Abstract
Intracellular bound Ca++ has been localized throughout mitosis and cytokinesis in two plant species by means of in situ precipitation with potassium antimonate and electron microscope visualization. Identification of Ca++ as the major cation precipitated was made by comparing solubility properties in water, EDTA, and EGTA of the intracellular deposits with respect to those of K+-, Mg++-, and Ca++- antimonate standards. In spermatogenous cells of the water fern, Marsilea vestita, and stomatal complex cells of barley, Hordeum vulgare, antimonate deposits have been found associated with the endoplasmic reticulum (ER), vacuoles, euchromatin/nucleoplasm, and mitochondria. The last contain a much higher density of precipitates in Marsilea than in Hordeum. Dictyosomes and the nuclear envelope of Marsilea also contain antimonate deposits, as do the plasmalemma, cell wall, and phragmoplast vesicles of Hordeum. Microtubule-organizing centers such as kinetochores and the blepharoplast of Marsilea do not stain. In spite of differences in associated antimonate between certain organelles of the two species, the presence of antimonate aong the ER throughout the cell cycle is common to both. Of particular interest are those precipitates seen along the tubules and cisternae of the extensive smooth ER that surrounds and invades the mitotic spindle in both species. The ability to bind divalent cations makes the mitotic apparatus (MA)-associated ER a likely candidate for regulation of free Ca++ levels in the immediate vicinity of structural components and processes that are Ca++-sensitive and proposed to be Ca++-regulated.
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- 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]
- Blaustein M. P., Ratzlaff R. W., Schweitzer E. S. Calcium buffering in presynaptic nerve terminals. II. Kinetic properties of the nonmitochondrial Ca sequestration mechanism. J Gen Physiol. 1978 Jul;72(1):43–66. doi: 10.1085/jgp.72.1.43. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Borle A. B. Calcium metabolism at the cellular level. Fed Proc. 1973 Sep;32(9):1944–1950. [PubMed] [Google Scholar]
- Brinley F. J., Jr, Tiffert T., Scarpa A. Mitochondria and other calcium buffers of squid axon studied in situ. J Gen Physiol. 1978 Jul;72(1):101–127. doi: 10.1085/jgp.72.1.101. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bruns D. E., McDonald J. M., Jarett L. Energy-dependent calcium transport in endoplasmic reticulum of adipocytes. J Biol Chem. 1976 Nov 25;251(22):7191–7197. [PubMed] [Google Scholar]
- Cramer E. B., Gallin J. I. Localization of submembranous cations to the leading end of human neutrophils during chemotaxis. J Cell Biol. 1979 Aug;82(2):369–379. doi: 10.1083/jcb.82.2.369. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dorée M., Moreau M., Guerrier P. Hormonal control of meiosis. In vitro induced release of calcium ions from the plasma membrane in starfish oocytes. Exp Cell Res. 1978 Sep;115(2):251–260. doi: 10.1016/0014-4827(78)90279-3. [DOI] [PubMed] [Google Scholar]
- Farber J. L., El-Mofty S. K., Schanne F. A., Aleo J. J., Jr, Serroni A. Intracellular calcium homeostasis in galactosamine-intoxicated rat liver cells. Active sequestration of calcium by microsomes and mitochondria. Arch Biochem Biophys. 1977 Jan 30;178(2):617–624. doi: 10.1016/0003-9861(77)90233-8. [DOI] [PubMed] [Google Scholar]
- Fulton B. P., Whittingham D. G. Activation of mammalian oocytes by intracellular injection of calcium. Nature. 1978 May 11;273(5658):149–151. doi: 10.1038/273149a0. [DOI] [PubMed] [Google Scholar]
- Harris P. The role of membranes in the ogranization of the mitotic apparatus. Exp Cell Res. 1975 Sep;94(2):409–425. doi: 10.1016/0014-4827(75)90507-8. [DOI] [PubMed] [Google Scholar]
- Hepler P. K. Membranes in the mitotic apparatus of barley cells. J Cell Biol. 1980 Aug;86(2):490–499. doi: 10.1083/jcb.86.2.490. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hepler P. K. The blepharoplast of Marsilea: its de novo formation and spindle association. J Cell Sci. 1976 Jul;21(2):361–390. doi: 10.1242/jcs.21.2.361. [DOI] [PubMed] [Google Scholar]
