Acharya Tusar Kanta, Pal Subhashis, Ghosh Arijit, Kumar Shamit, Kumar Satish, Chattopadhyay Naibedya, Goswami Chandan
National Institute of Science Education and Research, HBNI, School of Biological Sciences, Bhubaneswar, Odisha, India.
Training School Complex, Homi Bhabha National Institute, Mumbai, India.
Front Cell Dev Biol. 2023 Jun 12;11:1066788. doi: 10.3389/fcell.2023.1066788. eCollection 2023.
Different ion channels present in the osteoblast regulate the cellular functions including bio-mineralization, a process that is a highly stochastic event. Cellular events and molecular signaling involved in such process is poorly understood. Here we demonstrate that TRPV4, a mechanosensitive ion channel is endogenously present in an osteoblast cell line (MC3T3-E1) and in primary osteoblasts. Pharmacological activation of TRPV4 enhanced intracellular Ca-level, expression of osteoblast-specific genes and caused increased bio-mineralization. TRPV4 activation also affects mitochondrial Ca-levels and mitochondrial metabolisms. We further demonstrate that different point mutants of TRPV4 induce different mitochondrial morphology and have different levels of mitochondrial translocation, collectively suggesting that TRPV4-mutation-induced bone disorders and other channelopathies are mostly due to mitochondrial abnormalities. These findings may have broad biomedical implications.
成骨细胞中存在的不同离子通道调节细胞功能,包括生物矿化,这是一个高度随机的过程。人们对参与该过程的细胞事件和分子信号了解甚少。在这里,我们证明了机械敏感离子通道TRPV4内源性存在于成骨细胞系(MC3T3-E1)和原代成骨细胞中。TRPV4的药理学激活增强了细胞内钙水平、成骨细胞特异性基因的表达,并导致生物矿化增加。TRPV4激活还影响线粒体钙水平和线粒体代谢。我们进一步证明,TRPV4的不同点突变诱导不同的线粒体形态,并具有不同水平的线粒体易位,共同表明TRPV4突变引起的骨疾病和其他通道病主要是由于线粒体异常。这些发现可能具有广泛的生物医学意义。