Costimulatory markers in muscle of patients with idiopathic inflammatory myopathies and in cultured muscle cells

被引:77
作者
Nagaraju, K [1 ]
Raben, N
Villalba, ML
Danning, C
Loeffler, LA
Lee, E
Tresser, N
Abati, A
Fetsch, P
Plotz, PH
机构
[1] NIAMSD, Arthrit & Rheumatism Branch, NIH, Bethesda, MD 20892 USA
[2] NINDS, NIH, Bethesda, MD 20892 USA
[3] NCI, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
myositis; human skeletal muscle cells; costimulatory molecules; CD28; CTLA4; CD86; CD40; CD154;
D O I
10.1006/clim.1999.4743
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In an attempt to understand the mechanisms of cell injury in the inflammatory myopathies, we analyzed the expression of costimulatory molecules, CTLA4, CD28, CD86, CD40, and CD154 as well as HLA class I, HLA class II, and ICAM-I in normal muscle and in muscle biopsies from patients with polymyositis (PM) or dermatomyositis (DM). By immunohistochemical staining, DM and PM: biopsies showed the presence of CTLA4, CD28, CD86, and CD40 on inflammatory cells. More strikingly, however, low levels of CTLA4 and CD28 were observed on muscle cells. The expression of CTLA4 and CD28 on nonlymphoid cells has not been previously reported. These unexpected findings were confirmed in cultured normal human myoblasts: various proinflammatory cytokines induced the expression of CTLA4 and CD28 on normal human muscle cells. The sequences of the cDNAs were found to be identical to the sequences for these molecules in T cells. The data suggest a novel complexity in the network of cellular interactions between the infiltrated immune cells and the muscle cells in which the normal relationship between infiltrating inflammatory cells and target tissue is under a previously unrecognized set of controls.
引用
收藏
页码:161 / 169
页数:9
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