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CircRNA-1806 Decreases T Cell Apoptosis and Prolongs Survival of Mice After Cryptococcal Infection by Sponging miRNA-126

CircRNAs are a recently well-known regulator that mediates a variety of biological processes. Cryptococcus neoformans is an environmental fungal pathogen that can cause fatal cryptococcal meningitis in immunocompromised individuals. However, the involvement of circRNA in cryptococcal infection remai...

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Autores principales: Zhang, Lei, Zhang, Keming, Fang, Wenjie, Li, Hang, Li, Yingfang, Jiang, Weiwei, Hu, Dongying, Coelho, Carolina, Liu, Xiaogang, Cai, Liangqi, Liao, Wanqing, Pan, Weihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691421/
https://www.ncbi.nlm.nih.gov/pubmed/33281794
http://dx.doi.org/10.3389/fmicb.2020.596440
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author Zhang, Lei
Zhang, Keming
Fang, Wenjie
Li, Hang
Li, Yingfang
Jiang, Weiwei
Hu, Dongying
Coelho, Carolina
Liu, Xiaogang
Cai, Liangqi
Liao, Wanqing
Pan, Weihua
author_facet Zhang, Lei
Zhang, Keming
Fang, Wenjie
Li, Hang
Li, Yingfang
Jiang, Weiwei
Hu, Dongying
Coelho, Carolina
Liu, Xiaogang
Cai, Liangqi
Liao, Wanqing
Pan, Weihua
author_sort Zhang, Lei
collection PubMed
description CircRNAs are a recently well-known regulator that mediates a variety of biological processes. Cryptococcus neoformans is an environmental fungal pathogen that can cause fatal cryptococcal meningitis in immunocompromised individuals. However, the involvement of circRNA in cryptococcal infection remains unclear. In this study, high-throughput microarray was performed to identify the circRNA expression profile in cryptococcal meningitis patients. Circ_0001806 was significantly decreased in cryptococcal meningitis individuals. Then the effects of circ_0001806 and its interaction with miRNAs were explored in vivo and in vitro. The knock-down of circ_0001806 led to higher fungal infection and shorter survival in an experimental murine cryptococcosis model. Transcriptome analysis showed that decreased circ_0001806 regulated pathways related to the host antimicrobe response in T cells. Furthermore, in vitro experiments showed that circ_0001806 positively modulates ADM level, decreasing cell apoptosis and G1S arrest in T cells. Finally, we found circ_0001806 exerted its effects by sponging miRNA-126 in T cells. Taken together, our results reveal the role of circRNA-1806/miRNA-126 in the regulation of cell cycle and apoptosis in cryptococcal infection and can provide a new insights of the pathogenesis of cryptococcal infection.
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spelling pubmed-76914212020-12-04 CircRNA-1806 Decreases T Cell Apoptosis and Prolongs Survival of Mice After Cryptococcal Infection by Sponging miRNA-126 Zhang, Lei Zhang, Keming Fang, Wenjie Li, Hang Li, Yingfang Jiang, Weiwei Hu, Dongying Coelho, Carolina Liu, Xiaogang Cai, Liangqi Liao, Wanqing Pan, Weihua Front Microbiol Microbiology CircRNAs are a recently well-known regulator that mediates a variety of biological processes. Cryptococcus neoformans is an environmental fungal pathogen that can cause fatal cryptococcal meningitis in immunocompromised individuals. However, the involvement of circRNA in cryptococcal infection remains unclear. In this study, high-throughput microarray was performed to identify the circRNA expression profile in cryptococcal meningitis patients. Circ_0001806 was significantly decreased in cryptococcal meningitis individuals. Then the effects of circ_0001806 and its interaction with miRNAs were explored in vivo and in vitro. The knock-down of circ_0001806 led to higher fungal infection and shorter survival in an experimental murine cryptococcosis model. Transcriptome analysis showed that decreased circ_0001806 regulated pathways related to the host antimicrobe response in T cells. Furthermore, in vitro experiments showed that circ_0001806 positively modulates ADM level, decreasing cell apoptosis and G1S arrest in T cells. Finally, we found circ_0001806 exerted its effects by sponging miRNA-126 in T cells. Taken together, our results reveal the role of circRNA-1806/miRNA-126 in the regulation of cell cycle and apoptosis in cryptococcal infection and can provide a new insights of the pathogenesis of cryptococcal infection. Frontiers Media S.A. 2020-11-13 /pmc/articles/PMC7691421/ /pubmed/33281794 http://dx.doi.org/10.3389/fmicb.2020.596440 Text en Copyright © 2020 Zhang, Zhang, Fang, Li, Li, Jiang, Hu, Coelho, Liu, Cai, Liao and Pan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Zhang, Lei
Zhang, Keming
Fang, Wenjie
Li, Hang
Li, Yingfang
Jiang, Weiwei
Hu, Dongying
Coelho, Carolina
Liu, Xiaogang
Cai, Liangqi
Liao, Wanqing
Pan, Weihua
CircRNA-1806 Decreases T Cell Apoptosis and Prolongs Survival of Mice After Cryptococcal Infection by Sponging miRNA-126
title CircRNA-1806 Decreases T Cell Apoptosis and Prolongs Survival of Mice After Cryptococcal Infection by Sponging miRNA-126
title_full CircRNA-1806 Decreases T Cell Apoptosis and Prolongs Survival of Mice After Cryptococcal Infection by Sponging miRNA-126
title_fullStr CircRNA-1806 Decreases T Cell Apoptosis and Prolongs Survival of Mice After Cryptococcal Infection by Sponging miRNA-126
title_full_unstemmed CircRNA-1806 Decreases T Cell Apoptosis and Prolongs Survival of Mice After Cryptococcal Infection by Sponging miRNA-126
title_short CircRNA-1806 Decreases T Cell Apoptosis and Prolongs Survival of Mice After Cryptococcal Infection by Sponging miRNA-126
title_sort circrna-1806 decreases t cell apoptosis and prolongs survival of mice after cryptococcal infection by sponging mirna-126
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691421/
https://www.ncbi.nlm.nih.gov/pubmed/33281794
http://dx.doi.org/10.3389/fmicb.2020.596440
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