N-glycosylation of ICAM-2 is required for ICAM-2-mediated complete suppression of metastatic potential of SK-N-AS neuroblastoma cells
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Cell adhesion molecules (CAMs) are expressed ubiquitously. Each of the four families of CAMs is comprised of glycosylated, membrane-bound proteins that participate in multiple cellular processes including cell-cell communication, cell motility, inside-out and outside-in signaling, tumorigenesis, angiogenesis and metastasis. Intercellular adhesion molecule-2 (ICAM-2), a member of the immunoglobulin superfamily of CAMs, has six N-linked glycosylation sites at amino acids (asparagines) 47, 82, 105, 153, 178 and 187. Recently, we demonstrated a previously unknown function for ICAM-2 in tumor cells. We showed that ICAM-2 suppressed neuroblastoma cell motility and growth in soft agar, and induced a juxtamembrane distribution of F-actin in vitro. We also showed that ICAM-2 completely suppressed development of disseminated tumors in vivo in a murine model of metastatic NB. These effects of ICAM-2 on NB cell phenotype in vitro and in vivo depended on the interaction of ICAM-2 with the cytoskeletal linker protein α-actinin. Interestingly, ICAM-2 did not suppress subcutaneous growth of tumors in mice, suggesting that ICAM-2 affects the metastatic but not the tumorigenic potential of NB cells. The goal of the study presented here was to determine if the glycosylation status of ICAM-2 influenced its function in neuroblastoma cells.
Because it is well documented that glycosylation facilitates essential steps in tumor progression and metastasis, we investigated whether the glycosylation status of ICAM-2 affected the phenotype of NB cells. We used site-directed mutagenesis to express hypo- or non-glycosylated variants of ICAM-2, by substituting alanine for asparagine at glycosylation sites, and compared the impact of each variant on NB cell motility, anchorage-independent growth, interaction with intracellular proteins, effect on F-actin distribution and metastatic potential in vivo.
The in vitro and in vivo phenotypes of cells expressing glycosylation site variants differed from cells expressing fully-glycosylated ICAM-2 or no ICAM-2. Most striking was the finding that mice injected intravenously with NB cells expressing glycosylation site variants survived longer (P ≤ 0.002) than mice receiving SK-N-AS cells with undetectable ICAM-2. However, unlike fully-glycosylated ICAM-2, glycosylation site variants did not completely suppress disseminated tumor development.
Reduced glycosylation of ICAM-2 significantly attenuated, but did not abolish, its ability to suppress metastatic properties of NB cells.
KeywordsICAM-2 CD102 N-glycosylation Neuroblastoma Metastasis Cell motility
Intercellular adhesion molecule-2, CD102
Cell adhesion molecules
Glycosylation site variant
- IgLD-1 and IgLD-2
Two immunoglobulin-like C2 domains
- Asn N
- Ala A
Cell adhesion molecules (CAMs) participate in diverse functions in normal cells and tumor cells. These functions include cell-cell and cell-matrix adhesion, migration, oncogenesis, metastasis, tumor suppression or progression, and signal transduction [1, 2, 3, 4, 5]. Based on known functions, four major families of CAMs have been identified: integrins, cadherins, selectins, and immunoglobulin (Ig) superfamily. CAMs of the Ig superfamily contain one or more domains similar to the C2 type domains characteristic of a subset of Ig molecules (immunoglobulin-like C2 domain [IgLD]) .
Intercellular adhesion molecule-2 (ICAM-2), a 55-60 kDa transmembrane glycoprotein, belongs to the Ig superfamily of CAMs [7, 8]. In normal tissue, neovascular endothelial cells express the highest level of ICAM-2. Established vasculature and some leukocytes express a relatively low level of ICAM-2. Functionally, the extracellular domain (ED) of ICAM-2 mediates binding of ICAM-2 on vascular endothelial cells to β2-integrins on the surface of leukocytes, an initial step in immune responses [9, 10]. ICAM-2 also facilitates neutrophil binding to and migration through vascular endothelium as a component of immune reactions [11, 12]. In tumor cells, we recently identified a unique role for ICAM-2 when we demonstrated that ICAM-2 suppressed the metastatic phenotype neuroblastoma (NB) cells .
The ED of ICAM-2 contains six N-glycosylation sites (asparagines [Asn] residues; amino acids # 47, 82, 105, 153, 178 and 187) , a frequent post translational modification of CAM proteins and a modification known, in general, to influence CAM structure and function and to impact the phenotype of tumor cells [18, 19, 20]. For example, altered N-glycosylation of β1-integrin decreases cell migration , and aberrant N-glycosylation of E-cadherin increases discohesion of oral cancer cells . The effect of glycosylation of ICAM-2 on tumor cell function is unknown.
