|
|||||||||
|
|
|
|
|
|
|
|
|
|
|
CHEMOKINES
From the Department of Medicine, Divisions of
Hematology and Cardiology, and the Department of Pathology, The Mount
Sinai School of Medicine, New York, NY.
The CC chemokine receptor 8 (CCR8) is expressed on monocytes and
type 2 T lymphocytes. CCR8 is the sole receptor for the human CC
chemokine I-309, as well as for viral monocyte inflammatory protein-I
(vMIP-I), a human chemokine homologue induced in human cells by the
Kaposi sarcoma-related human herpesvirus-8. Recently it was found that
I-309 messenger RNA and protein are expressed by human umbilical vein
endothelial cells (HUVECs) and that the secretion of endothelial I-309
is stimulated by apolipoprotein(a). I-309, vMIP-I, and the conditioned
medium from apolipoprotein(a)-stimulated HUVECs induce endothelial
chemotaxis. A polyclonal anti-CCR8 antibody and a newly developed
murine monoclonal antibody against CCR8 inhibited this activity. The
G-protein inhibitor pertussis toxin also inhibited endothelial
chemotaxis, providing further evidence for a chemokine
receptor-mediated effect. Endothelial cells contain CCR8 mRNA as shown
by RNA blot analysis as well by direct sequence analysis.
Immunohistochemical studies identified CCR8 and I-309 on the
endothelium of human atherosclerotic plaques and in endothelial-derived spindle cells of Kaposi sarcoma. These results indicate that CCR8 is an
endothelial receptor that may modulate endothelial function.
(Blood. 2001;97:39-45) The CC chemokine receptor-8 (CCR8) has recently
been characterized.1-3 CCR8 is expressed on monocytes and
T lymphocytes1-3 and is preferentially expressed on type 2 T lymphocytes.4 CCR8 is a G-protein-coupled
7-transmembrane receptor that is the sole receptor for the human CC
chemokine I-309 and for the viral monocyte inflammatory protein-I
(vMIP-I), a human chemokine homologue induced by the human
herpesvirus-8 (HHV-8) that has been directly linked to Kaposi
sarcoma.5-7 CCR8 receptor is a coreceptor for diverse human immunodeficiency virus-1 (HIV-1) strains, and I-309 has been
found to inhibit HIV-1 envelope-mediated cell-cell fusion and virus
infection.8
I-309 is secreted by activated monocytes and
lymphocytes9,10 and is a potent chemoattractant for both
these cell types.11,12 Our prior studies have shown that
the apolipoprotein(a) (apo[a]) portion of the atherogenic lipoprotein
Lp(a) stimulates human vascular endothelial cells to produce a monocyte
chemotactic activity.13 We have recently identified I-309
as the principal monocyte chemoattractant secreted by human umbilical
vein endothelial cells (HUVECs) when incubated with
apo(a).14 I-309 was found in human atheromatous plaques in
the luminal endothelium, in macrophage-rich areas of the plaque, and in
acellular areas of the vessel wall matrix.
We now report that I-309, vMIP-I, and the endothelial conditioned
medium (CM) produced by incubating Lp(a) or a recombinant apo(a)
derivative with HUVECs induce endothelial chemotaxis. That CCR8 is the
receptor responsible for mediating endothelial chemotaxis was supported
by the demonstration that both a polyclonal and monoclonal antibody
directed against CCR8 inhibited endothelial chemotaxis and that
HUVECs expressed CCR8 messenger RNA (mRNA). Immunohistochemical studies
have identified CCR8 in the endothelium of human atherosclerotic
plaques and in the endothelial-derived spindle cells of Kaposi sarcoma.
These findings suggest that CCR8 may play a role in vascular biology
and participate in the genesis of Kaposi sarcoma.
Proteins and antibodies
Purification of Lp(a) and a recombinant apo(a)
derivative
Culture of HUVECs The HUVECs were harvested and cultured as described.13 For generating endothelial cell CM, cells from passages 2 through 5 were grown in 6-well plates. Either Lp(a) (100 µg/mL; 100 nM) or 6K apo(a) (20 µg/mL; 100 nM) were incubated with HUVECs for 6 hours at 37°C, and the CM frozen at 80°C until tested. Cell incubation mixtures contained 20 µg/mL
polymyxin B (Sigma, St Louis, MO) to inhibit endotoxin.
