| Project/Area Number |
15208034
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Applied molecular and cellular biology
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| Research Institution | Nagoya University |
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Principal Investigator |
KITAGAWA Yasuo Nagoya Univ., Grad. Sch. Bioagric. Sci., Professor, 大学院・生命農学研究科, 教授 (50101168)
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| Co-Investigator(Kenkyū-buntansha) |
TORII Shuhei Nagoya Univ., Grad. Sch. Medicine., Professor, 大学院・医学系研究科, 教授 (60115607)
鳥山 和宏 あいち小児保健医療センター, 医長
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| Project Period (FY) |
2003 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥52,260,000 (Direct Cost: ¥40,200,000、Indirect Cost: ¥12,060,000)
Fiscal Year 2005: ¥13,520,000 (Direct Cost: ¥10,400,000、Indirect Cost: ¥3,120,000)
Fiscal Year 2004: ¥13,520,000 (Direct Cost: ¥10,400,000、Indirect Cost: ¥3,120,000)
Fiscal Year 2003: ¥25,220,000 (Direct Cost: ¥19,400,000、Indirect Cost: ¥5,820,000)
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| Keywords | adipose tissues / age-dependency / autologous stem cells / fibroblast growth factor / humanized culture / low-serum medium / mesenchym / stromal vascular fraction / 幹細胞 / 幹細胞工学 / 幹細胞保育因子 / 再生医療 / 脂肪由来幹細胞 / 体性幹細胞 / 天井培養 / 間葉系幹細胞 / 成体幹細胞保育因子 / ラミニン / 形成外科 / 自家移植 / 末梢組織 / 大網 / ヒト血清培養 / 骨形成 |
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| Research Abstract |
Adipose tissues are abundant deposition sites of autologous stem cells with potential application for regenerative medicine and adipose-derived stromal vascular fraction (SVF) is a source of autologous stem cells with differentiation potential along mesenchymal, hematopoietic, neurogenic, angiogenic or epithelial lineage. By culturing SVF cells in high- or low- serum medium containing fibroblast growth factor (FGF)-2, we found that the cells grew faster in low-serum medium and could be subcultured unlimitedly. Cells expanded in low-serum medium showed higher potential of mesenchymal differentiation. We suggest that high-serum concentration is unfavorable for self-renewing of stem cells due to growth factors contained in the serum. When SVF cells from patients at different ages were culture in high-serum medium, stem cells with osteogenic potential were depleted at ages above 20 years, whereas they could be expanded in low-serum medium even from 82 years old patient. Since human adult serum could substitute for 2% fetal bovine serum to give even better proliferation and differentiation, we could humanized ex vivo expansion culture of human stem cells for immediate clinical applications. By our method, autologous stem cell population corresponding to 10^9 cells can be prepared within 3 weeks after obtaining 1 g of subcutaneous adipose tissue and 200 ml of blood from patients at any age.
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