ANATOMICAL AND ELECTROPHYSIOLOGICAL CHARACTERIZATION OF A POPULATION OF DI6 INTERNEURONS IN THE NEONATAL MOUSE SPINAL CORD
ANATOMICAL AND ELECTROPHYSIOLOGICAL CHARACTERIZATION OF A POPULATION OF DI6 INTERNEURONS IN THE NEONATAL MOUSE SPINAL CORD
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DOI:
10.1016/j.neuroscience.2017.08.031
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发表时间:
2017-10-24
期刊:
影响因子:
3.3
通讯作者:
Gosgnach, Simon
中科院分区:
文献类型:
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作者:
Griener, Anna;Zhang, Wei;Gosgnach, Simon
The locomotor central pattern generator is a neural network located in the ventral aspect of the caudal spinal cord that underlies stepping in mammals. While many genetically defined interneurons that are thought to comprise this neural network have been identified and characterized, the dI6 cells- which express the transcription factors WTI and/or DMRT3- are one population that settle in this region, are active during locomotion, whose function is poorly understood. These cells were originally hypothesized to be commissural premotor interneurons, however evidence in support of this is sparse. Here we characterize this population of cells using the TgDbx1(cre);R26(EFP); Dbx1(Lacz) transgenic mouse line, which has been shown to be an effective marker of dI6 interneurons. We show dI6 cells to be abundant in laminae VII and VIII along the entire spinal cord and provide evidence that subtypes outside the WT1/DMRT3 expressing dI6 cells may exist. Retrograde tracing experiments indicate that the majority of dI6 cells project descending axons, and some make monosynaptic or disynaptic contacts onto motoneurons on either side of the spinal cord. Analysis of their activity during non-resetting deletions, which occur during bouts of fictive locomotion, suggests that these cells are involved in both locomotor rhythm generation and pattern formation. This study provides a thorough characterization of the dI6 cells labeled in the TgDbx1(cre);R26(EFP);Dbx1(Lacz) transgenic mouse, and supports previous work suggesting that these cells play multiple roles during locomotor activity. (C) 2017 IBRO. Published by Elsevier Ltd. All rights reserved.