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先天性缺乏表达αβ型T细胞受体细胞的小鼠的淋巴细胞发育

Lymphoid development in mice congenitally lacking T cell receptor alpha beta-expressing cells.

作者信息

Philpott K L, Viney J L, Kay G, Rastan S, Gardiner E M, Chae S, Hayday A C, Owen M J

机构信息

Imperial Cancer Research Fund, London, United Kingdom.

出版信息

Science. 1992 Jun 5;256(5062):1448-52. doi: 10.1126/science.1604321.

Abstract

Vertebrate T cells express either an alpha beta or gamma delta T cell receptor (TCR). The developmental relatedness of the two cell types is unresolved. alpha beta + T cells respond to specific pathogens by collaborating with immunoglobulin-producing B cells in distinct lymphoid organs such as the spleen and Peyer's patches. The precise influence of alpha beta + T cells on B cell development is poorly understood. To investigate the developmental effects of alpha beta + T cells on B cells and gamma delta + T cells, mice homozygous for a disrupted TCR alpha gene were generated. The homozygotes showed elimination of alpha beta + T cells and the loss of thymic medullae. Despite this, gamma delta + T cells developed in normal numbers, and there was an increase in splenic B cells.

摘要

脊椎动物的T细胞表达αβ或γδT细胞受体(TCR)。这两种细胞类型在发育上的相关性尚未明确。αβ + T细胞通过在脾脏和派尔集合淋巴结等不同淋巴器官中与产生免疫球蛋白的B细胞协作来应对特定病原体。αβ + T细胞对B细胞发育的确切影响尚不清楚。为了研究αβ + T细胞对B细胞和γδ + T细胞发育的影响,制备了TCRα基因敲除的纯合小鼠。纯合子显示αβ + T细胞消失且胸腺髓质缺失。尽管如此,γδ + T细胞数量正常发育,并且脾脏B细胞有所增加。

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