Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1966 Feb 1;28(2):169–179. doi: 10.1083/jcb.28.2.169

STRUCTURE OF ISOLATED PLANT GOLGI APPARATUS REVEALED BY NEGATIVE STAINING

William P Cunningham 1, D James Morré 1, H H Mollenhauer 1
PMCID: PMC2106932  PMID: 4161888

Abstract

Sucrose-gradient-purified dictyosomes of plant Golgi apparatus appear, after glutaraldehyde stabilization, as stacks of highly fenestrate and tubate cisternae when negatively stained with phosphotungstic acid, shadowed with heavy metal, or OsO4-stained in thin section. The tubular proliferations (diameter 200 to 400 A) extend for several microns from the central region and are united at intervals into an anastomosing network. Associated with the tubules are two kinds of vesicles which are distinguishable on the basis of texture, size, shape, and staining characteristics. One vesicle type is rough-surfaced, nearly spherical, and of uniform dimensions (diameter approximately 600 A). Metal shadowing shows that these vesicles remain spherical after drying. The other vesicle type is smooth-surfaced and varies in both size and shape. Intercisternal elements are revealed, by negative staining, on the surface of internal cisternae after fragmentation of the dictyosome. The progressive differentiation of cisternae from the forming face to the maturing face is observed in thin sections of these isolated preparations. The morphological characteristics observed in negatively stained dictyosomes indicate regions of functional specialization within the dictyosome cisternae and reveal a dictyosome structure more extensive than that envisioned from sections.

Full Text

The Full Text of this article is available as a PDF (1.4 MB).

Selected References

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

  1. BRENNER S., HORNE R. W. A negative staining method for high resolution electron microscopy of viruses. Biochim Biophys Acta. 1959 Jul;34:103–110. doi: 10.1016/0006-3002(59)90237-9. [DOI] [PubMed] [Google Scholar]
  2. DANIELS E. W. ORIGIN OF THE GOLGI SYSTEM IN AMOEBAE. Z Zellforsch Mikrosk Anat. 1964 Sep 17;64:38–51. doi: 10.1007/BF00339184. [DOI] [PubMed] [Google Scholar]
  3. MOLLENHAUER H. H. PLASTIC EMBEDDING MIXTURES FOR USE IN ELECTRON MICROSCOPY. Stain Technol. 1964 Mar;39:111–114. [PubMed] [Google Scholar]
  4. MOLLENHAUER H. H. TRANSITION FORMS OF GOLGI APPARATUS SECRETION VESICLES. J Ultrastruct Res. 1965 Apr;12:439–446. doi: 10.1016/s0022-5320(65)80110-1. [DOI] [PubMed] [Google Scholar]
  5. MOLLENHAUER H. H., WHALEY W. G. An observation on the functioning of the Golgi apparatus. J Cell Biol. 1963 Apr;17:222–225. doi: 10.1083/jcb.17.1.222. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. MORRE D. J., MOLLENHAUER H. H., CHAMBERS J. E. GLUTARALDEHYDE STABILIZATION AS AN AID TO GOLGI APPARATUS ISOLATION. Exp Cell Res. 1965 Jun;38:672–675. doi: 10.1016/0014-4827(65)90392-7. [DOI] [PubMed] [Google Scholar]
  7. MORRE D. J., MOLLENHAUER H. H. ISOLATION OF THE GOLGI APPARATUS FROM PLANT CELLS. J Cell Biol. 1964 Nov;23:295–305. doi: 10.1083/jcb.23.2.295. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. SLAUTTERBACK D. B. CYTOPLASMIC MICROTUBULES. I. HYDRA. J Cell Biol. 1963 Aug;18:367–388. doi: 10.1083/jcb.18.2.367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. TURNER F. R., WHALEY W. G. INTERCISTERNAL ELEMENTS OF THE GOLGI APPARATUS. Science. 1965 Mar 12;147(3663):1303–1304. doi: 10.1126/science.147.3663.1303. [DOI] [PubMed] [Google Scholar]
  10. YAMAMOTO T. On the thickness of the unit membrane. J Cell Biol. 1963 May;17:413–421. doi: 10.1083/jcb.17.2.413. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES