Evidence map›Paper›PMID 21900683›Full record

ArticleBiology of reproduction2012

Immunoprotective properties of primary Sertoli cells in mice: potential functional pathways that confer immune privilege.

Timothy J Doyle, Gurvinder Kaur, Saroja M Putrevu, Emily L Dyson, Mathew Dyson, William T McCunniff, Mithun R Pasham, Kwan Hee Kim, Jannette M Dufour

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
7.4field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 112 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Article
  6. Article
  7. Article
  8. Transcription factorZoological research · 2023
    Article
  9. Review
  10. Article
  11. Mouse Sertoli Cells Inhibit Humoral-Based Immunity.International journal of molecular sciences · 2022
    Article
  12. Somatic-Immune Cells Crosstalk In-The-Making of Testicular Immune Privilege.Reproductive sciences (Thousand Oaks, Calif.) · 2022
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Characterization of rodent Sertoli cell primary cultures.Molecular reproduction and development · 2020
    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 3 institutions in 1 country.

Timothy J DoyleCenter for Reproductive Biology, School of Molecular Biosciences, Washington State University, Pullman, USA.
Gurvinder Kaur
Saroja M Putrevu
Emily L Dyson
Mathew Dyson
William T McCunniff
Mithun R Pasham
Kwan Hee Kim
Jannette M Dufour
Texas Tech University Health Sciences Center · USTexas Tech University · USWashington State University · US

Funding

Transplantation of Genetically Modified, Immune-privileged Steroli CellsR01HD067400 · NICHD · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI DUFOUR, JANNETTE M · 2010 to 2012
$663k
NICHD NIH HHS HD067400NICHD NIH HHS R01 HD067400
6 · The paper itself

Abstract

Primary Sertoli cells isolated from mouse testes survive when transplanted across immunological barriers and protect cotransplanted allogeneic and xenogeneic cells from rejection in rodent models. In contrast, the mouse Sertoli cell line (MSC-1) lacks immunoprotective properties associated with primary Sertoli cells. In this study, enriched primary Sertoli cells or MSC-1 cells were transplanted as allografts into the renal subcapsular area of naive BALB/c mice, and their survival in graft sites was compared. While Sertoli cells were detected within the grafts with 100% graft survival throughout the 20-day study, MSC-1 cells were rejected between 11 and 14 days, with 0% graft survival at 20 days posttransplantation. Nonetheless, the mechanism for primary Sertoli cell survival and immunoprotection remains unresolved. To identify immune factors or functional pathways potentially responsible for immune privilege, gene expression profiles of enriched primary Sertoli cells were compared with those of MSC-1 cells. Microarray analysis identified 2369 genes in enriched primary Sertoli cells that were differentially expressed at ±4-fold or higher levels than in MSC-1 cells. Ontological analyses identified multiple immune pathways, which were used to generate a list of 340 immune-related genes. Three functions were identified in primary Sertoli cells as potentially important for establishing immune privilege: suppression of inflammation by specific cytokines and prostanoid molecules, slowing of leukocyte migration by controlled cell junctions and actin polymerization, and inhibition of complement activation and membrane-associated cell lysis. These results increase our understanding of testicular immune privilege and, in the long-term, could lead to improvements in transplantation success.

Indexed as

Adherens JunctionsAnimalsApoptosisCell AdhesionCell LineGene Expression ProfilingGene Expression RegulationMaleMiceMice, Inbred BALB CMice, Inbred C57BLReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionSertoli CellsTight Junctions

Identifiers

PMID21900683
PMCPMC3313662
OpenAlexW2158211144

What OpenQuestion holds

Textmetadata
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.