Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1977 Oct 1;75(1):135–147. doi: 10.1083/jcb.75.1.135

Evidence that coated vesicles isolated from brain are calcium- sequestering organelles resembling sarcoplasmic reticulum

PMCID: PMC2111570  PMID: 144139

Abstract

Coated vesicles from the brain have been purified to near morphological homogeneity by a modification of the method of Pearse. These vesicles resemble sarcoplasmic reticulum fragments isolated from skeletal muscle. They contain proteins with 100,000- and 55,000-dalton mol wt which co-migrate on polyacrylamide gels, in the presence of sodium dodecyl sulfate, with the two major proteins of the sarcoplasmic reticulum fragment. These vesicles contain adenosine triphosphatase (ATPase) activity which is stimulated by calcium ions in the presence of Triton X-100 (Rohm & Haas Co., Philadelphia, Pa.), displaying maximal activity at 8 x 10(-7) M Ca ++. They take up calcium ions from the medium, and this uptake is stimulated by ATP and by potassium oxalate, a calcium-trapping agent. The 100,000-dalton protein of the coated vesicles displays immunological reactivity with an antiserum directed against the 100,000-dalton, calcium-stimulated ATPase of the sarcoplasmic reticulum. As with the sarcoplasmic reticulum fragment, this protein becomes radiolabeled when coated vesicles are briefly incubated with gamma-labeled [32P]ATP. The possible functions of coated vesicles as calcium-sequestering organelles are discussed.

