Blood Vessel Epicardial Substance (BVES), also known as POPDC1 (Popeye Domain Containing 1) or POP1, is a protein crucial in developing various tissues . BVES is expressed in cardiac and skeletal muscle and throughout the gastrointestinal epithelium . It functions as a cell adhesion molecule and is involved in maintaining tissue integrity and suppressing tumorigenesis . The recombinant form of pig BVES is produced for research purposes, allowing scientists to study its function and potential therapeutic applications in a controlled environment .
Recombinant pig BVES is typically produced in E. coli and tagged with histidine (His) to facilitate purification . The protein consists of 360 amino acids and has a high purity level (greater than 90%) . The recombinant protein is stored as a lyophilized powder in a Tris/PBS-based buffer with trehalose to maintain stability . Researchers can reconstitute the protein in sterile water for experimental use .
BVES, a member of the POP family of proteins, contains three putative transmembrane domains . It plays a crucial role in various cellular processes:
Cell Adhesion: BVES functions as a cell adhesion molecule, which is essential for maintaining tissue structure and integrity .
Cardiac Pacemaking: BVES is involved in cardiac pacemaking by modulating the affinity of cAMP interaction and interacting with the 2-pore domain potassium channel TREK-1 .
Epithelial Integrity: BVES regulates epidermal tight junction integrity . Mice lacking BVES exhibit worse intestinal injury and inflammation, indicating its role in preserving epithelial phenotypes .
Tumor Suppression: BVES is suppressed in gastrointestinal cancers, and its loss promotes tumor formation. BVES can regulate molecular pathways, including cAMP, WNT, and promoting the degradation of the oncogene, c-Myc .
Recombinant pig BVES is a valuable tool for various research applications:
Protein Structure and Function Studies: Researchers use recombinant BVES to study the protein's structure, interactions, and functions in vitro .
Drug Discovery: Recombinant BVES can screen potential therapeutic compounds that modulate BVES activity and target related diseases .
Cell Signaling Pathways: Recombinant BVES is employed to investigate BVES-related cell signaling pathways and their roles in different physiological and pathological conditions .
Understanding Disease Mechanisms: Studies using recombinant BVES can help elucidate the mechanisms underlying diseases related to BVES dysfunction, such as cancer and cardiovascular diseases .
BVES plays a significant role in cardiovascular function, particularly in cardiac pacemaking . Studies have identified a high-affinity cAMP binding domain within the POPEYE domain of BVES, which interacts with the 2-pore domain potassium channel TREK-1 . This interaction is sensitive to cAMP stimulation, suggesting that BVES recruits TREK-1 to the membrane to enhance current, modulated by cAMP levels . BVES knockout mice have impaired stress-induced bradycardia, indicating a sinus node defect .
BVES is recognized as a tumor suppressor in gastrointestinal cancers . Its expression is often suppressed in cancerous tissues, and the loss of BVES promotes tumor formation . BVES regulates several molecular pathways, including promoting the degradation of the oncogene c-Myc .
Research has identified recombinant enterovirus G (EV-G) viruses in pigs . Type 2 recombinant EV-Gs, which carry the torovirus PLCP gene, have been detected in pig farms . These viruses can undergo sequence changes over time due to persistent infection within pig farms or circulation between farms .
Recombinant Pig Blood Vessel Epicardial Substance (BVES) is a cell adhesion molecule crucial for maintaining cell integrity. It plays a vital role in forming and regulating the tight junction (TJ) paracellular permeability barrier in epithelial cells. Further, BVES is involved in VAMP3-mediated vesicular transport and receptor recycling through its interaction with VAMP3. It modulates cell shape and movement by influencing Rho-family GTPase activity via interaction with ARHGEF25/GEFT, inducing initial cell adhesion and aggregation independently of calcium. BVES is essential for skeletal muscle and heart development, contributing to striated muscle regeneration and repair and regulating cell spreading. Its role in maintaining cardiac function is significant, influencing heart rate dynamics potentially through cAMP binding and increased cell surface expression of the potassium channel KCNK2. Moreover, as a caveolae-associated protein, BVES is important for preserving caveolae structure and function, protecting the heart against ischemic injury.
KEGG: ssc:100153106
UniGene: Ssc.20392