4.7 Article

Cold-induced Yes-associated-protein expression through miR-429 mediates the browning of white adipose tissue

Journal

SCIENCE CHINA-LIFE SCIENCES
Volume 64, Issue 3, Pages 404-418

Publisher

SCIENCE PRESS
DOI: 10.1007/s11427-020-1779-2

Keywords

aging; browning; miR-429; UCP1; YAP

Categories

Funding

  1. National Key Research and Development Program of China [2019YFA0802502]
  2. National Natural Science Foundation of China [81770836, 81822006, 81700506]
  3. Natural Science Foundation of Tianjin [19JCQNJC10100]

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The study highlighted the importance of targeting the miR-429-YAP pathway in promoting the browning of subcutaneous white adipose tissue (sWAT) and potentially developing therapeutic strategies for age-related impairment of sWAT browning. Additionally, it was found that YAP overexpression could significantly improve impaired sWAT browning in middle-aged mice.
Targeting the white-to-brown fat conversion is important for developing potential strategies to counteract metabolic diseases; yet the mechanisms are not fully understood. Yes-associated-protein (YAP), a transcription co-activator, was demonstrated to regulate adipose tissue functions; however, its effects on browning of subcutaneous white adipose tissue (sWAT) are unclear. We demonstrated that YAP was highly expressed in cold-induced beige fat. Mechanistically, YAP was found as a target gene of miR-429, which downregulated YAP expression(in vivo)and(in vitro.)In addition, miR-429 level was decreased in cold-induced beige fat. Additionally, pharmacological inhibition of the interaction between YAP and transcriptional enhanced associate domains by verteporfin dampened the browning of sWAT. Although adipose tissue-specific YAP overexpression increased energy expenditure with increased basal uncoupling protein 1 expression, it had no additional effects on the browning of sWAT in young mice. However, we found age-related impairment of sWAT browning along with decreased YAP expression. Under these circumstances, YAP overexpression significantly improved the impaired WAT browning in middle-aged mice. In conclusion, YAP as a regulator of sWAT browning, was upregulated by lowering miR-429 level in cold-induced beige fat. Targeting the miR-429-YAP pathway could be exploited for therapeutic strategies for age-related impairment of sWAT browning.

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