Evidence map›Paper›PMID 42459078›Full record

ArticleCurrent medicinal chemistry2026

Effect of Melatonin and TNF-α on Differentiation of PDL Stem Cells.

Ting Liu, Liuyun Zheng, Dinesh Rokaya, Hao-Ying Li, Yang Cai

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Article in Current medicinal chemistry, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ting LiuDepartment of Stomatology, Guizhou Medical University, Guiyang, 550004, China.
Liuyun ZhengDepartment of Stomatology, School of Medicine, Guangzhou First People's Hospital, South China University of Technology, Guangzhou, China.
Dinesh RokayaClinical Sciences Department, College of Dentistry, Ajman University, Ajman, United Arab Emirates.ORCID 0000-0002-3854-667X
Hao-Ying LiInstitute of Pharmaceutical Science, King's College London, LondonSE1 9NH, United Kingdom.ORCID 0000-0001-6752-5328
Yang CaiDepartment of Stomatology, Guizhou Medical University, Guiyang, 550004, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMelatonin (MEL) has anti-inflammatory, antioxidant, and immune regulatory properties. This study aimed to evaluate MEL as an antioxidant in the osteogenesis process of the human periodontal ligament stem cells (hPDLSCs).

methodsThis is an in vitro experimental laboratory study using human periodontal ligament stem cells (hPDLSCs). were cultured and characterized in vitro. TNF-α was administered at 10 ng/ml. The ALP activity of hPDLSCs and the expressions of two genes, Runx2 and OPN, were also studied. ALP staining and activity assays were conducted on day 7 and day 14 to study the effects of TNF-α and MEL on bone formation.

resultsIt showed that MEL counteracted the ROS generation and the inhibitory osteogenesis of hPDLSCs induced by TNF-α, by upregulating the expression of antioxidases and downregulating the expression of oxidases. TNF-α treatment resulted in a decrease in ALP staining and activity, and MEL was able to result in TNF-α-induced impaired osteogenesis of hPDLSCs. Similarly, MEL inhibited the phosphorylation of p65 protein and blocked the degradation of IκBα protein. DISCUSSION: This study demonstrates that melatonin preserves the osteogenic potential of human periodontal ligament stem cells under TNF-α-induced inflammatory conditions. By reducing ROS, enhancing antioxidant defenses, and suppressing oxidases, melatonin restores ALP activity and increases Runx2 and OPN expression. These effects occur through inhibition of NF-κB signaling, indicating its protective role in inflammatory microenvironments.

conclusionMEL effectively attenuates TNF-α-induced oxidative stress and restores the osteogenic differentiation capacity of human periodontal ligament stem cells in an inflammatory microenvironment. Its antioxidant and anti-inflammatory properties support its potential use in periodontal regeneration therapies.

Indexed as

Cell DifferentiationMelatoninPeriodontal LigamentStem CellsTumor Necrosis Factor-alphaAntioxidantsCells, CulturedCore Binding Factor Alpha 1 SubunitHumansOsteogenesisReactive Oxygen SpeciesAntioxidantsCore Binding Factor Alpha 1 SubunitMelatoninReactive Oxygen SpeciesRUNX2 protein, humanTumor Necrosis Factor-alphaalveolar bone regenerationhuman periodontal ligament stem cellsMelatoninosteogenesisosteogenic differentiationoxidative stressperiodontitisTNF-α

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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 Socratic graph.