Literature DB >> 15494447

Dystrophin- and MLP-deficient mouse hearts: marked differences in morphology and function, but similar accumulation of cytoskeletal proteins.

James R Wilding1, Jürgen E Schneider, A Elizabeth Sang, Kay E Davies, Stefan Neubauer, Kieran Clarke.   

Abstract

In humans, cytoskeletal dystrophin and muscle LIM protein (MLP) gene mutations can cause dilated cardiomyopathy, yet these mutations may have different effects in mice, owing to increased accumulation of other, compensatory cytoskeletal proteins. Consequently, we characterized left-ventricular (LV) morphology and function in vivo using high-resolution cine-magnetic resonance imaging (MRI) in 2- to 3-month old dystrophin-deficient (mdx) and MLP-null mice, and their respective controls. LV passive stiffness was assessed in isolated, perfused hearts, and cytoskeletal protein levels were determined using Western blot analyses. In mdx mouse hearts, LV-to-body weight ratio, cavity volume, ejection fraction, stroke volume, and cardiac output were normal. However, MLP-null mouse hearts had 1.2-fold higher LV-to-body weight ratios (P<0.01), 1.5-fold higher end-diastolic volumes (P<0.01), and decreased ejection fraction compared with controls (25% vs. 66%, respectively, P<0.01), indicating dilated cardiomyopathy and heart failure. In both models, isolated, perfused heart end-diastolic pressure-volume relationships and passive left-ventricular stiffness were normal. Hearts from both models accumulated desmin and beta-tubulin, mdx mouse hearts accumulated utrophin and MLP, and MLP-null mouse hearts accumulated dystrophin and syncoilin. Although the increase in MLP and utrophin in the mdx mouse heart was able to compensate for the loss of dystrophin, accumulation of desmin, syncoilin and dystrophin were unable to compensate for the loss of MLP, resulting in heart failure.

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Year:  2004        PMID: 15494447     DOI: 10.1096/fj.04-1731fje

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  20 in total

1.  Osteopontin-stimulated expression of matrix metalloproteinase-9 causes cardiomyopathy in the mdx model of Duchenne muscular dystrophy.

Authors:  Saurabh Dahiya; Srikanth Givvimani; Shephali Bhatnagar; Natia Qipshidze; Suresh C Tyagi; Ashok Kumar
Journal:  J Immunol       Date:  2011-08-01       Impact factor: 5.422

2.  Overexpression of Jazf1 induces cardiac malformation through the upregulation of pro-apoptotic genes in mice.

Authors:  Ki Beom Bae; Myoung Ok Kim; Dong Hoon Yu; Mi Jung Shin; Hei Jung Kim; Hyung Soo Yuh; Young Rae Ji; Jae-Young Kim; Jin Man Kim; Byung Hwa Hyun; Hwi Cheul Lee; Won Kyong Chang; Soo Bong Park; Do Hyung Kim; Hyun-Shik Lee; Yeon-Sik Choo; Sanggyu Lee; Zae Young Ryoo
Journal:  Transgenic Res       Date:  2011-01-09       Impact factor: 2.788

3.  Cardiac micro-computed tomography for morphological and functional phenotyping of muscle LIM protein null mice.

Authors:  Cristian T Badea; Laurence W Hedlund; Julie F Boslego Mackel; Lan Mao; Howard A Rockman; G Allan Johnson
Journal:  Mol Imaging       Date:  2007 Jul-Aug       Impact factor: 4.488

4.  Early manifestation of alteration in cardiac function in dystrophin deficient mdx mouse using 3D CMR tagging.

Authors:  Wei Li; Wei Liu; Jia Zhong; Xin Yu
Journal:  J Cardiovasc Magn Reson       Date:  2009-10-22       Impact factor: 5.364

5.  Subcellular Ca2+ signaling in the heart: the role of ryanodine receptor sensitivity.

Authors:  Benjamin L Prosser; Christopher W Ward; W J Lederer
Journal:  J Gen Physiol       Date:  2010-08       Impact factor: 4.086

6.  Local energetic regulation of sarcoplasmic and myosin ATPase is differently impaired in rats with heart failure.

Authors:  Frederic Joubert; James R Wilding; Dominique Fortin; Valérie Domergue-Dupont; Marta Novotova; Renée Ventura-Clapier; Vladimir Veksler
Journal:  J Physiol       Date:  2008-09-11       Impact factor: 5.182

Review 7.  Alterations in mitochondrial function as a harbinger of cardiomyopathy: lessons from the dystrophic heart.

Authors:  Yan Burelle; Maya Khairallah; Alexis Ascah; Bruce G Allen; Christian F Deschepper; Basil J Petrof; Christine Des Rosiers
Journal:  J Mol Cell Cardiol       Date:  2009-09-18       Impact factor: 5.000

8.  Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation.

Authors:  Deborah Merrick; Lukas Kurt Josef Stadler; Dean Larner; Janet Smith
Journal:  Dis Model Mech       Date:  2009-06-17       Impact factor: 5.758

9.  Dystrophin-deficient cardiomyopathy in mouse: expression of Nox4 and Lox are associated with fibrosis and altered functional parameters in the heart.

Authors:  Christopher F Spurney; Susan Knoblach; Emidio E Pistilli; Kanneboyina Nagaraju; Gerard R Martin; Eric P Hoffman
Journal:  Neuromuscul Disord       Date:  2008-04-25       Impact factor: 4.296

10.  Syncoilin is required for generating maximum isometric stress in skeletal muscle but dispensable for muscle cytoarchitecture.

Authors:  Jianlin Zhang; Marie-Louise Bang; David S Gokhin; Yingchun Lu; Li Cui; Xiaodong Li; Yusu Gu; Nancy D Dalton; Maria Cecilia Scimia; Kirk L Peterson; Richard L Lieber; Ju Chen
Journal:  Am J Physiol Cell Physiol       Date:  2008-03-26       Impact factor: 4.249

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