Literature DB >> 2579814

Synchronous exocytosis in Paramecium cells. IV. Polyamino compounds as potent trigger agents for repeatable trigger-redocking cycles.

H Plattner, R Stürzl, H Matt.   

Abstract

We found that different polyamino compounds trigger the instantaneous and simultaneous release of trichocysts from Paramecium tetraurelia cells (monoxenically bacterized cultures), provided amino groups are spaced in intervals of approximately 1.0 nm; in this case even diamines or oligopeptides exert some trigger effect. The most potent trigger agent found was aminoethyldextran (AED, MW = 40 kDa) which was used mainly as a derivative with 40 -NH2/molecule. A maximal response (strain K401) was achieved at 1.38 X 10(-6) M, a half maximal response at 1.08 X 10(-6) M. AED acts by a dual effect, i.e., not only by statistically properly spaced amino groups but also by some additional effect of the dextran molecule, since this greatly enhances the effect of oligoamines, although it exerts no trigger effect per se. From a total of approximately 1120 or approximately 1230 trichocysts per cell (strain K401 or 7S) approximately 95% are releasable by AED. In these strains the number of non-releasable trichocysts corresponds closely to the number of undocked trichocysts floating in the cytoplasm, so that practically all trichocysts which are docked to the cell membrane, can be released. (We also analysed different mutant strains for their response to AED.) Massive trichocyst release does not impair cell viability or culture growth, and multiple release-redocking cycles can be performed; up to 5 trigger-docking cycles were tested with individual cells in 12 h intervals. AED-triggered exocytosis requires a free extracellular [Ca2+] of greater than or equal to 10(-5) M; it is inhibited by EGTA (ethyleneglycol-bis(beta-aminoethyl ether)-N,N'-tetraacetate), by a short pH 5.5 shock or by neomycin at 10(-5) M concentration.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1985        PMID: 2579814

Source DB:  PubMed          Journal:  Eur J Cell Biol        ISSN: 0171-9335            Impact factor:   4.492


  21 in total

1.  A cortical phosphoprotein ('PP63') sensitive to exocytosis triggering in Paramecium cells. Immunolocalization and quenched-flow correlation of time course of dephosphorylation with membrane fusion.

Authors:  B Höhne-Zell; G Knoll; U Riedel-Gras; W Hofer; H Plattner
Journal:  Biochem J       Date:  1992-09-15       Impact factor: 3.857

2.  Quantitative immuno-gold labelling and ultrastructural preservation after cryofixation (combined with different freeze-substitution and embedding protocols) and after chemical fixation and cryosectioning. Analysis of the secretory organelle matrix of Paramecium trichocysts.

Authors:  A G Bittermann; G Knoll; A Németh; H Plattner
Journal:  Histochemistry       Date:  1992

3.  Protein phosphatase and kinase activities possibly involved in exocytosis regulation in Paramecium tetraurelia.

Authors:  R Kissmehl; T Treptau; H W Hofer; H Plattner
Journal:  Biochem J       Date:  1996-07-01       Impact factor: 3.857

4.  Protein phosphatase 2B (PP2B, calcineurin) in Paramecium: partial characterization reveals that two members of the unusually large catalytic subunit family have distinct roles in calcium-dependent processes.

Authors:  D Fraga; I M Sehring; R Kissmehl; M Reiss; R Gaines; R Hinrichsen; H Plattner
Journal:  Eukaryot Cell       Date:  2010-04-30

5.  Identification of isoforms of the exocytosis-sensitive phosphoprotein PP63/parafusin in Paramecium tetraurelia and demonstration of phosphoglucomutase activity.

Authors:  K Hauser; R Kissmehl; J Linder; J E Schultz; F Lottspeich; H Plattner
Journal:  Biochem J       Date:  1997-04-01       Impact factor: 3.857

6.  Lectin binding sites in Paramecium tetraurelia cells. I. Labeling analysis predominantly of secretory components.

Authors:  N Lüthe; H Plattner; B Haacke; P Walther; M Müller
Journal:  Histochemistry       Date:  1986

7.  Seventeen a-subunit isoforms of paramecium V-ATPase provide high specialization in localization and function.

Authors:  Thomas Wassmer; Roland Kissmehl; Jean Cohen; Helmut Plattner
Journal:  Mol Biol Cell       Date:  2005-11-28       Impact factor: 4.138

8.  Novel types of Ca2+ release channels participate in the secretory cycle of Paramecium cells.

Authors:  Eva-Maria Ladenburger; Ivonne M Sehring; Iris Korn; Helmut Plattner
Journal:  Mol Cell Biol       Date:  2009-04-20       Impact factor: 4.272

9.  Lysozyme acts as a chemorepellent and secretagogue in Paramecium by activating a novel receptor-operated Ca++ conductance.

Authors:  T M Hennessey; M Y Kim; B H Satir
Journal:  J Membr Biol       Date:  1995-11       Impact factor: 1.843

10.  Veratridine triggers exocytosis in Paramecium cells by activating somatic Ca channels.

Authors:  H Plattner; C Braun; N Klauke; S Länge
Journal:  J Membr Biol       Date:  1994-11       Impact factor: 1.843

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