Salloum-Asfar Salam, Engelke Rudolf, Mousa Hanaa, Goswami Neha, Thompson I Richard, Palangi Freshteh, Kamal Kamal, Al-Noubi Muna N, Schmidt Frank, Abdulla Sara A, Emara Mohamed M
Neurological Disorders Research Center, Qatar Biomedical Research Institute (QBRI), Hamad Bin Khalifa University (HBKU), Education City, Qatar Foundation (QF), Doha, Qatar.
Proteomics Core, Weill Cornell Medical College-Qatar, Qatar Foundation, Doha, Qatar.
Stem Cells Int. 2021 Oct 15;2021:8274936. doi: 10.1155/2021/8274936. eCollection 2021.
Stress granules (SGs) are assemblies of selective messenger RNAs (mRNAs), translation factors, and RNA-binding proteins in small untranslated messenger ribonucleoprotein (mRNP) complexes in the cytoplasm. Evidence indicates that different types of cells have shown different mechanisms to respond to stress and the formation of SGs. In the present work, we investigated how human-induced pluripotent stem cells (hiPSCs/IMR90-1) overcome hyperosmotic stress compared to a cell line that does not harbor pluripotent characteristics (SH-SY5Y cell line). Gradient concentrations of NaCl showed a different pattern of SG formation between hiPSCs/IMR90-1 and the nonpluripotent cell line SH-SY5Y. Other pluripotent stem cell lines (hiPSCs/CRTD5 and hESCs/H9 (human embryonic stem cell line)) as well as nonpluripotent cell lines (BHK-21 and MCF-7) were used to confirm this phenomenon. Moreover, the formation of hyperosmotic SGs in hiPSCs/IMR90-1 was independent of eIF2 phosphorylation and was associated with low apoptosis levels. In addition, a comprehensive proteomics analysis was performed to identify proteins involved in regulating this specific pattern of hyperosmotic SG formation in hiPSCs/IMR90-1. We found possible implications of microtubule organization on the response to hyperosmotic stress in hiPSCs/IMR90-1. We have also unveiled a reduced expression of tubulin that may protect cells against hyperosmolarity stress while inhibiting SG formation without affecting stem cell self-renewal and pluripotency. Our observations may provide a possible cellular mechanism to better understand SG dynamics in pluripotent stem cells.
应激颗粒(SGs)是细胞质中未翻译的小信使核糖核蛋白(mRNP)复合物中选择性信使核糖核酸(mRNAs)、翻译因子和RNA结合蛋白的聚集体。有证据表明,不同类型的细胞对应激和SGs形成表现出不同的反应机制。在本研究中,我们研究了与不具有多能特性的细胞系(SH-SY5Y细胞系)相比,人诱导多能干细胞(hiPSCs/IMR90-1)如何克服高渗应激。NaCl的梯度浓度在hiPSCs/IMR90-1和非多能细胞系SH-SY5Y之间显示出不同的SG形成模式。使用其他多能干细胞系(hiPSCs/CRTD5和hESCs/H9(人胚胎干细胞系))以及非多能细胞系(BHK-21和MCF-7)来证实这一现象。此外,hiPSCs/IMR90-1中高渗SGs的形成独立于eIF2磷酸化,且与低凋亡水平相关。另外,进行了全面的蛋白质组学分析,以鉴定参与调节hiPSCs/IMR90-1中这种高渗SG形成特定模式的蛋白质。我们发现微管组织对hiPSCs/IMR90-1中高渗应激反应可能有影响。我们还揭示了微管蛋白表达的降低可能在抑制SG形成的同时保护细胞免受高渗应激,而不影响干细胞的自我更新和多能性。我们的观察结果可能为更好地理解多能干细胞中SG动态提供一种可能的细胞机制。