体外研究肠神经系统细胞的肠脱细胞基质

Schrenk S, Piccione M, Tasso A, D. R., Conconi Mt
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引用次数: 0

摘要

肠神经系统(ENS)细胞响应肠细胞外基质(ECM)信号,改变其增殖速率、迁移和分化。在这项研究中,我们在体外探索了原代ENS细胞培养物对肠道脱细胞基质(AM)刺激的适应性反应,确定了神经元功能标记物的基因表达谱。使用扫描电镜检测特定形态特征的获取。采用酶-洗涤剂处理制备肠道AM。采用酶促法从出生大鼠的肌肠丛中分离大鼠肠细胞,并在外源性神经营养因子存在的情况下将其植入肠AM。采用扫描电镜(SEM)和全量荧光染色对其形态学特征和特异性分化标志物的表达进行了评价。为了验证可溶性因子与AM的协同作用,在SM条件下培养的ENS细胞中,在AM存在或不存在的情况下,采用qPCR方法评估神经递质受体的基因表达。神经递质受体的表达和相互连接的神经节样结构的发展表明,ENS细胞工程肠基质可用于再生医学的医学应用或体外评估ENS三维培养系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut acellular matrix for the in vitro study of Enteric Nervous System cells
Enteric nervous system (ENS) cells respond to the intestinal extracellular matrix (ECM) signals changing their proliferation rate, migration and differentiation. In this study, we explored in vitro the adaptive response of primary ENS cell cultures to the stimulation of gut acellular matrix (AM) defining the gene expression profile of neuronal functionality markers. Scanning electron microscopy was used to detect the acquisition of specific morphological features. Intestinal AM was prepared using an enzyme-detergent treatment. Primary rat enteric cells were isolated from the myenteric plexus of postnatal rats using an enzymatic method and seeded on intestinal AM in the presence of exogenous neurotrophic factors. The morphological properties and the expression of specific differentiation markers were evaluated by Scanning Electron Microscopy (SEM) and wholemount fluorescent staining. In order to verify the synergic activity of soluble factors and AM, the gene expression of neurotransmitter receptors was evaluated by qPCR in ENS cells cultured in SM conditions in the presence or not of AM. The development of interconnected ganglion-like structures and the expression of neurotransmitter receptors suggested that gut matrix engineered with ENS cells could be useful for medical applications of regenerative medicine or for the in vitro assessment of tridimensional culture system of ENS.
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