Migration of osteoblastic cells on various guided bone regeneration membranes

被引:72
作者
Takata, T
Wang, HL
Miyauchi, M
机构
[1] Hiroshima Univ, Fac Dent, Dept Oral Pathol, Minami Ku, Hiroshima 7348553, Japan
[2] Univ Michigan, Sch Dent, Dept Periodont Prevent Geriatr, Ann Arbor, MI 48109 USA
关键词
guided bone regeneration; osteoblasts; cell migration; cell culture; barrier membranes; bioabsorbable; nonresorbable;
D O I
10.1034/j.1600-0501.2001.012004332.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
To evaluate the biological effects of guided bone regeneration (GBR) barrier : materials on osteoblastic cell migration, migration of mouse osteoprogenitor eel Is (MC3T3-E1) was examined, in vitro, on various membranes. Eight commercially available GBR membranes - bovine type I collagen (BioMend (TM); BM), porcine type I collagen (BioGide (R); BG), bovine type I atelocollagen (Tissue Guide (R); TC), polylactic acid (Epi-Guide (R); EC), copolymer of polylactic acid and polyglycolic acid (Resolute (R); RL, Resolut XT (R); RL-XT), expanded polytetrafluoroethylene (e-PTFE; Gore Tex (R); GT) and co-polymer of cellulose acetate and nitrocellulose (Millipore filter (R); MP) - were tested. A 3x5 mm section of the membrane was fixed to the bottom of a culture dish with double-sided adhesive tape, and half of the membrane was closely covered by PARAFILM (R) (American National Can (TM) )to leave an unexposed area for cell migration. The border between exposed and unexposed areas was marked as a baseline of cell migration. Membranes were then plated with 3 mi of cell suspension at an initial density of 1x10(5) cells/ml in alpha -MEM culture medium with 10% fetal bovine serum and ascorbic acid. After a 5-hour incubation, non-attached cells were completely washed out with phosphate buffered saline and the PARAFlLM (R) cover was removed. After 3 days cultivation, specimens were fixed with 10% buffered formalin and stained briefly with hematoxylin. The area of cell migration on a membrane was analyzed using a LA 500 Image Analysis System and migration area per unit length of the baseline (mm(2)/mm) was compared among membranes. Results demonstrated that cell migration was greater in the order: RL>RL-XT, BW, TC, MP > EG, BG. Membranes except for Bt, EG and GT showed the migration rate equal to or higher than a plastic culture cover slip (Celldesk (R)) (P <0.01) on which cells generally grow favorably Only a small number of the cells attached to CT, and the net cell migration for the membrane could not be determined. These results indicate that CBR barrier materials per se may influence the process of bone regeneration in vivo through the effects of their presence on cell migration.
引用
收藏
页码:332 / 338
页数:7
相关论文
共 17 条
[1]  
Brunette D M, 1988, Int J Oral Maxillofac Implants, V3, P231
[2]  
BURRIDGE K, 1986, Cancer Reviews, V4, P18
[3]  
BURRIDGE K, 1987, J CELL SCI, P211
[4]   Lateral ridge augmentation using autografts and barrier membranes: A clinical study with 40 partially edentulous patients [J].
Buser, D ;
Dula, K ;
Hirt, HP ;
Schenk, RK .
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 1996, 54 (04) :420-432
[5]   Regeneration and enlargement of jaw bone using guided tissue regeneration [J].
Buser, D. ;
Braegger, U. ;
Lang, N. P. ;
Nyman, S. .
CLINICAL ORAL IMPLANTS RESEARCH, 1990, 1 (01) :22-32
[6]  
Grinnell F, 1978, Int Rev Cytol, V53, P65
[7]  
Hämmerle CHF, 1999, PROCEEDINGS OF THE 3RD EUROPEAN WORKSHOP ON PERIODONTOLOGY: IMPLANT DENTISTRY, P468
[8]   Phenotype expression of gingival fibroblasts cultured on membranes used in guided tissue regeneration [J].
Locci, P ;
Calvitti, M ;
Belcastro, S ;
Pugliese, M ;
Guerra, M ;
Marinucci, L ;
Staffolani, N ;
Becchetti, E .
JOURNAL OF PERIODONTOLOGY, 1997, 68 (09) :857-863
[9]  
Nagahara K, 1995, Int J Oral Maxillofac Implants, V10, P109
[10]   Migration of human gingival fibroblasts over guided tissue regeneration barrier materials [J].
Payne, JM ;
Cobb, CM ;
Rapley, JW ;
Killoy, WJ ;
Spencer, P .
JOURNAL OF PERIODONTOLOGY, 1996, 67 (03) :236-244