Evidence map›Paper›PMID 24738045›Full record

ArticleBioMed research international2014

Differential gene expression profiling of enriched human spermatogonia after short- and long-term culture.

Sabine Conrad, Hossein Azizi, Maryam Hatami, Mikael Kubista, Michael Bonin, Jörg Hennenlotter, Markus Renninger, Thomas Skutella

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
6.4field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  5. Review
  6. Optimization ofFrontiers in veterinary science · 2022
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  11. Role of stem cells in fertility preservation: current insights.Stem cells and cloning : advances and applications · 2019
    Article
  12. Spermatogonial stem cells.Biology of reproduction · 2018
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. 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

8 authors at 4 institutions in 4 countries.

Sabine ConradInstitute of Anatomy, University of Tübingen, Österbergstraße 3, 72074 Tübingen, Germany.
Hossein AziziInstitute for Anatomy and Cell Biology, Medical Faculty, University of Heidelberg, Im Neuenheimer Feld 307, 69120 Heidelberg, Germany ; Amol University of Special Modern Technologies, Special Modern Technologies, P.O. Box 46168-49767, Amol, Iran ; Department of Stem Cells and Developmental Biology, Royan Institute, P.O. Box 19395-4644, Tehran, Iran.
Maryam HatamiInstitute for Anatomy and Cell Biology, Medical Faculty, University of Heidelberg, Im Neuenheimer Feld 307, 69120 Heidelberg, Germany.
Mikael KubistaTATAA Biocenter AB, Odinsgatan 28, 41103 Göteborg, Sweden and Institute of Biotechnology at the Czech Academy of Sciences, Vídenská 1083, 14220 Prague 4, Czech Republic.
Michael BoninInstitute of Anthropology and Human Genetics, Microarray Facility, University Clinic, Calwerstraße 7, 72076 Tübingen, Germany.
Jörg HennenlotterDepartment of Urology, University Clinic Tübingen, Hoppe-Seyler-Straße 3, 72076 Tübingen, Germany.
Markus RenningerDepartment of Urology, University Clinic Tübingen, Hoppe-Seyler-Straße 3, 72076 Tübingen, Germany.
Thomas SkutellaInstitute for Anatomy and Cell Biology, Medical Faculty, University of Heidelberg, Im Neuenheimer Feld 307, 69120 Heidelberg, Germany.
University Hospital Heidelberg · DEUniversity of Tübingen · DEHeidelberg University · DETataa Biocenter (Sweden) · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to provide a molecular signature for enriched adult human stem/progenitor spermatogonia during short-term (<2 weeks) and long-term culture (up to more than 14 months) in comparison to human testicular fibroblasts and human embryonic stem cells. Human spermatogonia were isolated by CD49f magnetic activated cell sorting and collagen(-)/laminin(+) matrix binding from primary testis cultures obtained from ten adult men. For transcriptomic analysis, single spermatogonia-like cells were collected based on their morphology and dimensions using a micromanipulation system from the enriched germ cell cultures. Immunocytochemical, RT-PCR and microarray analyses revealed that the analyzed populations of cells were distinct at the molecular level. The germ- and pluripotency-associated genes and genes of differentiation/spermatogenesis pathway were highly expressed in enriched short-term cultured spermatogonia. After long-term culture, a proportion of cells retained and aggravated the "spermatogonial" gene expression profile with the expression of germ and pluripotency-associated genes, while in the majority of long-term cultured cells this molecular profile, typical for the differentiation pathway, was reduced and more genes related to the extracellular matrix production and attachment were expressed. The approach we provide here to study the molecular status of in vitro cultured spermatogonia may be important to optimize the culture conditions and to evaluate the germ cell plasticity in the future.

Indexed as

AdultCell Culture TechniquesCell DifferentiationCells, CulturedCell SeparationEmbryonic Stem CellsFibroblastsGene Expression ProfilingHumansMaleMiddle AgedSpermatogenesisSpermatogoniaTestisTranscriptomeYoung Adult

Identifiers

PMID24738045
PMCPMC3971551
OpenAlexW1969312674

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LicenceCC BY
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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.