Počet záznamů: 1  

Long-Term Cultures of Spinal Cord Interneurons

  1. 1.
    0566895 - ÚEM 2023 RIV CH eng J - Článek v odborném periodiku
    Vargová, Ingrid - Kriška, Ján - Kwok, Jessica - Fawcett, James - Jendelová, Pavla
    Long-Term Cultures of Spinal Cord Interneurons.
    Frontiers in Cellular Neuroscience. Roč. 16, feb. (2022), č. článku 827628. E-ISSN 1662-5102
    Grant CEP: GA MŠMT(CZ) EF15_003/0000419
    Institucionální podpora: RVO:68378041
    Klíčová slova: spinal interneurons * culture * maturation * axon regeneration * laser axotomy
    Obor OECD: Neurosciences (including psychophysiology
    Impakt faktor: 5.3, rok: 2022
    Způsob publikování: Open access
    https://www.frontiersin.org/articles/10.3389/fncel.2022.827628/full

    Spinal cord interneurons (SpINs) are highly diverse population of neurons that play a significant role in circuit reorganization and spontaneous recovery after spinal cord injury. Regeneration of SpIN axons across rodent spinal injuries has been demonstrated after modification of the environment and neurotrophin treatment, but development of methods to enhance the intrinsic regenerative ability of SpINs is needed. There is a lack of described in vitro models of spinal cord neurons in which to develop new regeneration treatments. For this reason, we developed a new model of mouse primary spinal cord neuronal culture in which to analyze maturation, morphology, physiology, connectivity and regeneration of identified interneurons. Isolated from E14 mice, the neurons mature over 15 days in vitro, demonstrated by expression of maturity markers, electrophysiological patch-clamp recordings, and formation of synapses. The neurons express markers of SpINs, including Tlx3, Lmx1b, Lbx1, Chx10, and Pax2. The neurons demonstrate distinct morphologies and some form perineuronal nets in long-term cultivation. Live neurons in various maturation stages were axotomized, using a 900 nm multiphoton laser and their fate was observed overnight. The percentage of axons that regenerated declined with neuronal maturity. This model of SpINs will be a valuable tool in future regenerative, developmental, and functional studies alongside existing models using cortical or hippocampal neurons.
    Trvalý link: https://hdl.handle.net/11104/0338162

     
     
Počet záznamů: 1  

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