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Infection and Immunity, July 1999, p. 3390-3398, Vol. 67, No. 7
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Mycoplasmal Lipopeptide MALP-2 Induces the Chemoattractant
Proteins Macrophage Inflammatory Protein 1
(MIP-1
), Monocyte
Chemoattractant Protein 1, and MIP-2 and Promotes Leukocyte
Infiltration in Mice
Ursula
Deiters, and
Peter F.
Mühlradt*
Immunobiology Research Group, Gesellschaft
für Biotechnologische Forschung mbH, D-38124 Braunschweig,
Germany
Received 29 January 1999/Returned for modification 17 March
1999/Accepted 22 April 1999
Natural as well as experimental infections with pathogenic
mycoplasmas lead to cellular responses characterized by early
polymorphonuclear leukocyte influx, which in turn is followed by
infiltration of macrophages. Since some of the most potent leukocyte
chemoattractants are macrophage products, we investigated whether the
2-kDa macrophage-activating lipopeptide (MALP-2) from Mycoplasma
fermentans was capable of inducing chemoattractant chemokines and
initiating an in vivo inflammatory effect. MALP-2 was a potent in
vitro inducer of the chemokines macrophage inflammatory protein
1
(MIP-1
), monocyte chemoattractant protein 1 (MCP-1), and
MIP-2, yielding a maximal response at 0.1 ng/ml (5 × 10
11 M). Leukocyte infiltration was
determined after intraperitoneal injection of MALP-2,
liposome-encapsulated MALP-2, and heat-killed mycoplasmas. There was a
steady increase in the number of peritoneal cells over 72 h in
response to these agents. Polymorph counts were maximal by 24 to
48 h, decreasing thereafter. Monocytes/macrophages had
significantly increased after 3 days. MIP-1
, MCP-1, and MIP-2 levels
in serum or peritoneal lavage fluid were determined. MIP-1
and MCP-1
levels were elevated by 2 to 6 h after injection and were still
above control values after 24 h. In contrast, MIP-2 levels reached
their maximum at 2 h, dropping to control values after 24 h.
We conclude that macrophage-stimulating mycoplasmal lipoproteins,
exemplified by MALP-2, play an important role in the late phase of
phagocyte recruitment at sites of infection and that this is affected
by leukoattractive chemokines.
*
Corresponding author. Mailing address: Immunobiology
Research Group, Gesellschaft für Biotechnologische Forschung mbH,
Mascheroder Weg 1, D-38124 Braunschweig, Germany. Phone:
49-531-6181-240. Fax: 49-531-6181-284. E-mail: PFM{at}GBF.de.
Infection and Immunity, July 1999, p. 3390-3398, Vol. 67, No. 7
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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