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CD45R(Lp220)的缺失代表胸腺后T细胞分化事件。

Loss of CD45R (Lp220) represents a post-thymic T cell differentiation event.

作者信息

Serra H M, Krowka J F, Ledbetter J A, Pilarski L M

机构信息

Department of Immunology, University of Alberta, Edmonton, Canada.

出版信息

J Immunol. 1988 Mar 1;140(5):1435-41.

PMID:2964476
Abstract

CD45R+ and CDw29+ CD4+ T cells are widely regarded as separate functionally defined T cell lineages. The work described here indicates that they represent maturation stages within the same differentiation pathway. Purified populations of CD4+ or CD8+ T cells, after stimulation with PHA, lose cell surface expression of CD45R (Lp220) and gain an increased surface density of CDw29 (4B4). Clonal analysis demonstrated that individual CD4+ CD45R+ T cells lost CD45R and acquired CDw29 with time in culture. This effect was selective for the high Mr 220-kDa form of the T200 (CD45) complex because the density of CD45, detected by an antibody to common determinants, did not decrease. This strongly indicates that CD45R+ cells are an immature stage in a lineage that culminates in CDw29 expression. To further define the expression of CD45R and CDw29, we analyzed infant thymus cells. Thymocytes include only 4 to 6% CD45R+ cells, but 95% express CDw29 in moderate density. The CD45R+ set appears to include mainly single CD4+ or CD8+, CD3 "bright" medullary cells, although only 15 to 25% of thymocytes with medullary phenotype express CD45R. In vitro culture of thymocytes with Con A and T cell growth factor induces expression of CD45R but these cells differ from the peripheral CD45R+ set by virtue of their co-expression of a high density of CDw29 (4B4) Ag. We postulate that post-thymically CD45R (Lp200) and CDw29 (4B4) comprise a functional assembly on the surface of T cells that changes in composition after stimulation with Ag or mitogen. This may result in enhanced ability of an Ag-experienced T cell to respond effectively to Ag due perhaps to a more efficient signaling complex.

摘要

CD45R+和CDw29+ CD4+ T细胞被广泛认为是功能上不同的T细胞谱系。本文所述的研究表明,它们代表同一分化途径中的成熟阶段。纯化的CD4+或CD8+ T细胞群体在受到PHA刺激后,会失去CD45R(Lp220)的细胞表面表达,并增加CDw29(4B4)的表面密度。克隆分析表明,单个CD4+ CD45R+ T细胞在培养过程中会随着时间的推移失去CD45R并获得CDw29。这种效应对于T200(CD45)复合物的高分子量220-kDa形式具有选择性,因为针对共同决定簇的抗体检测到的CD45密度并未降低。这有力地表明,CD45R+细胞是一个谱系中的不成熟阶段,该谱系最终以CDw29表达为终点。为了进一步确定CD45R和CDw29的表达情况,我们分析了婴儿胸腺细胞。胸腺细胞中仅包含4%至6%的CD45R+细胞,但95%的细胞以中等密度表达CDw29。CD45R+细胞群似乎主要包括单个CD4+或CD8+、CD3“明亮”的髓质细胞,尽管只有15%至25%具有髓质表型的胸腺细胞表达CD45R。用Con A和T细胞生长因子对胸腺细胞进行体外培养可诱导CD45R的表达,但这些细胞与外周CD45R+细胞群不同,因为它们同时高表达CDw29(4B4)抗原。我们推测,胸腺后CD45R(Lp200)和CDw29(4B4)在T细胞表面构成一个功能组件,在受到抗原或有丝分裂原刺激后其组成会发生变化。这可能导致经历过抗原刺激的T细胞对抗原作出有效反应的能力增强,这或许是由于形成了更有效的信号复合物。

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