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Departments of
*
Microbiology and Immunology and
Endodontics and Periodontics, Tohoku University School of Dentistry, Sendai, Japan;
Department of Immunology, Saga Medical School, Saga, Japan; and
§
Division of Molecular Pathology, Department of Neuroscience and Immunology, Kumamoto University Graduate School of Medical Science, Kumamoto, Japan
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Abstract |
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 Top Abstract IntroductionMaterials and MethodsResultsDiscussionReferences |
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production by monocytes after HRGP
and KGP treatments was decreased at 1 ng/ml, but not at 20 µg/ml LPS,
indicating that gingipains inhibited a CD14-dependent cell activation.
These results suggest that gingipains preferentially cleave monocyte
CD14, resulting in attenuation of the cellular recognition of bacteria,
and as a consequence sustain chronic inflammation. |
Introduction |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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It is now clear that all of the trypsin-like proteinase activity of P. gingivalis is due to two cysteine proteinases (4). Two types of cysteine proteinases specific for Arg-X (50 and 95 kDa) (5) and Lys-X (105 kDa) bonds have been purified and characterized and are referred to as arginine-specific gingipain (RGP)3 (3) and lysine-specific gingipain (KGP), respectively (6). The 95-kDa high molecular mass RGP (HRGP or HRgpA) differs from the 50-kDa RGP (RGP2 or RgpB) in that the protein noncovalently complexes with the hemagglutinin/adhesin domain in the same manner as KGP. It has been shown that gingipains play a critical role in the onset of inflammation through enhancement of vascular permeability by activation of the kallikrein/kinin pathway (7, 8), dysregulation of plasma clot formation (9, 10, 11), activation of complement components (12), and modification of neutrophil function (13). Gingipains are also indispensable for the expression of P. gingivalis fimbriae, an important cell surface structure of this bacterium for adhesion and colonization, through normal processing of immature fimbrilin (14).
CD14, mainly expressed on monocytes, functions as a major receptor for LPS (15, 16). CD14 also exists in serum as a soluble protein (soluble CD14), and a complex of soluble CD14 and LPS activates CD14-negative cells, such as endothelial and epithelial cells (17, 18). We showed recently that human gingival fibroblasts heterogeneously express CD14 and the CD14-expressed fibroblasts secrete IL-8 in response to LPS in a CD14-dependent manner (19, 20). It was shown that CD14 acts as a pattern recognition receptor for many bacterial components in addition to LPS (21, 22). As CD14 is a 55-kDa GPI-anchored membrane protein that lacks transmembrane and cytoplasmic domains (23), CD14 itself does not elicit intracellular signaling (16). The Toll-like receptors (TLRs) of vertebrates, homologues of Drosophila Toll, have been implicated in the innate immune response in vertebrates (24), and it has recently been shown that TLR2 and TLR4 mediated the entry of LPS signal into the cells of human and mouse (25, 26, 27, 28, 29, 30).
Activation of monocytes through CD14/TLR by LPS and other bacterial components leads to the production of numerous inflammatory mediators, and the activated monocytes/macrophages and the released mediators function as the first line of defense against infectious bacteria. Adult periodontitis is characterized by the phases of chronic and sometimes active destruction of periodontal tissues with marked inflammation, followed by periods of remission, which leads to the hypothesis that P. gingivalis could evade immune surveillance by monocytes by cleaving bacterial recognition molecule(s) on monocytes using the bacterial proteinases and survive in periodontal tissues. In this study, we examined this hypothesis and showed that P. gingivalis cysteine proteinases, both KGP and RGP, preferentially cleave human monocyte CD14, but not TLR4, and as a consequence, inhibit a CD14-dependent monocyte activation pathway triggered by LPS.