Endothelial cell transmigration activity Cell transmigration was measured as described for mononuclear cells13,18 using a Neuroprobe chamber (Nucleopore, Pleasanton, CA) containing a polycarbonate filter with 5-µm pores. The filter was treated with 0.2% gelatin for 30 minutes at 37°C before the assay. For each assay, 29 µL of the chemokine to be tested or of HUVEC-conditioned culture medium was added to the wells of the lower chamber. Then 50 µL of HUVECs (1 × 106 cells/mL) was added to each well of the upper chamber. After a 4-hour incubation in 5% CO2 at 37°C, nonmigrating cells were scraped from the upper surface of the filter. Migrating cells on the lower surface were fixed with methanol and stained with Diff-Quik (Baxter Healthcare, Miami, FL). The number of HUVECs on the lower surface of the filter was determined by counting 3 microscopic fields per well under oil immersion (400 ×). To establish the effect of antibodies against CCR8, the purified antibodies or isotype controls were added to confluent HUVECs (1 µg IgG/mL) in 6-well tissue culture plates and incubated for 30 minutes at 37°C before the assay. After washing, the treated endothelial cells were harvested. To study the effects of pertussis and cholera toxins on endothelial cell transmigration induced by I-309, vMIP-I, and the CM from HUVECs incubated with Lp(a), the cells were cultured in the presence of 0.1 µg/mL pertussis toxin or 0.4 µg/mL cholera toxin for 16 hours before the assays.3 All samples were tested for endothelial cell transmigration in triplicate wells in the Neuroprobe chamber.Sequence analysis of HUVEC CCR8 complementary DNA Total RNA was isolated using the RNAeasy kit (Qiagen, Chatsworth, CA). Oligonucleotide primers (Operon Technologies, Alameda, CA) for CCR8 complementary DNA (cDNA) were designed as described.2 The sense 5'-TTATGTGTCTCTGTGACCAG and the antisense 5'-TAGTCTTCATTGATCCTCAC primers corresponded to positions 327-346 and 1425-1444 in the published sequence and span the entire coding region of TER1(CCR8) of 355 amino acids.19 For cDNA synthesis, the following reagents were added to Eppendorf tubes (20 µL total): RNA (1 µg), oligoT (500 µg/mL), DTT (0.01 M), dNTP (500 µM each), Superscript II (200 U) in buffer (50 mM Tris-HCl, pH 8.3; 75 mM KCl). The reaction mixture was incubated for 1 hour at 42°C. The cDNA (5 µL) products were added to tubes containing the following reaction mixtures at the indicated final concentrations: 200 µM dNTPs, 1.5 mM MgCl2, 0.2 µM sense primer, 0.2 µM antisense primer, 2.5 U AmpliTaq, and buffer (10 mM Tris-HCl, pH 8.3, 50 mM KCl) to a total volume of 50 µL. The mixture was preheated to 95°C for 5 minutes followed by 30 cycles of incubations at 94°C for 15 seconds, 62°C for 30 seconds, and 72°C for 15 seconds followed by a final extension step of 72°C for 10 minutes. The 1118-bp DNA fragment obtained was cloned in T/A cloning vector (InVitrogene, San Diego, CA) and sequenced using sequenase (US Biochemical, Cleveland, OH). The identity of the fragment as CCR8 mRNA was confirmed by sequence analysis (GenBank accession number U62556). Superscript II was excluded from the control reverse transcriptase-polymerase chain reaction (RT-PCR) to ensure that no DNA contamination was present.Northern blot analysis Samples of RNA were electrophoresed through 1.8% agarose gels containing formaldehyde, blotted, and cross-linked to Hybond-N nylon membranes (Amersham, Arlington Heights, IL). Levels of CCR8 mRNA were analyzed by prehybridization in buffer containing 5 × standard sodium citrate (SSC), 5 × Denhardts, 10 × dextran sulfate, 10% sodium dodecyl sulfate (SDS), and 1 µg/mL salmon sperm DNA for 2 hours at 42°C followed by hybridization with 32P-labeled probes and analyzed by autoradiography. The cDNA probes were labeled with [32P]dCTP by random priming to a specific activity of greater than 108 cpm/µL and used at 2 × 106 cpm/mL. The CCR8 probe was a 1118-kb RT-PCR fragment amplified from stimulated HUVECs. As a control, filters were hybridized with cDNA encoding the constitutively expressed glyceraldehyde-3-phosphate dehydrogenase (GAPDH).Immunohistochemistry Tissue samples from human coronary endarterectomy specimens and from Kaposi sarcoma biopsies were routinely processed and immunostained for CCR8, I-309, vWF, CD-68, and -actin using an avidin-biotin
technique.20 Tissue sections were blocked with ovalbumin
or, in some instances, with normal rabbit or horse serum before the
addition of the specific detecting antibody. Antigen retrieval was used
on some specimens.21 A positive control, nonimmune
negative, and processing controls were performed for each antigen
stain. Preabsorption of the CCR8 and I-309 antibody yielded
negative staining.
Statistical analysis Results of data are reported as the mean + SD. Levels of significance were determined by 2-tailed Student t test.
