We developed and characterized antibodies specific for FGF-2 and used
them to locate FGF-2 during chick embryo development. A series of micr
ographs demonstrated the progression of FGF-S staining during developm
ent of the different tissues and organs. FGF-2 was present in the ecto
derm covering the entire embryo, muscle cells, nervous system, neural
crest cells, and mesonephros. FGF-2 was also present in the limb from
initiation of budding through differentiation. The limb ectoderm and s
ubjacent mesoderm showed the strongest immunostaining, with lower leve
ls in the center of the bud. However, the distribution of FGF-2 positi
ve cells in the mesoderm was not homogeneous. This heterogeneity was n
ot due to cell cycle specific distribution of FGF-2 protein, as flow c
ytometric analysis showed that FGF-2-positive cells were distributed t
hroughout the cell cycle. However, the amount of anti-FGF-2 fluorescen
ce varied most during G1, consistent with the possibility that FGF-2 i
s low after M phase and increases during G1. A bioassay was used to de
monstrate FGF-S levels in the wing ectoderm were approximately 2.7-fol
d greater than in the mesoderm. We propose that the location of FGF-2
in the embryo is consistent with a role in epithelial-mesenchymal inte
ractions; in the limb bud it may prevent differentiation and permit li
mb outgrowth and subsequent expression of patterning events. (C) 1993
Wiley-Liss, Inc.