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利用牙囊细胞片结合牙本质基质支架实现牙根再生。

Tooth root regeneration using dental follicle cell sheets in combination with a dentin matrix - based scaffold.

机构信息

State Key Laboratory of Oral Diseases, Sichuan University, Chengdu 610041, PR China.

出版信息

Biomaterials. 2012 Mar;33(8):2449-61. doi: 10.1016/j.biomaterials.2011.11.074. Epub 2011 Dec 20.

Abstract

Stem cell mediated tissue engineering has been acknowledged as a prospective strategy for repairing and replacing damaged and lost tissues. However, the low survival rate of implanted stem cells proves to be a major challenge in the management of transplantation failures. While previous studies have indicated the effectiveness of tissue engineered cell sheets in improving the survival rate of implanted cells, we have recently demonstrated the use of treated dentin matrix (TDM) as a biological scaffold and dental follicle cells (DFCs) as the seeding cells for dentinogenesis and tooth root construction. This study proposes a strategy utilizing TDM with human dental follicle cell sheets (DFCSs) for root regeneration. The biological characteristics and changes of human DFCSs under the effect of TDM were studied with scanning electron microscopy, transmission electron microscopy, immunofluorescence microscopy, immunohistochemistry and quantitative real-time PCR. DFCSs combined with TDM were implanted subcutaneously into the dorsum of mice. Histological examination of the harvested grafts revealed a whirlpool-like alignment of the DFCs in multiple layers that were positive for COLI, integrinβ1, fibronectin and alkaline phosphatase (ALP), suggestive of the formation of a rich extracellular matrix. DFCSs, under the effect of TDM, highly expressed DMP-1 and bone sialoprotein (BSP), indicating their potential for odontogenesis and osteogenesis. Importantly, in vivo, TDM could induce and support DFCSs to develop new dentin-pulp like tissues and cementum-periodontal complexes that were positive for markers such as DSP, nestin and VIII factors, COLI and cementum attachment protein (CAP), implying successful root regeneration. Therefore, DFCSs combined with TDM may prove to be a better strategy for the construction of tooth root, and is a prospective approach that could be utilized for the treatment of root or tooth defect or loss in future.

摘要

干细胞介导的组织工程已被认为是修复和替代受损和丢失组织的有前途的策略。然而,植入的干细胞存活率低被证明是移植失败管理的主要挑战。虽然以前的研究表明组织工程细胞片在提高植入细胞存活率方面的有效性,但我们最近已经证明了使用处理牙本质基质 (TDM) 作为生物支架和牙滤泡细胞 (DFCs) 作为牙本质发生和牙根构建的种子细胞。本研究提出了一种利用 TDM 和人牙滤泡细胞片 (DFCS) 进行牙根再生的策略。通过扫描电子显微镜、透射电子显微镜、免疫荧光显微镜、免疫组织化学和实时定量 PCR 研究了 TDM 作用下的人 DFCS 的生物学特性和变化。将 DFCS 与 TDM 结合后,皮下植入小鼠背部。对收获移植物的组织学检查显示,DFC 呈多层漩涡状排列,COL1、整合素β1、纤连蛋白和碱性磷酸酶 (ALP) 阳性,提示形成丰富的细胞外基质。DFCS 在 TDM 的作用下高度表达 DMP-1 和骨涎蛋白 (BSP),表明其具有成牙和成骨的潜力。重要的是,在体内,TDM 可以诱导和支持 DFCS 形成新的牙髓样组织和牙骨质-牙周复合体,对 DSP、巢蛋白和 VIII 因子、COL1 和牙骨质附着蛋白 (CAP) 等标志物呈阳性,暗示成功的牙根再生。因此,DFCS 与 TDM 结合可能被证明是构建牙根的更好策略,并且是一种有前途的方法,可用于未来治疗牙根或牙齿缺陷或缺失。

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