دورية أكاديمية

Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells

التفاصيل البيبلوغرافية
العنوان: Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells
المؤلفون: Piffer, Alícia C., Santos, Francine M. dos, Thomé, Marcos P., Diehl, Camila, Garcia, Ane Wichine Acosta, Kinskovski, Uriel Perin, Schneider, Rafael de Oliveira, Gerber, Alexandra, Feltes, Bruno César, Schrank, Augusto, Vasconcelos, Ana Tereza R., Lenz, Guido, Kmetzsch, Lívia, Vainstein, Marilene H., Staats, Charley C.
المصدر: Genetics and Molecular Biology. January 2021 44(3)
بيانات النشر: Sociedade Brasileira de Genética, 2021.
سنة النشر: 2021
مصطلحات موضوعية: Macrophage, mTOR pathway, Cryptococcus, RNAseq, interatomic networks
الوصف: Cryptococcus neoformans and Cryptococcus gattii are the etiological agents of cryptococcosis, a high mortality disease. The development of such disease depends on the interaction of fungal cells with macrophages, in which they can reside and replicate. In order to dissect the molecular mechanisms by which cryptococcal cells modulate the activity of macrophages, a genome-scale comparative analysis of transcriptional changes in macrophages exposed to Cryptococcus spp. was conducted. Altered expression of nearly 40 genes was detected in macrophages exposed to cryptococcal cells. The major processes were associated with the mTOR pathway, whose associated genes exhibited decreased expression in macrophages incubated with cryptococcal cells. Phosphorylation of p70S6K and GSK-3β was also decreased in macrophages incubated with fungal cells. In this way, Cryptococci presence could drive the modulation of mTOR pathway in macrophages possibly to increase the survival of the pathogen.
نوع الوثيقة: article
وصف الملف: text/html
اللغة: English
تدمد: 1415-4757
DOI: 10.1590/1678-4685-gmb-2020-0390
URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572021000400702
حقوق: info:eu-repo/semantics/openAccess
رقم الأكسشن: edssci.S1415.47572021000400702
قاعدة البيانات: SciELO
الوصف
تدمد:14154757
DOI:10.1590/1678-4685-gmb-2020-0390