I-309, vMIP-I, and the CM from HUVECs incubated with 6K apo(a) induces chemotaxis of HUVECs The transmigration of endothelial cells in response to the human CC chemokine I-309 and to the Kaposi sarcoma-associated CC chemokine vMIP-I was studied in Neuroprobe chemotactic chambers using a 5-µm membrane coated with gelatin. In a preliminary study, concentrations of I-309 and vMIP-I from 0.01 to 500 ng/mL were used to induce endothelial transmigration. The response to increasing concentrations of I-309 and vMIP-I was bimodal (data not shown), a finding characteristic for a chemotactic response to CC chemokines. The maximum response occurred at 100 ng/mL (~10 nM) of the chemokines, a concentration that also induced maximum chemotactic response in cell lines transfected with CCR8.2To establish that the transmigration of endothelial cells in response
to the CC chemokines was chemotactic (directed), rather than
chemokinetic (nondirected), a checkerboard analysis was performed (Figure 1). I-309 (100 ng/mL), vMIP-I
(100 ng/mL), or the CM from 6K apo(a)-stimulated endothelial cells
(KCM) was placed in the bottom wells, in the top wells with the
indicator endothelial cells, or in both top and bottom wells of the
chemotaxis chamber. All 3 agonists increased endothelial cell
transmigration approximately 5-fold when placed in the bottom wells of
the chemotaxis chamber, as compared to the medium 199 control. In
contrast, the migration of endothelial cells was 3- to 4-fold less when
the agonists were added either to the top or to both top and bottom
wells. This checkerboard analysis indicates that the transmigration of
HUVECs in response to the agonists tested was primarily chemotactic. This study shows for the first time that I-309, vMIP-I, and apo(a) CM
are chemotactic for HUVECs.
Polyclonal antibody against CCR8 inhibits chemotaxis of HUVECs induced by I-309 and vMIP-I To examine the effect of blocking polyclonal antibodies against CCR8, I-309, and vMIP-I receptor, HUVECs were pretreated for 30 minutes at 37°C with 1 µg/mL normal goat IgG, goat anti-CCR8, or goat anti-CCR2, the MCP-1 receptor. These cells were then added to the top of the chemotaxis chamber. I-309 or vMIP-I (100 ng/mL each) was added to the bottom wells of the chamber and incubated as detailed in "Materials and methods." There was no significant difference in the chemotactic response of HUVECs in the presence of normal IgG or of antibody against CCR2. In contrast, antibody against CCR8 significantly inhibited endothelial chemotaxis (P < .001; Figure 2).
Polyclonal antibodies against I-309 or CCR8 inhibit endothelial chemotaxis induced by the conditioned medium from HUVECs incubated with Lp(a) or 6K apo(a) We tested the capacity of the CM from HUVECs incubated with either Lp(a) (LCM) or with recombinant 6K apo(a) (KCM) to induce endothelial chemotaxis. Lp(a) or the 6K apo(a) in the absence of incubation with HUVECs did not have significant endothelial chemotactic activity. LCM and KCM induced a 3-fold increase in endothelial transmigration as compared to the CM from endothelial cells incubated with medium 199 (P < .001; Figure 3). Blocking polyclonal antibodies directed against I-309 or CCR8 significantly inhibited chemotaxis induced by LCM or KCM, whereas the control goat IgG had no inhibitory effect.
A murine monoclonal antibody against the N-terminal extracellular domain of CCR8 inhibits HUVECs chemotaxis induced by I-309, vMIP-I, Lp(a) CM, but not by stromal cell-derived factor A murine monoclonal antibody was produced against a synthetic peptide from the N-terminal extracellular domain of CCR8 and tested for its effect on HUVEC chemotaxis. The monoclonal anti-CCR8 inhibited the endothelial chemotaxis induced by I-309, vMIP-I, and the Lp(a)-HUVEC CM (LCM), but did not inhibit endothelial chemotaxis induced by stromal cell-derived factor 1 (SDF-1; Figure 4). The murine IgG isotype control, IgG1, did not inhibit endothelial transmigration in response to the 3 chemokines. The HUVECs used in this experiment to study the endothelial response to LCM were derived from a different donor and demonstrated a lower background activity than did the HUVECs used for the 3 chemokines.
Pertussis toxin inhibits HUVEC chemotaxis induced by I-309, vMIP-I, and LCM To provide further evidence that the induction of endothelial chemotaxis by I-309, vMIP-I, and LCM was associated with a G-coupled chemokine receptor, the HUVECs were treated with the protein inhibitor pertussis toxin. Pertussis toxin inhibited endothelial transmigration induced by I-309, vMIP-I, and LCM (P < .001; Figure 5). Cholera toxin, in contrast, had no inhibitory effect on endothelial chemotaxis.
CCR8 mRNA is expressed in HUVECs RNA blot analysis with CCR8 cDNA demonstrated a single band in Jurkat cells as well as in confluent HUVECs (Figure 6). The identity of the DNA transcript as CCR8 was confirmed by sequence analysis as detailed in the "Materials and methods" (GenBank accession number U62556).
The endothelium in human atherosclerotic plaques contains CCR8 and I-309 The luminal endothelium of coronary endarterectomy specimens stained positively for CCR8 with both the polyclonal anti-CCR8 (Figure 7A) and the murine monoclonal anti-CCR8 (Figure 7C). The endothelium was identified by positive staining for vWF antigen (Figure 7D). Control goat IgG (not shown) and murine IgG1 used as an isotype control did not stain the arterial specimens (Figure 7F). I-309, as we have previously shown,14 stained the endothelium (Figure 7B). CCR8 and I-309 antigen was also detected in subendothelial tissue (Figure 7A-C). The luminal endothelium did not stain for the monocyte/macrophage antigen CD-68; however, some cells in the immediate subendothelium stained positively for CD-68 (Figure 7E). The staining of the endothelium by the CCR8 antisera was inhibited by absorption with the N-terminal peptide of CCR8, and the staining for I-309 was inhibited by absorption of the antibody with immobilized recombinant I-309.
