Artículo
Role of RAC3 coactivator in the adipocyte differentiation
Lira, María Cecilia
; Rosa, Francisco Damián
; Panelo, Laura Carolina
; Costas, Monica Alejandra
; Rubio, María Fernanda
Fecha de publicación:
12/2018
Editorial:
Nature Publishing Group
Revista:
Cell Death Discovery
e-ISSN:
2058-7716
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
RAC3 is a member of the p160 family of steroid receptor coactivators and it is highly expressed in several human cancers, contributing to enhanced cell proliferation and cellular transformation. In this work, we have studied the role of RAC3 in adipogenesis in L-929 cells. Adipogenesis is a highly regulated process, involving cell cycle arrest and changes in the gene expression pattern required for morphological remodelling. We found that RAC3 expression levels are downregulated during adipocyte differentiation induced by specific stimulus. In addition, cells constitutively expressing low levels of RAC3 (shRNA), showed enhanced adipocyte differentiation which was evidenced by the early detection of the adipocyte markers Perilipin, PPARγ and Oil Red O staining. Moreover, RAC3 downregulation favoured cell arrest and autophagy. Early and late autophagy inhibitors blocked adipocyte differentiation in control cells, but partially inhibited shRAC3 differentiation, demonstrating that although autophagy is required for adipogenesis, additional signals could be trigged by RAC3 downregulation. We conclude that RAC3 is a key regulator of adipogenesis, since its downregulation generates the cellular arrest and autophagic responses that are required steps for this process.
Palabras clave:
ADIPOGENESIS
,
RAC3
,
AUTOPHAGY
,
COACTIVATORS
Archivos asociados
Licencia
Identificadores
Colecciones
Articulos(IDIM)
Articulos de INST.DE INVEST.MEDICAS
Articulos de INST.DE INVEST.MEDICAS
Citación
Lira, María Cecilia; Rosa, Francisco Damián; Panelo, Laura Carolina; Costas, Monica Alejandra; Rubio, María Fernanda; Role of RAC3 coactivator in the adipocyte differentiation; Nature Publishing Group; Cell Death Discovery; 4; 1; 12-2018; 1-11
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