Ecto-Mesenchymal Stem Cells from Facial Process: Potential for Muscle Regeneration

被引:5
作者
Nie, Xin [1 ,2 ]
Xing, Yongjun [1 ,2 ]
Deng, Manjin [1 ,2 ]
Gang, Li [1 ,2 ]
Liu, Rui [1 ,2 ]
Zhang, Yongjie [3 ]
Wen, Xiujie [1 ,2 ]
机构
[1] Third Mil Med Univ, Daping Hosp, Dept Stomatol, Chongqing 400042, Peoples R China
[2] Third Mil Med Univ, Inst Surg Res, Chongqing 400042, Peoples R China
[3] Fourth Mil Med Univ, Qin Du Stomatol Coll, Ctr Tissue Engn, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
Ecto-mesenchymal stem cells; Muscle regeneration; Cell sheet; Transplantation; 1ST BRANCHIAL ARCH; NEURAL CREST; IN-VITRO; ECTOMESENCHYMAL CELLS; MULTILINEAGE DIFFERENTIATION; PROGENITOR CELLS; SATELLITE CELLS; EXPRESSION; PROTEINS; THERAPY;
D O I
10.1007/s12013-014-9964-x
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
Ecto-mesenchymal stem cells (EMSCs) originate from the cranial neural crest and participate in the formation of tooth, salivary, and muscle in early development stage. The transplantation of EMSCs, a potential source of myoblast stem cell, might improve muscle regeneration. The purpose of this study was to explore whether EMSCs have the potential to differentiate and display a myogenic phenotype in vitro the in vitro. Here, we characterized the EMSCs isolated from the facial process, and p75 + EMSCs were collected by a FACS calibur flow cytometer. In vitro, p75 + EMSCs induced by DMSO can accumulate and fuse into multinucleated myotubes and further differentiate into the skeletal muscle cells in form of cell sheet. Functional myoblast phenotypes of p75 + EMSCs were found in vivo model of muscle injury. The remarkable ability of stem cells to regenerate skeletal muscle indicated their potential role in the cell therapy and tissue engineering of the skeletal muscle.
引用
收藏
页码:615 / 622
页数:8
相关论文
共 30 条
[1]   Stem Cell Based Therapy for Skeletal Muscle Diseases [J].
Bhagavati, Satyakam .
CURRENT STEM CELL RESEARCH & THERAPY, 2008, 3 (03) :219-228
[2]   Neural crest and mesoderm lineage-dependent gene expression in orofacial development [J].
Bhattacherjee, Vasker ;
Mukhopadhyay, Partha ;
Singh, Saurabh ;
Johnson, Charles ;
Philipose, John T. ;
Warner, Courtney P. ;
Greene, Robert M. ;
Pisano, M. Michele .
DIFFERENTIATION, 2007, 75 (05) :463-477
[3]   Recent advances in craniofacial morphogenesis [J].
Chai, Yang ;
Maxson, Robert E., Jr. .
DEVELOPMENTAL DYNAMICS, 2006, 235 (09) :2353-2375
[4]   Widespread distribution and muscle differentiation of human fetal mesenchymal cells after intrauterine transplantation in dystrophic mdx mouse [J].
Chan, Jerry ;
Waddington, Simon N. ;
O'Donoghue, Keelin ;
Kurata, Hitoshi ;
Guillot, Pascale V. ;
Gotherstrom, Cecilia ;
Themis, Michael ;
Morgan, Jennifer E. ;
Fisk, Nicholas M. .
STEM CELLS, 2007, 25 (04) :875-884
[5]   Stem cell function, self-renewal, and behavioral heterogeneity of cells from the adult muscle satellite cell niche [J].
Collins, CA ;
Olsen, I ;
Zammit, PS ;
Heslop, L ;
Petrie, A ;
Partridge, TA ;
Morgan, JE .
CELL, 2005, 122 (02) :289-301
[6]   Aging, stem cells and tissue regeneration - Lessons from muscle [J].
Conboy, IM ;
Rando, TA .
CELL CYCLE, 2005, 4 (03) :407-410
[7]   A Multipotent Neural Crest-Derived Progenitor Cell Population Is Resident Within the Oral Mucosa Lamina Propria [J].
Davies, Lindsay C. ;
Locke, Matthew ;
Webb, Richard D. J. ;
Roberts, James T. ;
Langley, Martin ;
Thomas, David W. ;
Archer, Charles W. ;
Stephens, Phil .
STEM CELLS AND DEVELOPMENT, 2010, 19 (06) :819-830
[8]  
De B. C, 2003, J CELL BIOL, V160, P909
[9]   Defining properties of neural crest-derived progenitor cells from the apex of human developing tooth [J].
Degistirici, Oezer ;
Jaquiery, Claude ;
Schoenebeck, Bodo ;
Siemonsmeier, Juergen ;
Goetz, Werner ;
Martin, Ivan ;
Thie, Michael .
TISSUE ENGINEERING PART A, 2008, 14 (02) :317-U58
[10]   Effects of transforming growth factor β1 (TGFβ-1) and dentin non-collagenous proteins (DNCP) on human embryonic ectomesenchymal cells in a three-dimensional culture system [J].
Deng, MJ ;
Shi, J ;
Smith, AJ ;
Jin, Y .
ARCHIVES OF ORAL BIOLOGY, 2005, 50 (11) :937-945