Transient receptor potential vanilloid 1 and 4 double knockout leads to increased bone mass in mice

Haruki Nishimura1, Makoto Kawasaki1, Manabu Tsukamoto1

  • 1Department of Orthopaedic Surgery, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu 807-8555, Japan.

Bone Reports
|May 7, 2020
PubMed

Insights

Removing both TRPV1 and TRPV4 channels in mice significantly increases bone mass by suppressing bone-resorbing osteoclasts and promoting bone-building osteoblasts.

Area of Science:

  • Bone Biology
  • Ion Channels
  • Calcium Homeostasis

Background:

  • Calcium balance is crucial for bone homeostasis.
  • Transient Receptor Potential Vanilloid (TRPV) channels, including TRPV1 and TRPV4, regulate intracellular calcium signaling and bone cell function.
  • Individual deficiency in TRPV1 or TRPV4 increases bone mass, but the effect of combined deficiency is unknown.

Purpose of the Study:

  • To investigate the effect of combined TRPV1 and TRPV4 deficiency on bone mass and bone cell differentiation.
  • To evaluate bone mass and cellular mechanisms in TRPV1 and TRPV4 double knockout (DKO) mice.

Main Methods:

  • Utilized TRPV1 and TRPV4 double knockout (DKO) mice and wild-type (WT) littermates.
  • Assessed bone mass using dual-energy X-ray absorption, microcomputed tomography, and bone histomorphometry.
  • Evaluated osteoclast and osteoblast differentiation in vitro using bone marrow cells.

Main Results:

  • DKO mice exhibited significantly higher bone mass compared to WT mice.
  • DKO mice showed reduced numbers of multinucleated osteoclasts and decreased bone resorption.
  • Osteoclast differentiation was suppressed, while osteoblast differentiation was promoted in DKO mice.

Conclusions:

  • Combined deficiency of TRPV1 and TRPV4 leads to increased bone mass.
  • This increase is attributed to both suppressed osteoclast activity and enhanced osteoblast activity.
  • Both single and combined TRPV deficiencies impact bone mass, highlighting the complex role of TRPV channels in bone metabolism.