Conrad Rebecca, Jablonka Sibylle, Sczepan Teresa, Sendtner Michael, Wiese Stefan, Klausmeyer Alice
Institute for Cellmorphology and molecular Neurobiology, Group for Cellbiology, Ruhr-University Bochum.
J Vis Exp. 2011 Sep 15(55):3200. doi: 10.3791/3200.
Spinal motoneurons develop towards postmitotic stages through early embryonic nervous system development and subsequently grow out dendrites and axons. Neuroepithelial cells of the neural tube that express Nkx6.1 are the unique precursor cells for spinal motoneurons(1). Though postmitotic motoneurons move towards their final position and organize themselves into columns along the spinal tract(2,3). More than 90% of all these differentiated and positioned motoneurons express the transcription factors Islet 1/2. They innervate the muscles of the limbs as well as those of the body and the inner organs. Among others, motoneurons typically express the high affinity receptors for brain derived neurotrophic factor (BDNF) and Neurotrophin-3 (NT-3), the tropomyosin-related kinase B and C (TrkB, TrkC). They do not express the tropomyosin-related kinase A (TrkA)(4). Beside the two high affinity receptors, motoneurons do express the low affinity neurotrophin receptor p75(NTR). The p75(NTR) can bind all neurotrophins with similar but lower affinity to all neurotrophins than the high affinity receptors would bind the mature neurotrophins. Within the embryonic spinal cord, the p75(NTR) is exclusively expressed by the spinal motoneurons(5). This has been used to develop motoneuron isolation techniques to purify the cells from the vast majority of surrounding cells(6). Isolating motoneurons with the help of specific antibodies (panning) against the extracellular domains of p75(NTR) has turned out to be an expensive method as the amount of antibody used for a single experiment is high due to the size of the plate used for panning. A much more economical alternative is the use of lectin. Lectin has been shown to specifically bind to p75(NTR) as well(7). The following method describes an alternative technique using wheat germ agglutinin for a preplating procedure instead of the p75(NTR) antibody. The lectin is an extremely inexpensive alternative to the p75(NTR) antibody and the purification grades using lectin are comparable to that of the p75(NTR) antibody. Motoneurons from the embryonic spinal cord can be isolated by this method, survive and grow out neurites.
脊髓运动神经元在胚胎早期神经系统发育过程中向有丝分裂后阶段发展,随后长出树突和轴突。神经管中表达Nkx6.1的神经上皮细胞是脊髓运动神经元独特的前体细胞(1)。有丝分裂后的运动神经元虽然会迁移到它们的最终位置,并沿着脊髓束排列成柱(2,3)。所有这些已分化并定位的运动神经元中,超过90%表达转录因子Islet 1/2。它们支配四肢的肌肉以及身体和内脏的肌肉。其中,运动神经元通常表达脑源性神经营养因子(BDNF)和神经营养素-3(NT-3)的高亲和力受体、原肌球蛋白相关激酶B和C(TrkB、TrkC)。它们不表达原肌球蛋白相关激酶A(TrkA)(4)。除了这两种高亲和力受体外,运动神经元确实表达低亲和力神经营养素受体p75(NTR)。p75(NTR)能以与高亲和力受体结合成熟神经营养素类似但较低的亲和力结合所有神经营养素。在胚胎脊髓内,p75(NTR)仅由脊髓运动神经元表达(5)。这已被用于开发运动神经元分离技术,以便从绝大多数周围细胞中纯化细胞(6)。事实证明,借助针对p75(NTR)细胞外结构域的特异性抗体(淘选)分离运动神经元是一种昂贵的方法,因为由于用于淘选的培养皿尺寸较大,单次实验所用抗体量很高。一种更经济的替代方法是使用凝集素。已证明凝集素也能特异性结合p75(NTR)(7)。以下方法描述了一种替代技术,使用小麦胚芽凝集素进行预铺板程序,而不是p75(NTR)抗体。凝集素是p75(NTR)抗体极其廉价的替代品,使用凝集素的纯化等级与p75(NTR)抗体相当。通过这种方法可以分离胚胎脊髓中的运动神经元,使其存活并长出神经突。