Related Experiment Video
Updated: Mar 31, 2026

Author Spotlight: Advancing Tissue Regeneration and Disease Modeling with Dental Pulp Stem Cells
Published on: May 5, 2023
Purified Human Dental Pulp Stem Cells Promote Osteogenic Regeneration
T Yasui1, Y Mabuchi2, H Toriumi3
1Department of Physiology, Keio University School of Medicine, Tokyo, Japan Department of Dentistry and Oral Surgery, Keio University School of Medicine, Tokyo, Japan Department of Dentistry and Oral Surgery, Kawasaki Municipal Kawasaki Hospital, Kanagawa, Japan.
Researchers identified specific cell surface markers, LNGFR (CD271) and THY-1 (CD90), to isolate potent human dental pulp stem cells (hDPSCs). These prospectively isolated cells show promise for bone regeneration therapies.
Area of Science:
- Stem Cell Biology
- Regenerative Medicine
- Tissue Engineering
Background:
- Human dental pulp stem/progenitor cells (hDPSCs) are valuable for regenerative therapy due to their expansion potential.
- Plastic adherence isolation methods alter hDPSCs' surface markers and properties, obscuring original phenotypes.
- Identifying specific markers is crucial for understanding hDPSCs' in vivo functions and therapeutic applications.
Purpose of the Study:
- To identify specific cell-surface markers for prospectively isolating progenitor cells from human dental pulp.
- To characterize the biological properties and regenerative potential of these isolated cells.
- To evaluate the therapeutic efficacy of these cells in bone defect repair models.
Main Methods:
- Utilized cell surface marker expression profiles, specifically LNGFR (CD271) and THY-1 (CD90), for cell isolation.
- Assessed in vitro characteristics including clonogenicity, proliferation, and multilineage differentiation potential.
- Evaluated in vivo bone formation capacity in critical-size calvarial defects.
Main Results:
- Identified a dental pulp-specific cell population expressing low LNGFR and high THY-1 (LNGFR(Low+)THY-1(High+)).
- Prospectively isolated LNGFR(Low+)THY-1(High+) cells demonstrated high clonogenicity, long-term proliferation, and multilineage differentiation.
- These cells expressed mesenchymal markers and successfully promoted new bone formation in vivo, healing critical-size calvarial defects.
Conclusions:
- LNGFR(Low+)THY-1(High+) cells represent a highly enriched population of clonogenic progenitors within human dental pulp.
- These cells possess significant regenerative potential for bone formation.
- LNGFR(Low+)THY-1(High+) dental pulp-derived cells are a promising source for bone regenerative strategies.
More Related Videos
14:52Isolation, Characterization and Comparative Differentiation of Human Dental Pulp Stem Cells Derived from Permanent Teeth by Using Two Different Methods
Published on: November 24, 2012
02:33Isolation, Culture, and Characterization of Dental Pulp Stem Cells from Human Deciduous and Permanent Teeth
Published on: May 17, 2024