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μ阴性前B细胞上的Igα/Igβ异二聚体能够转导信号以诱导早期B细胞分化。

The Ig alpha/Igbeta heterodimer on mu-negative proB cells is competent for transducing signals to induce early B cell differentiation.

作者信息

Nagata K, Nakamura T, Kitamura F, Kuramochi S, Taki S, Campbell K S, Karasuyama H

机构信息

Department of Immunology, The Tokyo Metropolitan Institute of Medical Science, Japan.

出版信息

Immunity. 1997 Oct;7(4):559-70. doi: 10.1016/s1074-7613(00)80377-5.

Abstract

The immunoglobulin alpha (Ig alpha)/Ig beta heterodimer was detected on the surface of mu-negative proB cell lines in association with calnexin. The cross-linking of Ig beta on proB cells freshly isolated from bone marrow of recombination activating gene (RAG)-2-deficient mice induced a rapid and transient tyrosine-phosphorylation of Ig alpha as well as an array of intracellular proteins including Syk, PI3-kinase, Vav, and SLP-76. It also elicited the phosphorylation and activation of a MAP kinase ERK but not JNK/SAPK or p38. When RAG-2-deficient mice were treated with anti-Ig beta monoclonal antibody, developmentally arrested proB cells were induced to differentiate to the small preB cell stage as observed when the mu transgene was expressed in RAG-2-deficient mice. Thus, the cross-linking of Ig beta on proB cells appears to elicit differentiation signals analogous to those delivered by the preB cell receptor in normal B cell development.

摘要

在μ阴性前B细胞系表面检测到免疫球蛋白α(Igα)/Igβ异二聚体与钙连蛋白相关联。从重组激活基因(RAG)-2缺陷小鼠骨髓中新鲜分离的前B细胞上Igβ的交联诱导了Igα以及包括Syk、PI3激酶、Vav和SLP-76在内的一系列细胞内蛋白的快速且短暂的酪氨酸磷酸化。它还引发了丝裂原活化蛋白激酶ERK的磷酸化和激活,但未引发JNK/SAPK或p38的磷酸化和激活。当用抗Igβ单克隆抗体处理RAG-2缺陷小鼠时,发育停滞的前B细胞被诱导分化到小前B细胞阶段,这与在RAG-2缺陷小鼠中表达μ转基因时观察到的情况相同。因此,前B细胞上Igβ的交联似乎引发了类似于正常B细胞发育中前B细胞受体传递的分化信号。

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