感染不同柯萨奇病毒B4株的离体胰岛组织培养:病毒复制及对胰岛形态和胰岛素释放的影响

G. Frisk, H. Diderholm
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引用次数: 73

摘要

目的是研究柯萨奇病毒B4 (CBV-4)不同毒株是否能在体外感染人胰岛细胞并引起形态学和功能损伤。在组织培养中分离的胰岛感染了五种特征良好的CBV-4菌株。分析了培养基配比对病毒复制和胰岛素含量的影响。通过光镜检查感染和未感染的胰岛,以确定病毒诱导的细胞病变效应(CPE)的程度。结果表明,胰岛细胞对所有CBV-4菌株的感染均敏感,但感染结果不同。感染后48和72小时获得的病毒滴度在所有CBV-4菌株之间存在显著差异(p < 0.001),表明在胰岛细胞中复制的能力不同。5株CBV-4毒株中的4株诱导了弱CPE,部分原因是胰岛的来源(供体)。一个毒株(VD2921)尽管病毒滴度很高,但没有引起CPE。其中1株(V89-4557)均表现出明显的CPE。感染该菌株还会引起功能损伤,显著影响感染后48小时胰岛素对高糖的反应(p < 0.001)。与未感染的对照细胞相比,另一种CBV-4菌株(JVB)在胰岛细胞中的复制显著增加了胰岛素的释放(p < 0.001),表明β细胞的损伤导致胰岛素的泄漏。
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Tissue Culture of Isolated Human Pancreatic Islets Infected With Different Strains of Coxsackievirus B4: Assessment of Virus Replication and Effects on Islet Morphology and Insulin Release
The aim was to study whether different strains of Coxsackievirus B4 (CBV-4) are able to infect human pancreatic islet cells in vitro and cause morphological and functional damages. Isolated islets maintained in tissue culture were infected with five well- characterised strains of CBV-4. Aliquots of the culture medium were analysed with regard to virus replication and insulin content. Infected and uninfected islets were examined by light microscopy to determine the degree of virus-induced cytopathic effect (CPE). The results showed that the islet cells were susceptible to infection by all the strains of CBV-4 although the outcome of the infection differed. The virus titres obtained at 48 and 72 hours post infection differed significantly between all the CBV-4 strains (p < 0.001), indicating different ability to replicate in islet cells. Pronounced to weak CPE, which was partly due to the origin (donor) of the islets, was induced by four of the five CBV-4 strains. One strain (VD2921) replicated without causing CPE despite high virus titres. One (V89-4557) of the CBV-4 strains always revealed pronounced CPE. Infection by this strain also caused functional impairment that significantly affected insulin response to high glucose at 48 hours post infection (p < 0.001). Replication of another CBV-4 strain (JVB) in the islet cells significantly increased the release of insulin compared to non-infected control cells (p < 0.001) indicating damage of the β-cells leading to leakage of insulin.
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