Human alveolar bone cells interact with ProRoot and tooth-colored MTA

被引:70
作者
Al-Rabeah, Ebtehal [1 ]
Perinpanayagam, Hiran [1 ]
MacFarland, Don [1 ]
机构
[1] Univ Buffalo, Sch Dent Med, Dept Oral Biol, Buffalo, NY 14214 USA
关键词
alveolar bone; human osteoblast; mineral trioxide aggregate;
D O I
10.1016/j.joen.2006.03.019
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The cellular response to mineral trioxide aggregate (MTA) is important for the repair and regeneration of periradicular tissues. The purpose of this study was to analyze the response of human alveolar bone cells to MTA. A human alveolar bone chip was obtained from an oral surgical procedure and explant cultures harvested after 3 to 4 weeks of outgrowth in a-minimum essential medium supplemented with fetal calf serum. Cells in early passage were seeded onto preset ProRoot (gray) MTA, tooth-colored (white) MTA, and MTA prepared with local anesthetic solution. Scanning electron microscopy showed cells were attached and spread out onto MTA within 24 hours, and proliferated to form a matrix-like layer within 7 days. Cell attachment and cell-surface interactions with the gray and white MTA, and with the MTA prepared with local anesthetic were comparably propagated for 14 days. The surgically derived human alveolar bone cells provided a clinically relevant model that demonstrated the capacity of both ProRoot and tooth-colored MTA to support cell attachment, proliferation, and matrix formation.
引用
收藏
页码:872 / 875
页数:4
相关论文
共 16 条
[1]   An evaluation of accelerated Portland cement as a restorative material [J].
Abdullah, D ;
Ford, TRP ;
Papaioannou, S ;
Nicholson, J ;
McDonald, F .
BIOMATERIALS, 2002, 23 (19) :4001-4010
[2]   Attachment and morphological behavior of human periodontal ligament fibroblasts to mineral trioxide aggregate: A scanning electron microscope study [J].
Balto, HA .
JOURNAL OF ENDODONTICS, 2004, 30 (01) :25-29
[3]   Root-end filling materials alter fibroblast differentiation [J].
Bonson, S ;
Jeansonne, BG ;
Lallier, TE .
JOURNAL OF DENTAL RESEARCH, 2004, 83 (05) :408-413
[4]   Effects of sphingosine-1-phosphate and lysophosphatidic acid on human osteoblastic cells [J].
Dziak, R ;
Yang, BM ;
Leung, BW ;
Li, S ;
Marzec, N ;
Margarone, J ;
Bobek, L .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2003, 68 (03) :239-249
[5]   Engineering a bioactive matrix by modifications of calcium sulfate [J].
Intini, G ;
Andreana, S ;
Margarone, JE ;
Bush, PJ ;
Dziak, R .
TISSUE ENGINEERING, 2002, 8 (06) :997-1008
[6]   Cellular response to Mineral Trioxide Aggregate [J].
Koh, ET ;
McDonald, F ;
Ford, TRP ;
Torabinejad, M .
JOURNAL OF ENDODONTICS, 1998, 24 (08) :543-547
[7]  
Koh ET, 1997, J BIOMED MATER RES, V37, P432, DOI 10.1002/(SICI)1097-4636(19971205)37:3<432::AID-JBM14>3.0.CO
[8]  
2-D
[9]   Role of protein kinase C α in primary human osteoblast proliferation [J].
Lampasso, JD ;
Marzec, N ;
Margarone, J ;
Dziak, R .
JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 (11) :1968-1976
[10]   Sphingosine-1-phosphate effects on PKC isoform expression in human osteoblastic cells [J].
Lampasso, JD ;
Kamer, A ;
Margarone, J ;
Dziak, R .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2001, 65 (03) :139-146