首页> 外文期刊>Annals of Biomedical Engineering: The Journal of the Biomedical Engineering Society >Collagen-dependent neurite outgrowth and response to dynamic deformation in three-dimensional neuronal cultures.
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Collagen-dependent neurite outgrowth and response to dynamic deformation in three-dimensional neuronal cultures.

机译:三维神经元文化中的胶原依赖性神经突生长和对动态变形的响应。

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In vitro models of brain injury that use thick 3-D cultures and control extracellular matrix constituents allow evaluation of cell-matrix interactions in a more physiologically relevant configuration than traditional 2-D cultures. We have developed a 3-D cell culture system consisting of primary rat cortical neurons distributed throughout thick (>500 microm) gels consisting of type IV collagen (Col) conjugated to agarose. Neuronal viability and neurite outgrowth were examined for a range of agarose (AG) percentages (1.0-3.0%) and initial collagen concentrations ([Col](i); 0-600 microg/mL). In unmodified AG, 1.5% gels supported viable cultures with significant neurite outgrowth, which was not found at lower (< or =1.0%) concentrations. Varying [Col](i )in 1.25% AG revealed the formation of dense, 3-D neurite networks at [Col](i) of 300 microg/mL, while neurons in unmodified AG and at higher [Col](i) (600 microg/mL) exhibited significantly less neurite outgrowth; although, neuronal survival did not vary with [Col](i). The effect of [Col](i) on acute neuronal response following high magnitude, high rate shear deformation (0.50 strain, 30 s(-1) strain rate) was evaluated in 1.5% AG for [Col](i) of 30, 150, and 300 microg/mL, which supported cultures with similar baseline viability and neurite outgrowth. Conjugation of Col to AG also increased the complex modulus of the hydrogel. Following high rate deformation, neuronal viability significantly decreased with increasing [Col](i), implicating cell-matrix adhesions in acute mechanotransduction events associated with traumatic loading. These results suggest interrelated roles for matrix mechanical properties and receptor-mediated cell-matrix interactions in neuronal viability, neurite outgrowth, and transduction of high rate deformation. This model system may be further exploited for the elucidation of mechanotransduction mechanisms and cellular pathology following mechanical insult.
机译:使用厚3-D培养物并控制细胞外基质成分的体外脑损伤模型可以以比传统2-D培养物更生理相关的配置评估细胞-基质相互作用。我们已经开发了一个3-D细胞培养系统,该系统由原代大鼠皮质神经元组成,这些神经元分布在厚的(> 500微米)凝胶中,凝胶由与琼脂糖结合的IV型胶原(Col)组成。检查了一定范围的琼脂糖(AG)百分比(1.0-3.0%)和初始胶原蛋白浓度([Col](i); 0-600 microg / mL)的神经元活力和神经突生长。在未修饰的AG中,1.5%的凝胶支持具有明显神经突生长的可行培养物,在较低(<或= 1.0%)浓度下未发现。在1.25%AG中变化的[Col](i)显示在[Col](i)为300 microg / mL时,形成了密集的3-D神经突网络,而未修饰的AG和较高的[Col](i)中的神经元( 600微克/毫升)表现出明显更少的神经突增生;虽然,神经元的存活率并没有随[Col](i)的变化而变化。在[Col](i)为30时,在1.5%AG中评估了[Col](i)对高强度高速率剪切变形(0.50应变,30 s(-1)应变率)后急性神经元反应的影响。 150和300 microg / mL,可支持具有相似基线生存力和神经突生长的培养物。 Col与AG的缀合也增加了水凝胶的复数模量。高速率变形后,神经元活力随着[Col](i)的增加而显着降低,这暗示了与创伤负荷相关的急性机械转导事件中的细胞基质粘附。这些结果表明,在神经元活力,神经突长出和高速率变形的转导中,基质力学性能和受体介导的细胞-基质相互作用具有相互关联的作用。该模型系统可进一步用于阐明机械损伤后的机械转导机制和细胞病理学。

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