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FLASH GENE
Symbol CX3CR1 contributors: shn/npt/pgu - updated : 28-09-2020
HGNC name chemokine (C-X3-C motif) receptor 1
HGNC id 2558
Location 3p22.2      Physical location : 39.304.985 - 39.323.226
Synonym name
  • G protein-coupled receptor 13
  • fractalkine receptor CX3CR1
  • chemokine (C-C) receptor-like 1
  • chemokine (C-X3-C) receptor 1
  • chemokine, CX3C motif, receptor 1
  • Synonym symbol(s) CMKBRL1, CHEMR1, CCRL1, GPR13, CMKDR1, V28, C3X1, GPRV28,
    DNA
    TYPE functioning gene
    STRUCTURE 18.24 kb     2 Exon(s)
    10 Kb 5' upstream gene genomic sequence study
    MAPPING cloned Y linked N status confirmed
    Map pter - D3S3605 - D3S3593 - CX3CR1 - D3S3527 - D3S3522 - cen
    RNA
    TRANSCRIPTS type messenger
    identificationnb exonstypebpproduct
    ProteinkDaAAspecific expressionYearPubmed
    2 splicing 3160 - 387 - 2003 14607932
    2 splicing 3224 - 355 - 2003 14607932
    2 splicing 3264 - 355 - 2003 14607932
    2 splicing 3108 - 355 - 2003 14607932
    EXPRESSION
    Type widely
       expressed in (based on citations)
    organ(s)
    SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
    Endocrinepancreas     Homo sapiens
    Nervousbraindiencephalonhypothalamus highly
    Visualeyeretina  highly
    tissue
    SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
    Nervouscentral   
    Nervousperipherous   
    cells
    SystemCellPubmedSpeciesStageRna symbol
    Blood/Hematopoieticmonocyte Homo sapiens
    Endocrineislet cell (alpha,beta...) Homo sapiens
    Lymphoid/Immunedendritic cell Homo sapiens
    Lymphoid/Immunemacrophage Homo sapiens
    Lymphoid/ImmuneT cell Homo sapiens
    Nervousglia Homo sapiens
    Nervousneuron
    cell lineage
    cell lines
    fluid/secretion
    at STAGE
    PROTEIN
    PHYSICAL PROPERTIES
    STRUCTURE
    motifs/domains
  • seven transmembrane segments (7TM) receptor, carrying the chemokine domain on top of an extended mucin-like stalk
  • a binding site mapping to a region of greatest flexibility and structural variability
  • HOMOLOGY
    interspecies ortholog to CX3CR1, Pan troglodytes
    ortholog to Cx3cr1, Rattus norvegicus
    ortholog to Cx3cl1, Mus musculus
    Homologene
    FAMILY
  • G-protein coupled receptor superfamily
  • CX3C family
  • CATEGORY regulatory , signaling , receptor membrane G
    SUBCELLULAR LOCALIZATION     plasma membrane
    text multi-pass membrane protein
    basic FUNCTION
  • receptor for fractalkine and a coreceptor for HIV-1
  • chemokine (C-X3-C) receptor 1, mediating leukocyte migration and adhesion
  • involved in the pathogenesis of atherosclerotic disease
  • mediates both leukocyte migration and adhesion
  • neuronal CX3CR1 receptors mediate the neurotrophic effects of fractalkine, suggesting that fractalkine and its receptor are involved in a complex network of both paracrine and autocrine interactions between neurons and glia
  • control the clearance of entero-invasive pathogens by dendritic cells and may regulate immunological tolerance and inflammation
  • role in potentiating the rate of retinal microglial process dynamism and cellular migration
  • provides a survival signal to TH2 cells that is required for airway disease
  • CX3CR1 and CX3CL1 are required for the survival of both TH1 and TH2 cells in inflamed airways
  • key microglial pathway in protecting against Alzheimer disease-related cognitive deficits that are associated with aberrant microglial activation and elevated inflammatory cytokine
  • both CCR2 and CX3CR1 regulate arteriole growth, but only bone marrow-derived cell-expressed CX3CR1 impacts small venule growth
  • important pathogenic role of CX3CL1/CX3CR1 in atherogenesis and plaque destabilization
  • fractalkine-receptor/CX3CR1 distinguishes memory CD8(+) T cells with cytotoxic effector function from those with proliferative capacity, independent of tissue-homing properties
  • CX3CL1 and its receptor CX3CR1 play a fundamental role in the pathophysiology of stroke
  • neuronal CX3CR1 mediates neuronal apoptotic cell death in ischemia
  • CX3CL1/CX3CR1 communication system has anti-inflammatory and neuroprotective effects and plays an important role in maintaining autophagy activity
