Evidence map›Paper›PMID 35435578›Full record

ArticleAnatomical science international2022

Depletion of Ift88 in thymic epithelial cells affects thymic synapse and T-cell differentiation in aged mice.

Osamu Kutomi, Shigenori Nonaka, Katsuto Hozumi, Sén Takeda

Abstract read
PubMed Publisher
In one paragraph

Article in Anatomical science international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Ciliary and Non-Ciliary Roles of IFT88 in Development and Diseases.International journal of molecular sciences · 2025
    Review
  3. Article
  4. 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

4 authors at 4 institutions in 1 country.

Osamu KutomiDepartment of Anatomy and Cell Biology, Faculty of Medicine, University of Yamanashi, Chuo, Yamanashi, 409-3898, Japan. okutomi@yamanashi.ac.jp.ORCID http://orcid.org/0000-0003-2899-365X
Shigenori NonakaSpatiotemporal Regulations Group, Exploratory Research Center on Life and Living Systems, Okazaki, Aichi, 444-8585, Japan.
Katsuto HozumiDepartment of Immunology, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa, 259-1193, Japan.
Sén TakedaDepartment of Anatomy and Cell Biology, Faculty of Medicine, University of Yamanashi, Chuo, Yamanashi, 409-3898, Japan. takeda.sen.xm@teikyo-u.ac.jp.ORCID https://orcid.org/0000-0001-7090-2139
National Institute for Basic Biology · JPTokai University · JPUniversity of Fukui · JPUniversity of Yamanashi · JP

Funding

Cooperative Study Program of Exploratory Research Center on Life and Living Systems (JP) 19-403Cooperative Study Program of Exploratory Research Center on Life and Living Systems (JP) 20-406Japan Society for the Promotion of Science 16K18584Japan Society for the Promotion of Science 17K08511Japan Society for the Promotion of Science 20K16106Japan Society for the Promotion of Science 21K06753NIBB Collaborative Research Program (JP) 18-502
6 · The paper itself

Abstract

Primary cilia are ubiquitous hair-like organelles, usually projecting from the cell surface. They are essential for the organogenesis and homeostasis of various physiological functions, and their dysfunction leads to a plethora of human diseases. However, there are few reports on the role of primary cilia in the immune system; therefore, we focused on their role in the thymus that nurtures immature lymphocytes to full-fledged T cells. We detected primary cilia on the thymic epithelial cell (TEC) expressing transforming growth factor β (TGF-β) receptor in the basal body, and established a line of an intraflagellar transport protein 88 (Ift88) knockout mice lacking primary cilia in TECs (Ift88-TEC null mutant) to clarify their precise role in thymic organogenesis and T-cell differentiation. The Ift88-TEC null mutant mice showed stunted cilia or lack of cilia in TECs. The intercellular contact between T cells and the "thymic synapse" of medullary TECs was slightly disorganized in Ift88-TEC null mutants. Notably, the CD4- and CD8-single positive thymocyte subsets increased significantly. The absence or disorganization of thymic cilia downregulated the TGF-β signaling cascade, increasing the number of single positive thymocytes. To our knowledge, this is the first study reporting the physiological role of primary cilia and Ift88 in regulating the differentiation of the thymus and T cells.

Indexed as

Epithelial CellsT-LymphocytesTumor Suppressor ProteinsAgingAnimalsCell DifferentiationMiceMice, Inbred C57BLMice, KnockoutThymus GlandTransforming Growth Factor betaTg737Rpw protein, mouseTransforming Growth Factor betaTumor Suppressor ProteinsIft88Primary ciliaT cellTGF-β signalingThymic epithelial cells

Identifiers

PMID35435578
OpenAlexW4224106542

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.