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Effects of HSYA on the proliferation and apoptosis of MSCs exposed to hypoxic and serum deprivation conditions
As a primary active ingredient of safflor yellow, hydroxysafflor yellow A (HSYA) exhibits notable antioxidative and neuroprotective effects. The aim of the present study was to investigate the protective effects of HSYA in mesenchymal stem cells (MSCs) exposed to hypoxia (5% O(2)) and serum deprivat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996714/ https://www.ncbi.nlm.nih.gov/pubmed/29904409 http://dx.doi.org/10.3892/etm.2018.6125 |
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author | Song, Xiaoqing Su, Lining Yin, Haifeng Dai, Jin Wei, Huiping |
author_facet | Song, Xiaoqing Su, Lining Yin, Haifeng Dai, Jin Wei, Huiping |
author_sort | Song, Xiaoqing |
collection | PubMed |
description | As a primary active ingredient of safflor yellow, hydroxysafflor yellow A (HSYA) exhibits notable antioxidative and neuroprotective effects. The aim of the present study was to investigate the protective effects of HSYA in mesenchymal stem cells (MSCs) exposed to hypoxia (5% O(2)) and serum deprivation (H/SD), and to explore the mechanisms underlying HSYA-mediated protection. Under H/SD conditions, HSYA was applied to protect MSCs against injury. Cell viability, proliferation, apoptosis and reactive oxygen species (ROS) levels were determined using an 5-ethynyl-2′-deoxyuridine assay, MTT assay, Hoechst 33342/propidium iodide and 2′,7′-dichlorodihydrofluorescein diacetate staining, respectively. The results revealed that 160 mg/l HSYA significantly reduced apoptosis and ROS levels compared with the H/SD group; however, HSYA demonstrated minimal effects on cell proliferation. A western blot assay demonstrated that HSYA reduced cleaved caspase-3 expression and cytC release from the mitochondria to the cytoplasm when compared with the H/SD group. In addition, western blotting and RT-qPCR analyses revealed that HSYA treatment significantly increased the expression of hypoxia inducible factor-1α (HIF-1α) and vascular endothelial growth factor (VEGF). In conclusion, the results of the current study demonstrated that HSYA exerts protective effects against H/SD-induced apoptosis in MSCs potentially via activation of the HIF-1α/VEGF signaling pathway and stabilization of the mitochondrial membrane. |
format | Online Article Text |
id | pubmed-5996714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-59967142018-06-14 Effects of HSYA on the proliferation and apoptosis of MSCs exposed to hypoxic and serum deprivation conditions Song, Xiaoqing Su, Lining Yin, Haifeng Dai, Jin Wei, Huiping Exp Ther Med Articles As a primary active ingredient of safflor yellow, hydroxysafflor yellow A (HSYA) exhibits notable antioxidative and neuroprotective effects. The aim of the present study was to investigate the protective effects of HSYA in mesenchymal stem cells (MSCs) exposed to hypoxia (5% O(2)) and serum deprivation (H/SD), and to explore the mechanisms underlying HSYA-mediated protection. Under H/SD conditions, HSYA was applied to protect MSCs against injury. Cell viability, proliferation, apoptosis and reactive oxygen species (ROS) levels were determined using an 5-ethynyl-2′-deoxyuridine assay, MTT assay, Hoechst 33342/propidium iodide and 2′,7′-dichlorodihydrofluorescein diacetate staining, respectively. The results revealed that 160 mg/l HSYA significantly reduced apoptosis and ROS levels compared with the H/SD group; however, HSYA demonstrated minimal effects on cell proliferation. A western blot assay demonstrated that HSYA reduced cleaved caspase-3 expression and cytC release from the mitochondria to the cytoplasm when compared with the H/SD group. In addition, western blotting and RT-qPCR analyses revealed that HSYA treatment significantly increased the expression of hypoxia inducible factor-1α (HIF-1α) and vascular endothelial growth factor (VEGF). In conclusion, the results of the current study demonstrated that HSYA exerts protective effects against H/SD-induced apoptosis in MSCs potentially via activation of the HIF-1α/VEGF signaling pathway and stabilization of the mitochondrial membrane. D.A. Spandidos 2018-06 2018-05-03 /pmc/articles/PMC5996714/ /pubmed/29904409 http://dx.doi.org/10.3892/etm.2018.6125 Text en Copyright: © Song et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Song, Xiaoqing Su, Lining Yin, Haifeng Dai, Jin Wei, Huiping Effects of HSYA on the proliferation and apoptosis of MSCs exposed to hypoxic and serum deprivation conditions |
title | Effects of HSYA on the proliferation and apoptosis of MSCs exposed to hypoxic and serum deprivation conditions |
title_full | Effects of HSYA on the proliferation and apoptosis of MSCs exposed to hypoxic and serum deprivation conditions |
title_fullStr | Effects of HSYA on the proliferation and apoptosis of MSCs exposed to hypoxic and serum deprivation conditions |
title_full_unstemmed | Effects of HSYA on the proliferation and apoptosis of MSCs exposed to hypoxic and serum deprivation conditions |
title_short | Effects of HSYA on the proliferation and apoptosis of MSCs exposed to hypoxic and serum deprivation conditions |
title_sort | effects of hsya on the proliferation and apoptosis of mscs exposed to hypoxic and serum deprivation conditions |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996714/ https://www.ncbi.nlm.nih.gov/pubmed/29904409 http://dx.doi.org/10.3892/etm.2018.6125 |
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