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Materials and Methods |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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Phe-Pro-Arg-chloromethyl ketone (FPR-cmk) and benzyloxycarbonyl-Phe-Lys-chloromethyl ketone (Z-FK-cmk) were obtained from Bachem Bioscience (King of Prussia, PA). Phosphatidylinositol phospholipase C (PI-PLC) from Bacillus cereus and BSA fraction V were obtained from Boehringer Mannheim (Mannheim, Germany). Human leukocyte elastase (HLE) was obtained from Calbiochem-Novabiochem (San Diego, CA). Anti-TLR4 mAb HTA125 was raised by immunizing BALB/c mice with the Ba/F3 line expressing TLR4 and fusing spleen cells with SP2/0 (30). FITC-conjugated anti-CD14 mAb MY4 and all isotype control mAbs were obtained from Coulter (Miami, FL). Anti-CD18 FITC and anti-CD54 FITC were obtained from Becton Dickinson Immunocytometer System (San Jose, CA), and anti-CD59 FITC and anti-HLA-A, -B, -C FITC were obtained from PharMingen (San Diego, CA). Human rCD14 was obtained from Biometec (Geifswald, Germany). An ultrapurified LPS prepared from Salmonella abortusequi (Novo-Pyrexal) (31) was a gift from Dr. C. Galanos (Max Planck Institut für Immunbiologie, Freiburg, Germany). All other reagents were obtained from Sigma (St. Louis, MO), unless otherwise indicated.
Purification and activation of gingipains
Three forms of gingipains, 95-kDa HRGP, 50-kDa RGP2, and 105-kDa KGP, were purified from P. gingivalis HG66 culture supernatant, as described by Pike et al. (6). The amount of active enzyme in each purified proteinase was determined by active site titration using FPR-cmk and Z-FK-cmk for RGP and KGP, respectively (32). The concentration of fully activated gingipains with cysteine was calculated from the amount of inhibitors needed for complete inactivation of the proteinases. Therefore, the concentration of gingipains indicated in this study was represented as that of active gingipains. To activate gingipains, gingipains were diluted to 10 µM in 0.2 M HEPES, 5 mM CaCl2, and 10 mM cysteine, pH 8, and incubated at 37°C for 10 min. The activated gingipains were then diluted with medium or buffer. To block enzyme activity of gingipains, activated gingipains were incubated with the specific inhibitors, FPR-cmk and Z-FK-cmk, for 10 min at room temperature before use.
Cell and cell treatment
Human PBMCs were isolated from heparinized peripheral blood of healthy adult donors by Lympholyte-H (Cedarlane Laboratories, Ontario, Canada) gradient centrifugation at 800 x g for 20 min at room temperature (19). The isolated PBMCs were washed three times with PBS and suspended in RPMI 1640 medium (Nissui, Tokyo, Japan). PBMCs were treated with given concentrations of gingipains at 5 x 105 cells/50 µl at 37°C. After the treatment, cells were washed three times with ice-cold PBS at 4°C. For the inhibition experiment by human serum, gingipains and HLE were incubated with indicated doses of freshly isolated human serum at room temperature for 10 min before use. For the fixation of the cells, cells were treated with 1% w/v paraformaldehyde in PBS for 15 min at room temperature and then washed extensively. In some experiments, monocytes were purified from PBMCs by allowing them to adhere to plastic dishes (Falcon; Becton Dickinson Labware, Franklin Lakes, NJ) for 1 h at 37°C. After removal of nonadherent cells, monocytes were collected by treatment with 0.2% EDTA in PBS for 20 min at 4°C, and washed with ice-cold RPMI 1640 medium.
Flow cytometry
Flow-cytometric analyses were performed using a FACScan cytometer (Becton Dickinson, Mountain View, CA), as described (20). Briefly, cells were stained with FITC-conjugated mAbs or FITC-conjugated isotype-matched mouse IgG at 4°C for 30 min. For TLR4 staining, cells were stained with HTA125 or isotype control IgG at 4°C for 30 min, and then incubated with FITC-conjugated goat anti-mouse IgG (BioSource International, Camarillo, CA) at 4°C for an additional 30 min. The mean fluorescence intensity of monocytes was analyzed by gating on the basis of forward and side scatter characteristics.
