Vitronectin in human hepatic tumours contributes to the recruitment of lymphocytes in an αvβ3-independent manner

The degree of lymphocyte infiltration is a prognostic factor in liver cancer, but to date the mechanisms by which lymphocytes infiltrate into and are retained in hepatic tumours are poorly understood. We hypothesised that the extracellular matrix glycoprotein vitronectin, a major component of the stroma of hepatic tumours, might play a role in the recruitment and retention of tumour-infiltrating lymphocytes (TIL). Thus, we investigated the ability of vitronectin to support migration and adhesion of TIL isolated from hepatocellular carcinoma and colorectal hepatic metastases. Soluble vitronectin-induced dose-dependent migration of TIL in in vitro chemotaxis and haptotaxis assays and vitronectin in tissue sections was able to support TIL adhesion to tumour stroma. Neither adhesion nor migration was inhibited by a function blocking mAb against the major vitronectin receptor αvβ3 and we were unable to detect αvβ3 on TIL in vitro or in vivo on tumour tissue. However, TIL did express high levels of urokinase-type plasminogen activator receptor (uPAR) and inhibitory antibodies and amiloride both significantly inhibited TIL adhesion to vitronectin and reduced transendothelial migration of lymphocytes across liver endothelium in vitro. Thus, we provide evidence that vitronectin in liver tumours can support the recruitment and retention of effector lymphocytes by an uPAR-dependent mechanism.

Leucocyte recruitment into tissues from blood involves transmigration across the endothelium followed by migration through the extracellular matrix to sites of inflammation or residence within tissue. The composition of extracellular matrix differs between tissues and constitutes an organ-specific microenvironment with the ability to recruit and retain specific cell types (Hunt et al, 1996). Pathological conditions, including inflammation and cancer are associated with changes in the composition of extracellular matrix (Rojkind, 1988), and thus changes in the potential to recruit or retain inflammatory cells.
Vitronectin, a 75 kDa glycoprotein synthesised by hepatocytes, circulates (Felding-Habermann and Cheresh, 1993) predominantly as an internally folded and stabilised monomer (Stockmann et al, 1993). A minor fraction undergoes conformational change to adopt an open heparin-binding reactive form (Preissner, 1991;McKeown-Longo and Panetti, 1996), which can multimerise and bind to the extracellular matrix (Johansson, 1996;Francois et al, 1999b). Within the matrix, vitronectin can support cellular adhesion via interactions with the integrins avb1, avb3, avb5 and aIIbb3 (Preissner, 1991). Vitronectin is found at low concentrations in normal extracellular matrices, but is increased in chronic inflammatory liver disease where its deposition in the sinusoids is indicative of progressive fibrosis (Inuzuka et al, 1992;Kobayashi et al, 1994;Koukoulis et al, 2001). Vitronectin is also a major component of the stroma of primary hepatocellular carcinoma (HCC) and metastatic hepatic tumours, including colorectal hepatic metastases (CHM) (Jaskiewicz et al, 1993).
Vitronectin has promigratory properties for several cell types, and by activating avb3, it can promote a4b1-mediated adhesion of lymphocytes to VCAM-1 (Imhof et al, 1997;Legler et al, 2001). This may be particularly important in HCC where leucocyte accumulation cannot be accounted for by local proliferation because less than 5% of CD3 þ T cells within HCC are actively dividing , implying that increased recruitment and retention in the tumour also contribute.
In the present study, we demonstrate increased expression of vitronectin associated with areas of lymphocyte infiltration in chronically inflamed liver and in primary and metastatic tumours. Furthermore, we show for the first time that vitronectin can support the adhesion and migration of tumour-infiltrating lymphocytes (TIL). We conclude that vitronectin plays an important role in recruiting and positioning lymphocytes within inflamed and malignant liver tissue.

