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Cellular distribution and gene expression profile during flexor tendon graft repair: A novel tissue engineering approach*

机译:屈肌腱移植修复过程中的细胞分布和基因表达谱:一种新颖的组织工程方法*

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To understand scar and adhesion formation during postsurgical period of intrasynovial tendon graft healing, a murine model of flexor digitorum longus tendon graft repair was developed, by utilizing flexor digitorum longus tendon allograft from donor Rosa26/+ mouse, and the healing process at days 3, 7, 14, 21, 28, and 35 post surgery of host wild-type mouse was followed. Using X-gal staining, β-galactosidase positive cells of allograft origin were detectable in tissue sections of grafted tendon post surgery. Graft healing was assessed for the cellular density, scar and adhesion formation, and their interaction with surrounding tissue. From histological analysis, it was evident that the healing of intrasynovial flexor digitorum longus tendon graft takes place in an interactive environment of donor graft, host tendon, and host surrounding tissue. A total of 32 genes, analyzed by RNA analysis, expressed during healing process. Particularly, Alk1, Postn, Tnc, Tppp3, and Mkx will be further investigated for therapeutical value in reducing scars and adhesions.
机译:为了了解滑膜内腱移植修复术后期的瘢痕和粘连形成,通过使用供体Rosa26 / +小鼠的趾长屈肌腱同种异体移植,并建立了第3天的愈合过程,建立了趾长屈肌腱移植修复的小鼠模型,追踪宿主野生型小鼠的术后7、14、21、28和35。使用X-gal染色,可以在移植后的肌腱组织切片中检测到同种异体来源的β-半乳糖苷酶阳性细胞。评估移植修复的细胞密度,疤痕和粘连形成以及它们与周围组织的相互作用。从组织学分析,很明显,滑膜内屈指长肌腱移植物的愈合发生在供体移植物,宿主肌腱和宿主周围组织的相互作用环境中。通过RNA分析分析,共有32个基因在愈合过程中表达。特别是,将进一步研究Alk1,Postn,Tnc,Tppp3和Mkx在减少疤痕和粘连方面的治疗价值。

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