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Details

Autor(en) / Beteiligte
Titel
Modulation of calcium-induced cell death in human neural stem cells by the novel peptidylarginine deiminase–AIF pathway
Ist Teil von
  • Biochimica et biophysica acta, 2014-06, Vol.1843 (6), p.1162-1171
Ort / Verlag
Netherlands: Elsevier B.V
Erscheinungsjahr
2014
Link zum Volltext
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • PADs (peptidylarginine deiminases) are calcium-dependent enzymes that change protein-bound arginine to citrulline (citrullination/deimination) affecting protein conformation and function. PAD up-regulation following chick spinal cord injury has been linked to extensive tissue damage and loss of regenerative capability. Having found that human neural stem cells (hNSCs) expressed PAD2 and PAD3, we studied PAD function in these cells and investigated PAD3 as a potential target for neuroprotection by mimicking calcium-induced secondary injury responses. We show that PAD3, rather than PAD2 is a modulator of cell growth/death and that PAD activity is not associated with caspase-3-dependent cell death, but is required for AIF (apoptosis inducing factor)-mediated apoptosis. PAD inhibition prevents association of PAD3 with AIF and AIF cleavage required for its translocation to the nucleus. Finally, PAD inhibition also hinders calcium-induced cytoskeleton disassembly and association of PAD3 with vimentin, that we show to be associated also with AIF; together this suggests that PAD-dependent cytoskeleton disassembly may play a role in AIF translocation to the nucleus. This is the first study highlighting a role of PAD activity in balancing hNSC survival/death, identifying PAD3 as an important upstream regulator of calcium-induced apoptosis, which could be targeted to reduce neural loss, and shedding light on the mechanisms involved. [Display omitted] •PAD pathway is a novel regulator of cell death/survival in human neural stem cells.•PAD3 inhibition reduces calcium-induced cell death and cytoskeleton disassembly.•PAD3 is required for AIF (apoptosis inducing factor) translocation to the nucleus.•Targeting the PAD pathway could provide a novel strategy for neuroprotection.

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