TMCO1-mediated Ca<sup>2+</sup> leak underlies osteoblast functions via CaMKII signaling.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30962442.
- Also identified by DOI 10.1038/s41467-019-09653-5 and PMC identifier 6453895.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Transmembrane and coiled-coil domains 1 (TMCO1) is a recently identified Ca<sup>2+</sup> leak channel in the endoplasmic reticulum. TMCO1 dysfunction in humans is associated with dysmorphism, mental retardation, glaucoma and the occurrence of cancer. Here we show an essential role of TMCO1 in osteogenesis mediated by local Ca<sup>2+</sup>/CaMKII signaling in osteoblasts. TMCO1 levels were significantly decreased in bone from both osteoporosis patients and bone-loss mouse models. Tmco1<sup>-/-</sup> mice exhibited loss of bone mass and altered microarchitecture characteristic of osteoporosis. In the absence of TMCO1, decreased HDAC4 phosphorylation resulted in nuclear enrichment of HADC4, which leads to deacetylation and degradation of RUNX2, the master regulator of osteogenesis. We further demonstrate that TMCO1-mediated Ca<sup>2+</sup> leak provides local Ca<sup>2+</sup> signals to activate the CaMKII-HDAC4-RUNX2 signaling axis. The establishment of TMCO1 as a pivotal player in osteogenesis uncovers a novel potential therapeutic target for ameliorating osteoporosis.
Medical subject headings
- Calcium Channels
- Calcium-Calmodulin-Dependent Protein Kinase Type 2
- Membrane Proteins
- Osteoblasts
- Osteoporosis