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. 2011 Mar 2;31(5):1196–1210. doi: 10.1038/jcbfm.2011.26

Table 1. Summary of findings on BH3-only mice in seizure, ischemia, and trauma.

  Mechanism of activation Response to insult Knockout mouse phenotype and reference
Bid Cleaved to tBid Cleaved to tBid after seizure, ischemia, and TBI No protection (seizures) (Engel et al, 2010a)
      Smaller infarcts (ischemia) (Plesnila et al, 2001; Yin et al, 2002)
      Reduced lesion volume (TBI) (Bermpohl et al, 2006)
       
Bim Transcriptional induction (JNK, FoxO3a, CHOP) Upregulated after seizure and ischemia Mild protection in hippocampus but not cortex (seizures) (Murphy et al, 2010)
      Protection (ischemia) (Ness et al, 2006)
  Release from dynein light chain   Untested (TBI)
       
Puma Transcriptional induction (p53, FoxO3a, CHOP, ER stress) Upregulated after seizure and ischemia Strong protection (seizure) (Engel et al, 2010b, 2010c)
      No protection (ischemia) (Kuroki et al, 2009)
      Untested (TBI)

BH3, Bcl-2 homology domain 3; ER, endoplasmic reticulum; JNK, c-Jun N-terminal kinase; TBI, traumatic brain injury.