2010
DOI: 10.1016/j.neulet.2010.06.068
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Smoothened agonist augments proliferation and survival of neural cells

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Cited by 35 publications
(24 citation statements)
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“…It is possible that enhanced Shh ligand from the VDB may be transported via the septo-hippocampal pathway resulting in increased Shh signaling within the hippocampus (61), which is supported by the evidence of enhanced Ptc expression in the DG. In this context, it is noteworthy that T 3 administration is capable of increasing the postmitotic survival and neuronal differentiation of hippocampal progenitors (62), an effect that overlaps with the enhanced survival observed after treatment with Smo agonists (63). …”
Section: Discussionmentioning
confidence: 99%
“…It is possible that enhanced Shh ligand from the VDB may be transported via the septo-hippocampal pathway resulting in increased Shh signaling within the hippocampus (61), which is supported by the evidence of enhanced Ptc expression in the DG. In this context, it is noteworthy that T 3 administration is capable of increasing the postmitotic survival and neuronal differentiation of hippocampal progenitors (62), an effect that overlaps with the enhanced survival observed after treatment with Smo agonists (63). …”
Section: Discussionmentioning
confidence: 99%
“…Studies have specifically implicated Hh in the adult maintenance of hematopoietic stem cells40, epithelial stem cells in the gastrointestinal tract41, neuronal stem cells in the subventricular zone (SVZ) and the hippocampal dentate gyrus4243, hair follicle stem cells44, mammary stem cells45 and mesenchymal stem cells46. Besides its role in neurogenesis, Hh has also shown neurotrophic properties, in particular regarding dopaminergic neuron survival474849. Administration of Sonic Hedgehog reduced behavioral deficits in animal models of PD5051.…”
Section: Discussionmentioning
confidence: 99%
“…Further, our group has shown the neuroprotective effects of Shh pathway augmentation via a small molecule, smoothened agonist (SAG), against human immunodeficiency virus (HIV)-associated neuropathology in humanized mice (Singh et al 2016). Not only that, but SAG was also shown to prevent neuropathology in a rat model of spinal cord injury as well as a mouse model for Down’s syndrome(Bambakidis et al 2010; Bragina et al 2010), indicating that this approach might lead to timely identification of a neuroprotective drug in order to dampen ZIKV-associated neurological complications.…”
Section: Pharmacological Interventions Against Zikv Infectionmentioning
confidence: 99%