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DESCRIPTION (provided by applicant): Optical imaging is rapidly becoming one of the most versatile imaging modalities in biomedical research. The advantages of optical imaging compared to other imaging modalities include its non-ionizing low-energy radiation, high sensitivity for detecting objects in the micron range, and continuous data acquisition in real time and in an intact environment. The cost, space, and time demands associated with optical imaging are less than for other imaging modalities, and the speed and relative ease of imaging makes this modality attractive for potential clinical applications. The Athinoula A. Martinos Center for Biomedical Imaging at the Massachusetts General Hospital (MGH) strives to develop and apply breakthrough imaging approaches in clinically meaningful ways. Our continuing success relies on the integration of new and emerging technologies into our existing research imaging repertoire, which includes functional and high-resolution magnetic resonance imaging (fMRI and MRI), magnetoencephalography (MEG), positron emission tomography (PET), and homebuilt functional optical imaging instrumentation. New technologies enhance our ability to validate and interpret data from our existing imaging resources and to combine imaging modalities for novel multimodal imaging applications-capabilities that are particularly needed in the emerging field of molecular imaging. We propose to purchase a state-of-the-art optical imaging system capable of 3D molecular imaging in transmission fluorescence, reflectance fluorescence, and bioluminescence modes in vivo, ex vivo, and in vitro. Significant advantages of the optical techniques possible with this system include the potential for multichannel imaging by using multiple probes with different spectral characteristics; quick, easy, and relatively low-cost rapid testing of biological hypotheses and proofs of principle in living experimental models. Importantly, optical bioluminescence imaging has unique advantages for detection of very low levels of signal because of its virtually background-free light emission. With its ease of operation, short acquisition time (typically 10-60 sec), and potential high-throughput format in vitro (microplates) and in vivo (5 mice, 23 cm FOV), this innovative system also provides high-throughput imaging capabilities. The new optical system will be an important resource for many currently funded biomedical imaging research projects. Major projects include studies on neurodenenerative disorders and brain function, cancer, and pancreatic islets in diabetes and transplantation. With the new in vivo optical imaging system and our existing imaging facilities under one roof, we can feasibly perform in-vivo experiments using one or more imaging modalities in succession, or even in parallel. This system will be an invaluable resource for the rich body of interdisciplinary research at the Martinos center and the larger MGH research community, as well as at other institutions in the greater Boston area. PUBLIC HEALTH RELEVANCE: Acquiring of a state-of-the-art in vivo optical imaging system with fluorescence and bioluminescence capabilities will allow for fast, easy and cheap ways to rapidly test biological hypotheses and proofs of principle in living experimental models, which could be further utilized for in vivo drug screening, development of imaging reporters and versatile animal studies in cancer, neurological disorders, diabetes and cardiovascular pathologies.
期刊论文(20)
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科研奖励(0)
会议论文
DOI: 10.1002/ijc.28499
发表时间: 2014-04-01
期刊: INTERNATIONAL JOURNAL OF CANCER
影响因子: 6.4
作者: [Ghosh, Subrata K., Yigit, Mehmet V., Uchida, Masashi, Ross, Alana W., Barteneva, Natalie, Moore, Anna, Medarova, Zdravka]
通讯作者: Medarova, Zdravka
DOI: 10.1158/0008-5472.can-10-2070
发表时间: 2010-10-01
期刊: Cancer research
影响因子: 11.2
作者: [Kumar M, Yigit M, Dai G, Moore A, Medarova Z]
通讯作者: Medarova Z
DOI: 10.1371/journal.pone.0019362
发表时间: 2011-04-29
期刊: PloS one
影响因子: 3.7
作者: [Ran C, Zhao W, Moir RD, Moore A]
通讯作者: Moore A
DOI: 10.1093/noajnl/vdaa106
发表时间: 2020-01
期刊: Neuro-oncology advances
影响因子: --
作者: [Teng J, Lashgari G, Tabet EI, Tannous BA]
通讯作者: Tannous BA
13
    Novel Prostate cancer therapy based on m-aconitase inhibition
    • 批准号:
      10435673
    • 项目类别:
    • 资助金额:
      $23.5万
    • 财政年份:
      2022
    • 负责人:
      ANNA MOORE
    • 依托单位:
    Novel Prostate cancer therapy based on m-aconitase inhibition
    • 批准号:
      10580844
    • 项目类别:
    • 资助金额:
      $18.11万
    • 财政年份:
      2022
    • 负责人:
      ANNA MOORE
    • 依托单位:
    Large Animal Facility for Imaging and Image-guided Therapies at MSU
    • 批准号:
      10373769
    • 项目类别:
    • 资助金额:
      $672.12万
    • 财政年份:
      2021
    • 负责人:
      ANNA MOORE
    • 依托单位:
    Therapy for Metastatic breast cancer based on micro RNA silencing
    • 批准号:
      10434241
    • 项目类别:
    • 资助金额:
      $58.03万
    • 财政年份:
      2021
    • 负责人:
      ANNA MOORE
    • 依托单位:
    国内基金
    海外基金
    层出镰刀菌氮代谢调控因子AreA 介导伏马菌素 FB1 生物合成的作用机理
    • 批准号:
      2021JJ40433
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2021
    • 负责人:
      孙磊
    • 依托单位:
    寄主诱导梢腐病菌AreA和CYP51基因沉默增强甘蔗抗病性机制解析
    • 批准号:
      32001603
    • 项目类别:
      青年科学基金项目
    • 资助金额:
      24.0万元
    • 批准年份:
      2020
    • 负责人:
      段真珍
    • 依托单位:
    AREA国际经济模型的移植.改进和应用
    • 批准号:
      18870435
    • 项目类别:
      面上项目
    • 资助金额:
      2.0万元
    • 批准年份:
      1988
    • 负责人:
      史树中
    • 依托单位: