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首页> 外文期刊>Journal of Neuroscience Methods >A semi-automated image analysis method to quantify neurite preference/axon guidance on a patterned substratum.
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A semi-automated image analysis method to quantify neurite preference/axon guidance on a patterned substratum.

机译:一种半自动化的图像分析方法,用于量化图案化基质上的神经突偏好/轴突引导。

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摘要

Axon outgrowth and guidance are differentially promoted or inhibited by specific extracellular matrix (ECM) molecules. The effects of these molecules can be examined by culturing neuronal explants on patterned substrata consisting of alternating stripes adsorbed with the molecules of interest. While outgrowth on substrata adsorbed with homogenous molecules can be reliably quantified, current methods of quantifying neurite preference on patterned substrata are subjective, labor intensive, and overall less reliable. Here, we present a quick, semi-automated, lowly subjective macro-based method to quantify the effects of a change in substratum on axon extension and guidance. We plated chick dorsal root ganglion explants on a substratum consisting of alternating stripes of laminin-1 (outgrowth supportive) and chondroitin sulfate proteoglycans (CSPGs, outgrowth inhibitory). We evaluated neurite preference for laminin or CSPG-coated regions by measuring total neurite area, and produced an inhibition index. The quantitative data confirmed previous qualitative data showing that increasing concentrations of CSPGs induced increases in inhibition. The methods presented here: (1) require less stringent image capture criteria; (2) are quicker; (3) are less subjective compared to previously described methods; and (4) are versatile in that they can be used to assay neurite preference for any substratum-bound molecules in living or fixed cultures.
机译:轴突的生长和引导被特定的细胞外基质(ECM)分子差异地促进或抑制。这些分子的作用可以通过在图案化的基质上培养神经元外植体来检查,该图案化的基质由吸附有目标分子的交替条纹组成。尽管可以可靠地量化吸附在均质分子上的基质上的生长,但是目前的量化图案化基质上的神经突偏好的方法是主观的,费力的并且总体上不太可靠。在这里,我们提出了一种快速,半自动化,低主观的基于宏的方法,以量化基质变化对轴突延伸和引导的影响。我们将鸡背根神经节外植体接种在由层粘连蛋白-1(生长支持)和硫酸软骨素蛋白多糖(CSPG,抑制生长)的交替条纹组成的基质上。我们通过测量总的神经突面积,评估了对于层粘连蛋白或CSPG涂层区域的神经突偏好,并产生了抑制指数。定量数据证实了先前的定性数据,表明CSPG浓度的增加诱导了抑制作用的增加。这里介绍的方法:(1)要求不太严格的图像捕获标准; (2)速度更快; (3)与先前描述的方法相比主观性较差; (4)是通用的,因为它们可用于分析活体或固定培养物中任何与基质结合的分子的神经突偏好。

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