Infusion of Human Umbilical Cord Blood Cells in a Rat Model of Stroke Dose-Dependently Rescues Behavioral Deficits and Reduces Infarct Volume

Background and Purpose— Intravenously delivered human umbilical cord blood cells (HUCBC) have been previously shown to improve functional recovery of stroked rats. To extend these findings, we examined the behavioral recovery and stroke infarct volume in the presence of increasing doses of HUCBC after permanent middle cerebral artery occlusion (MCAO). Methods— Rats were subjected to MCAO and allowed to recover for 24 hours before intravenous infusion of 104 up to 3 to 5×107 HUCBC. Behavioral tests (spontaneous activity, step test, elevated body swing test) were performed 1 week before MCAO and at 2 and 4 weeks after HUCBC infusion. On completion of behavioral testing, animals were euthanized and brain infarct volumes quantified. HUCBC were identified by immunofluorescence for human nuclei and by polymerase chain reaction (PCR) using primers specific for human glycerol 3-phosphate dehydrogenase. Results— At 4 weeks after infusion, there was a significant recovery in behavioral performance when 106 or more HUCBC were delivered (p=0.001 to p=0.05). Infarct volume measurements revealed an inverse relationship between HUCBC dose and damage volume, which reached significance at the higher HUCBC doses (107 cells, p<0.01; 3 to 5×107 cells, p<0.05). Moreover, HUCBC were localized by immunohistochemistry and PCR analysis only in the injured brain hemisphere and spleen. Conclusions— These results extend previous observations of HUCBC infusion in the MCAO rat stroke model by demonstrating a dose relationship between HUCBC, behavioral improvement, and neuronal sparing.

[1]  P. Sanberg,et al.  Central Nervous System Entry of Peripherally Injected Umbilical Cord Blood Cells Is Not Required for Neuroprotection in Stroke , 2004, Stroke.

[2]  N. Rothwell,et al.  Peak plasma interleukin-6 and other peripheral markers of inflammation in the first week of ischaemic stroke correlate with brain infarct volume, stroke severity and long-term outcome , 2004, BMC neurology.

[3]  A. Straube,et al.  Expression of Neuronal Markers in Differentiated Marrow Stromal Cells and CD133+ Stem-Like Cells , 2003, Cell transplantation.

[4]  P. Sanberg,et al.  Intravenous versus intrastriatal cord blood administration in a rodent model of stroke , 2003, Journal of neuroscience research.

[5]  R. McCarron,et al.  Adoptive Transfer of Myelin Basic Protein–Tolerized Splenocytes to Naive Animals Reduces Infarct Size: A Role for Lymphocytes in Ischemic Brain Injury? , 2003, Stroke.

[6]  P. Sanberg,et al.  Human umbilical cord blood stem cells infusion in spinal cord injury: engraftment and beneficial influence on behavior. , 2003, Journal of hematotherapy & stem cell research.

[7]  P. Sanberg,et al.  Mobilized Peripheral Blood Cells Administered Intravenously Produce Functional Recovery in Stroke , 2003, Cell transplantation.

[8]  G. Starace,et al.  CD34-positive cells in human umbilical cord blood express nerve growth factor and its specific receptor TrkA , 2003, Journal of Neuroimmunology.

[9]  J. Živný,et al.  Expression of genes regulating angiogenesis in human circulating hematopoietic cord blood CD34+/CD133+ cells , 2003, European journal of haematology.

[10]  I. Lewis,et al.  Clinical and experimental uses of umbilical cord blood , 2002, Internal medicine journal.

[11]  Melitta Schachner,et al.  Neural stem cells display an inherent mechanism for rescuing dysfunctional neurons , 2002, Nature Biotechnology.

[12]  M. Chopp,et al.  Human marrow stromal cell therapy for stroke in rat: Neurotrophins and functional recovery , 2002, Neurology.

[13]  M. Chopp,et al.  Intravenous Administration of Human Umbilical Cord Blood Reduces Neurological Deficit in the Rat after Traumatic Brain Injury , 2002, Cell transplantation.

[14]  D. Reen,et al.  Interleukin 10, produced in abundance by human newborn T cells, may be the regulator of increased tolerance associated with cord blood stem cell transplantation , 2002, British journal of haematology.

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

[16]  P. Wernet,et al.  Phenotypic and functional comparison of monocytes from cord blood and granulocyte colony-stimulating factor-mobilized apheresis products. , 2001, Experimental hematology.

[17]  M. Chopp,et al.  Treatment of Traumatic Brain Injury in Adult Rats with Intravenous Administration of Human Bone Marrow Stromal Cells , 2001, Neurosurgery.

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

[19]  S. Watanabe,et al.  Cyclosporine A-Induced Hyperactivity in Rats: Is it Mediated by Immunosuppression, Neurotrophism, or Both? , 1999, Cell transplantation.

[20]  R. McKay,et al.  Transplantation of expanded mesencephalic precursors leads to recovery in parkinsonian rats , 1998, Nature Neuroscience.

[21]  Y. Olsson,et al.  Neurologic and neuropathologic outcome after middle cerebral artery occlusion in rats. , 1989, Stroke.

[22]  L. Pitts,et al.  Effect of opiate antagonists on middle cerebral artery occlusion infarct in the rat. , 1988, Journal of neurosurgery.

[23]  Daniel M. Rosenbaum,et al.  Efficacy and mechanism of action of a calcium channel blocker after global cerebral ischemia in rats. , 1988, Stroke.

[24]  D. Wall,et al.  Human umbilical cord blood cells can be induced to express markers for neurons and glia. , 2002, Cell transplantation.