Am. J. Respir. Cell Mol. Biol., Vol 11, No. 5, 11 1994, 568-576.
Primary and immortalized (BEAS 2B) human bronchial epithelial cells have significant antioxidative capacity in vitro
VL Kinnula, JR Yankaskas, L Chang, I Virtanen, A Linnala, BH Kang and JD Crapo
Department of Pulmonary Medicine, Duke University Medical Center, Durham, North Carolina 27710.
Antioxidant enzymes located in the bronchial epithelium can be expected to
be important in protecting these cells against both endogenous and
exogenous oxidants. In this study, human bronchial epithelial cells were
isolated and cultured from specimens obtained from donors for lung
transplantation. The levels and relative importance of different
antioxidant enzymes were also assessed using an immortalized human
bronchial epithelial cell line (BEAS 2B cells). Immunocytochemical studies
showed a similar pattern of intracellular localization with the moderate
degrees of labeling for Mn superoxide dismutase (SOD), CuZn SOD, and
catalase in freshly isolated bronchial epithelial cells, bronchial
epithelial cells in primary culture, and BEAS 2B cells. CuZn SOD and
catalase decreased in labeling density whereas Mn SOD was unchanged when
bronchial epithelial cells were placed in primary cultures. In contrast, Mn
SOD and catalase were decreased in BEAS 2B cells compared with primary
cultures. Although Mn SOD was low in BEAS 2B cells, it could be
significantly induced by tumor necrosis factor treatment. Biochemical
analysis showed remarkably similar catalase and glutathione reductase
activities in primary cultured epithelial cells and BEAS 2B cells.(ABSTRACT
TRUNCATED AT 250 WORDS)
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Copyright © 1994 American Thoracic Society.
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