1995
DOI: 10.1016/0165-3806(96)83482-1
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Phenotype plasticity and immunocytochemical evidence for ChAT and DβH co-localization in fetal pig superior cervical ganglion cells

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Cited by 10 publications
(6 citation statements)
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“…The co-localization of cholinergic and catecholaminergic markers has already been observed in STG neurons projecting to the pig bulbospongiosus muscle, 72 to the retractor penis muscle in the male pig 73 , and to the sow retractor clitoridis muscle 74 . Moreover, ChAT and DßH were found co-localized in the cranial cervical ganglion of fetal pig 75 . It is known that, during fetal development, some neurons transiently express the noradrenergic phenotype but subsequently lose their noradrenergic characteristics, becoming cholinergic cells 76-78 .…”
Section: Discussionmentioning
confidence: 72%
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“…The co-localization of cholinergic and catecholaminergic markers has already been observed in STG neurons projecting to the pig bulbospongiosus muscle, 72 to the retractor penis muscle in the male pig 73 , and to the sow retractor clitoridis muscle 74 . Moreover, ChAT and DßH were found co-localized in the cranial cervical ganglion of fetal pig 75 . It is known that, during fetal development, some neurons transiently express the noradrenergic phenotype but subsequently lose their noradrenergic characteristics, becoming cholinergic cells 76-78 .…”
Section: Discussionmentioning
confidence: 72%
“…Immunoreactivity for VIP has already been found, with distinct cranio-caudal differences, in some neurons of the pig cervical, 82 thoracolumbar 48,83 and sacral STG 75 . Quantitative differences in the positivity for this peptide have been found also within the pig UBT by different researchers.…”
Section: Discussionmentioning
confidence: 85%
“…Superior cervical ganglion (SCG) cells. Primary neuronal cultures were prepared from SCG from porcine fetuses collected at the slaughterhouse (gestation stage between 6?5 and 10 weeks) as adapted from Wang et al (1995).…”
Section: Cellsmentioning
confidence: 99%
“…Bovine liver was used as a positive control. Lymphocytes, isolated as previously described (42), were used as a negative control. PCR products were directly sequenced by an automated system using fluorescence-labeled dideoxynucleotides (Applied Biosystems, Foster City, CA).…”
Section: Methodsmentioning
confidence: 99%