Burmester G R, Jahn B, Rohwer P, Zacher J, Winchester R J, Kalden J R
J Clin Invest. 1987 Sep;80(3):595-604. doi: 10.1172/JCI113111.
The differential expression of Ia antigens was studied in freshly isolated rheumatoid nonlymphoid synovial lining cells (SLC) and rheumatoid synovial fibroblast cell lines cultured in the presence of Interferon-gamma, using a large panel of anti-Ia reagents with monomorphic or polymorphic specificities. All the HLA-DR or -DQ specificities detectable on the corresponding peripheral blood B cells were also expressed in freshly isolated SLC. However, in all instances, the number of DR-positive SLC exceeded the percentage of cells expressing DQ antigens. In addition, the epitope expression of Ia antigens varied within the DR or DQ populations of Ia molecules as revealed by polymorphic reagents. Double-label experiments or using the ingestion of Latex particles as a marker demonstrated that the synovial macrophages (type I SLC) primarily bear the DR+DQ+ phenotype, while there is an additional population of nonphagocytic SLC (previously termed type II SLC) that has a DR+ and monocyte marker negative phenotype but did not have detectable levels of DQ antigens as analyzed by both fluorescence microscopy and cell sorter analysis. This latter population frequently had a morphology showing dendritic processes and rapidly lost the expression of Ia antigens upon culture. Cells with a similar, primarily DR+ phenotype were readily obtained in synovial fibroblast cultures after treatment with Interferon-gamma. These data suggest that there are two populations of Ia+ synovial lining cells: the synovial macrophages (type I cells) with the DR+DQ+ phenotype, and cells probably related to fibroblasts with a DR+ phenotype without detectable DQ antigens (type II cells). The fact that the latter phenotype could be induced by Interferon-gamma treatment of cultured synovial fibroblasts suggests that this mediator may have a similar role in vivo in the activation of certain synovial cell populations.
使用大量具有单态或多态特异性的抗Ia试剂,研究了新鲜分离的类风湿性非淋巴细胞滑膜衬里细胞(SLC)和在γ干扰素存在下培养的类风湿性滑膜成纤维细胞系中Ia抗原的差异表达。在相应外周血B细胞上可检测到的所有HLA - DR或 - DQ特异性也在新鲜分离的SLC中表达。然而,在所有情况下,DR阳性SLC的数量超过表达DQ抗原的细胞百分比。此外,多态试剂显示,Ia抗原的表位表达在Ia分子的DR或DQ群体中有所不同。双标记实验或使用乳胶颗粒摄取作为标记表明,滑膜巨噬细胞(I型SLC)主要具有DR + DQ +表型,而存在另外一群非吞噬性SLC(以前称为II型SLC),其具有DR +且单核细胞标记阴性表型,但通过荧光显微镜和细胞分选分析均未检测到DQ抗原水平。后一群细胞的形态通常显示树突状突起,并且在培养后迅速失去Ia抗原的表达。用γ干扰素处理后,滑膜成纤维细胞培养物中很容易获得具有类似主要为DR +表型的细胞。这些数据表明,有两种Ia +滑膜衬里细胞群体:具有DR + DQ +表型的滑膜巨噬细胞(I型细胞),以及可能与成纤维细胞相关的具有DR +表型且未检测到DQ抗原的细胞(II型细胞)。后一种表型可通过γ干扰素处理培养的滑膜成纤维细胞诱导产生,这一事实表明该介质在体内可能对某些滑膜细胞群体的激活具有类似作用。