| Co-Investigator(Kenkyū-buntansha) |
HASE Koji RIKEN, Lab.for Epithelial Immunobiol., Researcher, 免疫系構築研究チーム, 研究員 (20359714)
MURAKAMI Takaya RIKEN, Lab.for Epithelial Immunobiol., Researcher, 免疫系構築研究チーム, 研究員 (10399446)
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| Budget Amount *help |
¥14,700,000 (Direct Cost: ¥14,700,000)
Fiscal Year 2005: ¥4,800,000 (Direct Cost: ¥4,800,000)
Fiscal Year 2004: ¥4,800,000 (Direct Cost: ¥4,800,000)
Fiscal Year 2003: ¥5,100,000 (Direct Cost: ¥5,100,000)
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| Research Abstract |
We investigated the roles of membrane traffic, especially AP complexes, in neurons and epithelial cells. The following has bee elucidated during the term of this grant.
1.Foxl1 is a transcription factor expressed in mesenchymes of gastrointestinal tract. Foxl1-KO mice suffer from hardly detectable gastric acid secretion. Upon stimulation, proton pump, H,K-ATPase, translocates from internal tubulovesicles to the plasma membrane in gastric parietal cells, which leads to gastric acid secretion. In foxl1-KO mice, however, this translocation does not occur. We found that the expression SNAP25, a SNARE involved in the fusion of tubulovesicules and the plasma membrane, was significantly reduced, which likely is a major problem involved in acid secretion insufficiency in these mice.
2.We established and analyzed KO mice for AP-3B, the neuron-specific AP complex. AP-3B-KO mice suffered from epileptic seizure. Structural abnormalities of synaptic terminals and synaptic vesicles were seen in AP-3B-KO mice. Consistent with the observation, release of the inhibitory neurotransmitter, GABA, was impaired, and abnormal excitability was observed in electrophysiological examinations, in these KO mice. Taken together, these observations suggest that insufficient release of GABA causes imbalance in neuroexcitability in AP-3B-KO mice, which ultimately leads to epileptic seizure in these mice.
3.Previous studies on cultured cells have suggested that the AP-2 complex, involved in endocytosis, is not essential for cell survival. However, there should still be a small, residual amount of AP-2 in these experimental conditions, which may be sufficient for cells to survive. To test this possibility, we have tried to establish AP-2-KO mice. To our surprise, no homozygous embryo has been recovered at embryonic day 3.5 or later, suggesting that AP-2 is essential for cell survival or embryonic development at very early stages.
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