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Three-dimensional reconstitution of embryonic cardiomyocytes in a collagen matrix: a new heart muscle model system.

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TLDR
The utility of this system as a test bed for genetic manipulation was demonstrated by infecting the CMPMs with a recombinant β‐galactosidase‐carrying adenovirus, and transduction efficiency increased from about 5% (MOI 0.1) to about 50% ( MOI 100).
Abstract
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.

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Fabrication of Pulsatile Cardiac Tissue Grafts Using a Novel 3-Dimensional Cell Sheet Manipulation Technique and Temperature-Responsive Cell Culture Surfaces

TL;DR: These results demonstrate that electrically communicative pulsatile 3-D cardiac constructs were achieved both in vitro and in vivo by layering cardiomyocyte sheets.
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Engineered heart tissue grafts improve systolic and diastolic function in infarcted rat hearts

TL;DR: This study provides evidence that large contractile cardiac tissue grafts can be constructed in vitro, can survive after implantation and can support contractile function of infarcted hearts.
Journal ArticleDOI

Tissue Engineering of a Differentiated Cardiac Muscle Construct

TL;DR: It is demonstrated that cardiac myocytes from neonatal rats, when mixed with collagen I and matrix factors, cast in circular molds, and subjected to phasic mechanical stretch, reconstitute ring-shaped EHTs that display important hallmarks of differentiated myocardium.
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Functional assembly of engineered myocardium by electrical stimulation of cardiac myocytes cultured on scaffolds.

TL;DR: It is hypothesized that excitation–contraction coupling, critical for the development of a normal heart, determines the development and function of engineered myocardium.
Journal ArticleDOI

Cell sheet engineering for myocardial tissue reconstruction

TL;DR: Novel tissue engineering methodology layering cell sheets to construct 3-D functional tissues without any artificial scaffolds is proposed and should have enormous potential for fabricating clinically applicable myocardial tissues and should promote tissue engineering research fields.
References
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Journal ArticleDOI

Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction

TL;DR: A new method of total RNA isolation by a single extraction with an acid guanidinium thiocyanate-phenol-chloroform mixture is described, providing a pure preparation of undegraded RNA in high yield and can be completed within 4 h.
Journal ArticleDOI

In vitro rapid organization of endothelial cells into capillary-like networks is promoted by collagen matrices.

TL;DR: Results showed that capillary endothelial cells have the capacity to form vessel-like structures with well-oriented cell polarity in vitro and suggest that an appropriate topological relationship of endothelium cells with collagen matrices has an inducive role on the expression of this potential.
Journal ArticleDOI

Cardiac hypertrophy. Mechanical, neural, and endocrine dependence.

TL;DR: Cardiac hypertrophy usually follows an increase in work load that is imposed on the heart, but increased pressure or volume work of the left ventricle is associated with increased release of neurotransmitters or plasma concentrations of hormones that may also have direct effects on cardiac myocyte growth.
Journal Article

A modification of the masson trichrome technique for routine laboratory purposes.

TL;DR: A striking modification of Mallory's connective tissue stain is devised by replacing fuchsin with a stable and exclusively nudear stain (Kernechtrot) which is a very brilliant carmine.
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