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2014 Fiscal Year Final Research Report

Molecular basis of intracellular cholesterol regulation in the maturation of canine erythroid cells.

Research Project

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Project/Area Number 25660234
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Veterinary medical science
Research InstitutionHokkaido University

Principal Investigator

SATO Kota  北海道大学, (連合)獣医学研究科, 准教授 (50283974)

Co-Investigator(Kenkyū-buntansha) INABA Mutsumi  北海道大学, 大学院獣医学研究科, 教授 (00183179)
Project Period (FY) 2013-04-01 – 2015-03-31
Keywordsコレステロール / 赤芽球 / 分化成熟 / 赤血球 / 犬
Outline of Final Research Achievements

Dog red cells show low intracellular K+ (LK) phenotype; however, some Japanese dogs have high intracellular K+ (HK) red cells which exhibit characteristics similar to reticulocytes. In the present study, we determined that TSPO2 was the candidate gene for the HK phenotype by genome-wide association study. HK dogs possessed two different mutant alleles in TSPO2 that resulted in amino acid substitutions: C40Y and the triple mutations V89F/ΔF98/T120I (VFT). Analysis of genomic DNA demonstrated that the dogs possessing HK red cells were homozygotes for the C40Y allele or compound heterozygotes for the C40Y and the VFT allele. In stable transfectants of K562 cells, the intracellular deposition of free cholesterol was evident in K562 cells expressing wild-type TSPO2 but not in cells expressing C40Y or VFT mutants. These findings suggest that impaired cholesterol metabolism during erythroid development and maturation are involved in the molecular cause of the HK red cell phenotype.

Free Research Field

臨床獣医学

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Published: 2016-09-02  

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