Isolation and culture of lymphocytes
Liver issue was obtained from the Liver Unit at the Queen Elizabeth Hospital with approval from the local Ethics Committee and consent of patients. Tissues were processed immediately after resection to extract lymphocytes. Lymphocytes were isolated from hepatic tumours and also nonmalignant liver tissue. Tissue was cut into 5 mm 3 pieces, washed in phosphate-buffered saline (PBS) and digested with 2 mg ml À1 collagenase type 1A (Sigma Aldrich Ltd, Gillingham, UK) under constant agitation at 371C. After 90 min, collagenase was inactivated with 10% FCS (Invitrogen, Paisley, UK) and the cell suspension was sieved, washed and lymphocytes enriched on Ficoll -Hypaque (Pharma, Oslo, Norway). When sufficient numbers of TIL were obtained, they were rested overnight in the medium without the addition of exogenous IL-2 and used as fresh, unexpanded cells in the migration assays. In most experiments, the low yield of TIL required us to expand them in IL-2 before carrying out the functional assays. In these cases, the TIL-enriched fraction was plated at 0.5 Â 10 6 cells ml À1 in 24-well plates in RPMI-1640 (Sigma, UK) with 2 mM L-glutamine, 60 mg ml À1 benzylpenicillin, 100 mg ml À1 streptomycin and 50 ng ml À1 amphotericin plus high-dose rIL-2 1000 IU ml À1 (Chiron, Liverpool, UK) and maintained at 371C in a humidified incubator for up to 20 days. Prior to experimentation, TIL were transferred to resting medium overnight (RPMI-1640 plus 10% FCS) to remove exogenous IL-2. Lymphocytes isolated from nonmalignant tissue specimens (liver-infiltrating lymphocytes (LIL)) were incubated overnight in resting media and used the next day for functional assays. Cell viability was tested by Trypan blue exclusion. Lymphoblasts were generated from peripheral blood lymphocytes (PBL) by culturing mononuclear cells in 24well plates coated with anti-CD3 (10 mg ml À1 , Dako, High Wycombe, UK) in RPMI plus high-dose rIL-2 and 10% FCS at 2 Â 10 5 cells ml À1 for 2 -3 days.

Immunohistochemistry
Immunohistochemistry was used to detect CD2 (MT910; Dako, High Wycombe, UK), avb3 (LM609) and vitronectin (MAB1945) (both from Chemicon International Inc., Temecula, CA, USA) (Yoong et al,. 1999) in primary HCC and hepatic metastases from colorectal cancer. Cryostat sections (5 mm) were cut from snapfrozen tissue, fixed in acetone (Fisher Scientific, Loughborough, UK) and incubated with primary antibody followed by rabbit anti-mouse immunoglobulin and a species-specific anti-immunoglobulin antibody conjugated with alkaline phosphatase. Alkaline phosphatase activity was developed with 0.1% Fast Red substrate in TBS (pH 8.2) plus N,N-dimethylformamide, napthol AS-MX phosphate and levamisole (all Sigma). Sections were counterstained with Mayer's haematoxylin (Sigma). Negative controls were stained with an isotype-matched antibody (Dako). Immunocytochemical analysis of cytospins used the same staining protocol.

Chemotaxis assay
Lymphocyte chemotaxis was measured in a modified Boyden chamber (Adams et al, 1994). Freshly isolated TIL or TIL cultured in high-dose IL-2 was rested overnight in RPMI/10% FCS. Dilutions of soluble vitronectin (BD Biosciences, Oxford, UK), CCL5/RANTES (R&D Systems, Oxford, UK) or control buffer were applied in quadruplicate to lower wells separated by a single 8 mm pore size polycarbonate membrane (Whatman International, Banbury, UK) from the cell suspension (1.5 Â 10 6 cells ml À1 ) in 50 ml aliquots to the upper wells. The chamber was incubated for 2 h at 371C and nonmigrated cells washed from the upper surface of the membrane. Migrated cells bound to the lower surface of the membrane were fixed in methanol and stained with Diff-Quik (Dade BehringAG, Düdingen, Switzerland). The number of migrated cells was counted in five high-power fields/well and an overall average for the four replicates calculated. This average value was divided by the basal level of migration as defined by the average number of cells that moved towards a control stimulus to yield a chemotactic index.

