Adherence and viability of primary human keratinocytes and primary human dermal fibroblasts on acrylonitrile-based copolymers with different concentrations of positively charged functional groups

被引:8
作者
Trescher, Karoline
Scharnagl, Nico
Kratz, Karl
Roch, Toralf
Lendlein, Andreas [1 ,2 ]
Jung, Friedrich
机构
[1] Helmholtz Zentrum Geesthacht, Ctr Biomat Dev, Polymer Res Inst, D-14513 Teltow, Germany
[2] Helmholtz Zentrum Geesthacht, Berlin Brandenburg Ctr Regenerat Therapies BCRT, Polymer Res Inst, D-14513 Teltow, Germany
关键词
Keratinocytes; fibroblasts; coculture; amine functional group; surface charge; SURFACE WETTABILITY; STEM-CELLS; IN-VITRO; ADHESION; ATTACHMENT; CULTIVATION; MEMBRANES; POLYMERS; CULTURE; SYSTEMS;
D O I
10.3233/CH-2012-1613
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
As shown in several studies, various properties of biomaterials such as stiffness, surface roughness, chemical composition or the amount of functional groups at the surface can influence adhesion, viability, proliferation and functionalities of cells. The aim of this work was to explore whether a cell-selective effect could be achieved for acrylonitrile-based copolymers containing different contents of positively charged functional groups, which were introduced by incorporation of methacrylic acid-2-aminoethylester hydrochloride (AEMA) units. The p(AN-co-AEMA) copolymers were synthesized by suspension polymerization in water and processed into disk shaped test specimen via a sintering process to ensure the absence of organic solvents in the copolymers. Copolymers with an AEMA content of 1.4, 1.6, and 4.4 mol-% were investigated according to their cell-selective capacity, which should support the adhesion, viability and proliferation of keratinocytes, while the adherence of fibroblasts should rather be disabled. The test samples were seeded with primary human keratinocytes and primary human dermal fibroblasts in monoas well as in co-cultures. Tissue culture plate polystyrene (TCP) was used to control the physiologic growth of the cells. Density and viability of attached and non-adherent cells were analyzed by live/dead staining, lactate dehydrogenase (LDH) assay and flow cytometry with DAPI staining. For the assured discrimination of adherent cell types in coculture a keratin/vimentin-staining was performed. On copolymers with 4.4 mol-% AEMA adherent keratinocytes in monoculture and cocultured keratinocytes and fibroblasts showed a higher viability, a lower impairment of cell membranes and higher densities of viable cells compared to both other copolymers. For adherent fibroblasts these parameters did not differ between the copolymers and an increasing ratio of keratinocytes to fibroblasts in cocultures were found with increasing AEMA content. The results showed that keratinocytes and fibroblasts can be influenced by copolymers with different contents of positively charged functional groups. Since the tendency of a better adherence and viability of keratinocytes with increasing amounts of positively charged functional groups was shown, the potential enhancement by further increase of the amount of positively charged functional groups shall be tested in a future study.
引用
收藏
页码:391 / 401
页数:11
相关论文
共 34 条
[1]   Isolation and cultivation of human keratinocytes from skin or plucked hair for the generation of induced pluripotent stem cells [J].
Aasen, Trond ;
Izpisua Belmonte, Juan Carlos .
NATURE PROTOCOLS, 2010, 5 (02) :371-382
[3]   Modulation of cell adhesion, proliferation and differentiation on materials designed for body implants [J].
Bacakova, Lucie ;
Filova, Elena ;
Parizek, Martin ;
Ruml, Tomas ;
Svorcik, Vaclav .
BIOTECHNOLOGY ADVANCES, 2011, 29 (06) :739-767
[4]   Membranes from acrylonitrile-based polymers for selective cultivation of human keratinocytes [J].
Boese, Gregor ;
Trimpert, Christiane ;
Albrecht, Wolfgang ;
Malsch, Gunter ;
Groth, Thomas ;
Lendlein, Andreas .
TISSUE ENGINEERING, 2007, 13 (12) :2995-3002
[5]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[6]   Designing tailored biomaterial surfaces to direct keratinocyte morphology, attachment, and differentiation [J].
Bush, K. A. ;
Driscoll, P. F. ;
Soto, E. R. ;
Lambert, C. R. ;
McGimpsey, W. G. ;
Pins, G. D. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2009, 90A (04) :999-1009
[7]   Melt-processable hydrophobic acrylonitrile-based copolymer systems with adjustable elastic properties designed for biomedical applications [J].
Cui, J. ;
Trescher, K. ;
Kratz, K. ;
Jung, F. ;
Hiebl, B. ;
Lendlein, A. .
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION, 2010, 45 (2-4) :401-411
[8]   Controlling the phenotype and function of mesenchymal stem cells in vitro by adhesion to silane-modified clean glass surfaces [J].
Curran, JM ;
Chen, R ;
Hunt, JA .
BIOMATERIALS, 2005, 26 (34) :7057-7067
[9]   Feeder layer- and animal product-free culture of neonatal foreskin keratinocytes: improved performance, usability, quality and safety [J].
De Corte, Peter ;
Verween, Gunther ;
Verbeken, Gilbert ;
Rose, Thomas ;
Jennes, Serge ;
De Coninck, Arlette ;
Roseeuw, Diane ;
Vanderkelen, Alain ;
Kets, Eric ;
Haddow, David ;
Pirnay, Jean-Paul .
CELL AND TISSUE BANKING, 2012, 13 (01) :175-189
[10]   Studies in vitro on the role of alpha v and beta 1 integrins in the adhesion of human dermal fibroblasts to provisional matrix proteins fibronectin, vibronectin, and fibrinogen [J].
Gailit, J ;
Clark, RAF .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 106 (01) :102-108