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Curr Opin Nephrol Hypertens. 2012 Mar;21(2):122-7. doi: 10.1097/MNH.0b013e3283503ce9.

Novel tyrosine kinase signaling pathways: implications in vascular remodeling.

Author information

1
Department of Medicine, Aab Cardiovascular Research Institute, University of Rochester School of Medicine and Dentistry, Rochester, New York, USA.

Abstract

PURPOSE OF REVIEW:

This review summarizes the recent advances in molecular mechanisms by which five classes of receptor tyrosine kinases (RTKs) contribute to vascular remodeling.

RECENT FINDINGS:

Recent findings have expanded our knowledge regarding RTK regulation. In particular, G-protein-coupled receptors, mineralocorticoid receptors, mechanical and oxidative stresses transactivate RTKs. These receptors are highly interactive with many downstream targets (including tyrosine kinases and other RTKs) and function as key regulatory nodes in a dynamic signaling network. Interactions between vascular and nonvascular (immune and neuronal) cells are controlled by RTKs in vascular remodeling. Inhibition of RTKs could be an advantageous therapeutic strategy for vascular disorders.

SUMMARY:

RTK-dependent signaling is important for regulation of key functions during vascular remodeling. However, current challenges are related to integration of the data on multiple RTKs in vascular pathology.

PMID:
22240445
PMCID:
PMC3609430
DOI:
10.1097/MNH.0b013e3283503ce9
[Indexed for MEDLINE]
Free PMC Article

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