TY - JOUR
T1 - Regulation of cardiac fibroblast cellular function by leukemia inhibitory factor
AU - Wang, Feng
AU - Trial, Jo Ann
AU - Diwan, Abhinav
AU - Gao, Feng
AU - Birdsall, Holly
AU - Entman, Mark
AU - Hornsby, Peter
AU - Sivasubramaniam, Natarajan
AU - Mann, Douglas
N1 - Funding Information:
The authors gratefully acknowledge the technical assistance of Dorellyn Lee-Jackson and the secretarial assistance of Ms Mary Helen Soliz. We would also like to thank Dr Andrew I. Schafer for his past and present support and guidance. This research was supported by research funds from the N.I.H. (P50 HL-O6H and RO1 HL58081-01, RO1 HL61543-01, HL-42250-10/10).
PY - 2002/10/1
Y1 - 2002/10/1
N2 - Background: Previous studies have shown that leukemia inhibitory factor (LIF) provokes hypertrophic and cytoprotective effects in cardiac myocytes. However, the effects of LIF in cardiac fibroblasts are not known. Given that the cardiac fibroblast is the most abundant cell type in the heart, we sought to examine the functional effects of LIF on cardiac fibroblasts in vitro. Results: Short-term LIF stimulation (24h) had no effect on fibroblast proliferation and/or cell differentiation. However, longer-term LIF stimulation (48-72 h) increased fibroblast proliferation, and significantly inhibited cardiac fibroblast differentiation into myofibroblasts. Moreover. 72 h of LIF stimulation significantly reduced collagen content in cardiac fibroblasts cultures, as well as decreased MMP activity in fibroblast culture supernatants. Conclusion: The results of this study suggest that LIF stimulation down-regulates several key components of the remodeling process, including collagen content and matrix metalloproteinase (MMP) activation, and thus suggest that LIF may play an important autocrine/paracrine role in preventing excessive extracellular matrix remodeling following acute myocardial injury.
AB - Background: Previous studies have shown that leukemia inhibitory factor (LIF) provokes hypertrophic and cytoprotective effects in cardiac myocytes. However, the effects of LIF in cardiac fibroblasts are not known. Given that the cardiac fibroblast is the most abundant cell type in the heart, we sought to examine the functional effects of LIF on cardiac fibroblasts in vitro. Results: Short-term LIF stimulation (24h) had no effect on fibroblast proliferation and/or cell differentiation. However, longer-term LIF stimulation (48-72 h) increased fibroblast proliferation, and significantly inhibited cardiac fibroblast differentiation into myofibroblasts. Moreover. 72 h of LIF stimulation significantly reduced collagen content in cardiac fibroblasts cultures, as well as decreased MMP activity in fibroblast culture supernatants. Conclusion: The results of this study suggest that LIF stimulation down-regulates several key components of the remodeling process, including collagen content and matrix metalloproteinase (MMP) activation, and thus suggest that LIF may play an important autocrine/paracrine role in preventing excessive extracellular matrix remodeling following acute myocardial injury.
KW - Cardiac fibroblast
KW - Collagen content
KW - Cytokine
KW - Differentiation
KW - Leukemia inhibitory factor
KW - MMP activity
KW - Proliferation
UR - http://www.scopus.com/inward/record.url?scp=0036772439&partnerID=8YFLogxK
U2 - 10.1016/S0022-2828(02)92059-6
DO - 10.1016/S0022-2828(02)92059-6
M3 - Article
C2 - 12392991
AN - SCOPUS:0036772439
SN - 0022-2828
VL - 34
SP - 1309
EP - 1316
JO - Journal of Molecular and Cellular Cardiology
JF - Journal of Molecular and Cellular Cardiology
IS - 10
ER -