紫外线辐射对角质形成细胞Ia表达的影响。

Photo-dermatology Pub Date : 1989-12-01
L K Roberts, B D Jun, A Gilhar, R V Anglin, J Corlett, M Emam, G G Krueger
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引用次数: 0

摘要

许多皮肤病,如移植物抗宿主病(GVHD),以皮肤淋巴细胞浸润为标志。这些疾病的严重程度通常与II类抗原(人、HLA-DR、;小鼠,Ia)通过角质形成细胞。这表明表达hla - dr的角质形成细胞可能参与了这些疾病的发病机制。由于其中一些疾病可以用紫外线辐射(UVR)有效治疗,因此本研究旨在确定UVR是否会改变II类抗原的角质细胞表达。为了验证这一假设,我们采用了2种实验诱导的角质形成细胞Ia表达模型。首先,将胸腺裸小鼠的一只耳朵用电工胶带保护,连续4天暴露在紫外线下(450j /m2/天)。然后静脉注射正常小鼠血清(NMS)诱导角质形成细胞Ia的表达。暴露在uvr下的动物皮肤中的角质形成细胞未被诱导表达Ia;然而,在被屏蔽的皮肤部位的表皮中观察到表达ia的角质形成细胞。同样,我们确定在裸鼠注射NMS后7天,UVR能够下调角质形成细胞Ia的表达。其次,通过临床相关的模型,我们发现在实验诱导的GVHD小鼠中,角化细胞的Ia表达被UVR治疗所消除。这似乎是UVR的直接作用,因为GVHD动物的屏蔽皮肤部位的角化细胞和肠上皮粘膜细胞显示表达Ia。这些数据为我们的假设提供了强有力的证据,即UVR治疗病变皮肤中角质形成细胞HLA-DR表达的降低是UVR发挥其治疗作用的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of ultraviolet radiation on Ia expression by keratinocytes.

Many skin diseases, such as graft-versus-host disease (GVHD), are marked by lymphocyte infiltrates in the skin. Severity of these diseases is often correlated with the induced expression of class II antigens (human, HLA-DR,; murine, Ia) by the keratinocytes. This suggests that HLA-DR-expressing keratinocytes may be involved in the pathogenesis of these diseases. Since some of these diseases are effectively treated with ultraviolet radiation (UVR), this study was conducted to determine whether UVR alters the keratinocyte expression of class II antigens. To test this hypothesis, 2 models of experimentally induced keratinocyte Ia expression were employed. First, athymic nude mice with one ear protected by electrical tape were exposed to UVR (450 J/m2/day on 4 consecutive days). They were then given an i.v. injection of normal mouse serum (NMS) to induce keratinocyte Ia expression. Keratinocytes in the UVR-exposed skin of these animals were not induced to express Ia; however, Ia-expressing keratinocytes were observed in the epidermis of shielded skin sites. Likewise, it was determined that UVR was capable of downregulating keratinocyte expression of Ia when administered to nude mice 7 d after receiving an injection of NMS. Second, employing a clinically relevant model, we found that Ia expression by keratinocytes in mice undergoing experimentally induced GVHD was abrogated by UVR treatment. This appeared to be a direct effect of the UVR, since keratinocytes in shielded skin sites and mucosal cells in the intestinal epithelium of animals with GVHD were shown to express Ia. These data provide compelling evidence for our hypothesis that decreased HLA-DR expression by keratinocytes in diseased skin treated with UVR is a mechanism by which UVR exerts its therapeutic effect.

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