scholarly journals BMP-2 mediates PGE2 -induced reduction of proliferation and osteogenic differentiation of human tendon stem cells

2011 ◽  
Vol 30 (1) ◽  
pp. 47-52 ◽  
Author(s):  
Jianying Zhang ◽  
James H-C. Wang
2018 ◽  
Vol 2018 ◽  
pp. 1-8 ◽  
Author(s):  
Sonia Bergante ◽  
Pasquale Creo ◽  
Marco Piccoli ◽  
Andrea Ghiroldi ◽  
Alessandra Menon ◽  
...  

Gangliosides, the sialic acid-conjugated glycosphingolipids present in the lipid rafts, have been recognized as important regulators of cell proliferation, migration, and apoptosis. Due to their peculiar localization in the cell membrane, they modulate the activity of several key cell receptors, and increasing evidence supports their involvement also in stem cell differentiation. In this context, herein we report the role played by the ganglioside GM1 in the osteogenic differentiation of human tendon stem cells (hTSCs). In particular, we found an increase of GM1 levels during osteogenesis that is instrumental for driving the process. In fact, supplementation of the ganglioside in the medium significantly increased the osteogenic differentiation capability of hTSCs. Mechanistically, we found that GM1 supplementation caused a reduction in the phosphorylation of the platelet-derived growth factor receptor-β (PDGFR-β), which is a known inhibitor of osteogenic commitment. These results were further corroborated by the observation that GM1 supplementation was able to revert the inhibitory effects on osteogenesis when the process was inhibited with exogenous PDGF.


PLoS ONE ◽  
2014 ◽  
Vol 9 (2) ◽  
pp. e87706 ◽  
Author(s):  
Jianying Zhang ◽  
James H-C. Wang

Author(s):  
Pietro Randelli ◽  
Alessandra Menon ◽  
Vincenza Ragone ◽  
Pasquale Creo ◽  
Umberto Alfieri Montrasio ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-11 ◽  
Author(s):  
Pietro Randelli ◽  
Alessandra Menon ◽  
Vincenza Ragone ◽  
Pasquale Creo ◽  
Sonia Bergante ◽  
...  

Increasing the success rate of rotator cuff healing remains tremendous challenge. Among many approaches, the possibility of activating resident stem cells in situ, without the need to isolate them from biopsies, could represent valuable therapeutic strategy. Along this line, it has been recently demonstrated that lipoaspirate product, Lipogems, contains and produces growth-factors that may activate resident stem cells. In this study, human tendon stem cells (hTSCs) from the rotator cuff were cocultured in a transwell system with the Lipogems lipoaspirate product and compared to control untreated cells in terms of cell proliferation, morphology, stem cell marker and VEGF expression, and differentiation and migration capabilities. Results showed that the Lipogems product significantly increases the proliferation rate of hTSCs without altering their stemness and differentiation capability. Moreover, treated cells increase the expression of VEGF, which is crucial for the neovascularization of the tissue during the healing process. Overall, this study supports that directly activating hTSCs with the Lipogems lipoaspirate could represent a new practical therapeutic approach. In fact, obtaining a lipoaspirate is easier, safer, and more cost-effective than harvesting cells from tendon or bone marrow biopsies, expanding them in GMP facility and then reinjecting them in the patient.


2021 ◽  
Author(s):  
Xiangzhou Liu ◽  
Ying Jin ◽  
Xiuqi Liu ◽  
Jiachen Peng

Abstract Background: Tendinopathy is currently the common clinical condition related to sports injury. The main pathological change in tendinopathy is ectopic ossification in tendon tissue, but the mechanisms have remained elusive. Studies have found that interleukin-6 (IL-6) is a major inflammatory mediator in chronic tendinopathy, and osteogenic differentiation of tendon stem cells (TSCs) is believed to be closely related to ectopic ossification of tendons. Methods: Rat tendon-derived stem cell (rTDSC) culture model, Lentivirus transfection, Alkaline phosphatase staining, Real-time PCR and Western blotting were performed in this study.Results: We showed that after IL-6 induction, the mRNA expression of Runx2, Alpl, Dlx5, and Wnt5a and the protein expression of phosphorylated STAT3, Runx2, and Wnt5a were increased in rTDSCs. Wnt5a shRNA and cDNA induced silencing and overexpression of Wnt5a inhibited and promoted osteogenic differentiation of rTDSCs, respectively. The addition of a STAT3 inhibitor inhibited osteogenic differentiation and Wnt5a mRNA and protein expression in rTDSCs, and this inhibition was reversed by cDNA induced Wnt5a overexpression. Conclusion: We concluded that IL-6 promotes osteogenic differentiation of rTDSCs through the STAT3/Wnt5a signalling pathway.


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