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Fig. 5. Ndst1 mutation disrupted Fgf10/Fgfr2b interaction and ectopic
lacrimal gland budding. (A-F) LACE assay of FGF/FGFR binding at the
lacrimal gland buds. Heparan sulfate mediated Fgf10/Fgfr2b and Fgf7/Fgfr2b
binding were observed in the tip of wild-type lacrimal gland buds, but not in
that of the Ndst1flox/flox;Le-Cre mutant embryos (arrow).
By contrast, ubiquitous Fgf1/Fgfr2b was present in both wild-type and mutant
embryos (arrowheads). (G-L) Ectopic lacrimal gland budding induced by
Fgf10. The control explant developed endogenous lacrimal gland in the presence
of BSA-containing beads (G, asterisks). By contrast, Fgf10 beads induced
additional ectopic lacrimal gland buds in both control and
Ndst1flox/flox;Le-Cre explants (J,K, arrowheads), whereas
no buds appeared in the Ndst1/2 double mutants (I,L). (M)
Lacrimal budding rate in explant cultures [Fisher's exact test: endogenous
budding in control and Ndst1flox/flox;Le-Cre mutants,
P<0.001; ectopic budding in control and Ndst1/2 double
mutants (Ndst1flox/flox;Ndst2-/-;Le-Cre),
P<0.02].