Background
CD26/dipeptidyl peptidase IV (DPPIV) is a 110–115 kD glycosylated protein that exists as a homodimer. It is a multifunctional membrane protein with three domains: extracellular, transmembrane, and cytoplasmic. It is widely expressed on a number of tissues and can regulate tumor growth and development [
1‐
7]. The interaction of CD26/DPPIV with other proteins, including collagen, fibronectin, and caveolin-1, likely influences its involvement in cell motility and invasion [
8,
9]. CD26 and its associated DPPIV enzyme activity play a key role in T-cell biology, serving as a marker of T-cell activation and participating in several signaling pathways [
10‐
13]. CD26 is also a marker of aggressive cancers, including T-cell malignancies [
14‐
20]. Interestingly, the cleaved form of CD26, which is present in plasma, is inversely correlated with several aggressive cancers [
21].
Our previous work showed that CD26-depleted human T-anaplastic large cell lymphoma (T-ALCL) Karpas 299 cells were unable to form tumors in SCID mice [
8], and that CD26 expression on two T-cell lines increased SDF-1-α-mediated invasion [
22]. We were interested in looking at CD26-associated gene products involved in cell motility and therefore conducted microarray analysis of genes involved in this pathway in parental Karpas 299 and CD26-depleted clones, and found that versican expression was associated with changes in CD26 level
. Microarray analysis revealed that mRNA level for versican was considerably lower in CD26-depleted Karpas 299 cells than parental Karpas 299 cells (1:88). Although mRNA levels for several other genes, including IGFBP3, tenascin C, and SPOCK1, were also lower in CD26-depleted cells than parental Karpas 299, Western blots confirmed a difference in protein expression for versican only, but not for the other three proteins. Versican is a large chondroitin sulfate proteoglycan involved in the regulation of adhesion, migration, invasion, and angiogenesis [
23]. Versican binds to ECM constituents including type I collagen, fibronectin, and hyaluronan (HA) [
24] and a number of cell-surface proteins, including CD44, integrin β1, and toll receptor 2 [
25,
26]. Versican levels are elevated in most malignancies, and correlated with poor patient outcome. Versican is secreted by peritumoral stromal cells and also by the individual cancer cells [
27,
28]. Four major isoforms exist that differ with respect to the number and position of GAG molecules attached, which are important for association with other proteins. Of note is that the V0 and V1 isoforms are reported to be the isoforms most closely associated with cancers.
In the present paper, we examined in detail CD26 involvement with cell migration and adhesion in T-cell lines. Expression array analyses of genes involved in extracellular matrix and adhesion pathways indicated that versican expression was significantly higher in parental T-ALCL Karpas 299 cells compared to CD26-depleted Karpas 299 cells. To further investigate the relationship between CD26 and versican, we conducted knock down studies of versican in Karpas 299 cells and evaluated for a potential effect on expression of signaling proteins and adhesion. We found that the use of shRNA to knock down versican expression in the parental Karpas 299 cells resulted in both lower MT1-MMP transcription and surface expression. To confirm that cell behavior was consistent with the observed change in MT1-MMP activity, several assays were performed; secretion and cleavage of CD44, collagenase I activity, and adhesion. In all three assays, parental Karpas 299 cells exhibited higher activity compared to cells in which CD26 or versican was knocked down. Finally, ERK activation, which is required for migration and invasion, was also highest in the parental Karpas 299 cell line.
Methods
Reagents
Bovine serum albumin (BSA), polybrene (hexadimethrine bromide), sodium dodecyl sulfate, glycine, sodium deoxycholate, trypsin, phosphate buffered saline, and dimethyl sulfoxide were from Sigma Life Science, St. Louis, MO. TX-100, NP-40, and Tween-20 were from Fisher Scientific, USA. Puromycin was from Life Technologies, USA. Rat tail collagen and bovine skin collagen were purchased from BD and Advanced Matrix, respectively. GM6001, a general MMP inhibitor was purchased from Calbiochem.
Cell culture
Karpas 299 cells were originally obtained from the American Type Culture Collection (ATCC, Manassas, VA) and maintained in RPMI-1640 (Hyclone, Logan, UT). Karpas 299 cells depleted of CD26 have been described previously [
8]. All cell media contained 10% fetal bovine serum (Hyclone), penicillin (100 u/ml) and streptomycin (100 μg/ml).
Expression arrays
GEArray express human extracellular matrix and adhesion molecule microarrays were carried out by SuperArray Bioscience Corporation on 10 μg total RNA isolated from parental Karpas 299 cells and Dep1, a cell line deficient in CD26 expression.
Real-time RT-PCR
Real-time RT-PCR was carried out on 10 ng total RNA (RNeasy kit, Qiagen). SYBR Green-based real-time RT-PCR was carried out using QuantiTect Primer Assays (Qiagen) for CD26 (Hs_DPP4_1_SG), Versican (Hs_VCAN_1_SG), and GAPDH (Hs_GAPDH_1_SG).
