Evidence map›Paper›PMID 23178507›Full record

ArticleAging2012

Aging affects epidermal Langerhans cell development and function and alters their miRNA gene expression profile.

Ying-Ping Xu, Rui-Qun Qi, Wenbin Chen, Yuling Shi, Zhi-Zhong Cui, Xing-Hua Gao, Hong-Duo Chen, Li Zhou, Qing-Sheng Mi

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

30 citing papers in PubMed, 56 citations in OpenAlex.

  1. What Do We Know About Immune System Aging from Human and Animal Studies?International journal of molecular sciences · 2026
    Review
  2. Article
  3. Review
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  5. Review
  6. Article
  7. Article
  8. Monocytes give rise to Langerhans cells that preferentially migrate to lymph nodes at steady state.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
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  15. Article
  16. The Role of microRNAs in Organismal and Skin Aging.International journal of molecular sciences · 2020
    Review
  17. Article
  18. Review
  19. Article
  20. 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 2 countries.

Ying-Ping XuHenry Ford Immunology Program, Henry Ford Health System, Detroit, MI 48202, USA.
Rui-Qun Qi
Wenbin Chen
Yuling Shi
Zhi-Zhong Cui
Xing-Hua Gao
Hong-Duo Chen
Li Zhou
Qing-Sheng Mi
Henry Ford Health System · USChina Medical University · CNShandong Agricultural University · CN

Funding

miRNAs and epidermal langerhans cell development and functionR21AR059976 · NIAMS · HENRY FORD HEALTH SYSTEM · PI MI, QING-SHENG · 2010 to 2011
$367k
NIAMS NIH HHS R21 AR059976NIAMS NIH HHS R21AR059976
6 · The paper itself

Abstract

Immunosenescence is a result of progressive decline in immune system function with advancing age. Epidermal Langerhans cells (LCs), belonging to the dendritic cell (DC) family, act as sentinels to play key roles in the skin immune responses. However, it has not been fully elucidated how aging affects development and function of LCs. Here, we systemically analyzed LC development and function during the aging process in C57BL/6J mice, and performed global microRNA (miRNA) gene expression profiles in aged and young LCs. We found that the frequency and maturation of epidermal LCs were significantly reduced in aged mice starting at 12 months of age, while the Langerin expression and ability to phagocytose Dextran in aged LCs were increased compared to LCs from < 6 month old mice. The migration of LCs to draining lymph nodes was comparable between aged and young mice. Functionally, aged LCs were impaired in their capacity to induce OVA-specific CD4+ and CD8+ T cell proliferation. Furthermore, the expression of miRNAs in aged epidermal LCs showed a distinct profile compared to young LCs. Most interestingly, aging-regulated miRNAs potentially target TGF-β-dependent and non- TGF-β-dependent signal pathways related to LCs. Overall, our data suggests that aging affects LCs development and function, and that age-regulated miRNAs may contribute to the LC developmental and functional changes in aging.

Indexed as

TranscriptomeAgingAnimalsEpidermisFlow CytometryImmunohistochemistryLangerhans CellsMiceMice, Inbred C57BLMicroRNAsReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionMicroRNAs

Identifiers

PMID23178507
PMCPMC3560442
OpenAlexW2097309414

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.