Orthogonal arrays are found on plasma membranes of glial cells, in the central nervous system, on muscle plasma membranes at neuromuscular junctions, and on a variety of epithelial cells. These structures have been correlated with ion flux. With the aid of freeze fracture technique, orthogonal particle arrays were found on plasma membranes on airway epithelial cells of rats and hamsters. They have been found in abundance at the base of secretory cells throughout normal airway epithelium. These structures were found to increase in number during regeneration in response to injury and they were found in great numbers on plasma membranes of all airway cells in response to acute and chronic NO2 exposure. The lateral and basal plasma membranes of the respiratory epithelium are a new source for studying orthogonal arrays. The normal number and distribution of these arrays can be perturbed in response to mechanical and chemical injury.Orthogonal particle assemblies (rectangular arrays) are closely packed 6-nm intramembrane particles arranged in a square lattice. These assemblies have been found on the P-face of freeze-fractured plasma membranes of a variety of cells (1-11). Mammalian astrocytes, in particular, can be identified in freeze fractures by the abundance of these structures on their plasma membrane (12).The biochemical nature of these particles and their function in the membrane have not been determined. It has been speculated that these structures are associated with ion flux, at least in astrocytes (13).In this report we describe a rich source for these orthogonal structures in respiratory epithelium of rats and hamsters. We also describe conditions that increase their abundance, thereby perhaps providing a mechanism whereby these structures could be biochemically characterized and their function determined.
MATERIALS AND METHODS20 male Syrian Golden hamsters weighing -60 g for the chronic study and 125 g for the acute study were divided into two groups. One group of eight animals was exposed to NO2:2 for 6 h, 2 for 24 h, 2 for 48 h, and the last 2 remained as controls breathing room air. The second group of 12 animals was exposed to NO2:2 for 1 mo, 2 for 5 mo, 2 for 9 mo, and the remaining six animals were used as unexposed age controls, two animals corresponding to each exposure period (1, 5, and 9 mo).Rationale for NOz Exposure: NO2 is a noxious gas that has been known to cause emphysematous lesions in rats (14) and hamsters (15). We have been using continuous NO2 exposure in hamsters as an animal model for the study of the development and progression of lesions caused by this agent in bronchioles and alveolar epithelium. During the studies in which we examined barrier function disruption of respiratory epithelium we made the observations reported in this manuscript.
NO2 Exposure Techniques:The exposure groups were treated with NO2 at concentrations of 30 ppm for 22 h per day, 7 d per wk. 30 ppm was chosen because it was low enough not to cause death and yet high enough to cause a consistent lesi...