Peripheral BDZ Receptor Biomarker of Neurontoxicity Grant

abstract

  • DESCRIPTION (provided by applicant): The long-term goal of this research is to continue the validation and application of the Translocator Protein 18 kDa (TSPO), previously called the peripheral benzodiazepine receptor as a biomarker of neurotoxicity, neuroinflammation and neurodegeneration. While TSPO is being used in preclinical and clinical studies to detect and monitor brain injury and inflammation, the function of TSPO in microglia and astrocytes, the glial cell types that express and upregulate TSPO levels is not currently known. The proposed studies have several inter-related goals. First, we have discovered that in primary microglia, TSPO may be associated with NADPH oxidase (NOX) and mechanistic studies proposed in Specific Aim 1 are planned to extend this finding and to further understand the TSPO/NOX interaction. In Specific Aim 2 we propose studies to understand the function of TSPO in astrocytes. While the function of TSPO in microglia may be associated with the innate immune response, we hypothesize that the function of TSPO in astrocytes may be associated with the synthesis of neurosteroids. An understanding of the function of TSPO in microglia and astrocytes will assist in devising therapeutic approaches for mitigating neuroinflammation in neurodegenerative disease. Finally in Specific Aim 3 we proposed studies to validate and apply TSPO as a biomarker of neurotoxicity in the fetal and early postnatal brain. While most studies to date have used brain tissue from adult animals or humans, we have evidence that TSPO may serve as a biomarker of brain injury in the fetal brain. These studies will use a novel TSPO-GFP mouse model that will significantly facilitate the detection of brain injury in vivo and ex vivo. Te development of novel methods to screen the neurotoxic potential of chemicals is of high priority as articulated by Dr. Francis Collins, the present director of the National Institutes of Health. Thus, the proposed studies have significant translational implications to the human condition. The proposed studies will use a variety of methodologies ranging from cell culture to imaging and are in line with research goals of the National Institute of Environmental Health Sciences and the National Toxicology Program.

date/time interval

  • January 1, 2016 - May 31, 2019

sponsor award ID

  • 5R01ES007062-19

local award ID

  • AWD000000006507

contributor

keywords

  • Adult
  • Animal Model
  • Animals
  • Antioxidants
  • Area
  • Astrocytes
  • Benzodiazepine Receptor
  • Biological Markers
  • Brain
  • Brain Injuries
  • Cell Culture Techniques
  • Cell Nucleus
  • Cell physiology
  • Chemicals
  • Cholesterol
  • Clinical Research
  • Cyclophosphamide
  • Detection
  • Development
  • Diagnosis
  • Disease model
  • Electron Transport Complex III
  • Encephalitis
  • Fluorescence
  • Genes
  • Goals
  • Grant
  • Green Fluorescent Proteins
  • Guidelines
  • Health
  • Histologic
  • Human
  • Image
  • Individual
  • Industrialization
  • Innate Immune Response
  • Investigation
  • Knowledge
  • Laboratories
  • Life
  • Ligands
  • Mediating
  • Methodology
  • Methods
  • Microglia
  • Microscopy
  • Molecular Chaperones
  • Monitor
  • Mus
  • NADPH Oxidase
  • National Institute of Environmental Health Sciences
  • National Toxicology Program
  • Nature
  • Nerve Degeneration
  • Neurodegenerative Disorders
  • Neuroglia
  • Neurologic
  • Neurotoxins
  • Optics
  • Peripheral
  • Process
  • Production
  • Progress Reports
  • Proteins
  • Recovery
  • Research
  • Risk
  • Role
  • Science
  • Teratogens
  • Testing
  • Therapeutic
  • Therapeutic Intervention
  • Time
  • Toxic effect
  • Toxicology
  • Translating
  • United States National Institutes of Health
  • Validation
  • Valproic Acid
  • Vision
  • Work
  • base
  • behavioral outcome
  • brain tissue
  • cell type
  • fetal
  • hazard
  • heme a
  • in utero
  • in vivo
  • interest
  • man
  • mature animal
  • mouse model
  • multidisciplinary
  • nervous system disorder
  • neuroinflammation
  • neurosteroids
  • neurotoxic
  • neurotoxicity
  • novel
  • novel strategies
  • postnatal
  • preclinical study
  • protein protein interaction
  • public health relevance
  • receptor
  • screening
  • specific biomarkers
  • therapeutic effectiveness
  • tool