Involvement of c-Jun N-terminal kinase in amyloid precursor protein-mediated neuronal cell death.
Hashimoto. Yuichi Y; Tsuji. Osahiko O; Niikura. Takako T; Yamagishi. Yohichi Y; Ishizaka. Miho M; Kawasumi. Masaoki M; Chiba. Tomohiro T; Kanekura. Kohsuke K; Yamada. Marina M; Tsukamoto. Emi E; Kouyama. Keisuke K; Terashita. Kenzo K; Aiso. Sadakazu S; Lin. Anning A; Nishimoto. Ikuo I
Key Findings
- APP triggers neuronal death via the JNK signaling pathway
- Blocking JNK with inhibitors or dominant‑negative forms prevents APP‑induced cell death
- Humanin peptide suppresses APP‑mediated neurotoxicity, likely by interfering with JNK signaling
Practical Outcomes
- Humanin appears to have neuroprotective properties against APP‑related toxicity, hinting it could be explored as a supplement for brain health. However, the evidence is limited to cell experiments, so no dosing or protocol recommendations can be made yet. Enthusiasts should watch for animal and human studies before considering practical use.
Summary
This study shows that a protein called APP can kill brain cells through a signaling pathway involving JNK, and that the tiny peptide Humanin can block this cell death, suggesting it might help protect neurons in conditions like Alzheimer’s, though the work was done in cells, not people.
Abstract
Amyloid precursor protein (APP), the precursor of Abeta, has been shown to function as a cell surface receptor that mediates neuronal cell death by anti-APP antibody. The c-Jun N-terminal kinase (JNK) can mediate various neurotoxic signals, including Abeta neurotoxicity. However, the relationship of APP-mediated neurotoxicity to JNK is not clear, partly because APP cytotoxicity is Abeta independent. Here we examined whether JNK is involved in APP-mediated neuronal cell death and found that: (i) neuronal cell death by antibody-bound APP was inhibited by dominant-negative JNK, JIP-1b and SP600125, the specific inhibitor of JNK, but not by SB203580 or PD98059; (ii) constitutively active (ca) JNK caused neuronal cell death and (iii) the pharmacological profile of caJNK-mediated cell death closely coincided with that of APP-mediated cell death. Pertussis toxin (PTX) suppressed APP-mediated cell death but not caJNK-induced cell death, which was suppressed by Humanin, a newly identified neuroprotective factor which inhibits APP-mediated cytotoxicity. In the presence of PTX, the PTX-resistant mutant of Galphao, but not that of Galphai, recovered the cytotoxic action of APP. These findings demonstrate that JNK is involved in APP-mediated neuronal cell death as a downstream signal transducer of Go.
Study Information
pubmed
2003
2003-02-01T00:00:00.000Z
10.1046/j.1471-4159.2003.01585.x
106
50