未折叠蛋白反应是病原真菌的潜在治疗靶点。

Hao Zhou, Jinping Zhang, Rong Wang, Ju Huang, Caiyan Xin, Zhangyong Song
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摘要

致病性真菌感染引起显著的发病率和死亡率,特别是在免疫功能低下的患者中。多药耐药菌株的频繁出现挑战了现有的抗真菌疗法,推动了研究针对新分子部分的新型抗真菌药物的需求。病原真菌在自然栖息地和宿主体内受到各种环境压力,包括pH值、温度和药理作用。这些应激源增加了内质网(ER)内错误折叠或未折叠蛋白质产生的风险,如果不及时减轻,可能导致内质网内这些蛋白质的积累。这种积累引发内质网应激反应,潜在地危及真菌的生存。未折叠蛋白反应(unedprotein response, UPR)是内质网应激激活后恢复蛋白折叠稳态的重要细胞防御机制。近年来,普遍定期审查在病原真菌中的调节作用引起了极大的关注,特别是它参与真菌适应、毒力调节和耐药性。本文对真菌和哺乳动物的UPR进行了比较分析,并探讨了UPR作为病原真菌分子抗真菌靶点的潜在用途。通过阐明UPR在病原真菌中的特异性和调控功能,我们强调了寻找潜在抗真菌治疗靶点的新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The unfolded protein response is a potential therapeutic target in pathogenic fungi.

Pathogenic fungal infections cause significant morbidity and mortality, particularly in immunocompromised patients. The frequent emergence of multidrug-resistant strains challenges existing antifungal therapies, driving the need to investigate novel antifungal agents that target new molecular moieties. Pathogenic fungi are subjected to various environmental stressors, including pH, temperature, and pharmacological agents, both in natural habitats and the host body. These stressors elevate the risk of misfolded or unfolded protein production within the endoplasmic reticulum (ER) which, if not promptly mitigated, can lead to the accumulation of these proteins in the ER lumen. This accumulation triggers an ER stress response, potentially jeopardizing fungal survival. The unfolded protein response (UPR) is a critical cellular defense mechanism activated by ER stress to restore the homeostasis of protein folding. In recent years, the regulatory role of the UPR in pathogenic fungi has garnered significant attention, particularly for its involvement in fungal adaptation, regulation of virulence, and drug resistance. In this review, we comparatively analyze the UPRs of fungi and mammals and examine the potential utility of the UPR as a molecular antifungal target in pathogenic fungi. By clarifying the specificity and regulatory functions of the UPR in pathogenic fungi, we highlight new avenues for identifying potential therapeutic targets for antifungal treatments.

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