Cell Biology of Megakaryocytes & Platelets GRC & GRS /Bridging the Divide Between Megakaryocytes and Platelets-

巨核细胞的细胞生物学

基本信息

  • 批准号:
    8901437
  • 负责人:
  • 金额:
    $ 1万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2015
  • 资助国家:
    美国
  • 起止时间:
    2015-04-15 至 2016-03-31
  • 项目状态:
    已结题

项目摘要

 DESCRIPTION (provided by applicant): Blood platelets play a critical role in the prevention of excessive blood loss at sites of tissue injury. They are formed from megakaryocytes in the bone marrow and circulate in the blood in a resting state, but undergo 'explosive' activation upon damage to the vasculature, supporting formation of a vascular plug. Conditions associated with a reduction in platelet number can lead to excessive bleeding. Platelets play a fundamental role in stroke and myocardial infarction, and contribute to the metastatic spread of cancer. The Gordon Research Conference (GRC) on the Cell Biology of Megakaryocytes and Platelets is the leading scientific meeting focused on the biology of platelets and their precursor cells, megakaryocytes. This will be the 6th biennial meeting that brings together two groups of scientists with complimentary goals and interests. Meeting topics will include emerging roles for platelets in biology, including immunity, tumor metastasis, and lymphatic development. Identification of novel signaling pathways that regulate MK development and platelet activation will also be a key theme, including an original session focused on membrane biology. Novel mechanisms for growing platelets in vitro as well as innovative ways to visualize MK and platelet biology will also come under the spotlight. The conference will also report on the latest findings in the regulation of circulating platelet numbers. In addition, there is a whole session devoted to presentations of Hot Topics, selected form submitted abstracts. There are several innovative aspects to the planned meeting, including 1. A session titled Blood Pharming: Making platelets in vitro, providing opportunities to learn about, and discuss new ideas about how novel megakaryocyte and platelet biology may transform the transfusion industry; 2. The sessions will combine both MK and platelet development and function, thus, forcing a union of two audiences with overlapping interests, further increasing exchange of ideas; 3. The bench to bedside potential is illustrated in a new session titled: Megakaryocytes and platelets breaking bad, and talks, such as on novel therapeutic options for low platelet counts; and 4. Inclusion, for the firs time, of a session titled: Platelets as the Swiss Army Knives of the Blood provides opportunities to learn about, and discuss new roles for platelets in other fields. The retention of the Gordon Research Seminar (GRS) for the 2015 meeting is a critical component. This venue encourages promising trainees to participate more visibly in the program and possibly be encouraged to continue and develop a career in MK and platelet biology. Abstracts submitted by trainees will be scored by a panel, and selected for oral presentations, of which some will also present under Hot Topics in the GRC. Open discussions with investigators will provide mentoring related to careers in academia and in pharmaceutical companies. The GRS/GRC take place from April 18-19th and 19-24th, 2015, at the Renaissance Tuscany II Ciocco Resort, Lucca (Barga), Italy.
 描述(由申请方提供):血小板在防止组织损伤部位失血过多方面发挥关键作用。它们由骨髓中的巨核细胞形成,并在静止状态下在血液中循环,但在血管系统受损时经历“爆炸性”激活,支持血管栓的形成。与血小板数量减少相关的疾病可导致过度出血。血小板在中风和心肌梗死中起着重要作用,并有助于癌症的转移扩散。关于巨核细胞和血小板的细胞生物学的戈登研究会议(GRC)是专注于血小板及其前体细胞巨核细胞生物学的领先科学会议。这将是第六届两年一度的会议,汇集了两组具有互补目标和兴趣的科学家。会议主题将包括血小板在生物学中的新兴作用,包括免疫,肿瘤转移和淋巴发育。识别调节MK发育和血小板活化的新型信号通路也将是一个关键主题,包括专注于膜生物学的原始会议。体外血小板生长的新机制以及可视化MK和血小板生物学的创新方法也将成为关注的焦点。会议还将报告关于调节循环血小板数量的最新发现。此外,还有一个专门讨论 热门话题的介绍,从提交的摘要中选出。计划中的会议有几个创新方面,包括1.一个会议题为血液制药:在体外制造血小板,提供机会了解,并讨论新的想法如何新的巨核细胞和血小板生物学可能会改变输血行业; 2。这些会议将联合收割机结合MK和血小板的发展和功能,从而迫使两个有重叠利益的观众联合起来,进一步增加思想交流; 3.在一个新的会议中说明了从实验室到床边的潜力,该会议的标题是:巨核细胞和血小板破裂不良,以及会谈,例如关于低血小板计数的新治疗选择;和4。第一次包括一个题为:血小板作为瑞士军队血液的补充,为了解和讨论血小板在其他领域的新作用提供了机会。保留戈登研究研讨会(GRS)的2015年会议是一个关键组成部分。这个场地鼓励有前途的学员更明显地参与该计划,并可能被鼓励继续和发展MK和血小板生物学的职业生涯。学员提交的摘要将由一个小组评分,并选择口头报告,其中一些也将在GRC的热门话题下提出。与调查人员的公开讨论将提供与学术界和制药公司职业相关的指导。GRS/GRC将于2015年4月18日至19日和19日至24日在意大利卢卡(巴尔加)的文艺复兴托斯卡纳II Ciocco度假村举行。

