Fukuda J, Kurata T, Yamamoto A, Yamaguchi K
Brain Res. 1983 Feb 28;262(1):79-89. doi: 10.1016/0006-8993(83)90471-7.
Adult guinea pigs were inoculated with type 2 herpes simplex virus (HSV) on the whole back skin, and nerve cells from the dorsal root ganglia (DRG) 6 days after infection were grown in tissue culture. Morphological and physiological properties of the cultured nerve cells from HSV-infected animals (HSV-NC) were compared to those of nerve cells of DRG from the control, non-virus infected animals (CON-NC). During the early period of the culture (0-4 days) growth of nerve cells and non-neuronal cells from the HSV infected animals was essentially the same as that from the control animals. HSV-antigen was present in only a small percentage of the HSV-NC by immunofluorescence (IF). Electrophysiological examination revealed that most of the HSV-NC exhibited a reduced capability of generating spikes, which was quantitatively described as a reduction in the Vmax of the Na spikes. This was interpreted as a reduction in the number of Na channel molecules in the plasma membrane of the HSV-NC, while the resting membrane properties of the same cells, such as the resting membrane potential, input resistance and capacitance, were essentially the same as those of the CON-NC. On 4-5 days in culture, some HSV-NC regained a full capability to generate Na spikes. We considered these nerve cells to have overcome the HSV infection and were now entering a latent period of HSV infection. About 1/3 of the HSV-NC still remained incapable of generating Na spikes. Viral antigen was detected in only 10% of the nerve cells. In the late stage of the culture, HSV infection in vitro was first observed as lysis of non-neuronal cells growing close to some HSV-NC. Nerve cells then started to lose their neurites and became spherical. Finally on 8-9 days most of the cells, including the nerve cells, were lost from the dishes as a result of a generalized infection of supporting cells, i.e. fibroblasts and Schwann cells. This study confirms our previous finding that the electrophysiological technique is much more sensitive than the IF method for the detection of HSV-infection in nerve cells. The results indicate that some nerve cells infected with HSV overcome the infection in vitro. This is interpreted as the entering of these nerve cells into a latent period of HSV infection in vitro.
将成年豚鼠整个背部皮肤接种2型单纯疱疹病毒(HSV),感染6天后从背根神经节(DRG)获取神经细胞并进行组织培养。将感染HSV动物(HSV-NC)培养的神经细胞的形态学和生理学特性与对照的未感染病毒动物(CON-NC)的DRG神经细胞的特性进行比较。在培养早期(0 - 4天),HSV感染动物的神经细胞和非神经细胞的生长与对照动物基本相同。通过免疫荧光(IF)检测,仅一小部分HSV-NC中存在HSV抗原。电生理检查显示,大多数HSV-NC产生动作电位的能力降低,这在数量上表现为Na动作电位的Vmax降低。这被解释为HSV-NC质膜中Na通道分子数量减少,而相同细胞的静息膜特性,如静息膜电位、输入电阻和电容,与CON-NC基本相同。在培养4 - 5天时,一些HSV-NC恢复了产生Na动作电位的全部能力。我们认为这些神经细胞已克服HSV感染,现在正进入HSV感染的潜伏期。约1/3的HSV-NC仍然无法产生Na动作电位。仅在10%的神经细胞中检测到病毒抗原。在培养后期,体外HSV感染首先表现为靠近一些HSV-NC生长的非神经细胞裂解。然后神经细胞开始失去其神经突并变成球形。最后在8 - 9天时,由于支持细胞(即成纤维细胞和雪旺细胞)的广泛感染,包括神经细胞在内的大多数细胞从培养皿中消失。本研究证实了我们先前的发现,即电生理技术在检测神经细胞中的HSV感染方面比IF方法更敏感。结果表明,一些感染HSV的神经细胞在体外克服了感染。这被解释为这些神经细胞在体外进入HSV感染的潜伏期。