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从健康和患病组织中分离的口腔间充质干细胞的比较评估

Comparative Assessment of Oral Mesenchymal Stem Cells Isolated from Healthy and Diseased Tissues.

作者信息

Páll Emöke, Florea Adrian, Soriţău Olga, Cenariu Mihai, Petruţiu Adrian S, Roman Alexandra

机构信息

1Department of Reproduction,Obstetrics and Veterinary Gynecology, Faculty of Veterinary Medicine,University of Agricultural Sciences and Veterinary Medicine,3-5 Mănăştur St.,400372 Cluj-Napoca,Romania.

3Department of Cell and Molecular Biology, Faculty of Medicine,"Iuliu Haţieganu" University of Medicine and Pharmacy,6 L. Pasteur St.,400349 Cluj-Napoca,Romania.

出版信息

Microsc Microanal. 2015 Oct;21(5):1249-63. doi: 10.1017/S1431927615014749. Epub 2015 Aug 28.

Abstract

The aim of the present study was to isolate human mesenchymal stem cells (MSCs) from palatal connective and periodontal granulation tissues and to comparatively evaluate their properties. MSCs were isolated using the explant culture method. Adherence to plastic, specific antigen makeup, multipotent differentiation potential, functionality, and ultrastructural characteristics were investigated. The frequency of colony-forming unit fibroblasts for palatal-derived mesenchymal stem cells (pMSCs) was significantly higher than that of granulation tissue-derived mesenchymal stem cells (gtMSCs). A significantly higher population doubling time and lower migration potential were recorded for gtMSCs than for pMSCs. Both cell lines were positive for CD105, CD73, CD90, CD44, and CD49f, and negative for CD34, CD45, and HLA-DR, but the level of expression was different. MSCs from both sources were relatively uniform in their ultrastructure. Generally, both cell lines possessed a large, irregular-shaped euchromatic nucleus, and cytoplasm rich in mitochondria, lysosomes, and endoplasmic reticulum. The periphery of the plasma membrane displayed many small filopodia. MSCs from both cell lines were successfully differentiated into osteogenic, adiopogenic, and chondrogenic lineages. Both healthy and diseased tissues may be considered as valuable sources of MSCs for regenerative medicine owing to the high acceptance and fewer complications during harvesting.

摘要

本研究的目的是从腭部结缔组织和牙周肉芽组织中分离人骨髓间充质干细胞(MSCs),并对其特性进行比较评估。采用组织块培养法分离MSCs。研究了细胞对塑料的贴壁能力、特异性抗原组成、多能分化潜能、功能及超微结构特征。腭部来源的间充质干细胞(pMSCs)的集落形成单位成纤维细胞频率显著高于肉芽组织来源的间充质干细胞(gtMSCs)。与pMSCs相比,gtMSCs的群体倍增时间显著更长,迁移潜能更低。两种细胞系CD105、CD73、CD90、CD44和CD49f均呈阳性,CD34、CD45和HLA-DR均呈阴性,但表达水平有所不同。两种来源的MSCs超微结构相对一致。一般来说,两种细胞系均具有大的、不规则形常染色质核,细胞质富含线粒体、溶酶体和内质网。质膜周边有许多小丝状伪足。两种细胞系的MSCs均成功分化为成骨、成脂和成软骨谱系。由于采集过程中接受度高且并发症少,健康组织和患病组织均可被视为再生医学中MSCs的宝贵来源。

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