Evidence map›Paper›PMID 40277146›Full record

ArticleInternational endodontic journal2025

Dental pulp lymphatic vessel dynamics during tooth development and pulp stimulation in rodents.

Kento Tazawa, Di Chen, Akira Fujimura, Philip D King, Hajime Sasaki

Abstract read
In one paragraph

Article in International endodontic journal, 2025. 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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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

5 authors.

Kento TazawaDepartment of Cariology, Restorative Sciences, and Endodontics, University of Michigan School of Dentistry, Ann Arbor, Michigan, USA.ORCID 0000-0001-9725-6034
Di ChenDepartment of Microbiology & Immunology, University of Michigan Medical School, Ann Arbor, Michigan, USA.ORCID 0000-0001-9509-2814
Akira FujimuraDivision of Dental Education, Department of Oral Medicine, School of Dentistry, Iwate Medical University, Iwate, Japan.
Philip D KingDepartment of Microbiology & Immunology, University of Michigan Medical School, Ann Arbor, Michigan, USA.ORCID 0000-0002-5598-2748
Hajime SasakiDepartment of Cariology, Restorative Sciences, and Endodontics, University of Michigan School of Dentistry, Ann Arbor, Michigan, USA.ORCID 0000-0003-3336-2537

Funding

Ras-MAPK Regulation of Lymphatic Vessel Valve DevelopmentR01HL120888 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PHILIP D KING · 2015 to 2026
$4.6M
Functional role of Serum Amyloid A in periapical inflammationR01DE024796 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SASAKI, HAJIME · 2015 to 2020
$2.1M
The Structure and Function of Dental Lymphatics (R21)R21DE030213 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KING, PHILIP D, SASAKI, HAJIME · 2021 to 2022
$429k
Functional role of serum amyloid A in periapical inflammation (R01 Renew)R56DE024796 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SASAKI, HAJIME · 2022 to 2022
$402k
NHLBI NIH HHS R01 HL120888NHLBI NIH HHS R01HL120888NIDCR NIH HHS R01 DE024796NIDCR NIH HHS R01DE024796NIDCR NIH HHS R21 DE030213NIDCR NIH HHS R21DE030213NIDCR NIH HHS R56 DE024796NIDCR NIH HHS R56DE024796Tokyo Medical and Dental University (TMDU) priority research area grant 3301019207
6 · The paper itself

Abstract

aimThe anatomy and functions of lymphatic vessels (LV) in mammals remain poorly understood compared to the blood vascular system. In particular, whether or not LV exist in the dental pulp is still controversial. This study aims to identify the existence of LV in the mouse dental pulp using a Prox1 (Prospero homeobox 1)-eGFP transgenic mouse model combined with a tissue-clearing technique. METHODOLOGY: Mandible or mandibular first molars of Prox1-eGFP mice were extracted, cleared for whole-mount observation and imaged using confocal microscopy. Dylight 594-lectin was injected intracardially to differentiate Prox1-eGFP+ LV from the blood vascular network. To further determine if pulpal LV act as an interstitial fluid drainage system, we examined ink absorption in surgically exposed dental pulp of mandibular first molars.

resultsAt the early stage of tooth development, abundant Prox1-eGFP+ LV distinct from lectin-labelled blood vessels were present in a dental pulp. However, after the initiation of root development, the expression of Prox1-eGFP in dental pulp decreased. In mature dental pulp, Prox1-eGFP+ LV was scattered with a discontinuous lumen. In response to a non-infectious transient pulp stimulation (TPS), the Prox1-eGFP+ LV increased in number and diameter with continuous lumen reaching the apical foramen. Ink particles applied to exposed dental pulp are distributed throughout the dental pulp via interstitial spaces and vessel-like structures. Histological evaluation revealed that ink particles were mainly present in the cell-free zone. However, due to TPS, ink particles were taken up into Prox1-eGFP+ LV.

conclusionOur findings suggest the presence of LV in the mature dental pulp that contributes to fluid drainage in this tissue together with the extravascular pathway.

Indexed as

Dental PulpLymphatic VesselsOdontogenesisAnimalsGreen Fluorescent ProteinsHomeodomain ProteinsMiceMice, TransgenicMicroscopy, ConfocalProspero-Related Homeobox 1 ProteinGreen Fluorescent ProteinsHomeodomain ProteinsProspero-Related Homeobox 1 Proteindental pulp developmentdental pulp stimulationlymphatic systemprospero‐related homeobox 1 protein (Prox1)three‐dimensional imaging

Identifiers

PMID40277146
PMCPMC12254533

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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.