Boucher R C
Environ Health Perspect. 1980 Apr;35:3-11. doi: 10.1289/ehp.80353.
The mucosal surface of the conducting airways has specialized structures for respiratory defense. Glands secret mucus that may act as a barrier to particle penetration and participate in particle clearance. Intraepithelial irritant receptors aid in particle clearance through airway constriction and cough. The epithelium acts as a barrier to the penetration of inhaled material into the airway wall. Morphologic studies have identified the tight junctions adjoining respiratory epithelial cells as the principal barrier to passive solute translocation across the airway. New approaches have been used to study airway epithelial function. Use of excised canine trachea mounted in Ussing chambers has permitted quantitative estimates of probe molecule permeation, the correlation of permeability with bioelectric properties, and estimation of equivalent pore radii. Probe molecule diffusion across canine trachea [mean transmucosal electric potential difference (PD) = 33 mV, lumen negative] is directly related to conductance (2.9 mS/cm2) and is compatible with an equivalent pore radius of 7.5 nm. Direct measurement of tracheal PD in vivo (-29 mV) facilitates study of the genesis of the biopotential in intact animals. Measurement of the movement of HRP by radioimmunoassay has allowed correlation of the rate of probe flow across airway walls in vivo with ultrastructure. These approaches lend themselves to the study of pharmacologic and toxicologic effects on epithelial function. Antigen challenge, diethyl ether, and unfractionated cigarette smoke have been shown to increase epithelial permeability to HRP accompanied by ultrastructural evidence of tight junctional damage. Application of pharmacologic agents, e.g. amphotericin, ouabain, onto the respiratory epithelium induces similar changes in in vitro and in vivo PD. We conclude that techniques that have been used to measure permeability and transport in other epithelia may help elucidate modes of action of environmental agents on airways.
传导气道的黏膜表面具有专门的呼吸防御结构。腺体分泌黏液,黏液可作为颗粒渗透的屏障并参与颗粒清除。上皮内刺激感受器通过气道收缩和咳嗽辅助颗粒清除。上皮作为吸入物质穿透气道壁的屏障。形态学研究已确定相邻呼吸上皮细胞间的紧密连接是被动溶质跨气道转运的主要屏障。已采用新方法来研究气道上皮功能。使用安装在尤斯灌流小室中的离体犬气管,可对探针分子渗透进行定量评估、渗透性与生物电特性的相关性研究以及等效孔径半径的估计。探针分子在犬气管上的扩散[平均跨黏膜电位差(PD)= 33 mV,管腔为负]与电导(2.9 mS/cm²)直接相关,且与7.5 nm的等效孔径半径相符。体内直接测量气管PD(-29 mV)有助于研究完整动物中生物电位的产生机制。通过放射免疫测定法测量辣根过氧化物酶(HRP)的移动,可使体内探针跨气道壁流动速率与超微结构相关联。这些方法有助于研究对上皮功能的药理和毒理作用。已表明抗原激发、乙醚和未分级香烟烟雾可增加上皮对HRP的通透性,并伴有紧密连接损伤的超微结构证据。将药理试剂,如两性霉素、哇巴因,应用于呼吸道上皮,可在体外和体内诱导PD发生类似变化。我们得出结论,用于测量其他上皮通透性和转运的技术可能有助于阐明环境因素对气道的作用方式。