Subcellular distribution and profiles of prosomes (proteasomes-MCP) during differentiation of human lymphoblastic cell line

被引:6
作者
Baz, A
Henry, L
Chateau, MT
Scherrer, K
Bureau, JP
机构
[1] Univ Montpellier I, Lab Biol Cellulaire & Cytogenet Mol, Fac Med, UPRES JE 1952, F-30900 Nimes, France
[2] Univ Paris 07, Inst Jacques Monod, CNRS, F-75251 Paris, France
关键词
leukemia; CCRF-CEM; prosomes; (proteasomes; MCP); differentiation; monoclonal antibodies; PMA; flow cytometry;
D O I
10.1016/S0145-2126(97)00091-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The human lymphoblastoid leukemic cell line (CCRF-CEM) was induced to differentiate with phorbol 12-myristate 13-acetate (PMA). During differentiation, assessed by monitoring the cluster of differentiation (CD) profile, the prosome (proteasomes, multi-catalytic proteinase) distribution and composition were studied by microscopy, flow cytometry and western blot analysis. Changes in prosome subunits were monitored using 3 monoclonal antibodies anti-p23K, p29K and p31K. There were changes in the subcellular distribution of prosome antigens in PMA treated cells compared to untreated cells. The amount of cytoplasmic prosomal antigens decreased during the first three days of differentiation and the membrane antigens increased; meanwhile there was an increase of p53 and no change in actin protein levels. As mitotic cyclins are degraded by the ubiquitin pathway and therefore via the prosome, the decrease observed in differentiated cells suggests that prosomes are involved in the cell cycle and thus in cell proliferation. (C) 1997 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1061 / 1070
页数:10
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