Literature DB >> 7767098

Alpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological confirmation by light and electron microscopy.

C Wallgren-Pettersson1, B Jasani, G R Newman, G E Morris, S Jones, S Singhrao, A Clarke, I Virtanen, C Holmberg, J Rapola.   

Abstract

To elucidate the protein composition of the nemaline bodies present in the muscle fibres of patients with congenital nemaline myopathy (CNM), we studied muscle biopsies with monoclonal antibodies against alpha-actinin and desmin in combination with a modified Gomori trichrome method. Electron microscopy of immunolabelled resin embedded sections was used for cytochemical localisation of alpha-actinin and desmin. Light microscopy of sections immunolabelled for alpha-actinin showed a cross-striation of the muscle fibres corresponding to the Z band pattern, focal thickening of the Z bands and additional reactivity with a granular pattern corresponding to the presence of nemaline bodies. Labelling of desmin did not show a similar pattern. Electron microscopy confirmed the presence of alpha-actinin in the nemaline bodies and Z bands, whereas desmin was only found in intermediate filaments around the Z bands. Western blots showed single, sharp alpha-actinin bands indistinguishable from normal. Our results provide direct evidence for the presence of alpha-actinin in nemaline bodies and a lack of quantitative or qualitative differences between the alpha-actinin of normal and CNM muscle.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7767098     DOI: 10.1016/0960-8966(94)00035-8

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  17 in total

Review 1.  Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy.

Authors:  K N North; N G Laing; C Wallgren-Pettersson
Journal:  J Med Genet       Date:  1997-09       Impact factor: 6.318

2.  Remodeling of the sarcomeric cytoskeleton in cardiac ventricular myocytes during heart failure and after cardiac resynchronization therapy.

Authors:  Justin G Lichter; Eric Carruth; Chelsea Mitchell; Andreas S Barth; Takeshi Aiba; David A Kass; Gordon F Tomaselli; John H Bridge; Frank B Sachse
Journal:  J Mol Cell Cardiol       Date:  2014-03-20       Impact factor: 5.000

3.  Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.

Authors:  J Moraczewska; N J Greenfield; Y Liu; S E Hitchcock-DeGregori
Journal:  Biophys J       Date:  2000-12       Impact factor: 4.033

4.  Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies.

Authors:  Ann E Davidson; Fazeel M Siddiqui; Michael A Lopez; Peter Lunt; Heather A Carlson; Brian E Moore; Seth Love; Donald E Born; Helen Roper; Anirban Majumdar; Suman Jayadev; Hunter R Underhill; Corrine O Smith; Maja von der Hagen; Angela Hubner; Philip Jardine; Andria Merrison; Elizabeth Curtis; Thomas Cullup; Heinz Jungbluth; Mary O Cox; Thomas L Winder; Hossam Abdel Salam; Jun Z Li; Steven A Moore; James J Dowling
Journal:  Brain       Date:  2013-02       Impact factor: 13.501

5.  Nemaline myopathy type 6: clinical and myopathological features.

Authors:  Montse Olivé; Lev G Goldfarb; Hee-Suk Lee; Zagaa Odgerel; Andre Blokhin; Laura Gonzalez-Mera; Dolores Moreno; Nigel G Laing; Nyamkhishig Sambuughin
Journal:  Muscle Nerve       Date:  2010-12       Impact factor: 3.217

6.  Cullin-3 dependent deregulation of ACTN1 represents a new pathogenic mechanism in nemaline myopathy.

Authors:  Jordan Blondelle; Kavya Tallapaka; Jane T Seto; Majid Ghassemian; Madison Clark; Jenni M Laitila; Adam Bournazos; Jeffrey D Singer; Stephan Lange
Journal:  JCI Insight       Date:  2019-04-16

7.  A recurrent copy number variation of the NEB triplicate region: only revealed by the targeted nemaline myopathy CGH array.

Authors:  Kirsi Kiiski; Vilma-Lotta Lehtokari; Ari Löytynoja; Liina Ahlstén; Jenni Laitila; Carina Wallgren-Pettersson; Katarina Pelin
Journal:  Eur J Hum Genet       Date:  2015-07-22       Impact factor: 4.246

8.  Reduced myofibrillar connectivity and increased Z-disk width in nebulin-deficient skeletal muscle.

Authors:  Paola Tonino; Christopher T Pappas; Bryan D Hudson; Siegfried Labeit; Carol C Gregorio; Henk Granzier
Journal:  J Cell Sci       Date:  2010-01-05       Impact factor: 5.285

9.  Evidence for myofibril remodeling as opposed to myofibril damage in human muscles with DOMS: an ultrastructural and immunoelectron microscopic study.

Authors:  Ji-Guo Yu; Lena Carlsson; Lars-Eric Thornell
Journal:  Histochem Cell Biol       Date:  2004-02-26       Impact factor: 4.304

10.  Mutation update: the spectra of nebulin variants and associated myopathies.

Authors:  Vilma-Lotta Lehtokari; Kirsi Kiiski; Sarah A Sandaradura; Jocelyn Laporte; Pauliina Repo; Jennifer A Frey; Kati Donner; Minttu Marttila; Carol Saunders; Peter G Barth; Johan T den Dunnen; Alan H Beggs; Nigel F Clarke; Kathryn N North; Nigel G Laing; Norma B Romero; Thomas L Winder; Katarina Pelin; Carina Wallgren-Pettersson
Journal:  Hum Mutat       Date:  2014-12       Impact factor: 4.878

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.