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表面免疫球蛋白交联后B细胞上I区相关抗原(Ia)表达增加。

Increased expression of I-region-associated antigen (Ia) on B cells after cross-linking of surface immunoglobulin.

作者信息

Mond J J, Seghal E, Kung J, Finkelman F D

出版信息

J Immunol. 1981 Sep;127(3):881-8.

PMID:6790620
Abstract

Both surface Ig (sIg) surface Ia (sIa) have been shown to have important roles in B lymphocyte activation. In order to investigate a possible relationship between these molecules, we studied the effects of cross-linking of sIg on the expression of sIa, as measured by fluorescence-activated cell sorter analysis of lymphoid cells stained with conventional anti-Ia anti-serum or with fluorescein-labeled anti-Ia antibodies. Exposure of cells for 24 hr in vitro to anti-delta, anti-mu, anti-kappa antibodies, or their F(ab')2 fragments induced a very dramatic increase in expression of sIa. Similarly, i.v. injection of anti-delta antibodies into adult mice induced a 2- to 3-fold increase in expression of B cell sIa on spleen, lymph node, and Peyer's patch lymphocytes. There was no increase under these conditions in expression of other B lymphocyte surface antigens, including H-2, 4B9, and 17C9. Furthermore, exposure of B lymphocytes to antibodies directed to B lymphocyte surface antigens other than sIg did not result in an increase in expression of sIa. The anti-Ig-induced increase in sIa expression appeared to be T independent, required cellular protein synthesis, and required more time to occur than did the cross-linking and removal of sIg. This increase in expression of sIa did not occur on B lymphocytes obtained from mice younger than 3 wk old. This increase in expression of sIa may reflect a proximal event in B lymphocyte activation that occurs after cross-linking of sIg by antigen and that may enhance subsequent cellular interactions involving B lymphocytes.

摘要

表面免疫球蛋白(sIg)和表面Ia抗原(sIa)在B淋巴细胞激活过程中均发挥着重要作用。为了探究这两种分子之间可能存在的关系,我们通过荧光激活细胞分选分析,利用传统抗Ia抗血清或荧光素标记的抗Ia抗体对淋巴细胞进行染色,研究了sIg交联对sIa表达的影响。体外将细胞暴露于抗δ、抗μ、抗κ抗体或其F(ab')2片段24小时,可诱导sIa表达显著增加。同样,给成年小鼠静脉注射抗δ抗体,可使脾脏、淋巴结和派伊尔结淋巴细胞上B细胞sIa的表达增加2至3倍。在这些条件下,包括H-2、4B9和17C9在内的其他B淋巴细胞表面抗原的表达并未增加。此外,将B淋巴细胞暴露于针对sIg以外的B淋巴细胞表面抗原的抗体中,不会导致sIa表达增加。抗Ig诱导的sIa表达增加似乎不依赖T细胞,需要细胞蛋白质合成,且与sIg的交联和去除相比,需要更长时间才会出现。3周龄以下小鼠的B淋巴细胞不会出现sIa表达的这种增加。sIa表达的这种增加可能反映了抗原使sIg交联后发生在B淋巴细胞激活过程中的一个近端事件,并且可能增强随后涉及B淋巴细胞的细胞间相互作用。

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