Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
1997-8-19
pubmed:abstractText
A method has been developed for culturing cardiac myocytes in a collagen matrix to produce a coherently contracting 3-dimensional model heart tissue that allows direct measurement of isometric contractile force. Embryonic chick cardiomyocytes were mixed with collagen solution and allowed to gel between two Velcro-coated glass tubes. During culture, the cardiomyocytes formed spontaneously beating cardiac myocyte-populated matrices (CMPMs) anchored at opposite ends to the Velcro-covered tubes through which they could be attached to a force measuring system. Immunohistochemistry and electron microscopy revealed a highly organized tissue-like structure of alpha-actin and alpha-tropomyosin-positive cardiac myocytes exhibiting typical cross-striation, sarcomeric myofilaments, intercalated discs, desmosomes, and tight junctions. Force measurements of paced or unpaced CMPMs were performed in organ baths after 6-11 days of cultivation and were stable for up to 24 h. Force increased with frequency between 0.8 and 2.0 Hz (positive "staircase"), increasing rest length (Starling mechanism), and increasing extracellular calcium. The utility of this system as a test bed for genetic manipulation was demonstrated by infecting the CMPMs with a recombinant beta-galactosidase-carrying adenovirus. Transduction efficiency increased from about 5% (MOI 0.1) to about 50% (MOI 100). CMPMs display more physiological characteristics of intact heart tissue than monolayer cultures. This approach, simpler and faster than generation of transgenic animals, should allow functional consequences of genetic or pharmacological manipulation of cardiomyocytes in vitro to be studied under highly controlled conditions.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0892-6638
pubmed:author
pubmed:issnType
Print
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
683-94
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9240969-Actins, pubmed-meshheading:9240969-Adenoviridae, pubmed-meshheading:9240969-Animals, pubmed-meshheading:9240969-Calcium, pubmed-meshheading:9240969-Cell Adhesion, pubmed-meshheading:9240969-Cell Culture Techniques, pubmed-meshheading:9240969-Cell Division, pubmed-meshheading:9240969-Cells, Cultured, pubmed-meshheading:9240969-Chick Embryo, pubmed-meshheading:9240969-Collagen, pubmed-meshheading:9240969-Electric Stimulation, pubmed-meshheading:9240969-Gels, pubmed-meshheading:9240969-Gene Transfer Techniques, pubmed-meshheading:9240969-Heart, pubmed-meshheading:9240969-Immunohistochemistry, pubmed-meshheading:9240969-Isometric Contraction, pubmed-meshheading:9240969-Microscopy, Electron, pubmed-meshheading:9240969-Myocardial Contraction, pubmed-meshheading:9240969-Myocardium, pubmed-meshheading:9240969-RNA, pubmed-meshheading:9240969-Signal Transduction, pubmed-meshheading:9240969-Thymidine, pubmed-meshheading:9240969-Tropomyosin, pubmed-meshheading:9240969-beta-Galactosidase
pubmed:year
1997
pubmed:articleTitle
Three-dimensional reconstitution of embryonic cardiomyocytes in a collagen matrix: a new heart muscle model system.
pubmed:affiliation
Abteilung Allgemeine Pharmakologie, Universitäts-Krankenhaus Eppendorf, Universität Hamburg, Germany.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't