Abstract
Adenophostin A, the most potent known agonist of inositol 1,4, 5-trisphosphate (InsP(3)) receptors, stimulated (45)Ca(2+) release from the intracellular stores of permeabilized hepatocytes. The concentration of adenophostin A causing the half-maximal effect (EC(50)) was 7.1+/-0.5 nM, whereas the EC(50) for InsP(3) was 177+/-26 nM; both responses were positively co-operative. In rapid superfusion analyses of (45)Ca(2+) release from the intracellular stores of immobilized hepatocytes, maximal concentrations of adenophostin A or InsP(3) evoked indistinguishable patterns of Ca(2+) release. The Ca(2+) release evoked by both agonists peaked at the same maximal rate after about 375 ms and the activity of the receptors then decayed to a stable, partially (60%) inactivated state with a half-time (t(1/2)) of 318+/-29 ms for adenophostin A and 321+/-22 ms for InsP(3). Dissociation rates were measured by recording rates of InsP(3)-receptor channel closure after rapid removal of agonist. The rate of adenophostin A dissociation (t(1/2), 840+/-195 ms) was only 2-fold slower than that of InsP(3) (t(1/2), 436+/-48 ms). We conclude that slow dissociation of adenophostin A from InsP(3) receptors does not underlie either its high-affinity binding or the reported differences in the Ca(2+) signals evoked by InsP(3) and adenophostin A in intact cells.
Full Text
The Full Text of this article is available as a PDF (147.3 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Adkins C. E., Taylor C. W. Lateral inhibition of inositol 1,4,5-trisphosphate receptors by cytosolic Ca(2+). Curr Biol. 1999 Oct 7;9(19):1115–1118. doi: 10.1016/s0960-9822(99)80481-3. [DOI] [PubMed] [Google Scholar]
- Beecroft M. D., Marchant J. S., Riley A. M., Van Straten N. C., Van der Marel G. A., Van Boom J. H., Potter B. V., Taylor C. W. Acyclophostin: a ribose-modified analog of adenophostin A with high affinity for inositol 1,4,5-trisphosphate receptors and pH-dependent efficacy. Mol Pharmacol. 1999 Jan;55(1):109–117. doi: 10.1124/mol.55.1.109. [DOI] [PubMed] [Google Scholar]
- Bird G. S., Takahashi M., Tanzawa K., Putney J. W., Jr Adenophostin A induces spatially restricted calcium signaling in Xenopus laevis oocytes. J Biol Chem. 1999 Jul 16;274(29):20643–20649. doi: 10.1074/jbc.274.29.20643. [DOI] [PubMed] [Google Scholar]
- Broad L. M., Armstrong D. L., Putney J. W., Jr Role of the inositol 1,4,5-trisphosphate receptor in Ca(2+) feedback inhibition of calcium release-activated calcium current (I(crac)). J Biol Chem. 1999 Nov 12;274(46):32881–32888. doi: 10.1074/jbc.274.46.32881. [DOI] [PubMed] [Google Scholar]
- DeLisle S., Marksberry E. W., Bonnett C., Jenkins D. J., Potter B. V., Takahashi M., Tanzawa K. Adenophostin A can stimulate Ca2+ influx without depleting the inositol 1,4,5-trisphosphate-sensitive Ca2+ stores in the Xenopus oocyte. J Biol Chem. 1997 Apr 11;272(15):9956–9961. doi: 10.1074/jbc.272.15.9956. [DOI] [PubMed] [Google Scholar]
- Hartzell H. C., Machaca K., Hirayama Y. Effects of adenophostin-A and inositol-1,4,5-trisphosphate on Cl- currents in Xenopus laevis oocytes. Mol Pharmacol. 1997 Apr;51(4):683–692. doi: 10.1124/mol.51.4.683. [DOI] [PubMed] [Google Scholar]
- He C. L., Damiani P., Ducibella T., Takahashi M., Tanzawa K., Parys J. B., Fissore R. A. Isoforms of the inositol 1,4,5-trisphosphate receptor are expressed in bovine oocytes and ovaries: the type-1 isoform is down-regulated by fertilization and by injection of adenophostin A. Biol Reprod. 1999 Oct;61(4):935–943. doi: 10.1095/biolreprod61.4.935. [DOI] [PubMed] [Google Scholar]
- Hirota J., Michikawa T., Miyawaki A., Takahashi M., Tanzawa K., Okura I., Furuichi T., Mikoshiba K. Adenophostin-medicated quantal Ca2+ release in the purified and reconstituted inositol 1,4,5-trisphosphate receptor type 1. FEBS Lett. 1995 Jul 17;368(2):248–252. doi: 10.1016/0014-5793(95)00659-w. [DOI] [PubMed] [Google Scholar]
- Hotoda H., Murayama K., Miyamoto S., Iwata Y., Takahashi M., Kawase Y., Tanzawa K., Kaneko M. Molecular recognition of adenophostin, a very potent Ca2+ inducer, at the D-myo-inositol 1,4,5-trisphosphate receptor. Biochemistry. 1999 Jul 20;38(29):9234–9241. doi: 10.1021/bi990114r. [DOI] [PubMed] [Google Scholar]
