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Vol. 11, Issue 7, 2497-2511, July 2000


and
*European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany; The simpler of the two infectious forms of vaccinia virus, the
intracellular mature virus (IMV) is known to infect cells less efficiently than the extracellular enveloped virus (EEV), which is
surrounded by an additional, TGN-derived membrane. We show here that
when the IMV binds HeLa cells, it activates a signaling cascade that is
regulated by the GTPase rac1 and rhoA, ezrin, and both tyrosine and
protein kinase C phosphorylation. These cascades are linked to the
formation of actin and ezrin containing protrusions at the plasma
membrane that seem to be essential for the entry of IMV cores. The
identical cores of the EEV also appear to enter at the cell surface,
but surprisingly, without the need for signaling and actin/membrane
rearrangements. Thus, in addition to its known role in wrapping the IMV
and the formation of intracellular actin comets, the membrane of the
EEV seems to have evolved the capacity to enter cells silently, without
a need for signaling.
Heinrich Pette Institute,
Martinistrasse 52, 2000 Hamburg, Germany; and
Beiersdorfs AG, Unnastrasse 48, 20245 Hamburg, Germany
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