Lithium blocks cell cycle transitions in the first cell cycles of sea urchin embryos, an effect rescued by myo-inositol

Development

Volumn 124, Issue 6, 1997, Pages 1099-1107

  Becchetti, Andrea ^a   Whitaker, Michael ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

Cell cycle; Lithium; Mitosis; myo inositol; Phosphoinositides; Sea urchin

Indexed keywords

INOSITOL; INOSITOL 1,4,5 TRISPHOSPHATE; LITHIUM; LITHIUM CHLORIDE; SEA WATER;

ANIMAL EXPERIMENT; ARTICLE; BLASTULA; CELL CYCLE; CELL DIVISION; CELL NUCLEUS MEMBRANE; CYTOKINESIS; EMBRYO; EMBRYO DEVELOPMENT; FERTILIZATION; MICROINJECTION; MITOSIS; NONHUMAN; PHOTOLYSIS; PRIORITY JOURNAL; SEA URCHIN;

ANIMALS; CELL CYCLE; EMBRYO, NONMAMMALIAN; FEMALE; FERTILIZATION; G2 PHASE; INOSITOL; INOSITOL 1,4,5-TRISPHOSPHATE; LITHIUM CHLORIDE; MALE; METAPHASE; MICROINJECTIONS; MITOSIS; NUCLEAR ENVELOPE; PHOSPHATIDYLINOSITOLS; SEA URCHINS; SECOND MESSENGER SYSTEMS; STEREOISOMERISM; TERATOGENS;

ANIMALIA; ECHINOIDEA; LYTECHINUS PICTUS;

EID: 0030894569     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (45)

