2007
DOI: 10.1074/jbc.m703099200
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Differential Regulation of Basic Helix-Loop-Helix Factors Mash1 and Olig2 by β-Amyloid Accelerates Both Differentiation and Death of Cultured Neural Stem/Progenitor Cells

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Cited by 34 publications
(28 citation statements)
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“…It is therefore of special interest in investigating the changes of Aβ or phosphorylated Tau protein levels in the STZ-treated and RCE -protected rats. Studies have already indicated that Aβ might cause deterioration of the brain microenvironment which is important for neurogenesis of NSCs [63], [64]. A recent study also showed that salidroside has protective effects against Aβ-induced oxidative stress in SH-SY5Y human neuroblastoma cells [48].…”
Section: Discussionmentioning
confidence: 99%
“…It is therefore of special interest in investigating the changes of Aβ or phosphorylated Tau protein levels in the STZ-treated and RCE -protected rats. Studies have already indicated that Aβ might cause deterioration of the brain microenvironment which is important for neurogenesis of NSCs [63], [64]. A recent study also showed that salidroside has protective effects against Aβ-induced oxidative stress in SH-SY5Y human neuroblastoma cells [48].…”
Section: Discussionmentioning
confidence: 99%
“…In AD, soluble species of A␤42 are more strongly correlated with disease symptoms than with amyloid plaques (5)(6)(7)(8)(9). A␤42 was also reported to have an effect on differentiation and death of cultured neural stem or progenitor cells (10). Intraneuronal A␤ accumulation in brains of patients with AD, in animal models, and in cultured cells has suggested a pathophysiological role specific for A␤40 and A␤42 (11).…”
mentioning
confidence: 99%
“…Mash1 or ASC1 is one of the basic helix-loop-helix (bHLH) transcription factors that heterodimerizes with the ubiquitous Class I bHLH E proteins to form complexes that are crucial in neurogenesis and neural differentiation during development (43 found in the adult cerebral cortex and giving rise to the ganglionic eminence and olfactory epithelium (44,45). A study using Mash1 null mutant mice showed that Mash1 is required for the generation of an early population of oligodendrocyte precursors (OPCs), which is involved in the regulation of synaptic transmission and adult neurogenensis (46).…”
Section: Discussionmentioning
confidence: 99%