Griebel P J, Ferrari G
Basel Institute for Immunology, Switzerland.
Eur J Immunol. 1994 Feb;24(2):401-9. doi: 10.1002/eji.1830240220.
Lymphoid follicles of the ileal Peyer's patch (PP) of young sheep function as the major source of B cells and a site of immunoglobulin (Ig) receptor diversification. However, extensive cell death in culture has restricted investigations of ileal PP follicular (iPf)B cell biology. We investigated the possibility that sustained iPfB cell proliferation may require an interaction with mesenchymal stromal cells (SC). Four SC lines, cloned from lymphoid follicles of the ileal PP, and various sheep and xenogeneic mesenchymal cells were used to characterize the nature of iPfB cell-SC interactions. A sustained proliferative response was unique to iPfB cells, required iPfB cell-SC contact, and SC membranes functioned as intact SC to either enhance or inhibit iPfB cell proliferative responses. The iPfB cell proliferation in SC co-cultures was accompanied by extensive cell death and a slow decline in viable cell number. Flow cytometric analysis confirmed that viable lymphocytes, present in SC co-cultures, were immature B cells that expressed surface IgM, with either lambda or kappa. Ig light chain, and that SC co-culture inhibited iPfB cell differentiation. Finally, addition of soluble anti-sheep Ig to iPfB cell-SC co-cultures did not inhibit SC-dependent iPfB cell proliferation or iPfB cell binding to SC. These data indicate that an interaction between specific SC membrane molecules and non-Ig molecules of iPfB cells either supported or inhibited a self-renewing proliferative response by immature (sIgMLo, BAQ44A-) iPfB cells. Finally, SC-dependent iPfB cell proliferation was independent of T cells and extrinsic antigen which further suggests that a functionally distinct B cell population resides in lymphoid follicles of the ileal PP.
幼羊回肠派尔集合淋巴结(PP)的淋巴滤泡是B细胞的主要来源以及免疫球蛋白(Ig)受体多样化的场所。然而,培养过程中广泛的细胞死亡限制了对回肠PP滤泡(iPf)B细胞生物学的研究。我们研究了持续的iPfB细胞增殖可能需要与间充质基质细胞(SC)相互作用的可能性。从回肠PP的淋巴滤泡中克隆出4种SC系,以及各种绵羊和异种间充质细胞,用于表征iPfB细胞与SC相互作用的性质。持续的增殖反应是iPfB细胞所特有的,需要iPfB细胞与SC接触,并且SC膜作为完整的SC发挥作用,以增强或抑制iPfB细胞的增殖反应。SC共培养中iPfB细胞的增殖伴随着广泛的细胞死亡以及活细胞数量的缓慢下降。流式细胞术分析证实,SC共培养中存在的活淋巴细胞是表达表面IgM、带有λ或κ Ig轻链的未成熟B细胞,并且SC共培养抑制iPfB细胞分化。最后,向iPfB细胞 - SC共培养物中添加可溶性抗绵羊Ig并不抑制SC依赖性iPfB细胞增殖或iPfB细胞与SC的结合。这些数据表明,特定SC膜分子与iPfB细胞的非Ig分子之间的相互作用要么支持要么抑制未成熟(sIgMLo,BAQ44A -)iPfB细胞的自我更新增殖反应。最后,SC依赖性iPfB细胞增殖独立于T细胞和外源性抗原,这进一步表明在回肠PP的淋巴滤泡中存在功能上不同的B细胞群体。