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Human dental pulp stem cells derived extracellular matrix promotes mineralization via Hippo and Wnt pathways.

Scientific reports (2024-03-22)
Chatvadee Kornsuthisopon, Nunthawan Nowwarote, Ajjima Chansaenroj, Suphalak Photichailert, Sunisa Rochanavibhata, Nuttha Klincumhom, Stephane Petit, Florent Dingli, Damarys Loew, Benjamin P J Fournier, Thanaphum Osathanon
RESUMEN

Extracellular matrix (ECM) is an intricate structure providing the microenvironment niche that influences stem cell differentiation. This study aimed to investigate the efficacy of decellularized ECM derived from human dental pulp stem cells (dECM_DPSCs) and gingival-derived mesenchymal stem cells (dECM_GSCs) as an inductive scaffold for osteogenic differentiation of GSCs. The proteomic analysis demonstrated that common and signature matrisome proteins from dECM_DPSCs and dECM_GSCs were related to osteogenesis/osteogenic differentiation. RNA sequencing data from GSCs reseeded on dECM_DPSCs revealed that dECM_DPSCs upregulated genes related to the Hippo and Wnt signaling pathways in GSCs. In the inhibitor experiments, results revealed that dECM_DPSCs superiorly promoted GSCs osteogenic differentiation, mainly mediated through Hippo and Wnt signaling. The present study emphasizes the promising translational application of dECM_DPSCs as a bio-scaffold rich in favorable regenerative microenvironment for tissue engineering.

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Millipore
JAK Inhibitor I, JAK Inhibitor I, CAS 457081-03-7, is a potent, reversible, cell-permeable, and ATP-competitive inhibitor of JAK 1 (IC₅₀ = 15 nM), JAK2 (IC₅₀ = 1 nM), JAK3 (Ki = 5 nM) and Tyk2 (IC₅₀ = 1 nM).
Sigma-Aldrich
2-Methylhippuric acid, 98%
Sigma-Aldrich
AS 604850, ≥98% (HPLC), solid