Identification of human hematopoietic stem cell regulators with HLA allele deficient cells behavior

鉴定具有 HLA 等位基因缺陷细胞行为的人类造血干细胞调节因子

基本信息

  • 批准号:
    24790968
  • 负责人:
  • 金额:
    $ 2.75万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
  • 财政年份:
    2012
  • 资助国家:
    日本
  • 起止时间:
    2012-04-01 至 2014-03-31
  • 项目状态:
    已结题

项目摘要

The percentage of 6pLOH was different among hematopoiesis stages in human bone marrow, and the progenitor cells showed much lower percentage of 6pLOH than that of MEP and GMP.I found approximately 30 times lower expression of CXCL12 which promotes the cell growth and proliferation cytokine than that of normal fraction with microarray analysis. As a result, I demonstrated the percentage of HLA deficient was significantly decreased, since the cell cycle was not promoted in the 6pLOH of CMP fraction with low CXCL12 and CXCR4 expression.
人骨髓造血不同阶段6pLOH的比例不同,6pLOH的比例在造血祖细胞中明显低于MEP和GMP,而促进细胞生长和增殖的细胞因子CXCL 12的表达比正常组份低约30倍。结果,我证明HLA缺陷的百分比显著降低,因为在具有低CXCL 12和CXCR 4表达的CMP组分的6pLOH中,细胞周期没有被促进。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Increased Gene Expression Of the Nr4A Family In Bone Marrow T Cells Of Patients With Early Stage Acquired Aplastic Anemia
早期获得性再生障碍性贫血患者骨髓 T 细胞中 Nr4A 家族基因表达增加
  • DOI:
  • 发表时间:
    2013
  • 期刊:
  • 影响因子:
    0
  • 作者:
    丸山 裕之;佐治 博夫;屋部登志雄;柏瀬 貢一;片桐 孝和;材木 義隆;斉藤 千鶴;細川 晃平;山崎 宏人;小川 誠司;中尾 眞二;Takamasa Katagiri;Kohei Hosokawa
  • 通讯作者:
    Kohei Hosokawa
Prevalence of HLA-A allele lacking leukocytes in patients with aplastic anemia at diagnosis
再生障碍性贫血患者诊断时缺乏白细胞的 HLA-A 等位基因的患病率
  • DOI:
  • 发表时间:
    2013
  • 期刊:
  • 影响因子:
    0
  • 作者:
    丸山 裕之;佐治 博夫;屋部登志雄;柏瀬 貢一;片桐 孝和;材木 義隆;斉藤 千鶴;細川 晃平;山崎 宏人;小川 誠司;中尾 眞二;Takamasa Katagiri;Kohei Hosokawa;Hiroyuki Maruyama;Tetsuichi Yoshizato;Takamasa Katagiri;Yoshiki Akatsuka;Chizuru Saito;Tetsuichi Yoshizato;Hiroyuki Maruyama
  • 通讯作者:
    Hiroyuki Maruyama
Immunologically escaped hematopoiesis caused by HLA allelic loss in patients with aplastic anemia
再生障碍性贫血患者 HLA 等位基因缺失导致免疫逃逸造血
  • DOI:
  • 发表时间:
    2012
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Takamasa Katagiri;Shinji Nakao
  • 通讯作者:
    Shinji Nakao
Evidence That GPI-AP-Specific CTLs Are Not Involved In The “escape” Of Piga mutant Hematopoietic Stem Cells In Aplastic Anemia
证据表明 GPI-AP 特异性 CTL 不参与再生障碍性贫血中 Piga 突变造血干细胞的“逃逸”
  • DOI:
  • 发表时间:
    2013
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Takamasa Katagiri;Hiroyuki Maruyama;Shigeki Ohtake;Chizuru Saito;Kohei Hosokawa;Seishi Ogawa;and Shinji Nakao
  • 通讯作者:
    and Shinji Nakao
Escape hematopoiesis by HSC with somatic SLIT1 mutaions in patients with acquired aplastic anemia
获得性再生障碍性贫血患者体细胞 SLIT1 突变的 HSC 逃逸造血
  • DOI:
  • 发表时间:
    2013
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Chizuru Saito;Kohei Hosokawa;Hiroyuki Maruyama;Takamasa Katagiri;Akinori Kanai;Hirotaka Matsui;Toshiya Inaba;Akari Kazami;Masafumi Taniwaki;Hirohito Yamazaki;Shinji Nakao
  • 通讯作者:
    Shinji Nakao
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KATAGIRI Takamasa其他文献

