Defining the Developmental Signals of the Cardiac Fibroblast
type: CreativeWork
description: Cardiac fibroblasts play a central role as a mediator of inflammatory and fibrotic response and also secrete extracellular matrix components that provide structural support for regeneration and remodeling of the wound. Despite the importance of the cardiac fibroblast in heart disease, very little is known about factors that are essential for differentiation along the cardiac fibroblast lineage. Using a combination of gene knockout and cardiac fibroblast-detecting methods, we have identified genes that are involved in the formation of cardiac fibroblasts. Our results demonstrate that in the absence of Tcf21, a basic helix-loop-helix transcription factor, cardiac fibroblast progenitors fail to migrate into the myocardium resulting in a specific loss of the cardiac fibroblast population. Loss of the receptor tyrosine kinase Pdgfra also results in loss of the cardiac fibroblast population. Interestingly, Tcf21 and Pdgfra are involved in the epithelial to mesenchymal transition (EMT) of epicardial cells. The epicardium (outer surface of the heart) functions as a pool of progenitor cells for the coronary vasculature and interstitial connective tissue during embryonic development. Although several signaling pathways have been identified that disrupt EMT, no component has been reported that negatively regulates EMT, which may also involved in the cardiac fibroblast development. Using a conditional knockout of neurofibromin 1 (Nf1) in the epicardium, we identified Nf1 as a key mediator of epicardial EMT. We found that the process of EMT occurred earlier in Nf1 mutant hearts, with an increase in epicardial cells entering the compact myocardium. Moreover, loss of Nf1 caused increased epicardial-derived cell proliferation and resulted in the expansion of cardiac fibroblasts and coronary vascular smooth muscle cells. In addition to revealing the function of Nf1, Tcf21 and Pdgfra in epicardial EMT and cardiac fibroblast development, we generated and established mouse models to st…
abstract: Cardiac fibroblasts play a central role as a mediator of inflammatory and fibrotic response and also secrete extracellular matrix components that provide structural support for regeneration and remodeling of the wound. Despite the importance of the cardiac fibroblast in heart disease, very little is known about factors that are essential for differentiation along the cardiac fibroblast lineage. Using a combination of gene knockout and cardiac fibroblast-detecting methods, we have identified genes that are involved in the formation of cardiac fibroblasts. Our results demonstrate that in the absence of Tcf21, a basic helix-loop-helix transcription factor, cardiac fibroblast progenitors fail to migrate into the myocardium resulting in a specific loss of the cardiac fibroblast population. Loss of the receptor tyrosine kinase Pdgfra also results in loss of the cardiac fibroblast population. Interestingly, Tcf21 and Pdgfra are involved in the epithelial to mesenchymal transition (EMT) of epicardial cells. The epicardium (outer surface of the heart) functions as a pool of progenitor cells for the coronary vasculature and interstitial connective tissue during embryonic development. Although several signaling pathways have been identified that disrupt EMT, no component has been reported that negatively regulates EMT, which may also involved in the cardiac fibroblast development. Using a conditional knockout of neurofibromin 1 (Nf1) in the epicardium, we identified Nf1 as a key mediator of epicardial EMT. We found that the process of EMT occurred earlier in Nf1 mutant hearts, with an increase in epicardial cells entering the compact myocardium. Moreover, loss of Nf1 caused increased epicardial-derived cell proliferation and resulted in the expansion of cardiac fibroblasts and coronary vascular smooth muscle cells. In addition to revealing the function of Nf1, Tcf21 and Pdgfra in epicardial EMT and cardiac fibroblast development, we generated and established mouse models to st…
author: Baek, Seung Tae
language: en
keywords: Cell Proliferation, Epithelial-mesenchymal transition, Pericardium
date published: 2012-12-21T16:31:07Z
date modified: 2026-07-24T05:52:31Z
provider: University of Texas Southwestern Medical Center
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: University of Texas Southwestern Medical Center

PropertyValue
property ID: Handle
value: https://hdl.handle.net/2152.5/1213