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一种与糖尿病相关的T细胞自身抗原定位于小鼠6号染色体的端粒位点。

A diabetes-associated T-cell autoantigen maps to a telomeric locus on mouse chromosome 6.

作者信息

Dallas-Pedretti A, McDuffie M, Haskins K

机构信息

Department of Immunology, University of Colorado Health Sciences Center, Denver 80262.

出版信息

Proc Natl Acad Sci U S A. 1995 Feb 28;92(5):1386-90. doi: 10.1073/pnas.92.5.1386.

Abstract

Identification of diabetes-associated T-cell autoantigens is important for understanding the immunopathology of diabetes and developing improved therapeutic strategies. We have used a genetic approach to move toward identifying the autoantigen recognized by a diabetogenic islet-specific T-cell clone from a nonobese diabetic (NOD) mouse. The unique antigen recognition pattern of this clone was utilized to map the gene encoding the antigen (or its expression) by genetic linkage analysis. In vitro analysis of T-cell proliferation by this clone showed that the capacity of the islets to stimulate T cells segregates as a single codominant gene in BALB/cByJ x (BALB/cByJ x NOD/Bdc) backcross mice. This phenotype was tightly linked to two microsatellites in the telomeric region of mouse chromosome 6.

摘要

鉴定与糖尿病相关的T细胞自身抗原对于理解糖尿病的免疫病理学以及制定改进的治疗策略至关重要。我们采用了一种遗传学方法,旨在从非肥胖糖尿病(NOD)小鼠中鉴定出一种致糖尿病胰岛特异性T细胞克隆所识别的自身抗原。利用该克隆独特的抗原识别模式,通过遗传连锁分析来定位编码该抗原(或其表达)的基因。该克隆对T细胞增殖的体外分析表明,胰岛刺激T细胞的能力在BALB/cByJ×(BALB/cByJ×NOD/Bdc)回交小鼠中作为一个单一的共显性基因进行分离。这种表型与小鼠6号染色体端粒区域的两个微卫星紧密连锁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6c/42524/e421e1cded7a/pnas01483-0150-a.jpg

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