Nishimura Haruki, Kawasaki Makoto, Tsukamoto Manabu, Menuki Kunitaka, Suzuki Hitoshi, Matsuura Takanori, Baba Kazuhiko, Motojima Yasuhito, Fujitani Teruaki, Ohnishi Hideo, Yamanaka Yoshiaki, Kosugi Kenji, Okada Yasuaki, Tokuda Kotaro, Tajima Takafumi, Yoshioka Toru, Okimoto Nobukazu, Ueta Yoichi, Sakai Akinori
Department of Orthopaedic Surgery, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu 807-8555, Japan.
Department of Orthopaedics, Shimura Hospital, 3-13 Funairimachi Naka-ku, Hiroshima 730-0841, Japan.
Bone Rep. 2020 Apr 23;12:100268. doi: 10.1016/j.bonr.2020.100268. eCollection 2020 Jun.
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 Ca 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 and double knockout (DKO) mice to evaluate their bone mass , and osteoclast and osteoblast differentiation . 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 , 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.
钙平衡在骨稳态中很重要。瞬时受体电位香草酸(TRPV)通道是一种对钙通透的非选择性阳离子通道,可被各种生理和药理刺激激活。特别是TRPV1和TRPV4在骨细胞的细胞内钙信号传导和细胞外钙稳态中起重要作用。TRPV1和TRPV4分别介导破骨细胞和成骨细胞分化,这些通道中任何一个的缺陷都会导致骨量增加。然而,在同时缺乏TRPV1和TRPV4的情况下骨量是否增加仍不清楚。在本研究中,我们使用TRPV1和TRPV4双敲除(DKO)小鼠来评估它们的骨量、破骨细胞和成骨细胞分化情况。我们的结果表明,DKO小鼠和野生型(WT)小鼠在体重和股骨长度上没有显著差异。然而,双能X线吸收法、显微计算机断层扫描和骨组织形态计量学的结果清楚地表明,DKO小鼠的骨量高于WT小鼠。此外,DKO小鼠的多核破骨细胞较少,骨吸收较低。另外,使用从小鼠股骨和胫骨冲洗出的骨髓进行细胞培养的结果表明,DKO小鼠中破骨细胞分化受到抑制,而成骨细胞分化得到促进。总之,我们的结果表明,DKO小鼠骨量的增加不仅是由破骨细胞分化和活性的抑制引起的,也是由成骨细胞分化和活性的增强引起的。我们的研究结果表明,TRPV单基因缺陷和TRPV同时缺陷都会导致骨量增加。此外,我们的数据表明,DKO小鼠和单基因敲除小鼠在破骨细胞和成骨细胞分化方面有不同的途径,因此,有必要就骨量增加对TRPV进行进一步研究,不仅要探索单个TRPV,还要探索TRPV的组合。