Cell Signaling & Neuroscience
Angiopoietins & Receptors
Slides
Programmed Cell Death
Activation and Inhibition of Apoptosis
Mitochondria in Apoptosis
ATM/p53 Signaling Pathway
Caspase Cascade
Caspase Activation Intrinsic Pathway
Granzyme B
FAS and Related Proteins
Fas Signaling
G1, and S Phases
G2 and M Phases
Regulatory Cascade
The p53 Signaling Pathway
Cytokines and Growth Factors
Structures of Activin and Inhibin
Structures of Chemokine Receptors
Angiopoietins
EGFR Signaling Pathway
Transmembrane Precursors of EGF
Possible Receptor Combos and Ligand
Actions of Flt-3/Flk-2
Hedgehog and BMI1
IGF Regulation of Apoptosis
IL-13 and IL-4 receptor
IL-18 Production
Neurotrophins and Their Receptors
TrkA
GDNF Family with Receptors
PDGF Receptors and Actions
TGF-beta Signaling
BMP Signaling
TNF Signaling
TNF-α and TNF-β
Proposed Balance Between TNF Superfamily
Structure of Receptors
VEGF Receptor and Ligands
Prolactin Regulation
Insulin Pathway
Glucocorticoid Receptor Signaling
Vascular Endothelial Cell Interactions
Integrin Signaling in Cell Survival
VEGF Receptor Signaling
MMPs and Cytokines
Events Leading to Angiogenesis
Transcription Factors
Nuclear Complex Targeting
Jak/Stat Pathway
STAT3
PPAR
Formation of Nucleosomes
DNA Compaction
Early Response Events
Cell Cycle Checkpoint
Linkage between DNA Repair and Chromatin Modification
Functions of WRN, BLM and MRE11
mRNP Transport
Importinα - Importinβ Pathway
Modular Structure of Transcription factors
Transcription Activation by Nuclear Receptors
Coupled RNA Splicing and Nuclear Export
RNA Polyadenylation
Mammalian mRNA Polyadenylation
RNA Maturation
Epigenetic Control
Phosphorylation-driven Initiation-Elongation
cAMP Metabolism
cGMP Metabolism
G-Protein Signaling
T Cell Receptor
B Cell Receptor
Monovalent Ion Channels
Activation/Inactivation
Ligand-Gated Ion Channel
Aquaporin Channel Structure
Calcium Channel Structure
Calcium Channel Pore Region
Chloride Channel
HCN Channel
2TM Potassium Channel Structure
6TM Potassium Channel Structure
Sodium Channel Structure
Sodium Channel Pore Region
PTEN Pathway
Lipids in Cell Signaling
Inositol Phosphates
Phosphatidic Acid
Inositol Phospholipids
ABC Transporters
ABC-ATPases
BSEP
MRP1
β-Amyloid Plaques
Notch Secretase
Second Messenger Systems
Limbic Reward Circuit
Major Pathways in the CNS
Endothelin Signaling
NPY and Catecholamines
Ascending Pain Pathway
Modulation of Pain Transmission
Mechanism of Action Fig. A
Mechanism of Action Fig. B
Drug Activation of Dopaminergic
GABAB Receptor
Oxidative Stress
nNOS
eNOS
iNOS
Nitric Oxide
Proteasome/Ubiquitination
Formation of Activated 20S Proteasome
Ubiquitin Pathway
MAP Kinase Cascades
AKT Signaling
Pathways Activated by VEGF
Angiopoietins and their receptors, Tie1 and Tie2
The angiopoietins were originally discovered as ligands for Tie receptors, a family of receptor tyrosine kinases (RTKs) that are selectively expressed within the vascular endothelium. + or - indicates either activation or antagonism of the Tie2 receptor by the individual angiopoietins. Potential interactions between the Tie1 receptor and the various angiopoietins have not yet been confirmed.
The Eph RTKs compromise the largest known family of growth factor receptors and are bound by the large family of ephrin ligands. The ephrins must be tethered to the membrane in order to activate their respective Eph receptors. Thus, they mediate cell:cell interactions. The signaling cascade can go both through the ligand and through the receptor. Only the several members that have been shown to be involved in vascular growth are displayed.
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References:
Beecken, W.D., et al., New molecular mediators in tumor angiogenesis. J. Cell. Mol. Med., 4 , 262-269 (2000).
Cheng, N., et al., The ephrins and Eph receptors in Angiogenesis. Cytokine Growth Factor Rev., 13 , 75-85 (2002).
Partanen, J., and Dumont, D.J., Functions of Tie1 and Tie2 receptor tyrosine kinases in vascular development. Curr. Top. Microbiol. Immunol., 237 , 159-172 (1999).