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通过直接激活gp130信号通路维持胚胎干细胞的多能性表型。

Maintenance of the pluripotential phenotype of embryonic stem cells through direct activation of gp130 signalling pathways.

作者信息

Yoshida K, Chambers I, Nichols J, Smith A, Saito M, Yasukawa K, Shoyab M, Taga T, Kishimoto T

机构信息

Institute for Molecular and Cellular Biology, Osaka University, Japan.

出版信息

Mech Dev. 1994 Feb;45(2):163-71. doi: 10.1016/0925-4773(94)90030-2.

Abstract

Propagation of the undifferentiated pluripotential phenotype of embryonic stem (ES) cells is dependent on the cytokine differentiation inhibiting activity/leukemia inhibitory factor (DIA/LIF). The DIA/LIF receptor complex is a heterodimer of DIA/LIF receptor (DIA/LIF-R) and gp130. The latter is also a component of the interleukin-6 (IL-6) receptor complex. We report that a combination of IL-6 and soluble IL-6 receptor (sIL-6R), which can induce homodimerisation of gp130 and activation of signalling processes, sustains self-renewal of pluripotential ES cells. Our findings indicate that the IL-6/sIL-6R complex acts on ES cells through gp130 alone, bypassing DIA/LIF-R, and therefore implicate gp130 as the key component in the signalling pathway responsible for stem cell renewal.

摘要

胚胎干细胞(ES细胞)未分化多能性表型的维持依赖于细胞因子分化抑制活性/白血病抑制因子(DIA/LIF)。DIA/LIF受体复合物是DIA/LIF受体(DIA/LIF-R)和gp130的异源二聚体。后者也是白细胞介素-6(IL-6)受体复合物的一个组成部分。我们报告,IL-6和可溶性IL-6受体(sIL-6R)的组合可诱导gp130同源二聚化并激活信号传导过程,从而维持多能性ES细胞的自我更新。我们的研究结果表明,IL-6/sIL-6R复合物仅通过gp130作用于ES细胞,绕过了DIA/LIF-R,因此表明gp130是负责干细胞更新的信号通路中的关键成分。

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