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Differential Expression of Exosomal microRNAs in Prefrontal Cortices of Schizophrenia and Bipolar Disorder Patients
Exosomes are cellular secretory vesicles containing microRNAs (miRNAs). Once secreted, exosomes are able to attach to recipient cells and release miRNAs potentially modulating the function of the recipient cell. We hypothesized that exosomal miRNA expression in brains of patients diagnosed with schi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559697/ https://www.ncbi.nlm.nih.gov/pubmed/23382797 http://dx.doi.org/10.1371/journal.pone.0048814 |
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author | Banigan, Meredith G. Kao, Patricia F. Kozubek, James A. Winslow, Ashley R. Medina, Juan Costa, Joan Schmitt, Andrea Schneider, Anja Cabral, Howard Cagsal-Getkin, Ozge Vanderburg, Charles R. Delalle, Ivana |
author_facet | Banigan, Meredith G. Kao, Patricia F. Kozubek, James A. Winslow, Ashley R. Medina, Juan Costa, Joan Schmitt, Andrea Schneider, Anja Cabral, Howard Cagsal-Getkin, Ozge Vanderburg, Charles R. Delalle, Ivana |
author_sort | Banigan, Meredith G. |
collection | PubMed |
description | Exosomes are cellular secretory vesicles containing microRNAs (miRNAs). Once secreted, exosomes are able to attach to recipient cells and release miRNAs potentially modulating the function of the recipient cell. We hypothesized that exosomal miRNA expression in brains of patients diagnosed with schizophrenia (SZ) and bipolar disorder (BD) might differ from controls, reflecting either disease-specific or common aberrations in SZ and BD patients. The sources of the analyzed samples included McLean 66 Cohort Collection (Harvard Brain Tissue Resource Center), BrainNet Europe II (BNE, a consortium of 18 brain banks across Europe) and Boston Medical Center (BMC). Exosomal miRNAs from frozen postmortem prefrontal cortices with well-preserved RNA were isolated and submitted to profiling by Luminex FLEXMAP 3D microfluidic device. Multiple statistical analyses of microarray data suggested that certain exosomal miRNAs were differentially expressed in SZ and BD subjects in comparison to controls. RT-PCR validation confirmed that two miRNAs, miR-497 in SZ samples and miR-29c in BD samples, have significantly increased expression when compared to control samples. These results warrant future studies to evaluate the potential of exosome-derived miRNAs to serve as biomarkers of SZ and BD. |
format | Online Article Text |
id | pubmed-3559697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35596972013-02-04 Differential Expression of Exosomal microRNAs in Prefrontal Cortices of Schizophrenia and Bipolar Disorder Patients Banigan, Meredith G. Kao, Patricia F. Kozubek, James A. Winslow, Ashley R. Medina, Juan Costa, Joan Schmitt, Andrea Schneider, Anja Cabral, Howard Cagsal-Getkin, Ozge Vanderburg, Charles R. Delalle, Ivana PLoS One Research Article Exosomes are cellular secretory vesicles containing microRNAs (miRNAs). Once secreted, exosomes are able to attach to recipient cells and release miRNAs potentially modulating the function of the recipient cell. We hypothesized that exosomal miRNA expression in brains of patients diagnosed with schizophrenia (SZ) and bipolar disorder (BD) might differ from controls, reflecting either disease-specific or common aberrations in SZ and BD patients. The sources of the analyzed samples included McLean 66 Cohort Collection (Harvard Brain Tissue Resource Center), BrainNet Europe II (BNE, a consortium of 18 brain banks across Europe) and Boston Medical Center (BMC). Exosomal miRNAs from frozen postmortem prefrontal cortices with well-preserved RNA were isolated and submitted to profiling by Luminex FLEXMAP 3D microfluidic device. Multiple statistical analyses of microarray data suggested that certain exosomal miRNAs were differentially expressed in SZ and BD subjects in comparison to controls. RT-PCR validation confirmed that two miRNAs, miR-497 in SZ samples and miR-29c in BD samples, have significantly increased expression when compared to control samples. These results warrant future studies to evaluate the potential of exosome-derived miRNAs to serve as biomarkers of SZ and BD. Public Library of Science 2013-01-30 /pmc/articles/PMC3559697/ /pubmed/23382797 http://dx.doi.org/10.1371/journal.pone.0048814 Text en © 2013 Kao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Banigan, Meredith G. Kao, Patricia F. Kozubek, James A. Winslow, Ashley R. Medina, Juan Costa, Joan Schmitt, Andrea Schneider, Anja Cabral, Howard Cagsal-Getkin, Ozge Vanderburg, Charles R. Delalle, Ivana Differential Expression of Exosomal microRNAs in Prefrontal Cortices of Schizophrenia and Bipolar Disorder Patients |
title | Differential Expression of Exosomal microRNAs in Prefrontal Cortices of Schizophrenia and Bipolar Disorder Patients |
title_full | Differential Expression of Exosomal microRNAs in Prefrontal Cortices of Schizophrenia and Bipolar Disorder Patients |
title_fullStr | Differential Expression of Exosomal microRNAs in Prefrontal Cortices of Schizophrenia and Bipolar Disorder Patients |
title_full_unstemmed | Differential Expression of Exosomal microRNAs in Prefrontal Cortices of Schizophrenia and Bipolar Disorder Patients |
title_short | Differential Expression of Exosomal microRNAs in Prefrontal Cortices of Schizophrenia and Bipolar Disorder Patients |
title_sort | differential expression of exosomal micrornas in prefrontal cortices of schizophrenia and bipolar disorder patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559697/ https://www.ncbi.nlm.nih.gov/pubmed/23382797 http://dx.doi.org/10.1371/journal.pone.0048814 |
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