- Hoffstein S. T. Ultrastructural demonstration of calcium loss from local regions of the plasma membrane of surface-stimulated human granulocytes. J Immunol. 1979 Sep;123(3):1395–1402. [PubMed] [Google Scholar]
- Lehninger A. L., Reynafarje B., Vercesi A., Tew W. P. Transport and accumulation of calcium in mitochondria. Ann N Y Acad Sci. 1978 Apr 28;307:160–176. doi: 10.1111/j.1749-6632.1978.tb41941.x. [DOI] [PubMed] [Google Scholar]
- Loewenstein W. R., Rose B. Calcium in (junctional) intercellular communication and a thought on its behavior in intracellular communication. Ann N Y Acad Sci. 1978 Apr 28;307:285–307. doi: 10.1111/j.1749-6632.1978.tb41958.x. [DOI] [PubMed] [Google Scholar]
- Mazia D., Petzelt C., Williams R. O., Meza I. A Ca-activated ATPase in the mitotic apparatus of the sea urchin egg (isolated by a new method). Exp Cell Res. 1972 Feb;70(2):325–332. doi: 10.1016/0014-4827(72)90143-7. [DOI] [PubMed] [Google Scholar]
- Moore L., Pastan I. Energy-dependent calcium uptake by fibroblast microsomes. Ann N Y Acad Sci. 1978 Apr 28;307:177–194. doi: 10.1111/j.1749-6632.1978.tb41942.x. [DOI] [PubMed] [Google Scholar]
- Moreau M., Guerrier P., Doree M., Ashley C. C. Hormone-induced release of intracellular Ca2+ triggers meiosis in starfish oocytes. Nature. 1978 Mar 16;272(5650):251–253. doi: 10.1038/272251a0. [DOI] [PubMed] [Google Scholar]
- Petzelt C., Auel D. Synthesis and activation of mitotic Ca2+-adenosinetriphosphatase during the cell cycle of mouse mastocytoma cells. Proc Natl Acad Sci U S A. 1977 Apr;74(4):1610–1613. doi: 10.1073/pnas.74.4.1610. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Requena J., DiPolo R., Brinley F. J., Jr, Mullins L. J. The control of ionized calcium in squid axons. J Gen Physiol. 1977 Sep;70(3):329–353. doi: 10.1085/jgp.70.3.329. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rose B., Loewenstein W. R. Calcium ion distribution in cytoplasm visualised by aequorin: diffusion in cytosol restricted by energized sequestering. Science. 1975 Dec 19;190(4220):1204–1206. doi: 10.1126/science.1198106. [DOI] [PubMed] [Google Scholar]
- Saetersdal T. S., Myklebust R., Berg Justesen N. P. Ultrastructural localization of calcium in the pigeon papillary muscle as demonstrated by cytochemical studies and x-ray microanalysis. Cell Tissue Res. 1974;155(1):57–74. doi: 10.1007/BF00220284. [DOI] [PubMed] [Google Scholar]
- Simson J. A., Spicer S. S. Selective subcellular localization of cations with variants of the potassium (pyro)antimonate technique. J Histochem Cytochem. 1975 Aug;23(8):575–598. doi: 10.1177/23.8.51037. [DOI] [PubMed] [Google Scholar]
- Siracusa G., Whittingham D. G., Codonesu M., De Felici M. Local anesthetics and phenothiazine tranquilizers induce parthenogenetic activation of the mouse oocyte. Dev Biol. 1978 Aug;65(2):531–535. doi: 10.1016/0012-1606(78)90048-9. [DOI] [PubMed] [Google Scholar]
- Somlyo A. P., Somlyo A. V., Shuman H., Sloane B., Scarpa A. Electron probe analysis of calcium compartments in cryo sections of smooth and striated muscles. Ann N Y Acad Sci. 1978 Apr 28;307:523–544. doi: 10.1111/j.1749-6632.1978.tb41980.x. [DOI] [PubMed] [Google Scholar]
- Stoeckel M. E., Hindelang-Gertner C., Dellmann H-D, Porte A., Stutinsky F. Subcellular localization of calcium in the mouse hypophysis. I. Calcium distribution in the adeno- and neurohypophysis under normal conditions. Cell Tissue Res. 1975;157(3):307–322. doi: 10.1007/BF00225522. [DOI] [PubMed] [Google Scholar]
- Weakley B. S. A variant of the pyroantimonate technique suitable for localization of calcium in ovarian tissue. J Histochem Cytochem. 1979 Jun;27(6):1017–1028. doi: 10.1177/27.6.88471. [DOI] [PubMed] [Google Scholar]
- Wooding F. B., Morgan G. Calcium localization in lactating rabbit mammary secretory cells. J Ultrastruct Res. 1978 Jun;63(3):323–333. doi: 10.1016/s0022-5320(78)80056-2. [DOI] [PubMed] [Google Scholar]