Transplantation of adult rat hippocampus-derived neural stem cells into retina injured by transient ischemia

Neurosci Lett. 2001 Jun 22;306(1-2):57-60. doi: 10.1016/s0304-3940(01)01857-2.

Abstract

Neural stem cells are capable of differentiating along multiple central nervous system cell-type lineages, and their use as graft material has provided new strategies for the treatment of neuronal damage. We transplanted adult rat hippocampus-derived neural stem cells into eyes of adult rats that underwent ischemia-reperfusion injury. As control, the cells were also injected into normal rats eyes without ischemic insult. The rats were sacrificed at 1, 2, 4, and 8 weeks, and the eyes were examined histochemically. In eyes with the insult, the transplanted cells were well integrated into the host retinas and expressed Map2ab. In the control, none of the cells migrated into the retina. These results suggest that neural stem cells may be used as donor cells for transplantation to repair ischemic-injured retina.

MeSH terms

  • Animals
  • Brain Ischemia / complications
  • Brain Ischemia / physiopathology
  • Brain Ischemia / surgery*
  • Brain Tissue Transplantation
  • Cell Differentiation / physiology
  • Cells, Cultured / cytology
  • Cells, Cultured / metabolism
  • Cells, Cultured / transplantation
  • Disease Models, Animal
  • Genes, Reporter / physiology
  • Graft Survival / physiology
  • Hippocampus / cytology
  • Hippocampus / metabolism
  • Hippocampus / transplantation*
  • Immunohistochemistry
  • Microtubule-Associated Proteins / metabolism
  • Neurons / cytology
  • Neurons / metabolism
  • Neurons / transplantation*
  • Rats
  • Rats, Inbred F344
  • Reperfusion Injury / complications
  • Reperfusion Injury / physiopathology
  • Reperfusion Injury / surgery*
  • Retina / injuries
  • Retina / pathology
  • Retina / surgery
  • Retinal Diseases / etiology
  • Retinal Diseases / physiopathology
  • Retinal Diseases / surgery*
  • Stem Cell Transplantation*
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Treatment Outcome
  • beta-Galactosidase / genetics
  • beta-Galactosidase / metabolism

Substances

  • Microtubule-Associated Proteins
  • beta-Galactosidase