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低剂量促红细胞生成素可激活大鼠血管平滑肌细胞中的丝裂原活化蛋白激酶,但不激活JAK2-STAT5。

Low doses of EPO activate MAP kinases but not JAK2-STAT5 in rat vascular smooth muscle cells.

作者信息

Ammarguellat F, Llovera M, Kelly P A, Goffin V

机构信息

INSERM Unit 344, Molecular Endocrinology, Faculté de Médecine Necker, 156 rue de Vaugirard, Paris Cedex 15, 75730, France.

出版信息

Biochem Biophys Res Commun. 2001 Jun 22;284(4):1031-8. doi: 10.1006/bbrc.2001.5085.

Abstract

Previous reports have shown a direct effect of erythropoietin (Epo) on vascular smooth muscle cells (VSMCs). Our aim was to assess expression of the Epo receptor (EpoR) on VSMCs and to study the activation of two major signaling cascades activated by Epo, namely JAK2/STAT5 and MAPK pathways. All experiments were performed in parallel using the Epo-responsive UT7 cell line. From semiquantitative RT-PCR experiments, VSMCs were estimated to express approximately 30-fold less EpoR mRNA than UT7 cells. Epo-induced phosphorylation of proteins involved in the EpoR/JAK2/STAT5 cascade could not be detected in VSMCs, even using pharmacological doses of Epo (250 IU/ml). In contrast, a strong activation of MAP kinase pathway was detected with as low as 10 IU/ml Epo. We suggest that MAPK activation reflects a physiologically relevant effect of Epo on VSMCs that may be correlated to cell proliferation.

摘要

先前的报告显示,促红细胞生成素(Epo)对血管平滑肌细胞(VSMC)有直接作用。我们的目的是评估VSMC上促红细胞生成素受体(EpoR)的表达,并研究Epo激活的两个主要信号级联反应,即JAK2/STAT5和MAPK途径。所有实验均使用对Epo有反应的UT7细胞系并行进行。通过半定量RT-PCR实验估计,VSMC表达的EpoR mRNA比UT7细胞少约30倍。即使使用药理剂量的Epo(250 IU/ml),也无法在VSMC中检测到Epo诱导的参与EpoR/JAK2/STAT5级联反应的蛋白质磷酸化。相反,低至10 IU/ml的Epo就能检测到MAP激酶途径的强烈激活。我们认为,MAPK激活反映了Epo对VSMC的生理相关作用,这可能与细胞增殖有关。

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