NGF (nerve growth factor) is a critical neurotrophin within the neurotrophin family, which also includes brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), and neurotrophin-4 (NT-4), all of which are secreted proteins essential for the development, survival, and functional maintenance of the nervous system. By binding to specific high-affinity tyrosine kinase receptors (Trk receptors) and the low-affinity p75 neurotrophin receptor, NGF primarily drives the growth, differentiation, and survival of sensory and sympathetic neurons, playing a pivotal role in both embryonic development and adult neural plasticity. Upon binding to its cognate receptor, TrkA, NGF activates downstream signaling cascades such as the PI3K/AKT and MAPK/ERK pathways, which regulate cell survival, axonal outgrowth, and synaptic plasticity. Disruptions in NGF signaling or its receptor pathway are implicated in various neurological conditions; for instance, mutations in the NGF or TrkA genes can lead to congenital insensitivity to pain due to the loss of sensory neurons, while impaired NGF signaling is associated with neurodegenerative disorders like Alzheimer’s disease. Conversely, aberrant overexpression of NGF can contribute to pathological states such as hyperalgesia and the progression of certain malignancies, including neuroblastoma, whereas reduced expression may result in neuronal apoptosis, sensory deficits, or cognitive impairment. Beyond its canonical roles in neurobiology, NGF also participates in immune regulation and inflammatory responses by modulating the function of mast cells and T cells, highlighting its broader physiological significance. The shared characteristics of the neurotrophin family, including their mechanism of action via Trk and p75 receptors and their regulation of neuronal homeostasis, underscore their potential as therapeutic targets for managing neurodegenerative diseases, chronic pain, and psychiatric disorders.
Subcellular localization of NGF (and its protein):
Gene Ontology (GO) terms for NGF:
| Interacting Gene | Interaction | Source/Score |
| Name |
|---|
| 4014 Ras signaling pathway [PATH:hsa04014] |
| 4015 Rap1 signaling pathway [PATH:hsa04015] |
| 4010 MAPK signaling pathway [PATH:hsa04010] |
| 4151 PI3K-Akt signaling pathway [PATH:hsa04151] |
| 4210 Apoptosis [PATH:hsa04210] |
| 4722 Neurotrophin signaling pathway [PATH:hsa04722] |
| 4750 Inflammatory mediator regulation of TRP channels [PATH:hsa04750] |
| Name |
|---|
| Activation of TRKA receptors |
| ARMS-mediated activation |
| Axonal growth stimulation |
| Cell death signalling via NRAGE, NRIF and NADE |
| Ceramide signalling |
| Frs2-mediated activation |
| NADE modulates death signalling |
| NF-kB is activated and signals survival |
| NFG and proNGF binds to p75NTR |
| NGF processing |
| NGF signalling via TRKA from the plasma membrane |
| NRAGE signals death through JNK |
| NRIF signals cell death from the nucleus |
| p75 NTR receptor-mediated signalling |
| p75NTR negatively regulates cell cycle via SC1 |
| p75NTR recruits signalling complexes |
| p75NTR regulates axonogenesis |
| p75NTR signals via NF-kB |
| PI3K/AKT activation |
| PLC-gamma1 signalling |
| Prolonged ERK activation events |
| Retrograde neurotrophin signalling |
| Signalling by NGF |
| Signalling to ERKs |
| Signalling to p38 via RIT and RIN |
| Signalling to RAS |
| Signalling to STAT3 |
| TRKA activation by NGF |
| Disease | Score | NofPmids | NofSnps | Source |
| Hereditary Sensory Autonomic Neuropathy, Type 5 | 0.360814326 | 4 | 1 | BeFree_CLINVAR_ORPHANET_UNIPROT |
| Inflammation | 0.20272435 | 3 | 0 | CTD_human_LHGDN_RGD |
| Cystitis | 0.2 | 2 | 0 | CTD_human_RGD |
| Overactive Bladder | 0.2 | 3 | 0 | CTD_human_RGD |
| Hyperalgesia | 0.2 | 4 | 0 | CTD_human_RGD |
| Glomerulonephritis | 0.12272435 | 2 | 0 | CTD_human_LHGDN |
| Hereditary Sensory and Autonomic Neuropathies | 0.122638474 | 2 | 0 | BeFree_CTD_human_GAD |
| Peripheral Neuropathy | 0.120271442 | 2 | 0 | BeFree_CTD_human |
| Heroin Dependence | 0.120271442 | 2 | 0 | BeFree_CTD_human |
| Neurodegenerative Disorders | 0.120271442 | 2 | 0 | BeFree_CTD_human |
No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong
Qilu Normal University · Genelibs Bioinformatics Lab
750 Shunhua Rd, Jinan
2F, Bldg F, University Science Park
Tel: 0531-88819269
Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.
Business Email
E-mail: product@genelibs.com