Griebel P, Hein W R, Dudler L, Ferrari G
Basel Institute for Immunology, Switzerland.
Stem Cells. 1993 Mar;11(2):130-43. doi: 10.1002/stem.5530110208.
The ileal Peyer's patch (PP) is the major site of B cell production and immunoglobulin diversification in lambs, but the factors which regulate these processes are poorly understood. As a first step toward identifying possible regulatory mechanisms, stable long-term cultures of ileal PP stromal cells were established at the clonal level. Four distinct cell types were identified by their phenotype and growth requirements. Immunohistochemical staining confirmed that all clones were mesenchymal (vimentin+; cytokeratin-) in origin and were negative for T cell, B cell, and macrophage markers. Three cell lines were negative for major histocompatibility complex (MHC) I and II molecules, but one cell line, SCN, expressed MHC I, MHC II and CD44 molecules, and a subpopulation of SCN cells expressed BAQ44A, a B cell differentiation molecule. The four cell lines produced different types and amounts of extracellular matrix proteins, and their growth was not influenced by exogenous human interleukin 1 (IL-1), IL-2, transforming growth factor beta 1 (TGF beta 1), or bovine fibroblast growth factor (FGF) but was influenced by serum. When tested for their capacity to support lymphocyte growth, all clones produced a soluble factor(s) that was mitogenic for ileal and jejunal PP cells and thymocytes. Similar growth promoting activity was observed with culture supernatants of murine, human and bovine fibroblasts but could not be reproduced using recombinant human cytokines. Furthermore, coculture of stromal cells with ileal PP follicular B cells elicited a proliferative response unique to each stromal cell line. Coculture with increasing numbers of SCN cells inhibited B cell proliferative responses, whereas coculture with SCG2 and SCF32 cells enhanced B cell proliferative response at both low and high stromal cell densities. Ileal PP follicular B cells rapidly bound to the surface of all stromal cell clones, and this interaction was specific when compared with thymocytes or peripheral blood lymphocytes. These results suggest that ileal PP stromal cells are a phenotypically and functionally heterogeneous population that may enhance or inhibit B lymphopoiesis in the ileal PP.
回肠派尔集合淋巴结(PP)是羔羊B细胞产生和免疫球蛋白多样化的主要部位,但调节这些过程的因素却知之甚少。作为确定可能调节机制的第一步,在克隆水平上建立了回肠PP基质细胞的稳定长期培养物。通过其表型和生长需求鉴定出四种不同的细胞类型。免疫组织化学染色证实,所有克隆均起源于间充质(波形蛋白阳性;细胞角蛋白阴性),且对T细胞、B细胞和巨噬细胞标志物呈阴性。三个细胞系对主要组织相容性复合体(MHC)I和II分子呈阴性,但一个细胞系SCN表达MHC I、MHC II和CD44分子,并且SCN细胞的一个亚群表达B细胞分化分子BAQ44A。这四个细胞系产生不同类型和数量的细胞外基质蛋白,它们的生长不受外源性人白细胞介素1(IL-1)、IL-2、转化生长因子β1(TGFβ1)或牛成纤维细胞生长因子(FGF)的影响,但受血清影响。当测试它们支持淋巴细胞生长的能力时,所有克隆都产生了一种可溶性因子,该因子对回肠和空肠PP细胞以及胸腺细胞具有促有丝分裂作用。在小鼠、人和牛成纤维细胞的培养上清液中观察到类似的生长促进活性,但使用重组人细胞因子无法重现。此外,基质细胞与回肠PP滤泡B细胞共培养引发了每个基质细胞系独特的增殖反应。与数量增加的SCN细胞共培养会抑制B细胞增殖反应,而与SCG2和SCF32细胞共培养在低和高基质细胞密度下均增强B细胞增殖反应。回肠PP滤泡B细胞迅速结合到所有基质细胞克隆的表面,与胸腺细胞或外周血淋巴细胞相比,这种相互作用具有特异性。这些结果表明,回肠PP基质细胞是一个表型和功能异质性的群体,可能增强或抑制回肠PP中的B淋巴细胞生成。