| Project/Area Number |
22790883
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Endocrinology
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| Research Institution | University of Yamanashi |
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Principal Investigator |
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| Project Period (FY) |
2010 – 2011
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| Project Status |
Completed (Fiscal Year 2011)
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| Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2011: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2010: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
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| Keywords | 内分泌学 / 膵臓 / 糖尿病 / 再生医療 / 核内ホルモン受容体 / 甲状腺 / 細胞周期 / 甲状腺ホルモン |
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| Research Abstract |
One goal of diabetic regenerative medicine is to instructively convert mature pancreatic exocrine cells into insulin-producing cells. We recently reported that liganded thyroid hormone receptorα(TRα) plays a critical role in expansion of theβ-cell mass during postnatal development.
AdTRαis a recombinant adenoviral vector that expresses human TRα1 under the control of the cytomegalovirus promoter. To analyze whether TRαgene transfer induces reprogramming of pancreatic exocrine cells to insulin-producing cells, AdTRαwere injected into the pancreas of immunodeficient mice. Rat pancreatic AR42J cells that possess exocrine and neuroendocrine properties were infected with AdTRα. The expression of transcription factors that are involved in the differentiation of pancreatic endocrine cells was then analyzed by quantitative RT-PCR, western blot or immunocytochemistry. To explore whether liganded-TRα-induced reprogramming of pancreatic exocrine cells is direct or indirect effect, AdTRα-infected AR42J cells were concomitantly transfected with siRNA of Ngn3 or MafA.
Small scattered clusters of insulin-producing cells, which also expressed lipase, were observed in AdTRα-infected mice. T3-treatment of AR42J cells that were infected with AdTRαand pretreated with activin A increased the mRNA and protein expression levels of Ngn3 and MafA, compared to no T3-treatment. Overexpression of TRαtogether with T3-treatment also induced insulin expression in activin A-treated AR42J cells. The siRNA-induced inhibition of expression of Ngn3 or MafA significantly inhibited AdTRα-induced reprogramming of AR42J cells into insulin-producing cells.
Conclusions : These results suggested that combination of liganded-TRαand activin A leads to reprogramming pancreatic exocrine cells to insulin-producing cells via induction of Ngn3 and MafA. Our findings also support the hypothesis that liganded-TRαplays a critical role inβ-cell regeneration during postnatal development.
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