Haptotaxis assay
This assay was designed to investigate whether TIL show migratory responses to immobilised vitronectin, that is, haptotaxis as well as chemotaxis or chemokinesis in response to soluble vitronectin (Hauzenberger et al, 1995). One microlitre of 0.02% BSA/RPMI as a control and different concentrations of vitronectin also in RPMI were applied to the surface of glass slides and then the chemotaxis membranes were coated by floating the membrane on the surface of the slide with the underside in contact with the coating solution overnight at 41C. The membranes were carefully lifted off the slide and the underside washed in PBS and allowed to air dry before being used in the chemotaxis assay as described in the section above.

Adhesion assays
Tissue-binding assay Adhesion of lymphocytes to liver tissue was assessed using a tissue-binding assay . Cryostat sections (10 mm) of tissue mounted on poly-L-lysine-coated slides were fixed in acetone and used as a substrate for adhesion. Antibody blockade was carried out by preincubating the sections or lymphocytes with blocking mAb for 30 min at 371C. For some experiments, the sections were incubated with function blocking antibody directed against vitronectin (10 mg ml À1 ) or an isotypematched control antibody (mouse IgG, 10 mg ml À1 , Dako, UK) for 60 min at room temperature. Specificity of the vitronectin antibody was confirmed by ELISA demonstration of binding to purified recombinant vitronectin, but not fibronectin or collagen (not shown). Excess unbound antibody was washed from the section prior to the addition of lymphocytes labelled with CD2 antibody to allow them to be distinguished from TIL within the tissue. In other experiments, TIL were incubated with blocking antibody against avb3 (20 mg ml À1 ; Chemicon, Chandlers Ford, UK) or b 2 -integrin chain (4 mg ml À1 ; BD Bioscience, UK) or an isotype-matched control for 30 min at 371C before application to the sections. In all experiments, lymphocytes were incubated on the sections for 30 min before fixing in acetone, washing and immunohistochemical staining to detect adherent cells. Lymphocyte adhesion was counted in 10 randomly selected high-power fields in both tumour tissue and in the associated normal tissue away from the tumour margin.
Adhesion to purified vitronectin Static adhesion assays were used to assess lymphocyte binding to immobilised purified vitronectin. Soluble vitronectin (2 -0.25 mg ml À1 ) was immobilised in 24-well plates overnight. Lymphocytes (1 Â 10 6 ml À1 ) were labelled with calcein AM (1 mM, Molecular Probes, UK) for 15 min at 371C prior to incubation in the vitronectin-coated wells in the presence or absence of function blocking anti-urokinase-type plasminogen activator receptor (uPAR) antibody (2.5 mg ml À1 , Chemicon, UK) or amiloride (100 mg ml À1 , Sigma). After 30 min, the nonadherent cells were washed off and adherent cells were measured using a plate reader.

Flow-based adhesion assays
To study the function of uPAR in lymphocyte transendothelial migration under the influence of physiological blood flow, primary human hepatic sinusoidal endothelial cells were cultured from human liver tissue as described previously (Lalor et al, 2002) and grown to confluence in glass capillary tubes. They were then stimulated for 24 h with TNF-a and IFN-g (both 10 ng ml À1 ; R&D Systems) and connected to the flow-based system as described previously (Curbishley et al, 2005). Liver-infiltrating lymphocytes were perfused through microslides at a physiologically relevant wall shear stress of 0.05 Pa. Adherent cells were visualised microscopically under phase contrast and a video link was used to record assays for offline analysis at a later date. The number of adherent cells was converted to adherent cells per millimetre squared and corrected for the number of cells perfused. The pattern of adhesion was analysed to determine the number of cells rolling, statically adherent or transmigrated. Cells appearing phase bright were above the endothelial monolayer, whereas those appearing phase dark had migrated through the monolayer. For functional studies, HSEC monolayers were incubated with blocking antibodies raised against uPAR or amiloride as described above for 90 min at 371C.