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)

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JOSEPH E ITALIANO其他文献

JOSEPH E ITALIANO的其他文献

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{{ truncateString('JOSEPH E ITALIANO', 18)}}的其他基金

The Centrosome as a master controller of platelet production.
中心体作为血小板生成的主控制器。
  • 批准号:
    10576942
  • 财政年份:
    2022
  • 资助金额:
    $ 1万
  • 项目类别:
The Centrosome as a master controller of platelet production.
中心体作为血小板生成的主控制器。
  • 批准号:
    10351290
  • 财政年份:
    2022
  • 资助金额:
    $ 1万
  • 项目类别:
Vascular Thiol Isomerases in Thrombosis
血栓形成中的血管硫醇异构酶
  • 批准号:
    9912828
  • 财政年份:
    2017
  • 资助金额:
    $ 1万
  • 项目类别:
Cytoskeletal Mechanisms of Platelet Formation
血小板形成的细胞骨架机制
  • 批准号:
    8786585
  • 财政年份:
    2001
  • 资助金额:
    $ 1万
  • 项目类别:
Cytoskeletal Mechanisms of Platelet Formation
血小板形成的细胞骨架机制
  • 批准号:
    8015560
  • 财政年份:
    2001
  • 资助金额:
    $ 1万
  • 项目类别:
Cytoskeletal Mechanisms of Platelet Formation
血小板形成的细胞骨架机制
  • 批准号:
    8979711
  • 财政年份:
    2001
  • 资助金额:
    $ 1万
  • 项目类别:
Cytoskeletal Mechanisms of Platelet Formation
血小板形成的细胞骨架机制
  • 批准号:
    10209279
  • 财政年份:
    2001
  • 资助金额:
    $ 1万
  • 项目类别:
Cytoskeletal Mechanisms of Platelet Formation
血小板形成的细胞骨架机制
  • 批准号:
    6365799
  • 财政年份:
    2001
  • 资助金额:
    $ 1万
  • 项目类别:
Cytoskeletal Mechanisms of Platelet Formation
血小板形成的细胞骨架机制
  • 批准号:
    6538082
  • 财政年份:
    2001
  • 资助金额:
    $ 1万
  • 项目类别:
Cytoskeletal Mechanisms of Platelet Formation
血小板形成的细胞骨架机制
  • 批准号:
    8399081
  • 财政年份:
    2001
  • 资助金额:
    $ 1万
  • 项目类别:

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