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. 1994 Apr;104(4):1131–1138. doi: 10.1104/pp.104.4.1131

Low Temperature-Induced Cytoplasmic Acidosis in Cultured Mung Bean (Vigna radiata [L.] Wilczek) Cells.

S Yoshida 1
PMCID: PMC159273  PMID: 12232153

Abstract

Cold-induced changes in vivo in the cytoplasmic pH of suspension-cultured cells of mung bean (Vigna radiata [L.] Wilczek) were investigated by fluorescence-ratio imaging cryomicroscopy with special reference to the variations in the chilling sensitivity of cells during the growth cycle. Because of the preferential localization of the fluorophore in the cytoplasm under specified conditions and the ideal response of fluorescence to pH, fluorescein diacetate allows measurements to be made of temporal changes in cytoplasmic pH at low temperature. A remarkable difference was demonstrated in the cold-induced changes in cytoplasmic pH between cells at the early and late stages of exponential growth. The cells at the early stage of exponential growth were most sensitive to chilling, and the cytoplasmic pH decreased dramatically within a short period of incubation at 0[deg]C, decreasing from 7.4 to 6.8 after 4 h and to 6.3 after 18 h. The cells at the late stage of exponential growth were chilling tolerant, and no significant decrease in the cytoplasmic pH was observed during the incubation at 0[deg]C for 24 h or even longer. From the results presented here, it appears that cold-induced cytoplasmic acidosis is characteristic of chilling-sensitive mung bean suspension-cultured cells.

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Selected References

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  1. Bright G. R., Fisher G. W., Rogowska J., Taylor D. L. Fluorescence ratio imaging microscopy: temporal and spatial measurements of cytoplasmic pH. J Cell Biol. 1987 Apr;104(4):1019–1033. doi: 10.1083/jcb.104.4.1019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Davies T. A., Dunn J. M., Simons E. R. Evaluation of changes in cytoplasmic pH in thrombin-stimulated human platelets. Anal Biochem. 1987 Nov 15;167(1):118–123. doi: 10.1016/0003-2697(87)90140-0. [DOI] [PubMed] [Google Scholar]
  3. Heiple J. M., Taylor D. L. Intracellular pH in single motile cells. J Cell Biol. 1980 Sep;86(3):885–890. doi: 10.1083/jcb.86.3.885. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Irving H. R., Gehring C. A., Parish R. W. Changes in cytosolic pH and calcium of guard cells precede stomatal movements. Proc Natl Acad Sci U S A. 1992 Mar 1;89(5):1790–1794. doi: 10.1073/pnas.89.5.1790. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Katsuhara M., Kuchitsu K., Takeshige K., Tazawa M. Salt Stress-Induced Cytoplasmic Acidification and Vacuolar Alkalization in Nitellopsis obtusa Cells : In VivoP-Nuclear Magnetic Resonance Study. Plant Physiol. 1989 Jul;90(3):1102–1107. doi: 10.1104/pp.90.3.1102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Roberts J. K., Callis J., Jardetzky O., Walbot V., Freeling M. Cytoplasmic acidosis as a determinant of flooding intolerance in plants. Proc Natl Acad Sci U S A. 1984 Oct;81(19):6029–6033. doi: 10.1073/pnas.81.19.6029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Rogers J., Hesketh T. R., Smith G. A., Metcalfe J. C. Intracellular pH of stimulated thymocytes measured with a new fluorescent indicator. J Biol Chem. 1983 May 25;258(10):5994–5997. [PubMed] [Google Scholar]
  8. Roos A., Boron W. F. Intracellular pH. Physiol Rev. 1981 Apr;61(2):296–434. doi: 10.1152/physrev.1981.61.2.296. [DOI] [PubMed] [Google Scholar]
  9. Saint-Ges V., Roby C., Bligny R., Pradet A., Douce R. Kinetic studies of the variations of cytoplasmic pH, nucleotide triphosphates (31P-NMR) and lactate during normoxic and anoxic transitions in maize root tips. Eur J Biochem. 1991 Sep 1;200(2):477–482. doi: 10.1111/j.1432-1033.1991.tb16207.x. [DOI] [PubMed] [Google Scholar]
  10. Slavík J. Intracellular pH of yeast cells measured with fluorescent probes. FEBS Lett. 1982 Apr 5;140(1):22–26. doi: 10.1016/0014-5793(82)80512-7. [DOI] [PubMed] [Google Scholar]
  11. Widholm J. M. The use of fluorescein diacetate and phenosafranine for determining viability of cultured plant cells. Stain Technol. 1972 Jul;47(4):189–194. doi: 10.3109/10520297209116483. [DOI] [PubMed] [Google Scholar]
  12. Yoshida S. Chilling-Induced Inactivation and Its Recovery of Tonoplast H-ATPase in Mung Bean Cell Suspension Cultures. Plant Physiol. 1991 Feb;95(2):456–460. doi: 10.1104/pp.95.2.456. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Yoshida S., Matsuura-Endo C. Comparison of Temperature Dependency of Tonoplast Proton Translocation between Plants Sensitive and Insensitive to Chilling. Plant Physiol. 1991 Feb;95(2):504–508. doi: 10.1104/pp.95.2.504. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Yoshida S., Matsuura C., Etani S. Impairment of Tonoplast H-ATPase as an Initial Physiological Response of Cells to Chilling in Mung Bean (Vigna radiata [L.] Wilczek). Plant Physiol. 1989 Feb;89(2):634–642. doi: 10.1104/pp.89.2.634. [DOI] [PMC free article] [PubMed] [Google Scholar]

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