Root-end filling materials alter fibroblast differentiation

被引:108
作者
Bonson, S
Jeansonne, BG
Lallier, TE
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Sch Dent,Dept Cell Biol & Anat, Ctr Excellence Oral & Craniofacial Biol, New Orleans, LA 70119 USA
[2] Louisiana State Univ, Hlth Sci Ctr, Sch Dent,Dept Endodont, Ctr Excellence Oral & Craniofacial Biol, New Orleans, LA 70119 USA
关键词
periodontal ligament; gingival fibroblast; cementogenesis; endodontics;
D O I
10.1177/154405910408300511
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Root-end filling materials are commonly used following endodontic surgical procedures; however, their effect on adjacent soft tissues is poorly understood. We predict that, due to the differences in their chemical composition, these materials will have profoundly different effects on the survival and differentiation of fibroblasts. Many of the root-end filling materials examined were initially cytotoxic to both PDL and gingival fibroblasts in co-culture experiments; however, this was reduced after the materials were washed in either mineral trioxide aggregate (MTA) or hybrid ionomere composite resin (HICR) for 2 wks. Additionally, PDL fibroblasts displayed enhanced proliferation on MTA and survival on amalgam when compared with gingival fibroblasts. MTA preferentially induced alkaline phosphatase expression and activity in both PDL and gingival fibroblasts. In contrast, HICR inhibited alkaline phosphatase expression and activity. In addition, MTA and HICR repressed pleiotrophin in PDL fibroblasts, while HICR repressed periostin in both fibroblasts. Thus, root-end filling materials differentially affect periodontal fibroblast differentiation. Abbreviations: mineral trioxide aggregate (MTA), zinc-oxide eugenol cement (ZOEC), hybrid ionomer composite resin ( HICR), reverse-transcriptase polymerase chain-reaction (RT-PCR).
引用
收藏
页码:408 / 413
页数:6
相关论文
共 26 条
[1]   Molecular and cell biology of the gingiva [J].
Bartold, PM ;
Walsh, LJ ;
Narayanan, S .
PERIODONTOLOGY 2000, 2000, 24 :28-55
[2]   Cloning and characterization of a novel β integrin-related cDNA coding for the protein TIED ("ten β integrin EGF-like repeat domains") that maps to chromosome band 13q33:: A divergent stand-alone integrin stalk structure [J].
Berg, RW ;
Leung, E ;
Gough, S ;
Morris, C ;
Yao, WP ;
Wang, SX ;
Ni, J ;
Krissansen, GW .
GENOMICS, 1999, 56 (02) :169-178
[3]   FORMATION OF NEW PERIODONTAL-LIGAMENT BY PERIODONTAL-LIGAMENT CELLS IMPLANTED INVIVO AFTER CULTURE INVITRO - A PRELIMINARY-STUDY OF TRANSPLANTED ROOTS IN THE DOG [J].
BOYKO, GA ;
MELCHER, AH ;
BRUNETTE, DM .
JOURNAL OF PERIODONTAL RESEARCH, 1981, 16 (01) :73-88
[4]   RETROGRADE FILLING MATERIALS - A RETROSPECTIVE SUCCESS-FAILURE STUDY OF AMALGAM, EBA, AND IRM [J].
DORN, SO ;
GARTNER, AH .
JOURNAL OF ENDODONTICS, 1990, 16 (08) :391-393
[5]  
Dragoo MR, 1997, INT J PERIODONT REST, V17, P74
[6]  
GARTNER A H, 1992, Dental Clinics of North America, V36, P357
[7]   Identification and characterization of a novel protein, periostin, with restricted expression to periosteum and periodontal ligament and increased expression by transforming growth factor β [J].
Horiuchi, K ;
Amizuka, N ;
Takeshita, S ;
Takamatsu, H ;
Katsuura, M ;
Ozawa, H ;
Toyama, Y ;
Bonewald, LF ;
Kudo, A .
JOURNAL OF BONE AND MINERAL RESEARCH, 1999, 14 (07) :1239-1249
[8]   Nidogen is nonessential and not required for normal type IV collagen localization in Caenorhabditis elegans [J].
Kang, SH ;
Kramer, JM .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (11) :3911-3923
[9]   Cellular response to Mineral Trioxide Aggregate [J].
Koh, ET ;
McDonald, F ;
Ford, TRP ;
Torabinejad, M .
JOURNAL OF ENDODONTICS, 1998, 24 (08) :543-547
[10]   Alkaline phosphatase activity is unregulated in regenerating human periodontal cells [J].
Kuru, L ;
Griffiths, GS ;
Petrie, A ;
Olsen, I .
JOURNAL OF PERIODONTAL RESEARCH, 1999, 34 (02) :123-127