Novel Autonomous Roles of CNS Angiogenesis

Information

  • Research Project
  • 10156492
  • ApplicationId
    10156492
  • Core Project Number
    R01NS100808
  • Full Project Number
    7R01NS100808-04
  • Serial Number
    100808
  • FOA Number
    PAS-15-029
  • Sub Project Id
  • Project Start Date
    9/30/2017 - 6 years ago
  • Project End Date
    7/31/2022 - a year ago
  • Program Officer Name
    RIDDLE, ROBERT D
  • Budget Start Date
    8/1/2020 - 3 years ago
  • Budget End Date
    7/31/2021 - 2 years ago
  • Fiscal Year
    2020
  • Support Year
    04
  • Suffix
  • Award Notice Date
    8/20/2020 - 3 years ago

Novel Autonomous Roles of CNS Angiogenesis

Abstract The central nervous system (CNS) acquires its vasculature by angiogenesis, a process that is critical for its development and repair. Our work has changed notions of cerebral vascularization which implied that blood vessels sprout passively into the brain parenchyma from pial vascular plexuses to meet metabolic needs of growing neuronal populations or treated endothelial cells of the CNS as a homogenous population. Based on origins, anatomical location, independent growth patterns and developmental regulation, forebrain vascular networks fall into two categories: pial and periventricular. The periventricular vascular network that develops in advance of and independent of neuronal development is strategically positioned to provide support and critical guidance cues to instruct neurogenesis and GABAergic interneuron migration in the developing telencephalon. These findings offer new solutions for transplanted primary neuronal precursors that are unable to migrate and integrate into regions requiring new neurons in the absence of proper guidance mechanisms. This application will explore this novel paradigm of neurovascular interactions in diverse ways. It will identify novel angiogenesis mechanisms underlying the origin and etiology of neuropsychiatric diseases. It aims to highlight the novel concept that endothelial GABA signaling is indispensable for brain development shaping postnatal and adult behavior. It attempts to rescue abnormal vascular GABA signaling during embryonic development as a therapeutic approach for long-lasting mental health outcomes. It will examine whether periventricular?like human endothelial cells promote human GABAergic neuronal migration to facilitate development of novel cell based therapies for GABA-related diseases. Results will have far-reaching effects on concepts and mechanisms of regulation of angiogenesis, offer new perspectives on telencephalic histogenesis principles and will lead to discoveries with unprecedented implications for regenerative medicine and treatment of many neurological and psychiatric diseases.

IC Name
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
  • Activity
    R01
  • Administering IC
    NS
  • Application Type
    7
  • Direct Cost Amount
    226864
  • Indirect Cost Amount
    113003
  • Total Cost
    339867
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    853
  • Ed Inst. Type
  • Funding ICs
    NINDS:339867\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    VCMB
  • Study Section Name
    Vascular Cell and Molecular Biology Study Section
  • Organization Name
    HUNTINGTON MEDICAL RESEARCH INSTITUTES
  • Organization Department
  • Organization DUNS
    077978898
  • Organization City
    PASADENA
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    911052606
  • Organization District
    UNITED STATES