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无淋巴细胞生成(aly)突变小鼠泪腺、唾液腺和肾脏中浸润性T细胞的T细胞受体库:干燥综合征的新模型

T-cell receptor repertoire of infiltrating T cells in lachrymal glands, salivary glands and kidneys from alymphoplasia (aly) mutant mice: a new model for Sjögren's syndrome.

作者信息

Furukawa M, Sakamoto A, Kita Y, Ohishi Y, Matsumura R, Tsubata R, Tsubata T, Iwamoto I, Saito Y, Sumida T

机构信息

Second Department of Internal Medicine, School of Medicine, Chiba University, Japan.

出版信息

Br J Rheumatol. 1996 Dec;35(12):1223-30. doi: 10.1093/rheumatology/35.12.1223.

Abstract

Alymphoplasia (aly) mice are thought to provide a new model for systemic Sjögren's syndrome (SS), since they reveal remarkable infiltration of mononuclear cells into salivary glands, lachrymal glands and kidneys, and show histological findings similar to those in patients with SS. Cell transfer experiments demonstrate that T cells induce the infiltration of mononuclear cells into several tissues in aly mice. To analyse the pathogenesis of cell infiltration in various tissues, we examined T-cell receptor (TCR) V beta usage of T cells in salivary glands, lachrymal glands and kidneys from aly mice, using family-polymerase chain reaction (PCR) and PCR-single-strand conformation polymorphism (SSCP) methods. The results of SSCP demonstrated that the infiltrating T cells in the three organs expanded clonally, suggesting that they proliferate by antigen-driven stimulation. Some TCR V beta genes (V beta 1, 3, 6, 11, 12, 16) were commonly used in salivary glands, lachrymal glands and kidneys, while the V beta 7 gene was specifically expressed in kidneys. SSCP also showed that there were a few shared T-cell clones (V beta 3- and V beta 6-positive cells) among the three tissues. Indeed, sequence analysis of accumulated T cells showed that a conserved amino acid (leucine) at position 98 in the TCR V beta complementary determining region (CDR) 3 was detected in all organs at high frequency (41-57%) and the amino acid sequence motif (LG) was specifically conserved at a frequency of 32% in the three organs. In conclusion, T cells that infiltrate into lachrymal glands, salivary glands and kidneys of aly mutant mice might recognize shared common epitopes in all three organs and a kidney-specific antigen.

摘要

无淋巴细胞形成(aly)小鼠被认为是系统性干燥综合征(SS)的一种新模型,因为它们显示出单核细胞显著浸润至唾液腺、泪腺和肾脏,并且呈现出与SS患者相似的组织学表现。细胞移植实验表明,T细胞可诱导单核细胞浸润至aly小鼠的多个组织。为分析不同组织中细胞浸润的发病机制,我们采用家族聚合酶链反应(PCR)和PCR-单链构象多态性(SSCP)方法,检测了aly小鼠唾液腺、泪腺和肾脏中T细胞的T细胞受体(TCR)Vβ使用情况。SSCP结果显示,三个器官中的浸润性T细胞呈克隆性扩增,提示它们通过抗原驱动的刺激而增殖。一些TCR Vβ基因(Vβ1、3、6、11、12、16)在唾液腺、泪腺和肾脏中共同使用,而Vβ7基因则在肾脏中特异性表达。SSCP还显示,三个组织中有一些共享的T细胞克隆(Vβ3和Vβ6阳性细胞)。事实上,对积累的T细胞进行序列分析表明,在TCR Vβ互补决定区(CDR)3的第98位保守氨基酸(亮氨酸)在所有器官中均以高频率(41%-57%)被检测到,并且氨基酸序列基序(LG)在三个器官中以32%的频率特异性保守。总之,浸润至aly突变小鼠泪腺、唾液腺和肾脏的T细胞可能识别所有三个器官中的共同表位以及肾脏特异性抗原。

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