Cellular apoptosis: An alternative mechanism of action for caspofungin against Candida glabrata

Cellular apoptosis: An alternative mechanism of action for caspofungin against Candida glabrata


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دانشگاه علوم پزشکی تبریز
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نویسندگان: نرگس اصلانی

کلمات کلیدی: Candida glabrata, Caspofungin, Flow cytometry, MCA1, NUC1

نشریه: 0 , 2 , 5 , 2019

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نویسنده ثبت کننده مقاله نرگس اصلانی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه بیماری های عفونی و گرمسیری
کد مقاله 67792
عنوان فارسی مقاله Cellular apoptosis: An alternative mechanism of action for caspofungin against Candida glabrata
عنوان لاتین مقاله Cellular apoptosis: An alternative mechanism of action for caspofungin against Candida glabrata
ناشر 9
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق) Current Medical Mycology
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح دو – PMC
آدرس لینک مقاله/ همایش در شبکه اینترنت

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Background and Purpose: Although the mechanism of action for echinocandins is known, the physiological mechanisms by which these antifungal agents cause cell death via the classical apoptotic pathways are not well-defined yet. Regarding this, the present study aimed to evaluate the mechanisms of caspofungin-induced Candida glabrata cell death. Materials and Methods: For the purpose of the study, the minimum inhibitory concentration (MIC) of caspofungin against C. glabrata (ATCC 90030) was determined using the broth microdilution reference method (CLSI M27-A2 and M27-S4). The annexin V and propidium iodide staining was performed to determine the way through which caspofungin acts against C. glabrata (i.e., through the induction of apoptosis and/or necrosis). Additionally, the possible effect of caspofungin on inducing the expression of two apoptotic genes, namely MCA1 and NUC, was studied using the realtime polymerase chain reaction assay. Results: According to the obtained MIC value (0.5 µg/mL), C. glabrata, exposed to 0.25, 0.5, and 1 µg/mL of caspofungin, exhibited the features of late apoptosis/necrosis after 18 h of incubation. Furthermore, the use of 0.25, 0.5, and 1 µg/ml caspofungin induced apoptosis (early/late) in 14.67%, 17.04%, and 15.89% of the cells, respectively. The results showed a significant difference between the percentages of early-apoptotic cells at the three concentrations (P<0.05). In addition, the rate of necrosis was significantly greater than that of apoptosis in response to caspofungin. Accordingly, necrosis occurred in 71.26%, 71.26%, and 61.26% of the cells at the caspofungin concentrations of 0.25, 0.5, and 1 µg/mL, respectively (P<0.05). The analysis of the data in the REST software demonstrated a significant increase in the expression of MCA1 and NUC1 genes (P<0.05). Conclusion: As the findings of the present study indicated, caspofungin promoted both necrosis and apoptosis of C. glabrata cells at concentrations higher than or equal to the MIC value.

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نرگس اصلانیسوم

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نام فایل تاریخ درج فایل اندازه فایل دانلود
2019, CMM, Cellular apoptosis.pdf1398/04/17596269دانلود