Zavrel Martin, Hoot Sam J, White Theodore C
University of Missouri-Kansas City, School of Biological Sciences, Cell Biology and Biophysics, Kansas City, MO, USA.
Eukaryot Cell. 2013 May;12(5):725-38. doi: 10.1128/EC.00345-12. Epub 2013 Mar 8.
Sterol import has been characterized under various conditions in three distinct fungal species, the model organism Saccharomyces cerevisiae and two human fungal pathogens Candida glabrata and Candida albicans, employing cholesterol, the sterol of higher eukaryotes, as well as its fungal equivalent, ergosterol. Import was confirmed by the detection of esterified cholesterol within the cells. Comparing the three fungal species, we observe sterol import under three different conditions. First, as previously well characterized, we observe sterol import under low oxygen levels in S. cerevisiae and C. glabrata, which is dependent on the transcription factor Upc2 and/or its orthologs or paralogs. Second, we observe sterol import under aerobic conditions exclusively in the two pathogenic fungi C. glabrata and C. albicans. Uptake emerges during post-exponential-growth phases, is independent of the characterized Upc2-pathway and is slower compared to the anaerobic uptake in S. cerevisiae and C. glabrata. Third, we observe under normoxic conditions in C. glabrata that Upc2-dependent sterol import can be induced in the presence of fetal bovine serum together with fluconazole. In summary, C. glabrata imports sterols both in aerobic and anaerobic conditions, and the limited aerobic uptake can be further stimulated by the presence of serum together with fluconazole. S. cerevisiae imports sterols only in anaerobic conditions, demonstrating aerobic sterol exclusion. Finally, C. albicans imports sterols exclusively aerobically in post-exponential-growth phases, independent of Upc2. For the first time, we provide direct evidence of sterol import into the human fungal pathogen C. albicans, which until now was believed to be incapable of active sterol import.
在三种不同的真菌物种中,即在模式生物酿酒酵母以及两种人类真菌病原体光滑念珠菌和白色念珠菌中,已经对甾醇的导入进行了多种条件下的研究,使用高等真核生物的甾醇胆固醇及其真菌等效物麦角甾醇。通过检测细胞内的酯化胆固醇证实了甾醇的导入。比较这三种真菌物种,我们观察到在三种不同条件下的甾醇导入情况。首先,如先前充分表征的那样,我们观察到酿酒酵母和光滑念珠菌在低氧水平下的甾醇导入,这依赖于转录因子Upc2及其直系同源物或旁系同源物。其次,我们仅在两种致病真菌光滑念珠菌和白色念珠菌中观察到有氧条件下的甾醇导入。摄取出现在指数生长后期,独立于已表征的Upc2途径,并且与酿酒酵母和光滑念珠菌中的厌氧摄取相比更慢。第三,我们观察到在光滑念珠菌的常氧条件下,在胎牛血清和氟康唑存在的情况下,Upc2依赖性甾醇导入可以被诱导。总之,光滑念珠菌在有氧和厌氧条件下都能导入甾醇,并且血清和氟康唑的存在可以进一步刺激有限的有氧摄取。酿酒酵母仅在厌氧条件下导入甾醇,表明其有氧甾醇排除。最后,白色念珠菌仅在指数生长后期有氧条件下导入甾醇,独立于Upc2。我们首次提供了甾醇导入人类真菌病原体白色念珠菌的直接证据;直到现在,人们一直认为它无法进行主动甾醇导入。