| Project/Area Number |
07807006
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
General physiology
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| Research Institution | Osaka University |
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Principal Investigator |
YAMASHITA Masayuki Osaka University Medical School, Associate Professor, 医学部, 助教授 (20183121)
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| Co-Investigator(Kenkyū-buntansha) |
MORIGIWA Katsuko Osaka University Medical School, Assistant Professor, 医学部, 助手 (00273665)
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| Project Period (FY) |
1995 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1996: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1995: ¥1,000,000 (Direct Cost: ¥1,000,000)
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| Keywords | Retina / Chick embryo / proliferation / Acetylcholine / development / calcium ion / fluorescence / Adenosine triphosphate / プリノセプター / アデノシンミリン酸 / アデノシン三りん酸 / 受容体 / 細胞内情報伝達 / 神経発生 |
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| Research Abstract |
Acetylcholine and adenosine triphosphate (ATP) raise intracellular Ca^<2+> concentration via muscarinic receptors and P_<2U> purinoceptors by releasing Ca^<2+> from intracellular Ca^<2+> stores in the neural retina of early embryonic chick. We studied the signal transduction mechanisms for the muscarinic and purinergic Ca^<2+> responses and developmental changes in the purinergic Ca^<2+> responses with fura-2 fluorescence measurements.
Pertussis toxin suppressed the ATP-induced Ca^<2+> rise, whereas no inhibition was observed on the muscarinic Ca^<2+> rise. U-73122, an inhibitor of phospholipase C,suppressed the Ca^<2+> rise to ATP,but its analog U-73343 did not suppress it. In contrast, both U-73122 and U-73343 suppressed the muscarinic Ca^<2+> rise. Li^+, which inhibits phosphatidylinositol metabolism, enhanced both the muscarinic and purinergic Ca^<2+> rises. Thapsigargin, an inhibitor of Ca^<2+>-ATPase of inositol trisphosphate (IP_3) -sensitive Ca^<2+> stores, abolished both the muscarinic and purinergic Ca^<2+> rises. Cross-talk occurred between the muscarinic and purinergic Ca^<2+> mobilizations but they were not occlusive. Our study suggests that both the muscarinic and purinergic Ca^<2+> mobilizations utilize IP_3-sensitive Ca^<2+> stores, but different signal transduction pathways are involved in between the muscarinic and purinergic Ca^<2+> responses.
The ATP-induced Ca^<2+> rise was the most prominent at E3, drastically declined towards E8 and further decreased until E11-13 before synapse formation. ATP might act as an intercellular messenger during the early period of neurogenesis in the chick retina.
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