| 研究課題/領域番号 |
22K20642
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| 研究種目 |
研究活動スタート支援
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| 配分区分 | 基金 |
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| 審査区分 |
0701:分子レベルから細胞レベルの生物学およびその関連分野
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| 研究機関 | 国立研究開発法人理化学研究所 |
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研究代表者 |
Vadivelu RajaKumar 国立研究開発法人理化学研究所, 開拓研究本部, 基礎科学特別研究員 (60963543)
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| 研究期間 (年度) |
2022-08-31 – 2024-03-31
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| 研究課題ステータス |
交付 (2022年度)
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| 配分額 *注記 |
2,860千円 (直接経費: 2,200千円、間接経費: 660千円)
2023年度: 1,430千円 (直接経費: 1,100千円、間接経費: 330千円)
2022年度: 1,430千円 (直接経費: 1,100千円、間接経費: 330千円)
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| キーワード | hIPSCs / Gastruloid / Cryogel / Mechanobiology / Neural Induction / Neuromesoderm / organogenesis / pluripotent / Embryonic Organoid / Neuromesodermal |
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| 研究開始時の研究の概要 |
The study will generate a mechanical microenvironment to direct iPSCs to generate embryo-like organoid called gastruloid without the use of exogenous chemical stimulation. The overall purpose to understand morphogenetic events taking place during tissue growth and elucidate neuromesodermal tissue specification.
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| 研究実績の概要 |
We aim to investigate how using cryogel sandwich model by embedding cell clusters with layer-by-layer cryogel could enhance mechanical constraints. First, we studied cryogel`s topology by using Hirox, and SEM microscope analysis revealed that cryogel surface topology consists of voids that appear as hill-valley-like structures composed of pockets like void space which can trap microbeads. Thus, cryogel facilitates spontaneous cell cohesion, leading to spherical-shaped aggregates within 24h. After cryogel embedding the aggregates acquire a teardrop-like shape. Eventually, on day 3 these aggregates showed up ovoid shape which resembles a symmetrical breaking process. Day 4 showed polarized aggregates with the posterior axis.
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| 現在までの達成度 (区分) |
現在までの達成度 (区分)
3: やや遅れている
理由
We focus on establishing methodological development to elucidate cryogel properties on stimulating mechanical input and impact iPSCs aggregation. For this purpose, we optimized cryogel fabrication at different freezing times and evaluate the topological features accordingly. The second optimization is determining the appropriate culture condition. We first optimized the 2D cell culture regime by using Matrigel and vitronectin. Along, with this we opt to find the suitable media either using Stem fit or E8. After establishing 2D cell culture regime we then determine the suitable growth condition of 3D culture. Then we tested the effect of ROCK inhibitor on the viability of the 3D culture. Also, include shifting from stem fit during 2D culture to E8 at the 3D growth phase.
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| 今後の研究の推進方策 |
Plan 1: The progressing research plan is to optimize the adequate and reproducible method in culturing iPSCs aggregates and how embedment method gives axial morphogenesis.
Plan 2: We will assess the impact of cryogel embedding on pluripotent exit and evaluate the localization of differentiated cells in the establishment of markers responsible for gastrulation. Particularly, the capacity to self-organize into a neural fate which is possibly rudimentary along the A-P axis. Next, we aim the examine the transition of core pluripotency protein Sox2+ cells to prime state pluripotency marked by Otx2 which is in the state of the stable epiblast. Later, we aim to identify mutually exclusive patterns between Otx2 and T-Bra with Sox2 that could occur.
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