Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1994 Apr;104(4):1177–1183. doi: 10.1104/pp.104.4.1177

Evidence for an Extracellular Reception Site for Abscisic Acid in Commelina Guard Cells.

B E Anderson 1, J M Ward 1, J I Schroeder 1
PMCID: PMC159278  PMID: 12232155

Abstract

The phytohormone abscisic acid (ABA) triggers stomatal closing as a physiological response to drought stress. Several basic questions limit an understanding of the mechanism of ABA reception in guard cells. Whether primary ABA receptors are located on the extracellular side of the plasma membrane, within the intracellular space of guard cells, or both remains unknown. Furthermore, it is not clear whether ABA must be transported into guard cells to exert control over stomatal movements. In the present study, a combination of microinjection into guard cells and physiological assays of stomatal movements have been performed to determine primary sites of ABA reception in guard cells. Microinjection of ABA into guard cells of Commelina communis L. resulted in injected cytosolic concentrations of 50 to 200 [mu]M ABA and in additional experiments in lower concentrations of approximately 1 [mu]M ABA. Stomata with ABA-loaded guard cells (n > 180) showed opening similar to stomata with uninjected guard cells. The viability of guard cells following ABA injection was demonstrated by neutral red staining as well as monitoring of stomatal opening. Extracellular application of 10 [mu]M ABA inhibited stomatal opening by 98% at pH 6.15 and by 57% at pH 8.0. The pH dependence of extracellular ABA action may suggest a contribution of an intracellular ABA receptor to stomatal regulation. The findings presented here show that intracellular ABA alone does not suffice to inhibit stomatal opening under the imposed conditions. Furthermore, these data provide evidence that a reception site for ABA-mediated inhibition of stomatal opening is on the extracellular side of the plasma membrane of guard cells.

Full Text

The Full Text of this article is available as a PDF (1.9 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Blatt M. R., Thiel G., Trentham D. R. Reversible inactivation of K+ channels of Vicia stomatal guard cells following the photolysis of caged inositol 1,4,5-trisphosphate. Nature. 1990 Aug 23;346(6286):766–769. doi: 10.1038/346766a0. [DOI] [PubMed] [Google Scholar]
  2. Gilroy S., Fricker M. D., Read N. D., Trewavas A. J. Role of Calcium in Signal Transduction of Commelina Guard Cells. Plant Cell. 1991 Apr;3(4):333–344. doi: 10.1105/tpc.3.4.333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Gilroy S., Read N. D., Trewavas A. J. Elevation of cytoplasmic calcium by caged calcium or caged inositol triphosphate initiates stomatal closure. Nature. 1990 Aug 23;346(6286):769–771. doi: 10.1038/346769a0. [DOI] [PubMed] [Google Scholar]
  4. Harris M. J., Outlaw W. H., Mertens R., Weiler E. W. Water-stress-induced changes in the abscisic acid content of guard cells and other cells of Vicia faba L. leaves as determined by enzyme-amplified immunoassay. Proc Natl Acad Sci U S A. 1988 Apr;85(8):2584–2588. doi: 10.1073/pnas.85.8.2584. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Kaiser W. M., Hartung W. Uptake and Release of Abscisic Acid by Isolated Photoautotrophic Mesophyll Cells, Depending on pH Gradients. Plant Physiol. 1981 Jul;68(1):202–206. doi: 10.1104/pp.68.1.202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Kearns E. V., Assmann S. M. The Guard Cell-Environment Connection. Plant Physiol. 1993 Jul;102(3):711–715. doi: 10.1104/pp.102.3.711. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lee H. J., Tucker E. B., Crain R. C., Lee Y. Stomatal Opening Is Induced in Epidermal Peels of Commelina communis L. by GTP Analogs or Pertussis Toxin. Plant Physiol. 1993 May;102(1):95–100. doi: 10.1104/pp.102.1.95. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. McAinsh M. R., Brownlee C., Hetherington A. M. Visualizing Changes in Cytosolic-Free Ca2+ during the Response of Stomatal Guard Cells to Abscisic Acid. Plant Cell. 1992 Sep;4(9):1113–1122. doi: 10.1105/tpc.4.9.1113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Schroeder J. I., Hagiwara S. Repetitive increases in cytosolic Ca2+ of guard cells by abscisic acid activation of nonselective Ca2+ permeable channels. Proc Natl Acad Sci U S A. 1990 Dec;87(23):9305–9309. doi: 10.1073/pnas.87.23.9305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Schroeder J. I., Hedrich R. Involvement of ion channels and active transport in osmoregulation and signaling of higher plant cells. Trends Biochem Sci. 1989 May;14(5):187–192. doi: 10.1016/0968-0004(89)90272-7. [DOI] [PubMed] [Google Scholar]
  11. Schwartz A., Ilan N., Grantz D. A. Calcium Effects on Stomatal Movement in Commelina communis L. : Use of EGTA to Modulate Stomatal Response to Light, KCl and CO(2). Plant Physiol. 1988 Jul;87(3):583–587. doi: 10.1104/pp.87.3.583. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES