Identification of APN/CD13 as the target antigen of FU3, a human monoclonal antibody that recognizes malignant fibrous histiocytoma
- Authors: Mikiko Aoki, Kazuki Nabeshima, Hiroyuki Hayashi, Makoto Hamasaki, Hiroshi Iwasaki
Published online on: Thursday, May 16, 2013
- Pages: 57-62
- DOI: 10.3892/ijo.2013.1940
Malignant fibrous histiocytoma (MFH), also called high grade undifferentiated sarcoma, collectively represent the most common types of sarcoma in the fifth and sixth decades of life. The overall incidence among adults approximates to 1–2 cases per 100,000 patients. Most MFH occur in the extremities and deep soft tissue (1). Approximately 5% of patients have metastases at presentation and MFH is aggressive with an overall 5-year survival probability of 50–60% (1). Surgical removal is presently the sole effective treatment and the goal of surgery is complete resection with negative margin.
Histopathologically, MFH shows a wide variety of morphological patterns. MFH commonly presents with marked cytological and nuclear pleomorphism, often with bizarre tumor giant cells, admixed with spindle cells and frequently with rounded histiocyte-like cells in varying proportions (2). MFH shows no evidence of true monocyte/macrophage/histiocytic differentiation. Several hypotheses suggest MFH arises from fibroblasts or primitive mesenchymal cells but current research does not show a definable line of differentiation. The diagnosis is controversial, but various cases are eligible for consideration as MFH (high grade undifferentiated sarcoma). At present, there are no useful immunohistochemical markers for the diagnosis of MFH; therefore, it is difficult to search for the origin of MFH.
Our laboratory generated monoclonal antibody FU3 using an MFH cell line as an immunogen. FU3 reacted strongly with the surface membrane of cultured MFH cells and with perivascular mesenchymal cells in frozen tissue sections. Accordingly, MFH may share common antigenicity with perivascular mesenchymal cells (3). Immuno-electron-microscopic studies demonstrated FU3-positive reactivity on the surface of cell membranes, which suggests that FU3 recognizes cell surface antigens (4–6).
The aim of this study was to identify the antigen recognized by FU3 antibody. Furthermore, we examined whether the antigen could be effectively applied to diagnosis and treatment of MFH.
Materials and methods
The MFH cell line SFT8503 was established in our laboratory, as described previously (6). The cell line was maintained in growth medium, Dulbecco’s modified Eagle’s medium/Ham’s F-12 (Wako, Japan), supplemented with 10% fetal calf serum, streptomycin (50 μg/ml) and penicillin G (50 U/ml).
Protein extraction and western blotting
The cultured cells were lysed in RIPA lysis buffer (50 mM Tris-HCl, pH 7.4, 150 mM NaCl, 1 mM EDTA, 1% NP-40; Millipore, Bedford, MA) and the lysed cells were sonicated on ice for 5 min three times and centrifuged at 15,000 rpm for 20 min at 4°C. The resultant supernatants were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). After electrophoresis, the proteins were transferred electrophoretically to Immobilon membrane (Millipore). Non-specific sites were blocked with 5% dry fat milk in Tris-buffered saline (TBS) at 37°C for 1 h and the membrane was incubated overnight at 4°C with monoclonal FU3 antibody or with commercially available CD13 antibody (Clone 38C12, ThermoScientific, Cheshire, UK). After washing with TBS-T (TBS containing 0.05% Tween-20), the membrane was incubated for 1 h with peroxidase-conjugated anti-mouse IgG. Color was developed with chemiluminescence reagents according to the instructions supplied by the manufacturer (DuPont New England Nuclear, Boston, MA).
Monoclonal antibody FU3, which was generated against MFH cells using a mouse hybridoma technique as previously described (3,4), was used to prepare an affinity column (7). We used cyanogen bromide CNBr-activated Sepharose 4B (GE Healthcare Ltd., UK) as an immunoaffinity matrix coupling to mouse FU3 antibody. The column was washed with phosphate buffered saline (PBS). Antigens bound to the matrix were then eluted from the column with 0.2 M glycine (pH 2.3). The eluted material was immediately neutralized with PBS and stored at 4°C. The eluted protein fraction of the column was purified by SDS-PAGE and immunoblotting. The purified protein was subjected to N-terminal amino acid sequencing (Takara Bio Inc. Otsu, Japan).
