Evidence map›Paper›PMID 42641051›Full record

ArticleStem cells translational medicine2026

Serum-induced recovery of proliferative capacity and differentiation potential in aged dental pulp stem cells.

Cho-Yeon Park, Joung-Ho Moon, Sang-Man Lee, Eun-Hye Lee, Joo-Young Park, Sun-Young Kim

Abstract read
In one paragraph

Article in Stem cells translational medicine, 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

6 authors.

Cho-Yeon ParkDepartment of Conservative Dentistry and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, 03080, South Korea.ORCID 0000-0002-6078-7306
Joung-Ho MoonDepartment of Conservative Dentistry and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, 03080, South Korea.
Sang-Man LeeDepartment of Conservative Dentistry and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, 03080, South Korea.
Eun-Hye LeeDepartment of Conservative Dentistry and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, 03080, South Korea.
Joo-Young ParkDepartment of Oral and Maxillofacial Surgery and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, 03080, South Korea.
Sun-Young KimDepartment of Conservative Dentistry and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, 03080, South Korea.

Funding

Biobank of Seoul National University Dental Hospital 2024ER050701Biotechnology R&D Program of the Ministry of Trade, Industry & Energy RS-2025-02309487National Research Foundation of Korea 2022M3A9F3082330National Research Foundation of Korea RS-2024-00334696
6 · The paper itself

Abstract

backgroundAging impairs the proliferative, survival, and differentiation capacities of dental pulp stem cells (DPSCs), thereby limiting their regenerative potential. This study systematically investigated whether high-serum preconditioning could promote serum-induced recovery of age-associated functional decline in rat and human DPSCs.

methodsYoung, older, and high-serum-conditioned DPSCs were compared using in vitro assays assessing proliferation, survival, colony-forming efficiency, and multilineage differentiation, together with in vivo functional regeneration models and transcriptomic profiling of human DPSCs.

resultsHigh-serum preconditioning significantly enhanced proliferation and colony-forming efficiency in older DPSCs and restored osteogenesis and neurogenesis through serum-induced recovery, approaching the levels of young cells. In vivo, transplantation of high-serum-conditioned DPSCs resulted in organized axonal regeneration accompanied by compact myelin formation, as well as improved bone regeneration in calvarial defect models, demonstrating functional recovery beyond in vitro outcomes. Human DPSCs cultured under high-serum conditions similarly exhibited increased proliferation, viability, and lineage-specific differentiation capacity while maintaining stable expression of mesenchymal stem cell markers. Transcriptomic analysis revealed extensive remodeling under high-serum conditions, including activation of stemness- and cell cycle-related gene programs and suppression of senescence-associated transcripts. However, global gene expression patterns indicated only partial convergence toward a youthful transcriptional state rather than complete rejuvenation.

conclusionsHigh-serum preconditioning promotes serum-induced recovery and partially restores the regenerative competence of older DPSCs through reconfiguration of functional and molecular programs without full reversion to a youthful state. This study provides preliminary insight into serum-induced recovery and a framework for identifying serum-derived factors for future stem cell-based regenerative applications.

Indexed as

Cell DifferentiationDental PulpSerumStem CellsAgingAnimalsCell ProliferationCells, CulturedCellular SenescenceHumansMaleOsteogenesisRatsagingdental pulp stem cellsneurogenesisosteogenesisserum recovery

Identifiers

PMID42641051
PMCPMC13505630

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.