Flow cytometry
FACS was used to phenotype TIL, PBL and the dermal microvascular endothelial cell line HMEC-1 (a gift of Dr E Ades (CDC Atlanta, GA, USA)) (Adams et al, 1997). HMEC-1 were grown as described before. Gentle trypsinisation was used to Figure 1 Vitronectin expression is increased in HCC. Immunohistochemical localisation of vitronectin and avb3 integrin in HCC. (A) Staining with an isotype-matched negative control monoclonal antibody. Extensive vitronectin deposits are located in the tumour stroma (B) and within sinusoidal-type endothelium (C and D). avb3 Integrin expression was restricted to some vessels within the tumour stroma (E), but was absent on infiltrating lymphocytes (F), which were identified by expression of CD2 (G).
prepare single-cell suspensions for analysis by flow cytometry. Cells were incubated with human immunoglobulin (Grifols, Cambridge, UK) to block Fc receptors, suspended at 10 6 cells/100 ml and incubated with mAb at predetermined optimal concentrations for 60 min followed by a 1 : 50 dilution of FITC-conjugated F(ab 0 ) 2 fragments of rabbit anti-mouse immunoglobulin (Dako) for 45 min. At this stage, HMEC-1 were fixed in 1% paraformaldehyde, whereas lymphocytes were incubated with 10% normal mouse serum to minimise nonspecific binding prior to a final incubation with Rphycoerythrin-conjugated mouse secondary antibodies (Dako) for 60 min and fixation in paraformaldehyde. Incubations were at 41C and followed by two washes with PBS plus 2% FCS and 0.02% sodium azide. Cells were analysed using a Coulter Epics XL flow cytometer (Beckman-Coulter, High Wycombe, UK) with a lymphocyte gate set to exclude dead cells and debris.

Vitronectin is expressed in liver tumours in association with infiltrating lymphocytes
In normal liver, vitronectin was restricted to the stroma of portal tracts and to the subendothelial matrix of central veins. In both HCC and CHM, strong vitronectin staining was detected in the tumour stroma. In HCC, sinusoidal-type vessels were positive for vitronectin ( Figure 1B -D) and avb3 was detected on tumour vessels but not on CD2 þ lymphocytes ( Figure 1E -G). In CHM, vitronectin was absent from vessels and avb3 was detected on tumour endothelium but not on TIL ( Figure 2D -F). In HCC, large numbers of TIL were seen within the tumour with marked perivascular cuffing in some areas, whereas in CHM, lymphocytes were localized to the stroma at tumour margins.

Vitronectin stimulates migration of TIL in vitro
Chemotaxis and chemokinesis Our finding that lymphocytes were associated with areas of increased vitronectin expression led us to investigate whether vitronectin might promote the recruitment or retention of lymphocytes. Lymphocytes were freshly isolated from tumours, rested overnight and either used without further stimulation or expanded in IL-2 before testing their ability to migrate towards soluble vitronectin in chemotaxis assays ( Figure 3). The majority of experiments were performed using IL-2-expanded TIL, as yields of cells were often insufficient to allow analysis on unexpanded TIL. However, on three occasions, we were able to assess the ability of vitronectin to stimulate the In all five patients, there was a response to 0.02 mg ml À1 vitronectin coating concentration, which did not increase at higher coating concentrations. In all four panels, values are given as chemotactic index with migration to control buffer assigned a value of 1. Indices greater than 2 indicate significant migration.

