In vivo effects of endotoxin on DNA synthesis in rat nasal epithelium

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Abstract
Airway inflammation in bacterial infections is characterized by the presence of neutrophils and often epithelial injury and repair. Release of endotoxin from bacteria may contribute to these processes. The purpose of this study was to determine the in vivo effects of repeated endotoxin exposure on DNA synthesis in rat nasal epithelium in the presence and absence of neutrophilic influx. Rats were intranally instilled, once a day for 3 days, with endotoxin or saline (controls). Before the first and third instillations, half of the saline and endotoxin‐instilled animals were depleted of circulating blood neutrophils by administering a rabbit anti‐rat neutrophil antiserum. Rats were sacrificed 6 or 24 h after the last instillation. Two hours prior to sacrifice, rats were intraperitoneally injected with bromodeoxyuridine (BrdU), an analog of thymidine that is incorporated in the nucleus of cells in the S‐phase of the cell cycle. Nasal tissues were processed for light microscopy and immunohistochemical detection of BrdU in nasal epithelial cells. The numbers of nasal epithelial cells, BrdU‐labeled epithelial nuclei, and neutrophils per millimeter of basal lamina in the epithelium lining the nasal turbinates in the proximal nasal passages were determined by morphometric analysis. We did not observe a neutrophilic influx in the nasal tissues of neutrophil‐depleted rats at 6 or 24 h after the last endotoxin instillation; however, the numbers of nasal epithelial cells and the BrdU‐labeling index were significantly increased compared to salineinstilled controls. In controls. In contrast, non‐neutrophil‐depleted rats instilled with endotoxin had a marked neutrophilic influx, but no significant differences in the number of nasal epithelial cells at 6 or 24 h, compared to controls. In addition, the BrdU‐labeling index in neutrophil‐sufficient rats was increased only 6 h after the last instillation, compared to controls. These results indicate that 1) endotoxin induces an increase in epithelial DNA synthesis that is neutrophil‐independent, and 2) without a neutrophilic influx, there is sustained epithelial proliferation, resulting in a hyperplastic epithelium after repeated endotoxin exposure. © 1993 Wiley‐Liss, Inc. †

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