Evidence map›Paper›PMID 35163399›Full record

ArticleInternational journal of molecular sciences2022

Role of Autophagy in Lysophosphatidylcholine-Induced Apoptosis of Mouse Ovarian Granulosa Cells.

Si Yang, Jie Chen, Bingchun Ma, Jinglei Wang, Jiaxiang Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.5field-weighted citation impact, top 5% of its field
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

14 citing papers in PubMed, 30 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Si YangDepartment of Physiology, School of Basic Medical Sciences, Nanchang University, Nanchang 330006, China.
Jie ChenDepartment of Physiology, School of Basic Medical Sciences, Nanchang University, Nanchang 330006, China.
Bingchun MaDepartment of Physiology, School of Basic Medical Sciences, Nanchang University, Nanchang 330006, China.
Jinglei WangDepartment of Physiology, School of Basic Medical Sciences, Nanchang University, Nanchang 330006, China.
Jiaxiang ChenDepartment of Physiology, School of Basic Medical Sciences, Nanchang University, Nanchang 330006, China.ORCID 0000-0003-0756-1647
Nanchang University · CN

Funding

Jiangxi Provincial Major Academic Disciplines and Technical Leaders Training Program 20204BCJ22031National Natural Science Foundation of China 81660246National Natural Science Foundation of China 81660255National Natural Science Foundation of China 82060278Natural Science Foundation of Jiangxi Province 20212ACB206036
6 · The paper itself

Abstract

Lysophosphatidylcholine (LPC), also known as lysolecithin, is one of the major components of oxidized low-density lipoproteins (ox-LDL). In the pathogenetic process of diverse diseases, LPC acts as a significant lipid mediator. However, no evidence shows that LPC can affect the female reproductive system. In our study, we found that LPC inhibited the cell viability of primary mouse ovarian granulosa cells. Meanwhile, LPC was shown to induce apoptosis, which is accompanied by an increase in apoptosis-related protein levels, such as cleaved caspase-3, cleaved caspase-8 and Bax, as well as a decrease in Bcl-2. The total numbers of early and late apoptotic cells also increased in the LPC-treated cells. These results indicated that LPC could induce apoptosis of mouse ovarian granulosa cells. Furthermore, the increase in autophagy-related protein levels and the number of autophagic vesicles suggested that LPC could induce autophagy. The inhibition of oxidative stress by N-acetyl-L-cysteine (NAC) could rescue the induction of apoptosis and autophagy by LPC, which indicated that oxidative stress was involved in LPC-induced apoptosis and autophagy. Interestingly, the inhibition of autophagy by 3-MA could reserve the inhibition of cell viability and the induction of apoptosis by LPC. In conclusion, oxidative stress was involved in LPC-induced apoptosis, whileautophagy of mouse ovarian granulosa cells and the inhibition of autophagy could alleviate LPC-induced apoptosis.

Indexed as

ApoptosisAutophagyAnimalsApoptosis Regulatory ProteinsFemaleGranulosa CellsLysophosphatidylcholinesMiceApoptosis Regulatory ProteinsLysophosphatidylcholinesapoptosisautophagylysophosphatidylcholineovarian granulosa cellsoxidative stress

Identifiers

PMID35163399
PMCPMC8835979
OpenAlexW4210600347

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.