Expression of vitronectin in hepatic tumours
S Edwards et al chemotactic activity of freshly isolated TIL ( Figure 3A). Tumourinfiltrating lymphocytes chemotaxis was compared with chemotaxis of PBL-derived lymphoblasts cultured under similar conditions. Chemotactic indices greater than 2 indicate significant migration when compared with migration to medium alone. Tumour-infiltrating lymphocytes from both CHM and HCC showed significant chemotactic responses to vitronectin, which peaked between 0.2 and 20 ng ml À1 (Figure 3B and C). Peripheral blood lymphocytes from HCC patients showed a similar response ( Figure 3B and C). We used checkerboard analysis to determine whether vitronectin acts by chemotaxis (migration to a gradient) or chemokinesis (nondirectional migration in the absence of a gradient, that is, when concentrations are the same in the upper and lower chambers). Vitronectin induced both chemotaxis and chemokinesis because increased migration occurred not only when the concentration was higher in the lower chambers but also in the absence of a gradient. The effect was specific because media had no effect on cell migration ( Figure 3D). These migration responses could not be inhibited using antibody raised against the vitronectin receptor avb3 (not shown). Haptotaxis To investigate whether immobilised vitronectin could also stimulate migratory responses in TIL, we used an assay of haptotaxis (migration on an immobilised substrate). Migration to immobilised vitronectin was compared with migration on membranes coated with 0.02%. BSA/RPMI. Vitronectin membranes were coated with 0.02 or 2 mg ml À1 vitronectin and the experiment conducted as before ( Figure 3E). Tumour-infiltrating lymphocytes showed increased migration to immobilised vitronectin compared with BSA control, although there was no increase with the higher coating concentration, suggesting that 0.02 mg ml À1 is sufficient for optimal coating of the chemotaxis membranes. The chemotactic index in response to immobilised vitronectin was 3.23 at 0.02 mg ml À1 and 2.85 at 2 mg ml À1 , which is similar to the level of response seen with the soluble vitronectin.

Vitronectin supports the adhesion of TIL to tumour tissue
Next, we demonstrated that vitronectin within tumour tissue can support lymphocyte adhesion using a modified Stamper -Woodruff tissue-binding assay (Stamper and Woodruff, 1976; on tissue sections of tumours. We compared adhesion of TIL to stromal areas, differentiated tumour tissue and surrounding, noninvolved tissue ( Figure 4). Tumour-infiltrating lymphocytes preferentially bound to stromal areas where strong expression of vitronectin was detected ( Figure 4A). Tumourinfiltrating lymphocyte adhesion to these vitronectin-rich regions was significantly inhibited by a function blocking antibody against vitronectin ( Figure 4A). Analysis of TIL adhesion to noninvolved tissue surrounding the tumour revealed that vitronectin supported adhesion to portal tracts where vitronectin expression was confined ( Figure 4B). However, consistent with the chemotaxis experiments, we were unable to block adhesion of TIL to vitronectin using antibodies against avb3 integrin despite good blocking with an antibody against vitronectin.

TIL do not express avb3 integrin
The failure of anti-avb3 integrin antibodies to block adhesion or migration to vitronectin was surprising and led us to analyse avb3 expression on TIL. Tumour-infiltrating lymphocytes that showed maximal responses to vitronectin in the chemotaxis assay were analysed by flow cytometry, and despite gating on both CD56 þ and CD3 þ populations, we were unable to demonstrate avb3 expression on TIL ( Figure 5A and B), despite strong staining of cultured dermal microvascular endothelial cells (HMEC-1; Figure 6C). Cytospins of TIL were also avb3 negative ( Figure 5D), suggesting that TIL do not express avb3.
TIL express the uPAR, which contributes to TIL adhesion to vitronectin and transendothelial migration of cells through liver endothelium ( Figure 6) We then looked for expression of the alternative vitronectin receptor uPAR, which has been detected on activated lymphocytes (Nykjaer et al, 1994;Bianchi et al, 1996). Figure 6A shows that TIL express moderate levels of uPAR, which is absent from freshly isolated PBL. We then investigated the effect of an anti-uPAR antibody or the uPAR inhibitor amiloride (Crowley et al, 1993) on TIL adhesion to immobilised vitronectin and found that both antibody uPAR and amiloride modestly but consistently inhibited TIL adhesion to immobilised vitronectin in a static adhesion assay ( Figure 6B). Because vitronectin was detected on the tumour sinusoidal vessels, we next tested the function of uPAR on freshly isolated liver-derived lymphocytes (without additional expansion in IL-2) in flow-based transendothelial migration assays using primary human sinusoidal endothelial cells ( Figure 6C). Under conditions of flow, the uPAR antibody and amiloride significantly reduced the levels of transendothelial migration, suggesting that uPAR can promote migration into the liver as well as migration and retention within the tumour.

