Evidence map›Paper›PMID 35366759›Full record

ArticleMolecular biology reports2022

Extracellular vesicles derived from human Sertoli cells: characterizations, proteomic analysis, and miRNA profiling.

Xiao-Hui Tan, Sheng-Ji Gu, Wen-Jie Tian, Wen-Peng Song, Yang-Yang Gu, Yi-Ming Yuan, Xue-Song Li, Zhong-Cheng Xin, Sae Woong Kim, Rui-Li Guan and 1 more

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In one paragraph

Article in Molecular biology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Role of Seminal Exosomes in Reproduction.Journal of cellular physiology · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Immune Regulation in the Testis and Epididymis.Advances in experimental medicine and biology · 2025
    Review
  9. Article
  10. Article
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

11 authors at 3 institutions in 2 countries.

Xiao-Hui Tan *Department of Urology, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Sheng-Ji Gu *Department of Urology, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Wen-Jie TianDepartment of Urology, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Wen-Peng SongInstitute of Urology, Peking University, Beijing, 100034, People's Republic of China.
Yang-Yang GuInstitute of Urology, Peking University, Beijing, 100034, People's Republic of China.
Yi-Ming YuanDepartment of Urology, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Xue-Song LiDepartment of Urology, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Zhong-Cheng XinDepartment of Urology, Peking University First Hospital, Beijing, 100034, People's Republic of China.
Sae Woong KimDepartment of Urology, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Rui-Li GuanDepartment of Urology, Peking University First Hospital, Beijing, 100034, People's Republic of China. guanruili@bjmu.edu.cn.ORCID http://orcid.org/0000-0003-0422-846X
Woong Jin BaeDepartment of Urology, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea. bwoong@catholic.ac.kr.
Peking University · CNCatholic University of Korea · KRCapital Medical University · CN

Funding

National Natural Science Foundation of China grant no. 81401194
6 · The paper itself

Abstract

backgroundExtracellular vesicles (EVs) contain thousands of proteins and nucleic acids, playing an important role in cell-cell communications. Sertoli cells have been essential in the testis as a "nurse cell". However, EVs derived from human Sertoli cells (HSerCs) have not been well investigated.

methodsEVs were isolated from HSerCs via ultracentrifugation and characterized by transmission electron microscopy, tunable resistive pulse sensing, and Western blotting. The cargo carried by HSerCs-EVs was measured via liquid chromatography-mass spectrometry and GeneChip miRNA Arrays. Bioinformatic analysis was performed to reveal potential functions of HSerCs-EVs.

resultsA total of 860 proteins with no less than 2 unique peptides and 88 microRNAs with high signal values were identified in HSerCs-EVs. Biological processes related to molecular binding, enzyme activity, and regulation of cell cycle were significantly enriched. Specifically, many proteins in HSerCs-EVs were associated with spermatogenesis and regulation of immune system, including Septins, Large proline-rich protein BAG6, Clusterin, and Galectin-1. Moreover, abundant microRNAs within HSerCs-EVs (miR-638, miR-149-3p, miR-1246, etc.) had a possible impact on male reproductive disorders such as asthenozoospermia and oligozoospermia.

conclusionsOur study has shown that HSerCs-EVs contain diverse components such as proteins and microRNAs. Further research is required to evaluate HSerCs-EVs in spermatogenesis, which are underutilized but highly potent resources with particular promise for male infertility.

Indexed as

Extracellular VesiclesMicroRNAsChromatography, LiquidHumansMaleMolecular ChaperonesProteinsProteomicsSertoli CellsBAG6 protein, humanMicroRNAsMIRN149 microRNA, humanMIRN638 microRNA, humanMolecular ChaperonesProteinsExtracellular vesiclesmicroRNAsProteomicsSertoli cellsSpermiogenesis

Identifiers

PMID35366759
OpenAlexW4225514432

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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.