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The Role of the Leukemia Inhibitory Factor (LIF) — Pathway in Derivation and Maintenance of Murine Pluripotent Stem Cells

机译:白血病抑制因子(LIF)的作用—途径在小鼠多能干细胞的衍生和维持中

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摘要

Developmental biology, regenerative medicine and cancer biology are more and more interested in understanding the molecular mechanisms controlling pluripotency and self-renewal in stem cells. Pluripotency is maintained by a synergistic interplay between extrinsic stimuli and intrinsic circuitries, which allow sustainment of the undifferentiated and self-renewing state. Nevertheless, even though a lot of efforts have been made in the past years, the precise mechanisms regulating these processes remain unclear. One of the key extrinsic factors is leukemia inhibitory factor (LIF) that is largely used for the cultivation and derivation of mouse embryonic and induced pluripotent stem cells. LIF acts through the LIFR/gp130 receptor and activates STAT3, an important regulator of mouse embryonic stem cell self-renewal. STAT3 is known to inhibit differentiation into both mesoderm and endoderm lineages by preventing the activation of lineage-specific differentiation programs. However, LIF activates also parallel circuitries like the PI3K-pathway and the MEK/ERK-pathway, but its mechanisms of action remain to be better elucidated. This review article aims at summarizing the actual knowledge on the importance of LIF in the maintenance of pluripotency and self-renewal in embryonic and induced pluripotent stem cells.
机译:发育生物学,再生医学和癌症生物学对理解控制干细胞多能性和自我更新的分子机制越来越感兴趣。多能性通过外在刺激与内在回路之间的协同相互作用来维持,从而维持未分化和自我更新的状态。然而,尽管在过去的几年中已经做出了很多努力,但是调节这些过程的确切机制仍然不清楚。关键的外在因素之一是白血病抑制因子(LIF),该因子主要用于小鼠胚胎和诱导多能干细胞的培养和衍生。 LIF通过LIFR / gp130受体起作用并激活STAT3,STAT3是小鼠胚胎干细胞自我更新的重要调节剂。已知STAT3通过阻止谱系特异性分化程序的激活而抑制分化为中胚层和内胚层谱系。但是,LIF也会激活并行电路,例如PI3K通路和MEK / ERK通路,但其作用机理仍有待进一步阐明。这篇综述文章旨在总结有关LIF在维持胚胎干细胞和诱导性多能干细胞的多能性和自我更新中的重要性的实际知识。

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