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Chondrogenically differentiated mesenchymal stromal cell pellets stimulate endochondral bone regeneration in critical-sized bone defects

机译:软骨分化的间充质基质细胞团刺激临界大小骨缺损中的软骨内骨再生

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Grafting bone defects or atrophic non-unions with mesenchymal stromal cells (MSCs)-based grafts is not yet successful. MSC-based grafts typically use undifferentiated or osteogenically differentiated MSCs and regenerate bone through intramembranous ossification. Endochondral ossification might be more potent but requires chondrogenic differentiation of MSCs. Here, we determined if chondrogenically differentiated MSC (ch-MSC) pellets could induce bone regeneration in an orthotopic environment through endochondral ossification. Undifferentiated MSC pellets (ud-MSC) and ch-MSC pellets were generated from MSCs of human donors cultured on chondrogenic medium for respectively 3 (ud-MSC) and 21 (ch-MSC) days. A 6 mm femoral bone defect was made and stabilised with an internal plate in 27 athymic rats. Defects were left empty for 6 weeks to develop an atrophic non-union before they were grafted with ch-MSC pellets or ud-MSC pellets. Micro-CT scans made 4 and 8 weeks after grafting showed that ch-MSC pellets resulted in significantly more bone than ud-MSC pellets. This regenerated bone could completely bridge the defect, but the amount of bone regeneration was donor-dependent. Histology after 7 and 14 days showed slowly mineralising pellets containing hypertrophic chondrocytes, as well as TRAP-positive and CD34-positive cells around the ch-MSC pellets, indicating osteoclastic resorption and vascularisation typical for endochondral ossification. In conclusion, grafting critical femoral bone defects with chondrogenically differentiated MSC pellets led to rapid and pronounced bone regeneration through endochondral ossification and may therefore be a more successful MSC-based graft to repair large bone defects or atrophic non-unions. But, since bone regeneration was donor-depend, the generation of potent chondrogenically differentiated MSC pellets for each single donor needs to be established first.
机译:用基于间充质基质细胞(MSCs)的移植物移植骨缺损或萎缩性骨不愈合尚未成功。基于MSC的移植物通常使用未分化或成骨分化的MSC,并通过膜内骨化来再生骨骼。软骨内骨化可能更有效,但需要分化成MSC。在这里,我们确定软骨形成分化的MSC(ch-MSC)颗粒是否可以通过软骨内骨化作用在原位环境中诱导骨再生。从在软骨形成培养基上分别培养3天(ud-MSC)和21天(ch-MSC)的人类供体的MSC产生未分化的MSC沉淀(ud-MSC)和ch-MSC沉淀。在27只无胸腺大鼠中制作了一个6毫米的股骨骨缺损并用内板稳定。将缺损留空6周以形成萎缩性不愈合,然后再将其植入ch-MSC沉淀或ud-MSC沉淀。嫁接后第4和第8周进行的Micro-CT扫描显示,与ud-MSC沉淀相比,ch-MSC沉淀产生的骨骼明显更多。再生的骨头可以完全弥补缺损,但骨骼的再生量取决于供体。 7天和14天后的组织学检查显示,缓慢沉淀的小球含有肥大的软骨细胞,以及ch-MSC小球周围的TRAP阳性和CD34阳性细胞,这表明软骨内骨化是典型的破骨细胞吸收和血管形成。总而言之,用软骨分化的MSC颗粒移植股骨严重骨缺损可通过软骨内骨化快速而明显地再生骨骼,因此可能是基于MSC的更成功的修复大骨缺损或萎缩性骨不连的移植物。但是,由于骨骼的再生取决于供体,因此首先需要为每个供体建立有效的软骨分化MSC颗粒。

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