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与富含纤维蛋白的质膜洗脱液接触的干细胞的增殖与分化。

Proliferation and differentiation of stem cells in contact with eluate from fibrin-rich plasma membrane.

作者信息

Souza Fernanda Gimenez de, Fernandes Beatriz Luci, Rebelatto Carmen Lucia Kuniyoshi, Aguiar Alessandra Melo de, Fracaro Letícia, Brofman Paulo Roberto Slud

机构信息

Pontifícia Universidade Católica do Paraná (PUC-PR), Curitiba, PR, Brazil.

Instituto Carlos Chagas, Fundação Oswaldo Cruz (Fiocruz), Curitiba, PR, Brazil.

出版信息

Rev Bras Ortop. 2017 Dec 12;53(1):45-52. doi: 10.1016/j.rboe.2017.12.004. eCollection 2018 Jan-Feb.

Abstract

OBJECTIVE

To evaluate the ability of the eluate from fibrin-rich plasma (FRP) membrane to induce proliferation and differentiation of isolated human adipose-derived stem cells (ASCs) into chondrocytes.

METHOD

FRP membranes were obtained by centrifugation of peripheral blood from two healthy donors, cut, and maintained in culture plate wells for 48 h to prepare the fibrin eluate. The SCATh were isolated from adipose tissue by collagenase digestion solution, and expanded . Cells were expanded and treated with DMEM-F12 culture, a commercial media for chondrogenic differentiation, and eluate from FRP membrane for three days, and labeled with BrdU for quantitative assessment of cell proliferation using the High-Content Operetta imaging system. For the chondrogenic differentiation assay, the SCATh were grown in micromass for 21 days and stained with toluidine blue and aggrecan for qualitative evaluation by light microscopy. The statistical analysis was performed using ANOVA and Tukey's test.

RESULTS

There was a greater proliferation of cells treated with the eluate from FRP membrane compared to the other two treatments, where the ANOVA test showed significance ( < 0.001). The differentiation into chondrocytes was visualized by the presence of mucopolysaccharide in the matrix of the cells marked in blue toluidine and aggrecan.

CONCLUSIONS

Treatment with eluate from FRP membrane stimulated cell proliferation and induced differentiation of the stem cells into chondrocytes, suggesting a potential application of FRP membranes in hyaline cartilage regeneration therapies.

摘要

目的

评估富含纤维蛋白血浆(FRP)膜洗脱液诱导分离的人脂肪来源干细胞(ASC)增殖并分化为软骨细胞的能力。

方法

通过离心两名健康供体的外周血获得FRP膜,切割后置于培养板孔中48小时以制备纤维蛋白洗脱液。通过胶原酶消化液从脂肪组织中分离出ASC,并进行扩增。细胞扩增后,用DMEM-F12培养基(一种用于软骨形成分化的商业培养基)和FRP膜洗脱液处理三天,并用BrdU标记,使用高内涵Operetta成像系统对细胞增殖进行定量评估。对于软骨形成分化试验,将ASC以微团形式培养21天,并用甲苯胺蓝和聚集蛋白聚糖染色,通过光学显微镜进行定性评估。采用方差分析和Tukey检验进行统计分析。

结果

与其他两种处理相比,用FRP膜洗脱液处理的细胞增殖更多,方差分析显示具有显著性(<0.001)。在甲苯胺蓝和聚集蛋白聚糖标记为蓝色的细胞基质中存在粘多糖,表明细胞分化为软骨细胞。

结论

FRP膜洗脱液处理可刺激细胞增殖并诱导干细胞分化为软骨细胞,提示FRP膜在透明软骨再生治疗中具有潜在应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7034/5771793/d519e1eab366/gr1.jpg

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