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Westbrook, G.

Publications and source records attributed to Westbrook, G..

3 recordsLinked to original sources

AMPAR immunization induces progressive autoimmune encephalitis with autoreactive B cells in the brain

AMPA and NMDA receptors are central to synaptic plasticity and cognitive function. In anti-NMDA receptor and anti-AMPA receptor (AMPAR) encephalitis, autoantibodies targeting these receptors disrupt synaptic signaling, leading to severe neuropsychiatric symptoms. However, the cellular autoimmune responses and source of pathogenic autoantibodies during onset and progression of central nervous system (CNS) pathology remain poorly understood. By immunizing mice with intact AMPARs in proteoliposomes, we developed a mouse model of anti-AMPAR encephalitis. Mice developed rapidly progressing neuropsychiatric deficits, autoantibodies targeting the AMPAR amino-terminal domain (ATD) and IgG deposition in the brain, accompanied by reduced AMPAR detection. Throughout disease onset and progression, AMPAR-ATD-specific non-proliferating plasma cells and plasmablasts accumulated in the brain and were predominantly localized in AMPAR-expressing brain parenchyma. In contrast, differentiated AMPAR-ATD specific B cells were far less enriched in peripheral lymphoid tissues. Our results suggest that humoral autoimmune responses directly in the CNS drives disease progression in anti-AMPAR encephalitis.

neuroscience↗

Biased synaptic activation of dentate granule cells by exercise reflects inputs from the lateral entorhinal cortex.

Hippocampal dentate granule cells receive multisensory information from the entorhinal cortex in a laminated and functionally segregated manner. We previously reported that brief periods of voluntary exercise in mice increased EPSCs and dendritic spines for inputs from the lateral, but not the medial, entorhinal cortex. Here we asked whether laminar specificity was due to molecular changes specific to distal granule cell dendrites or rather was dependent on upstream drive from the entorhinal cortex. Selective chemogenetic stimulation of either lateral entorhinal cortex (LEC) or the medial entorhinal cortex (MEC) increased granule cell dendritic spine density in the selected pathway. However, the preponderance of exercise-activated cells originated from LEC based on expression of an activity-dependent retrograde virus in Fos-TRAP mice. Our results indicate that the preferential activation by exercise reflects the drive of locomotor-related inputs from the lateral entorhinal cortex rather than selective molecular mechanisms in distal dendrites of dentate granule cells. How this activation pattern affects other salient stimuli involving contextual or spatial cues may underlie the benefits of exercise on learning and memory.

neuroscience↗

α2δ-2 is Required for Functional Postsynaptic Calcium Channel Nanodomain Signaling

2{delta} proteins (CACNA2D1-4) are required for normal neurological function, although how they control neuronal output remains unclear. Using whole-cell recordings of mouse Purkinje cells, we show 2{delta}-2 is required for functional coupling of postsynaptic voltage-dependent calcium entry with effector mechanisms controlling two different outputs, depolarization-induced suppression of excitation mediated by endocannabinoid signaling, and spike afterhyperpolarization generated by calcium-dependent potassium channels. Our findings indicate an important role for 2{delta}-2 proteins in regulating functional postsynaptic calcium channel-coupling in neurons. Significance StatementCalcium influx via membrane voltage-dependent calcium channels drives numerous neuronal processes by signaling through calcium-dependent effector molecules. Signal precision is achieved in part by calcium channel-effector coupling. In mouse Purkinje cell neurons, we show that neuronal 2{delta}-2 protein functionally couples calcium entry to two different postsynaptic calcium-dependent signals, retrograde endocannabinoid signaling and the action potential afterhyperpolarization. Our findings provide new insights about the control of calcium channel-effector coupling as well as new roles for 2{delta}-2 proteins in neurons.

neuroscience↗