Moriyama Yuko, Sekine Chiyoko, Koyanagi Akemi, Koyama Noriko, Ogata Hideko, Chiba Shigeru, Hirose Sachiko, Okumura Ko, Yagita Hideo
Department of Immunology, Biomedical Research Center, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
Int Immunol. 2008 Jun;20(6):763-73. doi: 10.1093/intimm/dxn034. Epub 2008 Apr 1.
Notch2 and Delta-like 1 (Dll1) have been implicated in the development of marginal zone B (MZB) cells. In the present study, we characterized the expression and function of mouse Notch receptors and ligands in the spleen by using newly generated mAbs. Although Notch2 was expressed on both B and T cells in the spleen, the highest expression was observed on precursors of marginal zone B and MZB cells. Dll1 was expressed on macrophage and erythroblasts in the red pulp, but not on B cells or marginal zone macrophage. Administration of a blocking mAb against Dll1 not only blocked the development of MZB cells in juvenile mice but also gradually depleted the pre-established MZB cells in adult mice, indicating a critical role for Dll1 in the maintenance of MZB cells in the spleen of normal mice. Interestingly, Dll1 was not necessary for the maintenance of MZB cells in lupus-prone (NZB x NZW) F1 mice particularly after the onset of the disease, suggesting that the Dll1 independence may be a feature of dysregulated MZB cells producing auto-antibodies.
Notch2和Delta样蛋白1(Dll1)与边缘区B(MZB)细胞的发育有关。在本研究中,我们通过使用新产生的单克隆抗体来表征小鼠Notch受体和配体在脾脏中的表达及功能。尽管Notch2在脾脏的B细胞和T细胞上均有表达,但在边缘区B细胞和MZB细胞的前体细胞上表达最高。Dll1在红髓中的巨噬细胞和成红细胞上表达,但在B细胞或边缘区巨噬细胞上不表达。给予抗Dll1阻断单克隆抗体不仅会阻断幼年小鼠中MZB细胞的发育,还会逐渐消耗成年小鼠中预先建立的MZB细胞,这表明Dll1在正常小鼠脾脏中MZB细胞的维持中起关键作用。有趣的是,Dll1对于易患狼疮的(NZB×NZW)F1小鼠中MZB细胞的维持并非必需,特别是在疾病发作后,这表明Dll1非依赖性可能是产生自身抗体的失调MZB细胞的一个特征。