Reexpression of CD14 after gingipain treatment
PBMCs (106 cells) were treated with or without 100 µl of 0.3 µM KGP or HRGP for 15 min at 37°C. After the treatment, cells were washed three times with ice-cold PBS at 4°C, and resuspended in 1 ml of RPMI 1640 medium supplemented with 10% FCS. Then cells were added in a 24-well plate (Falcon) and incubated at 37°C in a 5% CO2 incubator. At the time indicated, cells were collected by brief treatment with 0.25% trypsin/1 mM EDTA (Life Technologies, Grand Island, NY), and expression of CD14 on monocytes was analyzed by flow cytometry, as described above. Preliminary experiment showed that trypsinization did not affect the expression of CD14.
CD14 detection by Western blotting
Purified human monocytes were suspended at 5 x 105 cells/200 µl in a medium containing 0.3 µM KGP, 0.3 µM HRGP, or 1 U/ml PI-PLC, and treated for 15 min at 37°C. Reactions were stopped with 3 µM Z-FK-cmk for KGP and 3 µM FPR-cmk for HRGP. After centrifugation at 4°C, the medium was removed and dried by a vacuum centrifuge. Cell pellets and the dried materials were solubilized with Laemmli sample buffer (33). SDS-PAGE was performed in a 10% polyacrylamide slab gel containing 0.1% SDS under reducing conditions, according to the method of Laemmli (33). Proteins were transferred to a polyvinylidene difluoride (PVDF) membrane (ATTO, Tokyo, Japan) by a semidry transblot system (ATTO). The blot was blocked for 2 h with 3% BSA/PBS and incubated with 2 µg/ml sheep anti-human CD14 polyclonal Ab (Genzyme/Techne, Minneapolis, MN) in 3% BSA/PBS overnight at 4°C. The blot was washed four times with PBS and then incubated for 2 h with HRP-conjugated affinity-purified donkey anti-sheep IgG (Jackson ImmunoResearch, West Grove, PA) at 1:2000 in 3% BSA/PBS. After being washed, CD14 was visualized with diaminobenzidine. The Mr of the proteins was estimated by comparison with the position of a standard (Bio-Rad Laboratories, Hercules, CA).
Time course of digestion
For the enzymatic digestion of rCD14, a reaction mixture containing 364 nM rCD14 and 3.6 nM active enzymes at an enzyme:substrate (E:S) molar ratio of 1:100 in 0.1 M Tris-HCl, pH 7.6, containing 150 mM NaCl and 5 mM CaCl2, was incubated at 37°C. At the time point indicated, aliquots (2.5 µl) were removed and mixed with Laemmli sample buffer. Samples were then subjected to 12.5% SDS-PAGE under reducing conditions and transferred to a PVDF membrane. The membrane was probed with polyclonal anti-CD14 Ab.
TNF- production
PBMCs were treated with 0.3 µM gingipains at 1 x
106 cells/100 µl in the presence or absence of
3 µM specific inhibitors, i.e., Z-FK-cmk for KGP and FPR-cmk for
HRGP, for 15 min at 37°C. After the treatment, cells were washed
twice with RPMI 1640 medium, and seeded in a 96-well flat-bottom plate
(Falcon) at 5 x 105 cells/well in the
medium with 10% FCS. After 1-h incubation at 37°C, nonadherent cells
were removed by washing twice with warmed medium, and adherent
monocytes were stimulated with LPS for 3 h at 37°C. For the
inhibition experiment with anti-TLR4 mAb HTA125, adherent monocytes
were preincubated with HTA125 (10 µg/ml) or isotype control mouse
IgG2a (10 µg/ml) for 30 min at 37°C and then stimulated with LPS
for 3 h at 37°C. The TNF- concentration in the supernatant
was determined with an OptEIA human TNF- ELISA set (PharMingen),
according to the manufacturer’s protocol. Each sample was assayed in
triplicate.
Statistical analysis
All of the experiments in this study were conducted at least three times. The data shown are representative results. Experimental values are given as means ± SD. The statistical significance of differences between two means was evaluated by Student’s unpaired t test, and p values less than 0.05 were considered significant.
