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PMID: 4139163 Published · ppublish English Journal Article

Effects of phosphotungstate negative staining on the morphology of the isolated Golgi apparatus.

The Journal of cell biology ·Vol. 62 ·No. 2 ·1974-08-00 ·Pages 491-504

Cunningham WP, Staehelin LA, Rubin RW, Wilkins R, Bonneville M

Abstract

Isolated Golgi complexes can be recognized in phosphotungstate (PTA) negative stain as stacks of membranous plates surrounded by a complex anastomosing network of tubules and vesicles. The extent of this tubular network is, however, much greater than can be observed in thin sections of whole cells. To determine which of the steps leading to the final negatively stained image may produce the observed changes, we have monitored each of the steps by other electron microscope and biochemical methods. The first damage to the membranes seems to occur during the initial isolation procedure as judged by the appearance of smooth patches on the freeze-fractured membrane faces that are normally covered with particles. Subsequent suspension of the Golgi fraction in water, to dilute the sucrose for negative staining, leads to the disappearnce of the stacking, to some tubulation and some vesiculation of the membranes as judged by thin section and freeze-cleave microscopy. The latter technique also reveals an increase in smooth-cleaving membrane faces. Application of the negative stain to the water-washed Golgi fraction, finally, produces extensive tubular arrays and a simultaneous decrease in the remaining large membranous vesicles. The freeze-cleaved tubular membranes appear essentially smooth except for small patches of aggregated particles. Parallel gel electrophoresis studies of the membranes and of the water and negative stain wash extracts indicate that protein extraction is involved in these morphological changes. PTA seems to be a particularly effective solvent for certain membrane proteins that are not removed by the water wash. These observations suggest that removal of membrane proteins alters structural restraints on the membrane lipids so that they behave semiautonomously like myelinics and form new artificial structures. This does not eliminate the possibility, however, that some tubules also exist in the Golgi apparatus in vivo.

