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Human Papillomavirus Type 16 Entry: Retrograde Cell Surface Transport along Actin-Rich Protrusions

机译:人类乳头瘤病毒16型进入:沿富含肌动蛋白突起的细胞表面逆行转运

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摘要

The lateral mobility of individual, incoming human papillomavirus type 16 pseudoviruses (PsV) bound to live HeLa cells was studied by single particle tracking using fluorescence video microscopy. The trajectories were computationally analyzed in terms of diffusion rate and mode of motion as described by the moment scaling spectrum. Four distinct modes of mobility were seen: confined movement in small zones (30–60 nm in diameter), confined movement with a slow drift, fast random motion with transient confinement, and linear, directed movement for long distances. The directed movement was most prominent on actin-rich cell protrusions such as filopodia or retraction fibres, where the rate was similar to that measured for actin retrograde flow. It was, moreover, sensitive to perturbants of actin retrograde flow such as cytochalasin D, jasplakinolide, and blebbistatin. We found that transport along actin protrusions significantly enhanced HPV-16 infection in sparse tissue culture, cells suggesting a role for in vivo infection of basal keratinocytes during wound healing.
机译:通过使用荧光视频显微镜的单粒子跟踪研究了与活HeLa细胞结合的单个传入人类乳头瘤病毒16型假病毒(PsV)的横向迁移性。按照矩比例谱描述的方式,根据扩散速率和运动模式对轨迹进行了计算分析。可以看到四种不同的移动方式:在小区域(直径为30-60 nm)中的受限运动,缓慢漂移的受限运动,具有瞬态限制的快速随机运动以及长距离的线性定向运动。定向运动在富含肌动蛋白的细胞突起(如丝状伪足或缩回纤维)上最为突出,其速率与肌动蛋白逆行血流的速率相似。此外,它对肌动蛋白逆行流动的干扰物敏感,例如细胞松弛素D,jasplakinolide和blebbistatin。我们发现在稀疏组织培养中沿肌动蛋白突起的转运显着增强了HPV-16感染,提示在伤口愈合过程中细胞在体内感染基础角质形成细胞。

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