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Results |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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The effect of P. gingivalis cysteine proteinases, KGP,
HRGP, and RGP2, on the expression of CD14 on human monocytes was
evaluated by flow-cytometric analysis. When cells were treated with 0.3
and 1 µM KGP and HRGP, the binding of anti-CD14 mAb MY4 to
monocytes was almost completely abolished on 15-min treatment (Fig. 1
, A and B). Fig. 1A showed the representative FACS profiles of CD14
expression on monocytes after KGP and HRGP treatments for 15 min. HRGP
at 0.1 µM was still effective in elimination of MY4 binding to
monocytes, but this effect was weakened at 0.1 µM KGP. By contrast,
the effect of RGP2 on the elimination of MY4 binding to human monocytes
was weaker than that of KGP and HRGP, and 30-min treatment with 1 µM
RGP2 was required for the complete elimination of the binding. It is
notable that the cellular viability of PBMCs after treatments with all
three gingipain at 1 µM was more than 90% at 1 h and more than
80% at 2 h, as assessed by a 0.2% trypan blue exclusion test,
showing that gingipains have a weak potential cytotoxicity. The
elimination of surface molecules on monocytes by gingipain treatment
was preference for CD14, because the expressions of TLR4, and CD18,
CD54, CD59, and HLA-A, -B, -C were slightly increased and decreased,
respectively, by both 0.3 µM HRGP and KGP treatments (Fig. 2).
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To confirm that the elimination of MY4 binding was due to the
enzymatic activity of gingipains, inhibitors specific for gingipains,
as reported by Pike et al. (6) and Potempa et al.
(32), were employed. FPR-cmk, an effective inhibitor of
KGP and RGP, efficiently inhibited both KGP and HRGP activities at a
10-fold molar excess amount (Table I).
Z-FK-cmk, a specific inhibitor of KGP, completely inhibited KGP
activity, which was consistent with previous observations (6, 32). Because human serum is a rich source of various proteinase
inhibitors, the effect of human serum on CD14 reduction by KGP and HRGP
was examined. As shown in Fig. 3, the
reduction of CD14 by 0.3 µM KGP and HRGP for 15-min treatment was
still significantly effective in the presence of 10% v/v human serum.
By contrast, the reduction of CD14 induced by 1 µM HLE for 30-min
treatment, as reported previously (34), was completely
inhibited in the presence of 10% serum. After the treatment with KGP
and HRGP, CD14 was gradually reexpressed on the cell surface, and more
than 90% of the cell surface CD14 was recovered at 48 h (Fig. 4).
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These results suggested that the preferential reduction of CD14
most likely resulted from direct proteolysis, but raised two other
possible mechanisms of this effect. A possible mechanism of the effect
of gingipains is that CD14 is shed by an endogenous enzymatic activity
after monocyte activation by gingipains, as suggested by Bazil and
Strominger (35). To examine this possibility, the effect
of fixation with 1% paraformaldehyde on the elimination of MY4 binding
to monocytes was analyzed by flow cytometry. When cells were incubated
with 20 nM PMA for 60 min, a marked reduction in the binding was
observed, and fixation of the cells inhibited the down-modulation of
the surface CD14 (Fig. 5). These results
indicate that fixation blocked the shedding of surface CD14 by the
endogenous cellular enzymatic activity, as described (35).
By contrast, all three gingipains efficiently down-modulated the
binding of MY4 to fixed as well as unfixed monocytes, indicating that
gingipains directly cleave surface CD14 on the cells.
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Another possible explanation for the effect of gingipains is an
augmentation of CD14 internalization. To examine this possibility,
purified human monocytes were treated with KGP and HRGP, and cells and
the supernatants were analyzed by Western blotting using anti-CD14
polyclonal Ab. PI-PLC, an enzyme that specifically cleaves GPI-anchored
protein (23), was used as a positive control. Untreated
monocytes expressed a strong 55-kDa CD14 band, whereas the band was not
detected after 0.3 µM KGP and HRGP treatments and a strong reduction
of cell-associated CD14 was observed after 1 U/ml PI-PLC treatment
(Fig. 6A). In addition, five
bands with an Mr of about 50, 40, 26,
19, and 18 kDa and one band with an Mr
of about 19 kDa were revealed after 0.3 µM KGP and HRGP treatments
for 15 min, respectively. In the extracellular medium, a strong 55-kDa
band was detected after PI-PLC treatment, whereas a strong 48-kDa and a
weak 37-kDa band, and a strong 44-kDa and a weak 19-kDa band were
detected after 0.3 µM KGP and HRGP treatments for 15 min,
respectively (Fig. 6B). These results indicate that
gingipains directly cleave CD14 on monocytes and release CD14
fragments, and the digested fragments of CD14 still exist on the cell
surface especially after 0.3 µM KGP treatment for 15 min. The fact
that no 55-kDa CD14 was recovered from monocytes, that CD14 fragments
were detected in the extracellular medium after gingipain treatments,
and that the binding of MY4 to fixed monocytes was eliminated by
gingipains, as shown in Fig. 3
, rules out the possibility of CD14
internalization.
