Evidence map›Paper›PMID 42842136›Full record

ArticlePhotochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology2026

Light stimuli attenuates inflammatory activation in primary bone marrow-derived macrophages.

Brenda Gabriele da Silva, Bruna Araújo Milan, Laís Kawamata de Jesus, Robson Diego Calixto, Natália Pieretti Bueno, Márcia Martins Marques, Emanuela Prado Ferraz

Abstract read
PubMed Publisher
In one paragraph

Article in Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

7 authors.

Brenda Gabriele da SilvaBone Research Lab, Ribeirao Preto School of Dentistry, University of Sao Paulo, Café Avenue, Ribeirao Preto, SP, 14040-090, Brazil.
Bruna Araújo MilanBone Research Lab, Ribeirao Preto School of Dentistry, University of Sao Paulo, Café Avenue, Ribeirao Preto, SP, 14040-090, Brazil.
Laís Kawamata de JesusBone Research Lab, Ribeirao Preto School of Dentistry, University of Sao Paulo, Café Avenue, Ribeirao Preto, SP, 14040-090, Brazil.
Robson Diego CalixtoBone Research Lab, Ribeirao Preto School of Dentistry, University of Sao Paulo, Café Avenue, Ribeirao Preto, SP, 14040-090, Brazil.
Natália Pieretti BuenoSchool of Dentistry, University of Sao Paulo, Lineu Prestes Avenue, Sao Paulo, SP, 05508-000, Brazil.
Márcia Martins MarquesSchool of Dentistry, University of Sao Paulo, Lineu Prestes Avenue, Sao Paulo, SP, 05508-000, Brazil.
Emanuela Prado FerrazBone Research Lab, Ribeirao Preto School of Dentistry, University of Sao Paulo, Café Avenue, Ribeirao Preto, SP, 14040-090, Brazil. emanuelaferraz@usp.br.ORCID http://orcid.org/0000-0001-6833-4865

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001
6 · The paper itself

Abstract

Bone repair depends on a regulated macrophage-driven inflammatory response. Non-activated macrophages (M0) differentiate into pro-inflammatory (M1) or anti-inflammatory (M2) phenotypes in response to microenvironmental signals. This study evaluated, in vitro, the effects of photobiomodulation (PBM) on bone marrow-derived macrophage polarisation. Monocytes were isolated, differentiated into macrophages (M0), and induced to acquire M1- or M2-associated characteristics. Cells were irradiated using a PBM protocol for bone regeneration (equivalent dose of 2.1 E). Cells were analysed according to morphology, expression of M1 (iNOS, Tnf-α) or M2 markers (Arg1, Cd206), protein expression (iNOS and ARG1), and nitric oxide (NO) and reactive oxygen species (ROS) production. Data were analysed using 1-way analysis of variance or Student's t-test (p ≤ 0.05). PBM promoted selective and transient modulation of inflammatory and metabolic markers in M0, M1, and M2 macrophages. Compared to non-PBM-treated cells, M1

Indexed as

Bone repairMacrophages plasticityOsteoimmunologyPhotobiomodulation

Identifiers

PMID42842136

What OpenQuestion holds

Textmetadata
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.