4.5 Article

Selective Cre-mediated gene deletion identifies connexin 43 as the main connexin channel supporting olfactory ensheathing cell networks

期刊

JOURNAL OF COMPARATIVE NEUROLOGY
卷 527, 期 7, 页码 1278-1289

出版社

WILEY
DOI: 10.1002/cne.24628

关键词

Cre recombinase; connexin 43; gap junctions; olfactory ensheathing cells; proteolipid protein; RRID: AB_10000325; RRID: AB_141596; RRID: AB_2110187; RRID: AB_2533973; RRID: AB_2533979; RRID: AB_2576217; RRID: AB_561049; RRID: IMSR_JAX: 005975; RRID: IMSR_JAX: 007914; RRID: IMSR_JAX: 008039

资金

  1. Fondo para la Investigacion Cientifica y Tecnologica [PICT 2011-1650, PICT 2014-1954, PICT-PRH 2009 0053, PICT-PRH 2009-0053]
  2. National Institutes of Health, National Institute on Deafness and Other Communication Disorders [DC013791, DC015438]
  3. Consejo Nacional de Investigaciones Cientificas y Tecnicas [PIP 0332]
  4. Universidad de Buenos Aires [UBACYT 20020100100562]

向作者/读者索取更多资源

Many functions of glial cells depend on the formation of selective glial networks mediated by gap junctions formed by members of the connexin family. Olfactory ensheathing cells (OECs) are specialized glia associated with olfactory sensory neuron axons. Like other glia, they form selective networks, however, the connexins that support OEC connectivity in vivo have not been identified. We used an in vivo mouse model to selectively delete candidate connexin genes with temporal control from OECs and address the physiological consequences. Using this model, we effectively abolished the expression of connexin 43 (Cx43) in OECs in both juvenile and adult mice. Cx43-deleted OECs exhibited features consistent with the loss of gap junctions including reduced membrane conductance, largely reduced sensitivity to the gap junction blocker meclofenamic acid and loss of dye coupling. This indicates that Cx43, a typically astrocytic connexin, is the main connexin forming functional channels in OECs. Despite these changes in functional properties, the deletion of Cx43 deletion did not alter the density of OECs. The strategy used here may prove useful to delete other candidate genes to better understand the functional roles of OECs in vivo.

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