Cell transplantation for stroke

Cell transplantation has emerged as an experimental approach to restore brain function after stroke. Various cell types including porcine fetal cells, stem cells, immortalized cell lines, and marrow stromal cells are under investigation in experimental and clinical stroke trials. This review discusses the unique advantages and limitations of the different graft sources and emphasizes the current, limited knowledge about their biology. The survival, integration, and efficacy of neural transplants in stroke patients will depend on the type, severity, chronicity, adequacy of circulation, and location of the stroke lesion. Ann Neurol 2002;52:266–275

[1]  Bruce G. Jenkins,et al.  Embryonic stem cells develop into functional dopaminergic neurons after transplantation in a Parkinson rat model , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[2]  D. Jacoby,et al.  CNS Grafts for Treatment of Neurological Disorders , 2002 .

[3]  M. Chopp,et al.  Intravenous Administration of Human Umbilical Cord Blood Reduces Behavioral Deficits After Stroke in Rats , 2001, Stroke.

[4]  Michael Chopp,et al.  Expression of Neural Markers in Human Umbilical Cord Blood , 2001, Experimental Neurology.

[5]  C. Olanow,et al.  Transplantation of embryonic dopamine neurons for severe Parkinson's disease. , 2001, The New England journal of medicine.

[6]  T. Dawson,et al.  Neuroimmunophilins: Novel neuroprotective and neuroregenerative targets , 2001, Annals of neurology.

[7]  M. Chopp,et al.  Treatment of stroke in rat with intracarotid administration of marrow stromal cells , 2001, Neurology.

[8]  R. Rosqvist,et al.  Cortical Neurogenesis in Adult Rats After Transient Middle Cerebral Artery Occlusion , 2001, Stroke.

[9]  David A. Greenberg,et al.  Neurogenesis in dentate subgranular zone and rostral subventricular zone after focal cerebral ischemia in the rat , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[10]  M. Chopp,et al.  Therapeutic Benefit of Intravenous Administration of Bone Marrow Stromal Cells After Cerebral Ischemia in Rats , 2001, Stroke.

[11]  John S. Beech,et al.  Resolution of Stroke Deficits Following Contralateral Grafts of Conditionally Immortal Neuroepithelial Stem Cells , 2001, Stroke.

[12]  A. Buchan,et al.  Transplantation of cultured human neuronal cells for patients with stroke , 2001, Neurology.

[13]  R. Macdonald,et al.  Functional expression of L-, N-, P/Q-, and R-type calcium channels in the human NT2-N cell line. , 2000, Journal of neurophysiology.

[14]  Alan W Moore,et al.  NO EVIDENCE FOR INFECTION OF HUMAN CELLS WITH PORCINE ENDOGENOUS RETROVIRUS (PERV) AFTER EXPOSURE TO PORCINE FETAL NEURONAL CELLS1 , 2000, Transplantation.

[15]  M. Chopp,et al.  Intrastriatal Transplantation of Bone Marrow Nonhematopoietic Cells Improves Functional Recovery After Stroke in Adult Mice , 2000, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[16]  I. Black,et al.  Adult rat and human bone marrow stromal cells differentiate into neurons , 2000, Journal of neuroscience research.

[17]  P. Wester,et al.  Cortical Neurogenesis in Adult Rats after Reversible Photothrombotic Stroke , 2000, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[18]  W. Janssen,et al.  Adult Bone Marrow Stromal Cells Differentiate into Neural Cells in Vitro , 2000, Experimental Neurology.

[19]  I. Guillemain,et al.  Human NT2 neurons express a large variety of neurotransmission phenotypes in vitro , 2000, The Journal of comparative neurology.

[20]  A. Björklund,et al.  Cell replacement therapies for central nervous system disorders , 2000, Nature Neuroscience.

[21]  Human NT2/D1 cells differentiate into functional astrocytes. , 1999, Neuroreport.

[22]  M. Cunningham,et al.  Long‐term survival of fetal porcine lateral ganglionic eminence cells in the hippocampus of rats , 1999, Journal of neuroscience research.

[23]  Virginia M. Y. Lee,et al.  Functional synapses are formed between human NTera2 (NT2N, hNT) neurons grown on astrocytes , 1999, The Journal of comparative neurology.

[24]  D. Dawson,et al.  Targeting of marrow-derived astrocytes to the ischemic brain. , 1999, Neuroreport.

[25]  D. Prockop,et al.  Engraftment and migration of human bone marrow stromal cells implanted in the brains of albino rats--similarities to astrocyte grafts. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[26]  J. Trojanowski,et al.  Transplantation of Cryopreserved Human Embryonal Carcinoma-Derived Neurons (NT2N Cells) Promotes Functional Recovery in Ischemic Rats , 1998, Experimental Neurology.

[27]  J. Gray,et al.  Recovery of spatial learning by grafts of a conditionally immortalized hippocampal neuroepithelial cell line into the ischaemia-lesioned hippocampus , 1997, Neuroscience.

[28]  D. Prockop Marrow Stromal Cells as Stem Cells for Nonhematopoietic Tissues , 1997, Science.

[29]  P. Nowell,et al.  Long‐term integration and neuronal differentiation of human embryonal carcinoma cells (NT era‐2) transplanted into the caudoputamen of nude mice , 1996, The Journal of comparative neurology.

[30]  S. Dunnett,et al.  Survival and Differentiation of Rat and Human Epidermal Growth Factor-Responsive Precursor Cells Following Grafting into the Lesioned Adult Central Nervous System , 1996, Experimental Neurology.

[31]  T. Deacon,et al.  Transplanted xenogeneic neural cells in neurodegenerative disease models exhibit remarkable axonal target specificity and distinct growth patterns of glial and axonal fibres , 1995, Nature Medicine.

[32]  V. Lee,et al.  Proliferation, cell death, and neuronal differentiation in transplanted human embryonal carcinoma (NTera2) cells depend on the graft site in nude and severe combined immunodeficient mice. , 1995, Laboratory investigation; a journal of technical methods and pathology.

[33]  J. Trojanowski,et al.  Transplanted human neurons derived from a teratocarcinoma cell line (NTera‐2) mature, integrate, and survive for over 1 year in the nude mouse brain , 1995, The Journal of comparative neurology.

[34]  M. Chopp,et al.  Temporal Profile of in situ DNA Fragmentation after Transient Middle Cerebral Artery Occlusion in the Rat , 1995, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[35]  O. Isacson,et al.  Cytoarchitectonic Development, Axon-Glia Relationships, and Long Distance Axon Growth of Porcine Striatal Xenografts in Rats , 1994, Experimental Neurology.

[36]  Virginia M. Y. Lee,et al.  NTera 2 Cells: A human cell line which displays characteristics expected of a human committed neuronal progenitor cell , 1993, Journal of neuroscience research.

[37]  V. Lee,et al.  Inducible expression of neuronal glutamate receptor channels in the NT2 human cell line. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[38]  V M Lee,et al.  Pure, postmitotic, polarized human neurons derived from NTera 2 cells provide a system for expressing exogenous proteins in terminally differentiated neurons , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[39]  W. Young,et al.  Fetal cortical cells survive in focal cerebral infarct after permanent occlusion of the middle cerebral artery in adult rats. , 1992, Journal of neurotrauma.

[40]  N C Dracopoli,et al.  Pluripotent embryonal carcinoma clones derived from the human teratocarcinoma cell line Tera-2. Differentiation in vivo and in vitro. , 1984, Laboratory investigation; a journal of technical methods and pathology.

[41]  Daniel B Hier,et al.  Recovery of behavioral abnormalities after right hemisphere stroke , 1983, Neurology.