Role of inflammation in initiation and progression of clonal hematopoiesis
Project/Area Number |
18F18408
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Research Category |
Grant-in-Aid for JSPS Fellows
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Allocation Type | Single-year Grants |
Section | 外国 |
Review Section |
Basic Section 54010:Hematology and medical oncology-related
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Research Institution | Kumamoto University |
Principal Investigator |
滝澤 仁 (2018-2019) 熊本大学, 国際先端医学研究機構, 特別招聘教授 (10630866)
|
Co-Investigator(Kenkyū-buntansha) |
FAKRUDDIN MD 熊本大学, 国際先端医学研究機構, 特定事業研究員 (20816475)
FAKRUDDIN MD. 熊本大学, 国際先端医学研究機構, 外国人特別研究員
|
Project Period (FY) |
2018-10-12 – 2021-03-31
|
Project Status |
Completed (Fiscal Year 2020)
|
Budget Amount *help |
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 2020: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 2019: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 2018: ¥700,000 (Direct Cost: ¥700,000)
|
Keywords | Clonal / Hematopoiesis / Lineage / Tracing / Leukemia / Inflammation / clonal hematopoiesis / inflammation |
Outline of Annual Research Achievements |
Many labs around the world has been working to develop novel methods for lineage tracing employing different mechanisms. But, these methods cannot provide the information on clone size of the dys-regulated and expanded clones, which led us to design this study to develop a method to determine both clonality and clone size simultaneously. I designed, developed and evaluated the novel clonal tracing method in cell line transfected with sleeping beauty transposon vectors and analysis of data revealed that the method can detect around 500 clones (both expanded and non-expanded) with their respective clone size. Distribution of integration site analysis showed random and stochastic distribution of transposon integration in all the chromosomes. I also evaluated the method with cell number and with as low as 10000 cells, the method work well and can detect enough clones with their respective clone size. To apply this method in vivo, novel strains of mice were needed. So, I also generated two novel strains of mice- Rosa26-Hyper sleeping beauty (HSB), which contains transposase enzyme and polyIR mice, which contains multiple copy of IR transposon in silent locus of chromosome. Upon successful evaluation of the method developed in this study in mouse model, it will provide useful tools not only in the field of hematology but also in other biomedical research fields to trace lineage to single cell resolution. The knowledge obtained from this study is expected to provide contribution towards establishment of preventive methods for pre-leukemia initiation and progression.
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Research Progress Status |
令和2年度が最終年度であるため、記入しない。
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Strategy for Future Research Activity |
令和2年度が最終年度であるため、記入しない。
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Report
(2 results)
Research Products
(1 results)