2005
DOI: 10.1016/j.neuroscience.2005.06.040
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Interneurons transiently express the ERG K+ channels during development of mouse spinal networks in vitro

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Cited by 28 publications
(40 citation statements)
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“…The pH was adjusted to 7.4 with NaOH (osmolarity, 305 mOsm).Current-clamp recordings in the whole-cell configuration (patch-clamp) were obtained at room temperature (RT) (22 Ϯ 2°C) from visually identified ventral spinal neurons with pipettes (4 -6 M⍀) filled with a solution of the following composition (in mM): 120 K-gluconate, 20 KCl, 10 HEPES, 10 EGTA, 2 MgCl 2 , and 2 Na 2 ATP; pH 7.35 with KOH. In accordance with previous investigations (Streit et al, 1991;Ballerini and Galante, 1998;Ballerini et al, 1999;Galante et al, 2000;Rosato-Siri et al, 2002;Avossa et al, 2003;Furlan et al, 2005), neurons were empirically termed interneurons when their cell body diameter was between 10 and 20 m, thus making them clearly distinguishable from cells morphologically resembling motoneurons (30 -60 m diameter) and immunoreactive to the motoneuron marker SMI32 (supplemental Fig. 2, available at www.jneurosci.org as supplemental material).Unlike interneurons, motoneurons generated long processes that often terminated on the muscle fibers distributed laterally to the slice (Ballerini et al, 1999;Avossa et al, 2003).…”
Section: Methodssupporting
confidence: 67%
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“…The pH was adjusted to 7.4 with NaOH (osmolarity, 305 mOsm).Current-clamp recordings in the whole-cell configuration (patch-clamp) were obtained at room temperature (RT) (22 Ϯ 2°C) from visually identified ventral spinal neurons with pipettes (4 -6 M⍀) filled with a solution of the following composition (in mM): 120 K-gluconate, 20 KCl, 10 HEPES, 10 EGTA, 2 MgCl 2 , and 2 Na 2 ATP; pH 7.35 with KOH. In accordance with previous investigations (Streit et al, 1991;Ballerini and Galante, 1998;Ballerini et al, 1999;Galante et al, 2000;Rosato-Siri et al, 2002;Avossa et al, 2003;Furlan et al, 2005), neurons were empirically termed interneurons when their cell body diameter was between 10 and 20 m, thus making them clearly distinguishable from cells morphologically resembling motoneurons (30 -60 m diameter) and immunoreactive to the motoneuron marker SMI32 (supplemental Fig. 2, available at www.jneurosci.org as supplemental material).Unlike interneurons, motoneurons generated long processes that often terminated on the muscle fibers distributed laterally to the slice (Ballerini et al, 1999;Avossa et al, 2003).…”
Section: Methodssupporting
confidence: 67%
“…Organotypic slice cultures of spinal cord and dorsal root ganglia (DRG) were obtained from mouse embryos (F1 hybrid C57BL6ϫSJL) at days 12-13 of gestation, as described previously (Avossa et al, 2003;Furlan et al, 2005). Briefly, the fetuses were obtained by cesarean delivery from timedpregnant anesthetized mice (chloral hydrate 10.5%, 0.4 ml/100 g, i.m.)…”
Section: Methodsmentioning
confidence: 99%
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“…4 Among voltage-dependent K þ channels, the ERG subfamily is mainly involved in the control of cellular excitability, both in mammals and in invertebrates. 5,6 Moreover, macrophages and neutrophils are key cellular components of innate immunity and the GCA grancalcin gene, located between IFIH1 and KCNH7 genes, is highly expressed in both types of leukocytes. 7 More recently, association of this locus with Grave's disease was also found.…”
Section: Introductionmentioning
confidence: 99%