ABERRANT GENE-EXPRESSION IN CULTURED MAMMALIAN BONE-CELLS DEMONSTRATES AN OSTEOBLAST DEFECT IN OSTEOPETROSIS

被引:21
作者
JACKSON, ME [1 ]
SHALHOUB, V [1 ]
LIAN, JB [1 ]
STEIN, GS [1 ]
MARKS, SC [1 ]
机构
[1] UNIV MASSACHUSETTS, SCH MED, DEPT CELL BIOL, WORCESTER, MA 01655 USA
关键词
OSTEOCLAST; GENE REGULATION; RAT; SKELETON; OSTEOPONTIN; OSTEOCALCIN; MINERALIZATION;
D O I
10.1002/jcb.240550314
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Osteopetrosis is a skeletal condition in which a generalized radioopacity of bone is caused by reduced resorption of bone by osteoclasts. However, it has recently been shown that during skeletal development in several osteopetrotic rat mutations specific aberrations occur in gene expression reflecting the activity of the bone forming cells, osteoblasts, and the development of tissue organization. To evaluate their pathogenetic significance, progressive osteoblast differentiation was studied in vitro. Primary cultures of normal osteoblasts undergo a sequential expression of cell growth and tissue-related genes associated with development of skeletal tissue. We report that osteoblast cultures can be established from one of these mutants, toothless; that these cells in vitro exhibit similar aberrations in gene expression during cell proliferation and extracellular matrix formation and mineralization observed in vivo; and that an accelerated maturation sequence by mutant osteoblasts mimics the characteristic skeletal sclerosis of this disease. These data are the first direct evidence for an intrinsic osteoblast defect in osteopetrosis and establish an in vitro model for the study of heritable skeletal disorders. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:366 / 372
页数:7
相关论文
共 23 条
[1]  
ABE E, 1988, J BONE MINER RES, V3, P635
[2]   FACTORS THAT PROMOTE PROGRESSIVE DEVELOPMENT OF THE OSTEOBLAST PHENOTYPE IN CULTURED FETAL-RAT CALVARIA CELLS [J].
ARONOW, MA ;
GERSTENFELD, LC ;
OWEN, TA ;
TASSINARI, MS ;
STEIN, GS ;
LIAN, JB .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 143 (02) :213-221
[3]   MINERALIZED BONE NODULES FORMED INVITRO FROM ENZYMATICALLY RELEASED RAT CALVARIA CELL-POPULATIONS [J].
BELLOWS, CG ;
AUBIN, JE ;
HEERSCHE, JNM ;
ANTOSZ, ME .
CALCIFIED TISSUE INTERNATIONAL, 1986, 38 (03) :143-154
[4]  
COTTON WR, 1974, P SOC EXP BIOL MED, V146, P554, DOI 10.3181/00379727-146-38146
[5]   EXPRESSION OF DIFFERENTIATED FUNCTION BY MINERALIZING CULTURES OF CHICKEN OSTEOBLASTS [J].
GERSTENFELD, LC ;
CHIPMAN, SD ;
GLOWACKI, J ;
LIAN, JB .
DEVELOPMENTAL BIOLOGY, 1987, 122 (01) :49-60
[6]   IMPAIRED RECRUITMENT AND DIFFERENTIATION OF OSTEOCLAST PROGENITORS BY OSTEOCALCIN-DEPLETE BONE IMPLANTS [J].
GLOWACKI, J ;
LIAN, JB .
CELL DIFFERENTIATION, 1987, 21 (04) :247-254
[7]   FUNCTIONAL AND MOLECULAR-CHANGES IN COLONY STIMULATING FACTOR SECRETION BY OSTEOBLASTS [J].
HOROWITZ, MC ;
EINHORN, TA ;
PHILBRICK, W ;
JILKA, RL .
CONNECTIVE TISSUE RESEARCH, 1989, 20 (1-4) :159-168
[8]   OSTEOPETROSIS IN THE RAT - COEXISTENCE OF REDUCTIONS IN OSTEOCALCIN AND BONE-RESORPTION [J].
LIAN, JB ;
MARKS, SC .
ENDOCRINOLOGY, 1990, 126 (02) :955-962
[9]   RECRUITMENT OF OSTEOCLAST PRECURSORS BY PURIFIED BONE-MATRIX CONSTITUENTS [J].
MALONE, JD ;
TEITELBAUM, SL ;
GRIFFIN, GL ;
SENIOR, RM ;
KAHN, AJ .
JOURNAL OF CELL BIOLOGY, 1982, 92 (01) :227-230
[10]   ADMINISTRATION OF COLONY STIMULATING FACTOR-I CORRECTS SOME MACROPHAGE, DENTAL, AND SKELETAL DEFECTS IN AN OSTEOPETROTIC MUTATION (TOOTHLESS, TL) IN THE RAT [J].
MARKS, SC ;
WOJTOWICZ, A ;
SZPERL, M ;
URBANOWSKA, E ;
MACKAY, CA ;
WIKTORJEDRZEJCZAK, W ;
STANLEY, ER ;
AUKERMAN, SL .
BONE, 1992, 13 (01) :89-93