
Fibroblast Growth Factor‐2 Overexpression in Transplanted Neural Progenitors Promotes Perivascular Cluster Formation with a Neurogenic Potential
Author(s) -
Jenny Benoit,
Kanemitsu Michiko,
Tsupykov Oleg,
Potter Gael,
Salmon Patrick,
Zgraggen Eloisa,
Gascon Eduardo,
Skibo Galina,
Dayer Alexandre G.,
Kiss Jozsef Z.
Publication year - 2009
Publication title -
stem cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.159
H-Index - 229
eISSN - 1549-4918
pISSN - 1066-5099
DOI - 10.1002/stem.46
Subject(s) - progenitor cell , biology , fibroblast growth factor , neural stem cell , progenitor , microbiology and biotechnology , neurogenesis , neuroscience , stem cell , transplantation , basic fibroblast growth factor , growth factor , immunology , receptor , medicine , genetics
Stem/progenitor cell‐based therapies hold promises for repairing the damaged nervous system. However, the efficiency of these approaches for neuronal replacement remains very limited. A major challenge is to develop pretransplant cell manipulations that may promote the survival, engraftment, and differentiation of transplanted cells. Here, we investigated whether overexpression of fibroblast growth factor‐2 (FGF‐2) in grafted neural progenitors could improve their integration in the host tissue. We show that FGF‐2‐transduced progenitors grafted in the early postnatal rat cortex have the distinct tendency to associate with the vasculature and establish multiple proliferative clusters in the perivascular environment. The contact with vessels appears to be critical for maintaining progenitor cells in an undifferentiated and proliferative phenotype in the intact cortex. Strikingly, perivascular clusters of FGF‐2 expressing cells seem to supply immature neurons in an ischemic environment. Our data provide evidence that engineering neural progenitors to overexpress FGF‐2 may be a suitable strategy to improve the integration of grafted neural progenitor cells with the host vasculature thereby generating neurovascular clusters with a neurogenic potential for brain repair. S TEM C ELLS 2009;27:1309–1317