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• W2892292172 abstract "The enteric nervous system (ENS) is a network of neurons and glia found in the gut wall and governs this gastrointestinal function independently from the central nervous system (CNS). ENS comprises the myenteric plexus (MP) and the submucous plexus (SP). In this study, we examined the expression profile of neurofilament heavy chain (NF-H), neuron-specific enolase (NSE), calcyclin (S100A6), vimentin and glial fibril acidic protein (GFAP) in ovine ileal enteric neurons and enteric glia cells (EGCs) during prenatal development using an immunohistochemical method. The material of the study consisted of 15 different fetal ileum tissues obtained between days 60 and 150 of pregnancy. NF-H was observed in the majority of ganglion cells in SP and MP throughout the fetal period. It was determined that there was no NF-H reaction in some ganglion cells in Peyer’s patches of internal submucosal plexus (ISPF). In the early stage of pregnancy (60–90 days), there was no expression of NSE and S1006 in ileum. After this period, NSE and S1006 were expressed in the ganglion cells of the plexus, indicating an increase in the amount of expression towards the end of pregnancy. In the early period, vimentin expression was only detected in intramuscular interstitial cells (ICs) (60–90 days), but later (90–150 days) it was also seen in the cells around the ganglion cells in the plexus. On days 60–90 of gestation, GFAP expression only occurred in MP, but in later stages, staining was also detected in SP. In the plexus, an immunoreactivity was present in EGCs forming a network around the ganglion cell. During the last period of gestation (120–150 days), the number of GFAP-positive plexus increased, with the majority of these stained cells being observed in MP. Interestingly, weak staining or reaction did not occur in ISPF, unlike other plexuses. In conclusion, this is the first study that demonstrated the expression of NF-H, vimentin, S100A6, NSE and glial fibril acidic protein (GFAP) in ovine ileal ENS in the prenatal period. In the last period of gestation (120–150 days), the expression profile of ENS was similar to that of adult animals. The expression of the used markers increased toward the end of pregnancy. Our results suggest that neurons and EGCs show heterogeneity, and GFAP and NF-H cannot be used as panenteric glial or panneuronal markers, respectively. We also demonstrated, for the first time, the prenatal expression of S100A6 in enteric neurons and the possibility of using this protein for the identification of enteric neurons." @default.
• W2892292172 created "2018-09-27" @default.
• W2892292172 creator A5006371760 @default.
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• W2892292172 date "2018-11-01" @default.
• W2892292172 modified "2023-09-23" @default.
• W2892292172 title "Expression profile of some neuronal and glial cell markers in the ovine ileal enteric nervous system during prenatal development" @default.
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• W2892292172 cites W1725475117 @default.
• W2892292172 cites W1911440889 @default.
• W2892292172 cites W1966761529 @default.
• W2892292172 cites W1967827598 @default.
• W2892292172 cites W1975100390 @default.
• W2892292172 cites W1976310333 @default.
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• W2892292172 cites W2011848992 @default.
• W2892292172 cites W2013936060 @default.
• W2892292172 cites W2016905587 @default.
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• W2892292172 cites W2028885301 @default.
• W2892292172 cites W2030509467 @default.
• W2892292172 cites W2032984191 @default.
• W2892292172 cites W2036943768 @default.
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• W2892292172 cites W2162987671 @default.
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• W2892292172 doi "https://doi.org/10.1016/j.acthis.2018.09.002" @default.
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• W2892292172 hasPublicationYear "2018" @default.
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