| Literature DB >> 26709236 |
Nobuhito Nango1, Shogo Kubota2, Tomoka Hasegawa3, Wataru Yashiro4, Atsushi Momose5, Koichi Matsuo6.
Abstract
The mammalian skeleton stores calcium and phosphate ions in bone matrix. Osteocytes in osteocyte lacunae extend numerous dendrites into canaliculi less than a micron in diameter and which are distributed throughout bone matrix. Although osteoclasts are the primary bone-resorbing cells, osteocytes also reportedly dissolve hydroxyapatite at peri-lacunar bone matrix. However, robust three-dimensional evidence for peri-canalicular bone mineral dissolution has been lacking. Here we applied a previously reported Talbot-defocus multiscan tomography method for synchrotron X-ray microscopy and analyzed the degree of bone mineralization in mouse cortical bone around the lacuno-canalicular network, which is connected both to blood vessels and the peri- and endosteum. We detected cylindrical low mineral density regions spreading around canaliculi derived from a subset of osteocytes. Transmission electron microscopy revealed both intact and demineralized bone matrix around the canaliculus. Peri-canalicular low mineral density regions were also observed in osteopetrotic mice lacking osteoclasts, indicating that osteoclasts are dispensable for peri-canalicular demineralization. These data suggest demineralization can occur from within bone through the canalicular system, and that peri-canalicular demineralization occurs not uniformly but directed by individual osteocytes. Blockade of peri-canalicular demineralization may be a therapeutic strategy to increase bone mass and quality.Entities:
Keywords: Demineralization/remineralization; Mineral metabolism; Osteocyte canaliculus; Osteocytic osteolysis; Synchrotron radiation; Talbot-defocus multiscan tomography
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Year: 2015 PMID: 26709236 DOI: 10.1016/j.bone.2015.12.006
Source DB: PubMed Journal: Bone ISSN: 1873-2763 Impact factor: 4.398