Division of Genetic and Molecular Toxicology, U.S. Food and Drug Administration, National Center for Toxicological Research, Jefferson, AR 72079, USA.
Division of Genetic and Molecular Toxicology, U.S. Food and Drug Administration, National Center for Toxicological Research, Jefferson, AR 72079, USA.
Toxicology. 2018 Nov 1;409:119-128. doi: 10.1016/j.tox.2018.07.015. Epub 2018 Jul 24.
Many cigarette smoke-associated airway diseases involve alterations in mucin homeostasis. With the rationale that relevant tissue responses can be measured to evaluate the adverse health effects of tobacco products, we assessed changes in mucin secretion and the density and size of goblet cells in an in vitro human air-liquid-interface (ALI) airway tissue model after exposure to a tobacco smoke solution. Cultures were exposed daily for up to five consecutive days to a whole smoke solution (WSS) prepared by machine smoking Marlboro Red or Marlboro Silver cigarettes using the Canadian Intense (CI) protocol. Both WSSs induced concentration- and time-related hypersecretion of mucins 5AC and 5B, accompanied by up-regulation of the respective mucin genes. Mucin secretion returned to baseline levels following a 14-day recovery period. Mucin-secreting goblet cells exhibited increased cell density and decreased size after 5 daily treatments then recovered to their normal size, but with decreased cell density, 14 days after the last treatment. The beating frequency of ciliated cells, which plays a key role in mucociliary clearance, was increased by 5 daily treatments with the CI WSSs then reverted to baseline levels following a 7-day recovery. Taken together, our results indicate that ALI cultures can be used to measure the modulation of mucin production, secretion, and clearance, disturbances that are manifested in tobacco smoke-related diseases, such as chronic obstructive pulmonary disease. Measuring tissue responses directly relevant to the respiratory toxicity of cigarette smoke may provide useful information in support of science-based regulatory decisions.
许多与香烟烟雾相关的气道疾病都涉及粘蛋白动态平衡的改变。我们的基本原理是,可以通过测量相关组织反应来评估烟草制品对健康的不良影响,因此,我们评估了在体外人液-气界面 (ALI) 气道组织模型中,暴露于香烟烟雾溶液后粘蛋白分泌以及杯状细胞的密度和大小的变化。使用加拿大强化(CI)方案,通过机器吸烟万宝路红(Marlboro Red)或万宝路银(Marlboro Silver)香烟来制备全烟雾溶液(WSS),然后对培养物进行连续 5 天的每日暴露。两种 WSS 均诱导粘蛋白 5AC 和 5B 的浓度和时间依赖性高分泌,同时相应的粘蛋白基因上调。在 14 天恢复期后,粘蛋白分泌恢复到基线水平。在 5 天的治疗后,分泌粘蛋白的杯状细胞的细胞密度增加,细胞体积减小,而在最后一次治疗 14 天后,细胞恢复到正常大小,但细胞密度降低。纤毛细胞的跳动频率增加,纤毛细胞在粘液纤毛清除中起着关键作用,而在经过 5 天的 CI WSS 处理后,纤毛细胞的跳动频率又恢复到基线水平,然后在 7 天的恢复期后恢复到基线水平。总之,我们的研究结果表明,ALI 培养物可用于测量粘蛋白产生、分泌和清除的调节,这些调节在与香烟烟雾相关的疾病(如慢性阻塞性肺疾病)中表现出来。直接测量与香烟烟雾呼吸毒性相关的组织反应可能为基于科学的监管决策提供有用的信息。