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. 1992 Jan 1;116(1):147–156. doi: 10.1083/jcb.116.1.147

Reducing inositol lipid hydrolysis, Ins(1,4,5)P3 receptor availability, or Ca2+ gradients lengthens the duration of the cell cycle in Xenopus laevis blastomeres

PMCID: PMC2289269  PMID: 1309810

Abstract

We have microinjected a mAb specifically directed to phosphatidylinositol 4,5-bisphosphate (PIP2) into one blastomere of two- cell stage Xenopus laevis embryos. This antibody binds to endogenous PIP2 and reduces its rate of hydrolysis by phospholipase C. Antibody- injected blastomeres undergo partial or complete arrest of the cell cycle whereas the uninjected sister blastomeres divided normally. Since PIP2 hydrolysis normally produces diacylglycerol (DG) and inositol 1,4,5-triphosphate (Ins[1,4,5]P3), we attempted to measure changes in the levels of DG following stimulation of PIP2 hydrolysis in antibody- injected oocytes. The total amount of DG in antibody-injected oocytes was significantly reduced compared to that of water-injected ones following stimulation by either acetylcholine or progesterone indicating that the antibody does indeed suppress PIP2 hydrolysis. We also found that the PIP2 antibodies greatly reduced the amount of intracellular Ca2+ released in the egg cortex during egg activation. As an indirect test for Ins(1,4,5)P3 involvement in the cell cycle we injected heparin which competes with Ins(1,4,5)P3 for binding to its receptor, and thus inhibits Ins(1,4,5)P3-induced Ca2+ release. Microinjection of heparin into one blastomere of the two-cell stage embryo caused partial or complete arrest of the cell cycle depending upon the concentration of heparin injected. We further investigated the effect of reducing any [Ca2+]i gradients by microinjecting dibromo- BAPTA into the blastomere. Dibromo-BAPTA injection completely blocked mitotic cell division when a final concentration of 1.5 mM was used. These results suggest that PIP2 turnover as well as second messenger activity influence cell cycle duration during embryonic cell division in frogs.

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Selected References

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  1. Baker P. F., Warner A. E. Intracellular calcium and cell cleavage in early embryos of Xenopus laevis. J Cell Biol. 1972 May;53(2):579–581. doi: 10.1083/jcb.53.2.579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Baltus E., Hanocq-Quertier J., Hanocq F., Brachet J. Injection of an antibody against a p21 c-Ha-ras protein inhibits cleavage in axolotl eggs. Proc Natl Acad Sci U S A. 1988 Jan;85(2):502–506. doi: 10.1073/pnas.85.2.502. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Berridge M. J., Irvine R. F. Inositol phosphates and cell signalling. Nature. 1989 Sep 21;341(6239):197–205. doi: 10.1038/341197a0. [DOI] [PubMed] [Google Scholar]
  4. Broek D., Toda T., Michaeli T., Levin L., Birchmeier C., Zoller M., Powers S., Wigler M. The S. cerevisiae CDC25 gene product regulates the RAS/adenylate cyclase pathway. Cell. 1987 Mar 13;48(5):789–799. doi: 10.1016/0092-8674(87)90076-6. [DOI] [PubMed] [Google Scholar]
  5. Cataldi A., Miscia S., Lisio R., Rana R., Cocco L. Transient shift of diacylglycerol and inositol lipids induced by interferon in Daudi cells. Evidence for a different pattern between nuclei and intact cells. FEBS Lett. 1990 Sep 3;269(2):465–468. doi: 10.1016/0014-5793(90)81216-b. [DOI] [PubMed] [Google Scholar]
  6. Chafouleas J. G., Bolton W. E., Hidaka H., Boyd A. E., 3rd, Means A. R. Calmodulin and the cell cycle: involvement in regulation of cell-cycle progression. Cell. 1982 Jan;28(1):41–50. doi: 10.1016/0092-8674(82)90373-7. [DOI] [PubMed] [Google Scholar]