Kaposi sarcoma contains CCR8 and I-309 Ten human biopsy specimens of Kaposi sarcoma were immunostained for multiple antigens including CCR8, I-309, macrophage antigen CD-68 (KP-1), smooth muscle cell-actin, and vWF antigen. Sections from a
representative biopsy specimen are shown in Figure
8. The tissue section shown is comprised
mainly of endothelial-derived spindle cells that stain intensely and
diffusely for CCR8 with both the polyclonal antibody (Figure 8A) and
the murine monoclonal anti-CCR8 (Figure 8D). Similar positive staining
was documented for I-309 (Figure 8B). vWF antigen stained diffusely
indicating endothelial cell origin for the Kaposi tumor cells (Figure
8C). The Kaposi spindle cells also stained for CD-68 antigen (Figure 8E). Microvessels as identified by pericytes staining positively for
-actin are also scattered throughout the biopsy specimen (Figure
8F). Neither the secondary antibody (control, Figure 8G) nor the murine
IgG1 (Figure 8H) significantly stained the Kaposi tissue. In addition
to blocking the tissue sections with ovalbumin, the inclusion of horse
serum or rabbit serum did not inhibit immunostaining for CCR8 or I-309.
Absorption of the CCR8 with the N-terminal peptide of CCR8 blocked the
immunostaining (data not shown).
Endothelial cell migration in response to chemotactic signals appears to be required for angiogenesis, wound repair, and atherogenesis.22-25 A variety of factors including vascular endothelial growth factor23 and basic fibroblast growth factor26 can stimulate endothelial migration. Chemokines, which are low-molecular-weight proteins (8-10 kd), that have the capacity to direct leukocyte trafficking into areas of inflammation27,28 may also participate in endothelial cell migration. Chemokines are classified into 2 major families that are distinguished by the position of the first 2 of 4 conserved cysteines (CXC and CC). A CXC chemokine, SDF-1, is a potent inducer of endothelial chemotaxis,29 and its receptor CXCR4 has been reported as essential for vascularization of the gastrointestinal tract.30 The CC chemokine receptor CCR2 was recently identified on human endothelial cells, and its agonist, the CC chemokine MCP-1, was found to stimulate endothelial chemotaxis.31 In the present study we document for the first time that the CC chemokine I-309 and the HHV-8 encoded CC chemokine vMIP-I stimulate the transmigration of HUVECs. The results of checkerboard analysis indicate that the endothelial response to these agonists was due to chemotaxis rather than to chemokinesis. The CM from Lp(a)- or from 6K apo(a)-stimulated HUVECs, previously shown to contain I-309 and to be chemotactic for monocytes,14 was also chemotactic for endothelial cells. That the endothelial agonist was I-309 in the CM was supported by the observation that anti-I-309 antibody inhibited endothelial migration. It has been reported recently that vMIP-I is a specific agonist for CCR8.5,6 In a study using 65 recombinant chemokines to characterize the recognition properties of CCR8, only 2, I-309 and vMIP-I, acted as agonists as they bound to CCR8 and induced calcium flux.5 In another study, cell lines transfected with known or suspected chemokine receptors were tested for calcium flux response to 40 different chemokines. Only cells transfected with CCR8 (CCR8-Y3 cells) responded to vMIP-I and I-309.6 Cell lines stably transfected with 12 other chemokine receptors were tested and were found not to respond to either vMIP-I or I-309 emphasizing the specificity of CCR8. Thus our finding that I-309 and vMIP-I induce endothelial chemotaxis provides strong evidence that functional CCR8 is present on the endothelial surface. This concept is also supported by our finding that 2 different antibodies, a goat polyclonal antibody and a newly developed murine monoclonal antibody directed against the N-terminal extracellular portion of CCR8, inhibited the endothelial migration induced by I-309 and vMIP-I. In contrast, a polyclonal goat and a murine monoclonal antibody directed against CCR2, the MCP-1 receptor, did not inhibit endothelial chemotaxis induced by I-309, vMIP-I, or the LCM. The demonstration that the G-coupled protein inhibitor pertussis toxin inhibited the chemotaxis of HUVECs induced by I-309, vMIP-I, and LCM provides additional evidence that the endothelial chemotaxis induced by these agonists is mediated by a chemokine receptor. We have also documented by RNA blot analysis and more importantly by direct sequence analysis the presence of CCR8 cDNA in HUVECs. Our immunohistochemical studies of human coronary endarterectomy specimens demonstrate that CCR8 and I-309 are present on the luminal endothelium of the atherosclerotic plaque. We have also observed CCR8, I-309, and vWF antigen in subendothelial areas of the atherosclerotic plaque. The cellular source of these antigens in the intima are unknown at present. These findings support the possibility that the I-309 and its receptor, CCR8, may contribute to the atherogenic process. Kaposi sarcoma HHV-8 is causally linked to hematologic malignancies including all types of Kaposi sarcoma, primary effusion lymphomas, and to multicentric Castleman disease.7,32,33 HHV-8 has been found