Cargando…

LIF, a Novel Myokine, Protects Against Amyloid-Beta-Induced Neurotoxicity via Akt-Mediated Autophagy Signaling in Hippocampal Cells

BACKGROUND: Leukemia inhibitory factor, a novel myokine, is known to be associated with neural function, but the underlying molecular mechanism remains unclear. METHODS: HT-22 mouse hippocampal cells, primary hippocampal cells, and Drosophila Alzheimer’s disease model were used to determine the effe...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Hye Jeong, Lee, Jung Ok, Lee, Yong Woo, Kim, Shin Ae, Seo, Il Hyeok, Han, Jeong Ah, Kang, Min Ju, Kim, Su Jin, Cho, Yun-Ho, Park, Joong-Jean, Choi, Jong-Il, Park, Sun Hwa, Kim, Hyeon Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545540/
https://www.ncbi.nlm.nih.gov/pubmed/31125414
http://dx.doi.org/10.1093/ijnp/pyz016
_version_ 1783423400056717312
author Lee, Hye Jeong
Lee, Jung Ok
Lee, Yong Woo
Kim, Shin Ae
Seo, Il Hyeok
Han, Jeong Ah
Kang, Min Ju
Kim, Su Jin
Cho, Yun-Ho
Park, Joong-Jean
Choi, Jong-Il
Park, Sun Hwa
Kim, Hyeon Soo
author_facet Lee, Hye Jeong
Lee, Jung Ok
Lee, Yong Woo
Kim, Shin Ae
Seo, Il Hyeok
Han, Jeong Ah
Kang, Min Ju
Kim, Su Jin
Cho, Yun-Ho
Park, Joong-Jean
Choi, Jong-Il
Park, Sun Hwa
Kim, Hyeon Soo
author_sort Lee, Hye Jeong
collection PubMed
description BACKGROUND: Leukemia inhibitory factor, a novel myokine, is known to be associated with neural function, but the underlying molecular mechanism remains unclear. METHODS: HT-22 mouse hippocampal cells, primary hippocampal cells, and Drosophila Alzheimer’s disease model were used to determine the effect of leukemia inhibitory factor on neurons. Immunoblot analysis and immunofluorescence method were used to analyze biological mechanism. RESULTS: Leukemia inhibitory factor increased Akt phosphorylation in a phosphoinositide-3-kinase-dependent manner in hippocampal cells. Leukemia inhibitory factor also increased the phosphorylation of the mammalian target of rapamycin and the downstream S6K. Leukemia inhibitory factor stimulated the phosphorylation of signal transducer and activator of transcription via extracellular signal-regulated kinases. Leukemia inhibitory factor increased c-fos expression through both Akt and extracellular signal-regulated kinases. Leukemia inhibitory factor blocked amyloid β-induced neural viability suppression and inhibited amyloid β-induced glucose uptake impairment through the block of amyloid β-mediated insulin receptor downregulation. Leukemia inhibitory factor blocked amyloid β-mediated induction of the autophagy marker, microtubule-associated protein 1A/1B-light chain 3. Additionally, in primary prepared hippocampal cells, leukemia inhibitory factor stimulated Akt and extracellular signal-regulated kinase, demonstrating that leukemia inhibitory factor has physiological relevance in vivo. Suppression of the autophagy marker, light chain 3II, by leukemia inhibitory factor was observed in a Drosophila model of Alzheimer’s disease. CONCLUSIONS: These results demonstrate that leukemia inhibitory factor protects against amyloid β-induced neurotoxicity via Akt/extracellular signal-regulated kinase-mediated c-fos induction, and thus suggest that leukemia inhibitory factor is a potential drug for Alzheimer’s disease.
