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全反式维甲酸可诱导人胆脂瘤上皮细胞培养物中的黏液纤毛分化。

All-trans retinoic acid induces mucociliary differentiation in a human cholesteatoma epithelial cell culture.

作者信息

Choi Jae Young, Cho Kyu-Nam, Yoon Joo-Heon

机构信息

Department of Otorhinolaryngology, Yonsei University College of Medicine, Seoul, South Korea.

出版信息

Acta Otolaryngol. 2004 Jan;124(1):30-5. doi: 10.1080/00016480310002104.

Abstract

OBJECTIVES

Retinoic acid (RA) can prevent keratin formation and induce mucous differentiation in epithelia. In this study, we attempted to induce keratinizing squamous epithelium from human cholesteatoma epithelial (HCE) cells using an air-liquid interface (ALI) technique. We also examined the effect of RA on the phenotype of keratinizing HCE cells.

MATERIAL AND METHODS

HCE cells were cultured in RA-free defined media at an ALI or in a submerged state. We examined the morphological differences between ALI and submerged cultures, and histologically investigated the changes of phenotype after RA treatment. We also determined the effect of RA on the mRNA expressions of the cornifin-alpha and mucin genes as indicators of squamous and mucous differentiation, respectively.

RESULTS

Using an ALI technique, we were able to differentiate HCE cells into a keratinizing squamous epithelium. When we treated the keratinizing HCE cells with RA, the morphological phenotype progressively changed into mucociliary epithelium. In addition, the expression of cornifin-alpha mRNA was suppressed, and the expressions of mucin gene 5AC (MUC5AC) and MUC5B mRNA increased progressively with RA treatment.

CONCLUSION

We successfully developed a culturing system for keratinizing differentiation of HCE cells using the ALI technique in a defined medium. Our study also clearly showed that RA treatment led to mucociliary differentiation of HCE cells.

摘要

目的

维甲酸(RA)可阻止角质形成并诱导上皮细胞黏液分化。在本研究中,我们尝试使用气液界面(ALI)技术诱导人胆脂瘤上皮(HCE)细胞形成角化鳞状上皮。我们还研究了RA对角化HCE细胞表型的影响。

材料与方法

将HCE细胞在无RA的限定培养基中以ALI方式或在浸没状态下培养。我们检查了ALI培养和浸没培养之间的形态学差异,并通过组织学方法研究了RA处理后细胞表型的变化。我们还分别测定了RA对作为鳞状分化和黏液分化指标的角蛋白α和黏蛋白基因mRNA表达的影响。

结果

使用ALI技术,我们能够将HCE细胞分化为角化鳞状上皮。当我们用RA处理角化的HCE细胞时,其形态表型逐渐转变为黏液纤毛上皮。此外,角蛋白α mRNA的表达受到抑制,随着RA处理,黏蛋白基因5AC(MUC5AC)和MUC5B mRNA的表达逐渐增加。

结论

我们成功地在限定培养基中利用ALI技术开发了一种用于HCE细胞角化分化的培养系统。我们的研究还清楚地表明,RA处理导致HCE细胞发生黏液纤毛分化。

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