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肺炎链球菌免疫前后边缘区B细胞与滤泡B细胞以及独特型阳性边缘区B细胞的DNA微阵列基因表达谱

DNA microarray gene expression profile of marginal zone versus follicular B cells and idiotype positive marginal zone B cells before and after immunization with Streptococcus pneumoniae.

作者信息

Kin Nicholas W, Crawford Dianna M, Liu Jiabin, Behrens Timothy W, Kearney John F

机构信息

Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294.

Center for Immunology, Department of Medicine, University of Minnesota, Minneapolis, MN 55455.

出版信息

J Immunol. 2008 May 15;180(10):6663-6674. doi: 10.4049/jimmunol.180.10.6663.

DOI:10.4049/jimmunol.180.10.6663
PMID:18453586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3966313/
Abstract

Marginal zone (MZ) B cells play an important role in the clearance of blood-borne bacterial infections via rapid T-independent IgM responses. We have previously demonstrated that MZ B cells respond rapidly and robustly to bacterial particulates. To determine the MZ-specific genes that are expressed to allow for this response, MZ and follicular (FO) B cells were sort purified and analyzed via DNA microarray analysis. We identified 181 genes that were significantly different between the two B cell populations. Ninety-nine genes were more highly expressed in MZ B cells while 82 genes were more highly expressed in FO B cells. To further understand the molecular mechanisms by which MZ B cells respond so rapidly to bacterial challenge, Id-positive and -negative MZ B cells were sort purified before (0 h) or after (1 h) i.v. immunization with heat-killed Streptococcus pneumoniae, R36A, and analyzed via DNA microarray analysis. We identified genes specifically up-regulated or down-regulated at 1 h following immunization in the Id-positive MZ B cells. These results give insight into the gene expression pattern in resting MZ vs FO B cells and the specific regulation of gene expression in Ag-specific MZ B cells following interaction with Ag.

摘要

边缘区(MZ)B细胞通过快速的非依赖T细胞的IgM反应在清除血源细菌感染中发挥重要作用。我们之前已经证明MZ B细胞对细菌颗粒有快速且强烈的反应。为了确定为实现这种反应而表达的MZ特异性基因,对MZ和滤泡(FO)B细胞进行了分选纯化,并通过DNA微阵列分析进行了检测。我们鉴定出在这两种B细胞群体之间存在显著差异的181个基因。99个基因在MZ B细胞中表达更高,而82个基因在FO B细胞中表达更高。为了进一步了解MZ B细胞对细菌攻击反应如此迅速的分子机制,在用热灭活的肺炎链球菌R36A进行静脉内免疫之前(0小时)或之后(1小时),对Id阳性和阴性的MZ B细胞进行了分选纯化,并通过DNA微阵列分析进行了检测。我们鉴定出在Id阳性MZ B细胞免疫后1小时特异性上调或下调的基因。这些结果深入了解了静息MZ与FO B细胞中的基因表达模式,以及与抗原相互作用后抗原特异性MZ B细胞中基因表达的特定调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda0/3966313/ed9287c9ef1e/nihms-556235-f0007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bda0/3966313/ed9287c9ef1e/nihms-556235-f0007.jpg

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本文引用的文献

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CD36 is differentially expressed on B cell subsets during development and in responses to antigen.
J Immunol. 2008 Jan 1;180(1):230-7. doi: 10.4049/jimmunol.180.1.230.
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Follicular shuttling of marginal zone B cells facilitates antigen transport.边缘区B细胞的滤泡穿梭促进抗原转运。
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Regulatory T cells expressing interleukin 10 develop from Foxp3+ and Foxp3- precursor cells in the absence of interleukin 10.表达白细胞介素10的调节性T细胞在没有白细胞介素10的情况下由Foxp3 +和Foxp3-前体细胞发育而来。
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CD86 regulates IgG1 production via a CD19-dependent mechanism.CD86通过依赖CD19的机制调节IgG1的产生。
J Immunol. 2007 Aug 1;179(3):1516-23. doi: 10.4049/jimmunol.179.3.1516.
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RGS10-null mutation impairs osteoclast differentiation resulting from the loss of [Ca2+]i oscillation regulation.RGS10基因敲除突变会损害因细胞内钙离子浓度([Ca2+]i)振荡调节缺失而导致的破骨细胞分化。
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B cell regulation of CD4+CD25+ T regulatory cells and IL-10 via B7 is essential for recovery from experimental autoimmune encephalomyelitis.B细胞通过B7对CD4+CD25+调节性T细胞和白细胞介素-10的调节作用对于实验性自身免疫性脑脊髓炎的恢复至关重要。
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