in Kaposi sarcoma associated with acquired immunodeficiency syndrome, classic Kaposi sarcoma, endemic Kaposi sarcoma, and posttransplant Kaposi sarcoma32,33 indicating that Kaposi sarcoma can occur independently of HIV-1 infection. A hallmark of Kaposi sarcoma is intense angiogenesis, proliferation of endothelial cell-derived spindle cells and inflammation.34 The Kaposi sarcoma genome encodes 4 viral proteins including the CC chemokines vMIP-I, -II, and -III that share homology with human macrophage inflammatory protein (MIP-1), viral interleukin 6, and a G protein-coupled receptor (KSHV-GPR).35 The role of these viral chemokines in the etiology of Kaposi sarcoma is not known; however, both vMIP-I and vMIP-II were highly angiogenic in a chorioallantoic assay, suggesting a possible role in Kaposi sarcoma.36 The mechanisms underlying their angiogenic effect have not been defined; however, because CCR8 is preferentially expressed on Th2 lymphocytes,4 it was concluded that expression of vMIP-I by KSHV might alter the Th1/Th2 balance of the host immune response.6 The findings in the present study indicate that vMIP-I is directly chemotactic for endothelial cells. Immunohistochemical studies of Kaposi sarcoma biopsy specimens document diffuse staining for CCR8 associated with Kaposi sarcoma spindle cells. We also found intense and diffuse staining for I-309 in the Kaposi sarcoma lesion in a similar distribution to that of CCR8. Spindle cells appear to represent a mixed population of activated endothelial cells and macrophages,37 and these cells have been shown to stain for CD-68 antigen, as observed in the present study.38 These findings raise questions as to the possible role of I-309 and CCR8 in the formation of the Kaposi sarcoma lesion. Endothelial CCR8 may be in part responsible for the vasculogenic activity of vMIP-I previously documented in the chorioallantoic assay.36 Lipoprotein(a) has been shown to be an independent risk factor for atherosclerosis (reviewed in reference 39). Lp(a) consists of a low-density lipoprotein particle disulfide linked to apo(a),40,41 a glycoprotein of variable size that shares partial homology with plasminogen.42,43 The mechanisms by which Lp(a) participates in atherosclerosis are not defined. Our findings that Lp(a) stimulates endothelial chemotaxis by means of its capacity to induce endothelial I-309 production adds to our understanding of the pathophysiologic role for this lipoprotein.14 Because I-309 has been shown to be a chemoattractant for monocytes and for Th2 lymphocytes, it is reasonable to postulate that vessel wall-associated I-309 would attract these inflammatory cells into the forming atherosclerotic plaque. The present demonstration that CCR8 is present on vascular endothelial cells and that its stimulation by I-309 leads to endothelial migration indicates that I-309 may also function as an autocrine modulator of endothelial function. Two different angiogenesis inhibitors were found to reduce both intimal neovascularization and plaque growth in the apolipoprotein E-deficient mouse, providing evidence that new vessel formation is an important determinant of plaque growth.25 We have shown previously that I-309 is distributed widely in the human atheromatous plaque, appearing in the endothelium, in macrophages, and in the acellular matrix.14 We propose that I-309 in the plaque may provide an endothelial chemotactic stimulus, in addition to other inflammatory cytokines, to induce new vessel growth. The identification of CCR8 as an I-309 and vMIP-I receptor on vascular endothelial cells may be important to our understanding of the mechanisms underlying endothelial function in atherogenesis, in the formation of the lesions in Kaposi sarcoma, and as a novel target for the modulation of angiogenesis.
Submitted February 21, 2000; accepted September 6, 2000.
Supported in part by National Institutes of Health grant HL-54469.
The publication costs of this article were defrayed in part by page charge payment. Therefore, and solely to indicate this fact, this article is hereby marked "advertisement" in accordance with 18 U.S.C. section 1734.
Reprints: Peter C. Harpel, Box 1079, Mount Sinai School of Medicine, 1 Gustave L. Levy Place, New York, NY 10029; e-mail: peter.harpel{at}mssm.edu.
1.
Tiffany HL, Lautens LL, Gao JL, et al.
Identification of CCR8: a human monocyte and thymus receptor for the CC chemokine I-309.
J Exp Med.
1997;186:165-170
2.
Roos RS, Loetscher M, Legler DF, Clark-Lewis I, Baggiolini M, Moser B.
Identification of CCR8, the receptor for the human CC chemokine I-309.
J Biol Chem.
1997;272:17251-17254
3.
Goya I, Gutierrez J, Varona R, Kremer L, Zaballos A, Marquez G.
Identification of CCR8 as the specific receptor for the human beta- chemokine I-309: cloning and molecular characterization of murine CCR8 as the receptor for TCA-3.
J Immunol.
1998;160:1975-1981
4.
Zingoni A, Soto H, Hedrick JA, et al.
The chemokine receptor CCR8 is preferentially expressed in Th2 but not Th1 cells.
J Immunol.
1998;161:547-551
5.
Dairaghi DJ, Fan RA, McMaster BE, Hanley MR, Schall TJ.
HHV8-encoded vMIP-I selectively engages chemokine receptor CCR8. Agonist and antagonist profiles of viral chemokines.
