Literature DB >> 2713897

Substructure of cisternal organelles of neuronal perikarya in immature rat brains revealed by quick-freeze and deep-etch techniques.

T Gotow1, P H Hashimoto.   

Abstract

Membrane-bounded organelles possessing cisternae, i.e., rough endoplasmic reticulum and Golgi apparatus, in immature rat central neurons were examined by quick-freeze and deep-etch techniques to see how their intracisternal structures are organized and how ribosomes are associated with the membrane of the endoplasmic reticulum. Cisternae of endoplasmic reticulum, 60-100 nm wide, were bridged with randomly-distributed strands (trabecular strands, 12.5 nm in mean diameter). Luminal surfaces of cisternae of the endoplasmic reticulum were decorated with various-sized globular particles, some as small as intramembrane particles, and others as large as granules formed by soluble proteins seen in the cytoplasm. A closer examination revealed much thinner strands (3.3 nm in mean diameter). Such thin strands were short, usually winding toward the luminal surface, and sometimes touching the luminal surface with one end. Ribosomes appeared to be embedded into the entire thickness of cross-fractured membranes of endoplasmic reticulum, that is, their internal portions appeared to be situated at almost the same level as the cisternal luminal surface. From the internal portion of ribosomes, single thin strands occasionally protruded into the lumen, suggesting that these thin strands were newly synthesized polypeptides. A horizontal separation within ribosomes appeared to occur at the same level as the hydrophobic middle of the membrane of the endoplasmic reticulum. Interiors of the Golgi apparatus cisternae, which were much narrower than cisternae of endoplasmic reticulum, were similarly bridged with trabecular strands, but the Golgi trabecular strands were thinner and more frequent. Their cisternal lumina were also dotted with globular particles. No identifiable profiles corresponding to the thin strands in the endoplasmic reticulum were observed. Golgi cisternae showed a heterogeneous distribution of membrane granularity; the membrane in narrow cisternal space was granule-rich, while that in expanded space was granule-poor, suggesting a functional compartmentalization of the Golgi cisternae.

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Mesh:

Year:  1989        PMID: 2713897     DOI: 10.1007/BF00224718

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  31 in total

Review 1.  The structure and function of eukaryotic ribosomes.

Authors:  I G Wool
Journal:  Annu Rev Biochem       Date:  1979       Impact factor: 23.643

2.  Ultrastructural aspects of quick-freezing deep-etching replica images of the cytoskeletal system in anterior pituitary secretory cells of rats and mice.

Authors:  T Senda; H Fujita
Journal:  Arch Histol Jpn       Date:  1987-03

3.  Visualization of ribosomes by freeze-etching.

Authors:  J Wartiovaara; D Branton
Journal:  Exp Cell Res       Date:  1970-08       Impact factor: 3.905

4.  Heterogeneous distribution of filipin--cholesterol complexes across the cisternae of the Golgi apparatus.

Authors:  L Orci; R Montesano; P Meda; F Malaisse-Lagae; D Brown; A Perrelet; P Vassalli
Journal:  Proc Natl Acad Sci U S A       Date:  1981-01       Impact factor: 11.205

5.  Membrane differentiation in the Golgi complex of Micrasterias denticulata Bréb. visualized by freeze-etching.

Authors:  L A Staehelin; O Kiermayer
Journal:  J Cell Sci       Date:  1970-11       Impact factor: 5.285

6.  Ribosome binding sites visualized on freeze-fractured membranes of the rough endoplasmic reticulum.

Authors:  T H Giddings; L A Staehelin
Journal:  J Cell Biol       Date:  1980-04       Impact factor: 10.539

7.  Mobility of ribosomes bound to microsomal membranes. A freeze-etch and thin-section electron microscope study of the structure and fluidity of the rough endoplasmic reticulum.

Authors:  G K Ojakian; G Kreibich; D D Sabatini
Journal:  J Cell Biol       Date:  1977-03       Impact factor: 10.539

Review 8.  The Golgi apparatus (complex)-(1954-1981)-from artifact to center stage.

Authors:  M G Farquhar; G E Palade
Journal:  J Cell Biol       Date:  1981-12       Impact factor: 10.539

9.  Quick-freeze, deep-etch visualization of the cytoskeleton beneath surface differentiations of intestinal epithelial cells.

Authors:  N Hirokawa; J E Heuser
Journal:  J Cell Biol       Date:  1981-11       Impact factor: 10.539

10.  Ultrastructural localization of the mannose 6-phosphate receptor in rat liver.

Authors:  H J Geuze; J W Slot; G J Strous; A Hasilik; K Von Figura
Journal:  J Cell Biol       Date:  1984-06       Impact factor: 10.539

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  2 in total

1.  Three-dimensional studies of the cytoskeleton of cultured hepatocytes: a quick-freezing and deep-etching study.

Authors:  S Ohno; Y Fujii
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

2.  Subdomain-specific localization of CLIMP-63 (p63) in the endoplasmic reticulum is mediated by its luminal alpha-helical segment.

Authors:  D R Klopfenstein; J Klumperman; A Lustig; R A Kammerer; V Oorschot; H P Hauri
Journal:  J Cell Biol       Date:  2001-06-11       Impact factor: 10.539

  2 in total

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