کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5737875 | 1614733 | 2017 | 16 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Postnatal maturation of mouse medullo-spinal cerebrospinal fluid-contacting neurons
ترجمه فارسی عنوان
بلوغ پس از زایمان از نورون های تماس با مایع مغزی نخاعی مغز و نخاعی موش صحرایی
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کلمات کلیدی
DVCSC.caudal medullaPKD2L1phospho-CREBMAP-2Medulla oblongataPSA-NCAMNeuNIQRDcxImmunoreactivity - ایمنی فعالdoublecortin - دوچرخهBrainstem - ساقه مغزdentate gyrus - شکنج دندانه دارSpinal cord - طناب نخاعیCSF - مایع مغزی نخاعیCerebrospinal fluid - مایع مغزی نخاعیdorsal vagal complex - مجتمع وگال پشتیdegree of freedom - میزان آزادیCervical spinal cord - نخاع گردنیmicrotubule-associated protein 2 - پروتئین مرتبط با میکروتوبول 2neuronal nuclei protein - پروتئین هسته ای نورونolfactory bulb - پیاز بویاییcentral canal - کانال مرکزی
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب (عمومی)
چکیده انگلیسی
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 1Â month) 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.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience - Volume 343, 20 February 2017, Pages 39-54
Journal: Neuroscience - Volume 343, 20 February 2017, Pages 39-54
نویسندگان
Adeline Orts-Del'Immagine, Jérôme Trouslard, Coraline Airault, Jean-Philippe Hugnot, Baptiste Cordier, Thierry Doan, Anne Kastner, Nicolas Wanaverbecq,