1. Arndt-Jovin, D. J. and Jovin, T. M. (1989). Fluorescent labeling and microscopy of DNA. In Methods in Cell Biology (ed. D. Lansing Taylor and Y.-L. Wang), Vol. 30, pp. 417-448. San Diego, California, USA: Academic Press Inc.
2. Atack, J. R., Cook, S. M., Watt, A. P., Fletcher, S. R. and Ian Ragan, C. (1993). In vitro and in vivo inhibition of inositol monophosphatase by the bisphosphonate L-690,330. J. Neurochem. 60, 652-658.
3. + in the treatment of bipolar disorder. Trends Neurosci. 18, 343-349.
4. Balla, T., Enyedi, P., Hunyady, L. and Spat, A. (1984). Effects of lithium on angiotensin-stimulated phosphatidylinositol turnover and aldosterone production in adrenal glomerulosa cells: a possible causal relationship. FEBS Letts. 171, 179-182.
5. Berridge, M. J. and Fain, J. N. (1979). Inhibition of phosphatidylinositol synthesis and the inactivation of calcium entry after prolonged exposure of the blowfly salivary gland to 5-hydroxytryptamine. Biochem J. 178, 59-69.
6. Berridge, M. J., Downes, C. P. and Hanley, M. R. (1982). Lithium amplifies agonist-dependent phosphatidylinositol responses in brain and salivary glands. Biochem. J. 206, 587-595.
7. Berridge, M. J., Downes, C. P. and Hanley, M. R. (1989). Neural and developmental actions of lithium: a unifying hypothesis. Cell 59, 411-419.
8. Berridge, M. J. and Irvine, R. F. (1989). Inositol phosphates and cell signalling. Nature 341, 197-205.
9. Browne, C. I., Miller, A. L., Palazzo, R. E. and Jaffe, L. F. (1992). On the calcium pulse duringnuclear envelope breakdown (NEB) in sea urchin eggs. Biol. Bull. Mar. Biol. Lab., Woods Hole 177, 370-371.
10. Busa, W. B. (1988). Role for the phosphatidylinositol cycle in early development. Phil. Trans. Roy. Soc. (Land.) B 320, 415-426.
11. Busa, W. B. and Gimlich, R. L. (1989). Lithium-induced teratogenesis in frog embryos prevented by a phosphoinositide cycle intermediate or a diacylglycerol analog. Dev. Biol. 132, 315-324.
12. Chambers, E. L. (1976). Na is essential for activation of the inseminated sea urchin egg. J. Exp. Zool. 197, 149-154.
13. Ciapa, B., Borg, B. and Whitaker, M. (1992). Polyphosphoinositide metabolism during the fertilization wave in sea urchin eggs. Development 115, 187-195.
14. Ciapa, B. and Maggio, K. (1993). Effect of lithium on ionic balance and polyphosphoinositide metabolism during larval vegetalization of the sea urchin Paracentrotus lividus. Dev. Biol. 159, 114-121.
15. Ciapa, B., Pesando, D., Wilding, M. and Whitaker, M. (1994). Cell-cycle calcium transients driven by cyclic changes in inositol trisphosphate levels. Nature 368, 875-878.
16. Downes, C. P. and Stone, M. A. (1986). Lithium-induced reduction in intracellular inositol supply in cholinergically stimulated parotid gland. Biochem. J. 234, 199-204.
17. Ehrlich, B. E. and Diamond, J. (1980). Lithium, membranes, and manicdepressive illness. J. Membr. Biol. 52, 187-200.
18. Forer, A. and Sillers, P. (1987). The role of phosphatidylinositol cycle in mitosis in sea urchin zygotes. Exp. Cell Res. 170,42-55.
19. Galione, A., McDougall, A., Busa, W. B., Willmott, N. and Whitaker, M. J. (1993). Redundant mechanisms of calcium-induced calcium release underlie calcium waves during fertilization. Science 261, 348-352.
20. Godfrey, P. P. (1989). Potentiation by lithium of CMP-phosphatidate formation in carbachol-stimulated rat cerebral-cortical slices and its reversal by myoinositol. Biochem. J. 258, 621-624.
21. 2+ gradients lengthens the duration of the cell cycle in Xenopus laevis blastomeres. J. Cell Biol. 116. 147-156.
22. Hepler, P. H. (1992). Calcium and mitosis. Int. Rev. Cytol. 138, 239-268.
23. Hepler, P. H. (1994). The role of calcium in cell division. Cell Calcium 16, 322-330.
24. Herbst, C. (1892). Experimentelle Untersuchungen Uber den Einfluss der veranderten chemischen Zusammensetzung des Umgebenden Mediums auf die Entwicklung der Thiere. Z. Wins. Zool. 55, 446-578.
25. 2+ entry is blocked by antibodies to phosphatidylinositol 4.5-bisphosphate but not involve heparin-sensitive inositol 1,4,5-trisphosphate receptors. J. Biol. Chem. 266, 4045-4048.
26. + on preimplantation mouse embryos. J. Embryal. Exp. Morph. 67, 51 -58.
27. 2+ in mitotic progression of Swiss 3T3 fibroblasts. J. Cell Biol. 111, 183-196.
28. Kao, K. R., Masui, Y. and Elinson, P. (1986). Lithium-induced respecification of pattern in Xenopus laevis embryos. Nature 322, 371-373.
29. Livingston, B. T. and Wilt, F. H. (1989). Lithium evokes expression of vegetal-specific molecules in the animal blastomeres of sea urchin embryos. Proc. Nut. Acad. Sci. USA 86, 3669-3673.
30. Livingston, B. T. and Wilt, F. H. (1990). Determination of cell fate in sea urchin embryos. BioEssays 12, 115-119.
31. Markram, H. and Segal, M. (1992). The inositol 1,4,5-trisphosphate pathway mediates cholinergic potentiation of rat hippocampal neuronal responses to NMDA. J. Physiol. 447, 513-533.
32. Mazia, D., Petzelt, C., Williams, R. O. and Meza, I. (1972). A Ca-activated ATP-ase in the mitotic apparatus of the sea urchin egg (isolated by a new method). Exp. Cell Res. 70, 325-332.
33. 2. Science 239, 640-643.
34. Poenie, M., Alderton, J., Tsien, R. Y. and Steinhardt, R. A. (1985). Changes in free calcium with stages of the cell division cycle. Nature 315, 147-149.
35. Stachel, S. E., Grunwald, D. J. and Myers, P. Z. (1993). Lithium perturbation and goosecoid expression identify a dorsal specification pathway in the pregastrula zebrafish. Development 117, 1261-1274.
36. Stith, B. J., Goalstone, M., Silva, S. and Jaynes, C. (1993). Inositol 1.4,5-trisphosphate mass changes from fertilization through first cleavage in Xenopus laevis. Mol. Biol. Celll 4, 435-443.
37. Twigg, J., Patel, R. and Whitaker, M. (1988). Translational control of InsP3-induced chromatin condensation during the early cell cycles of sea urchin embryos. Nature 332, 366-369.
38. Uno, I., Fukami, K., Kato, H., Takenawa T. and Ishikawa, T. (1988). Essential role for phosphatidylinositol 4,5-bisphosphate in yeast cell proliferation. Nature 333, 188-190.
39. Whitaker, M. J. and Irvine, R. F. (1984). Inositol 1,4,5-trisphosphate microinjection activates sea urchin eggs. Nature 312, 636-639.
40. Whitaker M. and Patel, R. (1990). Calcium and cell cycle control. Development 108, 525-542.
41. Whitaker, M. J. and Swann, K. (1993). Lighting the fuse at fertilization. Development 117, 1-12.
42. Whitaker, M. (1995). Regulation of the cell division cycle by inositol trisphosphate and the calcium signaling pathway. In Advances in Second Messenger and Phosphoprotein Research Vol. 30. (ed. A. Means). New York: Raven Press Ltd.
43. Wilding, M., Wright, E.M., Patel, R., Ellis-Davis, G. and Whitaker, M. (1996). Local perinuclear calcium signals associated with mitosis-ENTRY in early sea urchin embryos. J. Cell Biol.
44. Wolniak, S. M. (1987). Lithium alters mitotic progression in stamen hair cells of Tradescantia in a time-dependent and reversible fashion. Eur. J. Cell Biol. 44, 286-293.
45. Wolniak, S. M. (1988). The regulation of mitotic spindle function. Biochem. Cell Biol. 66,490-514.