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17β-雌二醇抑制雌激素结合蛋白介导的白色念珠菌菌丝形成。

17β-Estradiol inhibits estrogen binding protein-mediated hypha formation in Candida albicans.

作者信息

Kurakado Sanae, Kurogane Rie, Sugita Takashi

机构信息

Department of Microbiology, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo, 204-8588, Japan.

Department of Microbiology, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo, 204-8588, Japan.

出版信息

Microb Pathog. 2017 Aug;109:151-155. doi: 10.1016/j.micpath.2017.05.038. Epub 2017 May 25.

Abstract

Candida albicans is one of the most prevalent and clinically important fungal pathogens. The ability to change form depending on environmental stress is an important microbial virulence factor. A survey of compounds that inhibit this morphological change identified various steroids, including 17β-estradiol. Interestingly, C. albicans has proteins capable of binding to steroids, including estrogen binding protein (Ebp1). Estrogens regulate cell differentiation and proliferation in humans through estrogen receptor proteins. To determine whether EBP1 regulates a virulence factor, we investigated the effect of 17β-estradiol on the morphological transition of C. albicans using an ebp1 deletion mutant. Treatment with 10 μg/mL of 17β-estradiol inhibited hypha formation, whereas its effect on the ebp1 deletion mutant was decreased compared to that on the wild-type and revertant strains. These data suggest a new pathway for the yeast-to-hypha transition via EBP1 in C. albicans.

摘要

白色念珠菌是最常见且临床上最重要的真菌病原体之一。根据环境压力改变形态的能力是一种重要的微生物毒力因子。一项对抑制这种形态变化的化合物的调查确定了各种类固醇,包括17β-雌二醇。有趣的是,白色念珠菌具有能够结合类固醇的蛋白质,包括雌激素结合蛋白(Ebp1)。雌激素通过雌激素受体蛋白调节人类细胞的分化和增殖。为了确定EBP1是否调节一种毒力因子,我们使用ebp1缺失突变体研究了17β-雌二醇对白色念珠菌形态转变的影响。用10μg/mL的17β-雌二醇处理可抑制菌丝形成,而与野生型和回复菌株相比,其对ebp1缺失突变体的影响有所降低。这些数据表明白色念珠菌中通过EBP1实现酵母到菌丝转变的新途径。

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