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在具有确定直径的聚乳酸-羟基乙酸共聚物(PLGA)微纤维上实现可控的细胞取向。

Controlled cellular orientation on PLGA microfibers with defined diameters.

作者信息

Hwang C M, Park Y, Park J Y, Lee K, Sun K, Khademhosseini A, Lee S H

机构信息

Department of Biomedical Engineering, College of Health Science, Korea University, Jeongneung-dong, Seongbuk-gu, Seoul 136-703, Republic of Korea.

出版信息

Biomed Microdevices. 2009 Aug;11(4):739-46. doi: 10.1007/s10544-009-9287-7.

Abstract

In this study, we investigated the effects of the diameter of microfibers on the orientation (angle between cells' major axis and the substrate fiber long axis) of adhered cells. For this purpose, mouse fibroblast L929 cells were cultured on the surface of PLGA fibers of defined diameters ranging from 10 to 242 mum, and their adhesion and alignment was quantitatively analyzed. It was found that the mean orientation of cells and the spatial variation of cell alignment angle directly related to the microfiber diameter. Cells that were cultured on microfibrous scaffolds oriented along the long axis of the microfiber and the orientation increased as the fiber diameter decreased. For the fiber diameter of 10 microm, the mean orientation was 3.0 +/- 0.2 degrees (mean +/- SE), whereas for a diameter of 242 microm, it decreased to 37.7 +/- 2.1 degrees . Using these studies we demonstrate that fibroblasts have a characteristic alignment on microscale fibers and that the microscale fiber diameter plays a critical role in cellular orientation. The ability to control cellular alignment on engineered tissue scaffold can be a potentially powerful approach to recreate the microscale architecture of engineered tissues. This may be important for engineering a variety of human tissues such as tendon, muscle and nerves as well as applications in 3D tissue culture and drug screening.

摘要

在本研究中,我们调查了微纤维直径对黏附细胞取向(细胞长轴与基质纤维长轴之间的夹角)的影响。为此,将小鼠成纤维细胞L929培养在直径范围为10至242微米的特定PLGA纤维表面,并对其黏附与排列进行了定量分析。结果发现,细胞的平均取向以及细胞排列角度的空间变化与微纤维直径直接相关。在微纤维支架上培养的细胞沿微纤维长轴取向,且随着纤维直径减小,取向增加。对于10微米的纤维直径,平均取向为3.0±0.2度(平均值±标准误),而对于242微米的直径,其降至37.7±2.1度。通过这些研究我们证明,成纤维细胞在微尺度纤维上具有特征性排列,并且微尺度纤维直径在细胞取向上起着关键作用。控制工程组织支架上细胞排列的能力可能是重建工程组织微尺度结构的一种潜在有力方法。这对于工程化多种人体组织(如肌腱、肌肉和神经)以及在3D组织培养和药物筛选中的应用可能很重要。

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