Our previous studies, however, document that fully glycosylated ICAM-2 suppresses the development of disseminated tumors in a murine model of metastatic NB. Importantly, and consistent with preclinical data, we also showed that primary human NB cells that express endogenous ICAM-2 have morphologic and histologic properties of NB cells recognized clinically to have limited metastatic potential . These observations suggest a functional role for ICAM-2 in primary tumor cells. Therefore, in order to identify domains of ICAM-2 that contribute significantly to its function in tumor cells, we generated four ICAM-2 constructs, encoding glycosylation site variants (gsv) of this protein. We expressed each construct in SK-N-AS NB cells, which have no detectable endogenous ICAM-2 and which display a metastatic phenotype in in vitro assays and in vivo models. We altered the glycosylation status of ICAM-2 by substitution of alanines for asparagines, to prevent glycosylation at specific residues that comprise N-linked glycosylation sites in situ; and then determined whether substitutions modulated the ability of ICAM-2 to suppress metastatic properties of NB cells. The data show that hypo-glycosylated variants of ICAM-2 have a significant impact on NB cell phenotype, but to a lesser extent than that seen with ICAM-2 WT.
Cell lines and culture conditions
The human neuroblastoma (NB) cell line SK-N-AS (American Type Culture Collection, Manassas, VA) was maintained in Dulbecco's Modified Eagle Medium (DMEM; Hyclone, Fisher Scientific, Savannah, GA) with 10% fetal bovine serum (Atlanta Biologicals, Lawrenceville, GA) and 2 mM L-glutamine (Hyclone, Fisher Scientific, Savannah, GA) at 37°C and 10% CO2. Parent SK-N-AS cells and stable transfectants were cultured under the same conditions. Human dermal microvascular endothelial cells (HDMVEC) were obtained from Lonza, Inc. (Allendale, NJ), and the human bone marrow endothelial cell line, HBMEC-28, was provided by Dr. E. van der Schoot (Sanquin Blood Supply Foundation, The Netherlands) . HDMVEC cells were grown in gelatin-coated culture flasks in Endothelial Cell Grown Medium (EGM) supplemented with 10% heat-inactivated FBS. HBMEC-28 cells were propagated in medium prepared using the EGM™ BulletKit™ (Lonza) according to the directions of the manufacturer.
Plasmids encoding human ICAM-2 and ICAM-2 variants
The plasmid encoding human ICAM-2 was generated as published . Briefly, cDNA encoding ICAM-2 was generated from RNA isolated from human umbilical vein endothelial cells (Clonetics, San Diego, CA). Primers for full length ICAM-2 were: forward (5'GCTTCCGCTGCCTGGATTCT3') and reverse (5'AAGTCCAGGTGTTGTATTC3'). Amplification was performed at 95°C for 1 min; then 30 cycles of 94°C for 30 sec, 55°C for 30 sec, 72°C for 1 min, followed by 72°C for 7 min. The resulting cDNA was isolated after electrophoresis in agarose gels, sequenced in its entirety by automated sequencing methods (St. Jude Hartwell Center for Bioinformatics, Memphis, TN), and subcloned into the BamH1 restriction site of the expression plasmid pIRESneo2 (Clontech, San Jose, CA) to generate pIRES.ICAM-2. Plasmid transfections were carried out using FuGene6 (Roche Diagnostics, Indianapolis, IN). Forty-eight hours after transfection, 750 μg/ml geneticin (G418; Roche Diagnostics Corporation, Indianapolis, IN) was added to select transfected cell populations. The use of a vector containing an internal ribosomal entry site (IRES) between the ICAM-2 cDNA and the gene encoding the G418 resistance protein eliminated the need to isolate and characterize multiple individual clonal cell lines. The ICAM-2 cDNA sequence was verified as error-free in the resulting cell line (SK-N-ASpIRES.ICAM-2) by the St. Jude Hartwell Center.
