粒细胞生成
中性粒细胞
生物
酪氨酸激酶
信号转导
个人识别码1
骨髓生成
激酶
免疫学
蛋白质酪氨酸磷酸酶
转录因子
受体酪氨酸激酶
细胞生物学
癌症研究
造血
磷酸化
丝氨酸
遗传学
干细胞
基因
作者
Hrishikesh Mehta,Seth J. Corey
标识
DOI:10.1016/j.smim.2021.101515
摘要
A considerable amount of continuous proliferation and differentiation is required to produce daily a billion new neutrophils in an adult human. Of the few cytokines and factors known to control neutrophil production, G-CSF is the guardian of granulopoiesis. G-CSF/CSF3R signaling involves the recruitment of non-receptor protein tyrosine kinases and their dependent signaling pathways of serine/threonine kinases, tyrosine phosphatases, and lipid second messengers. These pathways converge to activate the families of STAT and C/EBP transcription factors. CSF3R mutations are associated with human disorders of neutrophil production, including severe congenital neutropenia, neutrophilia, and myeloid malignancies. More than three decades after their identification, cloning, and characterization of G-CSF and G-CSF receptor, fundamental questions remain about their physiology.
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