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TRIB3 在巨核细胞生成中的调节作用的证据。

Evidence for a role of TRIB3 in the regulation of megakaryocytopoiesis.

机构信息

School of Health Sciences, Cardiff Metropolitan University, Cardiff, UK.

Estonian Biocentre, Tartu, Estonia.

出版信息

Sci Rep. 2017 Jul 27;7(1):6684. doi: 10.1038/s41598-017-07096-w.

Abstract

Megakaryocytopoiesis is a complex differentiation process driven by the hormone thrombopoietin by which haematopoietic progenitor cells give rise to megakaryocytes, the giant bone marrow cells that in turn break down to form blood platelets. The Tribbles Pseudokinase 3 gene (TRIB3) encodes a pleiotropic protein increasingly implicated in the regulation of cellular differentiation programmes. Previous studies have hinted that TRIB3 could be also involved in megakaryocytopoiesis but its role in this process has so far not been investigated. Using cellular model systems of haematopoietic lineage differentiation here we demonstrate that TRIB3 is a negative modulator of megakaryocytopoiesis. We found that in primary cultures derived from human haematopoietic progenitor cells, thrombopoietin-induced megakaryocytic differentiation led to a time and dose-dependent decrease in TRIB3 mRNA levels. In the haematopoietic cell line UT7/mpl, silencing of TRIB3 increased basal and thrombopoietin-stimulated megakaryocyte antigen expression, as well as basal levels of ERK1/2 phosphorylation. In primary haematopoietic cell cultures, silencing of TRIB3 facilitated megakaryocyte differentiation. In contrast, over-expression of TRIB3 in these cells inhibited the differentiation process. The in-vitro identification of TRIB3 as a negative regulator of megakaryocytopoiesis suggests that in-vivo this gene could be important for the regulation of platelet production.

摘要

巨核细胞生成是一个由激素血小板生成素驱动的复杂分化过程,造血祖细胞由此生成巨核细胞,即随后分解形成血小板的巨大骨髓细胞。Tribbles 假激酶 3 基因(TRIB3)编码一种多功能蛋白,越来越多地参与细胞分化程序的调控。先前的研究表明,TRIB3 也可能参与巨核细胞生成,但迄今为止尚未研究其在该过程中的作用。在这里,我们使用造血谱系分化的细胞模型系统证明,TRIB3 是巨核细胞生成的负调节剂。我们发现,在源自人类造血祖细胞的原代培养物中,血小板生成素诱导的巨核细胞分化导致 TRIB3 mRNA 水平随时间和剂量依赖性下降。在造血细胞系 UT7/mpl 中,沉默 TRIB3 增加了基础和血小板生成素刺激的巨核细胞抗原表达,以及 ERK1/2 磷酸化的基础水平。在原代造血细胞培养物中,沉默 TRIB3 促进了巨核细胞分化。相比之下,在这些细胞中过表达 TRIB3 抑制了分化过程。TRIB3 作为巨核细胞生成的负调节剂的体外鉴定表明,在体内,该基因可能对血小板生成的调节很重要。

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