Full Text

The Full Text of this article is available as a PDF (2.7 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Anderson R. G., Brown M. S., Goldstein J. L. Role of the coated endocytic vesicle in the uptake of receptor-bound low density lipoprotein in human fibroblasts. Cell. 1977 Mar;10(3):351–364. doi: 10.1016/0092-8674(77)90022-8. [DOI] [PubMed] [Google Scholar]
  2. Droller M. J., Roth T. F. An electron microscope study of yolk formation during oogenesis in Lebistes reticulatus guppyi. J Cell Biol. 1966 Feb;28(2):209–232. doi: 10.1083/jcb.28.2.209. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. 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]
  4. Fiehn W., Migala A. Calcium binding to sarcoplasmic membranes. Eur J Biochem. 1971 May 28;20(2):245–248. doi: 10.1111/j.1432-1033.1971.tb01387.x. [DOI] [PubMed] [Google Scholar]
  5. Franke W. W., Lüder M. R., Kartenbeck J., Zerban H., Keenan T. W. Involvement of vesicle coat material in casein secretion and surface regeneration. J Cell Biol. 1976 Apr;69(1):173–195. doi: 10.1083/jcb.69.1.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Fried R. C., Blaustein M. P. Synaptic vesicle recycling in synaptosomes in vitro. Nature. 1976 May 20;261(5557):255–256. doi: 10.1038/261255a0. [DOI] [PubMed] [Google Scholar]
  7. Gratzl M., Dahl G. Ca2+-induced fusion of golgi-derived secretory vesicles isolated from rat liver. FEBS Lett. 1976 Feb 15;62(2):142–145. doi: 10.1016/0014-5793(76)80038-5. [DOI] [PubMed] [Google Scholar]
  8. HASSELBACH W., MAKINOSE M. [The calcium pump of the "relaxing granules" of muscle and its dependence on ATP-splitting]. Biochem Z. 1961;333:518–528. [PubMed] [Google Scholar]
  9. Heuser J. E., Reese T. S. Evidence for recycling of synaptic vesicle membrane during transmitter release at the frog neuromuscular junction. J Cell Biol. 1973 May;57(2):315–344. doi: 10.1083/jcb.57.2.315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Ikemoto N. Transport and inhibitory Ca2+ binding sites on the ATPase enzyme isolated from the sarcoplasmic reticulum. J Biol Chem. 1975 Sep 25;250(18):7219–7224. [PubMed] [Google Scholar]
  11. Inesi G., Cohen J. A., Coan C. R. Two functional states of sarcoplasmic reticulum ATPase. Biochemistry. 1976 Nov 30;15(24):5293–5298. doi: 10.1021/bi00669a015. [DOI] [PubMed] [Google Scholar]
  12. Kanaseki T., Kadota K. The "vesicle in a basket". A morphological study of the coated vesicle isolated from the nerve endings of the guinea pig brain, with special reference to the mechanism of membrane movements. J Cell Biol. 1969 Jul;42(1):202–220. doi: 10.1083/jcb.42.1.202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Katz A. M., Repke D. I., Hasselbach W. Dependence of ionophore- and caffeine-induced calcium release from sarcoplasmic reticulum vesicles on external and internal calcium ion concentrations. J Biol Chem. 1977 Mar 25;252(6):1938–1949. [PubMed] [Google Scholar]
  14. Kendrick N. C., Blaustein M. P., Fried R. C., Ratzlaff R. W. ATP-dependent calcium storage in presynaptic nerve terminals. Nature. 1977 Jan 20;265(5591):246–248. doi: 10.1038/265246a0. [DOI] [PubMed] [Google Scholar]
  15. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  16. Lagunoff D., Curran D. E. Role of bristle-coated membrane in the uptake of ferritin by rat macrophages. Exp Cell Res. 1972 Dec;75(2):337–346. doi: 10.1016/0014-4827(72)90438-7. [DOI] [PubMed] [Google Scholar]
  17. Llinás R., Blinks J. R., Nicholson C. Calcium transient in presynaptic terminal of squid giant synapse: detection with aequorin. Science. 1972 Jun 9;176(4039):1127–1129. doi: 10.1126/science.176.4039.1127. [DOI] [PubMed] [Google Scholar]
  18. MacLennan D. H. Purification and properties of an adenosine triphosphatase from sarcoplasmic reticulum. J Biol Chem. 1970 Sep 10;245(17):4508–4518. [PubMed] [Google Scholar]
  19. Ockleford C. D. A three-dimensional reconstruction of the polygonal pattern on placental coated-vesicle membranes. J Cell Sci. 1976 Jun;21(1):83–91. doi: 10.1242/jcs.21.1.83. [DOI] [PubMed] [Google Scholar]
  20. Palade G. E., Bruns R. R. Structural modulations of plasmalemmal vesicles. J Cell Biol. 1968 Jun;37(3):633–649. doi: 10.1083/jcb.37.3.633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Pearse B. M. Clathrin: a unique protein associated with intracellular transfer of membrane by coated vesicles. Proc Natl Acad Sci U S A. 1976 Apr;73(4):1255–1259. doi: 10.1073/pnas.73.4.1255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Pearse B. M. Coated vesicles from pig brain: purification and biochemical characterization. J Mol Biol. 1975 Sep 5;97(1):93–98. doi: 10.1016/s0022-2836(75)80024-6. [DOI] [PubMed] [Google Scholar]
  23. Poste G., Allison A. C. Membrane fusion. Biochim Biophys Acta. 1973 Dec 28;300(4):421–465. doi: 10.1016/0304-4157(73)90015-4. [DOI] [PubMed] [Google Scholar]
  24. REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. ROTH T. F., PORTER K. R. YOLK PROTEIN UPTAKE IN THE OOCYTE OF THE MOSQUITO AEDES AEGYPTI. L. J Cell Biol. 1964 Feb;20:313–332. doi: 10.1083/jcb.20.2.313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Shainberg A., Yagil G., Yaffe D. Control of myogenesis in vitro by Ca 2 + concentration in nutritional medium. Exp Cell Res. 1969 Nov;58(1):163–167. doi: 10.1016/0014-4827(69)90127-x. [DOI] [PubMed] [Google Scholar]
  27. Weber K., Osborn M. The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis. J Biol Chem. 1969 Aug 25;244(16):4406–4412. [PubMed] [Google Scholar]
  28. Zakai N., Kulka R. G., Loyter A. Fusion of human erythrocyte ghosts promoted by the combined action of calcium and phosphate ions. Nature. 1976 Oct 21;263(5579):696–699. doi: 10.1038/263696a0. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES