Kretschmer Karsten, Jungebloud Anke, Stopkowicz Jana, Stoermann Britta, Hoffmann Reinhard, Weiss Siegfried
Molecular Immunology, German Research Center for Biotechnology, Braunschweig, Germany.
J Immunol. 2003 Aug 1;171(3):1192-201. doi: 10.4049/jimmunol.171.3.1192.
In L2 mice, a high expression level of the transgenic lambda2(315) L chain results in nearly complete exclusion of endogenous L chains and a predominance of B-1a cells. In this study, we show that splenic and peritoneal B-1a cells differ considerably in their Ab repertoire and gene expression profile. Splenic B-1a cells exhibit a more diversified repertoire under L chain limitation. Despite oligoclonal overlaps between both B-1a compartments, some B cell receptor specificities are clearly restricted to the peritoneum. The capacity of peritoneal B-1a cells to enter the splenic B-1a compartment was found to be very limited. Gene expression profiling revealed genes up-regulated in splenic B-1a cells that are involved in mediating specialized first-line-of-defense effector functions and interaction with T cells. Thus, splenic and peritoneal B-1a cells differ not only in their developmental program but also in functional properties.
在L2小鼠中,转基因λ2(315)轻链的高表达水平导致内源性轻链几乎完全被排斥,且B-1a细胞占主导地位。在本研究中,我们发现脾脏和腹膜B-1a细胞在抗体库和基因表达谱方面存在显著差异。在轻链受限的情况下,脾脏B-1a细胞表现出更多样化的抗体库。尽管两个B-1a细胞区室之间存在寡克隆重叠,但一些B细胞受体特异性明显局限于腹膜。发现腹膜B-1a细胞进入脾脏B-1a细胞区室的能力非常有限。基因表达谱分析揭示了在脾脏B-1a细胞中上调的基因,这些基因参与介导特殊的一线防御效应功能以及与T细胞的相互作用。因此,脾脏和腹膜B-1a细胞不仅在发育程序上不同,在功能特性上也不同。