Effects of ATP on the Intracellular Calcium Level in the Osteoblastic TBR31-2 Cell Line

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  • Nishii Naomi
    First Department of Biochemistry, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women's University
  • Nejime Namie
    Department of Pharmacology, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women's University
  • Yamauchi Chisako
    First Department of Biochemistry, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women's University
  • Yanai Nobuaki
    Department of Food and Nutritional Science, Faculty of Liberal Arts, Miyagi Gakuin Women's College
  • Shinozuka Kazumasa
    Department of Pharmacology, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women's University
  • Nakabayashi Toshikatsu
    First Department of Biochemistry, School of Pharmacy and Pharmaceutical Sciences, Mukogawa Women's University

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We investigated the effects of extracellular ATP on TBR31-2 cells established from the bone marrow of transgenic mice harboring the temperature-sensitive simian virus (SV) 40 T-antigen gene. These cells showed the capacity to differentiate toward osteoblasts and could be enhanced by bone morphogenetic protein (BMP)-2, an inducer of osteoblasts. The intracellular calcium ion level ([Ca2+]i) in differentiating TBR31-2 cells was measured by fluorescence confocal microscopic imaging using the Ca2+-sensitive probe, Calcium Green 1/AM. P2 receptor agonists, such as ATP (1 μM), uridine 5′-triphosphate (1 μM), and ADP (1 μM), significantly increased the [Ca2+]i of TBR31-2 cells in 2-d and 5-d cultures, but a potent P2X receptor agonist, α,β-methylene ATP (10 μM), did not increase [Ca2+]i. The increase in [Ca2+]i induced by ATP in the 2-d culture tended to be higher than in the 5-d culture. The increase in [Ca2+]i of both cultures was inhibited by pyridoxalphosphate-6-azophenyl-2′,4′-disulphonic acid, a P2 receptor antagonist. However, in an external Ca2+-free condition ATP-induced increase in [Ca2+]i was unchanged at either stage. U73122, phospholipase C inhibitor and Thapsigargin, a calcium-pump inhibitor, significantly inhibited the increase in [Ca2+]i at both stages. Reverse transcription-polymerase chain reaction analysis showed that the expression of P2Y receptor mRNA was higher in the 2-d culture than in the 5-d culture. These results indicate that ATP induces the increase in [Ca2+]i from the calcium store through activating P2Y receptors in TBR31-2 cells and that the 2-d culture can respond to ATP more than the 5-d culture due to the higher expression of P2Y receptors. This suggests that the physiological role of ATP in osteoblasts is altered during differentiation.

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