Early expression of bone matrix proteins in osteogenic cell cultures

被引:45
作者
de Oliveira, PT [1 ]
Zalzal, SF [1 ]
Irie, K [1 ]
Nanci, A [1 ]
机构
[1] Univ Montreal, Fac Dent, Dept Stomatol, Lab Study Calcified Tissues & Biomat, Montreal, PQ, Canada
关键词
rat; bone; calvarial cell culture; immunofluorescence; bone sialoprotein; collagen; fibronectin; osteopontin;
D O I
10.1177/002215540305100509
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Osteogenic cells express some matrix proteins at early culture intervals. The aim of this study was to determine if, and in what proportion, cells used for plating contain bone sialoprotein (BSP) and osteopontin (OPN), two matrix proteins associated with initial events in bone formation. Their pattern of expression, as well as that of fibronectin (FN) and type I pro-collagen, was also examined at 6 hr and at 1 and 3 days. The cells were obtained by enzymatic digestion of newborn rat calvariae, and grown on glass coverslips. Cytocentrifuge preparations of isolated cells and coverslips were processed for single or dual immunolabeling with monoclonal and/or polyclonal primary antibodies, followed by fluorochrome-conjugated antibodies. The cell labeling was mainly associated with perinuclear elements. OPN was also distinctively found at peripheral cytoplasmic sites. About 31% of isolated cells were OPN-positive and 18% were BSP-positive. After 1 day, almost 50% of cells were immunoreactive for OPN and for type I pro-collagen, and still less than 20% reacted for BSP. Approximately 7% exhibited peripheral staining for OPN. Almost all cells were associated with extracellular FN. However, only 15% showed intracellular labeling. These results indicate that an important proportion of cells used for plating contain BSP and OPN, a situation that should be taken into consideration in experimental analyses of osteoblast activity in vitro.
引用
收藏
页码:633 / 641
页数:9
相关论文
共 44 条
[1]   Immunocytochemical demonstration of extracellular matrix proteins in isolated osteocytes [J].
Aarden, EM ;
Wassenaar, AMM ;
Alblas, MJ ;
Nijweide, PJ .
HISTOCHEMISTRY AND CELL BIOLOGY, 1996, 106 (05) :495-501
[2]   Advances in the osteoblast lineage [J].
Aubin, JE .
BIOCHEMISTRY AND CELL BIOLOGY, 1998, 76 (06) :899-910
[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]   DETERMINATION OF NUMBERS OF OSTEOPROGENITORS PRESENT IN ISOLATED FETAL-RAT CALVARIA CELLS-INVITRO [J].
BELLOWS, CG ;
AUBIN, JE .
DEVELOPMENTAL BIOLOGY, 1989, 133 (01) :8-13
[5]   LOCALIZATION OF BONE SIALOPROTEIN (BSP) TO GOLGI AND POST-GOLGI SECRETORY STRUCTURES IN OSTEOBLASTS AND TO DISCRETE SITES IN EARLY BONE-MATRIX [J].
BIANCO, P ;
RIMINUCCI, M ;
SILVESTRINI, G ;
BONUCCI, E ;
TERMINE, JD ;
FISHER, LW ;
ROBEY, PG .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1993, 41 (02) :193-203
[6]   Activation of integrin αvβ3 regulates cell adhesion and migration to bone sialoprotein [J].
Byzova, TV ;
Kim, W ;
Midura, RJ ;
Plow, EF .
EXPERIMENTAL CELL RESEARCH, 2000, 254 (02) :299-308
[7]   Individual osteoblasts in the developing calvaria express different gene repertoires [J].
Candeliere, GA ;
Liu, F ;
Aubin, JE .
BONE, 2001, 28 (04) :351-361
[8]  
CHEN JK, 1992, J BONE MINER RES, V7, P987
[9]   Role of osteopontin in cellular signaling and toxicant injury [J].
Denhardt, DT ;
Giachelli, CM ;
Rittling, SR .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2001, 41 :723-749
[10]   The osteoblast: A sophisticated fibroblast under central surveillance [J].
Ducy, P ;
Schinke, T ;
Karsenty, G .
SCIENCE, 2000, 289 (5484) :1501-1504