Apoptosis in Sepsis: Regulation by TNF &delta-PKC

Information

  • Research Project
  • 7886287
  • ApplicationId
    7886287
  • Core Project Number
    R01GM064552
  • Full Project Number
    7R01GM064552-06
  • Serial Number
    64552
  • FOA Number
  • Sub Project Id
  • Project Start Date
    1/10/2002 - 23 years ago
  • Project End Date
    6/30/2009 - 15 years ago
  • Program Officer Name
    DUNSMORE, SARAH
  • Budget Start Date
    1/1/2009 - 16 years ago
  • Budget End Date
    6/30/2009 - 15 years ago
  • Fiscal Year
    2006
  • Support Year
    6
  • Suffix
  • Award Notice Date
    7/27/2009 - 15 years ago
Organizations

Apoptosis in Sepsis: Regulation by TNF &delta-PKC

Spontaneous apoptosis of neutrophils is attenuated during sepsis and inflammatory cytokines such as TNFalpha have been implicated. The pathophysiological mechanisms involved in TNFalpha-mediated attenuation of apoptosis are poorly understood but proposed to be mediated by the p60 TNF receptor (p60TNFR). In adherent neutrophils to engage beta2 integrins, TNFalpha triggers phosphorylation of the p60TNFR, activation of cell survival signaling pathways and inhibition of spontaneous apoptosis. Our studies implicate phosphatidylinositol 3-kinase (PI 3-kinase) in TNFalpha triggered NFkappaB activation and that TNFalpha activation of PI 3-kinase requires beta2 integrins. The protein kinase C isotype delta (delta-PKC) phosphorylates p60TNFR on serine residue(s) in TNFalpha activated neutrophils. Rottlerin, a delta-PKC inhibitor, suppressed the inhibitory effect of TNFalpha on neutrophil apoptosis and activation of the transcription factor NFkappaB suggesting that delta-PKC may regulate TNFalpha anti-apoptotic signaling. Our model proposes a selective role for delta-PKC in regulating anti-apoptotic signaling triggered by TNFalpha binding to the p60TNFR. The goal of this study is to establish a role for delta-PKC in TNFalpha mediated anti-apoptotic signaling through the p60TNFR using antisense technology to selectively deplete delta-PKC from HL60 cells differentiated to a neutrophilic phenotype. We will: 1: Determine whether delta-PKC regulates TNFalpha mediated anti- apoptotic signaling. Determine the effect of delta-PKC deletion on TNFalpha-mediated suppression of spontaneous apoptosis and activation of the antiapoptotic NFkappaB and the MAP kinases ERK1/2. 2: Assess the role of PI 3-kinase in TNFalpha mediated suppression of spontaneous apoptosis, and determine if delta-PKC is required for TNFalpha mediated activation of PI 3-kinase. 3: Identify the delta-PKC phosphorylation site on the p60TNFR and establish if phosphorylation is in the a) death domain, b) juxtamembrane region, or c) a novel domain. 4: Assess the role of delta-PKC in regulating the assembly of TNFalpha anti-apoptotic signaling complexes and their association with the p60TNFR.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R01
  • Administering IC
    GM
  • Application Type
    7
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    24071
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF MEDICINE
  • Funding ICs
    NIGMS:24071\
  • Funding Mechanism
  • Study Section
    SAT
  • Study Section Name
    Surgery, Anesthesiology and Trauma Study Section
  • Organization Name
    TEMPLE UNIVERSITY
  • Organization Department
    PHYSIOLOGY
  • Organization DUNS
  • Organization City
    PHILADELPHIA
  • Organization State
    PA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    19122
  • Organization District
    UNITED STATES