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首页> 外文期刊>Eukaryotic cell >The Calcineurin Pathway Inhibitor Tacrolimus Enhances the In Vitro Activity of Azoles against Mucorales via Apoptosis
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The Calcineurin Pathway Inhibitor Tacrolimus Enhances the In Vitro Activity of Azoles against Mucorales via Apoptosis

机译:钙调神经磷酸途径抑制剂他克莫司通过凋亡提高了唑类化合物对粘膜炎的体外活性。

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The calcineurin pathway regulates antifungal drug resistance and the virulence of several major human-pathogenic fungi, including the recalcitrant Mucorales. We hypothesized that the fungistatic triazoles posaconazole (PCZ) and itraconazole (ICZ) become fungicidal in the setting of the calcineurin inhibitor tacrolimus (TCR) and that such an effect is mediated through apoptosis. Fungicidal activity and apoptosis were studied using standard microbiological techniques and hyphal metabolic and vital dye reduction assays at 37°C in RPMI 1640. Apoptosis was characterized by detecting intracellular Ca2+, phosphatidylserine (PS) externalization, DNA fragmentation, plasma membrane integrity, chromatin condensation, reactive oxygen species (ROS) generation, caspase-like activity, ATP, and cytochrome c release. MICs for PCZ and ICZ alone were significantly higher (8 to 128 μg/ml) than those of PCZ or ICZ plus TCR (0.25 to 4 μg/ml) for Rhizopus oryzae, Cunninghamella bertholletiae, and Mucor circinelloides. Both PCZ and ICZ in combination with TCR became fungicidal, and their activity was mediated through increased apoptotic cell death of R. oryzae (10 to 50%), C. bertholletiae (5 to 50%), and M. circinelloides (5 to 55%) germlings, with morphological apoptotic changes characterized by externalization of PS, nuclear condensation, and DNA fragmentation. Moreover, activation of the caspase-like activity was correlated with cell death induced by TCR plus PCZ or ICZ. These changes correlated with elevated intracellular Ca2+ and ROS levels and disturbance of mitochondrial potential. We found that PCZ or ICZ in combination with TCR renders Mucorales sensitive to triazoles via apoptotic death. These observations could serve as a new paradigm for the development of new therapeutic strategies.
机译:钙调神经磷酸酶途径调节抗真菌药物的耐药性和几种主要的人类致病真菌(包括顽固的毛霉菌)的毒性。我们假设在钙调神经磷酸酶他克莫司(TCR)的环境中,抑菌三唑泊沙康唑(PCZ)和伊曲康唑(ICZ)成为杀真菌剂,并且这种作用是通过凋亡介导的。在37°C的RPMI 1640中,使用标准的微生物学技术和菌丝代谢和活性染料还原分析研究了杀真菌活性和凋亡。碎片,质膜完整性,染色质凝聚,活性氧(ROS)生成,半胱天冬酶样活性,ATP和细胞色素 c 释放。单独使用PCZ和ICZ的MICs(8至128μg/ ml)明显高于米根霉,Cunninghamella bertholletiae和 Circucellollides的PCZ或ICZ加TCR(0.25至4μg/ ml) 。 PCZ和ICZ均与TCR结合成为杀真菌剂,其活性是通过增加 R的凋亡细胞死亡来介导的。稻(10%至5​​0%),伯氏梭菌(5%至50%)和圆环分枝杆菌(5%至55%)的幼苗,具有形态学上的凋亡变化,其特征是PS外在化,核浓缩和DNA片段化。此外,胱天蛋白酶样活性的激活与TCR加PCZ或ICZ诱导的细胞死亡相关。这些变化与细胞内Ca 2 + 和ROS水平升高以及线粒体电位干扰有关。我们发现将PCZ或ICZ与TCR结合使用可使Mucorales通过细胞凋亡对三唑类药物敏感。这些观察结果可以作为开发新治疗策略的新范例。

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