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B细胞终末分化过程中NF-κB/Rel家族蛋白的顺序性诱导

Sequential induction of NF-kappa B/Rel family proteins during B-cell terminal differentiation.

作者信息

Liou H C, Sha W C, Scott M L, Baltimore D

机构信息

Rockfeller University, New York, New York 10021.

出版信息

Mol Cell Biol. 1994 Aug;14(8):5349-59. doi: 10.1128/mcb.14.8.5349-5359.1994.

Abstract

The NF-kappa B/Rel family of at least five transcription factor polypeptides is thought to function both as a developmental regulator in B cells and as a rapid response system in all cells. To examine this notion in more detail, we determined the protein contents of both the inducible and constitutive NF-kappa B/Rel activities in a pre-B-cell line, 70Z/3, and a mature B-cell line, WEHI 231. NF-kappa B p50/p65 is the major inducible nuclear complex after lipopolysaccharide or phorbol myristate acetate treatment of 70Z/3 cells. The constitutive and inducible complexes in WEHI 231 cells are mainly composed of p50 and Rel. The constitutive or induced activities are all sensitive to I kappa B-alpha, but this inhibitor is very short-lived in WEHI 231 cells, suggesting that the balance between synthesis and degradation of I kappa B-alpha determines whether a particular cell lineage has constitutive activity. A patterned expression of the NF-kappa B/Rel activator proteins emerges from an analysis of other B-lineage cell lines and splenic B cells: mainly p50 and p65 in pre-B (and non-B) cells, a predominance of Rel and p50 in mature B cells, and expression of p52 and RelB in plasmacytoma lines. This ordered pattern of regulators may reflect the requirement for expression of different genes during terminal B-cell differentiation because different combinations of NF-kappa B/Rel family members preferentially activate distinct kappa B sites in reporter constructs.

摘要

至少由五种转录因子多肽组成的NF-κB/Rel家族,被认为在B细胞中作为发育调节因子发挥作用,同时在所有细胞中作为快速反应系统发挥作用。为了更详细地研究这一概念,我们测定了前B细胞系70Z/3和成熟B细胞系WEHI 231中诱导型和组成型NF-κB/Rel活性的蛋白质含量。NF-κB p50/p65是脂多糖或佛波酯处理70Z/3细胞后主要的诱导型核复合物。WEHI 231细胞中的组成型和诱导型复合物主要由p50和Rel组成。组成型或诱导型活性均对IκB-α敏感,但该抑制剂在WEHI 231细胞中寿命很短,这表明IκB-α的合成与降解之间的平衡决定了特定细胞系是否具有组成型活性。通过对其他B系细胞系和脾B细胞的分析,出现了NF-κB/Rel激活蛋白的模式化表达:前B(和非B)细胞中主要是p50和p65,成熟B细胞中Rel和p50占优势,浆细胞瘤系中p52和RelB表达。这种有序的调节因子模式可能反映了终末B细胞分化过程中对不同基因表达的需求,因为NF-κB/Rel家族成员的不同组合优先激活报告构建体中不同的κB位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a60/359054/6237b41e3728/molcellb00008-0343-a.jpg

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