Matrix vesicles and calcification.

被引:414
作者
H. Clarke Anderson
机构
[1] Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, 2017 Wahl Hall West, 3901 Rainbow Boulevard, Kansas City, 66160-7410, KS
基金
美国国家卫生研究院;
关键词
Articular Cartilage; Growth Plate; Hypertrophic Chondrocytes; Matrix Vesicle; Growth Plate Chondrocytes;
D O I
10.1007/s11926-003-0071-z
中图分类号
学科分类号
摘要
Matrix vesicles (MVs) are extracellular, 100 nM in diameter, membrane-invested particles selectively located at sites of initial calcification in cartilage, bone, and predentin. The first crystals of apatitic bone mineral are formed within MVs close to the inner surfaces of their investing membranes. Matrix vesicle biogenesis occurs by polarized budding and pinching-off of vesicles from specific regions of the outer plasma membranes of differentiating growth plate chondrocytes, osteoblasts, and odontoblasts. Polarized release of MVs into selected areas of developing matrix determines the nonrandom distribution of calcification. Initiation of the first mineral crystals, within MVs (phase 1), is augmented by the activity of MV phosphatases (eg, alkaline phosphatase, adenosine triphosphatase and pyrophosphatase) plus calcium-binding molecules (eg, annexin I and phosphatidyl serine), all of which are concentrated in or near the MV membrane. Phase 2 of biologic mineralization begins with crystal release through the MV membrane, exposing preformed hydroxyapatite crystals to the extracellular fluid. The extracellular fluid normally contains sufficient Ca2+ and PO4(3-) to support continuous crystal proliferation, with preformed crystals serving as nuclei (templates) for the formation of new crystals by a process of homologous nucleation. In diseases such as osteoarthritis, crystal deposition arthritis, and atherosclerosis, MVs initiate pathologic calcification, which, in turn, augments disease progression.
引用
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页码:222 / 226
页数:4
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共 138 条
  • [1] Caswell AM(1987)Nucleoside triphosphate pyrophosphatase of rabbit matrix vesicles: a mechanism for the generation of inorganic pyrophosphate in epiphyseal cartilage Biochim Biophys Acta 924 276-283
  • [2] Ali SY(1962)Mechanism of calcification: inhibitory role of pyrophosphate Nature 195 911-911
  • [3] Russel RGG(1985)Role of proteoglycans in endochondral ossification: inhibition of calcification Calcif Tiss Int 37 360-564
  • [4] Fleisch H(1997)Spontaneous calcification of arteries and cartilage in mice lacking matrix Gla protein Nature 386 78-81
  • [5] Bisaz S(1995)Molecular biology of matrix vesicles Clin Orthop Rel Res 314 266-280
  • [6] Dziewaitkowski DD(1989)Cellular turnover at the chondroosseous junction of growth plate cartilage: analysis of serial sections at the light microscopic level J Orthop Res 7 654-666
  • [7] Majznerski LL(1978)The characterization of the tide mark in human articular cartilage Met Bone Dis Rel Res 1 115-118
  • [8] Luo G(1971)Phosphatases of epiphyseal cartilage studied by electron microscopic cytochemical methods J Histochem Cytochem 19 801-808
  • [9] Ducy P(1985)Immunolocalization of short chain cartilage collagen (type X) in Avian tissues J Cell Biol 100 598-605
  • [10] McKee MD(1987)Biochemistry of the glycosylphosphatidyl inositol membrane protein anchors Biochem J 244 1-13