Mutagenesis and nomenclature of ICAM-2 variants
The objective of this study was to evaluate the impact of the glycosylation status of ICAM-2 on the function in NB tumor cells. Therefore, mutagenesis by overlapping PCR, using Pfu polymerase (QuickChange mutagenesis kit; Stratagene-Agilent Tech, Wilmington, DE) and pIRES.ICAM-2 as a template, was performed to replace some or all of the six asparagine glycosylation sites with alanine residues at positions 47, 82, 105, 153, 176, and 187, each of which is glycosylated in the endogenous wild-type protein. Alanine was chosen for substitution at all six or of a subset of glycosylation sites to prevent glycosylation [24, 25, 26]. Plasmids encoding mutated variants of ICAM-2 cDNA were identified by restriction enzyme analysis and sequences confirmed by direct DNA sequencing. Transfection of plasmids encoding ICAM-2 variants into SK-N-AS cells, selection of transfected cells, and culture conditions were the same as for SK-N-ASpIRES.ICAM-2 transfectants. Plasmids and transfected cell lines are designated as glycosylation site variants (gsv) followed by the positions of the amino acids (asparagines) that were replaced with alanine. For example, gsv1,4,5 is non-glycosylated at amino acids 47, 153 and 176 (Figure 1). In Figures 2, 3, 4, 5, 6, 7 and 8, transfected SK-N-AS cell lines expressing variant forms of ICAM-2 are referred to as the specific variant expressed: gsv1,4,5; gsv1,2,5; gsv4,5; and gsv1-6. SK-N-AS cells expressing ICAM-2 WT are labeled in the Figures as “WT”. SK-N-ASpIRESneo2 control transfectants are labeled “neo”.
Cell proliferation assays (cell doubling time)
To determine if the growth rates of all SK-N-AS transfectants expressing ICAM-2 variants were comparable, 1×106 cells were plated in 75 cm2 flasks, and cell numbers determined daily thereafter, using a hemocytometer. Doubling times were calculated using http://www.doubling-time.com/compute.php.
Each well of a 6-well plate was plated with 1mL 0.8% Sea-plaque agarose in DMEM with 10% FBS, and cooled to 4°C overnight. NB cells were resuspended in soft agar (0.4%) in DMEM with 10% FBS at a density of 30,000 cells in 10 mL, and 1 mL of cell suspension was overlaid in the wells containing 0.8% agar. Plates were then incubated at 37°C for 14-21 days. Colonies of >20 cells were identified microscopically and the number of colonies/well recorded. Six replicate wells of each transfectant were included in at least three independent experiments, as published previously [13, 28].
Scratch assays (wound healing assays)
To assess the motility of transfectants expressing ICAM-2 variants, we performed scratch or wound healing assays . Cells were plated at an initial density of 1×106 cells per well in 6-well plates and allowed to grow to confluency. A centerline was marked on the underside of each well along its horizontal axis, to designate loci at which images would be acquired at each time point. Vertical linear defects (scratches) were introduced into cell monolayers using a 200 μL pipet tip. Each well received 3 scratches. Images were acquired at 0, 24, 48, and 72 hours post scratch, at 100× magnification at each intersection of the scratch wound (vertical defect) and the marked horizontal centerline using a Dr-5 digital camera (Southern Microscope) mounted t22232o a Nikon Eclipse TS100 inverted microscope. For each time point, 5 measurements were taken per well in each of 3 wells and the average the horizontal width of the linear defect in pixels calculated using Adobe Photoshop CS4 (version 11.0.2).
Biotinylation of surface proteins
Cells (SK-N-AS cells transfected to express ICAM-2 WT or variants gsv1,4,5; gsv1,2,5; gsv4,5; or gsv1-6) were plated in 175 cm2 tissue culture flasks (Corning) with standard growth medium (high glucose DMEM + 10%FBS + 2 mM L-glutamine) and grown to near-confluence. Cells were washed 3 times with ice-cold PBS (pH 8.0) and surface proteins biotinylated for 30 minutes at room temperature using 0.5 mg/ml EZ-Link® Sulfo-NHS-LC-Biotin (21335; Thermo Scientific/Pierce) reconstituted in PBS (pH 8.0). The biotinlyation reaction was quenched by washing the cells 3 times with 100 mM glycine in PBS (pH 7.2). Cells were then lysed with 0.5% NP-40 + complete Mini protease inhibitor (Roche) and homogenized. Biotinylated protein preparations were then incubated with 100 μl Pierce streptavidin® resin (6% crosslinked beaded agarose 50% aqueous slurry) at room temperature for 20 minutes with gentle rocking, and then centrifuged to separate membrane-associated, biotin-avidin precipitated proteins from unlabeled proteins. After unbound proteins (supernatant) were removed, beads were washed 3 times with cold lysis buffer, boiled in sample buffer, and subjected to SDS-PAGE. Following electrophoresis, standard immunoblots were performed.
