IGF2BP3 curbed by miR-15c-3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through AKT-Raf1-ERK1/2 signaling pathway
For commercial laying hens, the continuous high-intensity ovulation process leads to a significant accumulation of reactive oxygen species (ROS) in the granulosa cells, inducing oxidative stress, which accelerates ovarian aging and shortens the peak laying period. The molecular mechanisms underlying...
Saved in:
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2025-02-01
|
Series: | Poultry Science |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S0032579124013397 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1841560128207192064 |
---|---|
author | Zhongzhen Lin Yanrong Gong Chunlin Yu Chaowu Yang Lingqian Yin Donghao Zhang Yuan Tang Feng Xu Ye Wang Yiping Liu |
author_facet | Zhongzhen Lin Yanrong Gong Chunlin Yu Chaowu Yang Lingqian Yin Donghao Zhang Yuan Tang Feng Xu Ye Wang Yiping Liu |
author_sort | Zhongzhen Lin |
collection | DOAJ |
description | For commercial laying hens, the continuous high-intensity ovulation process leads to a significant accumulation of reactive oxygen species (ROS) in the granulosa cells, inducing oxidative stress, which accelerates ovarian aging and shortens the peak laying period. The molecular mechanisms underlying this process remain poorly understood. Therefore, we modeled the processes of oxidative stress and antioxidant in chicken granulosa cells. Small RNA sequencing revealed that miR-15c-3p expression was elevated by oxidative stress induction and attenuated by antioxidant curcumin. Functional validation with miR-15c-3p mimic and inhibitor confirmed the role of miR-15c-3p in exacerbating oxidative stress and resultant suppression of lipid droplet storage and progesterone secretion in chicken granulosa cells by targeting insulin-like growth factor 2 binding protein 3 (IGF2BP3). These regulatory effects were mediated through the sequential downstream signaling cascade of AKT-Raf1-ERK1/2. In conclusion, IGF2BP3 curbed by miR-15c-3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through AKT-Raf1-ERK1/2 signaling pathway. These findings offer new insights into the molecular mechanisms by which oxidative stress damages reproductive capacity and a theoretical basis for mitigating oxidative stress in laying hens through genetic improvement. |
format | Article |
id | doaj-art-9f69d1f3c3444b59b0f7f2b343de4e12 |
institution | Kabale University |
issn | 0032-5791 |
language | English |
publishDate | 2025-02-01 |
publisher | Elsevier |
record_format | Article |
series | Poultry Science |
spelling | doaj-art-9f69d1f3c3444b59b0f7f2b343de4e122025-01-05T04:27:45ZengElsevierPoultry Science0032-57912025-02-011042104761IGF2BP3 curbed by miR-15c-3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through AKT-Raf1-ERK1/2 signaling pathwayZhongzhen Lin0Yanrong Gong1Chunlin Yu2Chaowu Yang3Lingqian Yin4Donghao Zhang5Yuan Tang6Feng Xu7Ye Wang8Yiping Liu9State Key Laboratory of Swine and Poultry Breeding Industry, Key Laboratory of Livestock and Poultry Multi-omics, Ministry of Agriculture and Rural Affairs, and Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, ChinaState Key Laboratory of Swine and Poultry Breeding Industry, Key Laboratory of Livestock and Poultry Multi-omics, Ministry of Agriculture and Rural Affairs, and Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, ChinaAnimal Breeding and Genetics Key Laboratory of Sichuan Province, Sichuan Animal Science Academy, Chengdu, ChinaAnimal Breeding and Genetics Key Laboratory of Sichuan Province, Sichuan Animal Science Academy, Chengdu, ChinaState Key Laboratory of Swine and Poultry Breeding Industry, Key Laboratory of Livestock and Poultry Multi-omics, Ministry of Agriculture and Rural Affairs, and Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, ChinaState Key Laboratory of Swine and Poultry Breeding Industry, Key Laboratory of Livestock and Poultry Multi-omics, Ministry of Agriculture and Rural Affairs, and Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, ChinaState Key Laboratory of Swine and Poultry Breeding Industry, Key Laboratory of Livestock and Poultry Multi-omics, Ministry of Agriculture and Rural Affairs, and Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, ChinaState Key Laboratory of Swine and Poultry Breeding Industry, Key Laboratory of Livestock and Poultry Multi-omics, Ministry of Agriculture and Rural Affairs, and Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, ChinaSichuan Key Laboratory of Conservation Biology on Endangered Wildlife, Chengdu Research Base of Giant Panda Breeding, Chengdu, China; Corresponding authors.State Key Laboratory of Swine and Poultry Breeding