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牙龈间充质干细胞介导的骨组织再生治疗方法。

Gingiva-derived mesenchymal stem cell-mediated therapeutic approach for bone tissue regeneration.

机构信息

Department of Periodontology, School of Stomatology, Shandong University, Jinan, Shandong Province, People's Republic of China.

出版信息

Stem Cells Dev. 2011 Dec;20(12):2093-102. doi: 10.1089/scd.2010.0523. Epub 2011 Apr 27.

Abstract

Up to now, the gingiva-derived mesenchymal stem cells (GMSCs) as a new postnatal stem cells have been isolated and characterized with multipotential differentiation capabilities in vitro. However, the in vivo efficacy of utilizing the GMSCs in bone regeneration remains obscure. First of all, we identified canonical MSCs in human gingival tissue, which possessed homogenous immunophenotype (CD34(-)CD45(-)CD29(+)CD105(+)CD90(+) STRO-1(+)) and had tri-lineage differentiation potential (osteoblasts, adipocytes, and chondrocytes). Next, we examined the efficacy of utilizing these stem cells in bone tissue regeneration; the enhanced green fluorescent protein-labeled GMSCs seeded on type I collagen gel were implanted into the mandibular defects as well as the critical-sized calvarial defects in Sprague Dawley rats. We first demonstrated that GMSCs could repair the mandibular wounds and calvarial defects at 2 months in rats postsurgical reconstruction. Histomorphological analysis and image of fluorescence microscope certified that new bone in the defect areas was derived from the transplanted GMSCs. Immunohistochemical analysis of green fluorescent protein, human collagen I, and osteopontin further confirmed our conclusion. The above results implied that mesenchymal stem cells derived from gingival tissue could be a novel source for stem cell-based therapy in bone reconstruction in clinical applications.

摘要

迄今为止,牙龈来源的间充质干细胞(GMSCs)作为一种新的成体干细胞,已被分离并在体外证实具有多向分化潜能。然而,利用 GMSCs 进行骨再生的体内疗效尚不清楚。首先,我们鉴定了人牙龈组织中的经典 MSC,其具有同质的免疫表型(CD34(-)CD45(-)CD29(+)CD105(+)CD90(+)STRO-1(+)),并具有三系分化潜能(成骨细胞、脂肪细胞和成软骨细胞)。接下来,我们研究了利用这些干细胞进行骨组织再生的效果;将增强型绿色荧光蛋白标记的 GMSCs 种植在 I 型胶原凝胶上,然后植入下颌骨缺损以及 Sprague Dawley 大鼠的临界颅骨缺损中。我们首先证明,在大鼠手术后重建的 2 个月内,GMSCs 可以修复下颌骨伤口和颅骨缺损。组织形态学分析和荧光显微镜图像证实,缺损区域的新骨来源于移植的 GMSCs。绿色荧光蛋白、人胶原蛋白 I 和骨桥蛋白的免疫组织化学分析进一步证实了我们的结论。上述结果表明,牙龈来源的间充质干细胞可能成为临床应用中基于干细胞的骨重建治疗的新来源。

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