Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2563938 | Pharmacology & Therapeutics | 2008 | 25 Pages |
Abstract
The nerve growth factor (NGF) belongs to the neurotrophin family and induces its effects through activation of 2 distinct receptor types: the tropomyosin-related kinase A (TrkA) receptor, carrying an intrinsic tyrosine kinase activity in its intracellular domain, and the receptor p75 for neurotrophins (p75NTR), belonging to the death receptor family. Through activation of its TrkA receptor, NGF activates signalling pathways, including phospholipase Cγ (PLCγ), phosphatidyl-inositol 3-kinase (PI3K), the small G protein Ras, and mitogen-activated protein kinases (MAPK). Through its p75NTR receptor, NGF activates proapoptotic signalling pathways including the MAPK c-Jun N-terminal kinase (JNK), ceramides, and the small G protein Rac, but also activates pathways promoting cell survival through the transcription factor nuclear factor-κB (NF-κB). NGF was first described by Rita Levi-Montalcini and collaborators as an important factor involved in nerve differentiation and survival. Another role for NGF has since been established in inflammation, in particular of the airways, with increased NGF levels in chronic inflammatory diseases. In this review, we will first describe NGF structure and synthesis and NGF receptors and their signalling pathways. We will then provide information about NGF in the airways, describing its expression and regulation, as well as pointing out its potential role in inflammation, hyperresponsiveness, and remodelling process observed in airway inflammatory diseases, in particular in asthma.
Keywords
CREBEGFRNF-κBPI3KMMPEGFJnkCREMEF2MAGEbFGFEPOERKMAGCRDSHCNGFIP3CGRPGPCRAP-1ARMSPACAPp75NTRPKCinositol triphosphateIAPIKKAP-2GM-CSFPLCγEEA1PDZSOSSCFPKBPDGFOMgpTEFIFNγVDRGRB-2PDK1SH2TRAFTRPV-1SH3BH3CSF-1Bcl-2 homology domain 3APPLTrkA receptorMAPKKColony-stimulating factor-1Phosphatidyl-inositol 3-kinaseMelanoma-associated antigensFap-1GIPCCalcitonin gene-related proteinTGF-βA Disintegrin And Metalloprotease DomainPAI-ICAAT/enhancer binding proteinMKKKSC-1BDNFC/EBPc-Jun N-terminal kinaseIκB kinaseMAPKADAMAsthmaearly endosome antigen 1eosinophil peroxidaseAirway inflammationinterferon γinterleukinremodellingtransforming growth factor-βTrktropomyosin-related kinasetumor necrosis factor-αSrc homology domain 2Src homology domain 3diacylglycerolRaf kinaseDAGepidermal growth factorIRAKcAMP responsive elementtumor necrosis factor receptor-associated factorVascular endothelial growth factorVascular Endothelial Growth Factor (VEGF)platelet-derived growth factornerve growth factorbasic fibroblast growth factorStem Cell FactorBrain-derived neurotrophic factorTNF-αnuclear factor κBphospholipase Cγactivating protein 1granulocyte macrophage-colony stimulating factorMetalloproteaseMEKNRAGEinhibitor of apoptosisNadENeurotrophinHyperresponsivenesscAMP responsive element binding proteinProtein kinase Cmitogen-activated protein kinaseextracellular-regulated protein kinasemitogen-activated protein kinase kinasemitogen-activated protein kinase kinase kinaseson of sevenlesspituitary adenylate cyclase-activating peptideCARDInterleukin-1 receptor-associated kinaseMyelin-associated glycoproteinOligodendrocyte myelin glycoproteinCRIBEpidermal growth factor receptorvitamin D3 receptorG protein-coupled receptor
Related Topics
Health Sciences
Pharmacology, Toxicology and Pharmaceutical Science
Pharmacology
Authors
V. Freund-Michel, N. Frossard,