Our study included formalin-fixed, paraffin-embedded sections from 25 MFH [10 men, 15 women; age range, 26–81 (mean, 71) years], 9 synovial sarcoma [2 men, 7 women; age range, 20–88 (mean, 43) years], 10 liposarcoma [4 men, 6 women; age range, 20–74 (mean, 55) years], 10 leiomyosarcoma (4 men, 6 women; age range, 25–83 (mean, 62) years], 11 chondrosarcoma [7 men, 4 women; age range, 12–63 (mean, 42) years] and 5 osteosarcoma [5 women; age range, 14–57 (mean, 56) years], diagnosed at the Department of Pathology, Fukuoka University, Japan.
Immunohistochemical staining was performed using 4-μm thick paraffin-embedded sections, were deparaffinized and heated in a microwave oven (700 W) for 10 min to expose antigens in 10 mM Na-citrate buffer (pH 6.0; for CD13) or 1 mM EDTA/10 mM Tris-HCl buffer (pH 9.0; for FU3). The exposed antigen was detected using the labeled streptavidin-biotin method. The reaction was identified with naphthol AS-BI phosphate and counterstained with Mayer’s hematoxylin.
The staining results were evaluated semiquantitatively by two independent observers. Immunostaining was considered negative if stained tumor cells were <10%. In specimens considered positive, staining of the tumor was quantitated on a scale from 1–4 based on the percentage of positive tumor cells. The scale was structured as follows: 1+, 10–25% of cells positive; 2+, 25–50% of cells positive; 3+, 50–75% of cells positive; 4+, >75% of cells positive. In specimens considered high expression cases, staining of the tumor was quantified on scales 3+ and 4+.
Small interfering RNA (siRNA)
SFT8503 cells were grown to sub-confluence and treated with small interfering RNA (siRNA) for CD13 (Smart Pool, Dharmacon, Chicago, IL) or control siRNA (B-Bridge International, Sunnyvale, CA) using Lipofeamine 2000 (Invitrogen, Carlsbad, CA) accroding to the manufacturer’s instructions.
In vitro invasion assay
In vitro Matrigel invasion assay was performed by using 24-well Chemotaxicell chambers (pore size, 8 μm, Kubota Co., Tokyo, Japan) on 24-well culture plate. The upper and lower side of each chamber was coated with Matrigel (25 μg/filter, BD Biosciences). Hepatocyte growth factor (HGF; Peprotech Inc. Rocky Hill, NJ) was used as a chemoattractant. After incubation of cells for 72 h, the filters were fixed with formalin and stained with hematoxylin and the total number of cells that had invaded the Matrigel-coated filter were counted.
Immunoaffinity chromatography using FU3 antibody
Extracted proteins from SFT8503 MFH cells were purified using immunoaffinity chromatography with FU3 antibody, followed by immunoblotting. The N-terminal amino acid sequencing of the 150-kDa band (Fig. 1, arrow) revealed A-K-G-F-Y-I-S-K-S-L, which is identical to that of aminopeptidase N (APN)/CD13, known as an important zinc-dependent metallo-exopeptidase.
Western immunoblot analysis of whole ectracts (lane 1), flow through (lane 2), washings (lane 3) and elutes (lanes 4–10) immunostained with monoclonal antibody FU3 and showing the 150-kDa band.
The FU3 recognizing antigen is possibly aminopeptidase N (CD13)
To confirm the identity of FU3-reactive antigen as APN/CD13 we used immunoblotting and siRNA methods. First, by immunoblotting SFT8503 MFH whole cell extracts and an eluted protein from immunoaffinity chromatography columns, both CD13 and FU3 antibodies recognized an identical 150-kDa band (Fig. 2a).
