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CCL25 Gene
CCL25 (C-C Motif Chemokine Ligand 25)
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">CCL25 Gene</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td>CCL25</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>[6374](https://www.ncbi.nlm.nih.gov/gene/6374)</td>
</tr>
<tr>
<td class="label">Chromosome</td>
<td>19p13.2</td>
</tr>
<tr>
<td class="label">Protein Class</td>
<td>Chemokine</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~9.4 kDa</td>
</tr>
<tr>
<td class="label">Cell Type</td>
<td>Expression Level</td>
</tr>
<tr>
<td class="label">Thymic epithelial cells</td>
<td>High</td>
</tr>
<tr>
<td class="label">Small intestine</td>
<td>High</td>
</tr>
<tr>
<td class="label">Dendritic cells</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Brain</td>
<td>Low</td>
</tr>
<tr>
<td class="label">Astrocytes</td>
<td>Low-Medium</td>
</tr>
<tr>
<td class="label">Microglia</td>
<td>Low</td>
</tr>
<tr>
<td class="label">Endothelial cells</td>
<td>Variable</td>
</tr>
<tr>
<td class="label">Drug</td>
<td>Type</td>
</tr>
<tr>
<td class="label">CCX8037</td>
<td>Oral CCR9 antagonist</td>
</tr>
<tr>
<td class="label">CCX5216</td>
<td>Potent CCR9 antagonist</td>
</tr>
<tr>
<td class="label">Anti-CCL25 mAb</td>
<td>Neutralizing antibody</td>
</tr>
<tr>
<td class="label">GS-5740</td>
<td>Anti-CCL25 antibody<
CCL25 (C-C Motif Chemokine Ligand 25)
<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">CCL25 Gene</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td>CCL25</td>
</tr>
<tr>
<td class="label">NCBI Gene ID</td>
<td>[6374](https://www.ncbi.nlm.nih.gov/gene/6374)</td>
</tr>
<tr>
<td class="label">Chromosome</td>
<td>19p13.2</td>
</tr>
<tr>
<td class="label">Protein Class</td>
<td>Chemokine</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>~9.4 kDa</td>
</tr>
<tr>
<td class="label">Cell Type</td>
<td>Expression Level</td>
</tr>
<tr>
<td class="label">Thymic epithelial cells</td>
<td>High</td>
</tr>
<tr>
<td class="label">Small intestine</td>
<td>High</td>
</tr>
<tr>
<td class="label">Dendritic cells</td>
<td>Moderate</td>
</tr>
<tr>
<td class="label">Brain</td>
<td>Low</td>
</tr>
<tr>
<td class="label">Astrocytes</td>
<td>Low-Medium</td>
</tr>
<tr>
<td class="label">Microglia</td>
<td>Low</td>
</tr>
<tr>
<td class="label">Endothelial cells</td>
<td>Variable</td>
</tr>
<tr>
<td class="label">Drug</td>
<td>Type</td>
</tr>
<tr>
<td class="label">CCX8037</td>
<td>Oral CCR9 antagonist</td>
</tr>
<tr>
<td class="label">CCX5216</td>
<td>Potent CCR9 antagonist</td>
</tr>
<tr>
<td class="label">Anti-CCL25 mAb</td>
<td>Neutralizing antibody</td>
</tr>
<tr>
<td class="label">GS-5740</td>
<td>Anti-CCL25 antibody</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/aging" style="color:#ef9a9a">Aging</a>, <a href="/wiki/alzheimer" style="color:#ef9a9a">Alzheimer</a>, <a href="/wiki/autoimmune" style="color:#ef9a9a">Autoimmune</a>, <a href="/wiki/depression" style="color:#ef9a9a">Depression</a>, <a href="/wiki/inflammation" style="color:#ef9a9a">Inflammation</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">26 edges</a></td>
</tr>
</table>
Overview
CCL25 (C-C Motif Chemokine Ligand 25), also known as Thymus Expressed Chemokine (TECK), is a chemokine originally identified in the thymus that plays crucial roles in T cell development and mucosal immunity. CCL25 binds exclusively to CCR9, making it a unique target for therapeutic modulation. In the nervous system, CCL25/CCR9 signaling has been implicated in neuroinflammation, [gut-brain axis](/entities/gut-brain-axis) communication, and potentially in neurodegenerative diseases["@zabel1999"][@wurbel2001].
