Evidence map›Paper›PMID 42319490›Full record

ArticleCell and tissue research2026

Effects of gestational protein restriction on autophagy dynamics during odontogenesis.

Bruno Calsa, José Antônio Rocha Gontijo, Milton Santamaria-Jr, Patrícia Aline Boer

Abstract read
In one paragraph

Article in Cell and tissue research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Bruno CalsaFetal Programming and Hydroelectrolyte Metabolism Laboratory, Department of Internal Medicine, Faculty of Medical Sciences, Campinas State University (UNICAMP), Rua Cinco de Junho, 350, Cidade Universitária Zeferino Vaz, Campinas, SP, 13087-051, Brazil. calsabruno@gmail.com.
José Antônio Rocha GontijoFetal Programming and Hydroelectrolyte Metabolism Laboratory, Department of Internal Medicine, Faculty of Medical Sciences, Campinas State University (UNICAMP), Rua Cinco de Junho, 350, Cidade Universitária Zeferino Vaz, Campinas, SP, 13087-051, Brazil.
Milton Santamaria-JrDepartment of Social and Pediatric Dentistry, Institute of Science and Technology, College of Dentistry, São Paulo State University (UNESP), São José Dos Campos, SP, Brazil.
Patrícia Aline BoerFetal Programming and Hydroelectrolyte Metabolism Laboratory, Department of Internal Medicine, Faculty of Medical Sciences, Campinas State University (UNICAMP), Rua Cinco de Junho, 350, Cidade Universitária Zeferino Vaz, Campinas, SP, 13087-051, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico DOHaD-INCT (409165/2024- 7)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 88887.666525/2022-00Fundação de Amparo à Pesquisa do Estado de São Paulo 2013/07607-8Fundação de Amparo à Pesquisa do Estado de São Paulo 2024/06071-1
6 · The paper itself

Abstract

Autophagy is a cellular process essential for maintaining homeostasis and supporting development. Herein, we aimed to evaluate the effects of gestational protein restriction (GPR) on tooth germ autophagy. CAG-RFP-EGFP-LC3 female mice were mated and randomly assigned to normal protein or low-protein groups. Embryos were collected, and autophagy flux in the molar tooth germ was quantified. At the bud stage, GPR induced a decrease in autolysosomes in the condensed mesenchyme, alongside an increase in autophagosomes in the dental epithelium. At the cap stage, an increase in lysosome markers was observed in the dental papilla, while a decrease in autolysosomes was observed in enamel organ. By the bell stage, dental papilla exhibited a decrease in autolysosomes and an increase in lysosome markers. Similarly, inner enamel epithelium showed reduced autolysosomes and elevated lysosome markers. Bud stage was the most significantly affected; we further quantified apoptosis and mitosis, revealing impaired cell proliferation and enhanced apoptosis. Our data suggest that GPR block or delay acidification of autophagic vesicles, potentially impairing the recycling of cellular components critical for tooth germ proliferation and differentiation.

Indexed as

AutophagyOdontogenesisAnimalsApoptosisCell ProliferationFemaleLysosomesMicePregnancyTooth GermAutophagyDOHaDTooth developmentUndernutrition

Identifiers

PMID42319490
PMCPMC13282235

What OpenQuestion holds

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Registered trials

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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.