Different Cellular Mechanisms of Vasopressin Receptor V1 and V2 Subtype in Vasopression-Induced Adenosine 3′,5′-Monophosphate Formation in an Immortalized Renal Tubule Cell Line, TKC2

Kazuhisa Takeuchi, Nobuaki Yanai, Nobuyuki Takahashi, Takaaki Abe, Eikatsu Tsutsumi, Masuo Obinata, Keishi Abe

研究成果: Article査読

16 被引用数 (Scopus)

抄録

Vasopressin (VP) stimulates adenosine 3′,5′-monophosphate (cAMP) formation in an immortalized renal tubule cell line, TKC2, which is derived from transgenic mouse harboring temperature-sensitive SV40 T-antigen gene. VP (10-8 M)induced cAMP formation was significantly attenuated by either non-peptide vasopressin receptor V1 or V2 subtype antagonist, OPC-21268 (10-8 and 10-6 M) or OPC-31260 (10-8 and 10-6 M), respectively, and it was completely abolished by combination of both agents (10-6 M). VP (10-8 M) also induced an increase in cytosolic free Ca2+ and prostaglandin (PG) E2 synthesis, both of which were significantly inhibited by OPC-21268 (10-8 M), but not by OPC-31260 (10-6 M). Either OPC-21268 (10-8 M), depletion of extracellular Ca2+ or inhibition of cyclooxygenase attenuated both VP-induced PGE2 synthesis and cAMP formation. In conclusion, both V1 and V2 receptors can stimulate cAMP formation. V1 receptor, however, stimulates cAMP formation via Ca2+-dependent PGE2 synthesis, whereas V2 receptor may stimulate it directly.

本文言語English
ページ(範囲)680-687
ページ数8
ジャーナルBiochemical and biophysical research communications
202
2
DOI
出版ステータスPublished - 1994 1 1

ASJC Scopus subject areas

  • 生物理学
  • 生化学
  • 分子生物学
  • 細胞生物学

フィンガープリント

「Different Cellular Mechanisms of Vasopressin Receptor V1 and V2 Subtype in Vasopression-Induced Adenosine 3′,5′-Monophosphate Formation in an Immortalized Renal Tubule Cell Line, TKC2」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

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