信号通路在维持小鼠和人类胚胎干细胞多能性中的动态作用

IF 1.2 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Cellular reprogramming Pub Date : 2024-04-01 DOI:10.1089/cell.2024.0002
Anagha Oke, Sonal M Manohar
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引用次数: 0

摘要

体外培养小鼠和人类胚胎干细胞(ESC)是干细胞生物学领域的一大突破。这些模型之所以很快受到欢迎,主要是因为它们具有多能性。显而易见,小鼠和人类的干细胞因其多能性而共享典型的表型反应,如自我更新能力和效力。这些反应由保守的核心转录因子网络调控。然而,在这两个物种的 ESCs 中,这些核心多能性因子的表达和活性受明显不同的信号通路和上游转录网络调控。事实上,大量证据表明,在小鼠间充质干细胞中维持多能性的途径,在人类间充质干细胞中却能促进分化。在这篇综述中,我们讨论了与多能性和分化调控有关的典型信号通路在小鼠和人类 ESCs 中的作用。我们认为,了解这些不同的、有时是相反的机制,对干细胞生物学和再生医学领域的进步至关重要。
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Dynamic Roles of Signaling Pathways in Maintaining Pluripotency of Mouse and Human Embryonic Stem Cells.
Culturing of mouse and human embryonic stem cells (ESCs) in vitro was a major breakthrough in the field of stem cell biology. These models gained popularity very soon mainly due to their pluripotency. Evidently, the ESCs of mouse and human origin share typical phenotypic responses due to their pluripotent nature, such as self-renewal capacity and potency. The conserved network of core transcription factors regulates these responses. However, significantly different signaling pathways and upstream transcriptional networks regulate expression and activity of these core pluripotency factors in ESCs of both the species. In fact, ample evidence shows that a pathway, which maintains pluripotency in mouse ESCs, promotes differentiation in human ESCs. In this review, we discuss the role of canonical signaling pathways implicated in regulation of pluripotency and differentiation particularly in mouse and human ESCs. We believe that understanding these distinct and at times-opposite mechanisms-is critical for the progress in the field of stem cell biology and regenerative medicine.
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来源期刊
Cellular reprogramming
Cellular reprogramming CELL & TISSUE ENGINEERING-BIOTECHNOLOGY & APPLIED MICROBIOLOGY
CiteScore
2.50
自引率
6.20%
发文量
37
审稿时长
3 months
期刊介绍: Cellular Reprogramming is the premier journal dedicated to providing new insights on the etiology, development, and potential treatment of various diseases through reprogramming cellular mechanisms. The Journal delivers information on cutting-edge techniques and the latest high-quality research and discoveries that are transforming biomedical research. Cellular Reprogramming coverage includes: Somatic cell nuclear transfer and reprogramming in early embryos Embryonic stem cells Nuclear transfer stem cells (stem cells derived from nuclear transfer embryos) Generation of induced pluripotent stem (iPS) cells and/or potential for cell-based therapies Epigenetics Adult stem cells and pluripotency.
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