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Journal of Virology, August 2000, p. 7211-7220, Vol. 74, No. 16
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Lentivirus Infection in the Brain Induces Matrix
Metalloproteinase Expression: Role of Envelope Diversity
J. B.
Johnston,1
Y.
Jiang,1
G.
van
Marle,1
M. B.
Mayne,2
W.
Ni,1
J.
Holden,3
J. C.
McArthur,4 and
C.
Power1,2,*
Department of Clinical Neuroscience,
University of Calgary, Calgary, Alberta,1
Department of Pharmacology and Therapeutics, University of
Manitoba, Winnipeg, Manitoba,2 and
Department of Pathology, St. Paul's Hospital, Vancouver,
British Columbia,3 Canada, and
Department of Neurology, Johns Hopkins University,
Baltimore, Maryland4
Received 24 February 2000/Accepted 22 May 2000
Infection of the brain by lentiviruses, including human
immunodeficiency virus (HIV) and feline immunodeficiency virus (FIV), causes inflammation and results in neurodegeneration. Molecular diversity within the lentivirus envelope gene has been implicated in
the regulation of cell tropism and the host response to infection. Here, we examine the hypothesis that envelope sequence diversity modulates the expression of host molecules implicated in
lentivirus-induced brain disease, including matrix metalloproteinases
(MMP) and related transcription factors. Infection of primary
macrophages by chimeric HIV clones containing brain-derived envelope
fragments from patients with HIV-associated dementia (HAD) or
nondemented AIDS patients (HIV-ND) showed that MMP-2 and -9 levels in
conditioned media were significantly higher for the HAD clones.
Similarly, STAT-1 and JAK-1 levels were higher in macrophages infected
by HAD clones. Infections of primary feline macrophages by the
neurovirulent FIV strain (V1CSF), the less neurovirulent
strain (Petaluma), and a chimera containing the V1CSF
envelope in a Petaluma background (FIV-Ch) revealed that MMP-2 and -9 levels were significantly higher in conditioned media from
V1CSF- and FIV-Ch-infected macrophages, which was
associated with increased intracellular STAT-1 and JAK-1 levels. The
STAT-1 inhibitor fludarabine significantly reduced MMP-2 expression,
but not MMP-9 expression, in FIV-infected macrophages. Analysis of MMP
mRNA and protein levels in brain samples from HIV-infected persons or
FIV-infected cats showed that MMP-2 and -9 levels were significantly
increased in lentivirus-infected brains compared to those of uninfected
controls. Elevated MMP expression was accompanied by significant
increases in STAT-1 and JAK-1 mRNA and protein levels in the same brain
samples. The present findings indicate that two lentiviruses, HIV and
FIV, have common mechanisms of MMP-2 and -9 induction, which is
modulated in part by envelope sequence diversity and the STAT-1/JAK-1
signaling pathway.
*
Corresponding author. Mailing address: Department of
Clinical Neurosciences, HMRB 150, 3330 Hospital Dr. NW, University of Calgary, Calgary, Alberta T2N 4N1, Canada. Phone: (403) 220-5572. Fax:
(403) 283-8731. E-mail: power{at}ucalgary.ca.
Journal of Virology, August 2000, p. 7211-7220, Vol. 74, No. 16
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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