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Longitudinal imaging of HIV-1 spread in humanized mice with parallel 3D immunofluorescence and electron tomography

机译:平行3D免疫荧光和电子断层扫描在人源化小鼠中传播HIV-1的纵向成像

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Dissemination of HIV-1 throughout lymphoid tissues leads to systemic virus spread following infection. We combined tissue clearing, 3D-immunofluorescence, and electron tomography (ET) to longitudinally assess early HIV-1 spread in lymphoid tissues in humanized mice. Immunofluorescence revealed peak infection density in gut at 10–12 days post-infection when blood viral loads were low. Human CD4+ T-cells and HIV-1–infected cells localized predominantly to crypts and the lower third of intestinal villi. Free virions and infected cells were not readily detectable by ET at 5-days post-infection, whereas HIV-1–infected cells surrounded by pools of free virions were present in ~10% of intestinal crypts by 10–12 days. ET of spleen revealed thousands of virions released by individual cells and discreet cytoplasmic densities near sites of prolific virus production. These studies highlight the importance of multiscale imaging of HIV-1–infected tissues and are adaptable to other animal models and human patient samples.
机译:HIV-1在整个淋巴组织中的传播导致感染后全身病毒传播。我们结合组织清除,3D免疫荧光和电子断层扫描(ET)来纵向评估人源化小鼠中淋巴组织中早期HIV-1的传播。免疫荧光显示,当病毒载量低时,感染后10–12天肠道内的感染密度达到峰值。人类CD4 + T细胞和HIV-1感染的细胞主要位于隐窝和肠绒毛的下三分之一。在感染后5天,游离病毒颗粒和感染的细胞不易被ET检测到,而到10-12天,约10%的肠道隐窝中存在被游离病毒颗粒池包围的HIV-1感染细胞。脾的ET揭示了成千上万的病毒粒子被单个细胞释放,并且在多产病毒的产生部位附近具有离散的细胞质密度。这些研究凸显了对HIV-1感染组织进行多尺度成像的重要性,并且适用于其他动物模型和人类患者样品。

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