Recovery from paralysis in adult rats using embryonic stem cells

被引:203
作者
Deshpande, Deepa M.
Kim, Yun-Sook
Martinez, Tara
Carmen, Jessica
Dike, Sonny
Shats, Irina
Rubin, Lee L.
Drummond, Jennifer
Krishnan, Chitra
Hoke, Ahmet
Maragakis, Nicholas
Shefner, Jeremy
Rothstein, Jeffrey D.
Kerr, Douglas A.
机构
[1] Johns Hopkins Univ, Dept Neurol, Sch Med, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD USA
[3] Curis Inc, Cambridge, MA USA
[4] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD USA
[5] Upstate Med Univ, Dept Neurol, Syracuse, NY USA
关键词
D O I
10.1002/ana.20901
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: We explored the potential of embryonic stem cell-derived motor neurons to functionally replace those cells destroyed in paralyzed adult rats. Methods: We administered a phosphodiesterase type 4 inhibitor and dibutyryl cyclic adenosine monophosphate to overcome myelin-mediated repulsion and provided glial cell-derived neurotrophic factor within the sciatic nerve to attract transplanted embryonic stem cell-derived axons toward skeletal muscle targets. Results: We found that these strategies significantly increased the success of transplanted axons extending out of the spinal cord into ventral roots. Furthermore, transplant-derived axons reached muscle, formed neuromuscular junctions, were physiologically active, and mediated partial recovery from paralysis. Interpretation: We conclude that restoration of functional motor units by embryonic stem cells is possible and represents a potential therapeutic strategy for patients with paralysis. To our knowledge, this is the first report of the anatomical and functional replacement of a motor neuron circuit within the adult mammalian host.
引用
收藏
页码:32 / 44
页数:13
相关论文
共 39 条
[21]   Vesicular acetylcholine transporter can be a morphological marker for the reinnervation to muscle of regenerating motor axons [J].
Maeda, M ;
Ohba, N ;
Nakagomi, S ;
Suzuki, Y ;
Kiryu-Seo, S ;
Namikawa, K ;
Kondoh, W ;
Tanaka, A ;
Kiyama, H .
NEUROSCIENCE RESEARCH, 2004, 48 (03) :305-314
[22]   ELECTROPHYSIOLOGICAL ESTIMATION OF NUMBER OF MOTOR UNITS WITHIN A HUMAN MUSCLE [J].
MCCOMAS, AJ ;
FAWCETT, PRW ;
CAMPBELL, MJ ;
SICA, REP .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1971, 34 (02) :121-&
[23]   Functional properties of motoneurons derived from mouse embryonic stem cells [J].
Miles, GB ;
Yohn, DC ;
Wichterle, H ;
Jessell, TM ;
Rafuse, VF ;
Brownstone, RM .
JOURNAL OF NEUROSCIENCE, 2004, 24 (36) :7848-7858
[24]   Protein kinase A regulates the sensitivity of spinal commissural axon turning to netrin-1 but does not switch between chemoattraction and chemorepulsion [J].
Moore, SW ;
Kennedy, TE .
JOURNAL OF NEUROSCIENCE, 2006, 26 (09) :2419-2423
[25]   DEVELOPING MOTOR-NEURONS RESCUED FROM PROGRAMMED AND AXOTOMY-INDUCED CELL-DEATH BY GDNF [J].
OPPENHEIM, RW ;
HOUENOU, LJ ;
JOHNSON, JE ;
LIN, LFH ;
LI, LX ;
LO, AC ;
NEWSOME, AL ;
PREVETTE, DM ;
WANG, SW .
NATURE, 1995, 373 (6512) :344-346
[26]   cAMP and Schwann cells promote axonal growth and functional recovery after spinal cord injury [J].
Pearse, DD ;
Pereira, FC ;
Marcillo, AE ;
Bates, ML ;
Berrocal, YA ;
Filbin, MT ;
Bunge, MB .
NATURE MEDICINE, 2004, 10 (06) :610-616
[27]   GDNF triggers a novel Ret-independent Src kinase family-coupled signaling via a GPI-linked GDNF receptor α1 [J].
Poteryaev, D ;
Titievsky, A ;
Sun, YF ;
Thomas-Crusells, J ;
Lindahl, M ;
Billaud, M ;
Arumäe, U ;
Saarma, M .
FEBS LETTERS, 1999, 463 (1-2) :63-66
[28]   The use of statistical mune in a multicenter clinical trial [J].
Shefner, JM ;
Cudkowicz, ME ;
Zhang, H ;
Schoenfeld, D ;
Jillapalli, D .
MUSCLE & NERVE, 2004, 30 (04) :463-469
[29]   Comparison of incremental with multipoint mune methods in transgenic ALS mice [J].
Shefner, JM ;
Cudkowicz, ME ;
Brown, RH .
MUSCLE & NERVE, 2002, 25 (01) :39-42
[30]   MULTIPOTENT NEURAL CELL-LINES CAN ENGRAFT AND PARTICIPATE IN DEVELOPMENT OF MOUSE CEREBELLUM [J].
SNYDER, EY ;
DEITCHER, DL ;
WALSH, C ;
ARNOLDALDEA, S ;
HARTWIEG, EA ;
CEPKO, CL .
CELL, 1992, 68 (01) :33-51