@article {HuieENEURO.0091-15.2015, author = {J. Russell Huie and Ellen D. Stuck and Kuan H. Lee and Karen-Amanda Irvine and Michael S. Beattie and Jacqueline C. Bresnahan and James W. Grau and Adam R. Ferguson}, title = {AMPA receptor phosphorylation and synaptic co-localization on motor neurons drive maladaptive plasticity below complete spinal cord injury}, elocation-id = {ENEURO.0091-15.2015}, year = {2015}, doi = {10.1523/ENEURO.0091-15.2015}, publisher = {Society for Neuroscience}, abstract = {Clinical spinal cord injury (SCI) is accompanied by comorbid peripheral injury in 47\% of patients. Human and animal modeling data have shown that painful peripheral injuries undermine long-term recovery of locomotion through unknown mechanisms. Peripheral nociceptive stimuli induce maladaptive synaptic plasticity in dorsal horn sensory systems through AMPA receptor (AMPAR) phosphorylation and trafficking to synapses. Here we test whether ventral horn motor neurons in rats demonstrate similar experience-dependent maladaptive plasticity below a complete SCI in vivo. Quantitative biochemistry demonstrated that intermittent nociceptive stimulation (INS) rapidly and selectively increases AMPAR subunit GluA1 Serine 831 phosphorylation and localization to synapses in the injured spinal cord, while reducing synaptic GluA2. These changes predict motor dysfunction in the absence of cell death signaling, suggesting an opportunity for therapeutic reversal. Automated confocal time-course analysis of lumbar ventral horn motor neurons confirmed a time-dependent increase in synaptic GluA1 with concurrent decrease in synaptic GluA2. Optical fractionation of neuronal plasma membranes revealed GluA2 removal from extrasynaptic sites on motor neurons early after INS followed by removal from synapses 2 hours later. As GluA2-lacking AMPARs are canonical calcium-permeable AMPARs (CP-AMPARs), their stimulus- and time-dependent insertion provides a therapeutic target for limiting calcium-dependent dynamic maladaptive plasticity after SCI. Confirming this, a selective CP-AMPAR antagonist protected against INS-induced maladaptive spinal plasticity, restoring adaptive motor responses on a sensorimotor spinal training task. These findings highlight the critical involvement of AMPARs in experience-dependent spinal cord plasticity after injury and provide a pharmacologically-targetable synaptic mechanism by which early post-injury experience shapes motor plasticity.Significance Statement: Recent findings have demonstrated that painful stimuli below a spinal cord injury can affect future locomotor training and recovery in spinal cord injured patients (Bouffard et al. J Neuroscience 2014), as well as in animal models (Ferguson et al., J Neuroscience, 2008; Baumbauer et al., J Neuroscience, 2009). However the cellular and molecular mechanisms for this experience-dependent modulation of spinal cord plasticity are poorly understood. This work uncovers a novel synaptic mechanism by which peripheral nociceptive (painful) input following a spinal cord injury can undermine future adaptive spinal cord plasticity, providing a novel target for improving recovery after spinal cord injury, and mitigating aberrant forms of spinal neuroplasticity.}, URL = {https://www.eneuro.org/content/early/2015/10/30/ENEURO.0091-15.2015}, eprint = {https://www.eneuro.org/content/early/2015/10/30/ENEURO.0091-15.2015.full.pdf}, journal = {eNeuro} }