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Identification of MiR-205 As a MicroRNA That Is Highly Expressed in Medullary Thymic Epithelial Cells

Thymic epithelial cells (TECs) support T cell development in the thymus. Cortical thymic epithelial cells (cTECs) facilitate positive selection of developing thymocytes whereas medullary thymic epithelial cells (mTECs) facilitate the deletion of self-reactive thymocytes in order to prevent autoimmun...

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Autores principales: Khan, Imran S., Park, Chong Y., Mavropoulos, Anastasia, Shariat, Nikki, Pollack, Joshua L., Barczak, Andrea J., Erle, David J., McManus, Michael T., Anderson, Mark S., Jeker, Lukas T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535774/
https://www.ncbi.nlm.nih.gov/pubmed/26270036
http://dx.doi.org/10.1371/journal.pone.0135440
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author Khan, Imran S.
Park, Chong Y.
Mavropoulos, Anastasia
Shariat, Nikki
Pollack, Joshua L.
Barczak, Andrea J.
Erle, David J.
McManus, Michael T.
Anderson, Mark S.
Jeker, Lukas T.
author_facet Khan, Imran S.
Park, Chong Y.
Mavropoulos, Anastasia
Shariat, Nikki
Pollack, Joshua L.
Barczak, Andrea J.
Erle, David J.
McManus, Michael T.
Anderson, Mark S.
Jeker, Lukas T.
author_sort Khan, Imran S.
collection PubMed
description Thymic epithelial cells (TECs) support T cell development in the thymus. Cortical thymic epithelial cells (cTECs) facilitate positive selection of developing thymocytes whereas medullary thymic epithelial cells (mTECs) facilitate the deletion of self-reactive thymocytes in order to prevent autoimmunity. The mTEC compartment is highly dynamic with continuous maturation and turnover, but the genetic regulation of these processes remains poorly understood. MicroRNAs (miRNAs) are important regulators of TEC genetic programs since miRNA-deficient TECs are severely defective. However, the individual miRNAs important for TEC maintenance and function and their mechanisms of action remain unknown. Here, we demonstrate that miR-205 is highly and preferentially expressed in mTECs during both thymic ontogeny and in the postnatal thymus. This distinct expression is suggestive of functional importance for TEC biology. Genetic ablation of miR-205 in TECs, however, neither revealed a role for miR-205 in TEC function during homeostatic conditions nor during recovery from thymic stress conditions. Thus, despite its distinct expression, miR-205 on its own is largely dispensable for mTEC biology.
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spelling pubmed-45357742015-08-20 Identification of MiR-205 As a MicroRNA That Is Highly Expressed in Medullary Thymic Epithelial Cells Khan, Imran S. Park, Chong Y. Mavropoulos, Anastasia Shariat, Nikki Pollack, Joshua L. Barczak, Andrea J. Erle, David J. McManus, Michael T. Anderson, Mark S. Jeker, Lukas T. PLoS One Research Article Thymic epithelial cells (TECs) support T cell development in the thymus. Cortical thymic epithelial cells (cTECs) facilitate positive selection of developing thymocytes whereas medullary thymic epithelial cells (mTECs) facilitate the deletion of self-reactive thymocytes in order to prevent autoimmunity. The mTEC compartment is highly dynamic with continuous maturation and turnover, but the genetic regulation of these processes remains poorly understood. MicroRNAs (miRNAs) are important regulators of TEC genetic programs since miRNA-deficient TECs are severely defective. However, the individual miRNAs important for TEC maintenance and function and their mechanisms of action remain unknown. Here, we demonstrate that miR-205 is highly and preferentially expressed in mTECs during both thymic ontogeny and in the postnatal thymus. This distinct expression is suggestive of functional importance for TEC biology. Genetic ablation of miR-205 in TECs, however, neither revealed a role for miR-205 in TEC function during homeostatic conditions nor during recovery from thymic stress conditions. Thus, despite its distinct expression, miR-205 on its own is largely dispensable for mTEC biology. Public Library of Science 2015-08-13 /pmc/articles/PMC4535774/ /pubmed/26270036 http://dx.doi.org/10.1371/journal.pone.0135440 Text en © 2015 Khan 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
Khan, Imran S.
Park, Chong Y.
Mavropoulos, Anastasia
Shariat, Nikki
Pollack, Joshua L.
Barczak, Andrea J.
Erle, David J.
McManus, Michael T.
Anderson, Mark S.
Jeker, Lukas T.
Identification of MiR-205 As a MicroRNA That Is Highly Expressed in Medullary Thymic Epithelial Cells
title Identification of MiR-205 As a MicroRNA That Is Highly Expressed in Medullary Thymic Epithelial Cells
title_full Identification of MiR-205 As a MicroRNA That Is Highly Expressed in Medullary Thymic Epithelial Cells
title_fullStr Identification of MiR-205 As a MicroRNA That Is Highly Expressed in Medullary Thymic Epithelial Cells
title_full_unstemmed Identification of MiR-205 As a MicroRNA That Is Highly Expressed in Medullary Thymic Epithelial Cells
title_short Identification of MiR-205 As a MicroRNA That Is Highly Expressed in Medullary Thymic Epithelial Cells
title_sort identification of mir-205 as a microrna that is highly expressed in medullary thymic epithelial cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4535774/
https://www.ncbi.nlm.nih.gov/pubmed/26270036
http://dx.doi.org/10.1371/journal.pone.0135440
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