Genetic dissection of the final exocytosis steps in Paramecium tetraurelia cells: trigger analyses

A variety of trigger procedures were applied to analyse the exocytotic capability of different Paramecium tetraurelia strains. 7,S K 40I, kin 24I, and 9 (18 degrees C) are capable of exocytosis (permissive strains), in contrast to nd 6, nd 7, nd 9 (27 degrees C), tam 38 and ftb A, although all procedures used enhance [Ca2+]i in the cytoplasm of all strains tested and although strains nd 6, nd 7 and nd 9 (27 degrees C) contain a full set of morphologically normal trichocysts attended to the cell membrane. The results show that only those strains are permissive which were shown previously to contain a rosette of membrane-integrated particles and a Ca2+-ATPase activity in the cell membrane over the trichocyst attachment (exocytosis) sites. The results from trigger experiments with permissive and non-permissive strains would be compatible with a dual function of rosette particles as Ca2+ pumps and Ca2+ channels. Nevertheless, the latter aspect remains uncertain since we show that experiments along these lines published by others (introducing a Ca2+ ionophore from the outside) involve a solvent-induced artifact (pseudoexocytosis: matrix stretching in the absence of membrane fusion). In all strains, except for tam 38 and ftb A (which have abnormal trichocysts incapable of being attached to the cell membrane), the isolated trichocyst matrix can be transferred from the contracted to the expanded state in vitro with certain trigger procedures. Our data clearly show that an increase of [Ca2+]i in the cytoplasm is not sufficient for exocytosis to occur and that non-permissiveness is somehow due to an inability to perform membrane fusion. It remains open whether the lack of rosettes and Ca2+-ATPase activity at trichocyst attachment sites are primary cause of non-permissiveness.