Journal article

Expression of high affinity choline transporter during mouse development in vivo and its upregulation by NGF and BMP-4 in vitro


Authors listBerse, B; Szczecnska, W; Lopez-Coviella, I; Madziar, B; Zemelko, V; Kaminski, R; Kozar, K; Lips, KS; Pfeil, U; Blusztajn, JK

Publication year2005

Pages132-140

JournalDevelopmental brain research

Volume number157

Issue number2

ISSN0165-3806

DOI Linkhttps://doi.org/10.1016/j.devbrainres.2005.03.013

PublisherElsevier


Abstract
An important feature of cholinergic neurons is high-affinity choline transport, which allows them to reuse choline for the synthesis of ACh needed to support cholinergic neurotransmission. The choline transporter, designated CHT, was recently cloned. We applied RT/PCR to monitor the expression of CHT in the developing mouse CNS from embryonic day 14 (E14) to postnatal day 30 (P30). We found that CHT was expressed early in development, predominantly in the regions containing cholinergic neurons. In the spinal cord, CHT mRNA was present at close to adult levels at the earliest time point examined (E14) and showed almost no changes after birth. In the striatum and the septum, CHT mRNA increased steadily during embryonic stages and leveled off after birth. Surprisingly, CHT mRNA expression was also detected in other brain regions, notably in the cerebellum, where it peaked on E 19, and then rapidly declined during postnatal development. CHT protein was detected by Western blotting as a band of apparent molecular weight of 70 kDa. The accumulation of this protein during development lagged behind mRNA accumulation in all tissues. We also examined the effects of NGF and BMP-4, the potent inducers of choline acetyltransferase and vesicular acetylcholine transporter genes, on CHT expression. Both factors increased CHT mRNA accumulation in primary septal cultures. The effect of NGF was dependent on the PI3K signaling, as it was abolished by the PI3K inhibitor LY294002. This result indicates that some of the signals regulating other cholinergic-specific genes also control CHT expression. (C) 2005 Elsevier B.V. All rights reserved.



Citation Styles

Harvard Citation styleBerse, B., Szczecnska, W., Lopez-Coviella, I., Madziar, B., Zemelko, V., Kaminski, R., et al. (2005) Expression of high affinity choline transporter during mouse development in vivo and its upregulation by NGF and BMP-4 in vitro, Developmental brain research, 157(2), pp. 132-140. https://doi.org/10.1016/j.devbrainres.2005.03.013

APA Citation styleBerse, B., Szczecnska, W., Lopez-Coviella, I., Madziar, B., Zemelko, V., Kaminski, R., Kozar, K., Lips, K., Pfeil, U., & Blusztajn, J. (2005). Expression of high affinity choline transporter during mouse development in vivo and its upregulation by NGF and BMP-4 in vitro. Developmental brain research. 157(2), 132-140. https://doi.org/10.1016/j.devbrainres.2005.03.013



Keywords


ACID RECEPTOR-ALPHAbone morphogenetic proteinGROWTH-FACTORnerve growth factorSEPTAL CELL-LINEseptum

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