Bou-Gharios G, Osman J, Atherton A, Monoghan P, Vancheeswaran R, Black C, Olsen I
Cell Enzymology Unit, Kennedy Institute of Rheumatology, London, United Kingdom.
Ann Rheum Dis. 1995 Feb;54(2):111-6. doi: 10.1136/ard.54.2.111.
To examine the expression and concentrations of three ectopeptidases likely to be involved in regulating the functional levels of adhesion molecules and the turnover of connective tissue components, in patients with scleroderma (systemic sclerosis) (SSc) and in normal individuals.
Monoclonal antibodies against these antigens were used for immunoperoxidase staining of cryostat skin sections and for flow cytometric (fluorescence activated cell sorter) analysis of cultured dermal fibroblasts grown from SSc patients and normal controls.
Although neutral endopeptidase-24.11 (NEP) (CD10) was not detected in either SSc or normal skin, aminopeptidase N (APN) (CD13) and dipeptidyl peptidase IV (DPPIV) (CD26) were both readily visualised. However, DPPIV appeared to be present in smaller concentrations in the SSc biopsy specimens. Moreover, while fibroblasts grown in vitro from both SSc and normal skin also had similar concentrations of APN, the expression of DPPIV in the cultured SSc cells was found to be very much less than that present in the normal fibroblasts. It is noteworthy that NEP, which was not detected in the tissue sections, was nevertheless readily detected in fibroblasts in culture.
These results show that a number of cell surface proteases are expressed by dermal fibroblasts both in vivo and in vitro, and it is suggested that the marked downregulation of DPPIV in SSc could be at least partly responsible for the increased concentrations of adhesion molecules and matrix proteins associated with the molecular pathology of this disease.
检测三种可能参与调节黏附分子功能水平和结缔组织成分周转的外肽酶在硬皮病(系统性硬化症,SSc)患者和正常个体中的表达及浓度。
使用针对这些抗原的单克隆抗体对低温保存的皮肤切片进行免疫过氧化物酶染色,并对从SSc患者和正常对照者培养的真皮成纤维细胞进行流式细胞术(荧光激活细胞分选仪)分析。
尽管在SSc皮肤和正常皮肤中均未检测到中性内肽酶-24.11(NEP)(CD10),但氨肽酶N(APN)(CD13)和二肽基肽酶IV(DPPIV)(CD26)均易于观察到。然而,DPPIV在SSc活检标本中的浓度似乎较低。此外,虽然从SSc皮肤和正常皮肤体外培养的成纤维细胞中APN的浓度相似,但发现培养的SSc细胞中DPPIV的表达远低于正常成纤维细胞。值得注意的是,在组织切片中未检测到的NEP,在培养的成纤维细胞中却易于检测到。
这些结果表明,真皮成纤维细胞在体内和体外均表达多种细胞表面蛋白酶,并且提示SSc中DPPIV的显著下调可能至少部分导致了与该疾病分子病理学相关的黏附分子和基质蛋白浓度增加。