生长激素受体作用的信号转导机制

A. Herington, P. Lobie
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引用次数: 5

摘要

我们对生长激素及其受体GHR的作用机制的理解在过去十年中取得了显著进展,并提供了一些重要的惊喜。现在很清楚,GH-GHR轴激活了许多相互关联的信号通路,并不是所有的信号通路都像最初假设的那样依赖于细胞内酪氨酸激酶JAK2。通过Src家族激酶介导的jak2非依赖性通路,以及许多生长激素信号的负调节因子和与其他生长因子受体的新兴串扰机制,提供了一系列复杂的机制,能够以细胞环境依赖的方式微调对生长激素的反应。此外,现在也很清楚GH和GHR可以转移到靶细胞的细胞核,并启动尚未明确定义的核反应。继续强调阐明这些复杂的机制对于进一步了解生长激素的各种生理和病理生理作用至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Signal Transduction Mechanisms Underlying Growth Hormone ReceptorAction
Our understanding of the mechanisms of action of GH and its receptor, the GHR, has advanced significantly in the last decade and has provided some important surprises. It is now clear that the GH-GHR axis activates a number of inter-related signalling pathways, not all of which are dependent on the intracellular tyrosine kinase, JAK2 as originally postulated. JAK2-independent pathways, mediated via the Src family kinases, together with a number of negative regulators of GH signalling and emerging cross-talk mechanisms with other growth factor receptors, provide a complex array of mechanisms that are capable of fine-tuning responses to GH in a cell context dependent manner. Additionally, it is also now clear that GH and the GHR can translocate to the nucleus of target cells and initiate, as yet not well defined, nuclear responses. Continued emphasis on elucidation of these complex mechanisms is critical to provide further insights into the diverse physiological and pathophysiological effects of GH.
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