Crosstalk between erythropoiesis and iron homeostasis
| Project/Area Number |
26461400
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Hematology
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| Research Institution | Kanazawa Medical University (2016-2017)
Kyoto University (2014-2015) |
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Principal Investigator |
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| Co-Investigator(Renkei-kenkyūsha) |
TOMOSUGU Naohisa 金沢医科大学, 総合医学研究所, 教授 (80155580)
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| Research Collaborator |
MASUDA Taro
OISHI Shinya
SAKAMATO Soichoro
UCHIYAMA Tatsuki
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| Project Period (FY) |
2014-04-01 – 2018-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | 血液内科 / 鉄代謝 / ヘプシジン / フェリチン / 赤血球造血 / 血液内科学 / 無効造血 / エリスロフェロン / GDF15 / ヘモクロマトーシス / 鉄芽球性貧血 |
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| Outline of Final Research Achievements |
The erythropoietic system consumes a large amount of iron, and hepcidin regulates systemic iron homeostasis. We developed a hepcidin-promoter bioassay system and identified several compounds that inhibit hepcidin expression. Iron is mainly carried by transferrin in the circulation and taken up by cells through transferrin receptor 1. We found that H-ferritin, an iron storage protein, can be also taken up by the cells through the same receptor with different manners. H-ferritin suppressed BFU-erythroid colony formation in vitro. We also found that elevated pre-transplant serum hepcidin or ferritin levels are associated with poorer prognosis and delayed platelet engraftment in patients with hematologic malignancies.
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Report
(5 results)
Research Products
(18 results)
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[Journal Article] Overview2017
Author(s)
川端 浩
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Journal Title
Rinsho Ketsueki
Volume: 58
Issue: 4
Pages: 327-328
DOI
NAID
ISSN
0485-1439, 1882-0824
Related Report
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[Journal Article] The role of growth differentiation factor 15 in the pathogenesis of primary myelofibrosis.2015
Author(s)
Uchiyama T, Kawabata H, Miura Y, Yoshioka S, Iwasa M, Yao H, Sakamoto S, Fujimoto M, Haga H, Kadowaki N, Maekawa T, Takaori-Kondo A.
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Journal Title
Cancer Medicine
Volume: 4
Issue: 10
Pages: 1558-1572
DOI
NAID
Related Report
Peer Reviewed / Open Access
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