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PMID: 11909824 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Hypertrophic cardiomyopathy in cardiac myosin binding protein-C knockout mice.

Circulation research ·Vol. 90 ·No. 5 ·2002-03-22 ·Pages 594-601

Harris SP, Bartley CR, Hacker TA, McDonald KS, Douglas PS, Greaser ML, Powers PA, Moss RL

Abstract

Familial hypertrophic cardiomyopathy (FHC) is an inherited autosomal dominant disease caused by mutations in sarcomeric proteins. Among these, mutations that affect myosin binding protein-C (MyBP-C), an abundant component of the thick filaments, account for 20% to 30% of all mutations linked to FHC. However, the mechanisms by which MyBP-C mutations cause disease and the function of MyBP-C are not well understood. Therefore, to assess deficits due to elimination of MyBP-C, we used gene targeting to produce a knockout mouse that lacks MyBP-C in the heart. Knockout mice were produced by deletion of exons 3 to 10 from the endogenous cardiac (c) MyBP-C gene in murine embryonic stem (ES) cells and subsequent breeding of chimeric founder mice to obtain mice heterozygous (+/-) and homozygous (-/-) for the knockout allele. Wild-type (+/+), cMyBP-C(+/-), and cMyBP-C(-/-) mice were born in accordance with Mendelian inheritance ratios, survived into adulthood, and were fertile. Western blot analyses confirmed that cMyBP-C was absent in hearts of homozygous knockout mice. Whereas cMyBP-C(+/-) mice were indistinguishable from wild-type littermates, cMyBP-C(-/-) mice exhibited significant cardiac hypertrophy. Cardiac function, assessed using 2-dimensionally guided M-mode echocardiography, showed significantly depressed indices of diastolic and systolic function only in cMyBP-C(-/-) mice. Ca2+ sensitivity of tension, measured in single skinned myocytes, was reduced in cMyBP-C(-/-) but not cMyBP-C(+/-) mice. These results establish that cMyBP-C is not essential for cardiac development but that the absence of cMyBP-C results in profound cardiac hypertrophy and impaired contractile function.

MeSH Terms
Actin Cytoskeleton/drug effects,physiology Animals Blotting, Northern Blotting, Western Calcium/pharmacology Cardiomyopathy, Hypertrophic/diagnostic imaging,genetics,pathology Carrier Proteins/genetics,metabolism Echocardiography Gene Targeting Heterozygote Homozygote In Vitro Techniques Mice Mice, Knockout Muscle, Skeletal/metabolism Myocardium/metabolism,pathology,ultrastructure Phenotype RNA, Messenger/metabolism Reverse Transcriptase Polymerase Chain Reaction Ventricular Dysfunction, Left/etiology
Chemicals
Carrier Proteins RNA, Messenger myosin-binding protein C Calcium
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Harris Samantha P
Department of Physiology, Section of Cardiovascular Medicine, University of Wisconsin Medical School, Madison, Wis 53706, USA. spharris@physiology.wisc.edu
Bartley Christopher R
Hacker Timothy A
McDonald Kerry S
Douglas Pamela S
Greaser Marion L
Powers Patricia A
Moss Richard L
Article Info
Journal
Circulation research
Abbr.
Circ Res
ISSN
1524-4571
Published
2002-03-22
Pages
594-601
Language
English
Region
United States
NLM ID
0047103
Subset
IM
Grants
NHLBI NIH HHS · P01- HL47053 · United States
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