A novel cyclic peptide (Naturido) modulates glia-neuron interactions in vitro and reverses ageing-related deficits in senescence-accelerated mice.

The use of agents that target both glia and neurons may represent a new strategy for the treatment of ageing disorders. Here, we confirmed the presence of the novel cyclic peptide Naturido that originates from a medicinal fungus (Isaria japonica) grown on domestic silkworm (Bombyx mori). We found th...

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Main Authors: Shinichi Ishiguro, Tetsuro Shinada, Zhou Wu, Mayumi Karimazawa, Michimasa Uchidate, Eiji Nishimura, Yoko Yasuno, Makiko Ebata, Piyamas Sillapakong, Hiromi Ishiguro, Nobuyoshi Ebata, Junjun Ni, Muzhou Jiang, Masanobu Goryo, Keishi Otsu, Hidemitsu Harada, Koichi Suzuki
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0245235
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spelling doaj-1093fdd724644c2d8cd273661461c6a92021-05-21T04:31:02ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01161e024523510.1371/journal.pone.0245235A novel cyclic peptide (Naturido) modulates glia-neuron interactions in vitro and reverses ageing-related deficits in senescence-accelerated mice.Shinichi IshiguroTetsuro ShinadaZhou WuMayumi KarimazawaMichimasa UchidateEiji NishimuraYoko YasunoMakiko EbataPiyamas SillapakongHiromi IshiguroNobuyoshi EbataJunjun NiMuzhou JiangMasanobu GoryoKeishi OtsuHidemitsu HaradaKoichi SuzukiThe use of agents that target both glia and neurons may represent a new strategy for the treatment of ageing disorders. Here, we confirmed the presence of the novel cyclic peptide Naturido that originates from a medicinal fungus (Isaria japonica) grown on domestic silkworm (Bombyx mori). We found that Naturido significantly enhanced astrocyte proliferation and activated the single copy gene encoding the neuropeptide VGF and the neuron-derived NGF gene. The addition of the peptide to the culture medium of primary hippocampal neurons increased dendrite length, dendrite number and axon length. Furthermore, the addition of the peptide to primary microglial cultures shifted CGA-activated microglia towards anti-inflammatory and neuroprotective phenotypes. These findings of in vitro glia-neuron interactions led us to evaluate the effects of oral administration of the peptide on brain function and hair ageing in senescence-accelerated mice (SAMP8). In vivo analyses revealed that spatial learning ability and hair quality were improved in Naturido-treated mice compared with untreated mice, to the same level observed in the normal ageing control (SAMR1). These data suggest that Naturido may be a promising glia-neuron modulator for the treatment of not only senescence, but also Alzheimer's disease and other neurodegenerative diseases.https://doi.org/10.1371/journal.pone.0245235
collection DOAJ
language English
format Article
sources DOAJ
author Shinichi Ishiguro
Tetsuro Shinada
Zhou Wu
Mayumi Karimazawa
Michimasa Uchidate
Eiji Nishimura
Yoko Yasuno
Makiko Ebata
Piyamas Sillapakong
Hiromi Ishiguro
Nobuyoshi Ebata
Junjun Ni
Muzhou Jiang
Masanobu Goryo
Keishi Otsu
Hidemitsu Harada
Koichi Suzuki
spellingShingle Shinichi Ishiguro
Tetsuro Shinada
Zhou Wu
Mayumi Karimazawa
Michimasa Uchidate
Eiji Nishimura
Yoko Yasuno
Makiko Ebata
Piyamas Sillapakong
Hiromi Ishiguro
Nobuyoshi Ebata
Junjun Ni
Muzhou Jiang
Masanobu Goryo
Keishi Otsu
Hidemitsu Harada
Koichi Suzuki
A novel cyclic peptide (Naturido) modulates glia-neuron interactions in vitro and reverses ageing-related deficits in senescence-accelerated mice.
PLoS ONE
author_facet Shinichi Ishiguro
Tetsuro Shinada
Zhou Wu
Mayumi Karimazawa
Michimasa Uchidate
Eiji Nishimura
Yoko Yasuno
Makiko Ebata
Piyamas Sillapakong
Hiromi Ishiguro
Nobuyoshi Ebata
Junjun Ni
Muzhou Jiang
Masanobu Goryo
Keishi Otsu
Hidemitsu Harada
Koichi Suzuki
author_sort Shinichi Ishiguro
title A novel cyclic peptide (Naturido) modulates glia-neuron interactions in vitro and reverses ageing-related deficits in senescence-accelerated mice.
title_short A novel cyclic peptide (Naturido) modulates glia-neuron interactions in vitro and reverses ageing-related deficits in senescence-accelerated mice.
title_full A novel cyclic peptide (Naturido) modulates glia-neuron interactions in vitro and reverses ageing-related deficits in senescence-accelerated mice.
title_fullStr A novel cyclic peptide (Naturido) modulates glia-neuron interactions in vitro and reverses ageing-related deficits in senescence-accelerated mice.
title_full_unstemmed A novel cyclic peptide (Naturido) modulates glia-neuron interactions in vitro and reverses ageing-related deficits in senescence-accelerated mice.
title_sort novel cyclic peptide (naturido) modulates glia-neuron interactions in vitro and reverses ageing-related deficits in senescence-accelerated mice.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2021-01-01
description The use of agents that target both glia and neurons may represent a new strategy for the treatment of ageing disorders. Here, we confirmed the presence of the novel cyclic peptide Naturido that originates from a medicinal fungus (Isaria japonica) grown on domestic silkworm (Bombyx mori). We found that Naturido significantly enhanced astrocyte proliferation and activated the single copy gene encoding the neuropeptide VGF and the neuron-derived NGF gene. The addition of the peptide to the culture medium of primary hippocampal neurons increased dendrite length, dendrite number and axon length. Furthermore, the addition of the peptide to primary microglial cultures shifted CGA-activated microglia towards anti-inflammatory and neuroprotective phenotypes. These findings of in vitro glia-neuron interactions led us to evaluate the effects of oral administration of the peptide on brain function and hair ageing in senescence-accelerated mice (SAMP8). In vivo analyses revealed that spatial learning ability and hair quality were improved in Naturido-treated mice compared with untreated mice, to the same level observed in the normal ageing control (SAMR1). These data suggest that Naturido may be a promising glia-neuron modulator for the treatment of not only senescence, but also Alzheimer's disease and other neurodegenerative diseases.
url https://doi.org/10.1371/journal.pone.0245235
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