J Biol Chem.
1999;274:21569-21574
6.
Endres MJ, Garlisi CG, Xiao H, Shan L, Hedrick JA.
The Kaposi's sarcoma-related herpesvirus (KSHV)-encoded chemokine vMIP-I is a specific agonist for the CC chemokine receptor (CCR) 8.
J Exp Med
1999;189:1993-1998
7.
Sitas F, Carrara H, Beral V, et al.
Antibodies against human herpesvirus 8 in black South African patients with cancer.
N Engl J Med.
1999;340:1863-1871
8.
Horuk R, Hesselgesser J, Zhou Y, et al.
The CC chemokine I-309 inhibits CCR8-dependent infection by diverse HIV-1 strains.
J Biol Chem.
1998;273:386-391 9. Miller MD, Hata S, De Waal Malefyt R, Krangel MS. A novel polypeptide secreted by activated human T lymphocytes. J Immunol. 1989;143:2907-2916[Abstract]. 10. Miller MD, Wilson SD, Dorf ME, Seuanez HN, O'Brien SJ, Krangel MS. Sequence and chromosomal location of the I-309 gene: relationship to genes encoding a family of inflammatory cytokines. J Immunol. 1990;145:2737-2744[Abstract].
11.
Miller MD, Krangel MS.
The human cytokine I-309 is a monocyte chemoattractant.
Proc Natl Acad Sci U S A.
1992;89:2950-2954
12.
D'Ambrosio D, Iellem A, Bonecchi R, et al.
Selective up-regulation of chemokine receptors CCR4 and CCR8 upon activation of polarized human type 2 Th cells.
J Immunol.
1998;161:5111-5115
13.
Poon M, Zhang X, Dunsky KG, Taubman MB, Harpel PC.
Apolipoprotein(a) induces monocyte chemotactic activity in human vascular endothelial cells.
Circulation.
1997;96:2514-2519
14.
Haque N, Zhang X, French DL, et al.
The CC chemokine I-309 is the principle monocyte chemoattractant induced by apolipoprotein(a) in human vascular endothelial cells.
Circulation.
2000;102:786-792 15. Samson M, Stordeur P, Labbe O, Soularue P, Vassart G, Parmentier M. Molecular cloning and chromosomal mapping of a novel human gene, ChemR1, expressed in T lymphocytes and polymorphonuclear cells and encoding a putative chemokine receptor. Eur J Immunol. 1996;26:3021-3028[Medline] [Order article via Infotrieve]. 16. Koschinsky ML, Tomlinson JE, Zioncheck TF, Schwartz K, Eaton DL, Lawn RM. Apolipoprotein(a): expression and characterization of a recombinant form of the protein in mammalian cells. Biochem. 1991;30:5044-5051[CrossRef][Medline] [Order article via Infotrieve].
17.
Gabel BR, May LF, Marcovina SM, Koschinsky ML.
Lipoprotein(a) assembly: quantitative assessment of the role of apo(a) kringle IV types 2-10 in particle formation.
Arterioscler Thromb Vasc Biol.
1996;16:1559-1567
18.
Berliner JA, Territo M, Almada L, Carter A, Shafonsky E, Fogelman AM.
Monocyte chemotactic factor produced by large vessel endothelial cells in vitro.
Arteriosclerosis.
1986;6:254-258 19. Napolitano M, Zingoni A, Bernardini G, et al. Molecular cloning of TER1, a chemokine receptor-like gene expressed by lymphoid tissues. J Immunol. 1996;157:2759-2763[Abstract].
20.
Dangas G, Mehran R, Harpel PC, et al.
Lipoprotein(a) and inflammation in human coronary atheroma: association with the severity of clinical presentation.
J Am Coll Cardiol.
1998;32:2035-2042 21. Shi SR, Key ME, Kalra KL. Antigen retrieval in formalin-fixed, paraffin-embedded tissues: an enhancement method for immunohistochemical staining based on microwave oven heating of tissue sections. J Histochem Cytochem. 1991;39:741-748[Abstract].
22.
Folkman J, Klagsbrun M.
Angiogenic factors.
Science.
1987;235:442-447 23. Risau W. Mechanisms of angiogenesis. Nature. 1997;386:671-674[CrossRef][Medline] [Order article via Infotrieve].
24.
Ross R.
Atherosclerosis
25.
Moulton KS, Heller E, Konerding MA, Flynn E, Palinski W, Folkman J.
Angiogenesis inhibitors endostatin or TNP-470 reduce intimal neovascularization and plaque growth in apolipoprotein E-deficient mice.
Circulation.
1999;99:1726-1732 26. Lindner V, Majack RA, Reidy MA. Basic fibroblast growth factor stimulates endothelial regrowth and proliferation in denuded arteries. J Clin Invest. 1990;85:2004-2008.
27.
Rollins BJ.
Chemokines.
Blood.
1997;90:909-928
28.
Luster AD.
