Evidence map›Paper›PMID 38702372›Full record

ArticleScientific reports2024

Ovarian PERK/NRF2/CX43/StAR/progesterone pathway activation mediates female reproductive dysfunction induced by cold exposure.

Mengnan Ding, Yarong Lu, Qing Wen, Chen Xing, Xin Huang, Yifan Zhang, Wei Wang, Chongchong Zhang, Min Zhang, Fanfei Meng and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
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  5. Depletion ofInternational journal of molecular sciences · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Mengnan Ding *Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Yarong Lu *Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Qing WenBeijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Chen XingBeijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Xin HuangBeijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Yifan ZhangBeijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Wei WangBeijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Chongchong ZhangBeijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Min ZhangBeijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Fanfei MengBeijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Kun LiuBeijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Guangchao LiuHenan University Joint National Laboratory for Antibody Drug Engineering, Henan, 465004, China.
Lun SongBeijing Institute of Basic Medical Sciences, Beijing, 100850, China. lunsong0752@163.com.ORCID 0000-0001-7314-2649

Funding

Key Logistics Research Project of China XXX17J025
6 · The paper itself

Abstract

Ambient air temperature is a key factor affecting human health. Female reproductive disorders are representative health risk events under low temperature. However, the mechanism involving in cold-induced female reproductive disorders remains largely unknown. Female mice were intermittently exposed to cold conditions (4 °C) to address the health risk of low temperature on female reproductive system. Primary granulosa cells (GCs) were prepared and cultured under low temperature (35 °C) or exposed to β3-adrenoreceptor agonist, isoproterenol, to mimic the condition of cold exposure. Western-blot, RT-PCR, co-IP, ELISA, pharmacological inhibition or siRNA-mediated knockdown of target gene were performed to investigate the possible role of hormones, gap conjunction proteins, and ER stress sensor protein in regulating female reproductive disorders under cold exposure. Cold exposure induced estrous cycle disorder and follicular dysplasia in female mice, accompanying with abnormal upregulation of progesterone and its synthetic rate-limiting enzyme, StAR, in the ovarian granulosa cells. Under the same conditions, an increase in connexin 43 (CX43) expressions in the GCs was also observed, which contributed to elevated progesterone levels in the ovary. Moreover, ER stress sensor protein, PERK, was activated in the ovarian GCs after cold exposure, leading to the upregulation of downstream NRF2-dependent CX43 transcription and aberrant increase in progesterone synthesis. Most importantly, blocking PERK expression in vivo significantly inhibited NRF2/CX43/StAR/progesterone pathway activation in the ovary and efficiently rescued the prolongation of estrous cycle and the increase in follicular atresia of the female mice induced by cold stress. We have elucidated the mechanism of ovarian PERK/NRF2/CX43/StAR/progesterone pathway activation in mediating female reproductive disorder under cold exposure. Targeting PERK might be helpful for maintaining female reproductive health under cold conditions.

Indexed as

Cold TemperatureConnexin 43eIF-2 KinaseGranulosa CellsNF-E2-Related Factor 2ProgesteroneSignal TransductionAnimalsEstrous CycleFemaleMiceOvaryConnexin 43eIF-2 KinaseNfe2l2 protein, mouseNF-E2-Related Factor 2ProgesteroneColdCX43Female reproductive disordersNRF2PERKProgesterone

Identifiers

PMID38702372
PMCPMC11068861

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.