Gingiva-Derived Decellularised Extracellular Matrix Hydrogel Supports Osteogenic and Angiogenic Phenotypes of 3D STRO-1+ GMSC/HUVEC Spheroids In Vitro

INTRODUCTION AND AIMS: Stem cell-based bone tissue engineering is often limited by insufficient osteogenic differentiation and inadequate vascularisation, largely attributable to the absence of a biomimetic stem cell niche. This study aimed to develop a human gingiva-derived decellularised extracellular matrix hydrogel (G-dECM) as a supportive microenvironment for three-dimensional (3D) coculture spheroids of STRO-1⁺ gingival mesenchymal stem cells (sGMSC) and human umbilical vein endothelial cells (HUVEC), thereby promoting the expression of osteogenic and angiogenic markers. METHODS: Human gingival tissue was processed through decellularisation, enzymatic digestion, and sol-gel transformation to prepare G-dECM hydrogel. Composite 3D sGMSC/HUVEC spheroids (GHS) were generated and encapsulated within G-dECM. Morphological assessment, viability evaluation, and osteogenic differentiation analyses were conducted. Transcriptomic profiling was performed to identify G-dECM-associated regulatory signalling pathways. RESULTS: G-dECM exhibited a porous, collagen-rich structure enriched with bioactive ECM proteins. Encapsulation of GHS within G-dECM enhanced cellular viability, promoted the expression of osteogenic and angiogenic markers, and improved spheroid structural integrity compared with matrix-free controls. Transcriptomic analysis revealed activation of TGF-β/SMAD and BMP signalling pathways associated with osteogenic differentiation. CONCLUSION: G-dECM provides a biomimetic stem cell niche that supports the osteogenic and angiogenic phenotypes of 3D sGMSC/HUVEC spheroids, establishing an integrated regenerative graft system combining seed cells, scaffold, and endogenous signalling cues. CLINICAL RELEVANCE: This G-dECM-based composite graft strategy offers a promising translational approach for the regeneration of alveolar bone defects associated with periodontal disease, trauma, or tooth extraction.

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Journal
International Dental Journal
Published
2026-04-30
DOI
https://doi.org/10.1016/j.identj.2026.109603
Primary Topic
Tissue Engineering and Regenerative Medicine
Type
article
Field-Weighted Citation Impact
0.00

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article

Gingiva-Derived Decellularised Extracellular Matrix Hydrogel Supports Osteogenic and Angiogenic Phenotypes of 3D STRO-1+ GMSC/HUVEC Spheroids In Vitro

Yaqi Zhao, Yusen Lin, Yujian Gan, Shuyi Wen et al.
International Dental Journal
Tissue Engineering and Regenerative Medicine
article

Gingiva-Derived Decellularised Extracellular Matrix Hydrogel Supports Osteogenic and Angiogenic Phenotypes of 3D STRO-1+ GMSC/HUVEC Spheroids In Vitro

Yaqi Zhao, Yusen Lin, Yujian Gan, Shuyi Wen, Xufeng Huang, Xiao Zheng, Wei Qiao, Zhenyu Chen, Ruijie Wang, Mingdeng Rong, Yushan Liu
article en

Abstract

INTRODUCTION AND AIMS: Stem cell-based bone tissue engineering is often limited by insufficient osteogenic differentiation and inadequate vascularisation, largely attributable to the absence of a biomimetic stem cell niche. This study aimed to develop a human gingiva-derived decellularised extracellular matrix hydrogel (G-dECM) as a supportive microenvironment for three-dimensional (3D) coculture spheroids of STRO-1⁺ gingival mesenchymal stem cells (sGMSC) and human umbilical vein endothelial cells (HUVEC), thereby promoting the expression of osteogenic and angiogenic markers. METHODS: Human gingival tissue was processed through decellularisation, enzymatic digestion, and sol-gel transformation to prepare G-dECM hydrogel. Composite 3D sGMSC/HUVEC spheroids (GHS) were generated and encapsulated within G-dECM. Morphological assessment, viability evaluation, and osteogenic differentiation analyses were conducted. Transcriptomic profiling was performed to identify G-dECM-associated regulatory signalling pathways. RESULTS: G-dECM exhibited a porous, collagen-rich structure enriched with bioactive ECM proteins. Encapsulation of GHS within G-dECM enhanced cellular viability, promoted the expression of osteogenic and angiogenic markers, and improved spheroid structural integrity compared with matrix-free controls. Transcriptomic analysis revealed activation of TGF-β/SMAD and BMP signalling pathways associated with osteogenic differentiation. CONCLUSION: G-dECM provides a biomimetic stem cell niche that supports the osteogenic and angiogenic phenotypes of 3D sGMSC/HUVEC spheroids, establishing an integrated regenerative graft system combining seed cells, scaffold, and endogenous signalling cues. CLINICAL RELEVANCE: This G-dECM-based composite graft strategy offers a promising translational approach for the regeneration of alveolar bone defects associated with periodontal disease, trauma, or tooth extraction.

International Dental JournalVol. 76(4)
University of Debrecen (HU), Foshan University (CN), Guangdong Province Stomatological Hospital (CN), Stomatology Hospital (CN), University of Hong Kong - Shenzhen Hospital (CN), Southern Medical University (CN), University of Hong Kong (HK)
Natural Science Foundation of Guangdong Province, Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 17%
Tissue Engineering and Regenerative Medicine
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