Chemokines 29. Feil C, Augustin HG. Endothelial cells differentially express functional CXC-chemokine receptor-4 (CXCR-4/fusin) under the control of autocrine activity and exogenous cytokines. Biochem Biophys Res Commun. 1998;247:38-45[CrossRef][Medline] [Order article via Infotrieve]. 30. Tachibana K, Hirota S, Iizasa H, et al. The chemokine receptor CXCR4 is essential for vascularization of the gastrointestinal tract. Nature. 1998;393:591-594[CrossRef][Medline] [Order article via Infotrieve].
31.
Weber KS, Nelson PJ, Grone HJ, Weber C.
Expression of CCR2 by endothelial cells: implications for MCP-1 mediated wound injury repair and in vivo inflammatory activation of endothelium.
Arterioscler Thromb Vasc Biol.
1999;19:2085-2093
32.
Moore PS, Chang Y.
Kaposi's sarcoma (KS), KS-associated herpesvirus, and the criteria for causality in the age of molecular biology.
Am J Epidemiol.
1998;147:217-221 33. Boshoff C, Weiss RA. Kaposi's sarcoma-associated herpesvirus. Adv Cancer Res. 1998;75:57-86[Medline] [Order article via Infotrieve].
34.
Mesri EA.
Inflammatory reactivation and angiogenicity of Kaposi's sarcoma-associated herpesvirus/HHV8: a missing link in the pathogenesis of acquired immunodeficiency syndrome-associated Kaposi's sarcoma.
Blood.
1999;93:4031-4033
35.
Moore PS, Boshoff C, Weiss RA, Chang Y.
Molecular mimicry of human cytokine and cytokine response pathway genes by KSHV.
Science.
1996;274:1739-1744
36.
Boshoff C, Endo Y, Collins PD, et al.
Angiogenic and HIV-inhibitory functions of KSHV-encoded chemokines.
Science.
1997;278:290-294
37.
Monini P, Colombini S, Sturzl M, et al.
Reactivation and persistence of human herpesvirus-8 infection in B cells and monocytes by Th-1 cytokines increased in Kaposi's sarcoma.
Blood.
1999;93:4044-4058 38. Uccini S, Sirianni MC, Vincenzi L, et al. Co-expression of endothelial cell and macrophage antigens in Kaposi's sarcoma cells. J Pathol. 1994;173:23-31[CrossRef][Medline] [Order article via Infotrieve].
39.
Seman LJ, DeLuca C, Jenner JL, et al.
Lipoprotein(a)-cholesterol and coronary heart disease in the Framingham Heart Study.
Clin Chem.
1999;45:1039-1046
40.
Fless GM, ZumMallen ME, Scanu AM.
Physicochemical properties of apolipoprotein (a) and lipoprotein (a) derived from the dissociation of human plasma lipoprotein (a).
J Biol Chem.
1986;261:8712-8718 41. Gaubatz JW, Chari MV, Nava ML, Guyton JR, Morrisett JD. Isolation and characterization of the two major apoproteins in human lipoprotein(a). J Lipid Res. 1987;28:69-79[Abstract].
42.
Eaton DL, Fless GM, Kohr WJ, et al.
Partial amino acid sequence of apolipoprotein (a) shows that it is homologous to plasminogen.
Proc Natl Acad Sci U S A.
1987;84:3224-3228 43. McLean JW, Tomlinson JE, Kuang WJ, et al. cDNA sequence of human apolipoprotein(a) is homologous to plasminogen. Nature. 1987;330:132-137[CrossRef][Medline] [Order article via Infotrieve].
© 2001 by The American Society of Hematology.
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
 |
|
 |
|
  J. Hoover-Plow, E. Hart, Y. Gong, A. Shchurin, and T. Schneeman A Physiological Function for Apolipoprotein(a): A Natural Regulator of the Inflammatory Response Experimental Biology and Medicine, January 1, 2009; 234(1): 28 - 34. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 Y. B. Choi and J. Nicholas Autocrine and Paracrine Promotion of Cell Survival and Virus Replication by Human Herpesvirus 8 Chemokines J. Virol., July 1, 2008; 82(13): 6501 - 6513. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 H. R. Luttichau, A. H. Johnsen, J. Jurlander, M. M. Rosenkilde, and T. W. Schwartz Kaposi Sarcoma-associated Herpes Virus Targets the Lymphotactin Receptor with Both a Broad Spectrum Antagonist vCCL2 and a Highly Selective and Potent Agonist vCCL3 J. Biol. Chem., June 15, 2007; 282(24): 17794 - 17805. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. N'Diaye, E. Le Ferrec, D. Lagadic-Gossmann, S. Corre, D. Gilot, V. Lecureur, P. Monteiro, C. Rauch, M.-D. Galibert, and O. Fardel Aryl Hydrocarbon Receptor- and Calcium-dependent Induction of the Chemokine CCL1 by the Environmental Contaminant Benzo[a]pyrene J. Biol. Chem., July 21, 2006; 281(29): 19906 - 19915. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. M. Freeman, B.-C. Chiu, V. R. Stolberg, J. Hu, K. Zeibecoglou, N. W. Lukacs, S. A. Lira, S. L. Kunkel, and S. W. Chensue CCR8 Is Expressed by Antigen-Elicited, IL-10-Producing CD4+CD25+ T Cells, Which Regulate Th2-Mediated Granuloma Formation in Mice J. Immunol., February 15, 2005; 174(4): 1962 - 1970. