Author
Listed:
- Nuria Matesanz
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III)
- Edgar Bernardo
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III)
- Rebeca Acín-Pérez
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III)
- Elisa Manieri
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III
CSIC)
- Sonia Pérez-Sieira
(University of Santiago de Compostela-Instituto de Investigación Sanitaria
Travesía da Choupana)
- Lourdes Hernández-Cosido
(University of Salamanca)
- Valle Montalvo-Romeral
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III)
- Alfonso Mora
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III)
- Elena Rodríguez
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III)
- Luis Leiva-Vega
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III)
- Ana Victoria Lechuga-Vieco
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III
CIBER Enfermedades respiratorias (CIBERES))
- Jesús Ruiz-Cabello
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III
CIBER Enfermedades respiratorias (CIBERES)
Universidad Complutense de Madrid)
- Jorge L. Torres
(University Hospital of Salamanca-IBSAL)
- Maria Crespo-Ruiz
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III)
- Francisco Centeno
(Grupo GIEN (Grupo de Investigación en Enfermedades Neurodegenerativas))
- Clara V. Álvarez
(University of Santiago de Compostela-Instituto de Investigación Sanitaria)
- Miguel Marcos
(University Hospital of Salamanca-IBSAL)
- Jose Antonio Enríquez
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III
CIBER Fragilidad y Envejecimiento Saludable (CIBERFES))
- Ruben Nogueiras
(University of Santiago de Compostela-Instituto de Investigación Sanitaria
Travesía da Choupana)
- Guadalupe Sabio
(Fundación Centro Nacional de Investigaciones Cardiovasculares Carlos III)
Abstract
Increasing the thermogenic capacity of adipose tissue to enhance organismal energy expenditure is considered a promising therapeutic strategy to combat obesity. Here, we report that expression of the p38 MAPK activator MKK6 is elevated in white adipose tissue of obese individuals. Using knockout animals and shRNA, we show that Mkk6 deletion increases energy expenditure and thermogenic capacity of white adipose tissue, protecting mice against diet-induced obesity and the development of diabetes. Deletion of Mkk6 increases T3-stimulated UCP1 expression in adipocytes, thereby increasing their thermogenic capacity. Mechanistically, we demonstrate that, in white adipose tissue, p38 is activated by an alternative pathway involving AMPK, TAK, and TAB. Our results identify MKK6 in adipocytes as a potential therapeutic target to reduce obesity.
Suggested Citation
Nuria Matesanz & Edgar Bernardo & Rebeca Acín-Pérez & Elisa Manieri & Sonia Pérez-Sieira & Lourdes Hernández-Cosido & Valle Montalvo-Romeral & Alfonso Mora & Elena Rodríguez & Luis Leiva-Vega & Ana Vi, 2017.
"MKK6 controls T3-mediated browning of white adipose tissue,"
Nature Communications, Nature, vol. 8(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-00948-z
DOI: 10.1038/s41467-017-00948-z
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