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PROJECT SUMMARY/ABSTRACT The neurovascular interface fundamentally changes during CNS diseases due to increased blood-brain barrier permeability and influx of plasma proteins in the CNS parenchyma. Studying neurologic diseases through the multidisciplinary prism of vascular biology, immunology, and neuroscience could be critical for the identification of novel mechanisms of disease, discovery of imaging tools and therapeutic treatments for a wide range of neurologic diseases characterized by BBB disruption. In my laboratory we made unanticipated discoveries on the functional role of BBB disruption in CNS autoimmunity, glial cell activation, and neurodegeneration. We identified leakage of blood proteins in the brain and neurotrophin receptor signaling as novel molecular mediators at the neurovascular interface that regulate glial – neuron cross-talk and the communication between the brain and the immune system. Furthermore, we developed novel methods for high-resolution two-photon microscopy of the neurovascular interface in vivo. Our aim is to understand the mechanisms that control the communication between the brain, immune and vascular systems with the ultimate goal to design novel therapies for neurologic diseases. In this application we propose a multipronged approach to determine the role of neurovascular dysfunction in neurodegeneration, CNS repair, and glial cell biology and discover novel genetic regulatory circuits that control vascular-driven CNS innate immune mediated neurotoxicity. We use an innovative experimental design consisting of in vivo two-photon, super-resolution and electron microscopy of the neurovascular interface, electrophysiology, cell biology and signal transduction, new genetic tools and animal models, and genomic and proteomic approaches. The proposed studies will set the foundation how neurovascular dysfunction regulates brain functions and the outcomes of this research would be applicable for the understanding of the etiology and the development of new treatments for several neurologic diseases, such as multiple sclerosis, stroke, spinal cord and brain injury.
期刊论文(16)
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会议论文
Fractalkine Signaling Attenuates Perivascular Clustering of Microglia and Fibrinogen Leakage during Systemic Inflammation in Mouse Models of Diabetic Retinopathy.
分面信号传导减弱糖尿病性视网膜病变小鼠模型中全身性炎症过程中小胶质细胞和纤维蛋白原泄漏的血管周聚集。
DOI: 10.3389/fncel.2016.00303
发表时间: 2016
期刊: Frontiers in cellular neuroscience
影响因子: 5.3
作者: [Mendiola AS, Garza R, Cardona SM, Mythen SA, Lira SA, Akassoglou K, Cardona AE]
通讯作者: Cardona AE
Extensive and Persistent Extravascular Dermal Fibrin Deposition Characterizes Systemic Sclerosis.
广泛且持续的血管外真皮纤维蛋白沉积是系统性硬化症的特征。
DOI: 10.1101/2023.01.16.523256
发表时间: 2023
期刊: bioRxiv : the preprint server for biology
影响因子: --
作者: [Browning,JeffreyL, Bhawan,Jag, Tseng,Anna, Crossland,Nicholas, Bujor,AndreeaM, Akassoglou,Katerina, Assassi,Shervin, Skaug,Brian, Ho,Jonathan]
通讯作者: Ho,Jonathan
Plasminogen Deficiency Delays the Onset and Protects from Demyelination and Paralysis in Autoimmune Neuroinflammatory Disease.
纤溶酶原缺乏可延迟自身免疫性神经炎症疾病的发病并防止脱髓鞘和麻痹。
DOI: 10.1523/jneurosci.2932-15.2017
发表时间: 2017
期刊: The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子: --
作者: [Shaw,MaureenA, Gao,Zhen, McElhinney,KathrynE, Thornton,Sherry, Flick,MatthewJ, Lane,Adam, Degen,JayL, Ryu,JaeKyu, Akassoglou,Katerina, Mullins,EricS]
通讯作者: Mullins,EricS
Three-Dimensional Imaging of Fibrinogen and Neurovascular Alterations in Alzheimer's Disease.
阿尔茨海默病中纤维蛋白原和神经血管改变的三维成像。
DOI: 10.1007/978-1-0716-2655-9_5
发表时间: 2023
期刊: Methods in molecular biology (Clifton, N.J.)
影响因子: --
作者: [Merlini,Mario, Sozmen,ElifG, Subramanian,KeshavS, Nana,AlissaL, Seeley,WilliamW, Akassoglou,Katerina]
通讯作者: Akassoglou,Katerina
8
    Neurovascular Interactions: Mechanisms, imaging, therapeutic potential
    • 批准号:
      9765418
    • 项目类别:
    • 资助金额:
      $136.88万
    • 财政年份:
      2016
    • 负责人:
      Katerina Akassoglou
    • 依托单位:
    Neurovascular Interactions: Mechanisms, imaging, therapeutic potential
    • 批准号:
      10224346
    • 项目类别:
    • 资助金额:
      $141.6万
    • 财政年份:
      2016
    • 负责人:
      Katerina Akassoglou
    • 依托单位:
    Neurovascular Interactions: Mechanisms, imaging, therapeutic potential
    • 批准号:
      10019602
    • 项目类别:
    • 资助金额:
      $136.88万
    • 财政年份:
      2016
    • 负责人:
      Katerina Akassoglou
    • 依托单位:
    Neurovascular Interactions: Mechanisms, imaging, therapeutic potential
    • 批准号:
      10477958
    • 项目类别:
    • 资助金额:
      $141.6万
    • 财政年份:
      2016
    • 负责人:
      Katerina Akassoglou
    • 依托单位:
    国内基金
    海外基金
    Journal of Integrative Plant Biology
    • 批准号:
      31024801
    • 项目类别:
      专项基金项目
    • 资助金额:
      24.0万元
    • 批准年份:
      2010
    • 负责人:
      贺萍
    • 依托单位: