Mh. Deangelis et al., PROMOTION OF GASTRULATION BY MATERNAL GROWTH-FACTOR IN CULTURED RABBIT BLASTOCYSTS, Cell and tissue research, 282(1), 1995, pp. 147-154
Rabbit blastocysts of day 6 post coitum were cultured in a chemically
defined, protein-free medium for 24 h. Although the trophoblast contin
ued to grow, the embryonic disc degenerated. Addition of basic fibrobl
ast growth factor (FGF-2, of human recombinant or bovine origin, 10 ng
/ml) to the culture medium resulted in significant developmental progr
ess. The embryonic disc became pear-shaped showing a round anterior ed
ge and a posterior node. The primitive streak and Hensen's node indica
ted that gastrulation had begun. Mesoderm formation was confirmed from
histological sections and by localization of the expression of T-gene
transcripts in whole-mount preparations. FGF-2 mRNA was detected in b
oth day-6 endometrium and day 6-blastocysts using in vitro translation
followed by immunoprecipitation with a monoclonal antibody to FGF-2.
In the uterine secretions of day-6 pregnant and pseudopregnant animals
, several proteins exhibiting FGF-2 antigenicity were detected on West
ern blots following two-dimensional gel electrophoresis. As day-6 blas
tocysts required exogenous FGF-2 in vitro and as FGF-2 of uterine orig
in is present in the uterine secretion, the maternal growth factor can
promote gastrulation in vivo.