Ikai K, Danno K, Horio T, Narumiya S
J Invest Dermatol. 1985 Jul;85(1):82-4. doi: 10.1111/1523-1747.ep12275365.
The effect of UV irradiation on the skin was investigated in (WB-W/+) X (C57BL/6J-Wv/+)F1-W/Wv mice, which are genetically deficient in tissue mast cells. Their congenic littermates (+/+) and normal albino mice (ICR or BALB/c) were used as controls. Mice were irradiated with 500 mJ/cm2 of UVB and the increment of ear thickness was measured before and 6, 12, and 24 h after irradiation. Ear swelling in W/Wv mice at 12 and 24 h after irradiation was significantly smaller than that in +/+ and ICR mice. In contrast, the number of sunburn cells formed 24 h after UVB irradiation (200 or 500 mJ/cm2) was similar in W/Wv, +/+ and ICR mice. On the other hand, when mice were treated with 8-methoxy-psoralen (0.5%) plus UVA irradiation (4 J/cm2) (topical PUVA), ears of W/Wv and BALB/c mice, which were both white in color, were thickened similarly 72 h after treatment, but less swelling was observed in +/+ mice, which were black in skin color. The amount of prostaglandin D2 (PGD2) in ears, determined by radioimmunoassay specific for PGD2, was elevated 3-fold in +/+ and ICR mice at 3 h after irradiation with 500 mJ/cm2 of UVB in comparison with basal level without irradiation. However, such elevation was not observed in W/Wv mice. These results suggest that mast cells play an important role in UVB-induced inflammation, and PGs from mast cells are responsible at least in part for the development of this reaction. However, neither mast cells nor PGs contribute to the sunburn cell formation and ear swelling response by PUVA treatment.
在组织肥大细胞基因缺陷的(WB-W/+)×(C57BL/6J-Wv/+)F1-W/Wv小鼠中研究了紫外线照射对皮肤的影响。将其同基因的同窝小鼠(+/+)和正常白化小鼠(ICR或BALB/c)用作对照。用500 mJ/cm2的UVB照射小鼠,并在照射前以及照射后6、12和24小时测量耳厚度的增加。照射后12和24小时,W/Wv小鼠的耳部肿胀明显小于+/+和ICR小鼠。相反,UVB照射(200或500 mJ/cm2)24小时后形成的晒伤细胞数量在W/Wv、+/+和ICR小鼠中相似。另一方面,当用8-甲氧基补骨脂素(0.5%)加UVA照射(4 J/cm2)(外用PUVA)处理小鼠时,W/Wv和BALB/c小鼠(均为白色)的耳朵在处理后72小时增厚程度相似,但在皮肤为黑色的+/+小鼠中观察到的肿胀较小。通过对PGD2特异的放射免疫测定法测定,与未照射的基础水平相比,用500 mJ/cm2的UVB照射3小时后,+/+和ICR小鼠耳部的前列腺素D2(PGD2)量升高了3倍。然而,在W/Wv小鼠中未观察到这种升高。这些结果表明,肥大细胞在UVB诱导的炎症中起重要作用,并且肥大细胞产生的PGs至少部分负责这种反应的发展。然而,肥大细胞和PGs均不参与PUVA处理引起的晒伤细胞形成和耳部肿胀反应。