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大鼠中胸腺依赖性和非胸腺依赖性RT6⁺细胞的个体发生及免疫组织化学定位

Ontogeny and immunohistochemical localization of thymus-dependent and thymus-independent RT6+ cells in the rat.

作者信息

Waite D J, Appel M C, Handler E S, Mordes J P, Rossini A A, Greiner D L

机构信息

Department of Medicine, Diabetes Division, University of Massachusetts Medical Center, Worcester, Massachusetts 01605, USA.

出版信息

Am J Pathol. 1996 Jun;148(6):2043-56.

Abstract

RT6 is a cell surface alloantigen that identifies a regulatory subset of peripheral T cells in the rat. Diabetes-prone BB rats are deficient in peripheral RT6+ T cells and develop spontaneous autoimmune insulin-dependent diabetes mellitus. Diabetes-resistant BB rats have normal numbers of RT6+ T cells, and insulin-dependent diabetes mellitus can be induced in these animals by in vivo depletion of peripheral RT6+ cells. Athymic rats are also severely deficient in peripheral RT6+ T cells. Although very different with respect to the peripheral RT6+ cell compartment, normal, athymic, and diabetes-prone BB rats all generate RT6+ intestinal epithelial lymphocytes (IELs). The goal of these studies was to analyze the ontogeny of RT6+ IELs and peripheral lymphoid cells by in situ immunohistochemistry. We observed the following. 1) RT6+ IELs appear before alpha(beta) T-cell-receptor- expressing IELs in diabetes-prone BB, diabetes-resistant BB, and athymic WAG rats. 2) In vivo depletion of peripheral RT6+ T cells in diabetes-resistant BB rats using a cytotoxic monoclonal antibody is not accompanied by depletion of RT6+ IELs. 3) A population of RT6+ T-cell-receptor-negative IELs is present in normal, euthymic diabetes-resistant BB rats, constitutes a larger percentage of the euthymic but lymphopenic diabetes-prone BB rat IEL population, and is the predominant IEL phenotype in athymic WAG rats. These results suggest that RT6+ cells are composed of both thymus-dependent and thymus-independent cell subsets that have different developmental characteristics and may differ in function.

摘要

RT6是一种细胞表面同种异体抗原,可识别大鼠外周T细胞的一个调节亚群。易患糖尿病的BB大鼠外周RT6 + T细胞缺乏,并发展为自发性自身免疫性胰岛素依赖型糖尿病。抗糖尿病的BB大鼠RT6 + T细胞数量正常,通过体内清除外周RT6 +细胞可在这些动物中诱发胰岛素依赖型糖尿病。无胸腺大鼠外周RT6 + T细胞也严重缺乏。尽管在周围RT6 +细胞区室方面有很大差异,但正常、无胸腺和易患糖尿病的BB大鼠均产生RT6 +肠上皮淋巴细胞(IEL)。这些研究的目的是通过原位免疫组织化学分析RT6 + IEL和外周淋巴细胞的个体发生。我们观察到以下情况。1)在易患糖尿病的BB、抗糖尿病的BB和无胸腺WAG大鼠中,RT6 + IEL在表达α(β)T细胞受体的IEL之前出现。2)使用细胞毒性单克隆抗体在抗糖尿病的BB大鼠体内清除外周RT6 + T细胞,不会伴随RT6 + IEL的清除。3)在正常、有胸腺的抗糖尿病BB大鼠中存在一群RT6 + T细胞受体阴性的IEL,在有胸腺但淋巴细胞减少的易患糖尿病的BB大鼠IEL群体中占更大比例,并且是无胸腺WAG大鼠中主要的IEL表型。这些结果表明,RT6 +细胞由胸腺依赖性和胸腺非依赖性细胞亚群组成,它们具有不同的发育特征,功能可能也不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a28/1861642/a5392e3a2738/amjpathol00042-0319-a.jpg

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