4.8 Article

MKK6 controls T3-mediated browning of white adipose tissue

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NATURE COMMUNICATIONS
卷 8, 期 -, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-017-00948-z

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资金

  1. European Regional Development Fund (ERDF-FEDER)
  2. European Union's Seventh Framework Programme [ERC 260464]
  3. EFSD/Lilly
  4. MINECO-FEDER [SAF2016-79126-R]
  5. Comunidad de Madrid [S2010/BMD-2326, CAM/API1009]
  6. ISCIII
  7. FEDER [PI10/01692]
  8. Junta de Castilla y Leon [GRS 681/A/11]
  9. MINECO [BFU2015-70664-R]
  10. Xunta de Galicia [2015-CP080, PIE13/00024, ERC281408]
  11. Junta de Extremadura-FEDER [BR15164, BFU2013-46109-R]
  12. Ministry of Economy, Industry and Competitiveness (MEIC)
  13. Pro CNIC Foundation
  14. Severo Ochoa Center of Excellence [SEV-2015-0505]
  15. [UE0/MCA1108]
  16. [UE0/MCA1201]
  17. [I3SNS-INT12/049]
  18. European Foundation for the Study of Diabetes [Lilly 2016_5] Funding Source: researchfish

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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.

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