📗 Cite This Artifact
ACVR2B Gene
ACVR2B Gene
<div class="infobox infobox-gene">
| Property | Value |
|----------|-------|
| Gene Symbol | ACVR2B |
| Full Name | Activin A Receptor Type 2B |
| Chromosomal Location | 3p22.2 |
| NCBI Gene ID | 102 |
| OMIM ID | 602730 |
| Ensembl ID | ENSG00000121905 |
| UniProt ID | Q13705 |
| Encoded Protein | Activin receptor type-2B |
| Protein Family | TGF-beta receptor type II family |
| Molecular Weight | ~60 kDa |
| Tissue Expression | Brain, heart, lung, liver, skeletal muscle |
</div>
Overview
ACVR2B (Activin A Receptor Type 2B) encodes a type I serine/threonine kinase receptor that binds activin and other TGF-beta superfamily ligands. ACVR2B is a component of the larger TGF-beta signaling network, which plays essential roles in embryonic development, tissue homeostasis, and cellular function throughout the nervous system. The TGF-beta superfamily includes activins, inhibins, BMPs (bone morphogenetic proteins), and Nodal, each with distinct and overlapping functions [@acvr2b_tgfbeta].
ACVR2B functions as a type II receptor, meaning it binds ligand directly and initiates signaling by recruiting and phosphorylating type I receptors (also called ALKs - activin receptor-like kinases). The activated type I receptor then phosphorylates receptor-regulated SMADs (R-SMADs), which translocate to the nucleus to regulate gene expression. For activin signaling, the primary pathway involves SMAD2 and SMAD3, which form complexes with SMAD4 to regulate transcription [@acvr2b_smads].
ACVR2B Gene
<div class="infobox infobox-gene">
| Property | Value |
|----------|-------|
| Gene Symbol | ACVR2B |
| Full Name | Activin A Receptor Type 2B |
| Chromosomal Location | 3p22.2 |
| NCBI Gene ID | 102 |
| OMIM ID | 602730 |
| Ensembl ID | ENSG00000121905 |
| UniProt ID | Q13705 |
| Encoded Protein | Activin receptor type-2B |
| Protein Family | TGF-beta receptor type II family |
| Molecular Weight | ~60 kDa |
| Tissue Expression | Brain, heart, lung, liver, skeletal muscle |
</div>
Overview
ACVR2B (Activin A Receptor Type 2B) encodes a type I serine/threonine kinase receptor that binds activin and other TGF-beta superfamily ligands. ACVR2B is a component of the larger TGF-beta signaling network, which plays essential roles in embryonic development, tissue homeostasis, and cellular function throughout the nervous system. The TGF-beta superfamily includes activins, inhibins, BMPs (bone morphogenetic proteins), and Nodal, each with distinct and overlapping functions [@acvr2b_tgfbeta].
ACVR2B functions as a type II receptor, meaning it binds ligand directly and initiates signaling by recruiting and phosphorylating type I receptors (also called ALKs - activin receptor-like kinases). The activated type I receptor then phosphorylates receptor-regulated SMADs (R-SMADs), which translocate to the nucleus to regulate gene expression. For activin signaling, the primary pathway involves SMAD2 and SMAD3, which form complexes with SMAD4 to regulate transcription [@acvr2b_smads].
In the nervous system, ACVR2B-mediated signaling regulates neural development, synaptic plasticity, neurogenesis, and neuroprotection. Dysregulation of activin/ACVR2B signaling is implicated in Alzheimer's disease, Parkinson's disease, and other neurodegenerative conditions, making it a subject of significant research interest [@acvr2b_ad].
