Neutrophil serine proteases: specific regulators of inflammation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Energy Engineering and Power Technology,Fuel Technology
Link
http://www.nature.com/articles/nri1841.pdf
Reference104 articles.
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2. Faurschou, M. & Borregaard, N. Neutrophil granules and secretory vesicles in inflammation. Microbes Infect. 5, 1317–1327 (2003).
3. Belaaouaj, A. et al. Mice lacking neutrophil elastase reveal impaired host defense against gram negative bacterial sepsis. Nature Med. 4, 615–618 (1998). The first study to show that mice deficient in neutrophil elastase are more susceptible to infection with Gram-negative bacteria than wild-type mice.
4. Reeves, E. P. et al. Killing activity of neutrophils is mediated through activation of proteases by K+ flux. Nature 416, 291–297 (2002). This paper provides a new working model that features neutrophil serine proteases, not ROS, as the main agents responsible for the intracellular killing of bacteria.
5. Tkalcevic, J. et al. Impaired immunity and enhanced resistance to endotoxin in the absence of neutrophil elastase and cathepsin G. Immunity 12, 201–210 (2000). This study shows that, compared with wild-type mice, mice deficient in cathepsin G and neutrophil elastase are more susceptible to certain fungal infections but more resistant to LPS-induced septic shock.
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