Cleavage of N-linked glycans was carried out using Endo H (#P0702L; New England BioLabs, Ipswich, MA) and PNGase F (#P0704S; New England BioLabs, Ipswich, MA) according to the manufacturer’s instructions. In brief, 20 μg of protein from control cells (HBMEC-28) or NB cells expressing ICAM-2 WT or a variant were denatured at 100°C for 10 minutes with glycoprotein denaturing buffer (5% SDS, 0.4M DTT in PBS). After cooling, protein solutions were centrifuged and incubated for an additional hour at 37°C with 2 μl of either Endo H enzyme (plus G5 Reaction buffer, pH 5.5; New England Biolabs) or PNGase F enzyme (plus G7 reaction buffer, pH 7.5 plus 10% NP-40 ; New England Biolabs). Control samples were subjected to the same denaturing and digesting conditions, but substituting equivalent volumes of water for enzyme. Samples were then subjected to SDS-PAGE and immunoblot analyses.
Immunoprecipitations and immunoblots
Co-immunoprecipitations (IP) were done as described previously . The antibody used for IP of α-actinin was MAB1682 (Millipore, Fisher Scientific, Savannah, GA). Antibodies used for immunoblots (IB) for ICAM-2, α-actinin, and actin were AF244 (R&D Systems, Minneapolis, MN) and sc-1512 (Santa Cruz Biotech, Santa Cruz, CA), 4968 (Cell Signaling Technology, Danvers, MA), and A5316 (Sigma-Aldrich, St. Louis, MO), respectively. AF244 is a goat polyclonal IgG that recognizes the extracellular domain of ICAM-2. C-20 is a goat polyclonal IgG that recognizes the intracellular C-terminus of the ICAM-2 protein. Secondary HRP-conjugated anti-goat (AF244, sc-1512), anti-rabbit (4968) and anti-mouse (A5316) antibodies were purchased from Santa Cruz Biotech. The ECL system (Pierce ECL Chemiluminescent Substrate; Thermo Scientific) was used to detect presence of horseradish peroxidase (HRP) enzyme. Immunoblot result in Figure 2D was quantitated using Adobe Photoshop CS4 (San Jose, CA) by multiplying area by integrated intensity of the band of interest and normalizing that result to that of a control protein (actin) band.
Subcellular localization of F-actin
Actin fibers were visualized by fluorescence microscopy using standard methods . Briefly, cells were plated in chamber well slides (2 × 105 cells per chamber) and allowed to adhere. Approximately 18 hours after plating, cells were washed with PBS and fixed with 3.7% (w/v) paraformaldehyde in PBS for 10 minutes at room temperature. Remaining attached cells were washed with PBS, and permeabilized with 0.2% (v/v) Triton X-100 for 1 minute. Actin fibers were stained with 10 μg fluorescein isothiocyanate (FITC)-conjugated phalloidin (P5282; Sigma-Aldrich, St. Louis, MO) in 1 mL phosphate buffered saline (PBS) for 30 minutes. Phalloidin-stained fibers were visualized by confocal fluorescence microscope equipped with narrow band filters, by standard methods (Figure 5A) or by the Zeiss Axio Observer Z.1 microscope platform in conjunction with Zen 2011 Blue imaging software (Carl Zeiss)(insets in Figure 5A). DAPI (4’,6-diamidino-2-phenylindole; appears as blue fluorescence) was used to detect DNA.
Fluorescence-activated cell sorting (FACS)
Flow cytometric analyses were used to verify the cell membrane localization of ICAM-2 and ICAM-2 variants. Cells (1 × 106) were trypsinized, washed twice with PBS, and incubated for 30 min with goat serum (G9023, Sigma-Aldrich) diluted 1:10 in PBS. Cells were then incubated for 60 minutes on ice with mouse monoclonal anti-human ICAM-2 antibody (CBR-IC2/2, sc-23935 PE; Santa Cruz Biotech). A separate aliquot of cells was incubated with mouse isotope-matched IgG (sc-2025, Santa Cruz Biotech, Santa Cruz, CA) as a negative control. All samples were then washed twice with FACS buffer (1% BSA in PBS) and incubated for 60 minutes on ice with phycoerythrin (PE, sc-3798, Santa Cruz Biotech, Santa Cruz, CA)-conjugated goat anti-mouse IgG. Data were acquired on an LSR-II cytometer (BD Biosciences, San Jose, CA) and analyzed using FlowJo v 7.6.1 (TreeStar) software. Only intact cells, as identified by forward and side light scatter, were analyzed. Propidium iodide (5 μg/mL PBS; stored at 4°C in the dark) staining was also used as a parameter to exclude non-viable cells.
