Evidence map›Paper›PMID 34142719›Full record

ArticleJournal of periodontal research2021

Pyrophosphate inhibits periodontal ligament stem cell differentiation and mineralization through MAPK signaling pathways.

Yongxi Liang, Zhiai Hu, Qian Li, Xiaohua Liu

Open access · greenAbstract read
In one paragraph

Article in Journal of periodontal research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  6. Gli1Journal of dental research · 2024
    Article
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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 at 1 institution in 1 country.

Yongxi LiangDepartment of Biomedical Sciences, Texas A&M University College of Dentistry, Dallas, TX, USA.
Zhiai HuDepartment of Biomedical Sciences, Texas A&M University College of Dentistry, Dallas, TX, USA.
Qian LiDepartment of Biomedical Sciences, Texas A&M University College of Dentistry, Dallas, TX, USA.
Xiaohua LiuDepartment of Biomedical Sciences, Texas A&M University College of Dentistry, Dallas, TX, USA.ORCID https://orcid.org/0000-0003-0177-0886
Texas A&M University · US

Funding

Regeneration of Tubular Vascularized Pulpodentin ComplexR01DE024979 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI LIU, XIAOHUA · 2016 to 2020
$1.8M
MINE-MS for horizontal bone loss treatmentR01DE029808 · NIDCR · UNIVERSITY OF MISSOURI-COLUMBIA · PI LIU, XIAOHUA · 2021 to 2025
$1.8M
NIDCR NIH HHS DE024979NIDCR NIH HHS DE029808NIDCR NIH HHS R01 DE024979NIDCR NIH HHS R01 DE029808
6 · The paper itself

Abstract

BACKGROUND AND

objectivePeriodontal ligament stem cells (PDLSCs) are the primary cell source for the regeneration and remodeling of periodontal ligament (PDL). It is crucial to prevent PDLSCs from mineralization when using the PDLSCs for PDL regeneration. At present, little is known about how to inhibit PDLSC mineralization. This study investigates the effects of pyrophosphate (PPi) on inhibiting PDLSC osteogenic differentiation and mineralization as well as the underlying mechanism. MATERIALS AND

methodsHuman PDLSCs were cultured in an osteogenic differentiation medium with different PPi concentrations (0, 10, or 100 μM). The effects of PPi on osteogenic differentiation were assessed by ALP activity and the expressions of osteogenic related proteins (OPN, RUNX2, OSX, and DMP1). The mineralization formation was detected by alizarin red staining. The activation of MAPK signaling pathways (ERK1/2, JNK, and p38) was determined by western blotting and pathway blockade assays. The gene expressions of PPi's regulators (Ank, Enpp1, and Alpl) were assessed by real-time PCR.

resultsBoth low and high concentrations (10 μM and 100 μM) of PPi inhibited the mineralization of PDLSCs. The addition of PPi (10 μM or 100 μM) decreased the ALP activity of the PDLSCs to approximately two-thirds of the control group on day 3. PPi reduced the expressions of RUNX2, OSX, and DMP1 on days 7, 14, and 21, while it increased the expression of OPN at the three time points. PPi enhanced the phosphorylation of MAPK pathways, and the application of corresponding MAPK pathway inhibitors reversed the osteogenic inhibition effects of PPi.

conclusionPPi inhibits the osteogenic differentiation and mineralization of PDLSCs in vitro through activating ERK1/2, JNK, and p38 signaling pathways.

Indexed as

OsteogenesisPeriodontal LigamentCell DifferentiationCell ProliferationCells, CulturedDiphosphatesHumansMAP Kinase Signaling SystemDiphosphatesinhibitormineralizationosteogenic differentiationperiodontal ligament stem cellspyrophosphate

Identifiers

PMID34142719
PMCPMC10018283
OpenAlexW3168297087

What OpenQuestion holds

Textmetadata
LicenceTDM
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.