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To confirm that gingipains can degrade CD14, human rCD14 was
incubated with gingipains at an E:S molar ratio of 1:100 at 37°C for
up to 120 min. Fig. 7 shows that all
three gingipains were capable of degrading rCD14 within 5 min, and the
intensity of the rCD14 band was reduced in a time-dependent manner. The
rCD14 band disappeared at 30 min on KGP and HRGP treatment, but a faint
band remained until 120 min on RGP2 treatment. No fragments of rCD14,
however, were detected. These results indicate that soluble rCD14
functions as a substrate of gingipains and that gingipains digest rCD14
to small fragments.
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production from human monocytes
by gingipains
The observation that gingipains cleave monocyte CD14 raises the
question of whether gingipains inhibit the LPS-induced production of
TNF- by monocytes, one of the major proinflammatory cytokines
produced by the cells. Preincubation of human monocytes with 0.3 µM
HRGP and KGP for 15 min substantially suppressed TNF- production
triggered by 1 ng/ml LPS (Fig. 8A). Pretreatment of 0.3 µM
KGP and HRGP with 3 µM Z-FK-cmk and FPR-cmk, respectively, restored
TNF- production, suggesting that the proteolytic activity of
gingipains was required for the inhibitory activity. By contrast, when
KGP- and HRGP-pretreated human monocytes were stimulated with a higher
concentration of LPS (20 µg/ml), TNF- production was unchanged
(Fig. 8B), but TNF- production was significantly
inhibited by HTA125 (10 µg/ml) (Fig. 8C). Thus, these
results indicate that cleavage of CD14 on monocytes resulted in the
specific suppression of the cell activation elicited by a low
concentration of LPS, and that TLR4 is still functionally active after
gingipain treatment.
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Discussion |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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production
by the cells. The failure of MY4 to bind human monocytes resulted from
direct proteolysis of CD14, but could not be attributed to shedding or
internalization of CD14, because gingipains cleaved the CD14 on 1%
paraformaldehyde-fixed monocytes, and fragments of CD14 on monocytes
and in the extracellular medium were detected by Western blot analysis
using anti-CD14 polyclonal Ab. Human rCD14 was degraded by all
three gingipains, which confirmed that CD14 was a substrate for
gingipains.
Recently, Le-Barillec et al. (34) reported that HLE also
cleaves CD14 on human monocytes. They showed that 30-min treatment of
human monocytes with 3 µM HLE at 37°C was required for 95%
reduction of MY4 binding to the cells. The present study showed that
15-min exposure of the cells to 0.3 µM KGP and HRGP almost completely
eliminated the binding, indicating that bacterial proteinases,
gingipains, cleave CD14 on monocytes at least 20 times more efficiently
than a host proteinase, HLE. Gingipains were relatively resistant to
inhibition by human serum as compared with HLE (Fig. 4). HLE was
rapidly inactivated by 1-proteinase inhibitor
in the serum (36). By contrast, gingipains were inhibited
only by 2-macroglobulin in the serum and at a
slow rate, and KGP is still 50% active on exposure to
2-macroglobulin (37), suggesting
that gingipains function to cleave CD14 on monocytes more efficiently
than HLE in vivo. The concentration of gingipains in the gingival
crevicular fluid at inflamed sites of adult periodontitis patients was
about 0.1 µM, which was the lowest concentration used in this study,
and it was 10 times more than that from normal sites of these patients
using the same gingipain preparations as used in this study as a
standard control (K. Matsushita, T. Imamura, and I. Maruyama,
unpublished data). In addition to the secreted soluble gingipains,
gingipains are also either bound to the bacterial cell surface or
released as outer membrane blebs (13, 38). Therefore, it
is conceivable that the local concentration of gingipains around
P. gingivalis was much higher than that in the crevicular
fluid, and that down-regulation of CD14 on monocytes caused by
gingipains is likely to occur in vivo.
