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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.
Afiliación
  • Khan IS; UCSF Diabetes Center, University of California San Francisco, San Francisco, California, United States of America.
  • Park CY; UCSF Diabetes Center, University of California San Francisco, San Francisco, California, United States of America; WM Keck Center for Noncoding RNAs, University of California San Francisco, San Francisco, California, United States of America.
  • Mavropoulos A; UCSF Diabetes Center, University of California San Francisco, San Francisco, California, United States of America; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
  • Shariat N; UCSF Diabetes Center, University of California San Francisco, San Francisco, California, United States of America; WM Keck Center for Noncoding RNAs, University of California San Francisco, San Francisco, California, United States of America; Department of Microbiology and Immunology, University of
  • Pollack JL; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
  • Barczak AJ; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
  • Erle DJ; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
  • McManus MT; UCSF Diabetes Center, University of California San Francisco, San Francisco, California, United States of America; WM Keck Center for Noncoding RNAs, University of California San Francisco, San Francisco, California, United States of America; Department of Microbiology and Immunology, University of
  • Anderson MS; UCSF Diabetes Center, University of California San Francisco, San Francisco, California, United States of America.
  • Jeker LT; UCSF Diabetes Center, University of California San Francisco, San Francisco, California, United States of America; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America; Department of Pathology, University of California San Francisco, San
PLoS One ; 10(8): e0135440, 2015.
Article en En | MEDLINE | ID: mdl-26270036
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Asunto principal: Timo / Regulación de la Expresión Génica / MicroARNs / Células Epiteliales Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: Plos one Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Asunto principal: Timo / Regulación de la Expresión Génica / MicroARNs / Células Epiteliales Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: Plos one Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos