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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.
Abstract:
Calcium balance is important in bone homeostasis. The transient receptor potential vanilloid (TRPV) channel is a nonselective cation channel permeable to calcium and is activated by various physiological and pharmacological stimuli. TRPV1 and TRPV4, in particular, have important roles in intracellular Ca2+ signaling and extracellular calcium homeostasis in bone cells. TRPV1 and TRPV4 separately mediate osteoclast and osteoblast differentiation, and deficiency in any of these channels leads to increased bone mass. However, it remains unknown whether bone mass increases in the absence of both TRPV1 and TRPV4. In this study, we used TRPV1 and TRPV4 double knockout (DKO) mice to evaluate their bone mass in vivo, and osteoclast and osteoblast differentiation in vitro. Our results showed that DKO mice and wild type (WT) mice had no significant difference in body weight and femur length. However, the results of dual-energy X-ray absorption, microcomputed tomography, and bone histomorphometry clearly showed that DKO mice had higher bone mass than WT mice. Furthermore, DKO mice had less multinucleated osteoclasts and had lower bone resorption. In addition, the results of cell culture using flushed bone marrow from mouse femurs and tibias showed that osteoclast differentiation was suppressed, whereas osteoblast differentiation was promoted in DKO mice. In conclusion, our results suggest that the increase in bone mass in DKO mice was induced not only by the suppression of osteoclast differentiation and activity but also by the augmentation of osteoblast differentiation and activity. Our findings reveal that both the single deficiency of TRPVs and the concurrent deficiency of TRPVs result in an increase in bone mass. Furthermore, our data showed that DKO mice and single KO mice had varying approaches to osteoclast and osteoblast differentiation in vitro, and therefore, it is important to conduct further studies on TRPVs regarding the increase in bone mass to explore not only individual but also a combination of TRPVs.
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.