Transfected cells were seeded at a density of 15,000 cells/cm2 and maintained under standard culture conditions for 24-48 hours. Photomicrographs were acquired at 20× magnification using a Dr-5 digital camera (Southern Microscope) mounted to a Nikon Eclipse TS100 inverted microscope and archived with TSView software (version 7.1.04, Tucsen Imaging Technology Co./Southern Microscope, Inc., Haw River, NC).
Cells were washed three times with PBS at 4°C, and resuspended in Cell Lysis Buffer (10 mM HEPES, 10 mM NaCl, 1 mM KH2PO4, 5 mM NaHCO3, 1 mM CaCl2, and 0.5 mM MgCl2 solution ) + 1 mM EDTA + protease inhibitor (complete mini protease inhibitor tablets; Roche Applied Science, Indianapolis, IN) solution. Cells were allowed to swell for 5 minutes on ice and then homogenized using a Fisher Scientific Misonix XL2000 Ultrasonic Homogenizer (Fisher Scientific), and centrifuged at 7,500 rpm for 5 minutes. The resulting supernatant suspension contained both plasma membrane and cytosolic proteins. This suspension was then re-centrifuged at 25,000 rpm for 30 minutes to separate the plasma membrane (pellet) from the soluble protein fraction. The crude plasma membrane pellet was then resuspended in 40 μl PBS and standard assays done to determine the protein concentration of these suspensions. Samples were stored at -80°C until ready for use. Suspensions were verified as membrane-enriched by immunoblot analysis for the plasma membrane marker (ATP1A1; Novus, Novus Biologicals, Littleton, CO) .
Mouse model of metastatic neuroblastoma
Female Es1 e /SCID mice (6-8 weeks old) were obtained from St. Jude Children’s Research Hospital Animal Resources Center (ARC) (Memphis, TN), with the approval of Dr. Phil Potter . The in vivo animal studies were carried out in accordance with a protocol approved by the St. Jude Children’s Research Hospital Animal Care and Use Committee (Approval Number: 374). All mice were maintained in the Animal Resources Center at St. Jude and monitored daily for tumor growth. Mice were euthanized as soon as any animal that appeared to be in distress or discomfort. Animals were housed in an AAALAC accredited vivarium at St. Jude Children’s Research Hospital Animal Resources Center under the direction of Dr. Richard Rahija. Bedding and chow were autoclaved and cages changed twice weekly.
When injected intravenously into the tail veins of Es1 e /SCID mice, SK-N-AS NB cells (5 × 105 cells) produce disseminated tumors in 100% of mice. The number of cells administered was not toxic to Es1 e /SCID mice and no discomfort or death was seen at the time of injection. In this model, there is no “primary tumor” but the pattern of tumor development recapitulates the clinical dissemination of high-risk NB; tumors develop in multiple anatomic locations including lung, liver and bone marrow [33, 34]. Groups of 10 (neo and WT transfectants) or 5 mice (gsv1,4,5; gsv1,2,5; gsv4,5; gsv1-6 transfectants) were followed for 300 days after intravenous injection of tumor cells. Any animal that appeared to be in distress was euthanized and the day of euthanasia was recorded as the day of death.
Statistical analyses were performed using GraphPad Prism software, version 5.02 (GraphPad, San Diego, CA); graphs were generated using the same software. Two-tailed t tests were used to analyze results of soft agar assays and two-way ANOVA followed by Bonferroni post tests was used to analyze scratch assays. Soft agar assays and scratch (wound healing) assays were repeated a minimum of three times, with each experiment including six replicates of each cell line. Kaplan Meier survival data were used to calculate the 95% confidence interval for time-dependent fractional survival, using a log-rank (Mantel-Haenszel) test to compare survival of mice receiving vector control cells (neo), ICAM-2 WT, or gsv transfected cells.
Results and Discussion
Structural domains of ICAM-2 and ICAM-2 glycosylation site variants (gsv)
The schematic structure of ICAM-2 (Figure 1) reflects the complete 275 amino acid glycoprotein. The indicated domains of this extensively glycosylated protein were discussed in the Background section. The heavy glycosylation status of the ICAM-2 WT protein dictates its migration in SDS-PAGE gels as a diffuse band rather than as a discrete band of specific molecular mass. In this study, as the degree of glycosylation decreases when glycosylation sites are mutated, variants are predicted to migrate at different rates even though the number of amino acids remains unchanged (bottom panel of Figure 1). The non-glycosylated variant gsv1-6 has a predicted molecular mass of 30 kDa.