RT-PCR
RT-PCR was carried out on 10 ng of RNA isolated from parental Karpas 299 cells, Dep1, and Dep2 using the Titan One Tube RT-PCR system (Roche Applied Science). The primers were described previously [
29]. The sizes of the amplification products were 405 bp for V0 (forward: 5′- TCAACATCTCATGTTCCTCCC-3′ and reverse: 5′-TTC TTCACTGTGGGTATAGGTCTA-3′) and 336 bp for V1 (forward: 5′-GGCTTTGACCAGTGC GATTAC-3′ and reverse: 5′-TTCTTCACTGTGGGTATAGGTCTA-3′). The reverse transcription step was carried out at 50° for 30 min, followed by denaturation for 2 min at 94°, amplified by 35 cycles (94° for 30 s, 55° for 45 s, 68° for 45 s) and elongated for 7 min at 68°.
Flow cytometry
Cells were washed once with staining buffer (PBS containing 1% BSA) and incubated on ice for 30 minutes with antibodies specific for the activity domain of MT1-MMP (ab51074, Abcam, Cambridge, MA), then with FITC goat anti-rabbit Ig at 0.125 μg/106 cells (BD Pharmingen). After washing with staining buffer twice, the cells were resuspended in PBS. The optimum amount of MT1-MMP antibody was determined by titration.
Gene silencing
Transduction ready viral particles for gene silencing of versican (versican shRNA, Santa Cruz Biotechnology, Inc., Santa Cruz, CA) were used to infect Karpas cells at a ratio of 0.5 virus particles per cell. Cells were pelleted the following day, resuspended in fresh media, and 48 hrs following transduction, puromycin was added at a concentration of 2.5 ug/ml. Following selection, stable clones were isolated by limiting dilution. Knockdown was monitored by running whole cell lysates and/or spent media on gels and probing with versican antibodies as described in the Western Blot section.
Cell lysis
Cells were lysed using RIPA (1% NP40, 0.5% DOC, 0.1% SDS, 150 mM NaCl, 50 mM TrisCl, pH 8.0) or TX100 buffer (50 mM TrisCl, pH 8, 0.15 M NaCl, 1% TX-100) containing a protease/phosphatase inhibitor cocktail (Pierce, Rockford, IL). Protein concentration was determined using the bicinchoninic acid protein assay reagent (Pierce).
Isolation of vesicles from serum free media
Cells (8 × 10
6) were grown in serum free media for 48 hours, followed by centrifugation at 600 ×g for 15 min, then 1500 × g for 15 min, and the resulting supernatant was subsequently centrifuged at 100,000 × g for 1 hr at 4°C. Pelleted vesicles were suspended in PBS and assayed for protein [
30].
Western blots
Equal amounts of protein were run on 5.0, 7.5% or 10% polyacrylamide gels. For detection of versican, samples were combined with sample buffer without reducing agent. Following transfer, blots were blocked, then probed with one of the following antibodies: anti-CD26 (AF1180) and anti-CD44H (clone 2C5) were from R & D Systems, Inc., Minneapolis, MN; anti-versican (clone 2B1, Seikagaku, Tokyo, Japan); and anti-MT1-MMP (ab38971, Abcam). Anti-phospho-p44/42 MAPK (Erk ½) and anti-p44/42 MAPK (Erk ½) were from Cell Signaling Technology, Inc; anti-integrin alpha 5 chain (BD, cat# 610633). Precision Plus Protein Standards (Bio-Rad Laboratories, Hercules, CA) were run to estimate sizes of proteins of interest. Horseradish peroxidase-conjugated secondary antibodies and the detection reagent, SuperSignal West Dura Extended Duration Substrate, were from Pierce. Films were scanned using an Image Quant 400 (GE Healthcare, Piscataway, NJ).
Biotinylation and immunoprecipitation
Cells were suspended in PBS (2.5 × 107/ml) and incubated with 200 μl of 10 mM EZ-Link® Sulfo-NHS-LC-Biotin/ml cells for 30 min on ice. The cells were then washed 3× with PBS containing 100 mM glycine. Following lysis in TX100 buffer, 1 mg lysate was applied to a Streptavidin- Agarose spin column (Pierce), and following extensive washing, bound proteins were eluted with 2× sample buffer and heating at 100°C for 5 min. Eluates were run on 7.5% acrylamide gels and probed with anti-MT1-MMP antibody.
Collagen degradation in cultured cells
Collagen I degradation was monitored in live cells migrating through a native 3D collagen substrate. DQ™ collagen, type I from bovine skin, fluorescein conjugate (Molecular Probes) was copolymerized with rat-tail collagen type I, in RPMI media without phenol red (Life Technologies). After incubation for 48 hrs at 37°C, solid phase collagen and cells were pelleted and the supernatant analyzed for FITC using a Perkin-Elmer Victor
3 V multilabel counter [
31].
Collagen degradation in vesicles
The EnzChek collagenase assay (Life Technologies) was used to evaluate activity in vesicles isolated from conditioned media. In this assay, DQ™ collagen, type I from bovine skin, fluorescein conjugate (Molecular Probes) was used as substrate and the incubation was carried out at room temperature as described by the manufacturer. Each well of a 96 well plate contained 4.5 μg vesicle protein. Fluorescence was detected using the Perkin-Elmer instrument.
