Evidence map›Paper›PMID 34909124›Full record

ArticleWorld journal of stem cells2021

MKK7-mediated phosphorylation of JNKs regulates the proliferation and apoptosis of human spermatogonial stem cells.

Zeng-Hui Huang, Chuan Huang, Xi-Ren Ji, Wen-Jun Zhou, Xue-Feng Luo, Qian Liu, Yu-Lin Tang, Fei Gong, Wen-Bing Zhu

Open access · hybridAbstract read
In one paragraph

Article in World journal of stem cells, 2021. 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
1.5field-weighted citation impact, top 17% 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, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The lncRNA Gm8097 is associated with hypospermatogenesis.Clinical and experimental reproductive medicine · 2024
    Article
  5. Article
  6. Article
  7. Review
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

9 authors at 2 institutions in 1 country.

Zeng-Hui HuangInstitute of Reproductive and Stem Cell Engineering, Central South University, Changsha 410008, Hunan Province, China.
Chuan HuangDepartment of Sperm Bank, Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha 410008, Hunan Province, China.
Xi-Ren JiInstitute of Reproductive and Stem Cell Engineering, Central South University, Changsha 410008, Hunan Province, China.
Wen-Jun ZhouInstitute of Reproductive and Stem Cell Engineering, Central South University, Changsha 410008, Hunan Province, China.
Xue-Feng LuoInstitute of Reproductive and Stem Cell Engineering, Central South University, Changsha 410008, Hunan Province, China.
Qian LiuInstitute of Reproductive and Stem Cell Engineering, Central South University, Changsha 410008, Hunan Province, China.
Yu-Lin TangInstitute of Reproductive and Stem Cell Engineering, Central South University, Changsha 410008, Hunan Province, China.
Fei GongInstitute of Reproductive and Stem Cell Engineering, Central South University, Changsha 410008, Hunan Province, China.
Wen-Bing ZhuInstitute of Reproductive and Stem Cell Engineering, Central South University, Changsha 410008, Hunan Province, China.
Central South University · CNReproductive & Genetic Hospital CITIC-Xiangya · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman spermatogonial stem cells (SSCs) are the basis of spermatogenesis. However, little is known about the developmental regulatory mechanisms of SSC due to sample origin and species differences.

aimTo investigates the mechanisms involved in the proliferation of human SSC.

methodsThe expression of mitogen-activated protein kinase kinase 7 (MKK7) in human testis was identified using immunohistochemistry and western blotting (WB). MKK7 was knocked down using small interfering RNA, and cell proliferation and apoptosis were detected by WB, EdU, cell counting kit-8 and fluorescence-activated cell sorting. After bioinformatic analysis, the interaction of MKK7 with c-Jun N-terminal kinases ( JNKs ) was verified by protein co-immunoprecipitation and WB. The phosphorylation of JNKs was inhibited by SP600125, and the phenotypic changes were detected by WB, cell counting kit-8 and fluorescence-activated cell sorting.

resultsMKK7 is mainly expressed in human SSCs, and MKK7 knockdown inhibits SSC proliferation and promotes their apoptosis. MKK7 mediated the phosphorylation of JNKs, and after inhibiting the phosphorylation of JNKs, the phenotypic changes of the cells were similar to those after MKK7 downregulation. The expression of MKK7 was significantly downregulated in patients with abnormal spermatogenesis, suggesting that abnormal MKK7 may be associated with spermatogenesis impairment.

conclusionMKK7 regulates the proliferation and apoptosis of human SSC by mediating the phosphorylation of JNKs.

Indexed as

ApoptosisJNKsMKK7ProliferationSpermatogonial stem cell

Identifiers

PMID34909124
PMCPMC8641020
OpenAlexW3217079478

What OpenQuestion holds

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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.