Evidence map›Paper›PMID 20683063›Full record

ArticleHuman reproduction (Oxford, England)2010

Xenografting of human fetal testis tissue: a new approach to study fetal testis development and germ cell differentiation.

Rod T Mitchell, Philippa T K Saunders, Andrew J Childs, Claire Cassidy-Kojima, Richard A Anderson, W Hamish B Wallace, Chris J H Kelnar, Richard M Sharpe

Open access · bronzeAbstract read
In one paragraph

Article in Human reproduction (Oxford, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. The impact ofHuman reproduction open · 2025
    Review
  6. Article
  7. Article
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  9. Article
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  14. Characterization of Human Adrenal Steroidogenesis During Fetal Development.The Journal of clinical endocrinology and metabolism · 2019
    Article
  15. Article
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  17. 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 4 institutions in 1 country.

Rod T MitchellMRC Human Reproductive Sciences Unit, Centre for Reproductive Biology, The Queen's Medical Research Institute, University of Edinburgh, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.
Philippa T K Saunders
Andrew J Childs
Claire Cassidy-Kojima
Richard A Anderson
W Hamish B Wallace
Chris J H Kelnar
Richard M Sharpe
University of Edinburgh · GBMRC Centre for Reproductive Health · GBRoyal Hospital for Children · GBThe Queen's Medical Research Institute · GB

Funding

Medical Research Council MC_U127661055Medical Research Council MC_U127684422Medical Research Council MC_U127684439Medical Research Council MC_U127685844Medical Research Council U.1276.00.002(61055)Medical Research Council WBS U.1276.00.002.00001Medical Research Council WBS U.1276.00.003.00003.01
6 · The paper itself

Abstract

backgroundAbnormal fetal testis development can result in disorders of sex development (DSDs) and predispose to later testicular dysgenesis syndrome (TDS) disorders such as testicular germ cell tumours. Studies of human fetal testis development are hampered by the lack of appropriate model, and intervention systems. We hypothesized that human fetal testis xenografts can recapitulate normal development.

methodsHuman fetal testes (at 9 weeks, n = 4 and 14-18 weeks gestation, n = 6) were xenografted into male nude mice for 6 weeks, with or without hCG treatment of the host, and evaluated for normal cellular development and function using immunohistochemistry, triple immunofluorescence and testosterone assay. The differentiation and proliferation status of germ cells within xenografts was quantified and compared with age-matched controls.

resultsXenografts showed >75% survival with normal morphology. In the first-trimester xenografts seminiferous cord formation was initiated and in first- and second-trimester grafts normal functional development of Sertoli, Leydig and peritubular myoid cells was demonstrated using cell-specific protein markers. Grafts produced testosterone when hosts were treated with hCG (P = 0.004 versus control). Proliferation of germ cells and differentiation from gonocytes (OCT4(+)) into pre-spermatogonia (VASA(+)) occurred in grafts and quantification showed this progressed comparably with age-matched ungrafted controls.

conclusionsHuman fetal testis tissue xenografts demonstrate normal structure, function and development after xenografting, including normal germ cell differentiation. This provides an in vivo system to study normal human fetal testis development and its susceptibility to disruption by exogenous factors (e.g. environmental chemicals). This should provide mechanistic insight into the fetal origins of DSDs and TDS disorders.

Indexed as

SpermatogenesisAnimalsChorionic GonadotropinHumansLeydig CellsMaleMiceMice, NudeOctamer Transcription Factor-3Seminiferous EpitheliumSertoli CellsSpermatozoaTestisTestosteroneTransplantation, HeterologousChorionic GonadotropinOctamer Transcription Factor-3POU5F1 protein, humanTestosterone

Identifiers

PMID20683063
PMCPMC2939754
OpenAlexW2148926493

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.