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前体(蛋白酶体)在分化过程中的变化与诱导剂的类型有关。

Prosomes (proteasomes) changes during differentiation are related to the type of inducer.

作者信息

Bureau J P, Henry L, Baz A, Scherrer K, Château M T

机构信息

Laboratoire de Biologie Cellulaire et Cytogénétique Moléculaire (UPRES-JE 1952), Faculté de Médecine de Montpellier-Nîmes, Université Montpellier I, Nîmes, France.

出版信息

Mol Biol Rep. 1997 Mar;24(1-2):57-62. doi: 10.1023/a:1006856707793.

Abstract

The core of the 26S proteasome, the 20S prosome, is a highly organized multi-protein complex found in large amount in malignant cells. Differentiation of several cell lines, including the monoblastic U937 and the lymphoblastoid CCRF-CEM, is accompanied by a general decrease in the prosome concentration when phorbol-myrirtic-acetate (PMA) and retinoic acid plus dihydroxyvitamine D3 (RA+VD) are used. Incubation of U937 cells for three days with PMA or RA+VD causes differentiation, but the resulting patterns of prosome labeling in the cell and on the plasma membrane are not the same. In contrast, the same kind of prosome changes occur in U937 and CCRF-CEM cells when PMA is used as inducer. The intracellular distribution of prosomes is also linked to malignancy and differentiation. Prosomes are found in the nucleus and the cytoplasm of cancer cells; and treatment with RA+VD decreases the prosomes in the nucleus whereas PMA causes various prosome proteins changes. These results indicate that prosomes are important in cell regulation and in the expression of malignancy.

摘要

26S蛋白酶体的核心——20S前体,是一种高度有序的多蛋白复合物,在恶性细胞中大量存在。当使用佛波酯(PMA)、视黄酸加二羟基维生素D3(RA+VD)时,包括单核细胞样U937细胞系和淋巴母细胞样CCRF-CEM细胞系在内的几种细胞系的分化,伴随着前体浓度的普遍降低。用PMA或RA+VD培养U937细胞三天会导致分化,但细胞内和质膜上的前体标记结果模式并不相同。相反,当使用PMA作为诱导剂时,U937和CCRF-CEM细胞中会出现相同类型的前体变化。前体在细胞内的分布也与恶性肿瘤和分化有关。前体存在于癌细胞的细胞核和细胞质中;用RA+VD处理会减少细胞核中的前体,而PMA会导致各种前体蛋白发生变化。这些结果表明,前体在细胞调节和恶性肿瘤表达中很重要。

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