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Pregled bibliografske jedinice broj: 320900

Characterization of ionotrophic purinergic receptors in hepatocytes


Emmett, Daniel; Feranchak, Andrew; Kilić, Gordan; Puljak, Livia; Miller, Bonnie; Dolovčak, Svjetlana; McWilliams, Ryan; Doctor, Brian; Fitz, Gregory
Characterization of ionotrophic purinergic receptors in hepatocytes // Hepatology, 47 (2008), 2; 698-705 (međunarodna recenzija, članak, znanstveni)


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Naslov
Characterization of ionotrophic purinergic receptors in hepatocytes

Autori
Emmett, Daniel ; Feranchak, Andrew ; Kilić, Gordan ; Puljak, Livia ; Miller, Bonnie ; Dolovčak, Svjetlana ; McWilliams, Ryan ; Doctor, Brian ; Fitz, Gregory

Izvornik
Hepatology (0270-9139) 47 (2008), 2; 698-705

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
P2X receptors

Sažetak
Ionotrophic purinergic (P2X) receptors function as receptor-gated cation channels, where agonist binding leads to opening of a nonselective cation pore permeable to both Na(+) and Ca(2+). Based on evidence that extracellular adenosine 5'-triphosphate (ATP) stimulates glucose release from liver, these studies evaluate whether P2X receptors are expressed by hepatocytes and contribute to ATP-dependent calcium signaling and glucose release. Studies were performed in isolated hepatocytes from rats and mice and hepatoma cells from humans and rats. Transcripts and protein for both P2X4 and P2X7 were detectable, and immunohistochemistry of intact liver revealed P2X4 in the basolateral and canalicular domains. In whole cell patch clamp studies, exposure to the P2X4/P2X7 receptor agonist 2'3'-O-(4-benzoyl-benzoyl)-adenosine 5'-triphosphate (BzATP ; 10 microM) caused a rapid increase in membrane Na(+) conductance. Similarly, with Fluo-3 fluorescence, BzATP induced an increase in intracellular [Ca(2+)]. P2X4 receptors are likely involved because the calcium response to BzATP was inhibited by Cu(2+), and the P2X4 modulators Zn(2+) and ivermectin (0.3-3 microM) each increased intracellular [Ca(2+)]. Exposure to BzATP decreased cellular glycogen content ; and P2X4 receptor messenger RNA increased in glycogen-rich liver samples. CONCLUSION: These studies provide evidence that P2X4 receptors are functionally important in hepatocyte Na(+) and Ca(2+) transport, are regulated by extracellular ATP and divalent cation concentrations, and may constitute a mechanism for autocrine regulation of hepatic glycogen metabolism.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA


Ustanove:
Medicinski fakultet, Split

Profili:

Avatar Url Livia Puljak (autor)


Citiraj ovu publikaciju:

Emmett, Daniel; Feranchak, Andrew; Kilić, Gordan; Puljak, Livia; Miller, Bonnie; Dolovčak, Svjetlana; McWilliams, Ryan; Doctor, Brian; Fitz, Gregory
Characterization of ionotrophic purinergic receptors in hepatocytes // Hepatology, 47 (2008), 2; 698-705 (međunarodna recenzija, članak, znanstveni)
Emmett, D., Feranchak, A., Kilić, G., Puljak, L., Miller, B., Dolovčak, S., McWilliams, R., Doctor, B. & Fitz, G. (2008) Characterization of ionotrophic purinergic receptors in hepatocytes. Hepatology, 47 (2), 698-705.
@article{article, author = {Emmett, Daniel and Feranchak, Andrew and Kili\'{c}, Gordan and Puljak, Livia and Miller, Bonnie and Dolov\v{c}ak, Svjetlana and McWilliams, Ryan and Doctor, Brian and Fitz, Gregory}, year = {2008}, pages = {698-705}, keywords = {P2X receptors}, journal = {Hepatology}, volume = {47}, number = {2}, issn = {0270-9139}, title = {Characterization of ionotrophic purinergic receptors in hepatocytes}, keyword = {P2X receptors} }
@article{article, author = {Emmett, Daniel and Feranchak, Andrew and Kili\'{c}, Gordan and Puljak, Livia and Miller, Bonnie and Dolov\v{c}ak, Svjetlana and McWilliams, Ryan and Doctor, Brian and Fitz, Gregory}, year = {2008}, pages = {698-705}, keywords = {P2X receptors}, journal = {Hepatology}, volume = {47}, number = {2}, issn = {0270-9139}, title = {Characterization of ionotrophic purinergic receptors in hepatocytes}, keyword = {P2X receptors} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE





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