Evidence map›Paper›PMID 40379839›Full record

ArticleCommunications biology2025

Secretory leucocyte protease inhibitor regulates bone metabolism and inflammation in experimental mouse periodontitis.

Karin Sasagawa, Hisanori Domon, Satoru Hirayama, Tomoki Maekawa, Toshihito Isono, Koichi Tabeta, Yutaka Terao

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Karin SasagawaDivision of Microbiology and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.ORCID http://orcid.org/0009-0006-0016-3848
Hisanori DomonDivision of Microbiology and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Satoru HirayamaDivision of Microbiology and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Tomoki MaekawaDivision of Microbiology and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.ORCID http://orcid.org/0000-0002-4597-1316
Toshihito IsonoDivision of Microbiology and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Koichi TabetaDivision of Periodontology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Yutaka TeraoDivision of Microbiology and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan. terao@dent.niigata-u.ac.jp.ORCID http://orcid.org/0000-0002-4450-5583

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 20H03858[Terao]MEXT | Japan Society for the Promotion of Science (JSPS) 20K09903MEXT | Japan Society for the Promotion of Science (JSPS) 22H03267MEXT | Japan Society for the Promotion of Science (JSPS) 22K09923MEXT | Japan Society for the Promotion of Science (JSPS) 22K19614[Terao]MEXT | Japan Society for the Promotion of Science (JSPS) 22KJ1445MEXT | Japan Society for the Promotion of Science (JSPS) 23H00445[Terao]
6 · The paper itself

Abstract

Periodontitis is characterized by the activity of neutrophil elastase, a host defense factor that leads to the destruction of the epithelial barrier and bacterial invasion of the periodontal tissue. Secretory leukocyte protease inhibitors (SLPI), predominantly secreted by epithelial cells, diffuse into the mucosal surface and inhibit excessive tissue loss caused by elastase during inflammation. The SLPI level is high in healthy gingiva and low in severe periodontitis. In this study, we hypothesized that intragingival administration of SLPI inhibits periodontal tissue destruction caused by periodontitis. Administration of SLPI significantly reduced neutrophil elastase activity in periodontal tissue and alleviated alveolar bone loss in mice. Real-time PCR analysis revealed that SLPI administration downregulated the transcription of pro-inflammatory cytokines and osteoclast-related factors in the gingival tissue. Furthermore, in vitro treatment of bone marrow macrophages with SLPI resulted in the downregulation of osteoclast differentiation. SLPI treatment of MC3T3-E1 cells promoted osteoblast differentiation and bone formation. These findings suggest that SLPI protects against periodontal tissue damage by suppressing inflammation and bone resorption and promoting bone regeneration.

Indexed as

Bone and BonesPeriodontitisSecretory Leukocyte Peptidase InhibitorAlveolar Bone LossAnimalsCell DifferentiationDisease Models, AnimalInflammationLeukocyte ElastaseMaleMiceMice, Inbred C57BLOsteoclastsOsteogenesisLeukocyte ElastaseSecretory Leukocyte Peptidase InhibitorSlpi protein, mouse

Identifiers

PMID40379839
PMCPMC12084318

What OpenQuestion holds

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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.