• DocumentCode
    2272617
  • Title

    Activated astrocytes and TAT transduction after in vitro traumatic mechanical injury

  • Author

    Kang, Woo Hyeun ; Simon, Melissa J. ; Morrison, Barclay, III

  • Author_Institution
    Columbia Univ., New York, NY, USA
  • fYear
    2010
  • fDate
    26-28 March 2010
  • Firstpage
    1
  • Lastpage
    2
  • Abstract
    Activated astrocytes have been implicated in the deleterious cascade of events immediately following traumatic brain injury (TBI). In this study, primary astrocytes were activated by a well-characterized stretch injury model of TBI. Nitrite production, an outcome measure for activation in astrocytes, increased significantly after injury. Using the cell-penetrating peptide (CPP) TAT, delivery of a mock-therapeutic, green fluorescent protein (GFP), was enhanced after mechanical injury of primary astrocytes. GAG production also increased in injured astrocytes, suggesting a mechanism for enhanced delivery, confirming findings published in an earlier study. These results highlight the ability of TAT to target activated astrocytes via increased GAG content, which could lead to potential TAT-based targeted therapeutics for TBI.
  • Keywords
    biomembrane transport; brain; gene therapy; molecular biophysics; proteins; TAT transduction; activated astrocytes; cell-penetrating peptide; in vitro traumatic mechanical injury; mock-therapeutic green fluorescent protein; nitrite production; primary astrocytes; stretch injury model; traumatic brain injury; Brain injuries; Capacitive sensors; DNA; Diseases; Extraterrestrial measurements; Fluorescence; In vitro; Peptides; Production; Proteins;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioengineering Conference, Proceedings of the 2010 IEEE 36th Annual Northeast
  • Conference_Location
    New York, NY
  • Print_ISBN
    978-1-4244-6879-9
  • Type

    conf

  • DOI
    10.1109/NEBC.2010.5458144
  • Filename
    5458144