Evidence map›Paper›PMID 31359348›Full record

ArticleIn vitro cellular & developmental biology. Animal2019

ULK1 affects cell viability of goat Sertoli cell by modulating both autophagy and apoptosis.

Jing Pang, Le Han, Zifei Liu, Jian Zheng, Jie Zhao, Kaiping Deng, Feng Wang, Yanli Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

7 citing papers in PubMed, 23 citations in OpenAlex.

  1. Beclin1 Regulates Sertoli Cell Function to Maintain Mouse Spermatogenesis.Reproductive sciences (Thousand Oaks, Calif.) · 2026
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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.

Jing PangCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Le HanState Key Laboratory of Reproductive Medicine, Clinical Center of Reproductive Medicine, First Affiliated Hospital, Nanjing Medical University, Nanjing, 210029, China.
Zifei LiuCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Jian ZhengCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Jie ZhaoCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Kaiping DengCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Feng WangCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China.
Yanli ZhangCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, People's Republic of China. zhangyanli@njau.edu.cn.ORCID http://orcid.org/0000-0002-7901-7774
Nanjing Agricultural University · CNNanjing Medical University · CN

Funding

Chinese Fundamental Research Funds for the Central Universities KYDK201702the Natural Science Foundation of Jiangsu Province BK20161444
6 · The paper itself

Abstract

Sertoli cells (SCs) are necessary for proper germ cell development and viability. Unc-51 like autophagy activating kinase (ULK1) protein kinase is an important regulator of autophagy activation. This study aims to investigate the role of autophagy promoter ULK1 on cell viability of goat SCs. Our results showed that ULK1 knockdown in goat SCs decreased autophagy activation, which was confirmed by decreased expression of autophagy-related markers including LC3, Beclin1, Atg5, and Atg7 (P < 0.05). Meanwhile, lower ULK1 levels resulted in decreased expressions of goat SC marker genes ABP, AMH, FASL, and GATA4. However, a reverse trend of these parameters occurred when the goat SCs were transfected with ULK1 overexpression construct; higher ULK1 levels in goat SCs also decreased the ratio of Bax/Bcl-2. Moreover, ULK1 overexpression in goat SCs activated the autophagy levels when cells were exposed to an environmental contaminant bisphenol A (BPA). The above results indicated that ULK1 gene might play important roles in goat SC function by regulating cell viability.

Indexed as

ApoptosisAutophagyAnimalsAutophagosomesAutophagy-Related Protein-1 HomologBenzhydryl CompoundsBisphenol A CompoundsCell CycleCell SurvivalGenetic MarkersGenetic VectorsGoatsMalePhenolsRNA, Small InterferingSertoli CellsAutophagy-Related Protein-1 HomologBenzhydryl Compoundsbisphenol ABisphenol A CompoundsGenetic MarkersPhenolsRNA, Small InterferingApoptosisAutophagyGoatSertoli cellULK1

Identifiers

PMID31359348
OpenAlexW2966126028

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.