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派尔集合淋巴结生发中心细胞的表面表型与迁移能力

Surface phenotype and migratory capability of Peyer's patch germinal center cells.

作者信息

Butcher E C, Reichert R A, Coffman R L, Nottenburg C, Weissman I L

出版信息

Adv Exp Med Biol. 1982;149:765-72. doi: 10.1007/978-1-4684-9066-4_106.

Abstract

Peanut agglutinin (PNA) binds selectively to germinal center cells in mouse peripheral lymphoid organs. Using PNA as a marker, we have determined that Peyer's patch germinal center cells are B cells with a unique phenotype---they express a low level of surface immunoglobulin (about 85% Ig+), predominantly of the IgA class (70% alpha+), with only 10% bearing surface IgM, and few if any expressing IgD. This phenotype identifies murine Peyer's patch germinal center cells as fairly late cells in B cell differentiation, and suggests that they may be precursors of IgA-secreting plasma cells in the gut wall. In addition, we have described a means of purifying PNA+ Peyer's patch lymphocytes, and have demonstrated that these cells lack functional receptors for high endothelial venules and fail to migrate to lymphoid organs in vivo. It is speculated that PNA may be a general marker for nonmigratory lymphocyte populations undergoing local differentiation.

摘要

花生凝集素(PNA)可选择性地结合小鼠外周淋巴器官生发中心的细胞。以PNA作为标志物,我们已确定派尔集合淋巴结生发中心细胞是具有独特表型的B细胞——它们表面免疫球蛋白表达水平较低(约85%为Ig⁺),主要为IgA类(70%为α⁺),仅有10%带有表面IgM,几乎没有表达IgD的。这种表型将小鼠派尔集合淋巴结生发中心细胞鉴定为B细胞分化过程中相当晚期的细胞,并表明它们可能是肠壁中分泌IgA的浆细胞的前体。此外,我们描述了一种纯化PNA⁺派尔集合淋巴结淋巴细胞的方法,并证明这些细胞缺乏高内皮微静脉的功能性受体,且在体内无法迁移至淋巴器官。据推测,PNA可能是正在经历局部分化的非迁移性淋巴细胞群体的通用标志物。

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