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补体膜辅因子蛋白(CD46)在人白血病细胞系中的高表达:含STA结构域的可变剪接形式在CD46上调中的作用

High expression of membrane cofactor protein of complement (CD46) in human leukaemia cell lines: implication of an alternatively spliced form containing the STA domain in CD46 up-regulation.

作者信息

Hara T, Suzuki Y, Semba T, Hatanaka M, Matsumoto M, Seya T

机构信息

Department of Immunology, Center for Adult Diseases Osaka, Japan.

出版信息

Scand J Immunol. 1995 Dec;42(6):581-90. doi: 10.1111/j.1365-3083.1995.tb03700.x.

Abstract

Human membrane cofactor protein (MCP, CD46) is a receptor for the measles virus and serves as a complement regulator which protects host cells from autologous complement attack. MCP is highly polymorphic due to a variety of mRNA splice products. The levels of MCP expression on T and myeloid cell lines are usually two-eightfold higher than those on their normal counterparts, whereas Burkitt's lymphoma B cell lines express less MCP than B cell lineages carrying no EB virus. The molecule has a Ser/Thr-rich (ST) domain adjacent to the functional domain, namely short consensus repeats (SCR). The ST domain and a cytoplasmic tail (CYT) contribute to the MCP polymorphism. The ST domain is encoded by three exons (A, B and C) and major ST isoforms are STABC, STBC and STC. The authors investigated the relationship between the expression levels and isoform usage of MCP by flow cytometry using specific antibodies against STA and STC, by reverse transcriptase-polymerase chain reaction (RT-PCR) with size markers for each splice variant, and by RT-PCR/Southern blotting using a specific probe for STA. The results were (1) the profiles of mean shifts of myeloid and T cell lines were STC < STA on flow cytometry while those of B cell lines and normal blood cells were STA < STC; (2) all cell lines tested by RT-PCR expressed the messages for the isoforms STBC/CYT1, STC/CYT1, STBC/CYT2, and STC/CYT2. The band for STABC/CYT2 overlapped that for STC/CYT1, and the band for STABC/CYT1 was marginal in all cell lines examined; (3) semi-quantitative analysis of the STABC isoforms by Southern blotting indicated the presence of high levels of the STABC messages in myeloid and T-cell lines in comparison with B lymphoid cells and normal leucocytes. Thus, the quantity of MCP expressed parallels the STABC message level, which is up-regulated in T and myeloid leukaemia cell lines.

摘要

人膜辅因子蛋白(MCP,CD46)是麻疹病毒的受体,也是一种补体调节因子,可保护宿主细胞免受自身补体攻击。由于多种mRNA剪接产物,MCP具有高度多态性。T细胞系和髓细胞系上MCP的表达水平通常比其正常对应物高2至8倍,而伯基特淋巴瘤B细胞系表达的MCP比未携带EB病毒的B细胞谱系少。该分子在功能域(即短共有重复序列,SCR)附近有一个富含丝氨酸/苏氨酸的(ST)结构域。ST结构域和细胞质尾巴(CYT)导致了MCP的多态性。ST结构域由三个外显子(A、B和C)编码,主要的ST异构体是STABC、STBC和STC。作者通过使用针对STA和STC的特异性抗体进行流式细胞术、使用针对每个剪接变体的大小标记进行逆转录聚合酶链反应(RT-PCR)以及使用针对STA的特异性探针进行RT-PCR/ Southern印迹分析,研究了MCP的表达水平与异构体使用之间的关系。结果如下:(1)流式细胞术显示髓细胞系和T细胞系的平均位移谱为STC < STA,而B细胞系和正常血细胞的平均位移谱为STA < STC;(2)通过RT-PCR检测的所有细胞系均表达异构体STBC/CYT1、STC/CYT1、STBC/CYT2和STC/CYT2的信息。STABC/CYT2的条带与STC/CYT1的条带重叠,STABC/CYT1的条带在所有检测的细胞系中都很微弱;(3)通过Southern印迹对STABC异构体进行半定量分析表明,与B淋巴细胞和正常白细胞相比,髓细胞系和T细胞系中存在高水平的STABC信息。因此,MCP的表达量与STABC信息水平平行,而STABC信息水平在T细胞系和髓细胞白血病细胞系中上调。

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