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角质形成细胞在质膜上组成性表达CD95配体分子:对正常人皮肤超低温切片的原位免疫电子显微镜研究。

Keratinocytes constitutively express the CD95 ligand molecule on the plasma membrane: an in situ immunoelectron microscopy study on ultracryosections of normal human skin.

作者信息

de Panfilis G, Semenza D, Lavazza A, Mulder A A, Mommaas A M, Pasolini G

机构信息

Section of Dermatology, Department of Surgery, Parmi, Italy.

出版信息

Br J Dermatol. 2002 Jul;147(1):7-12. doi: 10.1046/j.1365-2133.2002.04746.x.

Abstract

BACKGROUND

Tissue homeostasis is mainly preserved by cytolytic functions. Cytolytic cells, when expressing the CD95 ligand (Fas-L) molecule on the cell membrane, are able to kill CD95 (Fas)-expressing target cells. Although cultured epidermal keratinocytes (KC) have been shown to express Fas-L, and normal skin has been shown to bear Fas-L mRNA, efforts so far to find possible constitutive Fas-L expression on the cell membrane by resting KC in normal human epidermis (i.e. in a functionally active location) have been inconclusive.

OBJECTIVES

The aim of the present study was therefore to show the constitutive expression of Fas-L on the plasma membrane of KC.

METHODS

Gold immunoelectronmicroscopy, a highly specific and sensitive immunodetection system, was performed in situ on skin sections obtained by ultracryomicrotomy, without previous embedding (i.e. in conditions strictly similar to the in vivo situation).

RESULTS

Relatively few (51.55 +/- 28.61), 10-nm colloidal gold particles were observed at the cell surface of KC in the basal layer of the epidermis and an even smaller (P < 0.005) number of gold granules was detected in the KC of the spinous layer.

CONCLUSIONS

Although scanty, the constitutive Fas-L expressed on the surface of KC can bind Fas expressed by possible occasional inflammatory cells entering the epidermis, and kill them, so preventing inflammation. Fas-L-expressing KC could moreover induce apoptosis of epidermal cells bearing viral or neoplastic antigens. Thus, the expression of Fas-L by KC may contribute to the preservation of epidermal homeostasis in vivo.

摘要

背景

组织稳态主要通过细胞溶解功能来维持。细胞溶解细胞在细胞膜上表达CD95配体(Fas-L)分子时,能够杀死表达CD95(Fas)的靶细胞。尽管已显示培养的表皮角质形成细胞(KC)表达Fas-L,且正常皮肤含有Fas-L mRNA,但迄今为止,试图在正常人类表皮(即在功能活跃部位)的静息KC细胞膜上找到可能的组成性Fas-L表达的研究尚无定论。

目的

因此,本研究的目的是证明KC质膜上Fas-L的组成性表达。

方法

采用金免疫电子显微镜技术,这是一种高度特异且敏感的免疫检测系统,对经超薄冷冻切片术获得的皮肤切片进行原位检测,无需预先包埋(即处于与体内情况严格相似的条件下)。

结果

在表皮基底层的KC细胞表面观察到相对较少(51.55±28.61)的10纳米胶体金颗粒,在棘层的KC中检测到的金颗粒数量甚至更少(P<0.005)。

结论

尽管数量稀少,但KC表面组成性表达的Fas-L可与偶尔进入表皮的炎性细胞所表达的Fas结合并将其杀死,从而预防炎症。此外,表达Fas-L的KC可能诱导携带病毒或肿瘤抗原的表皮细胞凋亡。因此,KC表达Fas-L可能有助于在体内维持表皮稳态。

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