JAML

JAML or Junctional Adhesion Molecule-Like, or AMICA1 is a JAM transmembrane protein family member.[1][2] It is composed of two extracellular immunoglobulin-like domains, a membrane-spanning region, and a cytoplasmic tail involved in activation signaling. A known ligand of JAML is Coxsackie virus and Adenovirus Receptor (CXADR in humans and CAR in mice) which has been shown to localize to the tight junctions of epithelial cells.

JAML
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Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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JAML-mediated activation of CAR is required for neutrophil extravasation[3] in addition to other leukocyte/epithelial cell interaction models.

Other members of the JAM family of transmembrane proteins include JAM1, JAM2 and JAM3.

References

  1. Clark HF, Gurney AL, Abaya E, Baker K, Baldwin D, Brush J, Chen J, Chow B, Chui C, Crowley C, Currell B, Deuel B, Dowd P, Eaton D, Foster J, Grimaldi C, Gu Q, Hass PE, Heldens S, Huang A, Kim HS, Klimowski L, Jin Y, Johnson S, Lee J, Lewis L, Liao D, Mark M, Robbie E, Sanchez C, Schoenfeld J, Seshagiri S, Simmons L, Singh J, Smith V, Stinson J, Vagts A, Vandlen R, Watanabe C, Wieand D, Woods K, Xie MH, Yansura D, Yi S, Yu G, Yuan J, Zhang M, Zhang Z, Goddard A, Wood WI, Godowski P, Gray A (Oct 2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
  2. "Entrez Gene: AMICA1 adhesion molecule, interacts with CXADR antigen 1".
  3. Zen, K.; Liu, Y; McCall, IC; Wu, T; Lee, W; Babbin, BA; Nusrat, A; Parkos, CA (2005). "Neutrophil Migration across Tight Junctions is Mediated by Adhesive Interactions between Epithelial Coxsackie and Adenovirus Receptor and a Junctional Adhesion Molecule-like Protein on Neutrophils". Molecular Biology of the Cell. 16 (6): 2694–703. doi:10.1091/mbc.E05-01-0036. PMC 1142417. PMID 15800062.

Further reading

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