Protein kinase D1, a new molecular player in VEGF signaling and angiogenesis

被引:21
作者
Ha, Chang Hoon
Jin, Zheng Gen [1 ]
机构
[1] Univ Rochester, Sch Med & Dent, Aab Cardiovasc Res Inst, Rochester, NY 14627 USA
关键词
angiogenesis; CAMK; endothelial cells; HDAC; MEF2; migration; PKC; PKD; VEGF; ENDOTHELIAL-GROWTH-FACTOR; PLECKSTRIN HOMOLOGY DOMAIN; INTESTINAL EPITHELIAL-CELLS; RECEPTOR TYROSINE KINASE; ACTIVATION LOOP SER(744); PHORBOL ESTER BINDING; TRANS-GOLGI NETWORK; C-DEPENDENT PATHWAY; D PKD ACTIVATION; TRANSDUCTION PATHWAY;
D O I
10.1007/s10059-009-0109-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vascular endothelial growth factor (VEGF) is essential for many angiogenic processes both in normal and pathological conditions. However, the signaling pathways involved in VEGF-induced angiogenesis are incompletely understood. The protein kinase D1 (PKD1), a newly described calcium/calmodulin-dependent serine/threonine kinase, has been implicated in cell migration, proliferation and membrane trafficking. Increasing evidence suggests critical roles for PKD1-mediated signaling pathways in endothelial cells, particularly in the regulation of VEGF-induced angiogenesis. Recent studies show that class IIa histone deacetylases (HDACs) are PKD1 substrates and VEGF signal-responsive repressors of myocyte enhancer factor-2 (MEF2) transcriptional activation in endothelial cells. This review provides a guide to PKD1 signaling pathways and the direct downstream targets of PKD1 in VEGF signaling, and suggests important functions of PKD1 in angiogenesis.
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页码:1 / 5
页数:5
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