  7. Chafouleas J. G., Lagacé L., Bolton W. E., Boyd A. E., 3rd, Means A. R. Changes in calmodulin and its mRNA accompany reentry of quiescent (G0) cells into the cell cycle. Cell. 1984 Jan;36(1):73–81. doi: 10.1016/0092-8674(84)90075-8. [DOI] [PubMed] [Google Scholar]
  8. Chilvers E. R., Batty I. H., Challiss R. A., Barnes P. J., Nahorski S. R. Determination of mass changes in phosphatidylinositol 4,5-bisphosphate and evidence for agonist-stimulated metabolism of inositol 1,4,5-trisphosphate in airway smooth muscle. Biochem J. 1991 Apr 15;275(Pt 2):373–379. doi: 10.1042/bj2750373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ciapa B., Whitaker M. Two phases of inositol polyphosphate and diacylglycerol production at fertilisation. FEBS Lett. 1986 Jan 20;195(1-2):347–351. doi: 10.1016/0014-5793(86)80191-0. [DOI] [PubMed] [Google Scholar]
  10. Cocco L., Gilmour R. S., Ognibene A., Letcher A. J., Manzoli F. A., Irvine R. F. Synthesis of polyphosphoinositides in nuclei of Friend cells. Evidence for polyphosphoinositide metabolism inside the nucleus which changes with cell differentiation. Biochem J. 1987 Dec 15;248(3):765–770. doi: 10.1042/bj2480765. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Cocco L., Martelli A. M., Gilmour R. S., Ognibene A., Manzoli F. A., Irvine R. F. Changes in nuclear inositol phospholipids induced in intact cells by insulin-like growth factor I. Biochem Biophys Res Commun. 1989 Mar 15;159(2):720–725. doi: 10.1016/0006-291x(89)90054-5. [DOI] [PubMed] [Google Scholar]
  12. Cocco L., Martelli A. M., Gilmour R. S., Ognibene A., Manzoli F. A., Irvine R. F. Rapid changes in phospholipid metabolism in the nuclei of Swiss 3T3 cells induced by treatment of the cells with insulin-like growth factor I. Biochem Biophys Res Commun. 1988 Aug 15;154(3):1266–1272. doi: 10.1016/0006-291x(88)90276-8. [DOI] [PubMed] [Google Scholar]
  13. Dargie P. J., Agre M. C., Lee H. C. Comparison of Ca2+ mobilizing activities of cyclic ADP-ribose and inositol trisphosphate. Cell Regul. 1990 Feb;1(3):279–290. doi: 10.1091/mbc.1.3.279. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Deshpande A. K., Kung H. F. Insulin induction of Xenopus laevis oocyte maturation is inhibited by monoclonal antibody against p21 ras proteins. Mol Cell Biol. 1987 Mar;7(3):1285–1288. doi: 10.1128/mcb.7.3.1285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Dumont J. N. Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals. J Morphol. 1972 Feb;136(2):153–179. doi: 10.1002/jmor.1051360203. [DOI] [PubMed] [Google Scholar]
  16. Ferguson J. E., Han J. K., Kao J. P., Nuccitelli R. The effects of inositol trisphosphates and inositol tetrakisphosphate on Ca2+ release and Cl- current pattern in the Xenopus laevis oocyte. Exp Cell Res. 1991 Feb;192(2):352–365. doi: 10.1016/0014-4827(91)90052-v. [DOI] [PubMed] [Google Scholar]
  17. Ferris C. D., Huganir R. L., Supattapone S., Snyder S. H. Purified inositol 1,4,5-trisphosphate receptor mediates calcium flux in reconstituted lipid vesicles. Nature. 1989 Nov 2;342(6245):87–89. doi: 10.1038/342087a0. [DOI] [PubMed] [Google Scholar]
  18. Fluck R. A., Miller A. L., Jaffe L. F. Slow calcium waves accompany cytokinesis in medaka fish eggs. J Cell Biol. 1991 Dec;115(5):1259–1265. doi: 10.1083/jcb.115.5.1259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Forer A., Sillers P. J. The role of the phosphatidylinositol cycle in mitosis in sea urchin zygotes. Lithium inhibition is overcome by myo-inositol but not by other cyclitols or sugars. Exp Cell Res. 1987 May;170(1):42–55. doi: 10.1016/0014-4827(87)90115-7. [DOI] [PubMed] [Google Scholar]