There are 21 Arg-X and 9 Lys-X bonds in the CD14 amino acid sequence
(23), which are possible sites of cleavage by RGP and KGP,
respectively, and it is suggested that the 65 N-terminal amino acids of
CD14 are critical for the binding of LPS to CD14 and subsequent signal
transduction (39, 40) and that deletion of amino acids
9–12 and 35–39 within this region eliminates MY4 binding
(39). The present study showed that gingipains cleave
CD14, resulting in the elimination of MY4 binding to human monocytes
and reducing the release of TNF- from the cells triggered by a low
concentration of LPS (Figs. 1 and 8), indicating that gingipains
efficiently eliminate at least the N-terminal regions of CD14 that are
important for MY4 and LPS binding. There were more bands after KGP than
after HRGP treatment for 15 min (Fig. 6A), which may be due
to the number of cleavage sites, i.e., the number of Arg-X and Lys-X
bonds in CD14. These observations also indicate that the elimination of
MY4 binding to monocytes by gingipains, as analyzed by flow cytometry,
closely correlated to the dysregulation of LPS responsiveness of
monocytes, even though fragments of CD14 were still expressed on
monocytes. Actually, Arg-X and Lys-X bonds existed within the 65
N-terminal sequence and around it in addition to other regions of CD14
(23). This possibility concurs with the evidence that MY4
is able to inhibit activation of monocytes initiated only by a low
concentration of LPS (34). In the extracellular medium,
relatively high molecular bands (48 and 37 kDa by KGP and 44 kDa by
HRGP) were detected (Fig. 6B), which indicates that
gingipains may generate long CD14 fragments in the medium after 15-min
treatment. By contrast, all three gingipains degraded soluble human
rCD14 within 5 min, and fragments of CD14 were not detectable at any
time point during digestion (Fig. 7). These observations also
suggest that gingipains efficiently digest CD14 to small fragments that
are not detected by Western blotting using anti-CD14 polyclonal Ab,
but we do not exclude the possibility that cleavage sites of
membrane-anchored CD14 may be distinct from those of soluble rCD14.
Taking into account these observations, in the ability to cleave CD14,
the three gingipains should rank HRGP>KGP>>RGP2. HRGP and KGP
differ from RGP2 in that the two proteinases have complexed with
hemagglutinin/adhesin domains. This domain can bind to fibrinogen,
fibronectin, and laminin (41), and reacted with
phospholipids (11). Therefore, this domain may have an
additional function, increasing the efficiency of the enzymatic
activity by helping to adhere to the cells or CD14 itself.
As gingipains proteolytically inactivate leukocyte C5aR
(12), it is possible that gingipains cleave other cell
surface molecules not only on monocytes, but on other cells, resulting
in dysregulation of the cells. The present study showed that
expressions of CD18, CD54, CD59, and MHC class I on monocytes were
reduced 20 to 30% after gingipain treatments (Fig. 2). CD59, another
GPI-anchored glycoprotein expressed on a wide range of cell types
including monocytes (42, 43), was not eliminated as
efficiently as CD14 by gingipains, which excluded the possibility that
gingipains preferentially cleave GPI-anchored molecules on the sell
surface. When cells were incubated for longer period and with higher
concentration (1 µM KGP and HRGP for 30 min), the expression of TLR4
was unchanged, and CD18, CD59, and HLA-A, -B, -C expressions were
reduced by about 10% compared with 0.3 µM KGP and HRGP, whereas CD54
(ICAM-1) was relatively sensitive, but about 50% still remains on the
cell surface after the treatment (data not shown). These results
indicate that gingipains had a preference for cleaving CD14 over other
polypeptides on human monocytes, although the underlying reason was
unclear. The expression of TLR4 on monocytes was slightly increased by
0.3 µM KGP and HRGP treatments for 15 min, but unchanged by the
gingipains after 1% paraformaldehyde fixation (data not shown),
suggesting that gingipains themselves may have a function to activate
monocytes, resulting in up-regulation of TLR4 expression. Experiments
are underway to clarify this point.
