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Journal: Journal of materials chemistry. B
Article Title: In vitro biological evaluation of epigallocatechin gallate (EGCG) release from three-dimensional printed (3DP) calcium phosphate bone scaffolds
doi: 10.1039/d2tb02210a
Figure Lengend Snippet: Effects of EGCG-loaded HA on coculture of hMSC-derived osteoblasts and monocyte derived osteoclasts were evaluated by SEM microscopy and relative gene expression.35 (A) SEM micrographs showed healthy osteoblast morphology in all samples at all time points. The control showed healthy maturation from differentiated monocytes (white circle) pre-osteoclast cells. The osteoclast cells bonded to form multi-nucleated mature osteoclasts at days 7 and 16. EGCG showed good adhesion and attachment of osteoclast cells, but inhibited maturation compared to the control at that time. (B)–(E) qRT-PCR results were presented as fold change compared to the control, which is standardized to a value of 1. GAPDH was used to normalize all gene expression data. Day 7 was the early time point to observe the effects of EGCG on coculture. The higher expression of (B) bone gamma-carboxyglutamic acid-containing protein (BGLAP) and (C) Runt-related transcription factor 2 (Runx2) in treatment than control implied that EGCG stimulated osteoblast differentiation and maturation on day 16. However, EGCG inhibited osteoclast differentiation and activity by upregulating (D) osteoprotegerin (OPG), a negative regulator of osteoclastogenesis, and downregulating (E) RANKL expression on day 16. (* denotes p value ≤ 0.05, ** denotes p value ≤ 0.001).
Article Snippet: Human mesenchymal stem cell (hMSC) osteogenic differentiation media was prepared using
Techniques: Derivative Assay, Microscopy, Gene Expression, Control, Quantitative RT-PCR, Expressing, Activity Assay
Journal: Stem Cells Translational Medicine
Article Title: Production of Mesenchymal Progenitor Cell-Derived Extracellular Vesicles in Suspension Bioreactors for Use in Articular Cartilage Repair
doi: 10.1093/stcltm/szab008
Figure Lengend Snippet: Alcian blue, type I/II/X collagen, and DAPI staining for chondrogenic pellets. 250000 MPCs were pelleted in each condition on day 0. The control condition contained chondrogenic basal medium without growth factor supplementation (negative control). The control + TGF-β3 condition contained control medium with the addition of 10ng/mL TGF-β3 (positive control). Static (Stat) and SSB (Dyn) conditions contained negative control medium with the addition of EVs from static and SSB (80rpm) culture conditions. Pellets were fixed after 30 days of culture, sectioned, and stained accordingly. Pellet quality scoring was identified by quantifying the MFI of each channel ( n = 6). Scale bars = 25 µM. Abbreviations: DAPI, 4ʹ,6-diamidino-2-phenylindole; EVs, extracellular vesicles; MFI, mean fluorescent intensity; MPCs, mesenchymal progenitor cells; SSB, stirred suspension bioreactor; TGF, transforming growth factor.
Article Snippet:
Techniques: Staining, Control, Negative Control, Positive Control, Suspension