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血小板生成素通过其在人白血病细胞系中的特异性受体c-Mpl支持体外红系分化。

Thrombopoietin supports in vitro erythroid differentiation via its specific receptor c-Mpl in a human leukemia cell line.

作者信息

Yamada M, Komatsu N, Kirito K, Kashii Y, Tomizuka H, Okada K, Endo T, Fukumaki Y, Shinjo K, Abe K, Miura Y

机构信息

Department of Medicine, Jichi Medical School, Tochigi, Japan.

出版信息

Cell Growth Differ. 1998 Jun;9(6):487-96.

PMID:9663467
Abstract

Thrombopoietin (TPO) acts on megakaryopoiesis and erythropoiesis in vitro and in vivo. We isolated a novel subline, UT-7/GMT, from the human leukemia cell line UT-7/GM (N. Komatsu, et al., Blood, 89: 4021-4033, 1997). A small population of UT-7/GM cells positively stained for hemoglobin (Hb) after a 7-day exposure to TPO. More than 50% of TPO-treated UT-7/GMT cells positively stained for Hb. Using UT-7/GMT cells, we examined how TPO promotes hemoglobinization. TPO induced tyrosine phosphorylation of the TPO receptor but not the erythropoietin (EPO) receptor. There was no competition between TPO and EPO for binding to EPO receptor. These findings suggest that TPO has a direct effect on hemoglobinization via a specific receptor on UT-7/GMT cells. Isoelectric focusing demonstrated that TPO induced fetal and adult Hb synthesis, whereas EPO induced embryonic, fetal, and adult Hb synthesis. Thus, our data suggest that TPO has a distinct action on erythropoiesis.

摘要

血小板生成素(TPO)在体内外均作用于巨核细胞生成和红细胞生成。我们从人白血病细胞系UT-7/GM中分离出一种新的亚系UT-7/GMT(N. 小松等人,《血液》,第89卷:4021 - 4033页,1997年)。一小部分UT-7/GM细胞在暴露于TPO 7天后血红蛋白(Hb)呈阳性染色。超过50%经TPO处理的UT-7/GMT细胞Hb呈阳性染色。利用UT-7/GMT细胞,我们研究了TPO如何促进血红蛋白化。TPO诱导TPO受体的酪氨酸磷酸化,但不诱导促红细胞生成素(EPO)受体的酪氨酸磷酸化。TPO与EPO在结合EPO受体方面不存在竞争。这些发现表明,TPO通过UT-7/GMT细胞上的特定受体对血红蛋白化有直接作用。等电聚焦显示,TPO诱导胎儿型和成人型Hb合成,而EPO诱导胚胎型、胎儿型和成人型Hb合成。因此,我们的数据表明TPO在红细胞生成中具有独特作用。

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