Osteocyte regulation of bone mineral: a little give and take

被引:128
作者
Atkins, G. J. [1 ]
Findlay, D. M. [1 ]
机构
[1] Univ Adelaide, Bone Cell Biol Grp, Discipline Orthopaed & Trauma, Adelaide, SA 5005, Australia
关键词
Mineralization; Osteocyte; RANKL; Sclerostin; VAN-BUCHEM-DISEASE; OSTEOCLASTOGENESIS-INHIBITORY FACTOR; HUMAN PRIMARY OSTEOBLASTS; DIFFERENTIATION IN-VITRO; MORPHOGENETIC PROTEIN; ACIDIC GLYCOPROTEIN-75; MATRIX MINERALIZATION; ALKALINE-PHOSPHATASE; PARATHYROID-HORMONE; ASARM-PEPTIDES;
D O I
10.1007/s00198-012-1915-z
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Osteocytes actively participate in almost every phase of mineral handling by bone. They regulate the mineralisation of osteoid during bone formation, and they are also a major RANKL-producing cell. Osteocytes are thus able to liberate bone mineral by regulating osteoclast differentiation and activity in response to a range of stimuli, including bone matrix damage, bone disuse and mechanical unloading, oestrogen deficiency, high-dose glucocorticoid and chemotherapeutic agents. At least some of these activities may be regulated by the osteocyte-secreted product, sclerostin. There is also mounting evidence that in addition to regulating phosphate homeostasis systemically, osteocytes contribute directly to calcium homeostasis in the mature skeleton. Osteocyte cell death and the local loss of control of bone mineralisation may be the cause of focal hypermineralisation of bone and osteopetrosis, as seen in aging and pathology. The sheer number of osteocytes in bone means that 'a little give and take' in terms of regulation of bone mineral content translates into a powerful whole organism effect.
引用
收藏
页码:2067 / 2079
页数:13
相关论文
共 127 条
[41]
Drilling k-wires, what about the osteocytes? An experimental study in rabbits [J].
Franssen, Bas B. G. M. ;
van Diest, Paul J. ;
Schuurman, Arnold H. ;
Kon, Moshe .
ARCHIVES OF ORTHOPAEDIC AND TRAUMA SURGERY, 2008, 128 (01) :83-87
[42]
Buried alive: How osteoblasts become osteocytes [J].
Franz-Odendaal, TA ;
Hall, BK ;
Witten, PE .
DEVELOPMENTAL DYNAMICS, 2006, 235 (01) :176-190
[43]
MICROPETROSIS [J].
FROST, HM .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1960, 42 (01) :144-150
[44]
Gaudin-Audrain C, 2008, HISTOL HISTOPATHOL, V23, P469, DOI 10.14670/HH-23.469
[45]
Canonical Wnt signaling in differentiated osteoblasts controls osteoclast differentiation [J].
Glass, DA ;
Bialek, P ;
Ahn, JD ;
Starbuck, M ;
Patel, MS ;
Clevers, H ;
Taketo, MM ;
Long, FX ;
McMahon, AP ;
Lang, RA ;
Karsenty, G .
DEVELOPMENTAL CELL, 2005, 8 (05) :751-764
[46]
Role of matrix vesicles in biomineralization [J].
Golub, Ellis E. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2009, 1790 (12) :1592-1598
[47]
Inhibition of Proprotein Convertase SKI-1 Blocks Transcription of Key Extracellular Matrix Genes Regulating Osteoblastic Mineralization [J].
Gorski, Jeff P. ;
Huffman, Nichole T. ;
Chittur, Sridar ;
Midura, Ronald J. ;
Black, Claudine ;
Oxford, Julie ;
Seidah, Nabil G. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (03) :1836-1849
[48]
Biomineralization of bone: a fresh view of the roles of non-collagenous proteins [J].
Gorski, Jeffrey Paul .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2011, 16 :2598-2621
[49]
Extracellular bone acidic glycoprotein-75 defines condensed mesenchyme regions to be mineralized and localizes with bone sialoprotein during intramembranous bone formation [J].
Gorski, JP ;
Wang, AM ;
Lovitch, D ;
Law, D ;
Powell, K ;
Midura, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (24) :25455-25463
[50]
Inhibition of MEPE cleavage by Phex [J].
Guo, R ;
Rowe, PSN ;
Liu, SG ;
Simpson, LG ;
Xiao, ZS ;
Quarles, LD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 297 (01) :38-45