Peripheral glial cell differentiation from neurospheres derived from adipose mesenchymal stem cells

被引:80
作者
Radtke, C. [1 ,2 ,3 ]
Schmitz, B. [1 ]
Spies, M. [4 ]
Kocsis, J. D. [2 ,3 ]
Vogt, P. M. [1 ]
机构
[1] Hannover Med Sch, Dept Plast Hand & Reconstruct Surg, D-30659 Hannover, Germany
[2] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06510 USA
[3] VA Connecticut Healthcare Syst, Neurosci & Regenerat Res Ctr, West Haven, CT 06516 USA
[4] Dept Plast Hand & Reconstruct Surg, Regensburg, Germany
关键词
Mesenchymal stem cells; Adipose tissue; Differentiation; Neurospheres; Glia cells; OLFACTORY ENSHEATHING CELLS; MARROW STROMAL CELLS; DEMYELINATED SPINAL-CORD; CEREBRAL-ISCHEMIA MODEL; BONE-MARROW; ADULT-RAT; SCHWANN-CELLS; IN-VITRO; CORTICOSPINAL TRACT; NERVE REGENERATION;
D O I
10.1016/j.ijdevneu.2009.08.006
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mesenchymal stem cells derived from bone marrow and adipose tissue are being considered for use in neural repair because they can differentiate after appropriate induction in culture into neurons and glia. The question we asked was if neurospheres could be harvested from adipose-derived stem cells and if they then could differentiate in culture to peripheral glial-like cells. Here, we demonstrate that adipose-derived mesenchymal stem cells can form nestin-positive non-adherent neurosphere cellular aggregates when cultured with basic fibroblast growth factor and epidermal growth factor. Dissociation of these neurospheres and removal of mitogens results in expression of the characteristic Schwann cell markers S100 and p75 nerve growth factor receptor and GFAP. The simultaneous expression of these glia markers are characteristic features of Schwann cells and olfactory ensheathing cells which have unique properties regarding remyelination and enhancement of axonal regeneration. When co-cultured with dorsal root ganglion neurons, the peripheral glial-like cells derived from adipose mesenchymal stem cells aligned with neuritis and stimulated neuritic outgrowth. These results indicate that neurospheres can be generated from adipose-derived mesenchymal stem cells, and upon mitogen withdrawal can differentiate into peripheral glial cells with neurotrophic effects. (C) 2009 ISDN. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:817 / 823
页数:7
相关论文
共 47 条
[1]   From marrow to brain: Expression of neuronal phenotypes in adult mice [J].
Brazelton, TR ;
Rossi, FMV ;
Keshet, GI ;
Blau, HM .
SCIENCE, 2000, 290 (5497) :1775-1779
[2]   Phenotypic and functional characteristics of mesenchymal stem cells differentiated along a Schwann cell lineage [J].
Caddick, Jenny ;
Kingham, Paul J. ;
Gardiner, Natalie J. ;
Wiberg, Mikael ;
Terenghi, Giorgio .
GLIA, 2006, 54 (08) :840-849
[3]   Protective effects of bone marrow stromal cell transplantation in injured rodent brain: Synthesis of neurotrophic factors [J].
Chen, Q ;
Long, Y ;
Yuan, XQ ;
Zou, LL ;
Sun, J ;
Chen, SD ;
Perez-Polo, JR ;
Yang, KY .
JOURNAL OF NEUROSCIENCE RESEARCH, 2005, 80 (05) :611-619
[4]  
Ciccolini F, 1998, J NEUROSCI, V18, P7869
[5]   NESTIN MESSENGER-RNA EXPRESSION CORRELATES WITH THE CENTRAL-NERVOUS-SYSTEM PROGENITOR-CELL STATE IN MANY, BUT NOT ALL, REGIONS OF DEVELOPING CENTRAL-NERVOUS-SYSTEM [J].
DAHLSTRAND, J ;
LARDELLI, M ;
LENDAHL, U .
DEVELOPMENTAL BRAIN RESEARCH, 1995, 84 (01) :109-129
[6]   Sciatic nerve regeneration in rats induced by transplantation of in vitro differentiated bone-marrow stromal cells [J].
Dezawa, M ;
Takahashi, I ;
Esaki, M ;
Takano, M ;
Sawada, H .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 14 (11) :1771-1776
[7]   Myelination and nodal formation of regenerated peripheral nerve fibers following transplantation of acutely prepared olfactory ensheathing cells [J].
Dombrowski, Mary A. ;
Sasaki, Masanori ;
Lankford, Karen L. ;
Kocsis, Jeffery D. ;
Radtke, Christine .
BRAIN RESEARCH, 2006, 1125 :1-8
[8]   The end of the beginning for pluripotent stem cells [J].
Donovan, PJ ;
Gearhart, J .
NATURE, 2001, 414 (6859) :92-97
[9]  
Franklin RJM, 1996, GLIA, V17, P217, DOI 10.1002/(SICI)1098-1136(199607)17:3<217::AID-GLIA4>3.0.CO
[10]  
2-Y