Evidence map›Paper›PMID 39123277›Full record

ArticleAging cell2024

B cell senescence promotes age-related changes in oral microbiota.

Hiroya Mizuno, Shimpei Kawamoto, Ken Uemura, Jeong Hoon Park, Nozomi Hori, Yumiko Okumura, Yusuke Konishi, Eiji Hara

Abstract read
In one paragraph

Article in Aging cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Article
  2. Review
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  4. [Aging-Associated Oral Microbiota Dysbiosis and Hypofunction: Their Role in Alzheimer's Disease Pathogenesis].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2026
    Review
  5. Review
  6. Review
  7. Review
  8. Review
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  11. 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.

Hiroya MizunoDepartment of Molecular Biology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Shimpei KawamotoDepartment of Molecular Biology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.ORCID 0000-0002-7033-671X
Ken UemuraDepartment of Molecular Biology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Jeong Hoon ParkDepartment of Molecular Biology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Nozomi HoriDepartment of Molecular Biology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Yumiko OkumuraDepartment of Molecular Biology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Yusuke KonishiDepartment of Molecular Biology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Eiji HaraDepartment of Molecular Biology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.ORCID 0000-0001-7821-3960

Funding

Foundation for Biomedical Research and InnovationJapan Agency for Medical Research and Development JP21gm5010001h0005Japan Agency for Medical Research and Development JP22ama221114h0001Japan Agency for Medical Research and Development JP22gm1710004h0001Japan Agency for Medical Research and Development JP22zf0127008h0001Japan Science and Technology Agency JPMJMS2022Japan Society for the Promotion of Science JP20K07446Japan Society for the Promotion of Science JP22H00457Japan Society for the Promotion of Science JP23K06481Kato Memorial Bioscience FoundationMitsubishi FoundationNaito FoundationPrincess Takamatsu Cancer Research FundTakeda Science FoundationUBE Foundation
6 · The paper itself

Abstract

In recent years, there has been increasing attention towards understanding the relationship between age-related alterations in the oral microbiota and age-associated diseases, with reports emphasizing the significance of maintaining a balanced oral microbiota for host health. However, the precise mechanisms underlying age-related changes in the oral microbiota remain elusive. We recently reported that cellular senescence of ileal germinal center (GC) B cells, triggered by the persistent presence of commensal bacteria, results in diminished IgA production with aging and subsequent alterations in the gut microbiota. Consequently, we hypothesize that a similar phenomenon may occur in the oral cavity, potentially contributing to age-related changes in the oral microbiota. Examination of p16-luc mice, wherein the expression of the senescent cell marker p16

Indexed as

AgingB-LymphocytesCellular SenescenceMicrobiotaAnimalsCyclin-Dependent Kinase Inhibitor p16Immunoglobulin AMiceMice, Inbred C57BLMouthCyclin-Dependent Kinase Inhibitor p16Immunoglobulin AB cellcellular senescenceimmunoglobulin Amicrobiotasaliva

Identifiers

PMID39123277
PMCPMC11634744

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.