format Online
Article
Text
id pubmed-6545540
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-65455402019-06-13 LIF, a Novel Myokine, Protects Against Amyloid-Beta-Induced Neurotoxicity via Akt-Mediated Autophagy Signaling in Hippocampal Cells Lee, Hye Jeong Lee, Jung Ok Lee, Yong Woo Kim, Shin Ae Seo, Il Hyeok Han, Jeong Ah Kang, Min Ju Kim, Su Jin Cho, Yun-Ho Park, Joong-Jean Choi, Jong-Il Park, Sun Hwa Kim, Hyeon Soo Int J Neuropsychopharmacol Regular Research Articles BACKGROUND: Leukemia inhibitory factor, a novel myokine, is known to be associated with neural function, but the underlying molecular mechanism remains unclear. METHODS: HT-22 mouse hippocampal cells, primary hippocampal cells, and Drosophila Alzheimer’s disease model were used to determine the effect of leukemia inhibitory factor on neurons. Immunoblot analysis and immunofluorescence method were used to analyze biological mechanism. RESULTS: Leukemia inhibitory factor increased Akt phosphorylation in a phosphoinositide-3-kinase-dependent manner in hippocampal cells. Leukemia inhibitory factor also increased the phosphorylation of the mammalian target of rapamycin and the downstream S6K. Leukemia inhibitory factor stimulated the phosphorylation of signal transducer and activator of transcription via extracellular signal-regulated kinases. Leukemia inhibitory factor increased c-fos expression through both Akt and extracellular signal-regulated kinases. Leukemia inhibitory factor blocked amyloid β-induced neural viability suppression and inhibited amyloid β-induced glucose uptake impairment through the block of amyloid β-mediated insulin receptor downregulation. Leukemia inhibitory factor blocked amyloid β-mediated induction of the autophagy marker, microtubule-associated protein 1A/1B-light chain 3. Additionally, in primary prepared hippocampal cells, leukemia inhibitory factor stimulated Akt and extracellular signal-regulated kinase, demonstrating that leukemia inhibitory factor has physiological relevance in vivo. Suppression of the autophagy marker, light chain 3II, by leukemia inhibitory factor was observed in a Drosophila model of Alzheimer’s disease. CONCLUSIONS: These results demonstrate that leukemia inhibitory factor protects against amyloid β-induced neurotoxicity via Akt/extracellular signal-regulated kinase-mediated c-fos induction, and thus suggest that leukemia inhibitory factor is a potential drug for Alzheimer’s disease. Oxford University Press 2019-04-10 /pmc/articles/PMC6545540/ /pubmed/31125414 http://dx.doi.org/10.1093/ijnp/pyz016 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of CINP. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Regular Research Articles
Lee, Hye Jeong
Lee, Jung Ok
Lee, Yong Woo
Kim, Shin Ae
Seo, Il Hyeok
Han, Jeong Ah
Kang, Min Ju
Kim, Su Jin
Cho, Yun-Ho
Park, Joong-Jean
Choi, Jong-Il
Park, Sun Hwa
Kim, Hyeon Soo
LIF, a Novel Myokine, Protects Against Amyloid-Beta-Induced Neurotoxicity via Akt-Mediated Autophagy Signaling in Hippocampal Cells
title LIF, a Novel Myokine, Protects Against Amyloid-Beta-Induced Neurotoxicity via Akt-Mediated Autophagy Signaling in Hippocampal Cells
title_full LIF, a Novel Myokine, Protects Against Amyloid-Beta-Induced Neurotoxicity via Akt-Mediated Autophagy Signaling in Hippocampal Cells
title_fullStr LIF, a Novel Myokine, Protects Against Amyloid-Beta-Induced Neurotoxicity via Akt-Mediated Autophagy Signaling in Hippocampal Cells
title_full_unstemmed LIF, a Novel Myokine, Protects Against Amyloid-Beta-Induced Neurotoxicity via Akt-Mediated Autophagy Signaling in Hippocampal Cells
title_short LIF, a Novel Myokine, Protects Against Amyloid-Beta-Induced Neurotoxicity via Akt-Mediated Autophagy Signaling in Hippocampal Cells
title_sort lif, a novel myokine, protects against amyloid-beta-induced neurotoxicity via akt-mediated autophagy signaling in hippocampal cells
topic Regular Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545540/
https://www.ncbi.nlm.nih.gov/pubmed/31125414
http://dx.doi.org/10.1093/ijnp/pyz016
work_keys_str_mv AT leehyejeong lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT leejungok lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT leeyongwoo lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT kimshinae lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT seoilhyeok lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT hanjeongah lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT kangminju lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT kimsujin lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT choyunho lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT parkjoongjean lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT choijongil lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT parksunhwa lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells
AT kimhyeonsoo lifanovelmyokineprotectsagainstamyloidbetainducedneurotoxicityviaaktmediatedautophagysignalinginhippocampalcells