FU3 recognizing antigen corresponds to the aminopeptidase N (CD13). (a) Western immunoblot analysis of whole cell extracts and immunoaffinity column-purified proteins. Both CD13 and FU3 recognizes identical 150-kDa protein. (b) CD13 siRNA (0.01 pmol/μl) treatment causes downregulation of both CD13 and FU-3-reactive protein at 72 h. NT, non-treated; cont, control siRNA.
Second, CD13-specific siRNA treatment (0.01 pmol/μl) of SFT8503 MFH cells caused significant downregulation of both CD13 and FU3-reactive 150 kDa proteins (Fig. 2b.). In view of the evidence, we considered that the FU3 reactive antigen was identical to APN/CD13.
CD13 expression in normal skin
Immunohistochemically, CD13 antibody stained perivascular mesenchymal cells, represented by small spindle or polygonal cells around small blood vessels, in normal skin (Fig. 3). A small number of fibroblasts also reacted with CD13 antibody; however, the stratified squamous epithelium and endothelial cells were not CD13 antibody-reactive. These findings were similar to those of FU3 reactive cells (3–6), supporting of the identification of FU3 antigen as APN/CD13.
Reactivity of normal skin cells with CD13. Perivascular mesenchymal cells in the normal dermis show staining, whereas epidermal cells and endothelial cells remain unstained. CD13-positive fibroblasts are also noted in part.
CD13 expression in MFH and soft tissue tumors
Expression of CD13 was examined immunohistochemically in 70 soft tissue tumors wich included 25 MFH and 45 other soft tissue tumors (Fig. 4 and Table I). Twenty cases of MFH (80%) were positive for CD13 and of these, there were 17 (68%) high expression cases. In MFH, CD13 expression pattern were classified into two types; perivascular (Fig. 4a and b) and diffuse types (Fig. 4c and d). Tissues of the perivascular type exhibited intense cytoplasmic and membrane staining of CD13 (Fig. 4b). In the diffuse type, almost all MFH cells had positively stained cytoplasms (Fig. 4d). Positive reactivity with CD13 was observed in several synovial sarcoma, leiomyosarcoma and osteosarcoma, but high-expression was found only in two cases of leiomyosarcoma (Table I).
Immunohistochemical expression of CD13 in MFH. Representative cases of perivascular (a and b) and diffuse (c and d) patterns. The perivascular type shows strong cytoplasmic staining along the membrane (b). The diffuse type shows moderate cytoplasmic reactivity (d). Original magnifications (a and c), ×40; (b and d), ×200.
Inhibition of MFH (SFT8503) cell invasion by CD13 siRNA
To investigate a biological role for APN/CD13 in MFH, we examined effect of CD13 siRNA treatment on MFH cell invasion. We used HGF as a chemoattractant factor because overexpression of HGF has been reported in MFH (8,9). Treatment of SFT8503 MFH cells with CD13 siRNA (0.01 and 0.02 pmol/μl) downregulated CD13 expression in a dose-dependent manner at 48 h (data not shown) and at 72 h (Fig. 5a) after transfection. HGF (100 ng/ml) induced greater SFT8503 cell invasion than serum-free medium. In the presence of CD13-targeted siRNA, HGF-stimulated MFH cell invasion was significantly attenuated as compared with that observed with control siRNA (Fig. 5b).
Expression of CD13 in SFT8503 cells and effect of CD13 siRNA on tumor invasion. (a) CD13 protein expression level by western blotting. Treatment with CD13 siRNA downregulated the level more severely at 0.02 pmol/μl than 0.01 pmol/μl at 72 h. (b) Tumor cell invasion of Matrigel was significantly suppressed by transfection of CD13 siRNA (0.02 pmol/μl) at 72 h. NT, non-treated; cont, control si RNA. *P<0.01 by Student’s t-test.
Development of an MFH recognizing FU3 antibody provided some important findings, especially on the cellular origin of MFH (4–6). The antibody, however, has not been widely used, one of the reasons may be that FU3 antibody is available only on frozen tissue sections but not on paraffin-embedded specimens. In this study, we demonstrated that the FU3 antibody recognizies an antigen identical to APN/CD13 using immunoaffinity chromatography and direct N-terminal amino acid sequencing. Immunohistochemically, greater amounts of APN/CD13 were observed more frequently in MFH tissues as compared with that observed in other sarcomas in paraffin-embedded specimens. Moreover, MFH cell invasion was significantly suppressed by transfection of APN/CD13 siRNA. The results from this study may point toward the use of APN/CD13, the FU3 antigen, as an important biomarker in the diagnosis and treatment of patients with MFH.
