Evidence map›Paper›PMID 42624975›Full record

ArticleOdontology2026

Spatiotemporal distribution of α-smooth muscle actin-positive mesenchymal cells during tooth development and mechanical remodeling of the murine periodontal ligament.

Haruhi Maruoka, Tomoka Hasegawa, Hiromi Hongo, Tomomaya Yamamoto, Miki Abe, Mai Kitakamae-Haraguchi, Kazuharu Irie, Toshihide Mizoguchi, Minqi Li, Akihiro Hosoya and 2 more

Abstract read
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Article in Odontology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Haruhi MaruokaUltrastructure of Hard Tissue, Faculty of Dental Medicine, Graduate School of Dental Medicine, Hokkaido University, Kita 13 Nishi 7 Kita-ku, Sapporo, 060-8586, Japan.
Tomoka HasegawaUltrastructure of Hard Tissue, Faculty of Dental Medicine, Graduate School of Dental Medicine, Hokkaido University, Kita 13 Nishi 7 Kita-ku, Sapporo, 060-8586, Japan. hasegawa@den.hokudai.ac.jp.ORCID http://orcid.org/0000-0003-0309-6637
Hiromi HongoUltrastructure of Hard Tissue, Faculty of Dental Medicine, Graduate School of Dental Medicine, Hokkaido University, Kita 13 Nishi 7 Kita-ku, Sapporo, 060-8586, Japan.
Tomomaya YamamotoUltrastructure of Hard Tissue, Faculty of Dental Medicine, Graduate School of Dental Medicine, Hokkaido University, Kita 13 Nishi 7 Kita-ku, Sapporo, 060-8586, Japan.
Miki AbeUltrastructure of Hard Tissue, Faculty of Dental Medicine, Graduate School of Dental Medicine, Hokkaido University, Kita 13 Nishi 7 Kita-ku, Sapporo, 060-8586, Japan.
Mai Kitakamae-HaraguchiUltrastructure of Hard Tissue, Faculty of Dental Medicine, Graduate School of Dental Medicine, Hokkaido University, Kita 13 Nishi 7 Kita-ku, Sapporo, 060-8586, Japan.
Kazuharu IrieDivision of Anatomy, Department of Oral Growth and Development, School of Dentistry, Health Sciences University of Hokkaido, Tobetsu-cho, Japan.
Toshihide MizoguchiOral Health Science Center, Tokyo Dental College, Tokyo, Japan.
Minqi LiDepartment of Bone Metabolism, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Research Center of Dental Materials and Oral Tissue Regeneration & Shandong Provincial Clinical Research Center for Oral Diseases, Shandong University, Jinan, China.
Akihiro HosoyaCraniofacial Development and Tissue Biology, Graduate School of Dentistry, Tohoku University, Sendai, Japan.
Yoshiaki SatoOrthodontics, Faculty of Dental Medicine, Hokkaido University, Sapporo, Japan.
Norio AmizukaUltrastructure of Hard Tissue, Faculty of Dental Medicine, Graduate School of Dental Medicine, Hokkaido University, Kita 13 Nishi 7 Kita-ku, Sapporo, 060-8586, Japan. amizuka@den.hokudai.ac.jp.

Funding

Japan Society for the Promotion of Science 24K19837Japan Society for the Promotion of Science 25K22678
6 · The paper itself

Abstract

The periodontal ligament (PDL) contains heterogeneous mesenchymal stem/progenitor cells that contribute to periodontal homeostasis and regeneration. However, the developmental origin and behavior of α-smooth muscle actin (αSMA)-positive cells remain poorly understood. This study investigated the spatiotemporal distribution of αSMA-positive cells during tooth development and their response to altered mechanical loading following extraction of the opposing mandibular molars in mice. Before tooth eruption, αSMA-positive cells were widely distributed throughout the dental follicles but became progressively restricted to the apical PDL during root formation and eruption. In contrast, c-kit immunoreactivity gradually disappeared from the apical PDL, whereas Gli1/tdTomato-positive cells partially co-localized with αSMA-positive cells. Following extraction of the opposing molars, the αSMA-positive area and the number of PCNA-positive cells transiently increased, while endomucin-positive blood vessels became dilated in the apical PDL. These findings demonstrate that αSMA-positive cells undergo dynamic developmental redistribution and rapidly respond to altered mechanical loading. Furthermore, the partial co-localization of αSMA and Gli1 suggests that at least a subset of αSMA-positive cells may represent a resident mechanosensitive mesenchymal progenitor population involved in periodontal homeostasis and remodeling, providing new insight into the biological basis of periodontal remodeling during orthodontic tooth movement and periodontal regeneration.

Indexed as

c-kitGli1Mechanical loadingPeriodontal ligamentαSMA

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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.