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Distinct physical condition and social behavior phenotypes of CD157 and CD38 knockout mice during aging

The ability of CD38 and CD157 to utilize nicotinamide adenine dinucleotide (NAD) has received much attention because the aging-induced elevation of CD38 expression plays a role in the senescence-related decline in NAD levels. Therefore, it is of interest to examine and compare the effects of age-ass...

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Autores principales: Gerasimenko, Maria, Lopatina, Olga, Shabalova, Anna A., Cherepanov, Stanislav M., Salmina, Alla B., Yokoyama, Shigeru, Goto, Hisanori, Okamoto, Hiroshi, Yamamoto, Yasuhiko, Ishihara, Katsuhiko, Higashida, Haruhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743928/
https://www.ncbi.nlm.nih.gov/pubmed/33326496
http://dx.doi.org/10.1371/journal.pone.0244022
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author Gerasimenko, Maria
Lopatina, Olga
Shabalova, Anna A.
Cherepanov, Stanislav M.
Salmina, Alla B.
Yokoyama, Shigeru
Goto, Hisanori
Okamoto, Hiroshi
Yamamoto, Yasuhiko
Ishihara, Katsuhiko
Higashida, Haruhiro
author_facet Gerasimenko, Maria
Lopatina, Olga
Shabalova, Anna A.
Cherepanov, Stanislav M.
Salmina, Alla B.
Yokoyama, Shigeru
Goto, Hisanori
Okamoto, Hiroshi
Yamamoto, Yasuhiko
Ishihara, Katsuhiko
Higashida, Haruhiro
author_sort Gerasimenko, Maria
collection PubMed
description The ability of CD38 and CD157 to utilize nicotinamide adenine dinucleotide (NAD) has received much attention because the aging-induced elevation of CD38 expression plays a role in the senescence-related decline in NAD levels. Therefore, it is of interest to examine and compare the effects of age-associated changes on the general health and brain function impairment of Cd157 and Cd38 knockout (CD157 KO and CD38 KO) mice. The body weight and behaviors were measured in 8-week-old (young adult) or 12-month-old (middle-aged) male mice of both KO strains. The locomotor activity, anxiety-like behavior, and social behavior of the mice were measured in the open field and three-chamber tests. The middle-aged CD157 KO male mice gained more body weight than young adult KO mice, while little or no body weight gain was observed in the middle-aged CD38 KO mice. Middle-aged CD157 KO mice displayed increased anxiety-like behavior and decreased sociability and interaction compared with young adult KO mice. Middle-aged CD38 KO mice showed less anxiety and hyperactivity than CD157 KO mice, similar to young adult CD38 KO mice. The results reveal marked age-dependent changes in male CD157 KO mice but not in male CD38 KO mice. We discuss the distinct differences in aging effects from the perspective of inhibition of NAD metabolism in CD157 and CD38 KO mice, which may contribute to differential behavioral changes during aging.
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spelling pubmed-77439282020-12-31 Distinct physical condition and social behavior phenotypes of CD157 and CD38 knockout mice during aging Gerasimenko, Maria Lopatina, Olga Shabalova, Anna A. Cherepanov, Stanislav M. Salmina, Alla B. Yokoyama, Shigeru Goto, Hisanori Okamoto, Hiroshi Yamamoto, Yasuhiko Ishihara, Katsuhiko Higashida, Haruhiro PLoS One Research Article The ability of CD38 and CD157 to utilize nicotinamide adenine dinucleotide (NAD) has received much attention because the aging-induced elevation of CD38 expression plays a role in the senescence-related decline in NAD levels. Therefore, it is of interest to examine and compare the effects of age-associated changes on the general health and brain function impairment of Cd157 and Cd38 knockout (CD157 KO and CD38 KO) mice. The body weight and behaviors were measured in 8-week-old (young adult) or 12-month-old (middle-aged) male mice of both KO strains. The locomotor activity, anxiety-like behavior, and social behavior of the mice were measured in the open field and three-chamber tests. The middle-aged CD157 KO male mice gained more body weight than young adult KO mice, while little or no body weight gain was observed in the middle-aged CD38 KO mice. Middle-aged CD157 KO mice displayed increased anxiety-like behavior and decreased sociability and interaction compared with young adult KO mice. Middle-aged CD38 KO mice showed less anxiety and hyperactivity than CD157 KO mice, similar to young adult CD38 KO mice. The results reveal marked age-dependent changes in male CD157 KO mice but not in male CD38 KO mice. We discuss the distinct differences in aging effects from the perspective of inhibition of NAD metabolism in CD157 and CD38 KO mice, which may contribute to differential behavioral changes during aging. Public Library of Science 2020-12-16 /pmc/articles/PMC7743928/ /pubmed/33326496 http://dx.doi.org/10.1371/journal.pone.0244022 Text en © 2020 Gerasimenko et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gerasimenko, Maria
Lopatina, Olga
Shabalova, Anna A.
Cherepanov, Stanislav M.
Salmina, Alla B.
Yokoyama, Shigeru
Goto, Hisanori
Okamoto, Hiroshi
Yamamoto, Yasuhiko
Ishihara, Katsuhiko
Higashida, Haruhiro
Distinct physical condition and social behavior phenotypes of CD157 and CD38 knockout mice during aging
title Distinct physical condition and social behavior phenotypes of CD157 and CD38 knockout mice during aging
title_full Distinct physical condition and social behavior phenotypes of CD157 and CD38 knockout mice during aging
title_fullStr Distinct physical condition and social behavior phenotypes of CD157 and CD38 knockout mice during aging
title_full_unstemmed Distinct physical condition and social behavior phenotypes of CD157 and CD38 knockout mice during aging
title_short Distinct physical condition and social behavior phenotypes of CD157 and CD38 knockout mice during aging
title_sort distinct physical condition and social behavior phenotypes of cd157 and cd38 knockout mice during aging
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743928/
https://www.ncbi.nlm.nih.gov/pubmed/33326496
http://dx.doi.org/10.1371/journal.pone.0244022
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