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人髓样细胞体外分化过程中白细胞介素-2受体γ链表达的差异调节

Differential regulation of the expression of interleukin-2 receptor gamma-chain during the in vitro differentiation of human myeloid cells.

作者信息

Morrone G, Bond H M, Cuomo C, Agosti V, Petrella A, Pagnano A M, Della Corte A, Marasco O, Venuta S

机构信息

Department of Experimental and Clinical Medicine, Faculty of Medicine, Catanzaro, Italy.

出版信息

Biochem J. 1995 Jun 15;308 ( Pt 3)(Pt 3):909-14. doi: 10.1042/bj3080909.

DOI:10.1042/bj3080909
PMID:8948450
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1136810/
Abstract

The common gamma-chain (gamma c) is a shared component of cell-surface receptors for the interleukins- 2, -4 and -7, and possibly others. We studied its expression in cells and cell lines of myeloid origin and found ubiquitous presence of gamma c mRNA in all cells examined. Differential regulation of gamma c expression was observed in myeloid cell lines induced to differentiate in vitro. In K-562 erythromyeloid cells, a sharp rise in the levels of gamma c mRNA and protein accompanied megakaryocytic, but not erythroid, differentiation. Surface binding of interleukin-2, as well as the transcripts for cognate receptor chains, were scarcely detectable in K-562 cells, whereas a significant increase in the binding of granulocyte-macrophage colony-stimulating factor specifically occurred during their megakaryocytic maturation. Our data indicate that expression of gamma c is a common feature of human myeloid cells, and suggest that its expression may be a requirement for human myelopoiesis.

摘要

共同γ链(γc)是白细胞介素-2、-4和-7以及可能其他细胞表面受体的共享成分。我们研究了其在髓系来源的细胞和细胞系中的表达,发现在所有检测的细胞中均普遍存在γc mRNA。在体外诱导分化的髓系细胞系中观察到γc表达的差异调节。在K-562红髓系细胞中,γc mRNA和蛋白质水平的急剧上升伴随着巨核细胞而非红细胞的分化。在K-562细胞中几乎检测不到白细胞介素-2的表面结合以及同源受体链的转录本,而在其巨核细胞成熟过程中,粒细胞-巨噬细胞集落刺激因子的结合显著增加。我们的数据表明γc的表达是人类髓系细胞的共同特征,并表明其表达可能是人类髓系造血的必要条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2191/1136810/3aea34331ae6/biochemj00061-0212-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2191/1136810/ce9985ceb71a/biochemj00061-0210-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2191/1136810/c45cefefcd91/biochemj00061-0211-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2191/1136810/98c1af431fc4/biochemj00061-0211-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2191/1136810/3aea34331ae6/biochemj00061-0212-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2191/1136810/ce9985ceb71a/biochemj00061-0210-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2191/1136810/c45cefefcd91/biochemj00061-0211-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2191/1136810/98c1af431fc4/biochemj00061-0211-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2191/1136810/3aea34331ae6/biochemj00061-0212-a.jpg

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