primary bone marrow mesenchymal stem cells bmscs  (ATCC)

Journal: Journal of Materials Science. Materials in Medicine

Article Title: Copper tannic acid coordination nanosheet as a potent in-situ antibiotic sustained-release carrier for chronic osteomyelitis

doi: 10.1007/s10856-025-06979-z

Figure Lengend Snippet: The effect of Van@CuTA on BMSCs and HUVECs. A CCK-8 assay demonstrated no toxicity of Van@CuTA toward BMSCs. B Representative images of alizarin red staining, revealing increased calcium deposition in BMSCs treated with Van@CuTA. C , D Representative images and statistical analysis of HUVECs migration assay demonstrating a significant increase in migrated cells following Van@CuTA treatment. E – G Tube formation assay images and corresponding quantifications of total tube length and node number per view indicated that Van@CuTA significantly promoted HUVECs’ tube formation. (* indicated p < 0.05)

Article Snippet: Primary bone marrow mesenchymal stem cells (BMSCs) and Human Umbilical Vein Endothelial Cells (HUVECs) were obtained from ATCC.

Techniques: CCK-8 Assay, Staining, Migration, Tube Formation Assay

Journal: Journal of Functional Biomaterials

Article Title: Cu-MOF-Decorated 3D-Printed Scaffolds for Infection Control and Bone Regeneration

doi: 10.3390/jfb16030083

Figure Lengend Snippet: Images of BMSCs extracted from rat bone marrow ( A ). Cytoskeleton staining of BMSCs grown on different scaffolds for 3 d ( B ). Live/dead staining of BMSCs grown on different scaffolds for 3 d ( C ). The proliferation of BMSCs on different composite scaffolds for 1, 4, and 7 d ( D ). * p < 0.05, ** p < 0.01.

Article Snippet: Primary bone marrow mesenchymal stem cells (BMSCs) were obtained from one-week-old Sprague-Dawley rats.

Techniques: Staining

Journal: Bioactive Materials

Article Title: Silver-quercetin-loaded honeycomb-like Ti-based interface combats infection-triggered excessive inflammation via specific bactericidal and macrophage reprogramming

doi: 10.1016/j.bioactmat.2024.09.012

Figure Lengend Snippet: Physicochemical characterization and biocompatibility assessment of the SQPdFT surfaces. (a) SEM images showing the surface morphology of Ti, 3DFT, PdFT, SPdFT, and SQPdFT. Scale bar: 500 nm and 100 nm, respectively. (b) EDS elemental mapping (Ag, O, C, and N) images of the SQPdFT surfaces. Scale bar: 1 μm. (c) Contact angles of the various surfaces. (d) XRD patterns of 3DFT, PdFT, SPdFT, and SQPdFT. (e) Raman shifts for 3DFT, PdFT, SPdFT, and SQPdFT. (f) FTIR spectra of PDA, Que, and SQPdFT. (g) Cell viability of RAW264.7 cells cultured on different Ti plates for 24, 48, and 72 h. Data represents the means ± S.D. (n = 5 per group). n.s. indicates no significance. (h) CLSM images of BMSCs adhered onto the different Ti sheet's surfaces. Scale bar: 200 μm, respectively.

Article Snippet: Primary bone marrow-derived mesenchymal stem cells (BMSCs) were isolated from the femur and tibial shafts of 4-week-old Sprague-Dawley rats using established cell isolation techniques.

Techniques: Cell Culture

Journal: Bioactive Materials

Article Title: Silver-quercetin-loaded honeycomb-like Ti-based interface combats infection-triggered excessive inflammation via specific bactericidal and macrophage reprogramming

doi: 10.1016/j.bioactmat.2024.09.012

Figure Lengend Snippet: Experimental validation of the PPARγ/NF-κB signaling pathway activated by Que and bone homeostasis indirectly regulated by SQPdFT in vitro. (a–e) Western blot analysis of macrophage polarization-related proteins. RAW264.7 cells were pretreated with LPS, Que, and various concentrations of Mifobate for 48 h. Data represent mean ± S.D. (n = 3 per group). ∗ indicates a statistical difference compared to the 0 μM group ( P < 0.05). (f) Images of immunofluorescence staining of iNOS and CD206 in different groups. Scale bar: 100 μm. (g) Diagram of the molecular mechanisms by which Que regulates macrophage polarization via the PPARγ/NF-κB pathway. (h) Schematic of the experimental protocol by which SQPdFT regulates osteoclast differentiation of BMMs in vitro. (i) TRAP staining of BMMs cultured in different induction media. Scale bar: 100 μm. (j) Schematic of the experimental protocol by which SQPdFT regulates osteogenic differentiation of BMSCs in vitro. (k) ALP staining and Alizarin red staining were performed to test the effect of different CM on the osteogenic differentiation of BMSC. Scale bar: 100 μm. (l, m) ALP activity and ARS absorbance detection of BMSCs in the groups of the control, Ti, 3DFT, PdFT, SPdFT, and SQPdFT groups. Data represent mean ± S.D. (n = 3 per group). n.s. indicates no significant, ∗ indicates a statistical difference compared to the control group ( P < 0.05). # indicates a statistical difference compared to the Ti group ( P < 0.05).

Article Snippet: Primary bone marrow-derived mesenchymal stem cells (BMSCs) were isolated from the femur and tibial shafts of 4-week-old Sprague-Dawley rats using established cell isolation techniques.

Techniques: Biomarker Discovery, In Vitro, Western Blot, Immunofluorescence, Staining, Cell Culture, Activity Assay, Control