Literature DB >> 6501420

Paramecium secretory granule content: quantitative studies on in vitro expansion and its regulation by calcium and pH.

R S Garofalo, B H Satir.   

Abstract

Ca2+-dependent secretion in Paramecium involves the exocytic release of a paracrystalline secretory product, the trichocyst matrix, which undergoes a characteristic structural change from a highly condensed storage form (Stage I) to an extended needle-like structure (Stage III) during release. We studied trichocyst matrix expansion in vitro to examine factors regulating the state of secretory organelle content. A new method for the isolation of membrane-free, condensed (Stage I) trichocyst matrices is described. These highly purified, condensed matrices were used to develop a rapid quantitative, spectrophotometric assay for matrix expansion to examine factors regulating the Stage I and Stage III transition. Expansion from Stages I to III was elicited in vitro by addition of Ca2+ and we found that at neutral pH, expansion required a Ca2+ concentration slightly above 10(-6)M. Previous studies indicate that calmodulin (CaM) antagonists inhibit matrix expansion in vivo. However, in vitro matrix expansion is normal even when trichocyst matrices are preincubated in CaM antagonists before stimulation. Thus, matrix components themselves are unlikely to be the site of CaM antagonist action in vivo. In vitro matrix expansion is also modulated by pH. Decreasing pH to 6.0 inhibits expansion, i.e., expansion requires higher Ca2+ concentration. Conversely, increasing pH to greater than 7.0 promotes expansion, allowing it to occur at a lower Ca2+ concentration. The pH sensitivity of the Ca2+ binding sites of the matrix suggests that, in vivo, the interior of the trichocyst vesicle may be maintained at an acidic pH. Exposure of cells to acridine orange, a fluorescent amine that accumulates in acidic intracellular compartments, leads to its uptake and concentration within trichocysts. Thus intratrichocyst pH appears to be acidic in vivo and may serve as a regulatory or "safety" mechanism to inhibit premature expansion.

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Year:  1984        PMID: 6501420      PMCID: PMC2113549          DOI: 10.1083/jcb.99.6.2193

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  23 in total

1.  Binding of trifluoperazine to the calcium-dependent activator of cyclic nucleotide phosphodiesterase.

Authors:  R M Levin; B Weiss
Journal:  Mol Pharmacol       Date:  1977-07       Impact factor: 4.436

2.  Energy-linked activities of the chromaffin granule membrane.

Authors:  C L Bashford; G K Radda; G A Ritchie
Journal:  FEBS Lett       Date:  1975-01-15       Impact factor: 4.124

3.  Properties and structure of isolated extrusive organelles.

Authors:  R Anderer; K Hausmann
Journal:  J Ultrastruct Res       Date:  1977-07

4.  The zymogen granule: intragranular organization and its functional significance.

Authors:  S S Rothman; S Burwen; C Liebow
Journal:  Adv Cytopharmacol       Date:  1974

5.  Molecular organization of rat prolactin secretory granules.

Authors:  A Zanini; G Giannattasio
Journal:  Adv Cytopharmacol       Date:  1974

6.  Physicochemical characteristics of insulin secretion granules.

Authors:  H G Coore; B Hellman; E Pihl; I B Täljedal
Journal:  Biochem J       Date:  1969-01       Impact factor: 3.857

7.  Ion permeability of isolated chromaffin granules.

Authors:  R G Johnson; A Scarpa
Journal:  J Gen Physiol       Date:  1976-12       Impact factor: 4.086

8.  Genetic analysis of membrane differentiation in Paramecium. Freeze-fracture study of the trichocyst cycle in wild-type and mutant strains.

Authors:  J Beisson; M Lefort-Tran; M Pouphile; M Rossignol; B Satir
Journal:  J Cell Biol       Date:  1976-04       Impact factor: 10.539

9.  Adenosinetriphosphate, calcium and temperature requirements for the final steps of exocytosis in Paramecium cells.

Authors:  H Matt; M Bilinski; H Plattner
Journal:  J Cell Sci       Date:  1978-08       Impact factor: 5.285

10.  Isolation and properties of secretory granules from rat islets of Langerhans. 3. Studies of the stability of the isolated beta granules.

Authors:  S L Howell; D A Young; P E Lacy
Journal:  J Cell Biol       Date:  1969-04       Impact factor: 10.539

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  2 in total

1.  The crystal lattice of Paramecium trichocysts before and after exocytosis by X-ray diffraction and freeze-fracture electron microscopy.

Authors:  L Sperling; A Tardieu; T Gulik-Krzywicki
Journal:  J Cell Biol       Date:  1987-10       Impact factor: 10.539

2.  A Ca2+ influx associated with exocytosis is specifically abolished in a Paramecium exocytotic mutant.

Authors:  D Kerboeuf; J Cohen
Journal:  J Cell Biol       Date:  1990-12       Impact factor: 10.539

  2 in total

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