Spatiotemporal expression dynamics of CD73 , CD90 , and CD105 based on scRNA ‐seq and immunofluorescence analysis of dental pulp toward establishing a triple‐positive population

Abstract Dental pulp stem cells (DPSCs), a subset of mesenchymal stem/progenitor cells, exhibit remarkable self‐renewal and multipotent differentiation capacity, making them promising candidates for regenerative applications. While their in vitro characteristics have been extensively studied, the in vivo dynamics and molecular regulation during development are much less known. This study examined the embryonic/prenatal (E16.5) and early postnatal (P3.5 and P7.5) stages of mouse molar development to trace the temporospatial expression and overlap of five key molecules associated with DPSC: a trio of positive markers (CD73/ Nt5e , CD90/ Thy1 , and CD105/ Eng ) and two negative markers (CD34/ Cd34 and CD45/ Ptprc ). Reanalysis of single‐cell RNA sequencing data revealed a triple‐positive and double‐negative population overlapping in the dental mesenchyme by P7.5. The results were confirmed by multiple immunofluorescence‐based in situ labeling. These findings contribute to the understanding of the spatiotemporal in vivo expression landscape and dynamics of DPSC markers, thus bridging the gap between in vitro characterization and the complex developmental reality of the dental pulp.

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Publication Details

Journal
The Anatomical Record
Published
2026-09-24
DOI
https://doi.org/10.1002/ar.70327
Primary Topic
Mesenchymal stem cell research
Type
article
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article

Spatiotemporal expression dynamics of CD73 , CD90 , and CD105 based on scRNA ‐seq and immunofluorescence analysis of dental pulp toward establishing a triple‐positive population

Shuntaro Yamada, Kateřina Holomková, Eva Matalová, Eva Janečková et al.
The Anatomical Record
Mesenchymal stem cell research
article

Spatiotemporal expression dynamics of CD73 , CD90 , and CD105 based on scRNA ‐seq and immunofluorescence analysis of dental pulp toward establishing a triple‐positive population

Shuntaro Yamada, Kateřina Holomková, Eva Matalová, Eva Janečková, Hervé Lesot, Sona Ayvazyan, Taleen Krikorian, Dino Azadians, Lidiia Bagdasarian, Jesica Hasmik Hovhannisyan, Eva Švandová
article en

Abstract

Abstract Dental pulp stem cells (DPSCs), a subset of mesenchymal stem/progenitor cells, exhibit remarkable self‐renewal and multipotent differentiation capacity, making them promising candidates for regenerative applications. While their in vitro characteristics have been extensively studied, the in vivo dynamics and molecular regulation during development are much less known. This study examined the embryonic/prenatal (E16.5) and early postnatal (P3.5 and P7.5) stages of mouse molar development to trace the temporospatial expression and overlap of five key molecules associated with DPSC: a trio of positive markers (CD73/ Nt5e , CD90/ Thy1 , and CD105/ Eng ) and two negative markers (CD34/ Cd34 and CD45/ Ptprc ). Reanalysis of single‐cell RNA sequencing data revealed a triple‐positive and double‐negative population overlapping in the dental mesenchyme by P7.5. The results were confirmed by multiple immunofluorescence‐based in situ labeling. These findings contribute to the understanding of the spatiotemporal in vivo expression landscape and dynamics of DPSC markers, thus bridging the gap between in vitro characterization and the complex developmental reality of the dental pulp.

The Anatomical Record
University of Veterinary Sciences Brno (CZ), King's College London (GB), Masaryk University (CZ), University of Veterinary Science (MM), Czech Academy of Sciences, Institute of Animal Physiology and Genetics (CZ), University of Bergen (NO), Glendale Community College (US)
Openalex Percentile: Top 12%
Mesenchymal stem cell research
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