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底物结合层粘连蛋白的梯度决定神经元的轴突特化。

Gradients of substrate-bound laminin orient axonal specification of neurons.

作者信息

Dertinger Stephan K W, Jiang Xingyu, Li Zhiying, Murthy Venkatesh N, Whitesides George M

机构信息

Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA.

出版信息

Proc Natl Acad Sci U S A. 2002 Oct 1;99(20):12542-7. doi: 10.1073/pnas.192457199. Epub 2002 Sep 17.

Abstract

Little is known about the influence of substrate-bound gradients on neuronal development, since it has been difficult to fabricate gradients over the distances typically required for biological studies (a few hundred micrometers). This article demonstrates a generally applicable technique for the fabrication of substrate-bound gradients of proteins with complex shapes, using laminar flows in microchannels. Gradients that range from pure laminin to pure BSA were formed in solution by using a network of microchannels, and these proteins were allowed to adsorb onto a homogeneous layer of poly-l-lysine. Rat hippocampal neurons were cultivated on these substrate-bound gradients. Analysis of optical images of these neurons showed that axon specification is oriented in the direction of increasing surface density of laminin. Linear gradients in laminin adsorbed from a gradient in solution having a slope of nabla [laminin] > about 0.06 microg (ml.microm)(-1) (defined by dividing the change of concentration of laminin in solution over the distance of the gradient) orient axon specification, whereas those with nabla [laminin] < about 0.06 microg (ml.microm)(-1) have no effect.

摘要

关于底物结合梯度对神经元发育的影响,人们所知甚少,因为在生物研究通常所需的距离(几百微米)上制造梯度一直很困难。本文展示了一种普遍适用的技术,利用微通道中的层流来制造形状复杂的蛋白质底物结合梯度。通过使用微通道网络在溶液中形成从纯层粘连蛋白到纯牛血清白蛋白的梯度,然后让这些蛋白质吸附到聚-L-赖氨酸的均匀层上。在这些底物结合梯度上培养大鼠海马神经元。对这些神经元的光学图像分析表明,轴突特化的方向是沿着层粘连蛋白表面密度增加的方向。从溶液梯度吸附的层粘连蛋白中的线性梯度,其斜率nabla [层粘连蛋白] > 约0.06微克(毫升·微米)⁻¹(通过将层粘连蛋白在溶液中的浓度变化除以梯度距离来定义)可使轴突特化,而nabla [层粘连蛋白] < 约0.06微克(毫升·微米)⁻¹的梯度则没有影响。

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