Evidence map›Paper›PMID 38492155›Full record

ArticleJournal of assisted reproduction and genetics2024

Extraction and identification of exosomes from three different sources of human ovarian granulosa cells and analysis of their differential miRNA expression profiles.

Xiaorong Li, Ting Gao, Xiaohong Ma, Jiawen Zhong, Ling Qin, Yan Nian, Xueyi Wang, Yuxue Luo

Open access · greenAbstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
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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 1 institution in 1 country.

Xiaorong Li *Department of the Center for Reproductive Medicine, General Hospital of Ningxia Medical University, No. 1106 of Shengli Road, Xingqin District, Yinchuan, 750004, China. lixiaoronglxr5@126.com.ORCID http://orcid.org/0009-0000-3533-9264
Ting Gao *Key Laboratory of Fertility Maintenance, Ningxia Medical University, Yinchuan, 750004, China.
Xiaohong MaDepartment of the Center for Reproductive Medicine, General Hospital of Ningxia Medical University, No. 1106 of Shengli Road, Xingqin District, Yinchuan, 750004, China.
Jiawen ZhongKey Laboratory of Fertility Maintenance, Ningxia Medical University, Yinchuan, 750004, China.
Ling QinKey Laboratory of Modernization of Hui Medicine, Ministry of Education, School of Traditional Chinese Medicine, Ningxia Medical University, Yinchuan, 750004, China.
Yan NianDepartment of the Center for Reproductive Medicine, General Hospital of Ningxia Medical University, No. 1106 of Shengli Road, Xingqin District, Yinchuan, 750004, China.
Xueyi WangKey Laboratory of Fertility Maintenance, Ningxia Medical University, Yinchuan, 750004, China.
Yuxue LuoKey Laboratory of Fertility Maintenance, Ningxia Medical University, Yinchuan, 750004, China.
Ningxia Medical University · CN

Funding

National Natural Science Foundation of China 81660806National Natural Science Foundation of China 82260947
6 · The paper itself

Abstract

objectiveAs important functional cells in the ovary, ovarian granulosa cells are involved in the regulation of oocyte growth and development and play an important role in the study of female fertility preservation. Based on the importance of granulosa cell functionalism, in this study, we analyzed the exosome secretion capacity of human ovarian granulosa cells (SVOG/KGN-cell line, PGC-primary cells) and the differences in their miRNA expression.

methodsCells were identified by hematoxylin-eosin staining (HE) and FSHR immunofluorescence staining; CCK8 and colony-forming assay were performed to compare cell proliferation capacity; exosomes were extracted and identified by ultra-high speed centrifugation, transmission electron microscopy (TEM), nanoparticle tracking analysis (NTA), and western blot analysis (WB), and the expression profile of each cellular exosomal miRNA was analyzed by miRNA high-throughput sequencing.

resultsThe proliferative abilities of the three granulosa cells differed, but all had the ability to secrete exosomes. In the exosomes of SVOG, KGN, and PGC cells, 218, 327, and 471 miRNAs were detected, respectively. When compared to the exosomal miRNAs of PGC cells, 111 miRNAs were significantly different in SVOG, and 70 miRNAs were washed two significantly different in KGN cells. These differential miRNA functions were mainly enriched in the cell cycle, cell division/differentiation, multicellular biogenesis, and protein binding.

conclusionHuman ovarian granulosa cells of different origins are capable of secreting exosomes, but there are still some differences in their exosomes and exosomal miRNAs, and experimental subjects should be selected rationally according to the actual situation.

Indexed as

Cell ProliferationExosomesGranulosa CellsMicroRNAsCell LineFemaleGene Expression ProfilingHumansMicroRNAsExosomesHigh-throughput sequencingmiRNAOvarian granulosa cells

Identifiers

PMID38492155
PMCPMC11143209
OpenAlexW4392881788

What OpenQuestion holds

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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.