Human adipose-derived mesenchymal stem cells: a better cell source for nervous system regeneration

被引:34
作者
Han Chao [1 ]
Zhang Liang [2 ]
Song Lin [1 ,3 ]
Liu Yang [1 ]
Zou Wei [4 ]
Piao Hua [5 ]
Liu Jing [1 ,6 ]
机构
[1] Dalian Med Univ, Affiliated Hosp 1, Regenerat Med Ctr, Dalian 116011, Liaoning, Peoples R China
[2] Capital Med Univ, Beijing Friendship Hosp, Dept Orthoped, Beijing 100050, Peoples R China
[3] Dalian Univ Technol, Sch Life Sci & Biotechnol, Dalian 116024, Liaoning, Peoples R China
[4] Liaoning Normal Univ, Coll Life Sci, Dalian 116011, Liaoning, Peoples R China
[5] Dalian Med Univ, Coll Basic Med Sci, Dalian 116027, Liaoning, Peoples R China
[6] Dalian Med Univ, Inst Integrat Med, Dalian 116027, Liaoning, Peoples R China
关键词
adipose derived stem cells; bone marrow mesenchymal stem cells; neuronal differentiation; rat brain-conditioned medium; HUMAN BONE-MARROW; STROMAL CELLS; ADULT-RAT; DIFFERENTIATION; TISSUE; NEURONS; CRYOPRESERVATION; PROGENITORS; CAPACITY; MUSCLE;
D O I
10.3760/cma.j.issn.0366-6999.20120064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background In order to suggest an ideal source of adult stem cells for the treatment of nervous system diseases, MSCs from human adipose tissue and bone marrow were isolated and studied to explore the differences with regard to cell morphology, surface markers, neuronal differentiation capacity, especially the synapse structure formation and the secretion of neurotrophic factors. Methods The neuronal differentiation capacity of human mesenchymal stem cells from adipose tissue (hADSCs) and bone marrow (hBMSCs) was determined based on nissl body and synapse structure formation, and neural factor secretion function. hADSCs and hBMSCs were isolated and differentiated into neuron-like cells with rat brain-conditioned medium, a potentially rich source of neuronal differentiation promoting signals. Specific neuronal proteins and neural factors were detected by immunohistochemistry and enzyme-linked immunosorbent assay analysis, respectively. Results Flow cytometric analysis showed that both cell types had similar phenotypes. Cell growth curves showed that hADSCs proliferated more quickly than hBMSCs. Both kinds of cells were capable of osteogenic and adipogenic differentiation. The morphology of hADSCs and hBMSCs changed during neuronal differentiation and displayed neuron-like cell appearance after 14 days' differentiation. Both hADSCs and hBMSCs were able to differentiate into neuron-like cells based on their production of neuron specific proteins including beta-tubulin-III, neuron-specific enolase (NSE), nissl bodies, and their ability to secrete brain derived neurotrophic factor (BDNF) and nerve growth factor (NGF). Assessment of synaptop hysin and growth-associated protein-43 (GAP-43) suggested synapse structure formation in differentiated hADSCs and hBMSCs. Conclusions Our results demonstrate that hADSCs have neuronal differentiation potential similar to hBMSC, but with a higher proliferation capacity than hBMSC. Adipose tissue is abundant, easily available and would be a potential ideal source of adult stem cells for neural-related clinical research and application.
引用
收藏
页码:329 / 337
页数:9
相关论文
共 37 条
[1]   Morphological differentiation of bone marrow stromal cells into neuron-like cells after co-culture with hippocampal slice [J].
Abouelfetouh, A ;
Kondoh, T ;
Ehara, K ;
Kohmura, E .
BRAIN RESEARCH, 2004, 1029 (01) :114-119
[2]   Human bone marrow stroma cells display certain neural characteristics and integrate in the subventricular compartment after injection into the liquor system [J].
Arnhold, Stefan ;
Klein, Helmut ;
Klinz, Franz-Josef ;
Absenger, Yvonne ;
Schmidt, Annette ;
Schinkoethe, Timo ;
Brixius, Klara ;
Kozlowski, Jolanta ;
Desai, Biren ;
Bloch, Wilhelm ;
Addicks, Klaus .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2006, 85 (06) :551-565
[3]   Neurogenic potential of human mesenchymal stem cells revisited: analysis by immunostaining, time-lapse video and microarray [J].
Bertani, N ;
Malatesta, P ;
Volpi, G ;
Sonego, P ;
Perris, R .
JOURNAL OF CELL SCIENCE, 2005, 118 (17) :3925-3936
[4]   Mesenchymal stem cells: Biology and potential clinical uses [J].
Deans, RJ ;
Moseley, AB .
EXPERIMENTAL HEMATOLOGY, 2000, 28 (08) :875-884
[5]   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
[6]   Adipose-derived adult stem cells: isolation, characterization, and differentiation potential [J].
Gimble, JM ;
Guilak, F .
CYTOTHERAPY, 2003, 5 (05) :362-369
[7]   Cryopreservation characteristics of adipose-derived stem cells: maintenance of differentiation potential and viability [J].
Goh, Brian C. ;
Thirumala, Sreedhar ;
Kilroy, Gail ;
Devireddy, Ram V. ;
Gimble, Jeffrey M. .
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2007, 1 (04) :322-324
[8]   Preserved proliferative capacity and multipotency of human adipose-derived stem cells after long-term cryopreservation [J].
Gonda, Koichi ;
Shigeura, Tomokuni ;
Sato, Takahiro ;
Matsumoto, Daisuke ;
Suga, Hirotaka ;
Inoue, Keita ;
Aoi, Noriyuki ;
Kato, Harunosuke ;
Sato, Katsujiro ;
Murase, Syoko ;
Koshima, Isao ;
Yoshimura, Kotaro .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2008, 121 (02) :401-410
[9]   Recovery of function following grafting of human bone marrow-derived stromal cells into the injured spinal cord [J].
Himes, B. Timothy ;
Neuhuber, Birgit ;
Coleman, Carl ;
Kushner, Robert ;
Swanger, Sharon A. ;
Kopen, Gene C. ;
Wagner, Joseph ;
Shumsky, Jed S. ;
Fischer, Itzhak .
NEUROREHABILITATION AND NEURAL REPAIR, 2006, 20 (02) :278-296
[10]   Bone marrow stromal cells protect and repair damaged neurons through multiple mechanisms [J].
Hokari, Masaaki ;
Kuroda, Satoshi ;
Shichinohe, Hideo ;
Yano, Shunsuke ;
Hida, Kazutoshi ;
Iwasaki, Yoshinobu .
JOURNAL OF NEUROSCIENCE RESEARCH, 2008, 86 (05) :1024-1035