Function
Receptor Structure and Activation
ACVR2B is a transmembrane receptor composed of extracellular, transmembrane, and intracellular kinase domains [@acvr2b_receptors]:
Extracellular Domain
- Ligand binding domain (~200 amino acids)
- Contains cysteine residues for disulfide bonds
- N-glycosylation sites for proper folding
Transmembrane Domain
- Single pass through the membrane
- anchors receptor in plasma membrane
- Connects extracellular and intracellular domains
Intracellular Domain
- Serine/threonine kinase domain
- C-terminal tail with regulatory sites
- Multiple phosphorylation sites
Activation Mechanism
SMAD Signaling
The primary downstream effectors of ACVR2B are SMAD2 and SMAD3 [@acvr2b_smads]:
SMAD2/3 Activation
- Type I receptor phosphorylates SMAD2/3 at C-terminal serines
- Phosphorylated SMADs form complexes with SMAD4
- Complexes translocate to the nucleus
Transcriptional Regulation
SMAD complexes regulate gene expression by:
- Binding to SMAD-binding elements (SBEs)
- Recruiting co-activators or co-repressors
- Chromatin remodeling
SMAD7 Feedback
SMAD7 is an inhibitory SMAD that provides negative feedback [@acvr2b_smad7]:
- Competes with SMAD2/3 for type I receptor binding
- Recruits ubiquitin ligases for receptor degradation
- Fine-tunes signaling intensity
Neural Development
ACVR2B signaling is crucial for multiple aspects of neural development [@acvr2b_development]:
Neurogenesis
- Regulates neural progenitor cell proliferation
- Controls differentiation timing
- Promotes neuronal commitment
Neuronal Migration
- Guides neuronal migration during cortical development
- Controls radial migration
- Regulates tangential migration
Axon Guidance
- Provides guidance cues for developing axons
- Responds to extracellular gradients
- Controls pathfinding decisions
Synaptogenesis
- Regulates synapse formation
- Controls synaptic connectivity
- Establishes appropriate circuits
Synaptic Plasticity
ACVR2B signaling modulates synaptic plasticity in the adult brain [@acvr2b_synapse]:
Long-Term Potentiation (LTP)
- Activin enhances LTP in hippocampus
- ACVR2B is required for LTP maintenance
- SMAD signaling participates in LTP consolidation
Long-Term Depression (LTD)
- Activin modulates LTD induction
- ACVR2B regulates AMPA receptor trafficking
- Participates in depression mechanisms
Synaptic Structure
- Controls dendritic spine morphology
- Regulates spine density
- Modulates synaptic stability
Hippocampal Function
ACVR2B is highly expressed in the hippocampus where it regulates [@acvr2b_hippocampus]:
Memory Formation
- Required for spatial memory
- Involved in contextual memory
- Supports consolidation
Adult Neurogenesis
- Promotes NPC proliferation in dentate gyrus
- Controls differentiation
- Supports new neuron integration
Circuit Function
- Modulates CA3-CA1 connectivity
- Regulates entorhinal cortical inputs
- Controls inhibitory/excitatory balance
Neuroprotection
ACVR2B signaling has neuroprotective properties:
Survival Promotion
- Activin promotes neuronal survival
- ACVR2B mediates anti-apoptotic effects
- Protects against excitotoxicity
Oxidative Stress
- Reduces oxidative damage
- Enhances antioxidant defenses
- Protects mitochondria
Inflammation Modulation
- Regulates neuroinflammatory responses
- Controls microglial activation
- Reduces cytokine production
Disease Associations
Alzheimer's Disease
ACVR2B is relevant to Alzheimer's disease through multiple mechanisms [@acvr2b_ad]:
TGF-beta Signaling Dysregulation
- TGF-beta signaling is altered in AD brain
- Activin levels are changed in AD
- ACVR2B expression may be affected
Neuroprotection
- Activin/ACVR2B is neuroprotective against Aβ toxicity
- Loss of signaling may increase vulnerability
- Restoring signaling may be therapeutic
Synaptic Function
- Activin modulates synaptic plasticity in AD
- ACVR2B signaling is impaired
- Contributes to synaptic failure
Neuroinflammation
- Activin regulates inflammatory responses
- ACVR2B dysfunction may exacerbate inflammation
Parkinson's Disease
ACVR2B has connections to Parkinson's disease [@acvr2b_pd]:
Dopaminergic Neurons
- ACVR2B is expressed in substantia nigra
- Activin promotes dopaminergic neuron survival
