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  • mProX™ Human GPR4 Stable Cell Line

    [CAT#: S01YF-0923-PY171]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Based on this stable cell line, we also provide cell-based in vitro assays to evaluate the effects of your compounds or antibodies.

    Sub Cat Product Name Target Protein Species Host Cell Type Assay Types Inquiry Datasheet
    S01YF-1122-KX800 Magic™ Mouse GPR4 in Vitro cAMP Assay Mouse 1321N1 cAMP Assay
    S01YF-1122-KX801 Magic™ Rat GPR4 in Vitro cAMP Assay Rat 1321N1 cAMP Assay

    Product Information

    Target Protein
    GPR4
    Target Family
    Orphan Family
    Target Protein Species
    Human
    Host Cell Type
    HBMECs;CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    Cancer Research
    Related Diseases
    Prolactin Producing Pituitary Tumor;Central Sleep Apnea
    Gene ID
    Human: 2828
    UniProt ID
    Human: P46093

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    GPR4, a proton-activated G-protein-coupled receptor, has been recognized for its role in various physiological processes. It has been associated with the development of osteoarthritis, where it modulates CXCL12/CXCR7 signaling. Furthermore, GPR4 has been implicated in the pH-dependent migration of melanoma cells within the tumor microenvironment. In the context of cardiovascular health, GPR4 has been suggested as a potential therapeutic target for COVID-19, where it might mitigate hyper-inflammatory responses and associated complications. Additionally, GPR4's role in regulating blood pressure and cardiovascular risk has been explored, emphasizing the importance of dietary fiber in modulating its activity.

    Protocols

    Please visit our protocols page.

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    FAQ

    chat Donna (Verified Customer)

    How is GPR4 related to inflammatory responses? Feb 19 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    GPR4 mediates tissue edema, inflammatory exudate formation, and leukocyte infiltration in inflamed tissue, playing a role in inflammatory responses, particularly in osteoarthritis​​. Feb 19 2022

    chat Laura (Verified Customer)

    Can GPR4 be studied using stable cell lines? Nov 15 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Yes, there are stable cell lines like the B16/GPR4 cell line, which is a stable GPR4-overexpressing cell line, used to investigate GPR4's role in melanoma cell spreading and adhesion. Additionally, HEK293 cells have been utilized to study GPR4 expression and function​​. Nov 15 2021

    Published Data

    Fig.1 LPC-stimulated monocyte transmigration is dependent on GPR4.

    HBMECs were cultivated to confluence on transwell filters and subjected to retrovirus-mediated siRNA-GPR4 infection, effectively silencing GPR4 expression, while a negative control group received retrovirus siRNA-LPA3. Subsequently, these HBMECs were exposed to 5 μM LPC for 1 hour, following which calcein-labeled human monocytes were introduced to the stimulated HBMEC monolayers to assess transendothelial migration. The results indicated a statistically significant difference (p < .05) compared to the non-LPC stimulated and non-infected group, with a sample size of n = 6.

    Ref: Huang, Fei, et al. "A novel lysophospholipid-and pH-sensitive receptor, GPR4, in brain endothelial cells regulates monocyte transmigration." Endothelium 14.1 (2007): 25-34.

    Pubmed: 17364894

    DOI: 10.1080/10623320601177288

    Research Highlights

    Li R, et al. "GPRASP1 loss-of-function links to arteriovenous malformations by endothelial ." Brain : a journal of neurology, 2023.
    This study examines the genetic pathogenesis of arteriovenous malformations (AVMs), which are a common cause of intracerebral hemorrhage in young adults. The researchers identified two missense variants of G protein-coupled receptor (GPCR) associated sorting protein 1 (GPRASP1) in AVM patients for the first time. These variants were found to be loss-of-function (LoF) in endothelial cells and resulted in endothelial dysfunction. The researchers also found a link between GPRASP1 and GPR4, another GPCR that is involved in causing endothelial disorders. They discovered that GPRASP1 plays a role in promoting GPR4 degradation, which leads to disturbed endothelial functions and contributes to vascular anomalies. The researchers suggest that targeting GPR4 with specific drugs could potentially help in treating AVMs.
    Pubmed: 37787182   DOI: 10.1093/brain/awad335

    Shu T, et al. "Effects of short-term water velocity stimulation on the biochemical and ." Frontiers in physiology, 2023.
    Since 2011, the ecological operation trials of the Three Gorges Reservoir (TGR) have been ongoing in order to enhance the spawning quantity of the four major Chinese carp species below the Gezhouba Dam. In particular, it is important to investigate the effects of short-term water velocity stimulation on the ovarian development of grass carp (Ctenopharyngodon idellus) in order to understand the response of natural reproduction to ecological flows. Through ovary histology analysis and biochemical assays on individuals under stimulation from running water, it was found that while there were no significant impacts on the ovarian development of grass carp, there were elevated levels of hormones including estradiol, progesterone, follicle-stimulating hormone (FSH), and triiodothyronine (T3). Further examination through RNA sequencing of ovarian tissues revealed that 221 and 741 genes were up- and downregulated, respectively, under short-term water velocity stimulation compared to a control group. The majority of these differentially expressed genes were enriched in pathways such as ABC transporters, cytokine-cytokine receptor interaction, ECM-receptor interaction, and steroid hormone biosynthesis. Important genes involved in ovarian development, including gpr4, vtg1, C-type lectin, hsd17b1, cyp19a1a, cyp17a1, and rdh12, were found to be regulated. These findings offer new insights and suggest potential regulatory genes and pathways involved in the ovarian development of grass carp under short-term water velocity stimulation, which could be beneficial for future ecological regulation strategies.
    Pubmed: 37719458   DOI: 10.3389/fphys.2023.1248999

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
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