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. Qu, E. W. Edwards, F. Tacke, V. Angeli, J. Llodra, G. Sanchez-Schmitz, A. Garin, N. S. Haque, W. Peters, N. van Rooijen, et al. Role of CCR8 and Other Chemokine Pathways in the Migration of Monocyte-derived Dendritic Cells to Lymph Nodes J. Exp. Med., November 15, 2004; 200(10): 1231 - 1241. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 P. A. Ruffini, A. Biragyn, M. Coscia, L. K. Harvey, S.-C. Cha, B. Bogen, and L. W. Kwak Genetic fusions with viral chemokines target delivery of nonimmunogenic antigen to trigger antitumor immunity independent of chemotaxis J. Leukoc. Biol., July 1, 2004; 76(1): 77 - 85. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 N. S. Haque, J. T. Fallon, J. J. Pan, M. B. Taubman, and P. C. Harpel Chemokine receptor-8 (CCR8) mediates human vascular smooth muscle cell chemotaxis and metalloproteinase-2 secretion Blood, February 15, 2004; 103(4): 1296 - 1304. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. Strasly, G. Doronzo, P. Capello, D. Valdembri, M. Arese, S. Mitola, P. Moore, G. Alessandri, M. Giovarelli, and F. Bussolino CCL16 activates an angiogenic program in vascular endothelial cells Blood, January 1, 2004; 103(1): 40 - 49. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 S. Senechal, P. de Nadai, N. Ralainirina, A. Scherpereel, H. Vorng, P. Lassalle, A.-B. Tonnel, A. Tsicopoulos, and B. Wallaert Effect of Diesel on Chemokines and Chemokine Receptors Involved in Helper T Cell Type 1/Type 2 Recruitment in Patients with Asthma Am. J. Respir. Crit. Care Med., July 15, 2003; 168(2): 215 - 221. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 L. A. Dourmishev, A. L. Dourmishev, D. Palmeri, R. A. Schwartz, and D. M. Lukac Molecular Genetics of Kaposi's Sarcoma-Associated Herpesvirus (Human Herpesvirus 8) Epidemiology and Pathogenesis Microbiol. Mol. Biol. Rev., June 1, 2003; 67(2): 175 - 212. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. E. DeVries, H. Cao, J. Wang, L. Xu, A. A. Kelvin, L. Ran, L. A. Chau, J. Madrenas, R. A. Hegele, and D. J. Kelvin Genomic Organization and Evolution of the CX3CR1/CCR8 Chemokine Receptor Locus J. Biol. Chem., March 28, 2003; 278(14): 11985 - 11994. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
I. Goya, R. Villares, A. Zaballos, J. Gutierrez, L. Kremer, J.-A. Gonzalo, R. Varona, L. Carramolino, A. Serrano, P. Pallares, et al. Absence of CCR8 Does Not Impair the Response to Ovalbumin-Induced Allergic Airway Disease J. Immunol., February 15, 2003; 170(4): 2138 - 2146. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
G. Spinetti, G. Bernardini, G. Camarda, A. Mangoni, A. Santoni, M. C. Capogrossi, and M. Napolitano The chemokine receptor CCR8 mediates rescue from dexamethasone-induced apoptosis via an ERK-dependent pathway J. Leukoc. Biol., January 1, 2003; 73(1): 201 - 207. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
C. D. Chung, F. Kuo, J. Kumer, A. S. Motani, C. E. Lawrence, W. R. Henderson Jr., and C. Venkataraman CCR8 Is Not Essential for the Development of Inflammation in a Mouse Model of Allergic Airway Disease J. Immunol., January 1, 2003; 170(1): 581 - 587. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
T. B. Huber, H. C. Reinhardt, M. Exner, J. A. Burger, D. Kerjaschki, M. A. Saleem, and H. Pavenstadt Expression of Functional CCR and CXCR Chemokine Receptors in Podocytes J. Immunol., June 15, 2002; 168(12): 6244 - 6252. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. Zheng, S. Deshpande, S. Lee, N. Ferrara, and B. T. Rouse Contribution of Vascular Endothelial Growth Factor in the Neovascularization Process during the Pathogenesis of Herpetic Stromal Keratitis J. Virol., October 15, 2001; 75(20): 9828 - 9835. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
 |
 |
 |
|||||||
 |
 |
 |
 |
 |
 |
 |
 |
||
| Copyright © 2001 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||
Top
Abstract
Introduction
; 100 ng/mL) and vMIP-I (
; 100 ng/mL) were tested for
endothelial cell chemotactic activity as detailed in "Materials and
methods." Prior to assay, the indicator HUVECs were incubated either
with normal goat IgG, goat polyclonal antibody against CCR8
(anti-CCR8), or goat polyclonal antibody against CCR2 (anti-CCR2) (1 µg/mL) for 30 minutes at 37°C. The anti-CCR8 significantly
inhibited endothelial chemotaxis as induced by I-309 and vMIP-I
(*P < .001). hpf, high power field.
an inflammatory disease.
N Engl J Med.
1999;340:115-126