DISCUSSION
In both HCC and CHM, prognosis is better if the tumour is infiltrated by lymphocytes (Emile et al, 2000;Gervaz et al, 2000;Okano et al, 2003), suggesting that immune responses partially contain these tumours. Thus, understanding the mechanisms involved in lymphocyte recruitment has therapeutic implications for adoptive immunotherapy as well as elucidating mechanisms of lymphocyte recruitment to inflamed tissue. Stromal cells and matrix proteins form the structural framework of an organ, which is critical for the functioning of resident cells and for the recruitment, retention and differentiation of cells that traffic through the tissue (Shimizu and Shaw, 1991). For example, splenic stroma has recently been shown to affect the function of infiltrating dendritic cells (Zhang et al, 2004) and gut stroma, the survival of activated lymphocytes (Sturm et al, 2004). Although changes in the tissue stroma are likely to be critical in the development of chronic inflammation, little is known about the role of matrix in regulating the recruitment and retention of lymphocytes (Schor et al, 2000). Many cancers stimulate an inflammatory response associated with changes in ECM components that recapitulate the changes of chronic inflammation (Coussens and Werb, 2002). This is illustrated by demonstration of increased vitronectin in both chronic inflammatory liver disease and in liver tumours (Jaskiewicz et al, 1993;Nejjari et al, 2002). In the present study, CHM were characterised by a stromal reaction around the tumour, which was heavily infiltrated by lymphocytes associated with strong staining for vitronectin, whereas the tumour itself did not express vitronectin and was largely devoid of lymphocytes. In contrast, vitronectin and infiltrating lymphocytes were detected both in peritumoural stroma and within the tumour itself, including on tumour vessels in HCC, where vitronectin is probably secreted by malignant hepatocytes (Inuzuka et al, 1992). Our findings confirm that liver cancer recapitulates chronic inflammatory change and suggested to us that vitronectin might play a role in the recruitment and retention of lymphocytes within tumours. This is particularly interesting since recent evidence suggests that proteolytic cleavage of vitronectin is enhanced in HCC to yield Tumour-infiltrating lymphocytes isolated from HCC express uPAR and demonstrate uPAR-dependent adhesion to vitronectin. Tumourinfiltrating lymphocytes isolated from HCC were cultured for up to 10 days in high-dose IL-2 and analysed for the expression of uPAR by flow cytometry. (A) All TIL in a representative experiment expressed uPAR. (B) When the same TIL were used in an adhesion assay, binding to immobilized vitronectin was modestly but significantly inhibited by pretreating the lymphocytes with amiloride (100 mg ml À1 ) or uPAR antibody (10 mg ml À1 ) for 20 min prior to assay. Data represent mean7s.e.m. of four experiments using vitronectin at concentrations ranging from 0.25 to 2 mg ml À1 . (C) Effect of uPAR on the transendothelial migration of liver-infiltrating lymphocytes across hepatic sinusoidal endothelium under flow. A function blocking mAb targeting uPAR or amiloride at a concentration of 100 mg ml À1 was used to treat LIL (PBL) and HSEC (EC) before the perfusion of LIL using a flow-based adhesion assay (at 0.05 Pa). HSEC were stimulated with TNF-a and IFN-g for 24 h before the assay. Transendothelial migration is shown as the percent of adherent cells that migrated across the endothelial monolayer under flow. Data represent mean7s.e.m. of four experiments. Paired samples t-test was used to calculate the statistical significance for adhesion events between control and treatment groups (* ¼ 2Po0.05).
high soluble levels of a vitronectin fragment in the serum, which can be used as a marker of disease progression (Paradis et al, 2005).