ICAM-2 glycosylation site variants (gsv) localize to cell membranes in transfected SK-N-AS neuroblastoma cells
Next, we examined ICAM-2 N-glycan sensitivity to endoglycosidase H (Endo H) and N-glycosidase F (PNGase F) since modification of glycosylation status can be detected using these enzymes. Endo H hydrolyzes high mannose and hybrid N-glycans synthesized in the endoplasmic reticulum (ER), while PNGase F hydrolyzes all N-linked glycans including complex glycans synthesized in the Golgi. ICAM-2 expressed by all transfectants and HBMEC-28 cells were sensitive to PNGase F and displayed increased electrophoretic mobility following a 1 hour incubation with PNGase F (Figure 2D), with non-glycosylated forms of ICAM-2 migrating at ~30 kDa. (The “nonspecific” band that appears at ~36kDa in all lanes marked + PNGase F is the PNGase F protein itself.) In contrast to results with PNGase F, results following incubation of cell lysates with Endo H differed for forms of ICAM-2 that were glycosylated at position 47 compared with those that were not glycosylated at this position. ICAM-2 WT and gsv4,5 and ICAM-2 from control HBMEC-28 cells were Endo H resistant, while gsv1,4,5 and gsv1,2,5 were Endo H sensitive. Potentially, N-glycans of ICAM-2 modify protein conformation thereby impacting protein stability, in addition to their documented roles in ligand recognition. Comparison of results from gsv4,5 with gsv1,2,5 and gsv1,4,5 suggests that N-glycans at amino acid 47 may be the most critical with respect to protein conformation and stability. Interestingly, quantitation of this experiment (Figure 2E) by densitometric scanning demonstrated that the level of gsv1,2,5 expressed was ~60% that of WT protein and the level of gsv1,4,5 was ~83% that of WT protein. Possibly this observation reflects a decreased protein stability of these variants, each of which contained an amino acid substitution at position 47 that prevented glycosylation at this site. Further, the robust level of expression of variant gsv4,5, the only variant that did not contain an amino acid substitution at position 47, is consistent with the hypothesis that N-glycosylation at this position may be critical to ICAM-2 protein structure and stability. Our data comparing Endo H and PNGase F sensitivities of ICAM-2 WT and variants suggest that N-glycosylation site at amino acid 47 may be the most critical N-glycan structure with respect to protein stability.
Next, we showed that similar to the WT protein, hypo-glycosylated ICAM-2 variants were associated with the plasma membrane (Figure 2F, 2G, 2H). We first isolated membrane-enriched fractions of each transfectant and performed immunoblots for ICAM-2 and also for the plasma membrane marker ATP1A1 (Na+/K+ transporting ATPase subunit alpha 1; Novus Biologicals, Littleton, CO). Membrane-enriched fractions contained readily detectable levels of ATP1A1 and also ICAM-2 proteins of the expected molecular mass using an antibody that recognizes the CD domain of ICAM-2 (sc-1512; Santa Cruz Biotech) (Figure 2F). To corroborate these data, we performed immunofluorescence staining using intact transfected cell lines and an antibody that recognized the ED of ICAM-2 (CBR-IC2/2-PE). Flow cytometric analysis of WT, neo and each of the four gsv transfectants demonstrated measurable levels of antibody reactivity (cell surface expression in intact cells) for ICAM-2 protein only for cells expressing WT and gsv4,5 (Figure 2G), even though gsv1,4,5, gsv1,2,5, and gsv1-6 were clearly seen by immunoblot. The CBR-IC2/2 antibody was generated using full length ICAM-2 (Santa Cruz Biotech). This antibody recognizes the LFA-1 binding domain of ICAM-2 which includes amino acid residues #42-63 within extracellular IgLD-1 domain [17, 35, 36, 37, 38], and inhibits binding of LFA-1 to ICAM-2. Our FACS results show that the CBR-IC2/2 did not react with any of the three variants containing an amino acid substitution at position 47 (gsv1,4,5, gsv1,2,5 and gsv1-6), suggesting that substitution at this position destroyed antibody recognition. However, since gsv4,5 contained the endogneous Asn at position 47, we used CBR-IC2/2 to confirm membrane localization of the expressed variant. The data are consistent with the previous report [17, 35, 36, 37, 38] that antibody CBR-IC2/2 recognizes amino acid residues within IgLD-1 and that an Asn residue at position 47 is essential for that recognition.
Next, cell surface protein biotinylation was performed to confirm cell membrane surface localization of all ICAM-2 variants. As shown in Figure 2H, biotinylation of proteins of intact cells showed readily detectable ICAM-2 proteins with the expected electrophoretic mobility for all cell lines. Data in Figures 2F, 2G, and 2H indicate that ICAM WT and variants localize to cell membranes.
