Mechanisms of neuroprotection by a novel rescue factor humanin from Swedish mutant amyloid precursor protein

Y Hashimoto, Y Ito, T Niikura, Z Shao, M Hata… - Biochemical and …, 2001 - Elsevier
Y Hashimoto, Y Ito, T Niikura, Z Shao, M Hata, F Oyama, I Nishimoto
Biochemical and biophysical research communications, 2001Elsevier
We report a novel gene, designated Humanin (HN) cDNA, that suppresses neuronal cell
death by K595N/M596L-APP (NL-APP), a mutant causing familial Alzheimer's disease
(FAD), termed Swedish mutant. Transfection of neuronal cells with HN cDNA or treatment
with the coding HN polypeptide abrogated cytotoxicity by NL-APP. HN suppressed
neurotoxicity by Aβ1-43 in the absence of N2 supplement, but could not inhibit Aβ secretion
from NL-APP. HN could also protect neuronal cells from death by NL-APP lacking the 41st …
We report a novel gene, designated Humanin (HN) cDNA, that suppresses neuronal cell death by K595N/M596L-APP (NL-APP), a mutant causing familial Alzheimer's disease (FAD), termed Swedish mutant. Transfection of neuronal cells with HN cDNA or treatment with the coding HN polypeptide abrogated cytotoxicity by NL-APP. HN suppressed neurotoxicity by Aβ1-43 in the absence of N2 supplement, but could not inhibit Aβ secretion from NL-APP. HN could also protect neuronal cells from death by NL-APP lacking the 41st and 42nd residues of the Aβ region. Therefore, HN suppressed neuronal cell death by NL-APP not through inhibition of Aβ42 secretion, but with two targets for its inhibitory action: (i) the intracellular toxic mechanism directly triggered by NL-APP and (ii) neurotoxicity by Aβ. HN will contribute to the development of curative therapy of AD, especially as a novel reagent that could mechanistically supplement Aβ-production inhibitors.
Elsevier