Strain Data Sheet

RBRC01939

Strain Information

Image
BRC No.RBRC01939
TypeTargeted MutationCartagena
SpeciesMus musculus
Strain nameB6.129X1-Trpv4<tm1Msz>
Former Common nameTRPV4KO
H-2 Haplotype
ES Cell lineRW4 [129X1/SvJ]
Background strainC57BL/6JJcl
Appearanceblack [a/a b/b C/C]
Strain developmentDeveloped by Makoto Suzuki, Jichi Medical School in 2001. The construct was electoroporated into RW4 ES cells derived from 129X1/SvJ. The mutant mice were backcrossed to C57BL/6J.
Strain descriptionTRPV4 (Trpv4, transient receptor potential cation channel, subfamily V, member 4) knockout mice. Exon 4 encodes the ankyrin-repeat domain was replaced with a neomycin resistance gene. The ion channel TRPV4 is a member of the TRP family, acts as a Ca2+-permeable cation channel in response to mechanical stress. Homozygous mutant mice are viable and fertile, but show a reduced responsiveness to pressure sensation and abnormal osmotic regulation.
Colony maintenanceHomozygote x Homozygote [or Crossing to C57BL/6JJcl]
References
Impaired osmotic sensation in mice lacking TRPV4.
Mizuno A, Matsumoto N, Imai M, Suzuki M
Am. J. Physiol. Cell Physiol., 285, C96-C101(2003). 12777254

Impaired pressure sensation in mice lacking TRPV4.
Suzuki M, Mizuno A, Kodaira K, Imai M
J. Biol. Chem., 278, 22664-22668 (2003). 12692122

Health Report

Examination Date / Room / Rack2024/10/07Room:3-ARack:I
2024/07/08Room:3-ARack:I
2024/04/08Room:3-ARack:I
2024/01/09Room:3-ARack:I
2023/10/10Room:3-ARack:I
2023/07/10Room:3-ARack:I
2023/04/10Room:3-ARack:I
2023/01/10Room:3-ARack:I

Gene

Gene SymbolGene NameChr.Allele SymbolAllele NameCommon NamesPromoterDiseases Related to This Gene
Trpv4transient receptor potential cation channel, subfamily V, member 45Trpv4targeted mutation 1, Makoto Suzuki
  • autosomal dominant brachyolmia(MedGEN)

  • avascular necrosis of femoral head, primary, 2(MedGEN)

  • Charcot-Marie-Tooth disease axonal type 2C(MedGEN)
  • more 7 Diseases
  • familial digital arthropathy-brachydactyly(MedGEN)

  • metatropic dysplasia(MedGEN)

  • neuronopathy, distal hereditary motor, autosomal dominant 8(MedGEN)

  • parastremmatic dwarfism(MedGEN)

  • scapuloperoneal spinal muscular atrophy, autosomal dominant(MedGEN)

  • spondyloepimetaphyseal dysplasia, Maroteaux type(MedGEN)

  • spondylometaphyseal dysplasia, Kozlowski type(MedGEN)
  • neoneomycin resistance gene (E. coli)5mouse phosphoglycerate kinase promoter (PGK promoter)
  • autosomal dominant brachyolmia(MedGEN)

  • avascular necrosis of femoral head, primary, 2(MedGEN)

  • Charcot-Marie-Tooth disease axonal type 2C(MedGEN)
  • more 7 Diseases
  • familial digital arthropathy-brachydactyly(MedGEN)

  • metatropic dysplasia(MedGEN)

  • neuronopathy, distal hereditary motor, autosomal dominant 8(MedGEN)

  • parastremmatic dwarfism(MedGEN)

  • scapuloperoneal spinal muscular atrophy, autosomal dominant(MedGEN)

  • spondyloepimetaphyseal dysplasia, Maroteaux type(MedGEN)

  • spondylometaphyseal dysplasia, Kozlowski type(MedGEN)
  • Phenotype

    Annotation by Mammalian phenotyhpe ontology
  • abnormal response to tactile stimuli(MP:0005316)

  • abnormal sensory capabilities/reflexes/nociception(MP:0002067)

  • impaired hearing(MP:0006325)

  • increased chemical nociceptive threshold(MP:0008531)

  • increased or absent threshold for auditory brainstem response(MP:0011967)
  • more 1 phenotypes
  • increased susceptibility to noise-induced hearing loss(MP:0004597)
  • Detailed phenotype data

    Ordering Information

    Donor DNAmouse Trpv4 genomic DNA, PGK-neo cassette (mouse phosphoglycerate kinase-1 promoter, E. coli aminoglycoside phosphotransferase cDNA)derived from the plasmid pKJ2.
    Research applicationSensorineural Research
    Specific Term and ConditionsIn publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the following literature(s) designated by the DEPOSITOR is requested. J, Biol. Chem., 278, 22664-22668 (2003). Am. J. Physiol. Cell Physiol., 285, C96-C101(2003).
    DepositorMakoto Suzuki (Jichi Medical University)
    Strain Statusan icon for Live miceLive mice
    an icon for Frozen embryosFrozen embryos
    an icon for Frozen spermFrozen sperm
    Strain AvailabilityCryopreserved sperm (within 1 month)
    Cryopreserved embryos (within 1 month)
    Live mouse (1 to 3 months)
    Additional Info.Necessary documents for ordering:
    1. Order form (Japanese / English)
    2. Category I MTA: MTA for distribution with RIKEN BRC (Japanese / English)
    3. Acceptance of responsibility for living modified organism (Japanese / English)

    Genotyping protocol -PCR-

    BRC mice in Publications

    Ueda T, Hoshikawa M, Shibata Y, Kumamoto N, Ugawa S.
    Basal cells express functional TRPV4 channels in the mouse nasal epithelium.
    Biochem Biophys Rep 4 169-174(2015) 29124201
    Sanjel B, Kim BH, Song MH, Carstens E, Shim WS.
    Glucosylsphingosine evokes pruritus via activation of 5-HT2A receptor and TRPV4 in sensory neurons.
    Br J Pharmacol 179(10) 2193-2207(2022) 34766332
    Schaller L, Gudermann T, Dietrich A.
    TRPV4 Mediates Alveolar Epithelial Barrier Integrity and Induces ADAM10-Driven E-Cadherin Shedding.
    Cells 13(20) (2024) 39451235
    Lee WJ, Shim WS.
    Cutaneous Neuroimmune Interactions of TSLP and TRPV4 Play Pivotal Roles in Dry Skin-Induced Pruritus.
    Front Immunol 12 772941(2021) 34925342
    Weber J, Rajan S, Schremmer C, Chao YK, Krasteva-Christ G, Kannler M, Yildirim AÖ, Brosien M, Schredelseker J, Weissmann N, Grimm C, Gudermann T, Dietrich A.
    TRPV4 channels are essential for alveolar epithelial barrier function as protection from lung edema.
    JCI Insight 5(20) (2020) 32931478