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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Defining the concentration gradient of nerve growth factor for guided neurite outgrowth.
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Defining the concentration gradient of nerve growth factor for guided neurite outgrowth.

机译:定义神经生长因子的浓度梯度,以指导神经突生长。

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The developing axon is believed to navigate towards its target tissue in response to a concentration gradient of neurotrophic factors, among other diffusible and surface-bound stimuli. However, the minimum concentration gradient required for guidance over the maximum distance is still unknown, largely because well-defined systems have not been utilized to address this question. In this study, a linear concentration gradient of nerve growth factor was achieved across a 5-mm agarose membrane that separated a nerve growth factor source compartment from a sink compartment. The concentrations in both compartments were maintained constant (and different). Both concentration and concentration gradient were well defined across the membrane, allowing us to study the relative importance of concentration gradient vs concentration for neurite guidance. The orientation of PC12 cell neurites was studied in response to a series of nerve growth factor concentration gradients in vitro. For effective guidance of PC12 cell neurite outgrowth, a minimum concentration gradient of 133ng/ml per mm was required, below which guidance was ineffective. Higher gradients were effective for guidance yet were limited by the concentration of nerve growth factor in the source compartment. At a nerve growth factor concentration of 995ng/ml, the PC12 cells' receptors were saturated, thereby limiting the maximum effective distance for guidance to less than 7.5mm in response to a diffusible nerve growth factor cue. This distance exceeds the 0.5-2mm distance observed by others for effective neurite guidance.Using this model system, we propose that the minimum concentration gradient can be defined for other cells and growth factors. Ultimately, it is anticipated that such concentration gradients could be included in a device to promote regeneration.
机译:据信发育中的轴突响应于神经营养因子以及其他可扩散的和表面结合的刺激物的浓度梯度而向其靶组织导航。然而,在最大距离上进行引导所需的最小浓度梯度仍然是未知的,这在很大程度上是因为尚未使用定义明确的系统来解决该问题。在这项研究中,神经生长因子的线性浓度梯度在5毫米琼脂糖膜上实现,该膜将神经生长因子源隔室与水槽隔室分隔开。两个隔室中的浓度均保持恒定(且不同)。整个膜上的浓度和浓度梯度均定义良好,这使我们能够研究浓度梯度与浓度对神经突引导的相对重要性。响应一系列神经生长因子浓度梯度体外研究了PC12细胞神经突的取向。为了有效指导PC12细胞神经突向外生长,要求最小浓度梯度为133ng / ml / mm,低于该指导无效。较高的梯度对引导有效,但受到源隔室中神经生长因子浓度的限制。在神经生长因子浓度为995ng / ml时,PC12细胞的受体饱和,从而将对弥散性神经生长因子提示的最大指导有效距离限制在7.5mm以下。该距离超过了其他人为有效的神经突引导所观察到的0.5-2mm的距离。使用此模型系统,我们建议可以为其他细胞和生长因子定义最小浓度梯度。最终,预期这种浓度梯度可以包含在促进再生的装置中。

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