- Huang Y., Takahashi M., Tanzawa K., Putney J. W., Jr Effect of adenophostin A on Ca2+ entry and calcium release-activated calcium current (Icrac) in rat basophilic leukemia cells. J Biol Chem. 1998 Nov 27;273(48):31815–31821. doi: 10.1074/jbc.273.48.31815. [DOI] [PubMed] [Google Scholar]
- Machaca K., Hartzell H. C. Adenophostin A and inositol 1,4,5-trisphosphate differentially activate Cl- currents in Xenopus oocytes because of disparate Ca2+ release kinetics. J Biol Chem. 1999 Feb 19;274(8):4824–4831. doi: 10.1074/jbc.274.8.4824. [DOI] [PubMed] [Google Scholar]
- Marchant J. S., Beecroft M. D., Riley A. M., Jenkins D. J., Marwood R. D., Taylor C. W., Potter B. V. Disaccharide polyphosphates based upon adenophostin A activate hepatic D-myo-inositol 1,4,5-trisphosphate receptors. Biochemistry. 1997 Oct 21;36(42):12780–12790. doi: 10.1021/bi971397v. [DOI] [PubMed] [Google Scholar]
- Marchant J. S., Parker I. Kinetics of elementary Ca2+ puffs evoked in Xenopus oocytes by different Ins(1,4,5)P3 receptor agonists. Biochem J. 1998 Sep 15;334(Pt 3):505–509. doi: 10.1042/bj3340505. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marchant J. S., Taylor C. W. Cooperative activation of IP3 receptors by sequential binding of IP3 and Ca2+ safeguards against spontaneous activity. Curr Biol. 1997 Jul 1;7(7):510–518. doi: 10.1016/s0960-9822(06)00222-3. [DOI] [PubMed] [Google Scholar]
- Marchant J. S., Taylor C. W. Rapid activation and partial inactivation of inositol trisphosphate receptors by inositol trisphosphate. Biochemistry. 1998 Aug 18;37(33):11524–11533. doi: 10.1021/bi980808k. [DOI] [PubMed] [Google Scholar]
- Marwood R. D., Riley A. M., Correa V., Taylor C. W., Potter B. V. Simplification of adenophostin A defines a minimal structure for potent glucopyranoside-based mimics of D-myo-inositol 1,4,5-trisphosphate. Bioorg Med Chem Lett. 1999 Feb 8;9(3):453–458. doi: 10.1016/s0960-894x(99)00006-2. [DOI] [PubMed] [Google Scholar]
- Missiaen L., Parys J. B., Sienaert I., Maes K., Kunzelmann K., Takahashi M., Tanzawa K., De Smedt H. Functional properties of the type-3 InsP3 receptor in 16HBE14o- bronchial mucosal cells. J Biol Chem. 1998 Apr 10;273(15):8983–8986. doi: 10.1074/jbc.273.15.8983. [DOI] [PubMed] [Google Scholar]
- Murphy C. T., Riley A. M., Lindley C. J., Jenkins D. J., Westwick J., Potter B. V. Structural analogues of D-myo-inositol-1,4,5-trisphosphate and adenophostin A: recognition by cerebellar and platelet inositol-1,4,5-trisphosphate receptors. Mol Pharmacol. 1997 Oct;52(4):741–748. doi: 10.1124/mol.52.4.741. [DOI] [PubMed] [Google Scholar]
- Nunn D. L., Taylor C. W. Luminal Ca2+ increases the sensitivity of Ca2+ stores to inositol 1,4,5-trisphosphate. Mol Pharmacol. 1992 Jan;41(1):115–119. [PubMed] [Google Scholar]
- Parys J. B., Bezprozvanny I. The inositol trisphosphate receptor of Xenopus oocytes. Cell Calcium. 1995 Nov;18(5):353–363. doi: 10.1016/0143-4160(95)90051-9. [DOI] [PubMed] [Google Scholar]
- Takahashi M., Tanzawa K., Takahashi S. Adenophostins, newly discovered metabolites of Penicillium brevicompactum, act as potent agonists of the inositol 1,4,5-trisphosphate receptor. J Biol Chem. 1994 Jan 7;269(1):369–372. [PubMed] [Google Scholar]
- Takahashi S., Kinoshita T., Takahashi M. Adenophostins A and B: potent agonists of inositol-1,4,5-trisphosphate receptor produced by Penicillium brevicompactum. Structure elucidation. J Antibiot (Tokyo) 1994 Jan;47(1):95–100. doi: 10.7164/antibiotics.47.95. [DOI] [PubMed] [Google Scholar]
- Taylor C. W. Inositol trisphosphate receptors: Ca2+-modulated intracellular Ca2+ channels. Biochim Biophys Acta. 1998 Dec 8;1436(1-2):19–33. doi: 10.1016/s0005-2760(98)00122-2. [DOI] [PubMed] [Google Scholar]
- Yoshida M., Sensui N., Inoue T., Morisawa M., Mikoshiba K. Role of two series of Ca2+ oscillations in activation of ascidian eggs. Dev Biol. 1998 Nov 1;203(1):122–133. doi: 10.1006/dbio.1998.9037. [DOI] [PubMed] [Google Scholar]