Matches in SemOpenAlex for { <https://semopenalex.org/work/W760441965> ?p ?o ?g. }
- W760441965 endingPage "142" @default.
- W760441965 startingPage "131" @default.
- W760441965 abstract "The floor plate (FP), a ventral midline structure of the developing neural tube, has differential neurogenic capabilities along the anterior–posterior axis. The midbrain FP, unlike the hindbrain and spinal cord floor plate, is highly neurogenic and produces midbrain dopaminergic (mDA) neurons. Canonical Wnt/beta-catenin signaling, at least in part, is thought to account for the difference in neurogenic capability. Removal of beta-catenin results in mDA progenitor specification defects as well as a profound reduction of neurogenesis. To examine the effects of excessive Wnt/beta-catenin signaling on mDA specification and neurogenesis, we have analyzed a model wherein beta-catenin is conditionally stabilized in the Shh + domain. Here, we show that the Foxa2 +/Lmx1a + domain is extended rostrally in mutant embryos, suggesting that canonical Wnt/beta-catenin signaling can drive FP expansion along the rostrocaudal axis. Although excess canonical Wnt/beta-catenin signaling generally promotes neurogenesis at midbrain levels, less tyrosine hydroxylase (Th)+, mDA neurons are generated, particularly impacting the Substantia Nigra pars compacta. This is likely because of improper progenitor specification. Excess canonical Wnt/beta-catenin signaling causes downregulation of net Lmx1b, Shh and Foxa2 levels in mDA progenitors. Moreover, these progenitors assume a mixed identity to that of Lmx1a +/Lmx1b +/Nkx6-1 +/Neurog1 + progenitors. We also show by lineage tracing analysis that normally, Neurog1 + progenitors predominantly give rise to Pou4f1 + neurons, but not Th + neurons. Accordingly, in the mutant embryos, Neurog1 + progenitors at the midline generate ectopic Pou4f1 + neurons at the expense of Th + mDA neurons. Our study suggests that an optimal dose of Wnt/beta-catenin signaling is critical for proper establishment of the mDA progenitor character. Our findings will impact embryonic stem cell protocols that utilize Wnt pathway reagents to derive mDA neuron models and therapeutics for Parkinson's disease." @default.
- W760441965 created "2016-06-24" @default.
- W760441965 creator A5001017141 @default.
- W760441965 creator A5008567079 @default.
- W760441965 creator A5011840167 @default.
- W760441965 creator A5036741347 @default.
- W760441965 creator A5047821770 @default.
- W760441965 creator A5051094403 @default.
- W760441965 creator A5053227531 @default.
- W760441965 creator A5082378596 @default.
- W760441965 date "2015-09-01" @default.
- W760441965 modified "2023-10-01" @default.
- W760441965 title "Excessive Wnt/beta-catenin signaling promotes midbrain floor plate neurogenesis, but results in vacillating dopamine progenitors" @default.
- W760441965 cites W1963783082 @default.
- W760441965 cites W1969276438 @default.
- W760441965 cites W1975703347 @default.
- W760441965 cites W1990251289 @default.
- W760441965 cites W1993209089 @default.
- W760441965 cites W1993634104 @default.
- W760441965 cites W1995626795 @default.
- W760441965 cites W1997187913 @default.
- W760441965 cites W2002526679 @default.
- W760441965 cites W2006852136 @default.
- W760441965 cites W2011083612 @default.
- W760441965 cites W2027764735 @default.
- W760441965 cites W2027969818 @default.
- W760441965 cites W2028326666 @default.
- W760441965 cites W2029150089 @default.
- W760441965 cites W2030285506 @default.
- W760441965 cites W2040079193 @default.
- W760441965 cites W2040538482 @default.
- W760441965 cites W2042408279 @default.
- W760441965 cites W2043269926 @default.
- W760441965 cites W2046867426 @default.
- W760441965 cites W2056413798 @default.
- W760441965 cites W2057335179 @default.
- W760441965 cites W2080936298 @default.
- W760441965 cites W2086046051 @default.
- W760441965 cites W2086723987 @default.
- W760441965 cites W2086809468 @default.
- W760441965 cites W2087625151 @default.
- W760441965 cites W2090863421 @default.
- W760441965 cites W2091040966 @default.
- W760441965 cites W2091134679 @default.
- W760441965 cites W2097295765 @default.
- W760441965 cites W2099270682 @default.
- W760441965 cites W2102130285 @default.
- W760441965 cites W2102512718 @default.
- W760441965 cites W2102678193 @default.
- W760441965 cites W2104135721 @default.
- W760441965 cites W2105643617 @default.
- W760441965 cites W2111525324 @default.
- W760441965 cites W2112763851 @default.
- W760441965 cites W2118259271 @default.
- W760441965 cites W2130128490 @default.
- W760441965 cites W2136440581 @default.
- W760441965 cites W2137927007 @default.
- W760441965 cites W2144216324 @default.
- W760441965 cites W2148512749 @default.
- W760441965 cites W2149288806 @default.
- W760441965 cites W2154069538 @default.
- W760441965 cites W2161282017 @default.
- W760441965 cites W2164223111 @default.
- W760441965 cites W2172099438 @default.
- W760441965 doi "https://doi.org/10.1016/j.mcn.2015.07.002" @default.
- W760441965 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4633300" @default.
- W760441965 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26164566" @default.
- W760441965 hasPublicationYear "2015" @default.
- W760441965 type Work @default.
- W760441965 sameAs 760441965 @default.
- W760441965 citedByCount "28" @default.
- W760441965 countsByYear W7604419652015 @default.
- W760441965 countsByYear W7604419652016 @default.
- W760441965 countsByYear W7604419652017 @default.
- W760441965 countsByYear W7604419652018 @default.
- W760441965 countsByYear W7604419652019 @default.
- W760441965 countsByYear W7604419652020 @default.
- W760441965 countsByYear W7604419652021 @default.
- W760441965 countsByYear W7604419652022 @default.
- W760441965 countsByYear W7604419652023 @default.
- W760441965 crossrefType "journal-article" @default.
- W760441965 hasAuthorship W760441965A5001017141 @default.
- W760441965 hasAuthorship W760441965A5008567079 @default.
- W760441965 hasAuthorship W760441965A5011840167 @default.
- W760441965 hasAuthorship W760441965A5036741347 @default.
- W760441965 hasAuthorship W760441965A5047821770 @default.
- W760441965 hasAuthorship W760441965A5051094403 @default.
- W760441965 hasAuthorship W760441965A5053227531 @default.
- W760441965 hasAuthorship W760441965A5082378596 @default.
- W760441965 hasBestOaLocation W7604419652 @default.
- W760441965 hasConcept C137183658 @default.
- W760441965 hasConcept C137620995 @default.
- W760441965 hasConcept C15729860 @default.
- W760441965 hasConcept C169760540 @default.
- W760441965 hasConcept C201750760 @default.
- W760441965 hasConcept C2779324961 @default.
- W760441965 hasConcept C2780938664 @default.
- W760441965 hasConcept C28328180 @default.