podoplanin | OKDB#: 4848 |
Symbols: | PDPN | Species: | human | ||
Synonyms: | T1A, GP36, GP40, Gp38, OTS8, T1A-2, AGGRUS, HT1A-1, PA2.26, | Locus: | 1p36.21 in Homo sapiens | HPMR |
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OMIM
Entrez Gene
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General Comment | NCBI Summary: This gene encodes a type-I integral membrane glycoprotein with diverse distribution in human tissues. The physiological function of this protein may be related to its mucin-type character. The homologous protein in other species has been described as a differentiation antigen and influenza-virus receptor. The specific function of this protein has not been determined but it has been proposed as a marker of lung injury. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008] | ||||
General function | Receptor, Cell adhesion molecule | ||||
Comment | |||||
Cellular localization | Plasma membrane | ||||
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Ovarian function | Luteolysis | ||||
Comment | Downregulation of Lymphatic Vessel Formation Factors in PGF2a-induced Luteolysis in the Cow. Nitta A et al. Prostaglandin F2a (PGF2a) induces luteolysis in cows and causes infiltration of immune cells, which resembles inflammatory immune response. Since the general immune response is mediated by the lymphatic system, we hypothesized that luteolysis is associated with generation of an immune response that involves lymphatic vessels in the bovine corpus luteum (CL). The CL was obtained from Holstein cows at the mid-luteal phase (days 10-12, ovulation = day 0) by ovariectomy at various time points after PGF2a injection. Lymphatic endothelial cell (LyEC) marker, endothelial hyaluronan receptor 1 (LYVE1), levels decreased significantly 12 h after PGF2a injection. Podoplanin, another LyEC marker, decreased from 15 min after PGF2a injection. PGF2a also diminished mRNA expression of lymphangiogenic factors, such as vascular endothelial growth factor (VEGF) C, VEGFD and VEGF receptor 3 (VEGFR3). During PGF2a-induced luteolysis, the levels of mRNA expression of tumor necrosis factor a (TNFa; the major pro-inflammatory cytokine) and chemokine (C-X-C motif) ligand 1 (neutrophil chemokine) were increased. On the other hand, chemokine (C-C motif) ligand 21, which regulates outflow of immune cells from tissues via the lymphatic vessels during an immune response, was decreased. This study demonstrated that the lymphatic network in the CL is disrupted during luteolysis and suggests that during luteolysis, immune cells can induce a local immune response in the CL without using the lymphatic vessels. | ||||
Expression regulated by | |||||
Comment | |||||
Ovarian localization | Luteal cells | ||||
Comment | |||||
Follicle stages | Corpus luteum | ||||
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Phenotypes | |||||
Mutations | 0 mutations | ||||
Genomic Region | show genomic region | ||||
Phenotypes and GWAS | show phenotypes and GWAS | ||||
Links |
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created: | April 5, 2013, 3:32 p.m. | by: |
hsueh email:
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last update: | April 5, 2013, 3:34 p.m. | by: | hsueh email: |
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