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PROGRESS IN PROTOZOOLOGY

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MEMBRANE FUSIONS <strong>IN</strong> PROTOZOA 269<br />

It is difficult to derive a time sequence or — even more — any possible<br />

functional implications of static snap shots one gets from membranes<br />

by cryofixation and freeze-fracturing. This holds even more if any such<br />

attempt is done after previous chemical pretreatments (aldehyde fixation,<br />

antifreeze impregnation). In retrospect it appears, as summarized<br />

by Plattner (1981), that much of the controversies (see below)<br />

between different groups, working with protozoa, and also other groups,<br />

working with metazoan systems, came from such preparative difficulties.<br />

Both Tetrahymena and Paramecium display "rosettes" already in<br />

the resting stage, i.e., without triggering. After exocytosis triggering<br />

by a Ca 2+ -ionophore, "rosettes" are no longer present, whereas the<br />

"rings" persist and collapse (Plattner 1974). This indicates that only<br />

"rosette" but not "ring" structures are directly involved in exocytosis<br />

performance; the "rings" merely delineate the potential fusion zones<br />

without participating in the fusion process. Even stronger evidence for<br />

this comes from freeze-fracture work with mutant strains of Paramecium<br />

tetraurelia (Beisson et al. 1976). A brief survey is given in Figs.<br />

2 and 3. Some mutations make no (tl) or grossly defective {ftA, tam 38)<br />

trichocysts which cannot be attached to the cell membrane. Other<br />

mutations (nd) allow the attachment but not the subsequent exocytotic<br />

discharge. Beisson et al. (1976) established that the discharge capacity<br />

is coupled with the presence of "rosettes". This has later been<br />

extended to further mutations (Beisson et al. 1980, Lefort-Tran<br />

et al. 1981).<br />

synthesis —<br />

packing<br />

transport<br />

attachment<br />

trigger }<br />

membrane fusion )<br />

discharge<br />

membrane resealing<br />

membrane detachment<br />

trichless<br />

tam 8. tam 38, ftb A<br />

nd 9 (27 °C)<br />

7S, K 401, kin 241<br />

( nd 6, nd 7 (all temperatures) I<br />

nd 9 {18 °C) = 'permissive'<br />

non-permissive<br />

Fig. 2. Sequence of events leading to exocytotic membrane fusion (left) and genetic<br />

dsturbances at different levels in various mutant strains of Paramecium<br />

tetraurelia. 7S is the wild type strain (K401, kin 241 are non-exocytotic mutations);<br />

for nd 9 see text. From Plattner et al. (1980)<br />

http://rcin.org.pl

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