A comparative analysis of strategies for isolation of matrix vesicles

被引:21
作者
Balcerzak, M.
Radisson, J.
Azzar, G.
Farlay, D.
Bolvin, G.
Pikula, S.
Buchet, R. [1 ]
机构
[1] Univ Lyon 1, CNRS, UMR 5013, Dept Chem Biochem, F-69622 Villeurbanne, France
[2] Polish Acad Sci, M Nencki Inst Expt Biol, Dept Cellular Biochem, PL-02093 Warsaw, Poland
[3] Univ Lyon 1, Fac Med R Laennec, INSERM, Unite 403, F-69372 Lyon, France
关键词
alkaline phosphatase; bone; calveolin; cholesterol; collagenase; hydroxyapatite; matrix vesicle; mineralization;
D O I
10.1016/j.ab.2006.10.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Matrix vesicles (MVs) are extracellular organelles involved in the initial steps of mineralization. MVs are isolated by two methods. The first isolation method of MVs starts with collagenase digestion of osseous tissues, followed by two differential centrifugations. The second isolation method does not use proteases but rather starts with differential centrifugation, followed by a fractionation on a sucrose gradient. The first method results in a homogeneous population of MVs with higher cholesterol/lipid content, alkaline phosphatase activity, and mineral formation rate as compared with MVs isolated by the second method. The second method leads to higher protein diversity as compared with MVs isolated according to the first method. Due to their distinct protein composition, lipid-to-protein and cholesterol-to-phospholipid ratios, and differences in rates of mineral formation, both types of isolated MVs are crucial for proteomic analysis and for understanding the regulation of mineralization process at the molecular level. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:176 / 182
页数:7
相关论文
共 33 条
[1]   ISOLATION AND CHARACTERIZATION OF CALCIFYING MATRIX VESICLES FROM EPIPHYSEAL CARTILAGE [J].
ALI, SY ;
SAJDERA, SW ;
ANDERSON, HC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1970, 67 (03) :1513-+
[2]   Phosphorylation-dependent phospholipase D activity of matrix vesicles [J].
Balcerzak, Marcin ;
Pikula, Slawomir ;
Buchet, Rene .
FEBS LETTERS, 2006, 580 (24) :5676-5680
[3]  
BARTLETT GR, 1959, J BIOL CHEM, V234, P466
[4]   CHARACTERIZATION, CLONING AND EXPRESSION OF THE 67-KDA ANNEXIN FROM CHICKEN GROWTH-PLATE CARTILAGE MATRIX VESICLES [J].
CAO, X ;
GENGE, BR ;
WU, LNY ;
BUZZI, WR ;
SHOWMAN, RM ;
WUTHIER, RE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 197 (02) :556-561
[5]  
Chen D, 2001, Penn Dent J (Phila), V101, P12
[6]  
CYBORON GW, 1981, J BIOL CHEM, V256, P7262
[7]   Authentic matrix vesicles contain active metalloproteases (MMP) -: A role for matrix vesicle-associated MMP-13 in activation of transforming growth factor-β [J].
D'Angelo, M ;
Billings, PC ;
Pacifici, M ;
Leboy, PS ;
Kirsch, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (14) :11347-11353
[8]   PROTEOGLYCAN INHIBITION OF CALCIUM-PHOSPHATE PRECIPITATION IN LIPOSOMAL SUSPENSIONS [J].
EANES, ED ;
HAILER, AW ;
MIDURA, RJ ;
HASCALL, VC .
GLYCOBIOLOGY, 1992, 2 (06) :571-578
[9]   INFRARED STUDIES OF APATITES .1. VIBRATIONAL ASSIGNMENTS FOR CALCIUM, STRONTIUM, AND BARIUM HYDROXYAPATITES UTILIZING ISOTOPIC-SUBSTITUTION [J].
FOWLER, BO .
INORGANIC CHEMISTRY, 1974, 13 (01) :194-207
[10]   Primary culture of rat growth plate chondrocytes: an in vitro model of growth plate histotype, matrix vesicle biogenesis and mineralization [J].
Garimella, R ;
Bi, XH ;
Camacho, N ;
Sipe, JB ;
Anderson, HC .
BONE, 2004, 34 (06) :961-970