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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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