MeSH Terms
Animals Buffers Cell Membrane/ultrastructure Electrophoresis, Polyacrylamide Gel Endoplasmic Reticulum/ultrastructure Golgi Apparatus/ultrastructure Hydrogen-Ion Concentration Male Microscopy, Electron Phosphotungstic Acid Rats Staining and Labeling Testis/ultrastructure
Chemicals
Buffers Phosphotungstic Acid
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Cunningham W P
Staehelin L A
Rubin R W
Wilkins R
Bonneville M
References (29)
29 references, click to expand
  1. Structure of isolated plant Golgi apparatus revealed by negative staining.
    J Cell Biol. 1966 Feb;28(2):169-79 PMID: 4161888
  2. Variation in membrane structure as revealed by negative staining technique.
    Exp Cell Res. 1966 Oct;44(1):31-45 PMID: 4162851
  3. Tubular connections between dictyosomes and forming secretory vesicles in plant Golgi apparatus.
    J Cell Biol. 1966 May;29(2):373-6 PMID: 5961348
  4. The effects of negative stains on lipids and proteins observed in the electron microscope.
    Protoplasma. 1967;63(1):212-3 PMID: 4166771
  5. [On the formation of pulsating vacuoles in Vacuolaria virescens (Chloromonadophyceae) from the Golgi apparatus].
    Arch Mikrobiol. 1966 Sep 8;54(3):229-36 PMID: 5998093
  6. Fenestrated cisternae in the Golgi apparatus of the epididymis.
    Anat Rec. 1969 Jan;163(1):39-53 PMID: 5763134
  7. Isolation and characterization of Golgi membranes from bovine liver.
    J Cell Biol. 1969 Oct;43(1):59-79 PMID: 4241907
  8. Isolation of a Golgi apparatus-rich fraction from rat liver. I. Method and morphology.
    J Cell Biol. 1970 Mar;44(3):484-91 PMID: 4905956
  9. Effects of phosphotungstic acid and silicotungstic acid on respiration and integrity of rat liver mitochondria.
    Biochem Biophys Res Commun. 1970 Feb 6;38(3):400-5 PMID: 4192036
  10. Cleavage of structural proteins during the assembly of the head of bacteriophage T4.
    Nature. 1970 Aug 15;227(5259):680-5 PMID: 5432063
  11. Membrane differentiation in the Golgi complex of Micrasterias denticulata Bréb. visualized by freeze-etching.
    J Cell Sci. 1970 Nov;7(3):787-92 PMID: 4923745
  12. Growth and differentiation of cytoplasmic membranes in the course of lipoprotein granule synthesis in the hepatic cell. I. Elaboration of elements of the Golgi complex.
    J Cell Biol. 1970 Dec;47(3):745-66 PMID: 5497550
  13. Changes in the golgi apparatus during spermiogenesis in the rat.
    Am J Anat. 1971 Mar;130(3):251-67 PMID: 4101823
  14. N-Acetylglucosaminyltransferase activity in liver, serum, and ovaries of domestic fowl.
    Can J Biochem. 1971 Jun;49(6):671-5 PMID: 4105584
  15. Golgi apparatus, GERL, and lysosomes of neurons in rat dorsal root ganglia, studied by thick section and thin section cytochemistry.
    J Cell Biol. 1971 Sep;50(3):859-86 PMID: 4329159
  16. Isolation of germ cell Golgi apparatus from seminiferous tubules of rat testes.
    J Cell Biol. 1971 Oct;51(1):273-85 PMID: 5111877
  17. Glycoproteins of cell surfaces. A comparative study of three different cell surfaces of the rat.
    J Biol Chem. 1971 Oct 25;246(20):6339-46 PMID: 4108384
  18. Electron microscopical studies on rat brain neurons. Localization of acid phosphatase and mode of formation of lipofuscin bodies.
    J Ultrastruct Res. 1972 Jan;38(1):1-15 PMID: 4333274
  19. The fluid mosaic model of the structure of cell membranes.
    Science. 1972 Feb 18;175(4023):720-31 PMID: 4333397
  20. An ultrastructural characterization of the endothelial cell in the rat liver sinusoid under normal and various experimental conditions, as a contribution to the distinction between endothelial and Kupffer cells.
    J Ultrastruct Res. 1972 Mar;38(5):528-62 PMID: 4335119
  21. Electron microscopic and histochemical evidence for a tubular innervation in the renal cortex of the monkey.
    J Ultrastruct Res. 1972 Dec;41(5):533-49 PMID: 4629670
  22. Partial purification and phosphotungstate solubilization of basal bodies and kinetodesmal fibers from Tetrahymena pyriformis.
    J Cell Biol. 1973 Jun;57(3):601-12 PMID: 4121523
  23. On a reticular derivative from Golgi bodies in the meristem of Anthroceros.
    J Biophys Biochem Cytol. 1960 Sep;8:221-31 PMID: 13766334
  24. MYELIN-LIKE FIGURES FORMED FROM MITOCHONDRIAL MATERIAL.
    Nature. 1964 Jun 13;202:1075-8 PMID: 14207197
  25. ISOLATION OF THE GOLGI APPARATUS FROM PLANT CELLS.
    J Cell Biol. 1964 Nov;23:295-305 PMID: 14228523
  26. THE FINE STRUCTURE OF STROMALYTIC FORMS PRODUCED BY OSMOTIC HEMOLYSIS OF RED BLOOD CELLS.
    J Ultrastruct Res. 1964 Dec;11:494-507 PMID: 14244173
  27. THE STRUCTURE OF THE HEAD, COLLAR AND BASE-PLATE OF 'T-EVEN' TYPE BACTERIOPHAGES.
    J Gen Microbiol. 1965 Mar;38:395-408 PMID: 14329966
  28. A negative staining method for high resolution electron microscopy of viruses.
    Biochim Biophys Acta. 1959 Jul;34:103-10 PMID: 13804200
  29. Structure and properties of hemocyanins. I. Electron micrographs of hemocyanin and apohemocyanin from Helix pomatia at different pH values.
    J Mol Biol. 1962 Jan;4:1-7 PMID: 13873917
Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1974-08-00
Pages
491-504
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2109383
Subset
IM
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