2012
DOI: 10.1371/journal.pone.0030790
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AKT Signaling Mediates IGF-I Survival Actions on Otic Neural Progenitors

Abstract: BackgroundOtic neurons and sensory cells derive from common progenitors whose transition into mature cells requires the coordination of cell survival, proliferation and differentiation programmes. Neurotrophic support and survival of post-mitotic otic neurons have been intensively studied, but the bases underlying the regulation of programmed cell death in immature proliferative otic neuroblasts remains poorly understood. The protein kinase AKT acts as a node, playing a critical role in controlling cell surviv… Show more

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Cited by 54 publications
(64 citation statements)
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“…The other genes were involved in two critical signaling pathway, namely PI3K/Akt pathway and Wnt signal pathway. The PI3K-Akt pathway participated in early infection of some exogenous avian leucosis viruses [46] and could mediate IGF-1 survival during the otic neuronal progenitor phase of early inner ear development [47]. The GPC1 gene involved in Wnt pathway was of great importance in chick, which can regulate the signaling mechanisms in early formation of the trigeminal sensory system and cell proliferation hence affected reproduction performance [48,49].…”
Section: Discussionmentioning
confidence: 99%
“…The other genes were involved in two critical signaling pathway, namely PI3K/Akt pathway and Wnt signal pathway. The PI3K-Akt pathway participated in early infection of some exogenous avian leucosis viruses [46] and could mediate IGF-1 survival during the otic neuronal progenitor phase of early inner ear development [47]. The GPC1 gene involved in Wnt pathway was of great importance in chick, which can regulate the signaling mechanisms in early formation of the trigeminal sensory system and cell proliferation hence affected reproduction performance [48,49].…”
Section: Discussionmentioning
confidence: 99%
“…During inner ear development, PI3K/Akt signaling has also been associated with insulin-like growth factor 1 (IGF-1). Mutation of the gene encoding its receptor (Igfr) is associated with severe cochlear defects and deafness [18], [19].…”
Section: Introductionmentioning
confidence: 99%
“…In addition, the fraction of injured urethras whose damage extended to corpus spongiosum tissue was the lowest in group 1, suggesting IGF‐1 prevented spongiofibrosis. IGF‐1 has been shown to have beneficial effects on antifibrosis and tissue regeneration, which are plausible explanations for this result . We should investigate the mechanisms of cell proliferation and antifibrotic effects of IGF‐1.…”
Section: Discussionmentioning
confidence: 95%