Wang B, Dong X, Yuan Z, Zuo Y, Wang J
Department of Dermatology, Peking Union Medical College Hospital, Beijing 100730, China.
Chin Med J (Engl). 1999 Jun;112(6):512-5.
To better understand the potential effect of ultraviolet light on the photosensitivity of patients with lupus erythematosus (LE), to elucidate the mechanisms of SSA/Ro antibody formation after UV exposure, and to investigate the role of this autoantibody in the pathogenesis of skin lesions.
Primary human keratinocytes were cultured in Medium-154. After ultraviolet-B light (UVB) irradiation, the keratinocytes were treated with affinity-purified anti-SSA/Ro sera and stained with FITC-labeled goat-anti-human IgG and propidium iodide (PI), followed by enzyme digestion with RNase, RNase-free DNase or RNase plus DNase. As target cells, the irradiated keratinocytes were incubated with affinity-purified anti-SSA/Ro sera, with or without fresh human sera as complement. The supernatants of irradiated keratinocytes were analyzed with ELISA method for SSA/Ro antigens.
UVB irradiation induced apoptotic blebs on the cell surface. The blebs were composed of ribonucleoproteins and contained SSA/Ro antigens. SSA/Ro antigens expressed on UVB irradiated keratinocytes bound to affinity-purified anti-SSA/Ro sera, leading to complement-dependent cytotoxicity. However, no SSA/Ro antigens were detected in the supernatants.
SSA/Ro, a ribonucleoprotein antigen expressed on UVB irradiated keratinocytes, may be recognized and presented to immune cells by a direct cell-cell contact other than be eliminated into the circulation.
为了更好地理解紫外线对红斑狼疮(LE)患者光敏性的潜在影响,阐明紫外线照射后SSA/Ro抗体形成的机制,并研究这种自身抗体在皮肤病变发病机制中的作用。
原代人角质形成细胞在154培养基中培养。用紫外线B(UVB)照射后,角质形成细胞用亲和纯化的抗SSA/Ro血清处理,并用异硫氰酸荧光素(FITC)标记的山羊抗人IgG和碘化丙啶(PI)染色,随后用核糖核酸酶(RNase)、无RNase的脱氧核糖核酸酶(DNase)或RNase加DNase进行酶消化。作为靶细胞,将照射后的角质形成细胞与亲和纯化的抗SSA/Ro血清一起孵育,有无新鲜人血清作为补体。用酶联免疫吸附测定(ELISA)法分析照射后角质形成细胞上清液中的SSA/Ro抗原。
UVB照射诱导细胞表面出现凋亡小泡。这些小泡由核糖核蛋白组成,并含有SSA/Ro抗原。UVB照射的角质形成细胞上表达的SSA/Ro抗原与亲和纯化的抗SSA/Ro血清结合,导致补体依赖性细胞毒性。然而,在上清液中未检测到SSA/Ro抗原。
UVB照射的角质形成细胞上表达的核糖核蛋白抗原SSA/Ro可能通过直接的细胞间接触被识别并呈递给免疫细胞,而不是被释放到循环中。