Lange-Wantzin G, Rothlein R, Kahn J, Faanes R B
J Immunol. 1987 Jun 1;138(11):3803-7.
The effect of UV-B irradiation on the expression of membrane-associated IL 1 (mIL 1) by rat pulmonary alveolar macrophages (PAM) was studied. We found that although there was an increase in secreted IL 1 by PAM exposed to UV-B, the expression of mIL 1 was inhibited in a dose-dependent manner. Furthermore, PAM that were allowed to express mIL 1 before UV-B irradiation had a faster decay of mIL 1 activity than unirradiated cells. These data suggested that mIL 1 expression is inhibited by UV-B irradiation, and that under normal circumstances, mIL 1 synthesis and degradation is at a steady state, with the half-life of mIL 1 activity being 24 hr when assayed in an IL 1-dependent cell line proliferation assay. These data indicate that secreted forms of IL 1 and mIL 1 are differentially regulated and that the therapeutic effects of UV irradiation may be due to its inhibition of mIL 1 activity.
研究了紫外线B(UV-B)照射对大鼠肺泡巨噬细胞(PAM)膜相关白细胞介素1(mIL-1)表达的影响。我们发现,虽然暴露于UV-B的PAM分泌的白细胞介素1有所增加,但mIL-1的表达却呈剂量依赖性抑制。此外,在UV-B照射前能够表达mIL-1的PAM,其mIL-1活性的衰减速度比未照射的细胞更快。这些数据表明,UV-B照射会抑制mIL-1的表达,并且在正常情况下,mIL-1的合成和降解处于稳定状态,在用依赖白细胞介素1的细胞系增殖试验进行检测时,mIL-1活性的半衰期为24小时。这些数据表明,白细胞介素1的分泌形式和mIL-1受到不同的调节,并且紫外线照射的治疗效果可能是由于其对mIL-1活性的抑制作用。