Myogenic potential of mesenchymal stem cells isolated from porcine adipose tissue

被引:20
作者
Milner, Derek J. [1 ,2 ]
Bionaz, Massimo [1 ,2 ]
Monaco, Elisa [1 ,2 ]
Cameron, Jo Ann [1 ,3 ]
Wheeler, Matthew B. [1 ,2 ]
机构
[1] Univ Illinois, Carl R Woese Inst Genom Biol, 1207 West Gregory Dr, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Anim Sci, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Cell & Dev Biol, Urbana, IL 61801 USA
关键词
Muscle regeneration; Porcine; Adipose-derived stem cells; Skeletal muscle; Myogenesis; RESTORE DYSTROPHIN EXPRESSION; MUSCLE SATELLITE CELL; HUMAN SKELETAL-MUSCLE; BONE-MARROW; IN-VITRO; DIFFERENTIATION; MOUSE; MYOBLASTS; TRANSPLANTATION; IDENTIFICATION;
D O I
10.1007/s00441-017-2764-z
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Advances in stem cell biology and materials science have provided a basis for developing tissue engineering methods to repair muscle injury. Among stem cell populations with potential to aid muscle repair, adipose-derived mesenchymal stem cells (ASC) hold great promise. To evaluate the possibility of using porcine ASC for muscle regeneration studies, we co-cultured porcine ASC with murine C2C12 myoblasts. These experiments demonstrated that porcine ASC display significant myogenic potential. Co-culture of ASC expressing green fluorescent protein (GFP) with C2C12 cells resulted in GFP(+) myotube formation, indicating fusion of ASC with myoblasts to form myotubes. The presence of porcine lamin A/C positive nuclei in myotubes and RTqPCR analysis of porcine myogenin and desmin expression confirmed that myotube nuclei derived from ASC contribute to muscle gene expression. Co-culturing GFP(+)ASC with porcine satellite cells demonstrated enhanced myogenic capability of ASC, as the percentage of labeled myotubes increased compared to mouse co-cultures. Enhancing myogenic potential of ASC through soluble factor treatment or expansion of ASC with innate myogenic capacity should allow for their therapeutic use to regenerate muscle tissue lost to disease or injury.
引用
收藏
页码:507 / 522
页数:16
相关论文
共 72 条
[1]   Myogenin expression, cell cycle withdrawal, and phenotypic differentiation are temporally separable events that precede cell fusion upon myogenesis [J].
Andres, V ;
Walsh, K .
JOURNAL OF CELL BIOLOGY, 1996, 132 (04) :657-666
[2]   Myogenic specification of side population cells in skeletal muscle [J].
Asakura, A ;
Seale, P ;
Girgis-Gabardo, A ;
Rudnicki, MA .
JOURNAL OF CELL BIOLOGY, 2002, 159 (01) :123-134
[3]   Myogenic Differentiation of Mesenchymal Stem Cells is Induced by Striated Muscle Influences in vitro [J].
Bajek, Anna ;
Drewa, Tomasz ;
Joachimiak, Romana ;
Spoz, Zaneta ;
Gagat, Maciej ;
Bodnar, Magdalena ;
Debski, Robert ;
Grzanka, Alina ;
Marszalek, Andrzej .
CURRENT SIGNAL TRANSDUCTION THERAPY, 2012, 7 (03) :220-227
[4]   Multipotential mesoangioblast stem cell therapy in the mdx/utrn-/- mouse model for Duchenne muscular dystrophy [J].
Berry, Suzanne E. ;
Liu, Jianming ;
Chaney, Eric J. ;
Kaufman, Stephen J. .
REGENERATIVE MEDICINE, 2007, 2 (03) :275-288
[5]   Identification of reference genes for quantitative real-time PCR in the bovine mammary gland during the lactation cycle [J].
Bionaz, Massimo ;
Loor, Juan J. .
PHYSIOLOGICAL GENOMICS, 2007, 29 (03) :312-319
[6]   The α7β1 integrin in muscle development and disease [J].
Burkin, DJ ;
Kaufman, SJ .
CELL AND TISSUE RESEARCH, 1999, 296 (01) :183-190
[7]   Transgenic pigs produced using in vitro matured oocytes infected with a retroviral vector [J].
Cabot, RA ;
Kühholzer, B ;
Chan, AWS ;
Lai, L ;
Park, KW ;
Chong, KY ;
Schatten, G ;
Murphy, CN ;
Abeydeera, LR ;
Day, BN ;
Prather, RS .
ANIMAL BIOTECHNOLOGY, 2001, 12 (02) :205-+
[8]  
Capetanaki Y, 1998, Subcell Biochem, V31, P463
[9]   Mesoangioblasts - vascular progenitors for extravascular mesodermal tissues [J].
Cossu, G ;
Bianco, P .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (05) :537-542
[10]   Skeletal myogenic progenitors originating from embryonic dorsal aorta coexpress endothelial and myogenic markers and contribute to postnatal muscle growth and regeneration [J].
De Angelis, L ;
Berghella, L ;
Coletta, M ;
Lattanzi, L ;
Zanchi, M ;
Cusella-De Angelis, MG ;
Ponzetto, C ;
Cossu, G .
JOURNAL OF CELL BIOLOGY, 1999, 147 (04) :869-877