Mesoporous silica films work as templates to form uniform nanoparticles of Au and Pt. The composite materials form an array of metal nanoparticles (diameter ca. 2.5 nm) in the one-dimensional mesopores (pore diameter 2.7 nm), showing an ordered structure in the TEM observation. The nanoparticles are isolated from the silica film by dissolving with a diluted HF solution, and in the presence of 1-dodecanethiol unsupported Au nanoparticles form a superlattice structure.
Complement-mediated pulmonary edema results from increases in lung capillary hydraulic conductivity (Lp), possibly by receptor-mediated mechanisms. We considered the Lp effects of vitronectin and the vitronectin-containing complement complex SC5b-9, which ligate the integrin α
v
β
3
. Vitronectin, SC5b-9, and SC5b-9–enriched zymosan-activated serum all rapidly increased Lp, as determined by the split-drop technique in single lung capillaries of rat lung. The Lp increases were inhibited by a monospecific (LM609) and a polyclonal (R838) antibody against the α
v
β
3
integrin but not by an irrelevant monoclonal antibody isotype matched with LM609, by a monoclonal antibody against the α
v
β
5
integrin, or by preimmune rabbit serum. Vitronectin monomers failed to increase Lp. The tyrosine kinase blockers genistein and methyl 2,5-dihydroxycinnamate caused significant concentration-dependent inhibitions of Lp increases due to vitronectin and zymosan-activated serum. By contrast, the protein kinase C blocker calphostin C had no major effect. We conclude that (1) multivalent ligation of the luminally located α
v
β
3
integrin of lung capillary endothelium increases transcapillary liquid flux, and (2) the dominant signal transduction pathway for this effect occurs through tyrosine kinase activation.
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