Literature DB >> 2653645

Immunocytochemical studies of spectrin in hamster cardiac tissue.

D A Messina1, L F Lemanski.   

Abstract

The spectrins are a family of cytoskeletal-membrane proteins that have a wide tissue distribution. In the present study, we employed polyclonal antibodies made against mammalian and avian erythroid spectrins as well as mammalian brain spectrin to assess their presence and distributions in the mammalian heart. Western blot analyses revealed that all three antibodies were specific for a 240,000 molecular weight alpha-spectrin subunit found in hamster erythrocyte ghost homogenates, whole hamster heart, and isolated hamster cardiac myofibril homogenates. Spectrin staining was absent from the Triton X-100-extracted supernatant fraction of myofibril preparations, suggesting that the protein is linked to the myofibril precipitate after exposure to the detergent. Frozen, unfixed, 2-microns-thick; sections of adult. Syrian golden hamster cardiac tissue exhibited strong immunofluorescent staining of intercalated discs and Z-bands using all three antibodies. In addition, the mammalian erythroid spectrin antibodies showed staining of the sarcolemma, and in cross section, revealed a delicate internal network of staining that appears to surround individual myofibrils. This may be T-tubule-associated staining. Myofibrils isolated from cardiac myocytes using Triton X-100 show positive Z-band staining using all three antibodies. Double staining with Texas Red-labeled monoclonal desmin and FITC-labeled polyclonal spectrin antibodies revealed that both stained the myofibrillar Z-line regions. These results demonstrate that spectrin is closely associated with the membranes, myofibrils, and intermediate filaments in the mammalian heart.

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Year:  1989        PMID: 2653645     DOI: 10.1002/cm.970120303

Source DB:  PubMed          Journal:  Cell Motil Cytoskeleton        ISSN: 0886-1544


  9 in total

1.  The transitional junction: a new functional subcellular domain at the intercalated disc.

Authors:  Pauline M Bennett; Alison M Maggs; Anthony J Baines; Jennifer C Pinder
Journal:  Mol Biol Cell       Date:  2006-02-15       Impact factor: 4.138

Review 2.  Diverse roles of the actin cytoskeleton in striated muscle.

Authors:  Anthony J Kee; Peter W Gunning; Edna C Hardeman
Journal:  J Muscle Res Cell Motil       Date:  2009-12-08       Impact factor: 2.698

3.  Cytochalasin D reduces Ca2+ sensitivity and maximum tension via interactions with myofilaments in skinned rat cardiac myocytes.

Authors:  S C Calaghan; E White; S Bedut; J Y Le Guennec
Journal:  J Physiol       Date:  2000-12-01       Impact factor: 5.182

4.  Localization of spectrin isoforms in the adult mouse heart.

Authors:  T Isayama; S R Goodman; I S Zagon
Journal:  Cell Tissue Res       Date:  1993-10       Impact factor: 5.249

5.  Characterization and expression of a heart-selective alternatively spliced variant of alpha II-spectrin, cardi+, during development in the rat.

Authors:  Yinghua Zhang; Wendy G Resneck; Pervis C Lee; William R Randall; Robert J Bloch; Jeanine A Ursitti
Journal:  J Mol Cell Cardiol       Date:  2010-01-28       Impact factor: 5.000

6.  Localization of dystrophin and beta-spectrin in vacuolar myopathies.

Authors:  J L De Bleecker; A G Engel; J C Winkelmann
Journal:  Am J Pathol       Date:  1993-10       Impact factor: 4.307

7.  Not just a plasma membrane protein: in cardiac muscle cells alpha-II spectrin also shows a close association with myofibrils.

Authors:  Pauline M Bennett; Anthony J Baines; Marie-Christine Lecomte; Alison M Maggs; Jennifer C Pinder
Journal:  J Muscle Res Cell Motil       Date:  2004       Impact factor: 2.698

8.  Costameres are sites of force transmission to the substratum in adult rat cardiomyocytes.

Authors:  B A Danowski; K Imanaka-Yoshida; J M Sanger; J W Sanger
Journal:  J Cell Biol       Date:  1992-09       Impact factor: 10.539

Review 9.  Riding the waves of the intercalated disc of the heart.

Authors:  Pauline M Bennett
Journal:  Biophys Rev       Date:  2018-07-09
  9 in total

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