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催乳素(PRL)依赖性锌指蛋白编码基因Gfi-1在Nb2淋巴瘤细胞中的表达:自主亚系中的组成型表达

Prolactin (PRL)-dependent expression of a zinc finger protein-encoding gene, Gfi-1, in Nb2 lymphoma cells: constitutive expression in autonomous sublines.

作者信息

Gilks C B, Porter S D, Barker C, Tsichlis P N, Gout P W

机构信息

Department of Pathology, University of British Columbia, Vancouver, Canada.

出版信息

Endocrinology. 1995 Apr;136(4):1805-8. doi: 10.1210/endo.136.4.7895694.

Abstract

The proliferation of cultured rat Nb2 lymphoma cells is dependent on prolactin (PRL) acting as the principal growth factor. Previously, PRL-independent Nb2 sublines were obtained by PRL starvation of the parent line and cloning of surviving cells. Development of PRL independence was in some cases found to be associated with a reciprocal translocation involving chromosome 14 at breakpoint 14p22. In the present study, a novel, 14p22 zinc finger protein-encoding gene, Gfi-1, has been examined for a role in Nb2 cell proliferation. PRL-dependent Nb2 cells expressed the gene during active growth; in comparison, in stationary, early G1-arrested cells obtained by an 18 hr lactogen starvation, Gfi-1 gene expression was markedly decreased. Addition of PRL to such stationary cells led to induction of Gfi-1 gene expression within a few hr with a maximum in late G1. Actively growing cells from 5 different PRL-independent Nb2 sublines, cultured in chemically defined, mitogen-free medium, expressed the gene constitutively. In two sublines, carrying the 14p22 rearrangement, the gene was markedly overexpressed. The results suggest the Gfi-1 gene product has a regulatory role in Nb2 cell mitogenesis and that unscheduled activation could contribute to loss of PRL dependency.

摘要

培养的大鼠Nb2淋巴瘤细胞的增殖依赖于催乳素(PRL)作为主要生长因子。以前,通过对亲代细胞系进行PRL饥饿处理并克隆存活细胞获得了不依赖PRL的Nb2亚系。在某些情况下,发现PRL独立性的发展与涉及14号染色体14p22断点的相互易位有关。在本研究中,已检测了一种新的、编码14p22锌指蛋白的基因Gfi-1在Nb2细胞增殖中的作用。依赖PRL的Nb2细胞在活跃生长期间表达该基因;相比之下,在通过18小时催乳素饥饿获得的静止、早期G1期停滞细胞中,Gfi-1基因表达明显降低。向此类静止细胞中添加PRL会在数小时内导致Gfi-1基因表达的诱导,在G1晚期达到最大值。在化学限定的无丝裂原培养基中培养的来自5个不同的不依赖PRL的Nb2亚系的活跃生长细胞持续表达该基因。在两个携带14p22重排的亚系中,该基因明显过表达。结果表明,Gfi-1基因产物在Nb2细胞有丝分裂中具有调节作用,且异常激活可能导致PRL依赖性丧失。

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