Evidence map›Paper›PMID 42866223›Full record

ArticleRegenerative therapy2026

Matrigel-embedded 3D culture maintains stemness and enhances hair-inductive capacity of human hair follicle epithelial stem cells.

Thuy Thi-Thanh Dao, Nhu Thi-Linh Trinh, Thi Xuan-Khanh Tran, Kim Hoang-Thien Dao, Loan Thi-Tung Dang

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Article in Regenerative therapy, 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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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Thuy Thi-Thanh DaoUniversity of Science, Ho Chi Minh City, Viet Nam.
Nhu Thi-Linh TrinhUniversity of Science, Ho Chi Minh City, Viet Nam.
Thi Xuan-Khanh TranUniversity of Science, Ho Chi Minh City, Viet Nam.
Kim Hoang-Thien DaoPham Ngoc Thach University of Medicine, Ho Chi Minh City, Viet Nam.
Loan Thi-Tung DangUniversity of Science, Ho Chi Minh City, Viet Nam.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Human hair follicle epithelial stem cells (hHF-EpSCs) represent a promising cell source for biomedical research. However, conventional 2D culture systems show limited efficacy in maintaining their stemness and proliferative capacity. Methods: In this study, we compared two 3D culture strategies: Embedding EpSCs in Matrigel (embedded culture) and seeding them on top of Matrigel (on-top culture). The formation, quantity, and size of the spheres were observed by microcscope. The cell viability and proliferation were assessed by staining Calcein AM/Propidium iodide (AM/PI) and Water-Soluble Tetrazolium 1 (Wst1) assay. The expression of EpSC specified markers such as CD200, CK19, CK15, CK10, CK5 were found via immunocytochemistry. The genes related to hair-induction, including Results: The embedded approach facilitated the formation of numerous cell aggregates with an average size below 200 μm, peaking in number on day 10 (88.33 ± 4.16 spheroids per microscopic field). In contrast, the on-top culture produced fewer aggregates (maximum 17.00 ± 1.00 per microscopic field on day 3), with larger average sizes (>200 μm). Cells cultured within Matrigel also exhibited higher viability and proliferation over 14 days. Both methods preserved the expression of key HF-EpSC markers, including CD200, CK19, CK15, CK10, and CK5. The upregulation of genes such as Conclusion: These findings suggest that 3D Matrigel-embedded culture is a promising approach for maintaining EpSCs, and promoting hair induction.

Indexed as

Cell culture techniquesCellularExtracellular matrixHair follicleSpheroidsStem cells

Identifiers

PMID42866223
PMCPMC13657106

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