Protein-coated poly(L-lactic acid) fibers provide a substrate for differentiation of human skeletal muscle cells

被引:67
作者
Cronin, EM
Thurmond, FA
Bassel-Duby, R
Williams, RS
Wright, WE
Nelson, KD
Garner, HR [1 ]
机构
[1] Univ Texas, SW Med Ctr, Joint Biomed Engn Program, Dallas, TX 75390 USA
[2] Univ Texas, Arlington, TX 76019 USA
[3] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75390 USA
[4] Univ Texas, SW Med Ctr, Dept Mol Biol, Dallas, TX 75390 USA
[5] Duke Univ, Sch Med, Off Dean, Durham, NC 27710 USA
[6] Univ Texas, SW Med Ctr, Dept Cell Biol, Dallas, TX 75390 USA
[7] Univ Texas, SW Med Ctr, McDermott Ctr Human Growth & Dev, Dallas, TX 75390 USA
[8] Univ Texas, SW Med Ctr, Ctr Biomed Intervent, Dallas, TX 75390 USA
关键词
skeletal muscle; differentiation; tissue engineering; poly L-lactic acid fiber scaffold; extracellular matrix proteins;
D O I
10.1002/jbm.a.30009
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Tissue engineering represents a potential method for repairing damaged skeletal muscle tissue. Extracellular matrix (ECM) proteins were evaluated for their ability to aid in cell attachment, whereas a poly(L-lactic acid) (PLLA) fiber scaffold was tested as a substrate for the differentiation of human skeletal muscle cells. In comparison to uncoated or gelatin-coated PLLA films, cell attachment increased significantly (p < 0.001) on PLLA films coated with ECM gel, fibronectin, or laminin. Myoblasts differentiated into multinucleated myofibers on ECM gel-coated PLLA fibers, and expressed muscle markers such as myosin and a-actinin. Oligonucleotide microarray analysis showed similar gene expression profiles for human skeletal muscle cells on ECM gel-coated PLLA fibers as to that observed for myofibers on tissue culture plates. Therefore, PLLA fibers coated with ECM proteins provide a scaffold for the development of skeletal muscle tissue for tissue engineering and cell transplantation applications. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:373 / 381
页数:9
相关论文
共 24 条
[1]   The growth and morphological behavior of salivary epithelial cells on matrix protein-coated biodegradable substrata [J].
Aframian, DJ ;
Cukierman, E ;
Nikolovski, J ;
Mooney, DJ ;
Yamada, KM ;
Baum, BJ .
TISSUE ENGINEERING, 2000, 6 (03) :209-216
[2]   BONE TISSUE ENGINEERING [J].
CRANE, GM ;
ISHAUG, SL ;
MIKOS, AG .
NATURE MEDICINE, 1995, 1 (12) :1322-1324
[3]   Excitability and contractility of skeletal muscle engineered from primary cultures and cell lines [J].
Dennis, RG ;
Kosnik, PE ;
Gilbert, ME ;
Faulkner, JA .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 280 (02) :C288-C295
[4]   DEVELOPMENT OF A BIOARTIFICIAL LIVER USING ISOLATED HEPATOCYTES [J].
DIXIT, V .
ARTIFICIAL ORGANS, 1994, 18 (05) :371-384
[5]   NEOCARTILAGE FORMATION INVITRO AND INVIVO USING CELLS CULTURED ON SYNTHETIC BIODEGRADABLE POLYMERS [J].
FREED, LE ;
MARQUIS, JC ;
NOHRIA, A ;
EMMANUAL, J ;
MIKOS, AG ;
LANGER, R .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1993, 27 (01) :11-23
[6]   Myogenic satellite cells: physiology to molecular biology [J].
Hawke, TJ ;
Garry, DJ .
JOURNAL OF APPLIED PHYSIOLOGY, 2001, 91 (02) :534-551
[7]   Molecular pathophysiology and targeted therapeutics for muscular dystrophy [J].
Hoffman, EP ;
Dressman, D .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2001, 22 (09) :465-470
[8]  
Humes HD, 1996, TRANSPLANT P, V28, P2032
[9]  
MILLER JB, 2001, DEV BIOL SKELETAL MU, P26
[10]  
Miller RG, 1997, MUSCLE NERVE, V20, P469, DOI 10.1002/(SICI)1097-4598(199704)20:4<469::AID-MUS10>3.0.CO