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人类胎儿肠道外植体培养物的HIV感染会诱导上皮细胞增殖。

HIV infection of human fetal intestinal explant cultures induces epithelial cell proliferation.

作者信息

Batman P A, Fleming S C, Sedgwick P M, MacDonald T T, Griffin G E

机构信息

Department of Histopathology, Bradford Royal Infirmary, UK.

出版信息

AIDS. 1994 Feb;8(2):161-7.

PMID:7913814
Abstract

OBJECTIVE

The concept that HIV infection per se alters small intestinal mucosal structure and function (HIV enteropathy) remains controversial and in this study we report in vitro experiments designed to elucidate the matter.

METHODS

Twenty pairs of human fetal intestinal tissue explants were maintained in vitro for up to 14 days; one explant of each pair was incubated and infected with HIV, and the other served as a matched uninfected control. At various times after infection, explant culture fluid and tissue were removed, p24 concentration was measured and tissue formalin fixed. Explant tissue was embedded in paraffin wax and sections stained by an immunoperoxidase method directed against proliferating cell nuclear antigen (PCNA). The percentage of proliferating crypt and villous epithelial cells, stained by PCNA, was calculated in paired samples. The difference between the percentage for paired samples was designated delta crypt proliferation (delta CP) and delta villous proliferation (delta VP), respectively. Epithelial cell proliferation was deemed to be enhanced if the percentage of PCNA-stained cells was greater in the HIV-infected than in the control tissue.

RESULTS

Explant culture fluid from tissue exposed to HIV showed a progressive rise in p24 antigen (Ag) level, indicating HIV infection of these explants. Fifteen pairs of explants showed progressively positive delta CP with time (P < 0.01) indicating crypt hyperplasia and all 20 pairs of explants showed positive delta VP, indicating hyperplasia of villous epithelial cells.

CONCLUSIONS

This study provides direct evidence that HIV stimulates epithelial cell proliferation in intestinal mucosa. HIV-infected human intestinal explants provide a model of crypt hyperplastic villous atrophy previously described as HIV enteropathy and detected in clinical biopsy specimens from HIV-infected patients.

摘要

目的

HIV感染本身会改变小肠黏膜结构和功能(HIV肠病)这一概念仍存在争议,在本研究中,我们报告了旨在阐明该问题的体外实验。

方法

将20对人胎儿肠道组织外植体在体外培养长达14天;每对中的一个外植体进行孵育并感染HIV,另一个作为配对的未感染对照。在感染后的不同时间,取出外植体培养液和组织,测量p24浓度并将组织用福尔马林固定。将外植体组织包埋在石蜡中,切片用针对增殖细胞核抗原(PCNA)的免疫过氧化物酶方法染色。计算配对样本中经PCNA染色的隐窝和绒毛上皮增殖细胞的百分比。配对样本百分比之间的差异分别称为隐窝增殖差异(δCP)和绒毛增殖差异(δVP)。如果HIV感染组织中PCNA染色细胞的百分比高于对照组织,则认为上皮细胞增殖增强。

结果

暴露于HIV的组织的外植体培养液显示p24抗原(Ag)水平逐渐升高,表明这些外植体被HIV感染。15对外植体随时间显示出逐渐增加的阳性δCP(P < 0.01),表明隐窝增生,所有20对外植体均显示阳性δVP,表明绒毛上皮细胞增生。

结论

本研究提供了直接证据,证明HIV刺激肠道黏膜上皮细胞增殖。感染HIV的人肠道外植体提供了一种隐窝增生性绒毛萎缩模型,该模型先前被描述为HIV肠病,并在HIV感染患者的临床活检标本中检测到。

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