Adhesion assays
Adhesion assays were carried out essentially as described [
8]. Cells (5 × 10
5/well) were seeded into 12 well collagen I coated plates and incubated overnight. Unattached cells were removed, plates were washed three times with PBS and the adhesive cells remaining were quantified using the MTS assay. The total cell number was determined using uncoated wells and serial dilutions were used to construct a standard curve to convert absorbance at 490 nm to cell number.
Discussion
In this paper, we have focused on the differential expression of versican in CD26-expressing Karpas 299 cells as compared to a CD26-depleted clone and the associated changes in various cellular activities as related to tumorigenesis. As a point of reference, we presented a working model at the beginning of the paper. The emphasis is placed on MT1-MMP (MMP-14), since it is known to have several important activities which could account for the ability of CD26-expressing Karpas 299 cells to form tumors in SCID mice as opposed to the inability of CD26-deficient Karpas 299 cells to develop tumors in the same animal model [
8]. We do note that this simplified model does not take into account the complex roles that MT1-MMP and other MMPs play in cancer progression. For example, in addition to degrading the extracellular matrix, MT1-MMP plays an important role in tumor angiogenesis [
47] through upregulation of VEGF [
48] and immunoregulation through its effect on the release and activation of cytokines such as TGF-β, a well-known suppressor of T-lymphocyte reaction against cancer [
49].
In addition to the difference in versican expression, there were differences in adhesion, MT1-MMP surface expression, CD44 cleavage and secretion, and collagenase I activity. Although CD26 is known to bind both collagen [
50,
51] and fibronectin [
52], versican also binds these proteins, and can further strengthen the binding of CD26-expressing cells to the extracellular matrix. This conclusion is consistent with our observation that MT1-MMP surface expression was increased in cells bound to collagen I. Since localization of MT1-MMP to the cell membrane is required for its ability to degrade the extracellular matrix [
32], the decreased surface expression of MT1-MMP associated with loss of versican would be predicted to have an effect on cell motility, and possibly, tumorigenesis by interfering with the ability of tumor cells to interact with the microenvironment.
Our present work also established a relationship between CD44, CD26 and versican, with CD44 cleavage/secretion being higher in parental Karpas 299 cells than in cells depleted of versican (both CD26-depleted cells as well as CD26-expressing/versican depleted cells). Interaction with and cleavage of CD44 by MT1-MMP has been shown to facilitate migration by indirectly linking MT1-MMP to the actin cytoskeleton [
35,
36]. The function of MT1-MMP is regulated in large part by its localization; MT1-MMP activity has been observed at invadopodia [
53‐
55], lamellipodia [
35], and focal adhesions [
56], with CD44 cleavage and secretion appearing to play a role in the localization of MT1-MMP to the invadopodia [
35].
Our data also indicated a higher level of ERK activation in parental Karpas 299 cells compared to CD26-depleted or CD26-expressiong/versican-depleted clones. ERK activation is required for migration, invasion [
44,
57,
58], and CD44 upregulation. The requirement for matrix proteins along with ERK activation suggests that integrins may be involved in MT1-MMP regulation [
59], a conclusion that is further supported by colocalization of integrins with MT1-MMP in vesicles [
46,
60] and the existence of common recycling pathways [
61]. In a recent study, intracellular trafficking of MT1-MMP was found to be coupled with trafficking of integrin α5, ERK activation, and phosphorylation of MT1-MMP at Thr
567[
38]. We also detected these three proteins in vesicles isolated from conditioned media; MT1-MMP and phosphorylated ERK were highest in the parental Karpas 299 cells, whereas the amount of α5 integrin was approximately the same in all three cell lines.
Although regulation of versican expression is not well understood, it has been shown to be a target of Wnt signaling, regulated by the phosphatidylinositol 3-kinase (PI3K) pathway in human embryonic carcinoma cells [
62]. It is possible that it is also regulated by this pathway in Karpas 299 cells, since activated Akt/PKB is higher in the parental Karpas 299 cells than in CD26-depleted or versican-depleted cells (unpublished observations, author).
In addition to its ability to form homodimers, CD26 can also form heterodimers with fibroblast activation protein alpha (FAP or Seprase) [
63], which shares 48% homology with CD26 [
64], but unlike CD26, can digest collagen. Although this protein complex has been detected at the invadopodia of migrating fibroblasts [
65], we did not explore the role of Seprase activity in the collagenase I activity of Karpas 299 cells. However, our Western blot assays for Seprase did not detect a difference among parental Karpas 299 cells, Dep1, and 6RD3 (data not shown). While it has been suggested that CD26 and related proteins, such as FAP, may serve as valuable biomarkers for selected malignancies, better in-depth understanding of the functional roles of these molecules in particular tumor types and their associated microenvironment will improve our knowledge of the implications of their expression in tumor behavior [
66].
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
PAH performed the research; PAH and NHD designed the research study, analyzed the data, and wrote the paper; KO, SI and CM contributed essential reagents and analyzed the data; LHD analyzed the data and critically revised the paper. All authors read and approved the final manuscript.