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1α,25(OH)(2)D(3) Promotes the Autophagy of Porcine Ovarian Granulosa Cells as a Protective Mechanism against ROS through the BNIP3/PINK1 Pathway
Vitamin D (VD) is one of the important nutrients required by livestock; however, VD deficiency is reported to be widespread. Earlier studies have suggested a potential role for VD in reproduction. Studies on the correlation between VD and sow reproduction are limited. The aim of the current study wa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10001661/ https://www.ncbi.nlm.nih.gov/pubmed/36901794 http://dx.doi.org/10.3390/ijms24054364 |
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author | Wang, Shiyou Yao, Qichun Zhao, Fan Cui, Wenfei Price, Christopher A. Wang, Yifan Lv, Jing Tang, Hong Jiang, Zhongliang |
author_facet | Wang, Shiyou Yao, Qichun Zhao, Fan Cui, Wenfei Price, Christopher A. Wang, Yifan Lv, Jing Tang, Hong Jiang, Zhongliang |
author_sort | Wang, Shiyou |
collection | PubMed |
description | Vitamin D (VD) is one of the important nutrients required by livestock; however, VD deficiency is reported to be widespread. Earlier studies have suggested a potential role for VD in reproduction. Studies on the correlation between VD and sow reproduction are limited. The aim of the current study was aimed to determine the role of 1,25-dihydroxy vitamin D(3) (1α,25(OH)(2)D(3)) on porcine ovarian granulosa cells (PGCs) in vitro to provide a theoretical basis for improving the reproductive efficiency of sows. We used chloroquine (autophagy inhibitor) and reactive oxygen species (ROS) scavenger N-acetylcysteine in conjunction with 1α,25(OH)(2)D(3) to explore the effect on PGCs. The results showed that 10 nM of 1α,25(OH)(2)D(3) increased PGC viability and ROS content. In addition, 1α,25(OH)(2)D(3) induces PGC autophagy according to the gene transcription and protein expression levels of LC3, ATG7, BECN1, and SQSTM1 and promotes the generation of autophagosomes. 1α,25(OH)(2)D(3)-induced autophagy affects the synthesis of E(2) and P(4) in PGCs. We investigated the relationship between ROS and autophagy, and the results showed that 1α,25(OH)(2)D(3)-induced ROS promoted PGC autophagy. The ROS-BNIP3-PINK1 pathway was involved in PGC autophagy induced by 1α,25(OH)(2)D(3). In conclusion, this study suggests that 1α,25(OH)(2)D(3) promotes PGC autophagy as a protective mechanism against ROS via the BNIP3/PINK1 pathway. |
format | Online Article Text |
id | pubmed-10001661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100016612023-03-11 1α,25(OH)(2)D(3) Promotes the Autophagy of Porcine Ovarian Granulosa Cells as a Protective Mechanism against ROS through the BNIP3/PINK1 Pathway Wang, Shiyou Yao, Qichun Zhao, Fan Cui, Wenfei Price, Christopher A. Wang, Yifan Lv, Jing Tang, Hong Jiang, Zhongliang Int J Mol Sci Article Vitamin D (VD) is one of the important nutrients required by livestock; however, VD deficiency is reported to be widespread. Earlier studies have suggested a potential role for VD in reproduction. Studies on the correlation between VD and sow reproduction are limited. The aim of the current study was aimed to determine the role of 1,25-dihydroxy vitamin D(3) (1α,25(OH)(2)D(3)) on porcine ovarian granulosa cells (PGCs) in vitro to provide a theoretical basis for improving the reproductive efficiency of sows. We used chloroquine (autophagy inhibitor) and reactive oxygen species (ROS) scavenger N-acetylcysteine in conjunction with 1α,25(OH)(2)D(3) to explore the effect on PGCs. The results showed that 10 nM of 1α,25(OH)(2)D(3) increased PGC viability and ROS content. In addition, 1α,25(OH)(2)D(3) induces PGC autophagy according to the gene transcription and protein expression levels of LC3, ATG7, BECN1, and SQSTM1 and promotes the generation of autophagosomes. 1α,25(OH)(2)D(3)-induced autophagy affects the synthesis of E(2) and P(4) in PGCs. We investigated the relationship between ROS and autophagy, and the results showed that 1α,25(OH)(2)D(3)-induced ROS promoted PGC autophagy. The ROS-BNIP3-PINK1 pathway was involved in PGC autophagy induced by 1α,25(OH)(2)D(3). In conclusion, this study suggests that 1α,25(OH)(2)D(3) promotes PGC autophagy as a protective mechanism against ROS via the BNIP3/PINK1 pathway. MDPI 2023-02-22 /pmc/articles/PMC10001661/ /pubmed/36901794 http://dx.doi.org/10.3390/ijms24054364 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Shiyou Yao, Qichun Zhao, Fan Cui, Wenfei Price, Christopher A. Wang, Yifan Lv, Jing Tang, Hong Jiang, Zhongliang 1α,25(OH)(2)D(3) Promotes the Autophagy of Porcine Ovarian Granulosa Cells as a Protective Mechanism against ROS through the BNIP3/PINK1 Pathway |
title | 1α,25(OH)(2)D(3) Promotes the Autophagy of Porcine Ovarian Granulosa Cells as a Protective Mechanism against ROS through the BNIP3/PINK1 Pathway |
title_full | 1α,25(OH)(2)D(3) Promotes the Autophagy of Porcine Ovarian Granulosa Cells as a Protective Mechanism against ROS through the BNIP3/PINK1 Pathway |
title_fullStr | 1α,25(OH)(2)D(3) Promotes the Autophagy of Porcine Ovarian Granulosa Cells as a Protective Mechanism against ROS through the BNIP3/PINK1 Pathway |
title_full_unstemmed | 1α,25(OH)(2)D(3) Promotes the Autophagy of Porcine Ovarian Granulosa Cells as a Protective Mechanism against ROS through the BNIP3/PINK1 Pathway |
title_short | 1α,25(OH)(2)D(3) Promotes the Autophagy of Porcine Ovarian Granulosa Cells as a Protective Mechanism against ROS through the BNIP3/PINK1 Pathway |
title_sort | 1α,25(oh)(2)d(3) promotes the autophagy of porcine ovarian granulosa cells as a protective mechanism against ros through the bnip3/pink1 pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10001661/ https://www.ncbi.nlm.nih.gov/pubmed/36901794 http://dx.doi.org/10.3390/ijms24054364 |
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