our results demonstrate that an adaptive UPR is a feature of megakaryocytic differentiation and that this response is not associated with ER stress-induced apoptosis. Differentiation did not alter the response to the canonical endoplasmic reticulum stressors DTT or thapsigargin. However, thapsigargin, but not DTT, inhibited differentiation, consistent with the involvement of Ca2+ signaling in megakaryocyte differentiation.

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巨核细胞的成熟涉及激活适应性未折叠蛋白反应。
内质网应激会触发未折叠蛋白反应(UPR),以促进细胞存活或凋亡。据报道,瞬时内质网应激激活可引发巨核细胞生成,而且据报道,UPR 激活是巨核细胞癌症的一个特征。然而,UPR 信号在巨核细胞生物学中的作用还不完全清楚。我们利用 PMA(光稳定剂 12-肉豆蔻酸 13-乙酸酯)诱导的巨核细胞系成熟和血栓生成素诱导的人类外周血祖细胞分化,研究了 UPR 在人类巨核细胞分化中的参与。我们的研究结果表明,适应性 UPR 是巨核细胞分化的一个特征,这种反应与 ER 应激诱导的细胞凋亡无关。分化不会改变对典型内质网应激物 DTT 或硫代硫甙的反应。然而,硫代加精(而非 DTT)抑制了分化,这与巨核细胞分化过程中 Ca2+ 信号的参与是一致的。
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来源期刊
Genes to Cells
Genes to Cells 生物-细胞生物学
CiteScore
3.40
自引率
0.00%
发文量
71
审稿时长
3 months
期刊介绍: Genes to Cells provides an international forum for the publication of papers describing important aspects of molecular and cellular biology. The journal aims to present papers that provide conceptual advance in the relevant field. Particular emphasis will be placed on work aimed at understanding the basic mechanisms underlying biological events.
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