Journal of Biological Chemistry · 2002 · 174 citations · 20 references
Life SciencesNeurosciencePharmacologyCell SignalingMolecular NeuroscienceSignal TransductionCholinergic PharmacologyCholinergic SignalingNeuroprotectionNeurotransmissionNeurotransmitter ReceptorsReceptor Signaling In NeuronsAmyloid-beta Induced ApoptosisNeuronal DysfunctionNeuroprotective MechanismsNeuroprotective SignalingNeurotransmitter-receptor InteractionsNicotinic Receptor PharmacologyPhosphoinositide 3-Kinase-akt ActivationReceptor-mediated Interactions
The molecular mechanisms of alpha7 nicotinic acetylcholine receptor (nAChR)-mediated neuroprotection remain unclear. In this study we provide evidence that nicotine stimulation of alpha7 nAChR transduces signals to phosphatidylinositol 3-kinase and Akt via Janus kinase 2 (JAK2) in a cascade, which results in neuroprotection. Exposure to beta-amyloid results in the activation of the apoptotic enzyme caspase-3 and cleavage of the DNA-repairing enzyme poly-(ADP-ribose) polymerase. This cascade is inhibited by nicotine through JAK2 activation, and these effects are blocked by preincubation with the JAK2-specific inhibitor AG-490. We also found that pretreatment of cells with angiotensin II blocks the nicotine-induced activation of JAK2 via the AT(2) receptor and completely prevents alpha7 nAChR-mediated neuroprotective effects further suggesting a pivotal role for JAK2. These findings identify novel mechanisms of receptor interactions relevant to neuronal viability and suggest novel therapeutic strategies to optimize neuroprotection.
20
Inhibition of acute lymphoblastic leukaemia by a Jak-2 inhibitor
Naftaly Meydan, T Grunberger, Harjit Dadi et al. · Nature · 1996 · 912 citations
Kelly T. Dineley, Marcus A. Westerman, Duc Thien Bui et al. · PubMed · 2001 · 516 citations · Full text
Kelly T. Dineley, Marcus A. Westerman, Duy Bui et al. · Journal of Neuroscience · 2001 · 462 citations · Full text