Description
GLP-2 is a 33-amino acid peptide hormone belonging to the proglucagon-derived peptide family, endogenously secreted by enteroendocrine L cells of the distal small intestine and colon. In experimental models, synthetic GLP-2 analogues are utilized to investigate the structural and functional dynamics of the GLP-2 receptor (GLP-2R), a G protein-coupled receptor expressed predominantly within the gastrointestinal tract.
Unlike general metabolic incretins such as GLP-1, GLP-2 is specifically recognized for its potent intestinotrophic actions. It is widely utilized in laboratory settings to map the downstream effects of GLP-2R activation, particularly regarding the stimulation of crypt cell proliferation, the reduction of enterocyte apoptosis, and the enhancement of intestinal barrier function and nutrient absorptive capacity.
Biochemical Characteristics
Chemically, GLP-2 functions as a synthetic polypeptide characterized by an amino acid sequence designed to interface with cell-surface receptors relevant to gut mucosal adaptation.
- Sequence/Structure: Synthetic polypeptide analogue of the 33-amino-acid endogenous GLP-2 hormone.
- Receptor Affinity: Binds specifically to the GLP-2 receptor (GLP-2R) located on subepithelial myofibroblasts, enteric neurons, and specific enteroendocrine cells.
- Stability: Supplied as a lyophilized salt to ensure long-term stability and prevent hydrolytic or proteolytic degradation during storage.
- Specificity: Utilized to selectively stimulate intestinal mucosal growth and cytoprotective pathways without the broader systemic insulinotropic effects characteristic of related incretins.
Chemical Properties
| Property |
Specification |
| Molecule Name |
GLP-2 |
| Synonyms |
Glucagon-Like Peptide 2 Analogue |
| Form |
Lyophilized Powder |
| Purity |
≥99% (Verified via HPLC) |
| Solubility |
Soluble in water and organic solvents (refer to SDS) |
| Documentation |
COA available per lot; SDS available |
(Note: Exact Molecular Weights and Formulas should be verified per lot COA/SDS).
GLP-2 is strictly for laboratory research and is commonly employed in the following investigational areas:
Intestinal Adaptation & Tissue Engineering Models
GLP-2 is extensively utilized as a chemical probe to study intestinal adaptive growth following structural resection or chemical injury. Researchers employ this peptide to quantify mucosal hyperplasia, increased crypt-villus height, and restored absorptive capacity in isolated gastrointestinal models.
Cellular Survival and Apoptosis Assays
In vitro studies employ GLP-2 to observe its cytoprotective impact on intestinal epithelial cells. Investigations focus on how GLP-2 receptor activation rapidly suppresses caspase-3 activation and upregulates Bcl-2, effectively reducing cellular apoptosis and increasing cell survival rates.
Gastrointestinal Barrier Function and Bioenergetics
Experimental models utilize this compound to study its role in reducing epithelial permeability and increasing mesenteric blood flow. Researchers investigate how GLP-2 modulates nitric oxide production and coordinates the transport of intracellular lipids and dietary nutrients across the apical membrane of enterocytes.
Pathway / Mechanistic Context
The primary mechanism of action for GLP-2 in research settings involves the targeted activation of the GLP-2 receptor (GLP-2R).
- Receptor Activation: Under experimental conditions, GLP-2 binds to GLP-2R, a G protein-coupled receptor predominantly localized in the subepithelial networks of the gut.
- Signal Transduction: This binding event stimulates adenylate cyclase, leading to the accumulation of intracellular cyclic AMP (cAMP) and subsequent protein kinase A (PKA) activation. It simultaneously triggers the extracellular signal-regulated kinase (ERK1/2) pathway.
- Resulting Flux: This divergent signaling cascade initiates cytoprotective mechanisms via the suppression of apoptotic factors, while also driving cellular proliferation and mediating localized expansion of the mucosal epithelium.
Preclinical Research Summary
Published preclinical literature documents investigations of GLP-2 across multiple experimental models for pathway characterization:
- Mucosal Growth: Studies in massive intestinal resection rat models demonstrate that GLP-2 administration significantly increases crypt-villus height, DNA and protein content, and overall mucosal mass in both the jejunum and ileum.
- Apoptosis Inhibition: Research indicates that early intracellular signaling following GLP-2 exposure effectively inhibits pro-apoptotic mechanisms in neonatal and adult intestinal cell models.
- Barrier Integrity: Data from in vivo assays suggest that sustained augmentation of GLP-2 signaling integrates nutrient-derived signals to optimize mucosal integrity, energy absorption, and adaptation to mucosal damage.
Form & Analytical Testing
This material is produced via robust chemical synthesis and supplied as a lyophilized (freeze-dried) powder.
- Lyophilization: Removes water content under vacuum to maintain compound integrity and extend shelf-life.
- Identity Verification: Each lot undergoes Mass Spectrometry (MS) to confirm molecular weight and identity.
- Purity Verification: High-Performance Liquid Chromatography (HPLC) is performed to ensure the product meets the ≥99% purity standard required for reproducible research data.
Referenced Citations
References are provided for informational purposes only and are not clinical claims.
- Drucker, D. J., & Yusta, B. (2014). Physiology and pharmacology of the enteroendocrine hormone glucagon-like peptide-2. Annual review of physiology, 76, 561-583. https://doi.org/10.1146/annurev-physiol-021113-170317
- Burrin, D. G., et al. (2006). GLP-2 rapidly activates divergent intracellular signaling pathways involved in intestinal cell survival and proliferation in neonatal piglets. American Journal of Physiology-Endocrinology and Metabolism.https://journals.physiology.org/doi/full/10.1152/ajpendo.00129.2006
- Scott, R. B., et al. (1998). GLP-2 augments the adaptive response to massive intestinal resection in rat. American Journal of Physiology-Gastrointestinal and Liver Physiology. https://doi.org/10.1152/ajpgi.1998.275.5.G911
- Drucker, D. J., et al. (2006). Glucagon-like Peptide-2. Annual Review of Nutrition, 26, 391-411.https://www.annualreviews.org/content/journals/10.1146/annurev.nutr.26.061505.111223
RESEARCH USE ONLY
This product is intended strictly for laboratory research use only. It is not for human or veterinary use. It is not intended for diagnosis, treatment, cure, or prevention of any disease. All purchases are subject to our Terms of Service and Purity Guarantee.
No COAs available for this product.
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