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指导红细胞生成的信号通路。

Signaling networks guiding erythropoiesis.

机构信息

Translational Research Institute.

Dermatology Institute, Academic Health System, Hamad Medical Corporation.

出版信息

Curr Opin Hematol. 2024 May 1;31(3):89-95. doi: 10.1097/MOH.0000000000000808. Epub 2024 Feb 7.

Abstract

PURPOSE OF REVIEW

Cytokine-mediated signaling pathways, including JAK/STAT, PI3K/AKT, and Ras/MAPK pathways, play an important role in the process of erythropoiesis. These pathways are involved in the survival, proliferation, and differentiation function of erythropoiesis.

RECENT FINDINGS

The JAK/STAT pathway controls erythroid progenitor differentiation, proliferation, and survival. The PI3K/AKT signaling cascade facilitates erythroid progenitor survival, proliferation, and final differentiation. During erythroid maturation, MAPK, triggered by EPO, suppresses myeloid genes, while PI3K is essential for differentiation. Pro-inflammatory cytokines activate signaling pathways that can alter erythropoiesis like EPOR-triggered signaling, including survival, differentiation, and proliferation.

SUMMARY

A comprehensive understanding of signaling networks is crucial for the formulation of treatment approaches for hematologic disorders. Further investigation is required to fully understand the mechanisms and interactions of these signaling pathways in erythropoiesis.

摘要

目的综述

细胞因子介导的信号通路,包括 JAK/STAT、PI3K/AKT 和 Ras/MAPK 通路,在红细胞生成过程中发挥重要作用。这些通路参与红细胞生成的存活、增殖和分化功能。

最新发现

JAK/STAT 通路控制红系祖细胞的分化、增殖和存活。PI3K/AKT 信号级联促进红系祖细胞的存活、增殖和最终分化。在红细胞成熟过程中,EPO 触发的 MAPK 抑制髓系基因,而 PI3K 对分化是必需的。促炎细胞因子激活信号通路,可以改变像 EPOR 触发的信号一样的红细胞生成,包括存活、分化和增殖。

总结

全面了解信号网络对于制定血液系统疾病的治疗方法至关重要。需要进一步研究以充分了解这些信号通路在红细胞生成中的机制和相互作用。

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