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Murali, A. R.

Publications and source records attributed to Murali, A. R..

2 recordsLinked to original sources

Activity-driven proprioceptive synaptic refinement in the developing spinal cord by complement signaling mechanisms

Proprioceptive group Ia afferents detect muscle stretch to guide effortless and purposeful movement and make monosynaptic connections with spinal a-motor neurons to mediate reflexes, such as the stretch reflex. It is thought that proprioceptive Ia afferents target motor neurons of the same spinal segment; yet, how this specificity, if any, is established during early development is unknown. Using ex vivo spinal cord electrophysiology preparations from neonatal mice of both sexes, we identified a developmental period during which proprioceptive la afferents evoke both segmental and intersegmental responses at monosynaptic latencies. We provide anatomical evidence that motor neurons in the lumbar segment 4 (L4) receive direct input from proprioceptive Ia afferents in L5 during early postnatal development. Intersegmental responses (L4/L5) were prominent at postnatal days (P) 4-7 but were virtually absent by P11-13. To test the role of proprioceptor activity on segmental specification, we analyzed NaV1.6 conditional knockout mice (NaV1.6cKO), in which proprioceptor signaling is impaired, and found that intersegmental responses persist up to P11-13 but were absent in age-matched floxed controls. We predict this is due to impaired activation of complement signaling pathways, as NaV1.6cKO mice showed reduced C1qA expression in the ventral spinal cord at P9. Consistent with this, C1qA knockout mice also retain intersegmental responses at P11-13. Collectively, these findings identify an important postnatal window during which segmental specificity of proprioceptive circuits emerges and suggest that proprioceptor activity induces C1qA-mediated elimination of excessive intersegmental connectivity. Key points summaryO_LIDuring the first ten days of postnatal development, the spinal monosynaptic reflex arc possesses intersegmental proprioceptive afferent projections onto motor neurons of an adjacent segment. C_LIO_LIThese exuberant Ia-motoneuron projections are accompanied by evocable intersegmental reflex responses. In normal conditions, the intersegmental response is lost by postnatal day 11. Conversely, in a mouse model of impaired proprioceptive signaling, the intersegmental response persists. C_LIO_LIWe find that impaired proprioceptive signaling through the monosynaptic reflex arc leads to low expression levels of the complement signaling protein, C1qA, near ChAT-positive motor neurons, whereas microglia recruitment is unaffected. This was consistent with the persistence of robust intersegmental responses in C1qA knockout mice. C_LIO_LICollectively, our results show that proprioceptor activity induces complement cascade signaling to prune exuberant intersegmental synapses in the spinal cord formed during early development, resulting in segmental restriction of the monosynaptic reflex arc by the end of the second postnatal week. C_LI

neuroscience↗

Differential encoding of mammalian proprioception by voltage-gated sodium channels

Animals that require purposeful movement for survival are endowed with mechanosensory neurons called proprioceptors that provide essential sensory feedback from muscles and joints to spinal cord circuits, which modulates motor output. Despite the essential nature of proprioceptive signaling in daily life, the mechanisms governing proprioceptor activity are poorly understood. Here, we have identified distinct and nonredundant roles for two voltage-gated sodium channels (NaVs), NaV1.1 and NaV1.6, in mammalian proprioception. Deletion of NaV1.6 in somatosensory neurons (NaV1.6cKO mice) causes severe motor deficits accompanied by complete loss of proprioceptive transmission, which contrasts with our previous findings using similar mouse models to target NaV1.1 (NaV1.1cKO). In NaV1.6cKO animals, loss of proprioceptive feedback caused non-cell- autonomous impairments in proprioceptor end-organs and skeletal muscle that were absent in NaV1.1cKO mice. We attribute the differential contribution of NaV1.1 and NaV1.6 in proprioceptor function to distinct cellular localization patterns. Collectively, these data provide the first evidence that NaV subtypes uniquely shape neurotransmission within a somatosensory modality. TeaserVoltage gated sodium channels differentially encode mammalian proprioception via distinct cellular localization patterns.

neuroscience↗