  • fractalkine/CX3CR1 axis regulates microglial activation and function, neuronal survival and synaptic function by controlling the release of inflammatory cytokines and synaptic plasticity in the course of the neurological disease
  • appears to play a mechanistic role in mediating viral infection of pediatric airway epithelial cells
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS immunity/defense , inflammation , cellular trafficking transport
    PATHWAY
    metabolism
    signaling signal transduction
    a component
  • CX3CL1-CX3CR1 axis is a highly adhesive pair involved in the firm adhesion of monocytes or lymphocytes on activated endothelium
  • INTERACTION
    DNA
    RNA
    small molecule
    protein
  • activating the protein kinase Akt and nuclear translocation of NFKB
  • chemokine (C-X3-C motif) ligand 1, CX3CL1
  • CCL26 is yet a functional ligand for CX3CR1, the receptor for fractalkine/CX3CL1, which is expressed by CD16(+) NK cells, cytotoxic effector CD8(+) T cells, and CD14(low)CD16(high) monocytes
  • CX3CL1/CX3CR1 axis acts in many physiological phenomena including those occurring in the central nervous system (CNS), by regulating the interactions between neurons, microglia, and immune cells
  • CX3CL1/CX3CR1 contributes positively to neuron protective as well as detrimental role in the course of the disease
  • CX3CR1 is a novel target for the clearance of extracellular MAPT
  • CX3CR1/CX3CL1 axis plays a key role in the phagocytosis of MAPT by microglia and that it is affected as Alzheimer disease progresses
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Other morbid association(s)
    TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
    constitutional     --over  
    in airway smooth muscle, lung endothelium and epithelium upon allergen challenge, in people with asthma
    constitutional       loss of function
    fractalkine signaling (CX3CL1/ CX3CR1) is deficient in the vulnerable regions of Alzheimer brains
    Susceptibility
  • to coronary artery disease
  • to brain infarction
  • to age-related macular degeneration
  • to autism spectrum disorder
  • to HIV-1 infection and rapid progression to AIDS
  • Variant & Polymorphism other
  • rapid progression of AIDS in HIV+ (Omim: 609423)
  • individuals homozygous for CXRCR1 (haplotype I249M280)
  • polymorphisms modulating its adhesive and signaling functions, associated with reduced risk of atherosclerotic cardiovascular disease(I249M)
  • I249 and M280 alleles were associated with an increased risk of brain infarction
  • prevalence of T280M polymorphism associated with retinal vasculitis in UK patients
  • polymorphisms increasing the risk of age-related macular degeneration
  • Candidate gene
    Marker
    Therapy target
    SystemTypeDisorderPubmed
    allergyasthm 
    CX3CR1 and CX3CL1 may represent attractive therapeutic targets in asthma
    cancermetastases 
    CX3CL1-CX3CR1 axis may be a novel target for the therapeutic intervention of bone resorbing diseases such as cancer bone metastasis
    osteoarticularboneostéoporosis
    CX3CL1-CX3CR1 axis may be a novel target for the therapeutic intervention of bone resorbing diseases such as rheumatoid arthritis, osteoporosis
    neurologyneurodegenerative 
    CX3CL1/CX3CR1 communication system is a therapeutic target for amyotrophic lateral sclerosis (ALS)patients
    neurosensorialvisualdegenerative
    CX3CL1-CX3CR1 signaling is a molecular mechanism capable of modulating microglial-mediated degeneration and represents a potential molecular target in therapeutic approaches to RP
    ANIMAL & CELL MODELS
  • CX3CR1(-/-) mice have a significant reduction in macrophage recruitment to the vessel wall and decreased atherosclerotic lesion formation
  • Retinal microglial density, distribution, cellular morphology, and overall retinal tissue anatomy were not altered in young CX3CR1(-/-) mice
  • deleting CX3CR1 in hAPP mice increased expression of inflammatory factors, such as TNF and IL6, and exacerbated plaque-independent neuronal dysfunction and cognitive deficits
  • in Cx3cr1-deficient (CX3CR1(GFP/GFP) ) rd10 mice microglial infiltration into the photoreceptor layer was significantly augmented and associated with accelerated photoreceptor apoptosis and atrophy