Adhesion, Proliferation and Migration of NIH/3T3 Cells on Modified Polyaniline Surfaces

被引:23
|
作者
Rejmontova, Petra [1 ]
Capakova, Zdenka [1 ]
Mikusova, Nikola [1 ]
Marakova, Nela [1 ]
Kasparkova, Vera [1 ]
Lehocky, Marian [1 ]
Humpolicek, Petr [1 ]
机构
[1] Tomas Bata Univ Zlin, Ctr Polymer Syst, Trida Tomase Bati 5678, Zlin 76001, Czech Republic
来源
关键词
polyaniline; fibroblast; cyto-compatibility; sulfamic acid; phosphotungstic acid; poly (2-acrylamido-2-methyl-1-propanesulfonic) acid; POLYMER; BIOCOMPATIBILITY; CONDUCTIVITY; CYTOTOXICITY; DISPERSIONS; FILMS;
D O I
10.3390/ijms17091439
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polyaniline shows great potential and promises wide application in the biomedical field thanks to its intrinsic conductivity and material properties, which closely resemble natural tissues. Surface properties are crucial, as these predetermine any interaction with biological fluids, proteins and cells. An advantage of polyaniline is the simple modification of its surface, e.g., by using various dopant acids. An investigation was made into the adhesion, proliferation and migration of mouse embryonic fibroblasts on pristine polyaniline films and films doped with sulfamic and phosphotungstic acids. In addition, polyaniline films supplemented with poly (2-acrylamido-2-methyl-1-propanesulfonic) acid at various ratios were tested. Results showed that the NIH/3T3 cell line was able to adhere, proliferate and migrate on the pristine polyaniline films as well as those films doped with sulfamic and phosphotungstic acids; thus, utilization of said forms in biomedicine appears promising. Nevertheless, incorporating poly (2-acrylamido-2-methyl-1-propanesulfonic) acid altered the surface properties of the polyaniline films and significantly affected cell behavior. In order to reveal the crucial factor influencing the surface/cell interaction, cell behavior is discussed in the context of the surface energy of individual samples. It was clearly demonstrated that the lesser the difference between the surface energy of the sample and cell, the more cyto-compatible the surface is.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] NIH/3T3 Fibroblasts Selectively Activate T Cells Specific for Posttranslationally Modified Collagen Type II
    Dzhambazov, Balik
    Batsalova, Tsvetelina
    Merky, Patrick
    Lange, Franziska
    Holmdahl, Rikard
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (13)
  • [22] Induction of cell proliferation in quiescent NIH 3T3 cells by oncogenic c-Raf-1
    Kerkhoff, E
    Rapp, UR
    MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (05) : 2576 - 2586
  • [23] The role of substrate flexibility in the proliferation of normal and ras-transformed NIH 3T3 cells.
    Wang, HB
    MOLECULAR BIOLOGY OF THE CELL, 1998, 9 : 168A - 168A
  • [24] Overexpression of T beta(4) in NIH 3T3 cells leads to increased cytoskeletal proteins and cell adhesion.
    Golla, R
    Collins, L
    Philp, N
    Safer, D
    Nachmias, VT
    MOLECULAR BIOLOGY OF THE CELL, 1996, 7 : 2192 - 2192
  • [25] RA induces the neural-like cells generated from epigenetic modified NIH/3T3 cells
    Xi-Mei Zhang
    Qiu-Ming Li
    Dong-Ju Su
    Ning Wang
    Zhi-Yan Shan
    Lian-Hong Jin
    Lei Lei
    Molecular Biology Reports, 2010, 37 : 1197 - 1202
  • [26] RA induces the neural-like cells generated from epigenetic modified NIH/3T3 cells
    Zhang, Xi-Mei
    Li, Qiu-Ming
    Su, Dong-Ju
    Wang, Ning
    Shan, Zhi-Yan
    Jin, Lian-Hong
    Lei, Lei
    MOLECULAR BIOLOGY REPORTS, 2010, 37 (03) : 1197 - 1202
  • [27] LPAR3 Is Associated with Migration of NIH 3T3 Cells and Progression to Malignant Cell Transformation during Carcinogenesis
    Lee, Michael
    Hwang, Sung-Hee
    Yeom, Hojin
    FASEB JOURNAL, 2020, 34
  • [28] The adhesion and seeding of NIH3T3 fibroblast on PHB surfaces
    Hu, J.
    Hu, P.
    Li, T.
    Jiang, L.
    Chen, J.
    Tao, Z.
    Shengwu Yixue Gongchengxue Zazhi/Journal of Biomedical Engineering, 2001, 18 (04): : 541 - 543
  • [29] CHARACTERIZATION OF METFORMIN TRANSPORT-SYSTEM IN NIH 3T3 CELLS
    KHAN, NA
    WIERNSPERGER, N
    QUEMENER, V
    HAVOUIS, R
    MOULINOUX, JP
    JOURNAL OF CELLULAR PHYSIOLOGY, 1992, 152 (02) : 310 - 316
  • [30] Enantioselective inhibition of neoplastic transformation in NIH 3T3 cells by ibuprofen
    Xiaotao, Q
    Dall, SD
    FASEB JOURNAL, 1997, 11 (03): : 1761 - 1761