CD14 as a GPI-anchored protein was not thought to participate directly
in signaling, and TLR4 has been shown to be an LPS signaling molecule
of human as well as murine cells (27, 28, 29, 30, 44, 45). It is
well known that LPS signals enter into the cells by a CD14-dependent
mechanism, but at very high, supraphysiological LPS concentrations, LPS
signaling occurs by CD14-independent mechanisms (16).
Pretreatment of human monocytes with KGP and HRGP markedly suppressed
TNF- production triggered by a low concentration of LPS, i.e., 1
ng/ml, but not by a high concentration of LPS, i.e., 20 µg/ml (Fig. 8, A and B), and anti-TLR4 mAb HTA125
significantly inhibited TNF- production from gingipain-treated
monocytes elicited by 20 µg/ml LPS (Fig. 8C). TNF-
production from untreated monocytes triggered by a low concentration of
LPS was also significantly inhibited by HTA125 as well as by MY4 (data
not shown). These results suggest that 1) TLR4 is still functionally
active after gingipain treatments, 2) TLR4 transduces LPS signal in
concert with CD14 at a low concentration of LPS and TLR4 can signal
independently of CD14 at a high concentration of LPS, and 3)
proteolysis of CD14 but not TLR4 by gingipains resulted in the specific
suppression of a CD14-dependent cell activation pathway.
Recent studies have shown that gingipains can cleave proinflammatory
cytokines such as TNF- (46) and IL-8 (38)
in addition to having a role in the onset of inflammation, as described
above, and are implicated in immune evasion, disrupting the host
cytokine network. Stimulation of gingipain-treated human monocytes with
LPS after removal of residual gingipains by washing (Fig. 8) excluded
the possibility that the reduced TNF- production was due to cleavage
of TNF- itself by gingipains. CD14 is shown to be a pattern
recognition receptor for many bacterial components in addition to LPS
(21, 22), and monocytes can phagocytose Gram-negative
bacteria by a CD14-dependent mechanism (47, 48).
Therefore, the present study further supports the above-mentioned
immune evasion mechanisms involving the cleaving of cell surface CD14
on human monocytes. CD14 is strongly detectable on the surface of
monocytes and macrophages (49, 50) and weakly detectable
on neutrophils (51) and human gingival fibroblasts
(19, 20), all of which exist in periodontal tissue with
periodontitis, indicating that these cell types are possibly subjected
to this regulation by gingipains. It is also possible that P.
gingivalis and other infective organisms may elaborate proteinases
that have similar functions to gingipains. In fact, a new cysteine
proteinase from P. gingivalis referred to as periodontain
was recently described (52). By using this mechanism,
P. gingivalis may cause chronic inflammation by surviving in
the periodontium. Recently, Genco et al. showed that preincubation of
P. gingivalis with a specific inhibitor, Z-FK-cmk, before
infection of mice resulted in a decrease in the recovery of P.
gingivalis from the mice, abdominal lesions, and death
(53), implying that an inhibitor of gingipains with low
toxicity may be useful as an agent for suppressing periodontal disease,
as the use of antibiotics unavoidably causes the induction of drug
resistance in bacteria.
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Acknowledgments |
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Footnotes |
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2 Address correspondence and reprint requests to Dr. Shunji Sugawara, Department of Microbiology and Immunology, Tohoku University School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan.
3 Abbreviations used in this paper: RGP, Arg-specific gingipain; E:S, enzyme:substrate; FPR-cmk, Phe-Pro-Arg-chloromethyl ketone; HLE, human leukocyte elastase; HRGP, high molecular mass Arg-specific gingipain; KGP, Lys-specific gingipain; PI-PLC, phosphatidylinositol phospholipase C; PVDF, polyvinylidene difluoride; TLR, Toll-like receptor; Z-FK-cmk, benzyloxycarbonyl-Phe-Lys-chloromethyl ketone.
Received for publication December 27, 1999. Accepted for publication April 12, 2000.
