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巨噬细胞通过 CXCL10/IP-10 诱导浆细胞分化。

Macrophages induce differentiation of plasma cells through CXCL10/IP-10.

机构信息

Baylor Institute for Immunology Research, Dallas, TX 75204, USA.

出版信息

J Exp Med. 2012 Sep 24;209(10):1813-23, S1-2. doi: 10.1084/jem.20112142. Epub 2012 Sep 17.

Abstract

In tonsils, CD138(+) plasma cells (PCs) are surrounded by CD163(+) resident macrophages (Ms). We show here that human Ms (isolated from tonsils or generated from monocytes in vitro) drive activated B cells to differentiate into CD138(+)CD38(++) PCs through secreted CXCL10/IP-10 and VCAM-1 contact. IP-10 production by Ms is induced by B cell-derived IL-6 and depends on STAT3 phosphorylation. Furthermore, IP-10 amplifies the production of IL-6 by B cells, which sustains the STAT3 signals that lead to PC differentiation. IP-10-deficient mice challenged with NP-Ficoll show a decreased frequency of NP-specific PCs and lower titers of antibodies. Thus, our results reveal a novel dialog between Ms and B cells, in which IP-10 acts as a PC differentiation factor.

摘要

在扁桃体中,CD138(+)浆细胞 (PCs) 被 CD163(+)固有巨噬细胞 (Ms) 包围。我们在这里表明,人类 Ms(从扁桃体中分离或体外由单核细胞生成)通过分泌的 CXCL10/IP-10 和 VCAM-1 接触,促使活化的 B 细胞分化为 CD138(+)CD38(++) PCs。Ms 中 IP-10 的产生由 B 细胞衍生的 IL-6 诱导,并依赖于 STAT3 磷酸化。此外,IP-10 扩增了 B 细胞产生的 IL-6,从而维持了导致 PC 分化的 STAT3 信号。用 NP-Ficoll 挑战的 IP-10 缺陷型小鼠显示出 NP 特异性 PCs 的频率降低和抗体滴度降低。因此,我们的结果揭示了 Ms 和 B 细胞之间的新型对话,其中 IP-10 作为 PC 分化因子发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06c7/3457728/f14f28fee5a2/JEM_20112142_Fig1.jpg

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