S
Satoru Funamoto
Researcher at Doshisha University
Publications - 33
Citations - 3203
Satoru Funamoto is an academic researcher from Doshisha University. The author has contributed to research in topics: Amyloid precursor protein & Presenilin. The author has an hindex of 18, co-authored 31 publications receiving 2988 citations. Previous affiliations of Satoru Funamoto include Hokkaido University & University of California, San Diego.
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Journal ArticleDOI
Spatial and temporal regulation of 3-phosphoinositides by PI 3-kinase and PTEN mediates chemotaxis
TL;DR: It is shown that chemotaxis pathways are activated along the lateral sides of cells and PI3K can initiate pseudopod formation, providing evidence for a direct instructional role ofPI3K in leading edge formation.
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gamma-Secretase: successive tripeptide and tetrapeptide release from the transmembrane domain of beta-carboxyl terminal fragment.
Mako Takami,Yu Nagashima,Yoshihisa Sano,Seiko Ishihara,Maho Morishima-Kawashima,Satoru Funamoto,Yasuo Ihara +6 more
TL;DR: Results strongly suggest that Aβ is generated through the stepwise processing of βCTF by γ-secretase, and that an induction period exists in the generation of peptides.
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Signaling pathways controlling cell polarity and chemotaxis
TL;DR: This review outlines the present understanding of Phosphoinositide 3-kinase's central and possibly pivotal role in establishing and maintaining cell polarity by regulating the subcellular localization and activation of downstream effectors that are essential for regulating cellPolarity and proper chemotaxis.
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Potent amyloidogenicity and pathogenicity of Aβ43
Takashi Saito,Takahiro Suemoto,Nathalie Brouwers,Kristel Sleegers,Satoru Funamoto,Naomi Mihira,Yukio Matsuba,Kazuyuki Yamada,Per Nilsson,Jiro Takano,Masaki Nishimura,Nobuhisa Iwata,Nobuhisa Iwata,Christine Van Broeckhoven,Yasuo Ihara,Takaomi C. Saido +15 more
TL;DR: The authors showed that Aβ43 showed a higher propensity to aggregate and was more neurotoxic than Aβ42, and other pathogenic presenilin mutations also caused overproduction of Aβ 43 in a manner correlating with Aβ 42 and with the age of disease onset.
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Role of Phosphatidylinositol 3′ Kinase and a Downstream Pleckstrin Homology Domain–Containing Protein in Controlling Chemotaxis inDictyostelium
TL;DR: PhdA is an adaptor protein that regulates F-actin localization in response to chemoattractants and links PI3K to the control of F-Actin polymerization at the leading edge during pseudopod formation, and it is suggested that PKB and PhdA lie downstream fromPI3K and control different downstream effector pathways that are essential for proper chemotaxis.