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紫外线A(UVA)和紫外线B(UVB)照射对通过ATP酶活性及单克隆抗体(OKT 6和抗Ia)所界定的人表皮朗格汉斯细胞膜标志物的影响。

Effect of UVA and UVB irradiation on human epidermal Langerhans cell membrane markers defined by ATPase activity and monoclonal antibodies (OKT 6 and anti-Ia).

作者信息

Koulu L, Jansén C T, Viander M

出版信息

Photodermatol. 1985 Dec;2(6):339-46.

PMID:2937025
Abstract

Healthy human volunteers were irradiated with graded doses of UVA and UVB radiation on the volar aspect of their forearms. The UVA doses ranged from 8 to 100 J/cm2, and the UVB doses from 37 to 416 mJ/cm2, corresponding to 5 to 52 mJ/cm2 of erythemally effective (300 nm) radiation (1/4-3 X MED). 7 days after irradiation, punch biopsy specimens were obtained from UVA and UVB irradiated spots. Epidermal sheets were stained for Langerhans cells (LC) using 3 different histochemical methods, viz: ATPase activity and immunoperoxidase staining with monoclonal antibodies against T6 and Ia antigens. A slightly higher control LC count was obtained with anti-T6 staining (848 cells/mm2) than with anti-Ia or ATPase staining (728 and 721 cells/mm2 respectively). No significant change in LC count was detected with any of the staining methods after UVA doses of up to 100 J/cm2. In contrast, UVB irradiation caused a dose-dependent decrease in the LC counts. The decrease was quite similar whether measured by anti-T6 or anti-Ia staining. With ATPase staining, the decrease in LC numbers was somewhat more pronounced at low to medium UVB doses, but at the dose of 416 mJ/cm2 (52 mJ of erythemally effective UVB, corresponding to approx. 3 X MED), the residual LC count as determined with any of the 3 histochemical methods was within the range of 23-30% of the control LC count. We conclude that the activity of the membrane-bound enzyme, ATPase, is more sensitive to abrogation by moderate UVB doses than the immunological reactivity of the 2 surface antigens, T6 and Ia.

摘要

健康人类志愿者的前臂掌侧接受了不同剂量的UVA和UVB辐射。UVA剂量范围为8至100 J/cm²,UVB剂量范围为37至416 mJ/cm²,相当于5至52 mJ/cm²的红斑有效(300 nm)辐射(1/4 - 3倍最小红斑量)。照射7天后,从UVA和UVB照射部位获取打孔活检标本。使用3种不同的组织化学方法对表皮片进行朗格汉斯细胞(LC)染色,即:ATP酶活性以及用抗T6和Ia抗原的单克隆抗体进行免疫过氧化物酶染色。抗T6染色获得的对照LC计数(848个细胞/mm²)略高于抗Ia或ATP酶染色(分别为728个和721个细胞/mm²)。在UVA剂量高达100 J/cm²后,用任何一种染色方法均未检测到LC计数有显著变化。相比之下,UVB照射导致LC计数呈剂量依赖性下降。无论通过抗T6还是抗Ia染色测量,下降情况都非常相似。用ATP酶染色时,在低至中等UVB剂量下LC数量的下降更为明显,但在416 mJ/cm²(52 mJ的红斑有效UVB,相当于约3倍最小红斑量)的剂量下,用3种组织化学方法中的任何一种测定的残余LC计数在对照LC计数的23% - 30%范围内。我们得出结论,膜结合酶ATP酶的活性比两种表面抗原T6和Ia的免疫反应性对中等剂量UVB的消除更敏感。

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