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Fig. 1. Effect of retinoic acid on whole sponges and primmorphs. (A) Untreated specimens of S. domuncula. (B,C) Induction of gemmules in animals by retinoic acid (50 µmol l–1). (B) Gemmules formed on a shell of the snail Trunculariopsis trunculus (incubation: 10 days) after retinoic acid treatment. (C) Group of gemmules arranged on the grooves of a shell. (D–G) Induction of canals in primmorphs. (D) Primmorphs formed in the absence of any organic matrix in the culture dish. The 3D-aggregates remained round and without canals. (E) Formation of canals by incubation of cells for 5 days on non-coated plates followed by 10 days on plates coated with galectin matrix. (F) Primmorphs with canals formed after for 5 days on non-coated plates followed by 10 days on poly-L-lysine plates. (G) Higher magnification of the canal system (> <) in the primmorphs developed for 20 days on the galectin matrix following 5 days incubation on non-coated plates. (H–L) Effect of retinoic acid on the canal system in primmorphs. (H,I) Incubation of canal-containing primmorphs (formed after a total incubation period of 15 days), cultured on the galectin matrix for 10 days, + 1 µmol l–1 of retinoic acid for an additional 5 days. (J–L) Incubation of the canal-containing primmorphs at the higher concentration of retinoic acid (50 µmol l–1) for the same period of time. For further details, see Materials and methods. Scale bars: 10 mm (except for C and G, 5 mm).





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