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Erythroid differentiation and iron metabolism in bone marrow of renal failure

Research Project

Project/Area Number 25461262
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Kidney internal medicine
Research InstitutionHyogo Medical University

Principal Investigator

NAKANISHI TAKESHI  兵庫医科大学, 医学部, 教授 (70217769)

Co-Investigator(Kenkyū-buntansha) KURAGANO TAKAHIRO  兵庫医科大学, 医学部, 准教授 (60411998)
HASUIKE YUKIKO  兵庫医科大学, 医学部, 講師 (80399146)
Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Keywordserythroblasts / differentiation / hepcidin / CD71 / 腎性貧血 / 鉄 / ヘプシジン / 骨髄細胞 / 脾臓 / ESA / フラタキシン
Outline of Final Research Achievements

Anemia in chronic renal failure has been believed to be mainly caused by inadequate EPO production, but the major cause has not been well clarified. In the present study, we examined the differentiation pattern of erythroid in the hematopoietic system of bone marrow (BM) using flow cytometry(FACS), and hepcidin expression in liver using mouse model of adenine-induced renal failure (RF). FACS showed the percentages of Pro erythroblast (CD71+/Ter119-) and Basophilic erythroblast(CD71+/Ter119+), those are in the steps of late differentiation, were decreased in the BM of femur of RF compared with Control(C). No change of erythroblast differentiation was observed in cells from spleen of RF. Hepatic Hamp mRNA expression was increased and serum hepcidin levels were also higher in RF than C. Finally we presumed that the increase in hepcidin expression could be associated with the dysregulated erythroblast differentiation and the decrease in CD71(TfR) expression in RF.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (1 results)

All 2016

All Presentation (1 results) (of which Int'l Joint Research: 1 results)

  • [Presentation] Pathophysiology of anemia in a mouse model of chronic kidney disease; hepcidin and erythropoiesis2016

    • Author(s)
      Tomoko Kimura, Kiyoko Yamamoto, Yuki Morikami, Sayuri Kawada, Takanori Nagai, Masayoshi Nanami, Yukiko Hasuike, Takahiro Kuragano, Takeshi Nakanishi.
    • Organizer
      53rd ERA-EDTA Congress in 2016
    • Place of Presentation
      Austria Center Vienna
    • Year and Date
      2016-05-21
    • Related Report
      2015 Annual Research Report
    • Int'l Joint Research

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Published: 2014-07-25   Modified: 2019-07-29  

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