Taken together, the data indicate that variable glycosylation does not affect the subcellular localization of ICAM-2 and that variants localize to the plasma membrane similar to the endogenous protein. As expected, control-transfected SK-N-AS cells showed no detectable ICAM-2 expression.
Morphology and cell doubling time of transfected gsv cell lines
Of particular interest, SK-N-ASpIRESneo cells and gsv transfectants appeared more discohesive and pleomorphic than cells expressing ICAM-2 WT. Also, SK-N-ASpIRESneo cells and gsv transfectants had relatively non-smooth borders compared to cells expressing ICAM-2 WT. Cells expressing gsv4,5 demonstrated a “drunken honey comb” appearance, a description frequently appropriate to malignant cells with decreased cohesiveness and non-smooth borders. Cells expressing gsv1-6, grew in smaller clusters than other transfectants. The most consistent findings were the relatively discohesive and pleomorphic characteristics of SK-N-AS cells expressing gsv transfectants, compared to ICAM-2 WT, possibly indicative of a more motile phenotype than that of cells expressing the WT protein.
To address this possibility and to more completely characterize the functional phenotype of the gsv transfectants, we characterized each transfectant using assays that reflect specific aspects or cellular functions involved in metastasis. These assays included cell motility (wound healing or scratch assays), anchorage-independent growth in soft agar, subcellular localization of actin fibers (F-actin), and development of disseminated tumors in an in vivo model of metastatic NB.
ICAM-2 variants altered tumor cell motility but did not affect actin fiber distribution in vitro
First, in standard scratch assays the width of the scratched area that remained free of cells at 24 hour intervals after introducing the scratch was quantitated in pixels. Results were expressed as the degree to which the scratch had closed, at 24 hour intervals post scratch (% scratch closure). SK-N-ASpIRESneo cells which express no detectable ICAM-2 completely closed the scratch within 72 hours (Figure 4A). In contrast, SK-N-ASpIRES.ICAM-2 cells migrated more slowly (P < 0.001, compared to SK-N-ASpIRESneo cells), with only 56% of the initial scratch filled at 72 hours (Figure 4B). In general, cells expressing the gsv ICAM-2 constructs migrated more slowly than control SK-N-ASpIRESneo cells and more rapidly than SK-N-ASpIRES.ICAM-2 (WT) cells. P values ranged from < 0.05-0.001 when cell lines expressing gsv constructs were compared with either control cell line. The single exception was the lack of a significant difference in the motility of cells expressing gsv4,5 and cells expressing no detectable ICAM-2 (neo, in Figure 4) at any time point. Simple differences in cell doubling times do not account for the apparent lack of function (failure to inhibit migration) of gsv4,5, as the doubling time for these cells did not differ from other transfectants.
gsv4,5 was the only construct evaluated that did not contain an Asn → Ala substitution at amino acid 47, suggesting that glycosylation at this site minimizes or circumvents the ability of ICAM-2 to inhibit NB cell motility. Possibly, glycosylation at position 47 inhibits adhesion, but this effect may be modulated by glycosylation at other sites in the WT protein. However, since ICAM-2 WT is glycosylated at this site and the WT protein significantly inhibits NB cell motility, the data are not consistent with a straightforward correlation between glycosylation of this specific residue and cell motility, as reflected by this assay. The data demonstrate that NB cell motility was most affected by fully glycosylated ICAM-2, but that three of the hypo-glycosylated ICAM-2 constructs retained an attenuated function compared to the endogenous fully-glycosylated protein.
Second, we performed phalloidin staining assays to determine the subcellular distribution of actin fibers. The ICAM-2-mediated decrease in NB cell motility suggested a possible involvement of the actin cytoskeletal network, a primary regulator of cell motility; and our previous work demonstrated a correlation between transverse distribution of actin fibers and a relatively motile metastatic phenotype in a panel of NB cell transfectants. As a preliminary assessment of actin cytoskeletal function, we examined the subcellular localization of actin fibers in cells expressing ICAM-2 variants. Fluorescence photomicrographs of F-actin in control cell lines (neo and WT cells in Figure 5)  stained with FITC-conjugated phalloidin demonstrated the expected contrast in distribution of actin fibers; relatively motile SK-N-ASpIRESneo cells harbored transverse actin fibers, while relatively non-motile SK-N-ASpIRES.ICAM-2 cells had juxtamembrane actin fibers. If the scratch assay and F-actin distribution accurately reflect cell motility, then scratch assay results would predict that cells expressing gsv4,5 would have transverse actin fibers and the other three constructs would have juxtamembrane fibers. FITC-conjugated phalloidin staining clearly demonstrated that this prediction did not hold true, and that cells expressing all four ICAM-2 variants had transverse actin fiber distribution (Figure 5 and data not shown). This assay does not provide a simple preliminary screen to assess the impact of ICAM-2 WT or gsv on NB cell motility in vitro.
