Literature DB >> 6147356

Preparation and morphology of sarcoplasmic reticulum terminal cisternae from rabbit skeletal muscle.

A Saito, S Seiler, A Chu, S Fleischer.   

Abstract

We have developed a procedure to isolate, from skeletal muscle, enriched terminal cisternae of sarcoplasmic reticulum (SR), which retain morphologically intact junctional "feet" structures similar to those observed in situ. The fraction is largely devoid of transverse tubule, plasma membrane, mitochondria, triads (transverse tubules junctionally associated with terminal cisternae), and longitudinal cisternae, as shown by thin-section electron microscopy of representative samples. The terminal cisternae vesicles have distinctive morphological characteristics that differ from the isolated longitudinal cisternae (light SR) obtained from the same gradient. The terminal cisternae consist of two distinct types of membranes, i.e., the junctional face membrane and the Ca2+ pump protein-containing membrane, whereas the longitudinal cisternae contain only the Ca2+ pump protein-containing membrane. The junctional face membrane of the terminal cisternae contains feet structures that extend approximately 12 nm from the membrane surface and can be clearly visualized in thin section through using tannic acid enhancement, by negative staining and by freeze-fracture electron microscopy. Sections of the terminal cisternae, cut tangential to and intersecting the plane of the junctional face, reveal a checkerboardlike lattice of alternating, square-shaped feet structures and spaces each 20 nm square. Structures characteristic of the Ca2+ pump protein are not observed between the feet at the junctional face membrane, either in thin section or by negative staining, even though the Ca2+ pump protein is observed in the nonjunctional membrane on the remainder of the same vesicle. Likewise, freeze-fracture replicas reveal regions of the P face containing ropelike strands instead of the high density of the 7-8-nm particles referable to the Ca2+ pump protein. The intravesicular content of the terminal cisternae, mostly Ca2+-binding protein (calsequestrin), is organized in the form of strands, sometimes appearing paracrystalline, and attached to the inner face of the membrane in the vicinity of the junctional feet. The terminal cisternae preparation is distinct from previously described heavy SR fractions in that it contains the highest percentage of junctional face membrane with morphologically well-preserved junctional feet structures.

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Year:  1984        PMID: 6147356      PMCID: PMC2113387          DOI: 10.1083/jcb.99.3.875

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  31 in total

1.  Isolation and characterization of two types of sarcoplasmic reticulum vesicles.

Authors:  G Meissner
Journal:  Biochim Biophys Acta       Date:  1975-04-21

2.  Reconstitution of a calcium pump using defined membrane components.

Authors:  G B Warren; P A Toon; N J Birdsall; A G Lee; J C Metcalfe
Journal:  Proc Natl Acad Sci U S A       Date:  1974-03       Impact factor: 11.205

3.  Effects of cation binding on the conformation of calsequestrin and the high affinity calcium-binding protein of sarcoplasmic reticulum.

Authors:  T J Ostwald; D H MacLennan; K J Dorrington
Journal:  J Biol Chem       Date:  1974-09-25       Impact factor: 5.157

4.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

5.  The sarcoplasmic reticulum and transverse tubules of the frog's sartorius.

Authors:  L D Peachey
Journal:  J Cell Biol       Date:  1965-06       Impact factor: 10.539

6.  Evidence for membrane microheterogeneity in the sarcoplasmic reticulum of fast twitch skeletal muscle.

Authors:  W B Van Winkle; R J Bick; D E Tucker; C A Tate; M L Entman
Journal:  J Biol Chem       Date:  1982-10-10       Impact factor: 5.157

7.  Calcium-induced calcium release at terminal cisternae of skeletal sarcoplasmic reticulum.

Authors:  H Miyamoto; E Racker
Journal:  FEBS Lett       Date:  1981-10-26       Impact factor: 4.124

8.  Ultrastructure of sarcoplasmic reticulum preparations.

Authors:  D W Deamer; R J Baskin
Journal:  J Cell Biol       Date:  1969-07       Impact factor: 10.539

9.  Localization of sarcoplasmic reticulum proteins in rat skeletal muscle by immunofluorescence.

Authors:  A O Jorgensen; V Kalnins; D H MacLennan
Journal:  J Cell Biol       Date:  1979-02       Impact factor: 10.539

10.  STUDIES OF THE TRIAD : I. Structure of the Junction in Frog Twitch Fibers.

Authors:  C Franzini-Armstrong
Journal:  J Cell Biol       Date:  1970-11-01       Impact factor: 10.539

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  181 in total

1.  Calsequestrin is an inhibitor of skeletal muscle ryanodine receptor calcium release channels.

Authors:  Nicole A Beard; Magdalena M Sakowska; Angela F Dulhunty; Derek R Laver
Journal:  Biophys J       Date:  2002-01       Impact factor: 4.033

2.  Electron tomography of frozen-hydrated isolated triad junctions.

Authors:  T Wagenknecht; C-E Hsieh; B K Rath; S Fleischer; M Marko
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

3.  CGP-37157 inhibits the sarcoplasmic reticulum Ca²+ ATPase and activates ryanodine receptor channels in striated muscle.

Authors:  Jake T Neumann; Paula L Diaz-Sylvester; Sidney Fleischer; Julio A Copello
Journal:  Mol Pharmacol       Date:  2010-10-05       Impact factor: 4.436

4.  Sparks and puffs in oligodendrocyte progenitors: cross talk between ryanodine receptors and inositol trisphosphate receptors.

Authors:  L L Haak; L S Song; T F Molinski; I N Pessah; H Cheng; J T Russell
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

5.  Molecular cloning, functional expression and tissue distribution of the cDNA encoding frog skeletal muscle calsequestrin.

Authors:  S Treves; B Vilsen; P Chiozzi; J P Andersen; F Zorzato
Journal:  Biochem J       Date:  1992-05-01       Impact factor: 3.857

Review 6.  Ion conduction and discrimination in the sarcoplasmic reticulum ryanodine receptor/calcium-release channel.

Authors:  A J Williams
Journal:  J Muscle Res Cell Motil       Date:  1992-02       Impact factor: 2.698

7.  Cryo-EM of the native structure of the calcium release channel/ryanodine receptor from sarcoplasmic reticulum.

Authors:  M Radermacher; T Wagenknecht; R Grassucci; J Frank; M Inui; C Chadwick; S Fleischer
Journal:  Biophys J       Date:  1992-04       Impact factor: 4.033

8.  Endogenously determined restriction of food intake overcomes excitation-contraction uncoupling in JP45KO mice with aging.

Authors:  Osvaldo Delbono; Maria Laura Messi; Zhong-Min Wang; Susan Treves; Barbara Mosca; Leda Bergamelli; Miyuki Nishi; Hiroshi Takeshima; Hang Shi; Bingzhong Xue; Francesco Zorzato
Journal:  Exp Gerontol       Date:  2012-01-25       Impact factor: 4.032

9.  Evidence for the transport of glutathione through ryanodine receptor channel type 1.

Authors:  Gábor Bánhegyi; Miklós Csala; Gábor Nagy; Vincenzo Sorrentino; Rosella Fulceri; Angelo Benedetti
Journal:  Biochem J       Date:  2003-12-15       Impact factor: 3.857

10.  Endogenous, Ca(2+)-dependent cysteine-protease cleaves specifically the ryanodine receptor/Ca2+ release channel in skeletal muscle.

Authors:  V Shoshan-Barmatz; S Weil; H Meyer; M Varsanyi; L M Heilmeyer
Journal:  J Membr Biol       Date:  1994-12       Impact factor: 1.843

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