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物理化学因子对小鼠表皮朗格汉斯细胞和Thy-1阳性树突状表皮细胞的影响。

Effects of physicochemical agents on murine epidermal Langerhans cells and Thy-1-positive dendritic epidermal cells.

作者信息

Aberer W, Romani N, Elbe A, Stingl G

出版信息

J Immunol. 1986 Feb 15;136(4):1210-6.

PMID:2868057
Abstract

The possibility that Thy-1-positive dendritic epidermal cells (Thy-1+DEC) may contribute to the immunologic functions of murine epidermal cells (EC) prompted us to simultaneously assess the effects of certain immunomodulating physicochemical agents on both Thy-1+DEC and Ia-bearing Langerhans cells (LC). C3H/He mice received one of the following treatment modalities: UV-B irradiation (four consecutive days); psoralen plus UV-A (PUVA; three times a week for three consecutive weeks); topically and systemically applied glucocorticosteroids (GCS). Beginning 2 days after the last treatment, animals were sacrificed and the structure and surface marker expression of Ia+EC and Thy-1+DEC were assessed by immunohistologic means on epidermal sheet preparations from ear skin by using appropriate monoclonal antibodies. Whereas low-dose UV-B irradiation (4 X 100 or 200 J/m2) had little, if any, effect on either Ia+EC or Thy-1+DEC, high-dose UV-B (4 X 700 or 1000 J/m2) or PUVA treatment led to an almost complete disappearance of both surface characteristics. Immunoelectron microscopic studies revealed that in the case of LC, high-dose UV-B or PUVA treatment results in the disappearance of their anti-Ia reactivity but leaves their ultrastructural morphology intact. In sharp contrast, Thy-1+DEC escape ultrastructural detection after PUVA treatment and are greatly reduced in number after high-dose UV-B. Ia+EC continuously reappeared with both treatment modalities over a course of 4 to 6 wk, whereas even after 14 to 22 wk Thy-1+DEC were present only in negligible numbers. Similar to high-dose UV-B or PUVA therapy, administration of GCS resulted in the disappearance of both anti-Thy-1- and anti-Ia-reactive cells. Ultrastructural studies disclosed, however, that these steroid-induced alterations in the surface characteristics were accompanied by a dramatic reduction of the LC population but were not paralleled by morphologic changes of Thy-1+DEC. In the course of 7 wk after cessation of steroid treatment, the number of both Ia+EC and Thy-1+DEC had returned to normal values. The selective removal of either of these two dendritic epidermal cell populations by physicochemical agents may provide an excellent strategy to further clarify the functional properties of both LC and Thy-1+DEC.

摘要

Thy-1阳性树突状表皮细胞(Thy-1+DEC)可能参与小鼠表皮细胞(EC)免疫功能的可能性,促使我们同时评估某些免疫调节理化因子对Thy-1+DEC和表达Ia的朗格汉斯细胞(LC)的影响。C3H/He小鼠接受以下治疗方式之一:UV-B照射(连续四天);补骨脂素加UV-A(PUVA;连续三周每周三次);局部和全身应用糖皮质激素(GCS)。在最后一次治疗后2天开始,处死动物,并使用适当的单克隆抗体通过免疫组织学方法在耳部皮肤的表皮片制备物上评估Ia+EC和Thy-1+DEC的结构和表面标志物表达。低剂量UV-B照射(4×100或200 J/m2)对Ia+EC或Thy-1+DEC几乎没有影响,而高剂量UV-B(4×700或1000 J/m2)或PUVA治疗导致这两种表面特征几乎完全消失。免疫电子显微镜研究表明,对于LC,高剂量UV-B或PUVA治疗导致其抗Ia反应性消失,但其超微结构形态保持完整。形成鲜明对比的是,PUVA治疗后Thy-1+DEC无法通过超微结构检测到,高剂量UV-B照射后其数量大幅减少。两种治疗方式在4至6周的过程中Ia+EC持续重新出现,而即使在14至22周后Thy-1+DEC的数量也仅可忽略不计。与高剂量UV-B或PUVA治疗相似,GCS给药导致抗Thy-1和抗Ia反应性细胞均消失。然而,超微结构研究表明,这些类固醇诱导的表面特征改变伴随着LC群体的显著减少,但Thy-1+DEC的形态学变化与之并不平行。在停止类固醇治疗后的7周内,Ia+EC和Thy-1+DEC的数量均恢复到正常水平。通过理化因子选择性去除这两种树突状表皮细胞群体中的任何一种,可能为进一步阐明LC和Thy-1+DEC的功能特性提供极佳策略。

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