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
[11]   Sulfated fibroin, a novel sulfated peptide derived from silk, inhibits human immunodeficiency virus replication in vitro [J].
Gotoh, K ;
Izumi, H ;
Kanamoto, T ;
Tamada, Y ;
Nakashima, H .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2000, 64 (08) :1664-1670
[12]   Migration of isogenic cell lines quantified by dynamic multivariate analysis of single-cell motility [J].
Harris, Mark P. ;
Kim, Eric ;
Weidow, Brandy ;
Wikswo, John P. ;
Quaranta, Vito .
CELL ADHESION & MIGRATION, 2008, 2 (02) :127-136
[13]   Silk fibroin as an organic polymer for controlled drug delivery [J].
Hofmann, S ;
Foo, CTWP ;
Rossetti, F ;
Textor, M ;
Vunjak-Novakovic, G ;
Kaplan, DL ;
Merkle, HP ;
Meinel, L .
JOURNAL OF CONTROLLED RELEASE, 2006, 111 (1-2) :219-227
[14]  
Ito E, 1998, J BIOMED MATER RES, V42, P148
[15]   Effects of RGDS sequence genetically interfused in the silk fibroin light chain protein on chondrocyte adhesion and cartilage synthesis [J].
Kambe, Yusuke ;
Yamamoto, Koji ;
Kojima, Katsura ;
Tamada, Yasushi ;
Tomita, Naohide .
BIOMATERIALS, 2010, 31 (29) :7503-7511
[16]   Characterization of a Silk-Resinified Compact Fabricated Using a Pulse-Energizing Sintering Device [J].
Kaneko, Atsushi ;
Tamada, Yasushi ;
Hirai, Shinji ;
Kuzuya, Toshihiro ;
Hashimoto, Tomoko .
MACROMOLECULAR MATERIALS AND ENGINEERING, 2012, 297 (03) :272-278
[17]   Structure and properties of silk hydrogels [J].
Kim, UJ ;
Park, JY ;
Li, CM ;
Jin, HJ ;
Valluzzi, R ;
Kaplan, DL .
BIOMACROMOLECULES, 2004, 5 (03) :786-792
[18]   BETA-IG-H3, A NOVEL SECRETORY PROTEIN INDUCIBLE BY TRANSFORMING GROWTH-FACTOR-BETA, IS PRESENT IN NORMAL SKIN AND PROMOTES THE ADHESION AND SPREADING OF DERMAL FIBROBLASTS IN-VITRO [J].
LEBARON, RG ;
BEZVERKOV, KI ;
ZIMBER, MP ;
PAVELEC, R ;
SKONIER, J ;
PURCHIO, AF .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 104 (05) :844-849
[19]  
LEVINE JH, 1993, AM J PATHOL, V143, P368
[20]   Mechanism of human dermal fibroblast migration driven by type I collagen and platelet-derived growth factor-BB [J].
Li, W ;
Fan, JH ;
Chen, M ;
Guan, SX ;
Sawcer, D ;
Bokoch, GM ;
Woodley, DT .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (01) :294-309