Quantitative Evaluation of Fibroblast Migration on a Silk Fibroin Surface and TGFBI Gene Expression

被引:17
作者
Hashimoto, Tomoko [1 ]
Kojima, Katsura [1 ]
Otaka, Akihisa [2 ]
Takeda, Yuji S. [2 ]
Tomita, Naohide [2 ]
Tamada, Yasushi [1 ]
机构
[1] Natl Inst Agrobiol Sci, Genetically Modified Organism Res Ctr, Silk Mat Res Unit, Tsukuba, Ibaraki 3058634, Japan
[2] Kyoto Univ, Grad Sch Engn, Dept Mech Engn, Sakyo Ku, Kyoto 6068501, Japan
关键词
Silk fibroin; cell migration; fibroblast; ECM; BONE REGENERATION; ADHESION; GROWTH; COLLAGEN; TISSUE; PROLIFERATION; BETA-IG-H3; POLYMER; CULTURE; PROTEIN;
D O I
10.1163/156856212X629025
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cell migration plays important roles in natural processes involving embryonic development, inflammation, wound healing, cancer metastasis and angiogenesis. Cell migration on various biomaterials is also believed to improve the rate of wound healing and implant therapies in the tissue-engineering field. This study measured the distance traversed, or mileage, of mouse fibroblasts on a silk fibroin surface. Fibroblasts on the fibroin surface moved with better progress during 24 h than cells on collagen or fibronectin surfaces. Results obtained by quantitative real-time reverse transcription-polymerase chain reaction (qRT-PCR) revealed that fibroblasts on the fibroin surface expressed transforming growth factor -induced protein (TGFBI), which is an extracellular matrix (ECM) protein, stronger than on other surfaces in the early cell-culture stages. These results demonstrate that the fibroin surface shows higher potential to enhance cell migration and the production of ECM than a collagen or fibronectin surface. (C) Koninklijke Brill NV, Leiden, 2012
引用
收藏
页码:158 / 169
页数:12
相关论文
共 36 条
[1]   Silk-based biomaterials [J].
Altman, GH ;
Diaz, F ;
Jakuba, C ;
Calabro, T ;
Horan, RL ;
Chen, JS ;
Lu, H ;
Richmond, J ;
Kaplan, DL .
BIOMATERIALS, 2003, 24 (03) :401-416
[2]  
Aoki H, 2003, BIO-MED MATER ENG, V13, P309
[3]   βig-h3 supports keratinocyte adhesion, migration, and proliferation through α3β1 integrin [J].
Bae, JS ;
Lee, SH ;
Kim, JE ;
Choi, JY ;
Park, RW ;
Park, JY ;
Park, HS ;
Sohn, YS ;
Lee, DS ;
Lee, EB ;
Kim, IS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 294 (05) :940-948
[4]   Toward guided tissue and bone regeneration: morphology, attachment, proliferation, and migration of cells cultured on collagen barrier membranes. A systematic review [J].
Behring, Jan ;
Junker, Ruediger ;
Walboomers, X. Frank ;
Chessnut, Betsy ;
Jansen, John A. .
ODONTOLOGY, 2008, 96 (01) :1-11
[5]   Functionality of endothelial cells on silk fibroin nets: Comparative study of micro- and nanometric fibre size [J].
Bondar, Borys ;
Fuchs, Sabine ;
Motta, Antonella ;
Migliaresi, Claudio ;
Kirkpatrick, Charles J. .
BIOMATERIALS, 2008, 29 (05) :561-572
[6]   Characterizing fibroblast migration on discrete collagen threads for applications in tissue regeneration [J].
Cornwell, KG ;
Downing, BR ;
Pins, GD .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 71A (01) :55-62
[7]   FINE STRUCTURE OF SILK FIBROIN [J].
DOBB, MG ;
FRASER, RDB ;
MACRAE, TP .
JOURNAL OF CELL BIOLOGY, 1967, 32 (02) :289-+
[8]   Imaging of cell migration [J].
Dormann, Dirk ;
Weijer, Cornelis J. .
EMBO JOURNAL, 2006, 25 (15) :3480-3493
[9]   Transforming growth factors beta 1, beta 2, and beta 3 and their receptors are differentially regulated during normal and impaired wound healing [J].
Frank, S ;
Madlener, M ;
Werner, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (17) :10188-10193
[10]   Dynamic processes involved in the pre-vascularization of silk fibroin constructs for bone regeneration using outgrowth endothelial cells [J].
Fuchs, Sabine ;
Jiang, Xin ;
Schmidt, Harald ;
Dohle, Eva ;
Ghanaati, Shahram ;
Orth, Carina ;
Hofmann, Alexander ;
Motta, Antonella ;
Migliaresi, Claudio ;
Kirkpatrick, Charles J. .
BIOMATERIALS, 2009, 30 (07) :1329-1338