Functionally Distinct Shed Subpopulations Detected After Magnetic-Activated Cell Sorting of CD71 and CD146

Mesenchymal stem cells derived from human exfoliated deciduous teeth (SHED) are a promising source for regenerative therapies due to their multipotency, proliferative capacity, and immunomodulatory properties. The present study aimed to isolate and characterize SHED subpopulations based on CD71 and CD146 expression and evaluate their multilineage differentiation potential. SHED were obtained from pediatric donors and separated into CD71<sup>+</sup>, CD71<sup>-</sup>, CD146<sup>+</sup>, and CD146<sup>-</sup> fractions using magnetic-activated cell sorting (MACS). CD71<sup>+</sup>/CD71<sup>-</sup> and CD146<sup>+</sup>/CD146<sup>-</sup> populations were isolated independently; no simultaneous double sorting for both markers was performed. Immunocytochemistry was employed to confirm the expression of surface and intracellular markers, including STRO-1, CD44, nestin, and vimentin. Multilineage differentiation assays toward osteogenic, adipogenic, and chondrogenic lineages revealed that CD71<sup>+</sup> cells exhibited reduced osteogenic capacity compared to CD71<sup>-</sup> cells, whereas CD146<sup>+</sup> cells showed enhanced osteogenic and adipogenic differentiation. Chondrogenic differentiation seemed unaffected by marker expression under the 2D conditions employed. These results highlight functional heterogeneity within SHED populations and indicate that CD71 and CD146 independently influence differentiation outcomes. The selective enrichment of CD146<sup>+</sup> SHED may enhance osteogenic and adipogenic regenerative applications, while CD71<sup>+</sup> subsets may serve as a valuable model for studying proliferation and paracrine effects. Limitations include the use of in vitro differentiation assays and the absence of in vivo validation; additionally, combined CD71/CD146 analysis may further clarify the relationship between metabolic activity and stem/progenitor niche characteristics. Overall, marker-based characterization of SHED subpopulations provides insight into their biological properties and potential utility in targeted cell-based therapeutic strategies.

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Journal
Cells
Published
2025-12-17
DOI
https://doi.org/10.3390/cells14242010
Primary Topic
Mesenchymal stem cell research
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article
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article

Functionally Distinct Shed Subpopulations Detected After Magnetic-Activated Cell Sorting of CD71 and CD146

Zornitsa Mihaylova, Vanio Mitev, Krasimir Hristov, Evgeniy Aleksiev et al.
Cells
Mesenchymal stem cell research
article

Functionally Distinct Shed Subpopulations Detected After Magnetic-Activated Cell Sorting of CD71 and CD146

Zornitsa Mihaylova, Vanio Mitev, Krasimir Hristov, Evgeniy Aleksiev, Emilia Karova, Nikolay Ishkitiev, Violeta Dogandzhiyska, Мirela Мarinova-Takorovа, Marina Miteva, Natalia Grancharova
article en

Abstract

Mesenchymal stem cells derived from human exfoliated deciduous teeth (SHED) are a promising source for regenerative therapies due to their multipotency, proliferative capacity, and immunomodulatory properties. The present study aimed to isolate and characterize SHED subpopulations based on CD71 and CD146 expression and evaluate their multilineage differentiation potential. SHED were obtained from pediatric donors and separated into CD71<sup>+</sup>, CD71<sup>-</sup>, CD146<sup>+</sup>, and CD146<sup>-</sup> fractions using magnetic-activated cell sorting (MACS). CD71<sup>+</sup>/CD71<sup>-</sup> and CD146<sup>+</sup>/CD146<sup>-</sup> populations were isolated independently; no simultaneous double sorting for both markers was performed. Immunocytochemistry was employed to confirm the expression of surface and intracellular markers, including STRO-1, CD44, nestin, and vimentin. Multilineage differentiation assays toward osteogenic, adipogenic, and chondrogenic lineages revealed that CD71<sup>+</sup> cells exhibited reduced osteogenic capacity compared to CD71<sup>-</sup> cells, whereas CD146<sup>+</sup> cells showed enhanced osteogenic and adipogenic differentiation. Chondrogenic differentiation seemed unaffected by marker expression under the 2D conditions employed. These results highlight functional heterogeneity within SHED populations and indicate that CD71 and CD146 independently influence differentiation outcomes. The selective enrichment of CD146<sup>+</sup> SHED may enhance osteogenic and adipogenic regenerative applications, while CD71<sup>+</sup> subsets may serve as a valuable model for studying proliferation and paracrine effects. Limitations include the use of in vitro differentiation assays and the absence of in vivo validation; additionally, combined CD71/CD146 analysis may further clarify the relationship between metabolic activity and stem/progenitor niche characteristics. Overall, marker-based characterization of SHED subpopulations provides insight into their biological properties and potential utility in targeted cell-based therapeutic strategies.

CellsVol. 14(24)
Medical University of Sofia (BG)
Openalex Percentile: Top 39%
Mesenchymal stem cell research
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