Literature DB >> 1317881

Dispositions of junctional feet in muscles of invertebrates.

K E Loesser1, L Castellani, C Franzini-Armstrong.   

Abstract

The structure and disposition of the feet occupying the junctions between sarcoplasmic reticulum (SR) and surface membrane/transverse tubules were studied in muscles from a variety of invertebrates. Feet were imaged by rotary shadowing of isolated junctional SR vesicles and by filtering of micrographs from grazing views of the junction in thin sections. The overall size and shape of invertebrate feet is the same as that of feet in skeletal and cardiac muscle of vertebrates. However, the arrangement of feet in invertebrate muscles differs from that in vertebrates. These findings are discussed in terms of known variations in properties of excitation-contraction coupling of the two phyla.

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Year:  1992        PMID： 1317881     DOI： 10.1007/BF01874153

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN： 0142-4319            Impact factor:   2.698


  49 in total

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Journal:  Nature       Date:  1989-11-09       Impact factor: 49.962

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Journal:  J Biol Chem       Date:  1987-02-05       Impact factor: 5.157

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Authors:  W H Fahrenbach
Journal:  J Cell Biol       Date:  1967-10       Impact factor: 10.539

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Authors:  C Franzini-Armstron
Journal:  J Cell Biol       Date:  1974-05       Impact factor: 10.539
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  18 in total

1.  The structure of Ca(2+) release units in arthropod body muscle indicates an indirect mechanism for excitation-contraction coupling.

Authors:  Hiroaki Takekura; Clara Franzini-Armstrong
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

2.  Dynamic interreceptor coupling: a novel working mechanism of two-dimensional ryanodine receptor array.

Authors:  Xin Liang; Xiao-Fang Hu; Jun Hu
Journal:  Biophys J       Date:  2006-12-01       Impact factor: 4.033

3.  Native structure and arrangement of inositol-1,4,5-trisphosphate receptor molecules in bovine cerebellar Purkinje cells as studied by quick-freeze deep-etch electron microscopy.

Authors:  E Katayama; H Funahashi; T Michikawa; T Shiraishi; T Ikemoto; M Iino; K Mikoshiba
Journal:  EMBO J       Date:  1996-09-16       Impact factor: 11.598

4.  Can the Arrangement of RyR2 in Cardiac Muscle Be Predicted?

Authors:  Clara Franzini-Armstrong
Journal:  Biophys J       Date:  2016-06-21       Impact factor: 4.033

5.  Modulation of the oligomerization of isolated ryanodine receptors by their functional states.

Authors:  Xiao-Fang Hu; Xin Liang; Ke-Ying Chen; Hong Xie; Yuhong Xu; Pei-Hong Zhu; Jun Hu
Journal:  Biophys J       Date:  2005-06-10       Impact factor: 4.033

6.  Excitation-contraction coupling in crustacea: do studies on these primitive creatures offer insights about EC coupling more generally?

Authors:  P Palade; S Györke
Journal:  J Muscle Res Cell Motil       Date:  1993-06       Impact factor: 2.698

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Authors:  H Takekura; X Sun; C Franzini-Armstrong
Journal:  J Muscle Res Cell Motil       Date:  1994-04       Impact factor: 2.698

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Authors:  M D Stern; L S Song; H Cheng; J S Sham; H T Yang; K R Boheler; E Ríos
Journal:  J Gen Physiol       Date:  1999-03       Impact factor: 4.086

9.  Type 3 ryanodine receptors of skeletal muscle are segregated in a parajunctional position.

Authors:  Edward Felder; Clara Franzini-Armstrong
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-29       Impact factor: 11.205

10.  The quantal nature of Ca2+ sparks and in situ operation of the ryanodine receptor array in cardiac cells.

Authors:  Shi Qiang Wang; Michael D Stern; Eduardo Ríos; Heping Cheng
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-02       Impact factor: 11.205
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