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Fig. 8. Rho and Cdc42, but not Rac 1, are involved in actin polymerization induced
by N. meningitidis. Confluent monolayers of HUVECs were either left
untreated (control), treated with 30 µM Y27632 prior to the infection and
during the infection (Y27632), microinjected with the recombinant exoenzyme C3
of C. botulinum 2 hours before cell infection (C3) or microinjected
with the cDNA encoding a dominant-negative form of Rac (RacN17) or
Cdc42 (Cdc42N17) 18 hours or 5 hours prior to infection of the
monolayer, respectively. Cells were then infected for 4 hours and labeled for
bacteria, F-actin and myc tag. The percentages of bacterial colonies
associated with polymerized actin were determined by immunofluorescence
analysis. Each condition was compared with non-treated cells infected in the
same conditions. Results correspond to counts of 1600 infected cells in 3 to
10 distinct experiments per condition.