Industry, Key Laboratory of Livestock and Poultry Multi-omics, Ministry of Agriculture and Rural Affairs, and Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, China; Corresponding authors.For commercial laying hens, the continuous high-intensity ovulation process leads to a significant accumulation of reactive oxygen species (ROS) in the granulosa cells, inducing oxidative stress, which accelerates ovarian aging and shortens the peak laying period. The molecular mechanisms underlying this process remain poorly understood. Therefore, we modeled the processes of oxidative stress and antioxidant in chicken granulosa cells. Small RNA sequencing revealed that miR-15c-3p expression was elevated by oxidative stress induction and attenuated by antioxidant curcumin. Functional validation with miR-15c-3p mimic and inhibitor confirmed the role of miR-15c-3p in exacerbating oxidative stress and resultant suppression of lipid droplet storage and progesterone secretion in chicken granulosa cells by targeting insulin-like growth factor 2 binding protein 3 (IGF2BP3). These regulatory effects were mediated through the sequential downstream signaling cascade of AKT-Raf1-ERK1/2. In conclusion, IGF2BP3 curbed by miR-15c-3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through AKT-Raf1-ERK1/2 signaling pathway. These findings offer new insights into the molecular mechanisms by which oxidative stress damages reproductive capacity and a theoretical basis for mitigating oxidative stress in laying hens through genetic improvement.http://www.sciencedirect.com/science/article/pii/S0032579124013397Lipid metabolismSteroid hormoneFecundityPoultry |
spellingShingle | Zhongzhen Lin Yanrong Gong Chunlin Yu Chaowu Yang Lingqian Yin Donghao Zhang Yuan Tang Feng Xu Ye Wang Yiping Liu IGF2BP3 curbed by miR-15c-3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through AKT-Raf1-ERK1/2 signaling pathway Poultry Science Lipid metabolism Steroid hormone Fecundity Poultry |
title | IGF2BP3 curbed by miR-15c-3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through AKT-Raf1-ERK1/2 signaling pathway |
title_full | IGF2BP3 curbed by miR-15c-3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through AKT-Raf1-ERK1/2 signaling pathway |
title_fullStr | IGF2BP3 curbed by miR-15c-3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through AKT-Raf1-ERK1/2 signaling pathway |
title_full_unstemmed | IGF2BP3 curbed by miR-15c-3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through AKT-Raf1-ERK1/2 signaling pathway |
title_short | IGF2BP3 curbed by miR-15c-3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through AKT-Raf1-ERK1/2 signaling pathway |
title_sort | igf2bp3 curbed by mir 15c 3p restores disrupted lipid storage and progesterone secretion in chicken granulosa cells under oxidative stress through akt raf1 erk1 2 signaling pathway |
topic | Lipid metabolism Steroid hormone Fecundity Poultry |
url | http://www.sciencedirect.com/science/article/pii/S0032579124013397 |
work_keys_str_mv | AT zhongzhenlin igf2bp3curbedbymir15c3prestoresdisruptedlipidstorageandprogesteronesecretioninchickengranulosacellsunderoxidativestressthroughaktraf1erk12signalingpathway AT yanronggong igf2bp3curbedbymir15c3prestoresdisruptedlipidstorageandprogesteronesecretioninchickengranulosacellsunderoxidativestressthroughaktraf1erk12signalingpathway AT chunlinyu igf2bp3curbedbymir15c3prestoresdisruptedlipidstorageandprogesteronesecretioninchickengranulosacellsunderoxidativestressthroughaktraf1erk12signalingpathway AT chaowuyang igf2bp3curbedbymir15c3prestoresdisruptedlipidstorageandprogesteronesecretioninchickengranulosacellsunderoxidativestressthroughaktraf1erk12signalingpathway AT lingqianyin igf2bp3curbedbymir15c3prestoresdisruptedlipidstorageandprogesteronesecretioninchickengranulosacellsunderoxidativestressthroughaktraf1erk12signalingpathway AT donghaozhang igf2bp3curbedbymir15c3prestoresdisruptedlipidstorageandprogesteronesecretioninchickengranulosacellsunderoxidativestressthroughaktraf1erk12signalingpathway AT yuantang igf2bp3curbedbymir15c3prestoresdisruptedlipidstorageandprogesteronesecretioninchickengranulosacellsunderoxidativestressthroughaktraf1erk12signalingpathway AT fengxu igf2bp3curbedbymir15c3prestoresdisruptedlipidstorageandprogesteronesecretioninchickengranulosacellsunderoxidativestressthroughaktraf1erk12signalingpathway AT yewang igf2bp3curbedbymir15c3prestoresdisruptedlipidstorageandprogesteronesecretioninchickengranulosacellsunderoxidativestressthroughaktraf1erk12signalingpathway AT yipingliu igf2bp3curbedbymir15c3prestoresdisruptedlipidstorageandprogesteronesecretioninchickengranulosacellsunderoxidativestressthroughaktraf1erk12signalingpathway |