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  • mProX™ Human CYSLTR1 Stable Cell Line

    [CAT#: S01YF-0923-PY94]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

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    Product Information

    Target Protein
    CYSLTR1
    Target Family
    Leukotriene Family
    Target Protein Species
    Human
    Host Cell Type
    SW480;HT-29;CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Target Research Area
    CNS Research
    Related Diseases
    Exercise-Induced Bronchoconstriction;Asthma
    Gene ID
    Human: 10800
    UniProt ID
    Human: Q9Y271

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Cysteinyl leukotriene receptor 1 (CYSLTR1) is a pivotal player in the realm of scientific research, particularly in the context of inflammatory responses. It is predominantly involved in mediating the effects of cysteinyl leukotrienes, which are lipid mediators implicated in various inflammatory conditions. Notably, CYSLTR1 has been linked to the pathogenesis of asthma, where it plays a role in bronchoconstriction, vascular permeability, and mucus secretion. Furthermore, its association with allergic rhinitis underscores its significance in allergic reactions. The therapeutic potential of targeting CYSLTR1 is evident, with antagonists being developed to treat asthma and allergic diseases.

    Protocols

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    FAQ

    chat Christopher (Verified Customer)

    What is the role of Cysteinyl Leukotriene Receptor-1 (CYSLTR1) in the immune system? May 05 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Cysteinyl leukotrienes (cysLTs) are predominantly produced by cells of the innate immune system, such as basophils, eosinophils, mast cells, and monocytes/macrophages. They have a proinflammatory effect due to their interactions with G-protein-coupled receptors, including CYSLTR1, which are expressed on various cell types. These interactions contribute to the immunopathogenesis of several inflammatory disorders, especially bronchial asthma. May 05 2020

    chat Ashley (Verified Customer)

    How do CYSLTR1 antagonists affect the immune response? Jun 13 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    CYSLTR1 antagonists, including montelukast, pranlukast, and zafirlukast, have been developed to target the proinflammatory activities of cysLTs. Apart from their primary action as CYSLTR1 antagonists, these agents also possess secondary anti-inflammatory activities that are particularly effective against neutrophils and monocytes/macrophages. These secondary mechanisms involve interference with cyclic nucleotide phosphodiesterases, 5'-lipoxygenase, and the proinflammatory transcription factor, nuclear factor kappa B. Jun 13 2023

    Published Data

    Fig.1 CysLT1R regulates PD-L1 expression in CC cells.

    Densitometric analysis compared CRISPR/Cas9-Ctrl and CRISPR/Cas9-CYSLTR1-transfected HT-29 and SW480 cells, both with and without IFNγ stimulation. Representative blots, denoting three replicates, illustrate the results, with corresponding densitometry graphs for HT-29 and SW480 cells under unstimulated and IFNγ-stimulated conditions.

    Ref: Satapathy, Shakti Ranjan, Souvik Ghatak, and Anita Sjölander. "The tumor promoter cysteinyl leukotriene receptor 1 regulates PD-L1 expression in colon cancer cells via the Wnt/β-catenin signaling axis." Cell Communication and Signaling 21.1 (2023): 1-15.

    Pubmed: 37316937

    DOI: 10.1186/s12964-023-01157-6

    Research Highlights

    Sayour NV, et al. "Droplet Digital PCR Is a Novel Screening Method Identifying Potential Cardiac ." International journal of molecular sciences, 2023.
    The need for improved outcomes in heart failure (HF) has prompted the search for novel drug targets. G-protein-coupled receptors (GPCRs) are the largest family of targets for approved drugs, which allows for potential repurposing. This study aimed to investigate differential expressions of 288 cardiac GPCRs using droplet digital PCR (ddPCR) and bulk RNA sequencing (RNAseq) in a rat model of left ventricular pressure-overload. Male Wistar rats subjected to transverse aortic constriction (TAC, n = 5) were compared to sham operated animals (SHAM, n = 5). Results showed significant systolic dysfunction in TAC rats compared to SHAM rats, as determined by echocardiography. RNAseq identified 69 differentially expressed GPCR mRNAs in TAC rats compared to SHAM rats, while ddPCR identified 27 differentially expressed GPCRs. Of these, 8 were identified by both methods, demonstrating correlation. Further investigation of the Prostaglandin-F2alpha-receptor (Ptgfr) using RNA-Scope revealed its presence on cardiomyocytes and fibroblasts in murine hearts. Antagonizing Ptgfr with AL-8810 showed potential for alleviating angiotensin-II-induced cardiomyocyte hypertrophy in vitro. Thus, this study presents a novel screening method using ddPCR to identify potential GPCR targets in HF, and suggests Ptgfr as a promising target for further investigation in HF treatment.
    Pubmed: 37762130   DOI: 10.3390/ijms241813826

    Zhao H, et al. "Identification of the shared gene signatures between pulmonary fibrosis and ." Frontiers in immunology, 2023.
    The present study aimed to identify common key genes and immune characteristics in Pulmonary Fibrosis (PF) and Pulmonary Hypertension (PH) through bioinformatics techniques. Expression profiles were retrieved from the Gene Expression Database and weighted gene co-expression network analysis was used to identify co-expression modules. The ClueGO software was used to enrich and analyze common genes in PF and PH, and a protein-protein interaction (PPI) network was obtained. Differential genes were screened in a separate cohort and intersected with the PPI network. Further, RT-PCR and immune infiltration analysis were performed on the intersecting genes. Results revealed lymphocyte activation as a common pathophysiological feature of PF and PH. Eight common characteristic genes and upregulation of resting CD4 memory T cells were identified. Using ImmPort database and RT-PCR analysis, IGF1 was identified as a potential therapeutic target for both diseases. Knockdown of IGF1 was found to reduce proliferation and apoptosis resistance in cells induced by hypoxia, platelet-derived growth factor-BB, and transforming growth factor-beta1. This study provides insight into common biomarkers and a potential candidate gene for targeted therapy of PF and PH.
    Pubmed: 37731513   DOI: 10.3389/fimmu.2023.1197752

    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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