KATAGIRI Takamasa的其他文献

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{{ truncateString('KATAGIRI Takamasa', 18)}}的其他基金

Elucidation of the pahogenesis of auto immune-bone marrow failure with human hematopoietic stem cells derived from iPS cells
利用 iPS 细胞衍生的人造血干细胞阐明自身免疫骨髓衰竭的发病机制
  • 批准号:
    17K09007
  • 财政年份:
    2017
  • 资助金额:
    $ 2.75万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Analysis of human haematopietic stem cell movement with PNH-type cell.
人类造血干细胞与PNH型细胞运动的分析。
  • 批准号:
    26860363
  • 财政年份:
    2014
  • 资助金额:
    $ 2.75万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)

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Immune escape mechanisms in BCOR/BCORL1 mutant hematopoietic stem cells from patients with aplastic anemia
再生障碍性贫血患者 BCOR/BCORL1 突变型造血干细胞的免疫逃逸机制
  • 批准号:
    23K15297
  • 财政年份:
    2023
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A Phase III Randomized Trial Comparing Unrelated Donor Bone Marrow Transplantation with Immune Suppressive Therapy for Newly Diagnosed Pediatric and Young Adult Patients with Severe Aplastic Anemia
一项针对新诊断患有严重再生障碍性贫血的儿童和年轻成人患者进行非亲缘供体骨髓移植与免疫抑制治疗比较的 III 期随机试验
  • 批准号:
    10722602
  • 财政年份:
    2022
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  • 项目类别:
A Phase III Randomized Trial Comparing Unrelated Donor Bone Marrow Transplantation with Immune Suppressive Therapy for Newly Diagnosed Pediatric and Young Adult Patients with Severe Aplastic Anemia
一项针对新诊断患有严重再生障碍性贫血的儿童和年轻成人患者进行非亲缘供体骨髓移植与免疫抑制治疗比较的 III 期随机试验
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Eltombopag: Novel Mode of Action on Normal and Aplastic Anemia Hematopoietic Stem Cells
Eltombopag:对正常和再生障碍性贫血造血干细胞的新作用模式
  • 批准号:
    10676888
  • 财政年份:
    2022
  • 资助金额:
    $ 2.75万
  • 项目类别:
1/2A Phase III Randomized Trial Comparing Unrelated Donor Bone Marrow Transplantation with Immune Suppressive Therapy for Newly Diagnosed Pediatric and Young Adult Patients with Severe Aplastic Anemia
1/2A III 期随机试验,比较无关供体骨髓移植与免疫抑制治疗对新诊断患有严重再生障碍性贫血的儿童和年轻成人患者的影响
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  • 项目类别:
The effects of somatic HLA class I allele mutations on antigen presentation in acquired aplastic anemia
体细胞 HLA I 类等位基因突变对获得性再生障碍性贫血抗原呈递的影响
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  • 财政年份:
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  • 项目类别:
1/2A Phase III Randomized Trial Comparing Unrelated Donor Bone Marrow Transplantation with Immune Suppressive Therapy for Newly Diagnosed Pediatric and Young Adult Patients with Severe Aplastic Anemia
1/2A III 期随机试验,比较无关供体骨髓移植与免疫抑制治疗对新诊断患有严重再生障碍性贫血的儿童和年轻成人患者的影响
  • 批准号:
    10370775
  • 财政年份:
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The effects of somatic HLA class I allele mutations on antigen presentation in acquired aplastic anemia
体细胞 HLA I 类等位基因突变对获得性再生障碍性贫血抗原呈递的影响
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    10545024
  • 财政年份:
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Identification of autoantigens presented by specific HLA class I alleles in aplastic anemia
再生障碍性贫血中特定 HLA I 类等位基因呈现的自身抗原的鉴定
  • 批准号:
    19H03686
  • 财政年份:
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    $ 2.75万
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    Grant-in-Aid for Scientific Research (B)
Functional analysis of novel genes related to aplastic anemia using mouse models.
使用小鼠模型对与再生障碍性贫血相关的新基因进行功能分析。
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    19K08297
  • 财政年份:
    2019
  • 资助金额:
    $ 2.75万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
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