  20. Fukami K., Matsuoka K., Nakanishi O., Yamakawa A., Kawai S., Takenawa T. Antibody to phosphatidylinositol 4,5-bisphosphate inhibits oncogene-induced mitogenesis. Proc Natl Acad Sci U S A. 1988 Dec;85(23):9057–9061. doi: 10.1073/pnas.85.23.9057. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Fukami K., Takenawa T. Quantitative changes in polyphosphoinositides 1,2-diacylglycerol and inositol 1,4,5-trisphosphate by platelet-derived growth factor and prostaglandin F2 alpha. J Biol Chem. 1989 Sep 5;264(25):14985–14989. [PubMed] [Google Scholar]
  22. Ghosh T. K., Eis P. S., Mullaney J. M., Ebert C. L., Gill D. L. Competitive, reversible, and potent antagonism of inositol 1,4,5-trisphosphate-activated calcium release by heparin. J Biol Chem. 1988 Aug 15;263(23):11075–11079. [PubMed] [Google Scholar]
  23. Gibbs J. B., Sigal I. S., Poe M., Scolnick E. M. Intrinsic GTPase activity distinguishes normal and oncogenic ras p21 molecules. Proc Natl Acad Sci U S A. 1984 Sep;81(18):5704–5708. doi: 10.1073/pnas.81.18.5704. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Grandin N., Charbonneau M. Intracellular free calcium oscillates during cell division of Xenopus embryos. J Cell Biol. 1991 Feb;112(4):711–718. doi: 10.1083/jcb.112.4.711. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. HIRAMOTO Y. Microinjection of the live spermatozoa into sea urchin eggs. Exp Cell Res. 1962 Sep;27:416–426. doi: 10.1016/0014-4827(62)90006-x. [DOI] [PubMed] [Google Scholar]
  26. Han J. K., Nuccitelli R. Inositol 1,4,5-trisphosphate-induced calcium release in the organelle layers of the stratified, intact egg of Xenopus laevis. J Cell Biol. 1990 Apr;110(4):1103–1110. doi: 10.1083/jcb.110.4.1103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Hepler P. K. Calcium restriction prolongs metaphase in dividing Tradescantia stamen hair cells. J Cell Biol. 1985 May;100(5):1363–1368. doi: 10.1083/jcb.100.5.1363. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Hepler P. K. Calcium transients during mitosis: observations in flux. J Cell Biol. 1989 Dec;109(6 Pt 1):2567–2573. doi: 10.1083/jcb.109.6.2567. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Hill T. D., Berggren P. O., Boynton A. L. Heparin inhibits inositol trisphosphate-induced calcium release from permeabilized rat liver cells. Biochem Biophys Res Commun. 1987 Dec 31;149(3):897–901. doi: 10.1016/0006-291x(87)90492-x. [DOI] [PubMed] [Google Scholar]
  30. Hirono C., Ito I., Sugiyama H. Neurotensin and acetylcholine evoke common responses in frog oocytes injected with rat brain messenger ribonucleic acid. J Physiol. 1987 Jan;382:523–535. doi: 10.1113/jphysiol.1987.sp016382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Huang C. L., Takenawa T., Ives H. E. Platelet-derived growth factor-mediated Ca2+ entry is blocked by antibodies to phosphatidylinositol 4,5-bisphosphate but does not involve heparin-sensitive inositol 1,4,5-trisphosphate receptors. J Biol Chem. 1991 Mar 5;266(7):4045–4048. [PubMed] [Google Scholar]
  32. Hughes D. A., Fukui Y., Yamamoto M. Homologous activators of ras in fission and budding yeast. Nature. 1990 Mar 22;344(6264):355–357. doi: 10.1038/344355a0. [DOI] [PubMed] [Google Scholar]
  33. Izant J. G. The role of calcium ions during mitosis. Calcium participates in the anaphase trigger. Chromosoma. 1983;88(1):1–10. doi: 10.1007/BF00329497. [DOI] [PubMed] [Google Scholar]
  34. Kao J. P., Alderton J. M., Tsien R. Y., Steinhardt R. A. Active involvement of Ca2+ in mitotic progression of Swiss 3T3 fibroblasts. J Cell Biol. 1990 Jul;111(1):183–196. doi: 10.1083/jcb.111.1.183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Keith C. H., Maxfield F. R., Shelanski M. L. Intracellular free calcium levels are reduced in mitotic Pt K2 epithelial cells. Proc Natl Acad Sci U S A. 1985 Feb;82(3):800–804. doi: 10.1073/pnas.82.3.800. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Keith C. H., Ratan R., Maxfield F. R., Bajer A., Shelanski M. L. Local cytoplasmic calcium gradients in living mitotic cells. 1985 Aug 29-Sep 4Nature. 316(6031):848–850. doi: 10.1038/316848a0. [DOI] [PubMed] [Google Scholar]
