Alveolar macrophages are thought to be important in immune or inflammatory reactions. We investigated the role of alveolar macrophages in defense against Pseudomonas aeruginosa infection in the lower respiratory tract. Intratracheal inoculation of formalin-inactivated P. aeruginosa (1 x 10(8)-1 x 10(10) organisms) into normal rats resulted in increase in the number of neutrophils in the bronchoalveolar lavage (BAL) fluid obtained 24 h later. The phagocytic activity of neutrophils for P. aeruginosa was higher than that of alveolar macrophages. These findings indicate that neutrophils are essential for phagocytosis of P. aeruginosa in the lower respiratory tract. On incubation with P. aeruginosa, alveolar macrophages released neutrophil chemotactic factor (NCF) dose-dependently. MDP-Lys(L18), a muramyl dipeptide analog, stimulated alveolar macrophages to phagocytize P. aeruginosa and stimulate the release of NCF from alveolar macrophages in vitro and enhanced the neutrophil response to inoculated P. aeruginosa in vivo. These results indicate that alveolar macrophages are important in initiating the neutrophil-dependent defense system against P. aeruginosa by releasing NCF and that MDP-Lys(L18) can amplify the defense system.

We fabricated sub-10-µm-class short-channel, top-gate carbon nanotube thin-film transistors using a flexographic printing technique, which is a high-speed printing technique that uses a flexible polymer plate. This device fabrication process is completely photolithography-free and vacuum-free as a result of the printing technique. The printing resolution was improved by using micro-flexo plates fabricated by a microprocessing technique. The fabricated device, with a channel length of 9.5 µm, exhibited a high on-current of 0.94 mA/mm. Hysteresis was suppressed by introducing a top-gate structure.

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