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人类白细胞抗原-DR分子在表皮朗格汉斯细胞和外分泌汗腺导管细胞上的细胞表面分布差异。

Differing cell surface distribution of human leukocyte antigen-DR molecules on epidermal Langerhans cells and eccrine duct cells.

作者信息

Imayama S, Yashima Y, Hori Y

机构信息

Department of Dermatology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

J Histochem Cytochem. 1992 Aug;40(8):1191-6. doi: 10.1177/40.8.1619281.

Abstract

Scanning electron microscopy (SEM) with immunogold labeling was employed to observe the undersurface of the human epidermis after it was split from dermal connective tissue, in an attempt to localize the molecules actually expressed on cell/tissue surfaces. We found that human leukocyte antigen-DR (HLA-DR) molecules were expressed on the surfaces of eccrine duct cells as well as those of epidermal Langerhans cells (LC) in normal skin. HLA-DR molecules, visualized by the deposition of gold particles, were distributed evenly on the LC surface but were present only along the interdigitating borders of the individual duct cells, thus producing a meshwork pattern on the duct surface. Transmission electron microscopy confirmed that the gold particles labeling cell surface HLA-DR molecules were seen only on the portions of duct cell membranes the interdigitated with neighboring duct cells. These findings suggest that the function of HLA-DR molecules may vary with their location and distribution. On the LC surface, the evenly distributed molecules seem to be well suited for promoting "accessory cell" functions. On duct cell surfaces, the HLA-DR molecules present along the intercellular spaces may be involved in trapping various peptide antigens that pass into the sweat gland filtrate and then are reabsorbed by the excretory duct, since these molecules have a highly permissive capacity for binding various peptides.

摘要

采用免疫金标记扫描电子显微镜(SEM)观察从真皮结缔组织分离后的人表皮下表面,试图定位细胞/组织表面实际表达的分子。我们发现,在正常皮肤中,人类白细胞抗原-DR(HLA-DR)分子在小汗腺导管细胞表面以及表皮朗格汉斯细胞(LC)表面均有表达。通过金颗粒沉积可视化的HLA-DR分子在LC表面均匀分布,但仅沿单个导管细胞的指状边界存在,从而在导管表面形成网状图案。透射电子显微镜证实,标记细胞表面HLA-DR分子的金颗粒仅见于与相邻导管细胞相互交错的导管细胞膜部分。这些发现表明,HLA-DR分子的功能可能随其位置和分布而变化。在LC表面,均匀分布的分子似乎非常适合促进“辅助细胞”功能。在导管细胞表面,沿细胞间隙存在的HLA-DR分子可能参与捕获进入汗腺滤液然后被排泄导管重新吸收的各种肽抗原,因为这些分子具有高度允许结合各种肽的能力。

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