  37. Kiehart D. P. Studies on the in vivo sensitivity of spindle microtubules to calcium ions and evidence for a vesicular calcium-sequestering system. J Cell Biol. 1981 Mar;88(3):604–617. doi: 10.1083/jcb.88.3.604. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Kline D., Kopf G. S., Muncy L. F., Jaffe L. A. Evidence for the involvement of a pertussis toxin-insensitive G-protein in egg activation of the frog, Xenopus laevis. Dev Biol. 1991 Feb;143(2):218–229. doi: 10.1016/0012-1606(91)90072-b. [DOI] [PubMed] [Google Scholar]
  39. Lacal J. C., Srivastava S. K., Anderson P. S., Aaronson S. A. Ras p21 proteins with high or low GTPase activity can efficiently transform NIH/3T3 cells. Cell. 1986 Feb 28;44(4):609–617. doi: 10.1016/0092-8674(86)90270-9. [DOI] [PubMed] [Google Scholar]
  40. Lacal J. C., de la Peña P., Moscat J., Garcia-Barreno P., Anderson P. S., Aaronson S. A. Rapid stimulation of diacylglycerol production in Xenopus oocytes by microinjection of H-ras p21. Science. 1987 Oct 23;238(4826):533–536. doi: 10.1126/science.2821623. [DOI] [PubMed] [Google Scholar]
  41. Levin D. E., Fields F. O., Kunisawa R., Bishop J. M., Thorner J. A candidate protein kinase C gene, PKC1, is required for the S. cerevisiae cell cycle. Cell. 1990 Jul 27;62(2):213–224. doi: 10.1016/0092-8674(90)90360-q. [DOI] [PubMed] [Google Scholar]
  42. Matuoka K., Fukami K., Nakanishi O., Kawai S., Takenawa T. Mitogenesis in response to PDGF and bombesin abolished by microinjection of antibody to PIP2. Science. 1988 Feb 5;239(4840):640–643. doi: 10.1126/science.2829356. [DOI] [PubMed] [Google Scholar]
  43. Miron M. J., Lanoix J., Paiement J. Cytological effects of the microinjection of antibody to ras p21 in early cleavage Xenopus embryos. Mol Reprod Dev. 1990 Apr;25(4):317–327. doi: 10.1002/mrd.1080250403. [DOI] [PubMed] [Google Scholar]
  44. Murray A. W., Kirschner M. W. Dominoes and clocks: the union of two views of the cell cycle. Science. 1989 Nov 3;246(4930):614–621. doi: 10.1126/science.2683077. [DOI] [PubMed] [Google Scholar]
  45. Newmark P. Events at the surface of the cell. Nature. 1985 Oct 3;317(6036):380–380. doi: 10.1038/317380a0. [DOI] [PubMed] [Google Scholar]
  46. Nishihara M., Keenan R. W. Inositol phospholipid levels of rat forebrain obtained by freeze-blowing method. Biochim Biophys Acta. 1985 Jul 9;835(2):415–418. doi: 10.1016/0005-2760(85)90300-5. [DOI] [PubMed] [Google Scholar]
  47. Oron Y., Dascal N., Nadler E., Lupu M. Inositol 1,4,5-trisphosphate mimics muscarinic response in Xenopus oocytes. Nature. 1985 Jan 10;313(5998):141–143. doi: 10.1038/313141a0. [DOI] [PubMed] [Google Scholar]
  48. Picard A., Cavadore J. C., Lory P., Bernengo J. C., Ojeda C., Dorée M. Microinjection of a conserved peptide sequence of p34cdc2 induces a Ca2+ transient in oocytes. Science. 1990 Jan 19;247(4940):327–329. doi: 10.1126/science.2153316. [DOI] [PubMed] [Google Scholar]
  49. Poenie M., Alderton J., Steinhardt R., Tsien R. Calcium rises abruptly and briefly throughout the cell at the onset of anaphase. Science. 1986 Aug 22;233(4766):886–889. doi: 10.1126/science.3755550. [DOI] [PubMed] [Google Scholar]
  50. Poenie M., Alderton J., Tsien R. Y., Steinhardt R. A. Changes of free calcium levels with stages of the cell division cycle. Nature. 1985 May 9;315(6015):147–149. doi: 10.1038/315147a0. [DOI] [PubMed] [Google Scholar]