APN/CD13, a 150-kDa metalloproteinase, is a multifunctional cell surface aminopeptidase. The human APN gene has been mapped to chromosome 15q25-26. APN/CD13 expression has been reported in hematopoietic cells of myeloid origin, fibroblasts, synaptic membranes in the central nervous system and epithelial cells of liver, kidney and intestine (10,11). High expression levels of APN/CD13 has been detected in various epithelial tumors and its expression correlates with increased clinical malignant behavior in pancreatic carcinoma and in colon and non-small lung cancer (12–14).
There is little information on the expression of APN/CD13 and its role in MFH. An immunohistochemical study of MFH demonstrated a positive reaction to APN/CD13 in six of ten cases (15). Another report showed four cell lines derived from an MFH expressed APN/CD13, using flow cytometric analysis (16). Immunohistochemically, APN/CD13 antibody showed strong reactivity with perivascular mesenchymal cells in the normal skin tissue and with MFH cells, to a similar extent seen with FU3. These findings lend support to our result that the FU3 recognizing antigen is identical to APN/CD13. Although we can not directly compare our results with those of previous results of APN/CD13 expression (15), owing to the differences in assessment methods, our findings were roughly consistent with previous studies on other soft tissues sarcomas. All our five cases of osteosarcoma were positive for APN/CD13, but no high expression cases were observed. Only two cases of leiomyosarcoma showed high expression. APN/CD13 immunostaining may be applicable to narrow the differential diagnosis of soft tissue sarcomas to MFH.
Our immunohistochemical study in normal skin demonstrated APN/CD13 expression in the perivascular cells and in some dermal fibroblasts. APN/CD13 expression in perivascular cells has also been reported in lung tissue; the majority of these CD13-positive cells were slender perivascular fibroblastic cells (17). Dermal fibroblasts express APN/CD13 to a relatively great degree in vitro (18,19). On the basis of immunoreactivity, MFH cells may have intimate relationship with perivascular cells and fibroblasts.
APN/CD13 might participate in tumor progression by regulating processes such as tumor invasion and angiogenesis (12,20–24). Our study, however, is the first to show that downregulation of APN/CD13 expression leads to marked suppression of invasion by MFH cells, although this is based on only in vitro data. In a previous study with osteosarcoma cell lines, CD13 siRNA treatment caused reduced cellular attachment to and increased proteolytic degeneration of the extracellular matrix (25). Anti-APN/CD13 antibody reduced the migratory activity of human dermal fibroblasts (19). These reduced activities may also occur in MFH cells and these possibilities are now under investigation in our laboratory.
Since the discovery in 1976 of the first APN enzymatic inhibitor bestatin, many APN inhibitors have been developed (26). Bestatin is already used clinically for the treatment of adult acute non-lymphocytic leukemia via peroral administration. Bestatin-mediated suppression of APN/CD13 activity in an APN/CD13-expressing ovarian carcinoma cells led to reduced migration, proliferation and peritoneal dissemination of tumor cells in a mouse model, which resulted in prolonged survival (27). Bestatin may also represent a new approach for improving the therapeutic efficacy of radiotherapy for uterine cervical carcinoma (28) and for enhancing paclitaxel chemosensitivity in ovarian carcinoma (29). Recently, some novel potent APN/CD13 inhibitors have also been reported, several of which show better inhibitory activity than bestatin against APN on human carcinoma cells (30,31).
In conclusion, our study indicates that APN/CD13 may be useful for diagnosing MFH and importantly, might serve as a new molecular target for therapy for patients with MFH.
We acknowledge the expert technical assistance of Ms. M. Onitsuka, M. Ishiguro and C. Fujita in immunohisto-chemical staining and in vitro studies.