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CD95(APO-1/Fas)介导的结肠上皮细胞凋亡:在溃疡性结肠炎中的可能作用。

CD95 (APO-1/Fas)-mediated apoptosis in colon epithelial cells: a possible role in ulcerative colitis.

作者信息

Sträter J, Wellisch I, Riedl S, Walczak H, Koretz K, Tandara A, Krammer P H, Möller P

机构信息

Department of Pathology, University of Ulm, Germany.

出版信息

Gastroenterology. 1997 Jul;113(1):160-7. doi: 10.1016/s0016-5085(97)70091-x.

Abstract

BACKGROUND & AIMS: Ligation of CD95 (APO-1/Fas) by antibody or CD95 ligand (CD95L) induces apoptosis and, in some cell lines, growth. Normal colonic epithelial cells constitutively express CD95. The function of CD95 on colonocytes is unknown. The aim of this study was to elucidate the role of epithelial CD95 in the normal colon and in ulcerative colitis.

METHODS

Intact colonic crypts were isolated, and the effects of CD95 ligation in vitro were studied. CD95L-expressing cells and apoptotic cells were detected in situ by RNA hybridization, immunohistochemistry, and DNA nick end labeling.

RESULTS

On CD95 ligation, isolated colonic crypt cells underwent apoptosis within 4 hours. No growth-promoting effect was observed. In normal colon, CD95L expression was restricted to few mononuclear cells randomly scattered within the lamina propria. Therefore, the CD95-CD95L system is very unlikely to operate in the regeneration of the colonic epithelium. However, in ulcerative colitis, the number of interstitial CD95L+ cells and the frequency of apoptosis in both lamina propria and epithelium were increased considerably. Further, a focal association of subepithelial CD95L+ mononuclear cells and epithelial apoptosis was observed.

CONCLUSIONS

In ulcerative colitis, soluble CD95L-mediated epithelial apoptosis may lead to a breakdown of the epithelial barrier function facilitating the invasion of pathogenic microorganisms.

摘要

背景与目的

用抗体或CD95配体(CD95L)连接CD95(APO-1/Fas)可诱导细胞凋亡,在某些细胞系中还可诱导生长。正常结肠上皮细胞组成性表达CD95。CD95在结肠细胞上的功能尚不清楚。本研究的目的是阐明上皮CD95在正常结肠和溃疡性结肠炎中的作用。

方法

分离完整的结肠隐窝,研究体外CD95连接的作用。通过RNA杂交、免疫组织化学和DNA缺口末端标记原位检测表达CD95L的细胞和凋亡细胞。

结果

连接CD95后,分离的结肠隐窝细胞在4小时内发生凋亡。未观察到促生长作用。在正常结肠中,CD95L表达仅限于固有层内随机散在的少数单核细胞。因此,CD95-CD95L系统极不可能在结肠上皮再生中起作用。然而,在溃疡性结肠炎中,固有层和上皮中间质CD95L+细胞的数量以及凋亡频率均显著增加。此外,观察到上皮下CD95L+单核细胞与上皮凋亡的局灶性关联。

结论

在溃疡性结肠炎中,可溶性CD95L介导的上皮凋亡可能导致上皮屏障功能破坏,促进致病微生物的侵袭。

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