Evidence map›Paper›PMID 33600795›Full record

ArticleThe Journal of biological chemistry

Heparan sulfate is essential for thymus growth.

Hsuan-Po Hsu, Yun-Tzu Chen, Yu-Ying Chen, Chih-Yu Lin, Po-Yu Chen, Shio-Yi Liao, Ciara Christianne Y Lim, Yu Yamaguchi, Chia-Lin Hsu, Ivan L Dzhagalov

Open access · goldAbstract read
In one paragraph

Article in The Journal of biological chemistry. 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
1.1field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Heparan Sulfate Proteoglycans in Immunity.Proteoglycan research · 2026
    Article
  2. Review
  3. Basic interactions responsible for thymus function explain the convoluted medulla shape.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Mesenchymal stromal cells in the thymus.Inflammation and regeneration · 2022
    Review
  9. Article
  10. Review
  11. 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

10 authors at 2 institutions in 2 countries.

Hsuan-Po HsuInstitute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.
Yun-Tzu ChenInstitute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.
Yu-Ying ChenInstitute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.
Chih-Yu LinInstitute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.
Po-Yu ChenInstitute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.
Shio-Yi LiaoInstitute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.
Ciara Christianne Y LimInstitute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.
Yu YamaguchiSanford Burnham Prebys Medical Discovery Institute, La Jolla, California, USA.
Chia-Lin HsuInstitute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan.
Ivan L DzhagalovInstitute of Microbiology and Immunology, National Yang-Ming University, Taipei, Taiwan. Electronic address: ivan.dzhagalov@ym.edu.tw.
National Yang Ming Chiao Tung University · TWSanford Burnham Prebys Medical Discovery Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thymus organogenesis and T cell development are coordinated by various soluble and cell-bound molecules. Heparan sulfate (HS) proteoglycans can interact with and immobilize many soluble mediators, creating fields or gradients of secreted ligands. While the role of HS in the development of many organs has been studied extensively, little is known about its function in the thymus. Here, we examined the distribution of HS in the thymus and the effect of its absence on thymus organogenesis and T cell development. We found that HS was expressed most abundantly on the thymic fibroblasts and at lower levels on endothelial, epithelial, and hematopoietic cells. To study the function of HS in the thymus, we eliminated most of HS in this organ by genetically disrupting the glycosyltransferase Ext1 that is essential for its synthesis. The absence of HS greatly reduced the size of the thymus in fetal thymic organ cultures and in vivo, in mice, and decreased the production of T cells. However, no specific blocks in T cell development were observed. Wild-type thymic fibroblasts were able to physically bind the homeostatic chemokines CCL19, CCL21, and CXCL12 ex vivo. However, this binding was abolished upon HS degradation, disrupting the CCL19/CCL21 chemokine gradients and causing impaired migration of dendritic cells in thymic slices. Thus, our results show that HS plays an essential role in the development and growth of the thymus and in regulating interstitial cell migration.

Indexed as

AnimalsCell DifferentiationCell MovementChemokine CCL19Chemokine CCL21Exostosin 1Heparan SulfateHeparan Sulfate ProteoglycansMiceMice, Inbred C57BLN-AcetylglucosaminyltransferasesThymus GlandT-LymphocytesChemokine CCL19Chemokine CCL21Exostosin 1Heparan SulfateHeparan Sulfate ProteoglycansN-Acetylglucosaminyltransferaseschemokinesfibroblastsheparan sulfateT cell developmentthymus

Identifiers

PMID33600795
PMCPMC7974028
OpenAlexW3133270999

What OpenQuestion holds

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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.