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SVF cell sheets: A new multicellular material-based strategy for promoting angiogenesis and regeneration in diced cartilage grafts

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Abstract Autologous diced cartilage, while biocompatible and easy to shape, is limited in clinical application due to its high resorption rate and challenges in establishing timely and effective neovascularization post-surgery. In this study, we produced SVF cell sheets from adipose-derived stromal vascular fraction (SVF) via enzymatic digestion, employing a temperature-sensitive culture system. Our in vivo and in vitro experiments validated that SVF cell sheets, when wrapped around granular cartilage, exhibited a notable promotion of cartilage regeneration and mitigated granular cartilage resorption in a rabbit diced cartilage graft model. Our findings demonstrate that SVF cell sheets facilitated effective neovascularization and timely cartilage block formation by secreting VEGF and Ang-1 while also suppressing the expression of pyroptotic proteins like NLRP3, Caspase1, and GSDMD. As a biofilm, derived from a multicellular source, SVF cell sheets hold promise in promoting neovascularization and cartilage regeneration in diced cartilage grafts while also preventing chondrocyte pyroptosis, presenting a potential novel approach for autologous diced cartilage transplantation.
Title: SVF cell sheets: A new multicellular material-based strategy for promoting angiogenesis and regeneration in diced cartilage grafts
Description:
Abstract Autologous diced cartilage, while biocompatible and easy to shape, is limited in clinical application due to its high resorption rate and challenges in establishing timely and effective neovascularization post-surgery.
In this study, we produced SVF cell sheets from adipose-derived stromal vascular fraction (SVF) via enzymatic digestion, employing a temperature-sensitive culture system.
Our in vivo and in vitro experiments validated that SVF cell sheets, when wrapped around granular cartilage, exhibited a notable promotion of cartilage regeneration and mitigated granular cartilage resorption in a rabbit diced cartilage graft model.
Our findings demonstrate that SVF cell sheets facilitated effective neovascularization and timely cartilage block formation by secreting VEGF and Ang-1 while also suppressing the expression of pyroptotic proteins like NLRP3, Caspase1, and GSDMD.
As a biofilm, derived from a multicellular source, SVF cell sheets hold promise in promoting neovascularization and cartilage regeneration in diced cartilage grafts while also preventing chondrocyte pyroptosis, presenting a potential novel approach for autologous diced cartilage transplantation.

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