The Hippo signal transduction network for exercise physiologists

J Appl Physiol (1985). 2016 May 15;120(10):1105-17. doi: 10.1152/japplphysiol.01076.2015. Epub 2016 Mar 3.

Abstract

The ubiquitous transcriptional coactivators Yap (gene symbol Yap1) and Taz (gene symbol Wwtr1) regulate gene expression mainly by coactivating the Tead transcription factors. Being at the center of the Hippo signaling network, Yap and Taz are regulated by the Hippo kinase cassette and additionally by a plethora of exercise-associated signals and signaling modules. These include mechanotransduction, the AKT-mTORC1 network, the SMAD transcription factors, hypoxia, glucose homeostasis, AMPK, adrenaline/epinephrine and angiotensin II through G protein-coupled receptors, and IL-6. Consequently, exercise should alter Hippo signaling in several organs to mediate at least some aspects of the organ-specific adaptations to exercise. Indeed, Tead1 overexpression in muscle fibers has been shown to promote a fast-to-slow fiber type switch, whereas Yap in muscle fibers and cardiomyocytes promotes skeletal muscle hypertrophy and cardiomyocyte adaptations, respectively. Finally, genome-wide association studies in humans have linked the Hippo pathway members LATS2, TEAD1, YAP1, VGLL2, VGLL3, and VGLL4 to body height, which is a key factor in sports.

Keywords: Hippo; Yap; exercise; hypertrophy; skeletal muscle.

Publication types

  • Review

MeSH terms

  • Animals
  • Exercise / physiology*
  • Humans
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / physiology
  • Physical Conditioning, Animal / physiology*
  • Protein Serine-Threonine Kinases / metabolism*
  • Signal Transduction / physiology*
  • Transcription Factors / metabolism

Substances

  • Transcription Factors
  • Protein Serine-Threonine Kinases