Evidence map›Paper›PMID 37298716›Full record

ArticleInternational journal of molecular sciences2023

Effects of Red LED Irradiation in Enhancing the Mineralization of Human Dental Pulp Cells In Vitro.

Ying Yang, Ok-Su Kim, Guo Liu, Bin-Na Lee, Danyang Liu, Wenqi Fu, Siyu Zhu, Jae-Seok Kang, Byunggook Kim, Okjoon Kim

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. 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

10 authors.

Ying YangDental Implant Center, School and Hospital of Stomatology, Wenzhou Medical University, Wenzhou 325027, China.ORCID 0000-0002-8234-6421
Ok-Su KimDepartment of Periodontology, School of Dentistry, Chonnam National University, Gwangju 61186, Republic of Korea.ORCID 0000-0001-8528-9314
Guo LiuDepartment of Endodontics, School and Hospital of Stomatology, Wenzhou Medical University, Wenzhou 325027, China.ORCID 0000-0001-5254-362X
Bin-Na LeeDepartment of Conservative Dentistry, School of Dentistry, Dental Science Research Institute, Chonnam National University, Gwangju 61186, Republic of Korea.ORCID 0000-0001-8017-1835
Danyang LiuDepartment of Oral Pathology, School of Dentistry, Chonnam National University, Gwangju 61186, Republic of Korea.
Wenqi FuDepartment of Oral Pathology, School of Dentistry, Chonnam National University, Gwangju 61186, Republic of Korea.
Siyu ZhuDepartment of Oral Pathology, School of Dentistry, Chonnam National University, Gwangju 61186, Republic of Korea.
Jae-Seok KangDepartment of Oral Pathology, School of Dentistry, Chonnam National University, Gwangju 61186, Republic of Korea.
Byunggook KimDepartment of Oral Medicine, School of Dentistry, Chonnam National University, Gwangju 61186, Republic of Korea.
Okjoon KimDepartment of Oral Pathology, School of Dentistry, Chonnam National University, Gwangju 61186, Republic of Korea.ORCID 0000-0002-6347-1411

Funding

National Research Foundation of Korea 2022R1F1A1068614
6 · The paper itself

Abstract

Dentin regeneration is the preferred method used to preserve dental pulp vitality after pulp exposure due to caries. Red light-emitting diode irradiation (LEDI), which is based on photobiomodulation (PBM), has been used to promote hard-tissue regeneration. However, the underlying mechanism still needs elucidation. This study aimed to explore the mechanism involved in red LEDI affecting dentin regeneration. Alizarin red S (ARS) staining revealed that red LEDI induced mineralization of human dental pulp cells (HDPCs) in vitro. We further distinguished the cell proliferation (0-6 d), differentiation (6-12 d), and mineralization (12-18 d) of HDPCs in vitro and treated cells either with or without red LEDI in each stage. The results showed that red LEDI treatment in the mineralization stage, but not the proliferation or differentiation stages, increased mineralized nodule formation around HDPCs. Western blot also indicated that red LEDI treatment in the mineralization stage, but not the proliferation or differentiation stages, upregulated the expression of dentin matrix marker proteins (dentin sialophosphoprotein, DSPP; dentin matrix protein 1, DMP1; osteopontin, OPN) and an intracellular secretory vesicle marker protein (lysosomal-associated membrane protein 1, LAMP1). Therefore, the red LEDI might enhance the matrix vesicle secretion of HDPCs. On the molecular level, red LEDI enhanced mineralization by activating the mitogen-activated protein kinase (MAPK) signaling pathways (ERK and P38). ERK and P38 inhibition reduced mineralized nodule formation and the expression of relevant marker proteins. In summary, red LEDI enhanced the mineralization of HDPCs by functioning to produce a positive effect in the mineralization stage in vitro.

Indexed as

Dental PulpOdontoblastsAlkaline PhosphataseCell DifferentiationCell ProliferationCells, CulturedExtracellular Matrix ProteinsHumansMAP Kinase Signaling SystemPhosphoproteinsAlkaline PhosphataseExtracellular Matrix ProteinsPhosphoproteinsdentin regenerationERKP38photobiomodulationred LEDI

Identifiers

PMID37298716
PMCPMC10253352

What OpenQuestion holds

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LicenceCC BY
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.