Transforming growth factor-β isoform expression in mature human healthy and carious molar teeth

被引:76
作者
Sloan, AJ [1 ]
Perry, H [1 ]
Matthews, JB [1 ]
Smith, AJ [1 ]
机构
[1] Univ Birmingham, Sch Dent, Birmingham, W Midlands, England
来源
HISTOCHEMICAL JOURNAL | 2000年 / 32卷 / 04期
关键词
D O I
10.1023/A:1004007202404
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transforming growth factor (TGF)-beta isoforms have been implicated in cellular signalling during tooth development and repair, but little is known of their cellular localisation or distribution within the dental tissues in the mature tooth. This study investigated the presence of TGF-beta 1, beta 2 and beta 3 isoforms in tissues of sound and carious human molar teeth, to understand better the expression of TGF-beta s during health and disease. In healthy tissues, odontoblasts, cells of the cell rich layer, pulpal fibroblasts and endothelial cells were stained to varying degrees for all isoforms, with TGF-beta 3 showing the greatest intensity and TGF-beta 1 the weakest intensity. Similar patterns of staining were observed in carious teeth; however, TGF-beta 1 showed significantly increased staining intensity within odontoblasts and pulpal cells of carious teeth (p < 0.001). Biochemical analysis showed greater amounts of TGF-beta 1 in tertiary dentine than in primary dentine samples. The expression of TGF-beta s in odontoblasts and the increased presence of TGF-beta 1 in tertiary dentine suggest that these isoforms may be important in odontoblast behaviour and the modulation of the tissue response to injury.
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页码:247 / 252
页数:6
相关论文
共 32 条
[1]  
BEGUEKIRN C, 1994, INT J DEV BIOL, V38, P405
[2]   Physicochemical Activation of Recombinant Latent Transforming Growth Factor-beta's 1, 2, and 3 [J].
Brownh, Peter D. ;
Wakefiel, Lalage M. ;
Levinson, Arthur D. ;
Sporn, Michael B. .
GROWTH FACTORS, 1990, 3 (01) :35-43
[3]   IMMUNOLOCALIZATION OF TRANSFORMING GROWTH FACTOR-BETA-1 AND EPIDERMAL GROWTH-FACTOR RECEPTOR EPITOPES IN MOUSE INCISORS AND MOLARS WITH A DEMONSTRATION OF INVITRO PRODUCTION OF TRANSFORMING ACTIVITY [J].
CAM, Y ;
NEUMANN, MR ;
RUCH, JV .
ARCHIVES OF ORAL BIOLOGY, 1990, 35 (10) :813-822
[4]   Distribution of transforming growth factor-beta(1)-binding proteins and low-affinity receptors during odontoblast differentiation in the mouse [J].
Cam, Y ;
Lesot, H ;
Colosetti, P ;
Ruch, JV .
ARCHIVES OF ORAL BIOLOGY, 1997, 42 (05) :385-391
[5]   Comparative analysis of transforming growth factor-beta isoforms 1-3 in human and rabbit dentine matrices [J].
Cassidy, N ;
Fahey, M ;
Prime, SS ;
Smith, AJ .
ARCHIVES OF ORAL BIOLOGY, 1997, 42 (03) :219-223
[6]   SPECIFIC TRANSFORMING GROWTH-FACTOR-BETA SUBTYPES REGULATE EMBRYONIC MOUSE MECKELS CARTILAGE AND TOOTH DEVELOPMENT [J].
CHAI, Y ;
MAH, A ;
CROHIN, C ;
GROFF, S ;
BRINGAS, P ;
LE, T ;
SANTOS, V ;
SLAVKIN, HC .
DEVELOPMENTAL BIOLOGY, 1994, 162 (01) :85-103
[7]   DIFFERENTIAL REGULATION OF THE EXPRESSION OF TRANSFORMING GROWTH FACTOR-BETA-S-1 AND FACTOR-BETA-2 BY RETINOIC ACID, EPIDERMAL GROWTH-FACTOR, AND DEXAMETHASONE IN NRK-49F AND A549 CELLS [J].
DANIELPOUR, D ;
KIM, KY ;
WINOKUR, TS ;
SPORN, MB .
JOURNAL OF CELLULAR PHYSIOLOGY, 1991, 148 (02) :235-244
[8]  
FINKELMAN RD, 1990, J BONE MINER RES, V5, P717
[9]   Transforming growth factors beta 1, beta 2, and beta 3 and their receptors are differentially regulated during normal and impaired wound healing [J].
Frank, S ;
Madlener, M ;
Werner, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (17) :10188-10193
[10]   Differential changes in transforming growth factor-β isoform expression during postnatal cardiac growth [J].
Haworth, RS ;
Brooks, G ;
Cummins, P ;
Dobie, K ;
Chilton, DC ;
Avkiran, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 245 (03) :923-927