Defining the Mechanisms by Which Plateletes Regulate Angiogenesis

描述（由申请人提供）：该提案需要一个5年的职业发展计划，以实现血液学的学术生涯。主要研究者已经完成了内科和血液学/肿瘤学奖学金的住院治疗，现在正在通过一个基础科学和翻译方面的项目来扩展她的研究技能。该项目是血小板生物学和血管生成领域的整合。Joseph Italiano博士和Nancy Berliner博士将担任主要研究者的共同导师。Italiano博士是巨核细胞和血小板生物学领域公认的领导者。为了加强该计划的学术指导方面，布里格姆妇女医院（BWH）血液科主任南希·柏林博士将担任共同导师。除了她作为主任的角色，她在骨髓生成方面拥有长期的专业知识，并指导了大量年轻的研究人员。此外，主要研究者还组建了一个咨询委员会，该委员会具有各种科学和临床兴趣，以提供科学和学术职业建议。该项目将重点关注血小板在血管生成中的作用。最近的证据表明，血小板将血管生成调节蛋白组织成不同的α颗粒和形态学上不同的α颗粒群，然后在血小板活化时对差异调节敏感。这项建议将需要建立组织的血管生成调节蛋白的α颗粒和理解机制的差异释放。还将在恶性肿瘤患者以及接受抗血管生成治疗的患者中研究血小板颗粒内的血管生成平衡。具体目标是：1.明确血管生成调节蛋白在血小板中的储存和隔离机制; 2.研究这些蛋白质进行差异释放的机制; 3.探讨血小板在储存、输送和抗血管生成治疗中的作用。相关性（见说明书）：已知血小板携带许多蛋白质，这些蛋白质在称为血管生成的血管生长过程中很重要。在这项研究中，我们试图确定血小板如何组织蛋白质，调节血管生成，以及这些过程在恶性肿瘤患者中的差异，其中血管生成有助于肿瘤生长。 (End摘要）

DESCRIPTION (provided by applicant): The proposal entails a 5 year career development plan for attaining an academic career in Hematology. The principle investigator has completed both residency in Internal Medicine and Hematology/Oncology Fellowship and now is expanding her research skills through a project with both basic science and translational aspects. The project is an integration of the fields of platelet biology and angiogenesis. Dr. Joseph Italiano and Dr. Nancy Berliner will act as co-mentors for the principal investigator. Dr. Italiano is a well recognized leader in the field of megakaryocyte and platelet biology. To enhance the academic mentoring aspects of the program, Dr. Nancy Berliner, Chair of the Division of Hematology at Brigham and Women's Hospital (BWH) will serve as a co-mentor. In addition to her role as Director, she has a long-term expertise in myelopoiesis and has mentored a large number of young investigators. In addition, the principle investigator has assembled an advisory committee with varied scientific and clinical interests to provide scientific and academic career advice. The project will focus on the role of the platelet in angiogenesis. Recent evidence suggests that platelets organize angiogenic regulatory proteins into pharmacologically and morphologically distinct populations of alpha granules, which are then susceptible to differential regulation upon platelet activation. This proposal will entail establishing the organization of angiogenic regulatory proteins in alpha granules and understanding mechanisms of differential release. The angiogenic balance within platelet granules will also be investigated in patients with malignancy as well as those receiving anti-angiogenic therapies. The specific aims are: 1. To define how angiogenesis regulatory proteins are sequestered and stored in platelets; 2. To investigate the mechanisms by which these proteins undergo differential release; and 3. To investigate the role of the platelet in storage, delivery, and function of ant-angiogenic therapy. RELEVANCE (See instructions): Platelets are known to carry a number of proteins important in the process of growing blood vessels termed angiogenesis. In this grant we try to determine how platelets organize the proteins, regulate angiogenesis, and how these processes differ in patients with malignancy in which angiogenesis is instrumental for tumor growth. (End of Abstract)