We isolated lymphocytes from both HCC and CHM , which were expanded (Seljelid, 1997) in vitro to generate sufficient numbers for functional studies. We studied their migratory and adhesive interactions with vitronectin. Tumour-infiltrating lymphocytes migrated towards soluble vitronectin by chemotaxis at low concentrations and at higher concentrations stimulated chemokinesis. Migration assays using immobilised vitronectin demonstrated that TIL also show a haptotactic response to vitronectin, that is, migration in response to an immobilised substrate. Thus, soluble vitronectin can act to direct migration and to stimulate general motility of lymphocytes, and this response may be further stimulated when the lymphocyte interacts with immobilised vitronectin in the tumour stroma. Thus, vitronectin may promote the accumulation of lymphocytes within the tumour stroma. To our surprise, this migration was not inhibited by antibodies against the classical vitronectin receptor avb3, which we were unable to detect on TIL using three different methods, flow cytometry, immunocytochemistry and immunohistochemistry. The molecule was appropriately expressed on an endothelial cell line. Lack of expression on TIL is consistent with our previous published work showing a lack of avb3 on TIL isolated from malignant melanoma (Adams et al, 1997). Other integrins that can bind vitronectin are not found at high levels on lymphocytes (Nejjari et al, 2002), but the uPAR, which can either modulate the function of other integrins or act directly as an adhesion receptor for vitronectin has been demonstrated on activated lymphocytes and reported to mediate migration (Nykjaer et al, 1994;Wei et al, 1994;Bianchi et al, 1996;Blasi, 1997). We were able to inhibit TIL adhesion to immobilised vitronectin with anti-uPAR antibodies or the uPAR inhibitor amiloride. Because we detected strong vitronectin on tumour endothelium in HCC in sinusoidal-like vessels, we also tested the function of uPAR in another migration system in which fresh liver-derived lymphocytes were tested for their ability to undergo transendothelial migration across monolayers of human hepatic sinusoidal endothelium under flow. In this system, antibodies to uPAR and amiloride both inhibited adhesion and transendothelial migration. Activated T cells also express the uPA, which binds soluble vitronectin allowing the complex to activate uPAR (Nykjaer et al, 1994;Preissner et al, 2000;. In melanoma cells, adhesion to vitronectin is enhanced in the presence of uPA, and soluble uPAR inhibits this effect, indicating that uPA/uPAR functions as a vitronectin receptor that can promote cell attachment  In contrast, plasminogen activator inhibitor I stimulates melanoma cell migration on vitronectin, presumably either by inhibiting uPA/ uPAR-mediated cell adhesion or by direct effects on the cytoskeleton (Waltz et al, 1997). Our data suggest that a similarly complex interaction with vitronectin and the uPA system might contribute to adhesion and migration of lymphocytes. These mechanisms may be particularly relevant in the liver because uPA/ PAI-1 and vitronectin are colocalised at areas of inflammatory damage in liver disease (Inuzuka et al, 1992).
Leucocytes may encounter vitronectin either as a soluble protein or immobilised within the extracellular matrix or on tumour vessels. Our data suggest that all of these interactions can stimulate TIL migration and motility (Francois et al, 1999a;Preissner et al, 2000). In order to determine that native, tissue-bound vitronectin could mediate direct adhesion of TIL, we used tissue-binding assays to demonstrate that vitronectin in liver tumours can support the adhesion of TIL. Tumour-infiltrating lymphocytes adhesion to the vitronectin-rich stromal regions of hepatic tumours was blocked using an antibody to vitronectin, but once again antibodies against avb3 had no effect. We detected TIL adhesion to the portal tracts in adjacent noninvolved liver tissue, which was again blocked by antibodies against vitronectin, suggesting that vitronectin in the native liver can also support lymphocyte adhesion. Thus, vitronectin can combine with other adhesive proteins  expressed within the tumour microenvironment to support the recruitment and retention of lymphocytes within liver tumours and inflamed liver tissue. Our studies also have implications for chronic inflammatory liver diseases in which lymphocyte infiltration is associated with areas of increased vitronectin deposition (Inuzuka et al, 1992;Jaskiewicz et al, 1993;Kobayashi et al, 1994;Koukoulis et al, 2001).