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Role of membrane immunoglobulin (Ig) crosslinking in membrane Ig-mediated, major histocompatibility-restricted T cell-B cell cooperation.膜免疫球蛋白(Ig)交联在膜Ig介导的、主要组织相容性限制的T细胞 - B细胞协作中的作用。
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In vitro activation and nuclear translocation of NF-kappa B catalyzed by cyclic AMP-dependent protein kinase and protein kinase C.环磷酸腺苷依赖性蛋白激酶和蛋白激酶C催化的核因子κB的体外激活及核转位
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Interleukin 1 and cyclic AMP induce kappa immunoglobulin light-chain expression via activation of an NF-kappa B-like DNA-binding protein.白细胞介素1和环磷酸腺苷通过激活一种类核因子κB的DNA结合蛋白诱导κ免疫球蛋白轻链表达。
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Tumor necrosis factor alpha and interleukin 1 stimulate the human immunodeficiency virus enhancer by activation of the nuclear factor kappa B.肿瘤坏死因子α和白细胞介素1通过激活核因子κB来刺激人类免疫缺陷病毒增强子。
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B细胞中T细胞依赖性诱导核因子-κB

T cell-dependent induction of NF-kappa B in B cells.

作者信息

Lalmanach-Girard A C, Chiles T C, Parker D C, Rothstein T L

机构信息

Department of Medicine, Boston University Medical Center, Massachusetts 02118.

出版信息

J Exp Med. 1993 Apr 1;177(4):1215-9. doi: 10.1084/jem.177.4.1215.

DOI:10.1084/jem.177.4.1215
PMID:8459216
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2190960/
Abstract

In comparison to B cell stimulation mediated by surface immunoglobulin (Ig) antigen receptor ligation, little is known about the intracellular events associated with T cell-dependent B cell responses. A model for the efferent phase of T cell-B cell interaction was used to examine the capacity of activated T cells to trigger nuclear expression of the trans-acting transcription factor, NF-kappa B, in B cells. Fixed, activated, but not fixed, resting Th2 cells were found to induce increased binding activity for a kappa B site-containing oligonucleotide in a time-dependent manner. This induction of NF-kappa B was eliminated by an antibody directed against a 39-kD cell interaction protein on activated T cells as well as by a soluble form of B cell CD40. Of particular relevance to intracellular signaling, NF-kappa B induction was not diminished by prior depletion of B cell protein kinase C (PKC) with phorbol myristate acetate. These results strongly suggest that T cell-dependent B cell stimulation is associated with NF-kappa B induction via p39-CD40 interaction and that this is brought about by non-PKC dependent signaling, in marked contrast to the previously documented requirement for PKC in sIg receptor-mediated stimulation. This suggest that NF-kappa B responds to more than one receptor-mediated intracellular signaling pathway in B cells and may be part of a "final common pathway" for B cell stimulation.

摘要

与由表面免疫球蛋白(Ig)抗原受体连接介导的B细胞刺激相比,对于与T细胞依赖性B细胞应答相关的细胞内事件了解甚少。采用T细胞 - B细胞相互作用传出阶段的模型,来检测活化T细胞触发B细胞核内反式作用转录因子NF-κB表达的能力。发现固定的活化Th2细胞(而非固定的静止Th2细胞)能以时间依赖性方式诱导含κB位点的寡核苷酸结合活性增加。针对活化T细胞上一种39-kD细胞相互作用蛋白的抗体以及可溶性形式的B细胞CD40,均可消除这种NF-κB的诱导。与细胞内信号传导特别相关的是,预先用佛波酯肉豆蔻酸酯耗尽B细胞蛋白激酶C(PKC),并不会减弱NF-κB的诱导。这些结果强烈表明,T细胞依赖性B细胞刺激与通过p39 - CD40相互作用诱导NF-κB有关,并且这是由非PKC依赖性信号传导引起的,这与之前记录的sIg受体介导的刺激中对PKC的需求形成鲜明对比。这表明NF-κB对B细胞中不止一种受体介导的细胞内信号传导途径有反应,并且可能是B细胞刺激“最终共同途径”的一部分。