Gene Overview
Function
CCL25 has distinct functions in immune development and homeostasis:
Immune System
- T cell development: Critical for thymocyte migration and T cell development in the thymus[@uehara2002]
- Gut homing: Guides α4β7+ T cells to intestinal lamina propria via CCR9
- Mucosal immunity: Important for immune surveillance of gastrointestinal tract
Nervous System
- Neuroinflammation: Modulates inflammatory responses in CNS
- Gut-brain axis: Potential pathway for gut-immune-brain communication
- [Blood-brain barrier](/entities/blood-brain-barrier): May influence BBB function under inflammatory conditions
Receptor
CCL25 has a unique receptor profile:
- CCR9 (CC Chemokine Receptor 9): The sole receptor for CCL25
- Expression: High on small intestinal T cells, thymocytes, and some inflammatory cells
- Alternative: Can also bind to CCR9 splice variants
CCR9 Signaling
CCL25/CCR9 activates characteristic chemokine signaling[@zlotnik2005][@zhou2023]:
CCR9 Expression in Disease
CCR9 is over-expressed in several disease contexts[@mendelsohn2019]:
- Inflammatory bowel disease
- Colorectal cancer metastasis
- Certain leukemias
- Autoimmune conditions
Signaling Pathways
CCL25/CCR9 activates characteristic chemokine signaling:
CCL25/CCR9 in the Gut-Brain Axis
The CCL25/CCR9 axis plays a significant role in the gut-brain communication pathway, which has emerged as a critical factor in neurodegenerative disease pathogenesis[@li2022].
Gut-Associated Lymphoid Tissue (GALT)
- CCL25 is highly expressed in the small intestine, particularly in the crypt epithelium
- CCR9+ T cells home to the intestinal lamina propria under homeostatic conditions
- The intestinal immune system communicates with the CNS through multiple pathways:
- Vagal afferent nerves
- Circulating immune mediators
- Microbial metabolites (short-chain fatty acids, bile acids)
- Endocrine signaling
Microbial Modulation of CCL25/CCR9
- Gut microbiota can influence CCL25 expression in intestinal epithelial cells
- Dysbiosis alters CCR9+ T cell trafficking and may affect systemic inflammation
- Probiotic interventions may modulate CCL25/CCR9 axis in therapeutic contexts
Intestinal Permeability
- CCL25/CCR9 signaling affects tight junction integrity in intestinal epithelium
- Increased intestinal permeability ("leaky gut") associated with neuroinflammation
- Potential for CCL25-targeted interventions to restore barrier function
Disease Associations
Neurodegenerative Diseases
Alzheimer's Disease
In Alzheimer's disease, the CCL25/CCR9 axis contributes to neuroinflammation through several mechanisms[@chen2016][@heppner2015]:
- Amyloid-beta effects: Aβ peptides can induce CCL25 expression in astrocytes and microglia
- Microglial activation: CCR9 signaling modulates microglial phenotypic polarization
- T cell trafficking: Peripheral T cells expressing CCR9 may enter the CNS in AD
- Blood-brain barrier: CCL25 may affect BBB permeability through endothelial cell activation
Research has shown elevated CCL25 levels in cerebrospinal fluid of AD patients compared to controls, suggesting potential as a biomarker[@ch书信2021].
