TY - JOUR
T1 - Transforming growth factor β2 is a neuronal death-inducing ligand for amyloid-β precursor protein
AU - Hashimoto, Yuichi
AU - Chiba, Tomohiro
AU - Yamada, Marina
AU - Nawa, Mikiro
AU - Kanekura, Kohsuke
AU - Suzuki, Hiroaki
AU - Terashita, Kenzo
AU - Aiso, Sadakazu
AU - Nishimoto, Ikuo
AU - Matsuoka, Masaaki
PY - 2005/11
Y1 - 2005/11
N2 - APP, amyloid β precursor protein, is linked to the onset of Alzheimer's disease (AD). We have here found that transforming growth factor β2 (TGFβ2), but not TGFβ1, binds to APP. The binding affinity of TGFβ2 to APP is lower than the binding affinity of TGFβ2 to the TGFβ receptor. On binding to APP, TGFβ2 activates an APP-mediated death pathway via heterotrimeric G protein Go, c-Jun N-terminal kinase, NADPH oxidase, and caspase 3 and/or related caspases. Overall degrees of TGFβ2-induced death are larger in cells expressing a familial AD-related mutant APP than in those expressing wild-type APP. Consequently, superphysiological concentrations of TGFβ2 induce neuronal death in primary cortical neurons, whose one allele of the APP gene is knocked in with the V642I mutation. Combined with the finding indicated by several earlier reports that both neural and glial expression of TGFβ2 was upregulated in AD brains, it is speculated that TGFβ2 may contribute to the development of AD-related neuronal cell death.
AB - APP, amyloid β precursor protein, is linked to the onset of Alzheimer's disease (AD). We have here found that transforming growth factor β2 (TGFβ2), but not TGFβ1, binds to APP. The binding affinity of TGFβ2 to APP is lower than the binding affinity of TGFβ2 to the TGFβ receptor. On binding to APP, TGFβ2 activates an APP-mediated death pathway via heterotrimeric G protein Go, c-Jun N-terminal kinase, NADPH oxidase, and caspase 3 and/or related caspases. Overall degrees of TGFβ2-induced death are larger in cells expressing a familial AD-related mutant APP than in those expressing wild-type APP. Consequently, superphysiological concentrations of TGFβ2 induce neuronal death in primary cortical neurons, whose one allele of the APP gene is knocked in with the V642I mutation. Combined with the finding indicated by several earlier reports that both neural and glial expression of TGFβ2 was upregulated in AD brains, it is speculated that TGFβ2 may contribute to the development of AD-related neuronal cell death.
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U2 - 10.1128/MCB.25.21.9304-9317.2005
DO - 10.1128/MCB.25.21.9304-9317.2005
M3 - Article
C2 - 16227582
AN - SCOPUS:27144443047
SN - 0270-7306
VL - 25
SP - 9304
EP - 9317
JO - Molecular and Cellular Biology
JF - Molecular and Cellular Biology
IS - 21
ER -