首页> 外文期刊>Journal of Medical Virology >HPV-DNA is not detectable in outgrowing cells from explant cultures of skin lesions established at the air-liquid-interface.
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HPV-DNA is not detectable in outgrowing cells from explant cultures of skin lesions established at the air-liquid-interface.

机译:在气液界面处建立的皮肤损伤的外植体培养物中,在外生细胞中无法检测到HPV-DNA。

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摘要

Keratinocyte cultures established from HPV containing skin cancers were described earlier to lose their HPV DNA after passaging in vitro. A different approach was therefore used in this study. Explant cultures were generated by depositing small pieces of various benign and (pre)malignant skin specimens of renal transplant recipients and non-immunosuppressed patients on fibroblast-populated collagen lattices or on de-epidermized dermis. Subsequently, the cultures were maintained at the air-liquid interface. At various time points, samples were collected for both HPV analysis, using a nested PCR approach, and morphology. The outgrowing keratinocytes developed into multilayered epithelial structures showing terminal differentiation. No histological differences were observed between cultures established from HPV positive and negative lesions. Eighteen biopsy specimens were tested for their HPV content before and after culture. Before culture 11 out of these skin specimens contained DNA of the Epidermodysplasia Verruciformis-related HPV types (EV-HPV). Comparison of the HPV types detected in two different parts of the same skin specimen before culture was strongly suggestive for a non-homogeneous distribution of EV-HPV in the lesions. From the explant cultures derived from the 11 HPV-positive biopsies, 31 samples from the originally explanted pieces of tissue and 38 samples from the outgrowing multilayered epithelial sections were collected. HPV DNA was detected in 10 of the 31 and in 3 of the 38 samples (Chi-square test, P = 0.01), respectively. These results indicate that EV-HPV positive keratinocytes do not efficiently proliferate or lose their HPV DNA in this culture system or EV-HPV DNA is present in only a few basal cells, making it improbable that these cells are located at the outgrowing margins. Copyright 2000 Wiley-Liss, Inc.
机译:先前描述了从含有HPV的皮肤癌中建立的角质形成细胞培养物在体外传代后会丢失其HPV DNA。因此,本研究使用了不同的方法。外植体培养物是通过将肾移植受者和非免疫抑制患者的各种良性和(恶性)皮肤样本的小块放置在成纤维细胞填充的胶原蛋白晶格或去表皮的真皮上而产生的。随后,将培养物保持在气-液界面。在不同的时间点,使用巢式PCR方法收集样品进行HPV分析,并进行形态学分析。向外生长的角质形成细胞发展成多层上皮结构,显示出终末分化。从HPV阳性和阴性病变建立的培养物之间未观察到组织学差异。培养前后分别检查了18个活检标本的HPV含量。在培养之前,这些皮肤样本中有11个含有与疣状表皮发育相关的HPV类型(EV-HPV)的DNA。培养前在同一皮肤样本的两个不同部位检测到的HPV类型的比较强烈提示EV-HPV在病变中的分布不均匀。从源自11例HPV阳性活检组织的外植体培养物中,收集了31份来自最初植入的组织切片的样品和38份来自向外生长的多层上皮切片的样品。在31个样品中的10个和38个样品中的3个中分别检测到HPV DNA(卡方检验,P = 0.01)。这些结果表明,EV-HPV阳性角质形成细胞在该培养系统中不能有效增殖或丢失其HPV DNA,或者EV-HPV DNA仅存在于少数基础细胞中,因此不可能将这些细胞定位在向外生长的边缘。版权所有2000 Wiley-Liss,Inc.

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