Literature DB >> 8126223

Differentiation of membrane systems during development of slow and fast skeletal muscle fibres in chicken.

H Takekura1, H Shuman, C Franzini-Armstrong.   

Abstract

The disposition of transverse (T) tubules, sarcoplasmic reticulum (SR) and T-SR junctions (triads) and the width of Z lines are matched to contractile properties in adult muscle fibres. We have studied the development of the membrane systems in the slow anterior (ALD) and the fast posterior (PLD) latissimus dorsi of the chicken in ovo (E14-E21) and after hatching (D1-D30). T tubules, SR, triads and Z lines were visualized using DiIC16[3] labelling for confocal microscopy and either Ca-osmium-ferrocyanide or standard procedures for electron microscopy. Anterior latissimus dorsi and PLD have similar, slow twitches in early development (E14-E16), but PLD suddenly becomes faster starting at E17-E18. We find that in coincidence with the differentiation of faster contraction properties (starting at E18-E19) density of triads is significantly higher and width of Z lines is narrower in PLD. The SR also begins to acquire fibre-type specific characteristics at this time. Early development of T tubules, on the other hand, is quite similar in the two muscles. Peripherally-located, longitudinally-oriented T tubules, and the first T networks crossing the fibre center appear earlier in ALD (E14-E15 and E16) than in PLD (E14-E16 and E17), but have similar dispositions. The final fibre-type specific distribution of T tubules is achieved after hatching. Some T tubules-rich fibres in the ALD, presumably future fast fibres, develop extensive T tubules networks at early stages. Location of triads at the Z line in pectoralis occurs in three steps: an initial location of longitudinally oriented triads at the A-I junction; a subsequent move to the Z lines and finally a rotation to a transverse orientation.

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Year:  1993        PMID: 8126223     DOI: 10.1007/bf00141560

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


  42 in total

1.  Some properties of avian skeletal muscle fibres with multiple neuromuscular junctions.

Authors:  B L GINSBORG
Journal:  J Physiol       Date:  1960-12       Impact factor: 5.182

2.  A comparative freeze-etch study of the sarcoplasmic reticulum of avian fast and slow muscle fibers.

Authors:  D F Bray; D G Rayns
Journal:  J Ultrastruct Res       Date:  1976-12

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Authors:  T Gordon; G Vrbová
Journal:  Pflugers Arch       Date:  1975-11-14       Impact factor: 3.657

4.  Laser confocal scanning microscopy of the surface membrane/T-tubular system and the sarcoplasmic reticulum in insect striated muscle stained with DilC18(3).

Authors:  O Baumann; T Kitazawa; A P Somlyo
Journal:  J Struct Biol       Date:  1990 Oct-Dec       Impact factor: 2.867

Review 5.  Dynamic properties of mammalian skeletal muscles.

Authors:  R I Close
Journal:  Physiol Rev       Date:  1972-01       Impact factor: 37.312

6.  Antigenic specificity of red and white muscle myosin.

Authors:  I Arndt; F A Pepe
Journal:  J Histochem Cytochem       Date:  1975-03       Impact factor: 2.479

7.  The biosynthesis of sarcoplasmic reticulum.

Authors:  A Martonosi; D Roufa; D B Ha; R Boland
Journal:  Fed Proc       Date:  1980-05-15

Review 8.  The ultrastructure of the mammalian cardiac muscle cell--with special emphasis on the tubular membrane systems. A review.

Authors:  J R Sommer; R A Waugh
Journal:  Am J Pathol       Date:  1976-01       Impact factor: 4.307

9.  Regulation of expression of avian slow myosin heavy-chain isoforms.

Authors:  S K Reid; J M Kennedy; N Shimizu; A Stewart; G Vrbova; R Zak
Journal:  Biochem J       Date:  1989-06-01       Impact factor: 3.857

10.  Discrimination between fast- and slow-twitch fibres of guinea pig skeletal muscle using the relative surface density of junctional transverse tubule membrane.

Authors:  C Franzini-Armstrong; D G Ferguson; C Champ
Journal:  J Muscle Res Cell Motil       Date:  1988-10       Impact factor: 2.698

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  16 in total

1.  Differential response of the membrane systems involved in excitation-contraction coupling to early and later postnatal denervation in rat skeletal muscle.

Authors:  H Takekura; N Kasuga
Journal:  J Muscle Res Cell Motil       Date:  1999-04       Impact factor: 2.698

2.  Assembly of transverse tubule architecture in the middle and myotendinous junctional regions in developing rat skeletal muscle fibers.

Authors:  Susumu Yamashita; Kelly F McGrath; Atsumu Yuki; Hiroyuki Tamaki; Norikatsu Kasuga; Hiroaki Takekura
Journal:  J Muscle Res Cell Motil       Date:  2007-07-04       Impact factor: 2.698

3.  Influences of sarcomere length and selective elimination of myosin filaments on the localization and orientation of triads in rat muscle fibres.

Authors:  H Takekura; N Kasuga; T Yoshioka
Journal:  J Muscle Res Cell Motil       Date:  1996-04       Impact factor: 2.698

4.  Morphological changes in the triads and sarcoplasmic reticulum of rat slow and fast muscle fibres following denervation and immobilization.

Authors:  H Takekura; N Kasuga; K Kitada; T Yoshioka
Journal:  J Muscle Res Cell Motil       Date:  1996-08       Impact factor: 2.698

5.  Development of the excitation-contraction coupling apparatus in skeletal muscle: peripheral and internal calcium release units are formed sequentially.

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

6.  Eccentric exercise-induced morphological changes in the membrane systems involved in excitation-contraction coupling in rat skeletal muscle.

Authors:  H Takekura; N Fujinami; T Nishizawa; H Ogasawara; N Kasuga
Journal:  J Physiol       Date:  2001-06-01       Impact factor: 5.182

7.  Plasticity of the transverse tubules following denervation and subsequent reinnervation in rat slow and fast muscle fibres.

Authors:  Hiroaki Takekura; Hiroyuki Tamaki; Tomie Nishizawa; Norikatsu Kasuga
Journal:  J Muscle Res Cell Motil       Date:  2003       Impact factor: 2.698

8.  T-tubule formation in cardiacmyocytes: two possible mechanisms?

Authors:  Alessandro Di Maio; Kimberly Karko; Rose M Snopko; Rafael Mejía-Alvarez; Clara Franzini-Armstrong
Journal:  J Muscle Res Cell Motil       Date:  2007-10-17       Impact factor: 2.698

9.  Structural differentiation of skeletal muscle fibers in the absence of innervation in humans.

Authors:  Simona Boncompagni; Helmut Kern; Katia Rossini; Christian Hofer; Winfried Mayr; Ugo Carraro; Feliciano Protasi
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-27       Impact factor: 11.205

10.  Reversible vacuolation of the transverse tubules of frog skeletal muscle: a confocal fluorescence microscopy study.

Authors:  S A Krolenko; W B Amos; J A Lucy
Journal:  J Muscle Res Cell Motil       Date:  1995-08       Impact factor: 2.698

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