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  A. Uehara, M. Naito, T. Imamura, J. Potempa, J. Travis, K. Nakayama, and H. Takada Dual regulation of interleukin-8 production in human oral epithelial cells upon stimulation with gingipains from Porphyromonas gingivalis J. Med. Microbiol., April 1, 2008; 57(4): 500 - 507. [Abstract] [Full Text] [PDF]
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 K. Popadiak, J. Potempa, K. Riesbeck, and A. M. Blom Biphasic Effect of Gingipains from Porphyromonas gingivalis on the Human Complement System J. Immunol., June 1, 2007; 178(11): 7242 - 7250. [Abstract] [Full Text] [PDF]
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A. Uehara, K. Muramoto, T. Imamura, K. Nakayama, J. Potempa, J. Travis, S. Sugawara, and H. Takada Arginine-Specific Gingipains from Porphyromonas gingivalis Stimulate Production of Hepatocyte Growth Factor (Scatter Factor) through Protease-Activated Receptors in Human Gingival Fibroblasts in Culture J. Immunol., November 1, 2005; 175(9): 6076 - 6084. [Abstract] [Full Text] [PDF]
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S. Tancharoen, K. P. Sarker, T. Imamura, K. K. Biswas, K. Matsushita, S. Tatsuyama, J. Travis, J. Potempa, M. Torii, and I. Maruyama Neuropeptide Release from Dental Pulp Cells by RgpB via Proteinase-Activated Receptor-2 Signaling J. Immunol., May 1, 2005; 174(9): 5796 - 5804. [Abstract] [Full Text] [PDF]
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 R. Mezyk-Kopec, M. Bzowska, J. Potempa, M. Bzowska, N. Jura, A. Sroka, R. A. Black, and J. Bereta Inactivation of Membrane Tumor Necrosis Factor Alpha by Gingipains from Porphyromonas gingivalis Infect. Immun., March 1, 2005; 73(3): 1506 - 1514. [Abstract] [Full Text] [PDF]
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R. Takii, T. Kadowaki, A. Baba, T. Tsukuba, and K. Yamamoto A Functional Virulence Complex Composed of Gingipains, Adhesins, and Lipopolysaccharide Shows High Affinity to Host Cells and Matrix Proteins and Escapes Recognition by Host Immune Systems Infect. Immun., February 1, 2005; 73(2): 883 - 893. [Abstract] [Full Text] [PDF]
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A. Ozawa, H. Tada, Y. Sugawara, A. Uehara, T. Sasano, H. Shimauchi, H. Takada, and S. Sugawara Endogenous IL-15 Sustains Recruitment of IL-2R{beta} and Common {gamma} and IL-2-Mediated Chemokine Production in Normal and Inflamed Human Gingival Fibroblasts J. Immunol., October 15, 2004; 173(8): 5180 - 5188. [Abstract] [Full Text] [PDF]
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 S.-M. Lin, C. W. Frevert, O. Kajikawa, M. M. Wurfel, K. Ballman, S. Mongovin, V. A. Wong, A. Selk, and T. R. Martin Differential Regulation of Membrane CD14 Expression and Endotoxin-Tolerance in Alveolar Macrophages Am. J. Respir. Cell Mol. Biol., August 1, 2004; 31(2): 162 - 170. [Abstract] [Full Text] [PDF]
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 N. Cohen, J. Morisset, and D. Emilie Induction of Tolerance by Porphyromonas gingivalis on APCs: a Mechanism Implicated in Periodontal Infection J. Dent. Res., May 1, 2004; 83(5): 429 - 433. [Abstract] [Full Text] [PDF]
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 S. Fukuda and G. W. Schmid-Schonbein Regulation of CD18 expression on neutrophils in response to fluid shear stress PNAS, November 11, 2003; 100(23): 13152 - 13157. [Abstract] [Full Text] [PDF]
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H. Tada, S. Sugawara, E. Nemoto, T. Imamura, J. Potempa, J. Travis, H. Shimauchi, and H. Takada Proteolysis of ICAM-1 on Human Oral Epithelial Cells by Gingipains J. Dent. Res., October 1, 2003; 82(10): 796 - 801. [Abstract] [Ful |
