Transplantation of a novel human cord blood-derived neural-like stem cell line in a rat model of cortical infarct

Stem Cells Dev. 2007 Jun;16(3):481-8. doi: 10.1089/scd.2007.9993.

Abstract

Umbilical cord blood can be a rich source of stem/progenitor cells, not only for hematopoetic but also for other tissue-specific lineages. Recently, we have developed a novel, self-renewed neural-like stem cell line named HUCB-NSC from human cord blood. To test if HUCB-NSCs can supply brain in need of regeneration, we injected these cells into immunosuppressed intact rat forebrain and to animals suffering from a photothrombotic cortical lesion at 48 h after injury. The survival, migration, and differentiation of the transplanted HUCB-NSCs were measured at 7 and 30 days post-transplantation by immunohistochemical methods. Results show survival and extensive migration of transplanted neural-like progenitors into damaged brain cortex during the first week of post-stroke recovery. The donor cells accumulated mainly in peri-infarct area and then differentiated showing a strong co-expression of neuronal (NF-200) but only moderate of astrocytic (GFAP) cell markers. However, the paucity of HUCB-NSCs detected within post-ischemic rat brain at the end of a 1 month period, as well as acute rejection of grafted cells by intact, yet cyclosporin A (CsA) immunosuppressed, rat brain tissue, suggests development of a severe adverse host reaction to the presence of alien donor cells and an urgent need for further study of the immunological response evoked by xenotransplantations of human cord blood-derived cells in animal experimental models.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / anatomy & histology
  • Brain / pathology
  • Cell Differentiation
  • Cell Line
  • Cell Movement
  • Cell Survival
  • Cerebral Infarction / pathology
  • Cerebral Infarction / therapy*
  • Disease Models, Animal
  • Fetal Blood / cytology*
  • Humans
  • Male
  • Rats
  • Rats, Wistar
  • Stem Cell Transplantation*
  • Stem Cells / cytology
  • Stem Cells / physiology*