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Local NGF and GDNF levels modulate morphology and function of porcine DRG neurites, In Vitro

机译:局部NGF和GDNF水平体外调节猪DRG神经突的形态和功能

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摘要

Nerve terminals of primary sensory neurons are influenced by their environment through target derived trophic factors, like nerve growth factor (NGF) or glial cell line-derived neurotrophic factor (GDNF). In mice, subpopulations of DRG neurons express receptors either for NGF or GDNF and therefore differentially respond to these neurotrophic factors. We probed neurite endings from porcine DRG neurons cultured in either NGF or GDNF and examined their shape, elongation and stimulus-evoked CGRP release. A compartmentalized culture system was employed allowing spatial separation of outgrown neurites from their somata and use of different growth factors in the compartments. We show that neurites of GDNF cultured somata extend into lateral compartments without added growth factor, unlike neurites of NGF cultured ones. Neurites of NGF cultured somata extend not only into NGF- but also into GDNF-containing compartments. GDNF at the site of terminals of NGF responsive somata led to a strong neurite arborization and formation of large growth cones, compared to neurites in medium with NGF. Functionally, we could detect evoked CGRP release from as few as 7 outgrown neurites per compartment and calculated release per mm neurite length. CGRP release was detected both in neurites from NGF and GDNF cultured somata, suggesting that also the latter ones are peptidergic in pig. When neurites of NGF cultured somata were grown in GDNF, capsaicin evoked a lower CGRP release than high potassium, compared to those grown in NGF. Our experiments demonstrate that the compartmented culture chamber can be a suitable model to assess neurite properties from trophic factor specific primary sensory neurons. With this model, insights into mechanisms of gain or loss of function of specific nociceptive neurites may be achieved.
机译:初级感觉神经元的神经末梢受到靶标衍生的营养因子(如神经生长因子(NGF)或神经胶质细胞系衍生的神经营养因子(GDNF))的环境影响。在小鼠中,DRG神经元的亚群表达NGF或GDNF的受体,因此对这些神经营养因子有不同的反应。我们探查了在NGF或GDNF中培养的猪DRG神经元的神经突末端,并检查了它们的形状,延伸率和刺激诱发的CGRP释放。采用隔间培养系统,可以将生长迟缓的神经突与其躯体空间分离,并在隔间内使用不同的生长因子。我们显示,与NGF培养的神经突不同,GDNF培养的躯体的神经突延伸到外侧腔室而没有增加的生长因子。 NGF培养的躯体的神经突不仅延伸到NGF区域,而且延伸到包含GDNF的区域。与具有NGF的培养基中的神经突相比,位于NGF响应​​性躯体末端的GDNF导致强烈的神经突乔化并形成大的生长锥。从功能上讲,我们可以从每个隔室少至7个生长迟缓的神经突中检测诱发的CGRP释放,并计算每毫米神经突长度的释放。在NGF和GDNF培养的体细胞瘤的神经突中都检测到了CGRP释放,这表明后者在猪中也是肽能的。当在NGNF中培养NGF培养的躯体神经突时,与在NGF中生长的那些相比,辣椒素引起的CGRP释放要比高钾低。我们的实验表明,隔室培养室可以作为评估营养因子特异的初级感觉神经元神经突特性的合适模型。使用此模型,可以了解特定伤害感受神经突功能的获得或丧失机理。

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