Evidence map›Paper›PMID 31966494›Full record

ArticleInternational journal of clinical and experimental pathology2017

Accumulated autophagosomes and excessive apoptosis during the luteal development of pregnant rats.

Zonghao Tang, Yuxiu Huang, Zhenghong Zhang, Yedong Tang, Jiajie Chen, Fengqi Sun, Hongqin Yang, Zhengchao Wang

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In one paragraph

Article in International journal of clinical and experimental pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 9 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

8 authors at 2 institutions in 1 country.

Zonghao TangProvincial Key Laboratory for Developmental Biology and Neurosciences, College of Life Sciences, Fujian Normal University Fuzhou, China.
Yuxiu HuangDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Fujian Medical University Fuzhou, China.
Zhenghong ZhangProvincial Key Laboratory for Developmental Biology and Neurosciences, College of Life Sciences, Fujian Normal University Fuzhou, China.
Yedong TangProvincial Key Laboratory for Developmental Biology and Neurosciences, College of Life Sciences, Fujian Normal University Fuzhou, China.
Jiajie ChenProvincial Key Laboratory for Developmental Biology and Neurosciences, College of Life Sciences, Fujian Normal University Fuzhou, China.
Fengqi SunProvincial Key Laboratory for Developmental Biology and Neurosciences, College of Life Sciences, Fujian Normal University Fuzhou, China.
Hongqin YangKey Laboratory of Optoelectronic Science and Technology for Medicine of Ministry of Education, Institute of Laser and Optoelectronics Technology, Fujian Normal University Fuzhou, China.
Zhengchao WangProvincial Key Laboratory for Developmental Biology and Neurosciences, College of Life Sciences, Fujian Normal University Fuzhou, China.
Fujian Normal University · CNFujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy plays an important role in the regression of pseudopregnant corpus luteum, whereas the involvement of autophagy in the pregnant luteolysis still remains unknown. Therefore, the present study was designed to investigate the levels and effects of accumulated autophagosomes on excessive apoptosis during the luteal development of pregnant rats. Ovaries were obtained from the female rats at the early, middle or late phase of the pregnancy, which correspondingly had three groups; including the early (ELP), middle (MLP) and late luteal phase (LLP). The results of autophagy-associated protein LC-3 clearly showed that autophagy expressed during the pregnant CL and significantly increased at LLP, while the expression changes of apoptosis related proteins cleaved caspase-3 and Bax were similar with LC-3 expression changes, indicating autophagy may be involved in the initiation of pregnant luteolysis through the induction of cellular apoptosis at LLP of pregnant ovaries. The present study was further examined the expressions of other two autophagy-associated proteins p62 and LAMP-2, since the degradation failure of autophagosomes contributed to cellular apoptosis. The results demonstrated p62 protein was accumulated at LLP while its mRNA was maintained during the whole luteal development of pregnant rats. Interestingly, the expressions of LAMP-2 mRNA and premature protein were significantly increased at MLP and LLP, while the expression of mature LAMP-2 increased at MLP and then decreased at LLP, implying autophagosomes were accumulated at LLP. Together, to our knowledge, the present study firstly demonstrated that the insufficient of lysosomal functions contributed to the impaired degradation of autophagosomes and then activated caspase-3 dependent apoptotic pathway during the pregnant luteolysis of rat ovaries, which will provide a new insight into the important mechanism regulating the luteolysis of the pregnant ovaries in mammals.

Indexed as

Autophagosomecellular apoptosiscorpus luteumlysosomal functionpregnant rat

Identifiers

PMID31966494
PMCPMC6966024
OpenAlexW3014175018

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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.