首页> 外文期刊>The Journal of Comparative Neurology >Differences in developmental cell death between somatic and autonomic motor neurons of rat spinal cord.
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Differences in developmental cell death between somatic and autonomic motor neurons of rat spinal cord.

机译:大鼠脊髓体细胞神经和自主神经运动神经元发育细胞死亡的差异。

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Considerable knowledge concerning developmental cell death has come from the study of somatic motor neurons (SMNs), but a related set of spinal neurons, the autonomic motor neurons (AMNs), have been studied less extensively in this respect. In the present study, we used three different approaches to determine the amount of AMN cell death during normal development in the rat. First, target dependency was studied in organotypic slice cultures, and it was found that AMNs survived for at least 12 days after removal of their postsynaptic targets. No factors were added to the serum-free medium to substitute for the ablated targets, indicating that AMNs were able to survive without target-derived trophic factors. Such target-independent survival is not characteristic of neurons that undergo typical developmental cell death. Second, AMNs were counted in double-stained choline acetyltransferase immunocytochemical and NADPH diaphorase histochemical preparations at ages (postnatal days 4-22) encompassing the period when AMN postsynaptic target cells undergo developmental death. Neuron numbers were essentially identical at all ages examined, indicating that no AMN cell death occurred postnatally. Finally, from embryonic day 13 to postnatal day 22, animals were analyzed by using terminal transferase-mediated nick-end labeling to identify dying cells. Many fewer labeled cells were observed among AMNs than among SMNs. Thus, all three approaches indicated that there is a significant SMN/AMN difference in developmental cell death. The phenotypic trait(s) that underlies this difference may also be important in the relative resistance of AMNs to pathological conditions that induce death of SMNs, e.g., those involved in amyotrophic lateral sclerosis and excitotoxicity.
机译:有关发育细胞死亡的大量知识来自于体动神经元(SMN)的研究,但是在这方面,对相关的一组脊柱神经元,即自主神经元(AMN)的研究较少。在本研究中,我们使用三种不同的方法来确定大鼠正常发育过程中AMN细胞的死亡数量。首先,在器官型切片培养物中研究了靶标依赖性,发现AMNs在去除其突触后靶标后至少存活了12天。没有因素被添加到无血清培养基中以替代消融的靶标,这表明AMNs能够在没有靶标衍生的营养因子的情况下生存。这种不依赖靶标的存活不是经历典型发育细胞死亡的神经元的特征。第二,在包括AMN突触后靶细胞发育死亡的时期(出生后4-22天)的年龄(双染胆碱乙酰转移酶免疫细胞化学和NADPH心肌黄酶组织化学制剂)中对AMNs进行计数。在所有检查的年龄段,神经元数量基本相同,表明出生后未发生AMN细胞死亡。最后,从胚胎的第13天到出生后的第22天,通过使用末端转移酶介导的切口末端标记来分析动物,以鉴定死亡的细胞。在AMN中观察到的标记细胞要比在SMN中少得多。因此,所有三种方法都表明发育细胞死亡中存在显着的SMN / AMN差异。造成这种差异的表型性状也可能对AMNs对导致SMNs死亡的病理状况(例如,与肌萎缩性侧索硬化症和兴奋性中毒有关)的相对抵抗具有重要意义。

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