Extensive neuronal differentiation of human neural stem cell grafts in adult rat spinal cord

被引:181
作者
Yan, Jun
Xu, Leyan
Welsh, Annie M.
Hatfield, Glen
Hazel, Thomas
Johe, Karl
Koliatsos, Vassilis E. [1 ]
机构
[1] Johns Hopkins Med Inst, Div Neuropathol, Dept Pathol, Baltimore, MD 21205 USA
[2] Neuralstem, Rockville, MD USA
[3] Johns Hopkins Med Inst, Dept Neurol, Baltimore, MD 21205 USA
[4] Johns Hopkins Med Inst, Dept Neurosci, Baltimore, MD 21205 USA
[5] Johns Hopkins Med Inst, Dept Psychiat & Behav Sci, Baltimore, MD 21205 USA
关键词
D O I
10.1371/journal.pmed.0040039
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Effective treatments for degenerative and traumatic diseases of the nervous system are not currently available. The support or replacement of injured neurons with neural grafts, already an established approach in experimental therapeutics, has been recently invigorated with the addition of neural and embryonic stem-derived precursors as inexhaustible, self-propagating alternatives to fetal tissues. The adult spinal cord, i.e., the site of common devastating injuries and motor neuron disease, has been an especially challenging target for stem cell therapies. In most cases, neural stem cell (NSC) transplants have shown either poor differentiation or a preferential choice of glial lineages. Methods and Findings In the present investigation, we grafted NSCs from human fetal spinal cord grown in monolayer into the lumbar cord of normal or injured adult nude rats and observed large-scale differentiation of these cells into neurons that formed axons and synapses and established extensive contacts with host motor neurons. Spinal cord microenvironment appeared to influence fate choice, with centrally located cells taking on a predominant neuronal path, and cells located under the pia membrane persisting as NSCs or presenting with astrocytic phenotypes. Slightly fewer than one-tenth of grafted neurons differentiated into oligodendrocytes. The presence of lesions increased the frequency of astrocytic phenotypes in the white matter. Conclusions NSC grafts can show substantial neuronal differentiation in the normal and injured adult spinal cord with good potential of integration into host neural circuits. In view of recent similar findings from other laboratories, the extent of neuronal differentiation observed here disputes the notion of a spinal cord that is constitutively unfavorable to neuronal repair. Restoration of spinal cord circuitry in traumatic and degenerative diseases may be more realistic than previously thought, although major challenges remain, especially with respect to the establishment of neuromuscular connections.
引用
收藏
页码:318 / 332
页数:15
相关论文
共 60 条
[1]  
ANDESOMPELE J, 2002, GENOME BIOL, V3, DOI UNSP RESEARCH0034.1-RESEARCH034.11
[2]  
Arsenijevic Y, 1998, J NEUROSCI, V18, P2118
[3]   VEGF delivery with retrogradely transported lentivector prolongs survival in a mouse ALS model [J].
Azzouz, M ;
Ralph, GS ;
Storkebaum, E ;
Walmsley, LE ;
Mitrophanous, KA ;
Kingsman, SM ;
Carmeliet, P ;
Mazarakis, ND .
NATURE, 2004, 429 (6990) :413-417
[4]   MESENCEPHALIC DOPAMINERGIC-NEURONS PROTECTED BY GDNF FROM AXOTOMY-INDUCED DEGENERATION IN THE ADULT BRAIN [J].
BECK, KD ;
VALVERDE, J ;
ALEXI, T ;
POULSEN, K ;
MOFFAT, B ;
VANDLEN, RA ;
ROSENTHAL, A ;
HEFTI, F .
NATURE, 1995, 373 (6512) :339-341
[5]   Pluripotent stem cells engrafted into the normal or lesioned adult rat spinal cord are restricted to a glial lineage [J].
Cao, QL ;
Zhang, YP ;
Howard, RM ;
Walters, WM ;
Tsoulfas, P ;
Whittemore, SR .
EXPERIMENTAL NEUROLOGY, 2001, 167 (01) :48-58
[6]   Differentiation of engrafted neuronal-restricted precursor cells is inhibited in the traumatically injured spinal cord [J].
Cao, QL ;
Howard, RM ;
Dennison, JB ;
Whittemore, SR .
EXPERIMENTAL NEUROLOGY, 2002, 177 (02) :349-359
[7]   Human neural stem cells differentiate and promote locomotor recovery in spinal cord-injured mice [J].
Cummings, BJ ;
Uchida, N ;
Tamaki, SJ ;
Salazar, DL ;
Hooshmand, M ;
Summers, R ;
Gage, FH ;
Anderson, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (39) :14069-14074
[8]  
Davies KJA, 1999, IUBMB LIFE, V48, P41, DOI 10.1080/152165499307404
[9]   Regeneration of adult axons in white matter tracts of the central nervous system [J].
Davies, SJA ;
Fitch, MT ;
Memberg, SP ;
Hall, AK ;
Raisman, G ;
Silver, J .
NATURE, 1997, 390 (6661) :680-683
[10]   Recovery from paralysis in adult rats using embryonic stem cells [J].
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. .
ANNALS OF NEUROLOGY, 2006, 60 (01) :32-44