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TRPV4 regulates osteoblast differentiation and mitochondrial function that are relevant for channelopathy.
Acharya, Tusar Kanta; Pal, Subhashis; Ghosh, Arijit; Kumar, Shamit; Kumar, Satish; Chattopadhyay, Naibedya; Goswami, Chandan.
Affiliation
  • Acharya TK; National Institute of Science Education and Research, HBNI, School of Biological Sciences, Bhubaneswar, Odisha, India.
  • Pal S; Training School Complex, Homi Bhabha National Institute, Mumbai, India.
  • Ghosh A; Division of Endocrinology and Center for Research in Anabolic Skeletal Target in Health and Illness (ASTHI), Central Drug Research Institute (CDRI), Council of Scientific and Industrial Research (CSIR), Lucknow, India.
  • Kumar S; National Institute of Science Education and Research, HBNI, School of Biological Sciences, Bhubaneswar, Odisha, India.
  • Kumar S; Training School Complex, Homi Bhabha National Institute, Mumbai, India.
  • Chattopadhyay N; National Institute of Science Education and Research, HBNI, School of Biological Sciences, Bhubaneswar, Odisha, India.
  • Goswami C; Training School Complex, Homi Bhabha National Institute, Mumbai, India.
Front Cell Dev Biol ; 11: 1066788, 2023.
Article in En | MEDLINE | ID: mdl-37377733
ABSTRACT
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 Ca2+-level, expression of osteoblast-specific genes and caused increased bio-mineralization. TRPV4 activation also affects mitochondrial Ca2+-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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Cell Dev Biol Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Cell Dev Biol Year: 2023 Document type: Article