Parkinson's Disease
The CCL25/CCR9 axis is implicated in Parkinson's disease through gut-brain axis mechanisms[@chen2020][@cryan2020][@li2022]:
- Enteric nervous system: CCR9+ T cells accumulate in the gut in PD
- Alpha-synuclein propagation: Gut inflammation may accelerate synucleinopathy spread
- Dopaminergic neurons: CCL25 may directly affect survival of dopaminergic neurons
- Microbiota-gut-brain axis: CCL25 expression modulated by gut microbiome alterations
Multiple Sclerosis
CCL25 plays complex roles in multiple sclerosis[@owensby2018]:
- T cell recruitment: CCR9+ T cells may traffic to CNS lesions
- Intestinal immune dysfunction: MS patients often exhibit gut immune abnormalities
- Therapeutic potential: CCR9 antagonists explored for MS treatment
- Remyelination: CCL25 may influence oligodendrocyte precursor cell function
Neuroinflammation
CCL25 participates in neuroinflammatory processes[@aguzzi2014][@hansson2019][@eraky2023][@zhou2023]:
- Modulates T cell trafficking into CNS
- Influences blood-brain barrier permeability
- May interact with other chemokines in inflammatory cascades
- Potential role in autoimmune encephalitis
- Cytokine storm modulation in neuroinflammatory conditions
Other Conditions
- Inflammatory bowel disease (Crohn's disease particularly)
- Celiac disease
- Type 1 diabetes
- Certain cancers (colorectal, pancreatic)
- HIV infection
- Graft-versus-host disease
Expression
CCL25 expression is tissue-specific:
Regulation of Expression
CCL25 expression is dynamically regulated:
- Inflammatory cytokines: TNF-α, IL-1β, and IFN-γ upregulate CCL25
- Microbial signals: TLR agonists can induce CCL25 expression
- Hormonal regulation: Estrogen may modulate CCL25 levels
- Epigenetic control: DNA methylation patterns affect CCL25 transcription
Therapeutic Potential
The CCL25/CCR9 axis is a therapeutic target with multiple intervention strategies[@foster2007][@stolz2018][@zhou2023]:
Therapeutic Strategies
Clinical Applications
The CCL25/CCR9 axis has been targeted in several clinical contexts[yokota2006][@marsal2015]:
- Inflammatory Bowel Disease: CCR9 antagonists in Phase I/II trials showed efficacy in Crohn's disease
- Celiac Disease: CCL25-blocking strategies investigated for refractory disease
- Asthma: Investigated for eosinophilic airway inflammation
- Cancer Metastasis: CCR9 inhibition to prevent tumor spread, particularly in colorectal cancer
- Transplant: CCR9 blockade to prevent graft-versus-host disease
Drug Development Pipeline
Several CCR9-targeted agents have been developed[@marsal2015][@stolz2018]:
Emerging Applications in Neurodegeneration
- Alzheimer's disease: CCR9 antagonists may reduce neuroinflammation and Aβ-induced damage
- Parkinson's disease: Modulation of gut-brain axis inflammation through CCL25 inhibition
- Multiple sclerosis: CCR9 blockade may reduce CNS-infiltrating T cells
- Amyotrophic lateral sclerosis: Potential for modulating inflammatory responses
Challenges and Considerations
- BBB penetration: Ensuring therapeutic agents reach CNS targets
- Homeostatic vs. inflammatory roles: Targeting CCL25 without disrupting normal immune function
- Biomarker development: Identifying patient subgroups most likely to benefit
- Combination therapies: Potential synergies with other immunomodulatory agents
Cross-References
- [Parkinson's Disease](/diseases/parkinsons-disease) - Gut-brain axis
- [Alzheimer's Disease](/diseases/alzheimers-disease)
- [Neuroinflammation](/mechanisms/neuroinflammation)
- [Chemokine Signaling](/mechanisms/chemokine-signaling)
- [Gut-Brain Axis](/mechanisms/gut-brain-axis)
See Also
- [Parkinson's Disease](/diseases/parkinsons-disease)
- [Alzheimer's Disease](/diseases/alzheimers-disease)
- [Neuroinflammation](/mechanisms/neuroinflammation)
- [Chemokine Signaling](/mechanisms/chemokine-signaling)
- [Gut-Brain Axis](/mechanisms/gut-brain-axis)
External Links
- [NCBI Gene: 6374](https://www.ncbi.nlm.nih.gov/gene/6374)
References
Pathway Diagram
The following diagram shows the key molecular relationships involving CCL25 Gene discovered through SciDEX knowledge graph analysis:
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | genes-ccl25 |
| kg_node_id | CCL25 |
| entity_type | gene |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-6bbb8172b2c9 |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'genes-ccl25'} |
| _schema_version | 1 |
No provenance edges found
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[CCL25 Gene](http://scidex.ai/artifact/wiki-genes-ccl25)
http://scidex.ai/artifact/wiki-genes-ccl25