Glycosaminoglycan Chains and Axon Regeneration
نویسندگان
چکیده
Specific sensory input to neocortex arrives in layer 4, whereas nonspecific input, such as information about salience or novelty, is thought to arrive in layer 1. This scheme might imply a slower arrival of inputs to layer 1. In this issue, Zhu and Zhu examine this question using paired whole-cell recording in vivo from layer 1 nonpyramidal cells and the dendrites of the output pyramidal neurons in layer 5. They measured the latency of EPSCs evoked by natural stimulation of whiskers. Surprisingly, the latency in layer 1 was 5–7 msec, the same as in layer 4. As expected, layer 1 cells had larger receptive fields responding to 6 –15 whiskers. Because concurrent signals in layers 1 and 4 lower the threshold for dendritic calcium action potentials and thus enhance burst firing in the output cells in layer 5, the authors postulate that the concurrent inputs may serve as a coincidence detector.
منابع مشابه
A novel DNA enzyme reduces glycosaminoglycan chains in the glial scar and allows microtransplanted dorsal root ganglia axons to regenerate beyond lesions in the spinal cord.
CNS lesions induce production of ECM molecules that inhibit axon regeneration. One major inhibitory family is the chondroitin sulfate proteoglycans (CSPGs). Reduction of their glycosaminoglycan (GAG) chains with chondroitinase ABC leads to increased axon regeneration that does not extend well past the lesion. Chondroitinase ABC, however, is unable to completely digest the GAG chains from the pr...
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Chondroitin sulfate proteoglycans (CSPGs) play important roles in the developing and mature nervous system, where they guide axons, maintain stable connections, restrict synaptic plasticity, and prevent axon regeneration following CNS injury. The chondroitin sulfate glycosaminoglycan (CS GAG) chains that decorate CSPGs are essential for their functions. Through these sugar chains, CSPGs are abl...
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Chondroitin sulfate proteoglycans (CSPGs) are upregulated in the CNS after injury and participate in the inhibition of axon regeneration mainly through their glycosaminoglycan (GAG) side chains. In the present study, we have identified a new way to alleviate the inhibition of axonal regeneration by CSPG GAGs. We have successfully decreased the amount of CSPG GAG produced by astrocytes by target...
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