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. 1980 Aug 1;86(2):490–499. doi: 10.1083/jcb.86.2.490

Membranes in the miotic apparatus of barley cells

PK Hepler
PMCID: PMC2111505  PMID: 7400216

Abstract

Membranes in the mitotic apparatus have been investigated ultrastructually in dividing cells of barley (Hordeum vulgare). After osmium tetroxide- potassium ferricyanide or ferrocyanide postfixation (OsFeCN) of material that had been fixed in glutaraldehyde in the presence of Ca(++), the nuclear envolope (NE)-endoplasmic reticulum (ER) complex is selectively stained, permitting observations on the cellular pattern and structural ramifications of this membrane system that have not been previously recognized. Specifically, it is observed that membrane system that have not been previously recognized. Specifically, it is observed that during mitosis the NE-ER forms a continuous membrane system that ensheathes and isolates the mitotic apparatus (MA). Elements of ER progressively accumulate in the region of the spindle pole, becoming most concentrated by early anaphase. Within the MA itself, there are striking spindle- membrane associations; in particular, tubular elements of predominantly smooth NE-ER invade the spindle interior selectively along kinetochore microtubules. The membrane elements at the pole and surrounding the MA consist of tubular reticulum and fenestrated lamellae. Membranes of the MA thus resemble in considerable detail the tubular network and fenestrated elements of the sarcoplasmic reticulum of muscle. It is suggested that the NE-ER of the dividing barley cell may function in one or both of the following ways: (a) to control the concentration of free Ca(++) in the MA and (b) to serve as an anchor to chromosome motion.

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Selected References

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  1. Brinkley B. R., Cartwright J., Jr Cold-labile and cold-stable microtubules in the mitotic spindle of mammalian cells. Ann N Y Acad Sci. 1975 Jun 30;253:428–439. doi: 10.1111/j.1749-6632.1975.tb19218.x. [DOI] [PubMed] [Google Scholar]
  2. Brinkley B. R., Stubblefield E., Hsu T. C. The effects of colcemid inhibition and reversal on the fine structure of the mitotic apparatus of Chinese hamster cells in vitro. J Ultrastruct Res. 1967 Jul;19(1):1–18. doi: 10.1016/s0022-5320(67)80057-1. [DOI] [PubMed] [Google Scholar]
  3. Clarke M., Spudich J. A. Nonmuscle contractile proteins: the role of actin and myosin in cell motility and shape determination. Annu Rev Biochem. 1977;46:797–822. doi: 10.1146/annurev.bi.46.070177.004053. [DOI] [PubMed] [Google Scholar]
  4. Endo M. Calcium release from the sarcoplasmic reticulum. Physiol Rev. 1977 Jan;57(1):71–108. doi: 10.1152/physrev.1977.57.1.71. [DOI] [PubMed] [Google Scholar]
  5. Forbes M. S., Plantholt B. A., Sperelakis N. Cytochemical staining procedures selective for sarcotubular systems of muscle: modifications and applications. J Ultrastruct Res. 1977 Sep;60(3):306–327. doi: 10.1016/s0022-5320(77)80016-6. [DOI] [PubMed] [Google Scholar]
  6. Goldstein M. A., Entman M. L. Microtubules in mammalian heart muscle. J Cell Biol. 1979 Jan;80(1):183–195. doi: 10.1083/jcb.80.1.183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. 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]
  8. Hepler P. K., McIntosh J. R., Cleland S. Intermicrotubule bridges in mitotic spindle apparatus. J Cell Biol. 1970 May;45(2):438–444. doi: 10.1083/jcb.45.2.438. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. 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]
  10. 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]
  11. PORTER K. R., MACHADO R. D. Studies on the endoplasmic reticulum. IV. Its form and distribution during mitosis in cells of onion root tip. J Biophys Biochem Cytol. 1960 Feb;7:167–180. doi: 10.1083/jcb.7.1.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Peachey L. D. The sarcoplasmic reticulum and transverse tubules of the frog's sartorius. J Cell Biol. 1965 Jun;25(3 Suppl):209–231. doi: 10.1083/jcb.25.3.209. [DOI] [PubMed] [Google Scholar]
  13. Petzelt C. Ca 2+ -activated APTase during the cell cycle of the sea urchin Strongylocentrotus purpuratus. Exp Cell Res. 1972 Feb;70(2):333–339. doi: 10.1016/0014-4827(72)90144-9. [DOI] [PubMed] [Google Scholar]
  14. Petzelt C. Further evidence that a Ca 2+ -activated ATPase is connected with the cell cycle. Exp Cell Res. 1972 Sep;74(1):156–162. doi: 10.1016/0014-4827(72)90491-0. [DOI] [PubMed] [Google Scholar]
  15. Petzelt C., von Ledebur-Villiger M. Ca2+-stimulated ATPase during the early development of parthenogenetically activated eggs of the sea urchin Paracentrotus lividus. Exp Cell Res. 1973 Sep;81(1):87–94. doi: 10.1016/0014-4827(73)90114-6. [DOI] [PubMed] [Google Scholar]
  16. Silver R. B., Cole R. D., Cande W. Z. Isolation of mitotic apparatus containing vesicles with calcium sequestration activity. Cell. 1980 Feb;19(2):505–516. doi: 10.1016/0092-8674(80)90525-5. [DOI] [PubMed] [Google Scholar]
  17. Weisenberg R. C. Microtubule formation in vitro in solutions containing low calcium concentrations. Science. 1972 Sep 22;177(4054):1104–1105. doi: 10.1126/science.177.4054.1104. [DOI] [PubMed] [Google Scholar]
  18. Welsh M. J., Dedman J. R., Brinkley B. R., Means A. R. Tubulin and calmodulin. Effects of microtubule and microfilament inhibitors on localization in the mitotic apparatus. J Cell Biol. 1979 Jun;81(3):624–634. doi: 10.1083/jcb.81.3.624. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. White D. L., Mazurkiewicz J. E., Barrnett R. J. A chemical mechanism for tissue staining by osmium tetroxide-ferrocyanide mixtures. J Histochem Cytochem. 1979 Jul;27(7):1084–1091. doi: 10.1177/27.7.89155. [DOI] [PubMed] [Google Scholar]
  20. Wick S. M., Hepler P. K. Localization of Ca++-containing antimonate precipitates during mitosis. J Cell Biol. 1980 Aug;86(2):500–513. doi: 10.1083/jcb.86.2.500. [DOI] [PMC free article] [PubMed] [Google Scholar]

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