Danno K, Horio T
Br J Dermatol. 1985 Oct;113(4):391-6. doi: 10.1111/j.1365-2133.1985.tb02352.x.
The purpose of this study was to investigate whether 8-methoxypsoralen (8-MOP) plus long-wave ultraviolet (UV-A) light irradiation (PUVA) had a direct effect on the expression of epidermal cell and basement membrane zone (BMZ) markers without altering intracellular metabolic pathways. Cryostat sections of guinea-pig skin were covered with an 8-MOP solution and irradiated in vitro with UV-A light. Treated sections were stained subsequently with various membrane markers including pemphigus sera, pemphigoid sera (BMZ marker) and a group of biotin-labelled lectins (Concanavalin-A, peanut agglutinin, soybean agglutinin, Ulex europeus agglutinin (UEA) and wheat germ agglutinin). Fluorescent staining with all reagents except for UEA was reduced appreciably in intensity by PUVA radiation at higher energy doses (20 micrograms/ml of 8-MOP plus 20-30 J/cm2 of UV-A). Radiation with lower energy doses did not affect membrane marker staining. Weakened or abolished marker staining was restored to normal when scavengers of oxygen intermediates such as superoxide dismutase (540-5400 units/ml) or sodium azide (10-200 mM) were added to the 8-MOP solution during UV-A irradiation. UEA staining was negative in both PUVA-irradiated and untreated guinea-pig skin. PUVA at higher energy doses appeared to cause tissue damage by photodynamic reactions, resulting in decrease in membrane marker staining.
本研究的目的是调查8-甲氧基补骨脂素(8-MOP)加长波紫外线(UV-A)照射(PUVA)是否对表皮细胞和基底膜带(BMZ)标志物的表达有直接影响,而不改变细胞内代谢途径。将豚鼠皮肤的冰冻切片用8-MOP溶液覆盖,并在体外进行UV-A照射。随后用各种膜标志物对处理过的切片进行染色,包括天疱疮血清、类天疱疮血清(BMZ标志物)和一组生物素标记的凝集素(刀豆球蛋白A、花生凝集素、大豆凝集素、欧洲荆豆凝集素(UEA)和麦胚凝集素)。在较高能量剂量(20微克/毫升的8-MOP加20-30焦/平方厘米的UV-A)下,PUVA辐射使除UEA外的所有试剂的荧光染色强度明显降低。较低能量剂量的辐射不影响膜标志物染色。当在UV-A照射期间向8-MOP溶液中加入氧中间体清除剂如超氧化物歧化酶(540-5400单位/毫升)或叠氮化钠(10-200毫摩尔)时,减弱或消除的标志物染色恢复正常。在PUVA照射和未处理的豚鼠皮肤中,UEA染色均为阴性。较高能量剂量的PUVA似乎通过光动力反应导致组织损伤,从而导致膜标志物染色减少。