Houchin-Ray Tiffany, Zelivyanskaya Marina, Huang Alyssa, Shea Lonnie D
Department of Chemical and Biological Engineering, Northwestern University, 2145 Sheridan Rd E156 Evanston, Illinois 60208-3120, USA.
Biotechnol Bioeng. 2009 Aug 1;103(5):1023-33. doi: 10.1002/bit.22311.
Gene delivery from tissue engineering scaffolds can induce expression of tissue inductive factors to stimulate the cellular processes required for regeneration. Transfected cells secrete diffusible proteins that can create local concentration gradients, depending on the number, distribution, and expression level of transfected cells. These gradients are linked to cellular organization and tissue architecture during embryogenesis. In this report, we investigate neuronal architecture and neurite guidance in response to the concentration gradients achieved by localized secretion of a neurotrophic factor from transfected cells. A co-culture model was employed to examine neuronal responses to multiple transfection profiles, which affects the local concentration of secreted nerve growth factor (NGF). Neuronal architecture, as defined by number of neurites per neuron and length of neurites, was influenced by the transfection profile. Low levels of NGF production by few transfected cells produced longer primary neurites with less branching relative to the higher expression levels or increased numbers of transfected cells. Furthermore, for low NGF production by few transfected cells, the growth cone of the axons was marked by longer extensions and larger surface area, suggesting the presence of a guidance cue. Control studies with varying NGF concentrations did not substantially alter the neuronal architecture, further supporting an effect of localized concentration gradients, and not simply the concentration. Mathematical modeling of NGF diffusion was employed to predict the concentration gradients produced by the transfection profiles, and the resultant gradients were correlated to the cellular response. This report connects the transfection profile, concentration gradients, and the resulting cellular architecture, suggesting a critical design consideration for the application of gene delivery to regenerative medicine.
来自组织工程支架的基因传递可诱导组织诱导因子的表达,以刺激再生所需的细胞过程。转染细胞分泌可扩散的蛋白质,这些蛋白质可根据转染细胞的数量、分布和表达水平产生局部浓度梯度。这些梯度在胚胎发育过程中与细胞组织和组织结构相关联。在本报告中,我们研究了神经元结构和神经突导向对转染细胞局部分泌神经营养因子所形成的浓度梯度的反应。采用共培养模型来检测神经元对多种转染模式的反应,这些模式会影响分泌的神经生长因子(NGF)的局部浓度。由每个神经元的神经突数量和神经突长度所定义的神经元结构受转染模式的影响。相对于较高的表达水平或增加的转染细胞数量,少量转染细胞产生的低水平NGF会产生更长且分支更少的初级神经突。此外,对于少量转染细胞产生的低水平NGF,轴突的生长锥具有更长的延伸和更大的表面积,表明存在导向信号。用不同NGF浓度进行的对照研究并未显著改变神经元结构,这进一步支持了局部浓度梯度的作用,而不仅仅是浓度的作用。采用NGF扩散的数学模型来预测转染模式产生的浓度梯度,并将所得梯度与细胞反应相关联。本报告将转染模式、浓度梯度和由此产生的细胞结构联系起来,为基因传递在再生医学中的应用提出了关键的设计考量。