Cardiac fibroblasts influence cardiomyocyte phenotype in vitro
Cardiac fibroblasts influence cardiomyocyte phenotype in vitro
Cardiac fibroblasts impact myocardial development and remodeling through intercellular contact with cardiomyocytes, but less is known about noncontact, profibrotic signals whereby fibroblasts alter cardiomyocyte behavior. Fibroblasts and cardiomyocytes were harvested from newborn rat ventricles and separated by serial digestion and gradient centrifugation. Cardiomyocytes were cultured in 1) standard medium, 2) standard medium diluted 1:1 with PBS, or 3) standard medium diluted 1:1 with medium conditioned > or =72 h by cardiac fibroblasts. Serum concentrations were held constant under all media conditions, and complete medium exchanges were performed daily. Cardiomyocytes began contracting within 24 h at clonal or mass densities with <5% of cells expressing vimentin. Immunocytochemical analysis revealed progressive expression of alpha-smooth muscle actin in cardiomyocytes after 24 h in all conditions. Only cardiomyocytes in fibroblast-conditioned medium stopped contracting by 72 h. There was a significant, sustained increase in vimentin expression specific to these cultures (means +/- SD: conditioned 46.3 +/- 6.0 vs. control 5.3 +/- 2.9%, P < 0.00025) typically with cardiac myosin heavy chain coexpression. Proteomics assays revealed 10 cytokines (VEGF, GRO/KC, monocyte chemoattractant protein-1, leptin, macrophage inflammatory protein-1alpha, IL-6, IL-10, IL-12p70, IL-17, and tumor necrosis factor-alpha) at or below detection levels in unconditioned medium that were significantly elevated in fibroblast-conditioned medium. Latent transforming growth factor-beta and RANTES were present in unconditioned medium but rose to higher levels in conditioned medium. Only granulocyte-macrophage colony-stimulating factor was present above threshold levels in standard medium but decreased with fibroblast conditioning. These data indicated that under the influence of fibroblast-conditioned medium, cardiomyocytes exhibited marked hypertrophy, diminished contractile capacity, and phenotype plasticity distinct from the dedifferentiation program present under standard culture conditions.
proteomics, myosin heavy chain, vimentin, myofibroblast, primary culture, dedifferentiation, plasticity
C1799-C1808
LaFramboise, W.A.
3d4885e7-9c4e-4b43-94f1-6fdbd4a192eb
Scalise, D.
827caf5c-0762-4bc9-b775-f835a4b256aa
Stoodley, P.
08614665-92a9-4466-806e-20c6daeb483f
Graner, S.R.
d4444db6-e48d-4f18-b379-9b18a444d226
Guthrie, R.D.
e0fed28e-4847-4751-8392-22d798f4701c
Magovern, J.A.
b9b8dc11-4884-40b8-9858-761454c15ee6
Becich, M.J.
7bf0df0a-2a98-4a8e-a266-c51d6fe94218
17 January 2007
LaFramboise, W.A.
3d4885e7-9c4e-4b43-94f1-6fdbd4a192eb
Scalise, D.
827caf5c-0762-4bc9-b775-f835a4b256aa
Stoodley, P.
08614665-92a9-4466-806e-20c6daeb483f
Graner, S.R.
d4444db6-e48d-4f18-b379-9b18a444d226
Guthrie, R.D.
e0fed28e-4847-4751-8392-22d798f4701c
Magovern, J.A.
b9b8dc11-4884-40b8-9858-761454c15ee6
Becich, M.J.
7bf0df0a-2a98-4a8e-a266-c51d6fe94218
LaFramboise, W.A., Scalise, D., Stoodley, P., Graner, S.R., Guthrie, R.D., Magovern, J.A. and Becich, M.J.
(2007)
Cardiac fibroblasts influence cardiomyocyte phenotype in vitro.
American Journal of Physiology: Cell Physiology, 292 (5), .
(doi:10.1152/ajpcell.00166.2006).
Abstract
Cardiac fibroblasts impact myocardial development and remodeling through intercellular contact with cardiomyocytes, but less is known about noncontact, profibrotic signals whereby fibroblasts alter cardiomyocyte behavior. Fibroblasts and cardiomyocytes were harvested from newborn rat ventricles and separated by serial digestion and gradient centrifugation. Cardiomyocytes were cultured in 1) standard medium, 2) standard medium diluted 1:1 with PBS, or 3) standard medium diluted 1:1 with medium conditioned > or =72 h by cardiac fibroblasts. Serum concentrations were held constant under all media conditions, and complete medium exchanges were performed daily. Cardiomyocytes began contracting within 24 h at clonal or mass densities with <5% of cells expressing vimentin. Immunocytochemical analysis revealed progressive expression of alpha-smooth muscle actin in cardiomyocytes after 24 h in all conditions. Only cardiomyocytes in fibroblast-conditioned medium stopped contracting by 72 h. There was a significant, sustained increase in vimentin expression specific to these cultures (means +/- SD: conditioned 46.3 +/- 6.0 vs. control 5.3 +/- 2.9%, P < 0.00025) typically with cardiac myosin heavy chain coexpression. Proteomics assays revealed 10 cytokines (VEGF, GRO/KC, monocyte chemoattractant protein-1, leptin, macrophage inflammatory protein-1alpha, IL-6, IL-10, IL-12p70, IL-17, and tumor necrosis factor-alpha) at or below detection levels in unconditioned medium that were significantly elevated in fibroblast-conditioned medium. Latent transforming growth factor-beta and RANTES were present in unconditioned medium but rose to higher levels in conditioned medium. Only granulocyte-macrophage colony-stimulating factor was present above threshold levels in standard medium but decreased with fibroblast conditioning. These data indicated that under the influence of fibroblast-conditioned medium, cardiomyocytes exhibited marked hypertrophy, diminished contractile capacity, and phenotype plasticity distinct from the dedifferentiation program present under standard culture conditions.
This record has no associated files available for download.
More information
Published date: 17 January 2007
Keywords:
proteomics, myosin heavy chain, vimentin, myofibroblast, primary culture, dedifferentiation, plasticity
Organisations:
Engineering Mats & Surface Engineerg Gp
Identifiers
Local EPrints ID: 157165
URI: http://eprints.soton.ac.uk/id/eprint/157165
ISSN: 0363-6143
PURE UUID: a19b59dc-01ee-43ec-8338-6bb49c453a78
Catalogue record
Date deposited: 07 Jun 2010 08:48
Last modified: 14 Mar 2024 02:55
Export record
Altmetrics
Contributors
Author:
W.A. LaFramboise
Author:
D. Scalise
Author:
S.R. Graner
Author:
R.D. Guthrie
Author:
J.A. Magovern
Author:
M.J. Becich
Download statistics
Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.
View more statistics