We then also addressed whether the observed differences in actin fiber distribution could be attributed to differences in cell density. We plated neo transfectants at twice the original density and ICAM-2 cells at half the original density shown in the insets of the two upper panels in Figure 5A. Altering cell density did not affect actin fiber distribution. Actin fiber distribution appeared to be unrelated to cell density. As an alternative approach to examine the effect of cell density on F-actin distribution in the neo and ICAM-2 WT transfectancts we again performed a scratch assay as shown in Figure 4, but just prior to complete closure of the scratch by neo transfectants (~72 hours post scratch), we fixed both neo and ICAM-2 WT transfectants and incubated the cells with FITC-conjugated phalloidin. The question to be addressed was whether the F-actin distribution of cells at the leading edge of migration would be similar to its distribution in non-migrating cells. Fluorescence photomicrographs in Figure 5B show that both non-migrating and migrating SK-N-ASpIRESneo cells display transverse actin fibers and both non-migrating and migrating SK-N-ASpIRES.ICAM-2 cells display juxtamembrane actin fibers.
All four ICAM-2 variants inhibited colony growth in anchorage-independent growth assays
ICAM-2 WT and all four variants associate with α-actinin and actin
In interpreting the IP/IB data, we note that the data are qualitative and do not necessarily reflect the ratio in which these proteins associate for several reasons. Firstly, immunoblots for glycosylated ICAM-2 give an area x density signal approximately 300% - 400% greater than that for the same amount of de-glycosylated ICAM-2 (Figure 2C). Secondly, α-actinin induces actin self-association , resulting in variable numbers of actin molecules associated with a single α-actinin molecule. Thirdly, the necessary use of mono- and polyclonal antibodies likely allows binding of secondary antibodies to a variable number of recognition sites on primary antibodies. However, the data do clearly indicate that all four variants associate with α-actinin, an interaction essential to ICAM-2-mediated suppression of metastatic potential. Based on this mechanistic consideration and on cell function assays (Figures 4 and 6), we would predict that all hypo-glycosylated ICAM-2 variants retain at least partial function, in suppressing metastatic properties of NB cells. Next, we tested this hypothesis in a murine model of metastatic NB. Of note, based on co-IP data in Figure 7, ICAM-2 WT and gsv4,5 appear to interact more readily with α-actinin than do the other three hypo-glycosylated ICAM-2 variants. We next evaluated the function of ICAM-2 WT and variants in an in vivo model of metastatic neuroblastoma.
Hypo- and non-glycosylated ICAM-2 delay tumor progression in a preclinical model of metastatic neuroblastoma
While in vitro cell motility (scratch assay) most accurately predicted cell phenotype in vivo, no single in vitro assay consistently predicted results in vivo for all ICAM-2 variants. In general, the morphology, anchorage-independent growth, and motility of cells expressing hypo- or non-glycosylated variants of ICAM-2 were intermediate to characteristics of negative and positive control transfectants expressing no detectable ICAM-2 or the WT protein. In vivo results for all transfectants were also intermediate to these control cell lines, in that expression of gsv transfectants significantly delayed but did not prevent the occurrence of disseminated disease in a model of metastatic NB. In addition, our results from Endo H sensitivity studies suggest that glycosylation at position 47 may be critical to protein folding or conformation, and that glycosylation at this position likely affects protein stability. Potentially, a decrease in ICAM-2 protein stability leads to lower levels of membrane-associated ICAM-2, which, in turn, impacts the novel role of ICAM-2 in suppressing metastatic properties. We conclude that the glycosylation status of ICAM-2 significantly affects the function of this protein in SK-N-AS NB cells.
We are indebted to Dr. Mary K. Danks for her support and discussions. We thank Dr. Phil M. Potter for his support, helpful discussions, and for allowing us to use the mouse strain developed in his laboratory. We are also grateful to Joanna S. Remack, Doris A. Phelps, and Rebecca A. Bush for their outstanding technical assistance. We thank Dr. E. van der Schoot (CLB, Sanquin Blood Supply Foundation, The Netherlands) for her gracious gift of the HBMEC-28 bone marrow endothelial cells. This work was supported by the NIH Cancer Center Core Grant (CA21765); and the University of Alabama at Birmingham-Comprehensive Cancer Center- Young Supporter’s Board-New Faculty Development Award (YSB-NFDA).
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