Interactions of acinar cells on biomaterials with various surf ace properties

被引:29
作者
Chen, MH
Hsu, YH
Lin, CP
Chen, YJ
Young, TH
机构
[1] Natl Taiwan Univ, Coll Med, Inst Biomed Engn, Taipei 100, Taiwan
[2] Natl Taiwan Univ, Coll Engn, Taipei 100, Taiwan
[3] Natl Taiwan Univ Hosp, Taipei 100, Taiwan
[4] Natl Taiwan Univ, Coll Med, Sch Dent, Taipei 100, Taiwan
关键词
acinar cells; PVDF; hydrophilicity; artificial salivary gland;
D O I
10.1002/jbm.a.30376
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The purpose of this study is to evaluate the interactions of rat parotid acinar cells on biomaterials with different surface properties. The biomaterials used in this study included polyvinyl alcohol (PVA), chitosan, poly (ethylene-co-vinyl alcohol) (EVAL), and polyvinylidene fluoride (PVDF). Cell morphology was observed by photomicroscope. Cell growth and differentiated characteristic function were separately assayed with 3-(4,5-dimethylthiazol-2-yl)2,5-diphenyl tetrazolium bromide (MTT) reduction activity and amylase activity. Results indicated that behaviors of acinar cells on materials might differ to a great extent depending on the surface hydrophilicity and morphology of the materials. On the relatively hydrophobic materials, the abilities of acinar cells to adhere and proliferate increased simultaneously. In addition, porous PVDF had higher cell growth compared with dense PVDF. Therefore, the hydrophobic PVDF with a porous structure was the best substrate for culturing acinar cells. According to our findings, a tubular PVDF scaffold with dense outer surface to prevent saliva leakage and with porous inner surface for the cell growth was proposed to serve as an artificial salivary gland for future use in the treatment of patients with salivary hypofunction. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:254 / 262
页数:9
相关论文
共 24 条
[2]   Proliferation and phenotypic preservation of rat parotid acinar cells [J].
Chen, MH ;
Chen, RS ;
Hsu, YH ;
Chen, YJ ;
Young, TH .
TISSUE ENGINEERING, 2005, 11 (3-4) :526-534
[3]   Establishment of a convenient system for the long-term culture and study of non-neoplastic human salivary gland epithelial cells [J].
Dimitriou, ID ;
Kapsogeorgou, EK ;
Abu-Helu, RF ;
Moutsopoulos, HM ;
Manoussakis, MN .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2002, 110 (01) :21-30
[4]   Acquired salivary dysfunction - Drugs and radiation [J].
Fox, PC .
SALIVARY GLAND BIOGENESIS AND FUNCTION, 1998, 842 :132-137
[5]  
Grinnell F, 1978, Int Rev Cytol, V53, P65
[6]   Identification of neurite outgrowth promoting sites on the laminin α3 chain G domain [J].
Kato, K ;
Utani, A ;
Suzuki, N ;
Mochizuki, M ;
Yamada, M ;
Nishi, N ;
Matsuura, H ;
Shinkai, H ;
Nomizu, M .
BIOCHEMISTRY, 2002, 41 (35) :10747-10753
[7]  
Kikkawa Y, 1996, IN VITRO CELL DEV-AN, V32, P46
[8]   TISSUE ENGINEERING [J].
LANGER, R ;
VACANTI, JP .
SCIENCE, 1993, 260 (5110) :920-926
[9]  
LEE HB, 1995, ENCY HDB BIOMATERIAL, V1, P371
[10]   Interaction of cells on chargeable functional group gradient surfaces [J].
Lee, JH ;
Lee, JW ;
Khang, G ;
Lee, HB .
BIOMATERIALS, 1997, 18 (04) :351-358