Copyright © 2007, European Society of Cardiology
ERK signaling is a central regulator for BMP-4 dependent capillary sprouting
aDepartment of Cardiology, University of Freiburg, Germany
bDivision of Cardiology, Carolina Cardiovascular Biology Center, Chapel Hill, NC, USA
*Corresponding author. Department of Cardiology, University of Freiburg, Hugstetterstr. 55, 79106 Freiburg, Germany. Tel.: +49 761 270 3401; fax: +49 761 270 3254. moserm{at}medizin.ukl.uni-freiburg.de
Objective Bone Morphogenetic Protein-4 (BMP-4) and Extracellular-Signal Regulated Kinases (ERK) play crucial roles in vascular diseases. Here, we demonstrate that BMP-4 not only signals through the classical Smad cascade but also activates ERK phosphorylation as an alternative pathway in human umbilical vein endothelial cells (HUVEC) and that Smad and ERK pathways communicate through signal crosstalk.
Methods HUVECs were treated with BMP-4 and/or MEK inhibitors. Smad 6 and constitutively active (ca) MEK1 were overexpressed. Loss of function of Smad 4 and Smad 6 was achieved by specific siRNA transfection. Cell lysates were analyzed by western blotting for Smad and ERK phosphorylation. HUVEC spheroids were generated for angiogenesis quantification.
Results Treatment with BMP-4 results in a dose- and time-dependent activation of the MEK–ERK 1/2 pathway in addition to activation of the Smad pathway and is blocked by MEK inhibitors. Quantitative in-gel angiogenesis assays in the presence or absence of MEK inhibitors demonstrate that ERK signals are necessary for BMP-4 induced capillary sprouting. Furthermore sprouting is not blocked by inhibition of the Smad signaling pathway. Overexpression of the inhibitory Smad 6 inhibits ERK phosphorylation and ERK-induced capillary sprouting, whereas loss of function of Smad 4 has no effect.
Conclusions We demonstrate that ERK1/2 functions as an alternative pathway in BMP-4 signaling in HUVECs. Capillary sprouting induced by BMP-4 is dependent on ERK phosphorylation. ERK is essential for efficient transduction of BMP signals and serves as a positive feedback mechanism. On the other hand, stimulation of Smad 6 inhibits ERK activation and thus results in a negative feedback loop to fine-tune BMP signaling in HUVECs.
KEYWORDS BMP-4 ERK 1/2; In-gel angiogenesis; HUVEC; Signal transduction
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  T. Helbing, F. Volkmar, U. Goebel, J. Heinke, P. Diehl, H. L. Pahl, C. Bode, C. Patterson, and M. Moser Kruppel-like factor 15 regulates BMPER in endothelial cells Cardiovasc Res, October 18, 2009; (2009) cvp314v2. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 K. Kunimasa, M.-R. Ahn, T. Kobayashi, R. Eguchi, S. Kumazawa, Y. Fujimori, T. Nakano, T. Nakayama, K. Kaji, and T. Ohta Brazilian Propolis Suppresses Angiogenesis by Inducing Apoptosis in Tube-forming Endothelial Cells through Inactivation of Survival Signal ERK1/2 Evid. Based Complement. Altern. Med., April 7, 2009; (2009) nep024v1. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. Heinke, L. Wehofsits, Q. Zhou, C. Zoeller, K.-M. Baar, T. Helbing, A. Laib, H. Augustin, C. Bode, C. Patterson, et al. BMPER Is an Endothelial Cell Regulator and Controls Bone Morphogenetic Protein-4-Dependent Angiogenesis Circ. Res., October 10, 2008; 103(8): 804 - 812. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. T. Holderfield and C. C.W. Hughes Crosstalk Between Vascular Endothelial Growth Factor, Notch, and Transforming Growth Factor-{beta} in Vascular Morphogenesis Circ. Res., March 28, 2008; 102(6): 637 - 652. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. T. Rizzo ERK and Smads: Getting together for angiogenic sprouting Cardiovasc Res, December 1, 2007; 76(3): 375 - 376. [Full Text] [PDF]
|
|