Institute of Immunology, Biomedical Sciences Research Center Alexander Fleming, 16672 Vari, Greece.
J Immunol. 2011 Jun 15;186(12):6860-70. doi: 10.4049/jimmunol.1001833. Epub 2011 May 13.
Bone morphogenetic protein (BMP) signaling is increasingly implicated in immune cell differentiation and function; however, direct in vivo evidence for such a role is still missing. In this article, we report that Twisted gastrulation (TWSG1), an extracellular regulator of BMP signaling, is expressed in activated B cells and regulates T-independent B cell responses in the mouse. Twsg1-deficient B cells mount stronger T-independent type 2 responses reflected as increased IgM levels and numbers of Ag-specific IgM-secreting cells. BCR stimulation of Twsg1-deficient B cells results in hyperproliferation, hyperresponsiveness, and decreased apoptosis, whereas TLR stimulation results in hyperproliferation and increased IgG3 production. These changes are reflected on the molecular level by increased transcription of Bcl-6, Pax5, and the BMP-responsive gene Id-2. The TWSG1 effects on B cells appear to be cell intrinsic, suggesting that Twsg1 expression in B cells serves to interpret BMP signals on a per-cell basis. In summary, our observations on the role of TWSG1 in B cell function is opening new paths toward the exploration of the role of BMP signaling in immunological processes.
骨形态发生蛋白(BMP)信号通路越来越多地被认为与免疫细胞的分化和功能有关;然而,直接的体内证据仍然缺乏。在本文中,我们报告了 Twisted gastrulation(TWSG1),一种 BMP 信号通路的细胞外调节剂,在活化的 B 细胞中表达,并调节小鼠中的 T 细胞非依赖性 B 细胞反应。Twsg1 缺陷的 B 细胞产生更强的 T 细胞非依赖性 2 型反应,表现为 IgM 水平升高和抗原特异性 IgM 分泌细胞数量增加。BCR 刺激 Twsg1 缺陷的 B 细胞导致过度增殖、过度反应和凋亡减少,而 TLR 刺激导致过度增殖和 IgG3 产生增加。这些变化在分子水平上反映为 Bcl-6、Pax5 和 BMP 反应基因 Id-2 的转录增加。TWSG1 对 B 细胞的影响似乎是细胞内的,这表明 B 细胞中 Twsg1 的表达用于在单个细胞的基础上解释 BMP 信号。总之,我们对 TWSG1 在 B 细胞功能中的作用的观察为探索 BMP 信号在免疫过程中的作用开辟了新的途径。