- Loss of signaling may contribute to degeneration
α-Synuclein
- TGF-beta signaling interacts with α-synuclein
- ACVR2B may affect aggregation
- Protective effects against toxicity
Neuroinflammation
- Activin modulates microglial activation
- May influence inflammatory environment
Amyotrophic Lateral Sclerosis
ACVR2B has relevance to ALS:
- Motor neuron survival
- Glial interactions
- [Neuroinflammation](/mechanisms/neuroinflammation)
Stroke and CNS Injury
ACVR2B is protective in CNS injury:
- Ischemic damage
- Traumatic injury
- Potential for regeneration
Expression
Tissue Distribution
ACVR2B is expressed in many tissues:
- Brain (neurons, glia)
- Heart
- Lung
- Liver
- Skeletal muscle
- Kidney
Brain Expression
In the brain, ACVR2B is expressed in:
Neurons
- Pyramidal neurons in cortex
- Hippocampal neurons (CA1, CA3, dentate gyrus)
- Dopaminergic neurons in substantia nigra
- Cerebellar Purkinje cells
Glia
- Astrocytes [@acvr2b_astrocyte]- [Oligodendrocytes](/cell-types/oligodendrocytes)r2b_microglia]
- [Oligodendrocytes](/cell-types/oligodendrocytes)
Subcellular Localization
- Plasma membrane: Primary receptor location
- Endosomes: Signaling compartments
- Nucleus: Some SMAD-dependent nuclear localization
Regulation
ACVR2B expression is regulated:
- Transcription: Activity-dependent
- Post-translation: Receptor internalization and degradation
- Signaling: Feedback regulation
Signaling Pathways
Primary Pathway
ACVR2B activates the canonical SMAD pathway:
Cross-Talk
ACVR2B signaling intersects with other pathways [@acvr2b_bmp]:
BMP Signaling
- Shared SMAD4
- Competition and cooperation
- Balanced regulation
MAPK Pathways
- ERK activation
- JNK/p38 modulation
- Non-SMAD pathways
PI3K/AKT
- AKT can be activated
- Survival signaling
- Cross-inhibition
Non-SMAD Pathways
ACVR2B can signal through non-SMAD mechanisms:
- MAPK activation
- PI3K signaling
- Calcium signaling
Mechanisms in Neurodegeneration
Loss of Neuroprotection
In neurodegeneration, reduced ACVR2B signaling contributes to:
Synaptic Dysfunction
ACVR2B signaling is important for synaptic function, and its loss contributes to:
- Reduced plasticity
- Spine loss
- Transmission deficits
Neuroinflammation
Dysregulated ACVR2B signaling may contribute to:
- Increased inflammation
- Microglial activation
- Cytokine production
Impaired Regeneration
ACVR2B signaling is important for neural repair [@acvr2b_regeneration]:
- Reduced regeneration capacity
- Impaired repair
- Limited recovery
Therapeutic Implications
ACVR2B signaling represents a potential therapeutic target:
Activin Agonists
Receptor Modulation
SMAD Modulation
Challenges
- Delivery to the brain
- Receptor specificity
- Off-target effects
- Dose optimization
Key Publications
Mechanism Map
See Also
- [Alzheimer's Disease](/diseases/alzheimers-disease)
- [Parkinson's Disease](/diseases/parkinsons-disease)
- [TGF-beta Signaling](/mechanisms/ad-neuroinflammation-microglia-pathway)
- [Synaptic Plasticity](/mechanisms/activity-dependent-synaptic-plasticity)
- [Adult Neurogenesis](/mechanisms/adult-neurogenesis-neurodegeneration)
External Links
- [NCBI Gene: ACVR2B](https://www.ncbi.nlm.nih.gov/gene/102)
- [Ensembl: ENSG00000121905](https://www.ensembl.org/Homo_sapiens/Gene/Summary?g=ENSG00000121905)
- [UniProt: Q13705](https://www.uniprot.org/uniprot/Q13705)
- [GeneCards: ACVR2B](https://www.genecards.org/cgi-bin/carddisp.pl?gene=ACVR2B)
- [OMIM: ACVR2B](https://omim.org/entry/602730)
- [Allen Brain Atlas: ACVR2B](https://human.brain-map.org/microarray/search/show?search_term=ACVR2B)
References
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | genes-acvr2b |
| kg_node_id | ACVR2B |
| entity_type | gene |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-21d5b8af0a4c |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'genes-acvr2b'} |
| _schema_version | 1 |
No provenance edges found
Use ?embed=1 to load the artifact without SciDEX chrome — suitable for iframing into wiki pages or external sites.
<iframe src="http://scidex.ai/artifact/wiki-genes-acvr2b?embed=1" width="100%" height="600" style="border:0;border-radius:8px"></iframe>
[ACVR2B Gene](http://scidex.ai/artifact/wiki-genes-acvr2b)
http://scidex.ai/artifact/wiki-genes-acvr2b