Neural stem cell-conditioned medium ameliorates Aβ25–35-induced damage in SH-SY5Y cells by protecting mitochondrial function
Inhibition of amyloid β (Aβ)-induced mitochondrial damage is considered crucial for reducing the pathological damage in Alzheimer’s disease (AD). We evaluated the effect of neural stem cell-conditioned medium (NSC-CDM) on Aβ25–35-induced damage in SH-SY5Y cells. An in vitro model of AD was establis...
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Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina
2021-04-01
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Series: | Biomolecules & Biomedicine |
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Online Access: | https://www.bjbms.org/ojs/index.php/bjbms/article/view/4570 |
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author | Guoyong Jia Zengyan Diao Ying Liu Congcong Sun Cuilan Wang |
author_facet | Guoyong Jia Zengyan Diao Ying Liu Congcong Sun Cuilan Wang |
author_sort | Guoyong Jia |
collection | DOAJ |
description |
Inhibition of amyloid β (Aβ)-induced mitochondrial damage is considered crucial for reducing the pathological damage in Alzheimer’s disease (AD). We evaluated the effect of neural stem cell-conditioned medium (NSC-CDM) on Aβ25–35-induced damage in SH-SY5Y cells. An in vitro model of AD was established by treating SH-SY5Y cells with 40 µM Aβ25–35 for 24 h. SH-SY5Y cells were divided into control, Aβ25–35 (40 µM), Aβ25–35 (40 µM) + NSC-CDM, and Aβ25–35 (40 µM) + neural stem cell-complete medium (NSC-CPM) groups. Cell viability was detected by CCK-8 assay. Apoptosis, reactive oxygen species (ROS) production, and mitochondrial membrane potential (MMP) were detected by flow cytometry. Malondialdehyde content was detected by ELISA assay. Western blot analysis was used to detect cytochrome c release and apoptosis-related proteins. Transmission electron microscopy was used to observe mitochondrial morphology. Cell viability significantly decreased and apoptosis significantly increased in SH-SY5Y cells treated with Aβ25–35, and both effects were rescued by NSC-CDM. In addition, NSC-CDM reduced ROS production and significantly inhibited the reduction of MMP caused by Aβ25–35. Furthermore, NSC-CDM ameliorated Aβ25–35-induced reduction in Bcl-2 expression levels and increased the expression levels of cytochrome c, caspase-9, caspase-3, and Bax. Moreover, Aβ25–35 induced the destruction of mitochondrial ultrastructure and this effect was reversed by NSC-CDM. Collectively, our findings demonstrated the protective effect of NCS-CDM against Aβ25–35-induced SH-SY5Y cell damage and clarified the mechanism of action of Aβ25–35 in terms of mitochondrial maintenance and mitochondria-associated apoptosis signaling pathways, thus providing a theoretical basis for the development of novel anti-AD treatments.
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first_indexed | 2024-04-24T23:39:37Z |
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issn | 2831-0896 2831-090X |
language | English |
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series | Biomolecules & Biomedicine |
spelling | doaj.art-f246ac8d37c54bafb1f9fbf5af9bbe132024-03-15T13:44:23ZengAssociation of Basic Medical Sciences of Federation of Bosnia and HerzegovinaBiomolecules & Biomedicine2831-08962831-090X2021-04-0121210.17305/bjbms.2020.4570Neural stem cell-conditioned medium ameliorates Aβ25–35-induced damage in SH-SY5Y cells by protecting mitochondrial functionGuoyong Jia0https://orcid.org/0000-0002-7418-0628Zengyan Diao1Ying Liu2Congcong Sun3Cuilan Wang4Department of Neurology, Qilu Hospital, Shandong University, Jinan, ChinaDepartment of Neurology, Qilu Hospital, Shandong University, Jinan, ChinaDepartment of Neurology, Qilu Hospital, Shandong University, Jinan, ChinaDepartment of Neurology, Qilu Hospital, Shandong University, Jinan, ChinaDepartment of Neurology, Qilu Hospital, Shandong University, Jinan, China Inhibition of amyloid β (Aβ)-induced mitochondrial damage is considered crucial for reducing the pathological damage in Alzheimer’s disease (AD). We evaluated the effect of neural stem cell-conditioned medium (NSC-CDM) on Aβ25–35-induced damage in SH-SY5Y cells. An in vitro model of AD was established by treating SH-SY5Y cells with 40 µM Aβ25–35 for 24 h. SH-SY5Y cells were divided into control, Aβ25–35 (40 µM), Aβ25–35 (40 µM) + NSC-CDM, and Aβ25–35 (40 µM) + neural stem cell-complete medium (NSC-CPM) groups. Cell viability was detected by CCK-8 assay. Apoptosis, reactive oxygen species (ROS) production, and mitochondrial membrane potential (MMP) were detected by flow cytometry. Malondialdehyde content was detected by ELISA assay. Western blot analysis was used to detect cytochrome c release and apoptosis-related proteins. Transmission electron microscopy was used to observe mitochondrial morphology. Cell viability significantly decreased and apoptosis significantly increased in SH-SY5Y cells treated with Aβ25–35, and both effects were rescued by NSC-CDM. In addition, NSC-CDM reduced ROS production and significantly inhibited the reduction of MMP caused by Aβ25–35. Furthermore, NSC-CDM ameliorated Aβ25–35-induced reduction in Bcl-2 expression levels and increased the expression levels of cytochrome c, caspase-9, caspase-3, and Bax. Moreover, Aβ25–35 induced the destruction of mitochondrial ultrastructure and this effect was reversed by NSC-CDM. Collectively, our findings demonstrated the protective effect of NCS-CDM against Aβ25–35-induced SH-SY5Y cell damage and clarified the mechanism of action of Aβ25–35 in terms of mitochondrial maintenance and mitochondria-associated apoptosis signaling pathways, thus providing a theoretical basis for the development of novel anti-AD treatments. https://www.bjbms.org/ojs/index.php/bjbms/article/view/4570Alzheimer’s diseaseneural stem cell-conditioned mediumAβ25–35mitochondriaapoptosis |
spellingShingle | Guoyong Jia Zengyan Diao Ying Liu Congcong Sun Cuilan Wang Neural stem cell-conditioned medium ameliorates Aβ25–35-induced damage in SH-SY5Y cells by protecting mitochondrial function Biomolecules & Biomedicine Alzheimer’s disease neural stem cell-conditioned medium Aβ25–35 mitochondria apoptosis |
title | Neural stem cell-conditioned medium ameliorates Aβ25–35-induced damage in SH-SY5Y cells by protecting mitochondrial function |
title_full | Neural stem cell-conditioned medium ameliorates Aβ25–35-induced damage in SH-SY5Y cells by protecting mitochondrial function |
title_fullStr | Neural stem cell-conditioned medium ameliorates Aβ25–35-induced damage in SH-SY5Y cells by protecting mitochondrial function |
title_full_unstemmed | Neural stem cell-conditioned medium ameliorates Aβ25–35-induced damage in SH-SY5Y cells by protecting mitochondrial function |
title_short | Neural stem cell-conditioned medium ameliorates Aβ25–35-induced damage in SH-SY5Y cells by protecting mitochondrial function |
title_sort | neural stem cell conditioned medium ameliorates aβ25 35 induced damage in sh sy5y cells by protecting mitochondrial function |
topic | Alzheimer’s disease neural stem cell-conditioned medium Aβ25–35 mitochondria apoptosis |
url | https://www.bjbms.org/ojs/index.php/bjbms/article/view/4570 |
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