Olfactory ensheathing glia (EG) from adult rat proliferate slowly in vitro
without added mitogens. The potential future use of EG in transplantation w
ithin the central nervous system to improve neural repair is dependent on i
dentifying mitogens that will effectively expand EG without altering their
phenotype. The mitogenic effects of heregulin (HRG), fibroblast growth fact
or 2 (FGF-2), platelet-derived growth factor BE (PDGF-BB), insulin-like gro
wth factor 1 (IGF-1), and forskolin (FSK) on cultured adult-derived rat EG
were monitored by tritiated-thymidine labeling and p75 immunostaining. In s
erum-containing medium, HRG, FGF-2, PDGF-BB, IGF-1, and FSK were capable of
stimulating EG proliferation, and the stimulation by these growth factors
was potentiated by FSK. The combinations of HRG + FGF-2, HRG + PDGF-BB, HRG
+ IGF-1, FGF-2 + PDGF-BB, and FGF-2 + IGF-1 all promoted EG proliferation
in an additive manner. In serum-free medium, HRG and FGF-2 were mitogenic,
but PDGF-BB, IGF-1 and FSK were not; however, FSK potentiated the stimulati
on by HRG and FGF-2, and the combination of HRG + FGF-2 promoted EG prolife
ration in an additive manner. This new information will be useful for the d
esign of protocols to achieve sufficient numbers of adult-derived EG for cl
inical purposes. This study also further establishes similarities between E
G and Schwann cells. GLIA 33:334-342, 2001. (C) 2001 Wiley-Liss Inc.