Literature DB >> 4016893

Intracellular levels and distribution of Ca2+ in digitonin-permeabilized cells.

G Fiskum.   

Abstract

Digitonin and other saponins can be used to selectively permeabilize the plasma membrane of a wide variety of cells without significantly affecting the gross structure and function of Ca2+-sequestering organelles such as mitochondria and endoplasmic reticulum. These characteristics have allowed digitonin to be used in the determination of the intracellular levels and distribution of Ca2+, as well as the measurement of Ca2+ fluxes by organelles "in situ". Studies conducted with several different types of digitonin-permeabilized cells indicate that the endoplasmic reticulum functions as a high affinity and low-capacity intracellular Ca2+ buffer, whereas mitochondria operate as a relatively low affinity but high capacity Ca2+ buffering system. However, recent findings suggest that mitochondria have a comparable affinity for net Ca2+ uptake in the presence of physiological concentrations of polyamines. The use of permeabilized cells has also been important in the identification of the endoplasmic reticulum as a site at which the recently discovered second messenger inositol trisphosphate acts to bring about an increase in the cytosolic free Ca2+ concentration. Thus, the selective permeabilization of cells with digitonin and its analogues has been a powerful yet simple tool in the study of intracellular Ca2+ homeostasis.

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Year:  1985        PMID: 4016893     DOI: 10.1016/0143-4160(85)90032-6

Source DB:  PubMed          Journal:  Cell Calcium        ISSN: 0143-4160            Impact factor:   6.817


  20 in total

1.  Regulation of cytosolic free calcium concentration by intrasynaptic mitochondria.

Authors:  A Martínez-Serrano; J Satrústegui
Journal:  Mol Biol Cell       Date:  1992-02       Impact factor: 4.138

2.  Calcium-containing organelles display unique reactivity to chemical stimulation in cultured hippocampal neurons.

Authors:  E Korkotian; M Segal
Journal:  J Neurosci       Date:  1997-03-01       Impact factor: 6.167

3.  Oxidative phosphorylation in myocardial mitochondria 'in situ': a calorimetric study on permeabilized cardiac muscle preparations.

Authors:  D Köhnke; M Schramm; J Daut
Journal:  Mol Cell Biochem       Date:  1997-09       Impact factor: 3.396

4.  Monitoring of the mitochondrial and plasma membrane potentials in human fibroblasts by tetraphenylphosphonium ion distribution.

Authors:  M Rugolo; G Lenaz
Journal:  J Bioenerg Biomembr       Date:  1987-12       Impact factor: 2.945

5.  Characterization of Ca2+ fluxes in rat liver plasma-membrane vesicles.

Authors:  C Dargemont; M Hilly; M Claret; J P Mauger
Journal:  Biochem J       Date:  1988-11-15       Impact factor: 3.857

6.  Cytosolic alkalinization mediated by abscisic Acid is necessary, but not sufficient, for abscisic Acid-induced gene expression in barley aleurone protoplasts.

Authors:  R van der Veen; S Heimovaara-Dijkstra; M Wang
Journal:  Plant Physiol       Date:  1992-10       Impact factor: 8.340

7.  Plasma membrane Ca2+-ATPase mRNA expression in murine hepatocarcinoma and regenerating liver cells.

Authors:  Blanca Delgado-Coello; Juan Santiago-García; Angel Zarain-Herzberg; Jaime Mas-Oliva
Journal:  Mol Cell Biochem       Date:  2003-05       Impact factor: 3.396

8.  Effects of inositol trisphosphate on calcium mobilization in bone cells.

Authors:  R Falsafi; D N Tatakis; S Hagel-Bradway; R Dziak
Journal:  Calcif Tissue Int       Date:  1991-11       Impact factor: 4.333

9.  Oxidative damage to sarcoplasmic reticulum Ca(2+)-pump induced by Fe2+/H2O2/ascorbate is not mediated by lipid peroxidation or thiol oxidation and leads to protein fragmentation.

Authors:  R F Castilho; P C Carvalho-Alves; A E Vercesi; S T Ferreira
Journal:  Mol Cell Biochem       Date:  1996-06-21       Impact factor: 3.396

10.  Dual effect of spermine on mitochondrial Ca2+ transport.

Authors:  S Lenzen; W Münster; I Rustenbeck
Journal:  Biochem J       Date:  1992-09-01       Impact factor: 3.857

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