| Literature DB >> 27188440 |
Chengzhu Zhao1, Atsuhiko Ichimura2, Nianchao Qian1, Tsunaki Iida1, Daiju Yamazaki1, Naruto Noma3, Masataka Asagiri3, Koji Yamamoto3, Shinji Komazaki4, Chikara Sato5, Fumiyo Aoyama6, Akira Sawaguchi6, Sho Kakizawa1, Miyuki Nishi1, Hiroshi Takeshima7.
Abstract
The trimeric intracellular cation (TRIC) channels TRIC-A and TRIC-B localize predominantly to the endoplasmic reticulum (ER) and likely support Ca(2+) release from intracellular stores by mediating cationic flux to maintain electrical neutrality. Deletion and point mutations in TRIC-B occur in families with autosomal recessive osteogenesis imperfecta. Tric-b knockout mice develop neonatal respiratory failure and exhibit poor bone ossification. We investigated the cellular defect causing the bone phenotype. Bone histology indicated collagen matrix deposition was reduced in Tric-b knockout mice. Osteoblasts, the bone-depositing cells, from Tric-b knockout mice exhibited reduced Ca(2+) release from ER and increased ER Ca(2+) content, which was associated with ER swelling. These cells also had impaired collagen release without a decrease in collagen-encoding transcripts, consistent with a defect in trafficking of collagen through ER. In contrast, osteoclasts, the bone-degrading cells, from Tric-b knockout mice were similar to those from wild-type mice. Thus, TRIC-B function is essential to support the production and release of large amounts of collagen by osteoblasts, which is necessary for bone mineralization.Entities:
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Year: 2016 PMID: 27188440 DOI: 10.1126/scisignal.aad9055
Source DB: PubMed Journal: Sci Signal ISSN: 1945-0877 Impact factor: 8.192