  51. Rakow T. L., Shen S. S. Multiple stores of calcium are released in the sea urchin egg during fertilization. Proc Natl Acad Sci U S A. 1990 Dec;87(23):9285–9289. doi: 10.1073/pnas.87.23.9285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Ratan R. R., Shelanski M. L., Maxfield F. R. Transition from metaphase to anaphase is accompanied by local changes in cytoplasmic free calcium in Pt K2 kidney epithelial cells. Proc Natl Acad Sci U S A. 1986 Jul;83(14):5136–5140. doi: 10.1073/pnas.83.14.5136. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Rink T. J., Tsien R. Y., Warner A. E. Free calcium in Xenopus embryos measured with ion-selective microelectrodes. Nature. 1980 Feb 14;283(5748):658–660. doi: 10.1038/283658a0. [DOI] [PubMed] [Google Scholar]
  54. Robinson L. C., Gibbs J. B., Marshall M. S., Sigal I. S., Tatchell K. CDC25: a component of the RAS-adenylate cyclase pathway in Saccharomyces cerevisiae. Science. 1987 Mar 6;235(4793):1218–1221. doi: 10.1126/science.3547648. [DOI] [PubMed] [Google Scholar]
  55. Shih T. Y., Papageorge A. G., Stokes P. E., Weeks M. O., Scolnick E. M. Guanine nucleotide-binding and autophosphorylating activities associated with the p21src protein of Harvey murine sarcoma virus. Nature. 1980 Oct 23;287(5784):686–691. doi: 10.1038/287686a0. [DOI] [PubMed] [Google Scholar]
  56. Silver R. B. Nuclear envelope breakdown and mitosis in sand dollar embryos is inhibited by microinjection of calcium buffers in a calcium-reversible fashion, and by antagonists of intracellular Ca2+ channels. Dev Biol. 1989 Jan;131(1):11–26. doi: 10.1016/s0012-1606(89)80034-x. [DOI] [PubMed] [Google Scholar]
  57. Speksnijder J. E., Miller A. L., Weisenseel M. H., Chen T. H., Jaffe L. F. Calcium buffer injections block fucoid egg development by facilitating calcium diffusion. Proc Natl Acad Sci U S A. 1989 Sep;86(17):6607–6611. doi: 10.1073/pnas.86.17.6607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Steinhardt R. A., Alderton J. Intracellular free calcium rise triggers nuclear envelope breakdown in the sea urchin embryo. Nature. 1988 Mar 24;332(6162):364–366. doi: 10.1038/332364a0. [DOI] [PubMed] [Google Scholar]
  59. Tsien R. Y. New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures. Biochemistry. 1980 May 27;19(11):2396–2404. doi: 10.1021/bi00552a018. [DOI] [PubMed] [Google Scholar]
  60. Twigg J., Patel R., Whitaker M. Translational control of InsP3-induced chromatin condensation during the early cell cycles of sea urchin embryos. Nature. 1988 Mar 24;332(6162):366–369. doi: 10.1038/332366a0. [DOI] [PubMed] [Google Scholar]
  61. Uno I., Fukami K., Kato H., Takenawa T., Ishikawa T. Essential role for phosphatidylinositol 4,5-bisphosphate in yeast cell proliferation. Nature. 1988 May 12;333(6169):188–190. doi: 10.1038/333188a0. [DOI] [PubMed] [Google Scholar]
  62. Wasserman W. J., Freedman A. B., LaBella J. J. sn-1,2-diacylglycerol levels increase in progesterone-stimulated Xenopus laevis oocytes. J Exp Zool. 1990 Jul;255(1):63–71. doi: 10.1002/jez.1402550109. [DOI] [PubMed] [Google Scholar]
  63. Whitaker M., Patel R. Calcium and cell cycle control. Development. 1990 Apr;108(4):525–542. doi: 10.1242/dev.108.4.525. [DOI] [PubMed] [Google Scholar]
  64. Worley P. F., Baraban J. M., Supattapone S., Wilson V. S., Snyder S. H. Characterization of inositol trisphosphate receptor binding in brain. Regulation by pH and calcium. J Biol Chem. 1987 Sep 5;262(25):12132–12136. [PubMed] [Google Scholar]
  65. Zhang D. H., Callaham D. A., Hepler P. K. Regulation of anaphase chromosome motion in Tradescantia stamen hair cells by calcium and related signaling agents. J Cell Biol. 1990 Jul;111(1):171–182. doi: 10.1083/jcb.111.1.171. [DOI] [PMC free article] [PubMed] [Google Scholar]

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