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通过简单的几何变换描述成纤维细胞在带凹槽表面上的排列。

Alignment of fibroblasts on grooved surfaces described by a simple geometric transformation.

作者信息

Dunn G A, Brown A F

出版信息

J Cell Sci. 1986 Jul;83:313-40. doi: 10.1242/jcs.83.1.313.

Abstract

The response of chick heart fibroblasts to grooved substrata was studied using microfabricated grooves and new measures of shape and alignment derived from the moments of cell shapes. Cell shape and alignment were measured on 23 different sets of regular, parallel grooves, which ranged in width from 1.65 to 8.96 micron, and in repeat spacing from 3.0 to 32.0 micron. The grooves were of constant depth, 0.69 micron. Digitized video images were analysed to extract the zero-, first- and second-order moments of the cell shapes, from which were calculated three measures of cell shape, and three measures of cell alignment. Regression analyses of the measures against parameters of the substratum such as groove width, repeat spacing and the ridge width between grooves show that ridge width is the main parameter affecting cell alignment (alignment being inversely proportional to ridge width), although groove width has a small additional effect. All the differences in cell shape between the different grooves can be summarized to a very good approximation as simple geometrical stretch transformations of the shapes of cells on planar surfaces. Our principal measure of cell alignment, paraxial elongation, is a measure of the necessary transformation. This finding has the interesting biological implication that the shape and orientation adopted by cells, in response to the grooves, are not governed by independent cellular mechanisms.

摘要

利用微加工凹槽以及从细胞形状矩得出的形状和排列新测量方法,研究了鸡心脏成纤维细胞对带凹槽基质的反应。在23组不同的规则平行凹槽上测量细胞形状和排列,这些凹槽宽度从1.65微米到8.96微米不等,重复间距从3.0微米到32.0微米不等。凹槽深度恒定,为0.69微米。分析数字化视频图像以提取细胞形状的零阶、一阶和二阶矩,由此计算出三种细胞形状测量值和三种细胞排列测量值。对这些测量值与基质参数(如凹槽宽度、重复间距和凹槽之间的脊宽度)进行回归分析表明,脊宽度是影响细胞排列的主要参数(排列与脊宽度成反比),尽管凹槽宽度有较小的附加影响。不同凹槽之间细胞形状的所有差异都可以很好地近似总结为平面上细胞形状的简单几何拉伸变换。我们主要的细胞排列测量值——近轴伸长,就是这种必要变换的一种测量。这一发现具有有趣的生物学意义,即细胞响应凹槽所采用的形状和方向并非由独立的细胞机制控制。

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