Literature DB >> 27939302

Postnatal maturation of mouse medullo-spinal cerebrospinal fluid-contacting neurons.

Adeline Orts-Del'Immagine1, Jérôme Trouslard1, Coraline Airault1, Jean-Philippe Hugnot2, Baptiste Cordier3, Thierry Doan3, Anne Kastner1, Nicolas Wanaverbecq4.   

Abstract

The central canal along the spinal cord (SC.) and medulla is characterized by the presence of a specific population of neurons that contacts the cerebrospinal fluid (CSF). These medullo-spinal CSF-contacting neurons (CSF-cNs) are identified by the selective expression of the polycystin kidney disease 2-like 1 ionic channel (PKD2L1 or polycystin-L). In adult, they have been shown to express doublecortin (DCX) and Nkx6.1, two markers of juvenile neurons along with the neuron-specific nuclear protein (NeuN) typically expressed in mature neurons. They were therefore suggested to remain in a rather incomplete maturation state. The aim of this study was to assess whether such juvenile state is stable in postnatal animals or whether CSF-cNs may reach maturity at older stages than neurons in the parenchyma. We show, in the cervical SC. and the brainstem that, in relation to age, CSF-cN density declines and that their cell bodies become more distant from the cc, except in its ventral part. Moreover, in adults (from 1month) by comparison with neonatal mice, we show that CSF-cNs have evolved to a more mature state, as indicated by the increase in the percentage of cells positive for NeuN and of its level of expression. In parallel, CSF-cNs exhibit, in adult, lower DCX immunoreactivity and do not express PSA-NCAM and TUC4, two neurogenic markers. Nevertheless, CSF-cNs still share in adult characteristics of juvenile neurons such as the presence of phospho-CREB and DCX while NeuN expression remained low. This phenotype persists in 12-month-old animals. Thus, despite a pursuit of neuronal maturation during the postnatal period, CSF-cNs retain a durable low differentiated state.
Copyright © 2016 IBRO. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  CSF-contacting neurons; PKD2L1; brainstem; central canal; cervical spinal cord; maturity markers

Mesh:

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Year:  2016        PMID: 27939302     DOI: 10.1016/j.neuroscience.2016.11.028

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  4 in total

1.  GABAB receptors modulate Ca2+ but not G protein-gated inwardly rectifying K+ channels in cerebrospinal-fluid contacting neurones of mouse brainstem.

Authors:  Nina Jurčić; Ghizlane Er-Raoui; Coraline Airault; Jérôme Trouslard; Nicolas Wanaverbecq; Riad Seddik
Journal:  J Physiol       Date:  2018-12-10       Impact factor: 5.182

2.  The Neural Stem Cell Properties of PKD2L1+ Cerebrospinal Fluid-Contacting Neurons in vitro.

Authors:  Shuo Wang; Yuqi He; Huiqian Zhang; Li Chen; Liang Cao; Leiluo Yang; Chunqing Wang; Yujie Pan; Qian Tang; Wei Tan; Xiaowei Dou; Qing Li
Journal:  Front Cell Neurosci       Date:  2021-03-15       Impact factor: 5.505

Review 3.  Regulating Endogenous Neural Stem Cell Activation to Promote Spinal Cord Injury Repair.

Authors:  Emily A B Gilbert; Nishanth Lakshman; Kylie S K Lau; Cindi M Morshead
Journal:  Cells       Date:  2022-03-01       Impact factor: 6.600

4.  The neural stem cell properties of Pkd2l1+ cerebrospinal fluid-contacting neurons in vivo.

Authors:  Liang Cao; Ming-Zhi Huang; Qiang Zhang; Zhang-Rong Luo; Yi Zhang; Ping-Jiang An; Lei-Luo Yang; Wei Tan; Chun-Qing Wang; Xiao-Wei Dou; Qing Li
Journal:  Front Cell Neurosci       Date:  2022-09-09       Impact factor: 6.147

  4 in total

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