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人外周血B细胞中Cα1和Cα2种系及成熟mRNA转录本的差异调节

Differential regulation of C alpha 1 and C alpha 2 germ-line and mature mRNA transcripts in human peripheral blood B cells.

作者信息

Kitani A, Strober W

机构信息

Mucosal Immunity Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.

出版信息

J Immunol. 1994 Aug 15;153(4):1466-77.

PMID:8046226
Abstract

In this study, we investigated the regulation of germ-line and mature C alpha mRNA transcript expression in human peripheral blood B cells. In initial studies, we found that C alpha germ-line and mature transcripts were constitutively expressed in total peripheral blood B cells but not in high density surface IgM+ (surface IgA-) B cells; the latter cells were therefore used in subsequent studies. Focusing first on regulation of germ-line (I alpha-C alpha) transcripts, we showed that C alpha 1 germ-line transcripts are induced by TGF-beta 1 alone but such induction is enhanced by Staphylococcus aureus, Cowan I (SAC). In contrast, C alpha 2 germ-line transcripts are optimally induced by TGF-beta 1 in the absence of a B cell stimulus. In addition, although SAC alone induced both C alpha 1 and C alpha 2 germ-line transcripts, such induction is dependent on endogenous (B cell-derived) TGF-beta 1 production, because no induction is detected in cells cultured in the presence of neutralizing anti-TGF-beta 1. Turning next to mature (VDJ-C alpha) transcripts we showed that SAC plus TGF-beta 1 induces mature C alpha 1 transcripts, and such induction is IL-10 dependent because it is enhanced by exogenous IL-10 and abrogated by the presence of anti-IL-10. In contrast, SAC plus TGF-beta 1 does not induce C alpha 2 mature transcripts, even in the presence of exogenous IL-10; such transcripts are induced, however, by T cell stimuli such as anti-CD40 (presented by CDw32-transfected L cells) in the presence of TGF-beta 1/IL-10 or by PWM-activated T cells. In summary, these studies show that C alpha 1 and C alpha 2 germ-line transcript induction is differentially regulated, in keeping with previous studies of differences in germ-line CH transcript induction in the first and second IgH duplication units. Furthermore, C alpha 1 and C alpha 2 mature transcript induction is also differentially regulated, with C alpha 2 requiring a T cell signal such as that delivered by the CD40 ligand. Finally, IL-10 appears to be uniquely supportive of the induction of both C alpha 1 and C alpha 2 mature transcripts.

摘要

在本研究中,我们调查了人类外周血B细胞中生殖系和成熟Cα mRNA转录本表达的调控情况。在初步研究中,我们发现Cα生殖系和成熟转录本在总外周血B细胞中组成性表达,但在高密度表面IgM+(表面IgA-) B细胞中不表达;因此,后一种细胞被用于后续研究。首先关注生殖系(Iα-Cα)转录本的调控,我们发现Cα1生殖系转录本仅由TGF-β1诱导,但金黄色葡萄球菌Cowan I(SAC)可增强这种诱导作用。相比之下,Cα2生殖系转录本在无B细胞刺激的情况下由TGF-β1最佳诱导。此外,虽然单独的SAC可诱导Cα1和Cα2生殖系转录本,但这种诱导依赖于内源性(B细胞来源)TGF-β1的产生,因为在存在中和性抗TGF-β1的情况下培养的细胞中未检测到诱导作用。接下来转向成熟(VDJ-Cα)转录本,我们发现SAC加TGF-β1可诱导成熟Cα1转录本,且这种诱导依赖于IL-10,因为外源性IL-10可增强诱导作用,而抗IL-10的存在可消除这种诱导作用。相比之下,SAC加TGF-β1即使在存在外源性IL-10的情况下也不诱导Cα2成熟转录本;然而,在TGF-β1/IL-10存在的情况下,T细胞刺激如抗CD40(由CDw32转染的L细胞呈递)或PWM激活的T细胞可诱导这种转录本。总之,这些研究表明,Cα1和Cα2生殖系转录本的诱导受到不同调控,这与先前关于第一和第二个IgH重复单元中生殖系CH转录本诱导差异的研究一致。此外,Cα1和Cα2成熟转录本的诱导也受到不同调控,Cα2需要T细胞信号,如由CD40配体传递的信号。最后,IL-10似乎独特地支持Cα1和Cα2成熟转录本的诱导。

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