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From the Departments of Human Anatomy and Cell Science,* Obstetrics, Gynecology, and Reproductive Sciences, and Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada; the Division of Stem Cell and Developmental Biology,|| Ontario Cancer Institute, University Health Network, University of Toronto, Toronto, Ontario, Canada; Biomedical Sciences,** University of Guelph, Guelph, Canada; and the Clinics of General, Visceral, and Vascular Surgery, and the Departments of Physiological Chemistry and Pathology,¶ Martin Luther University, Halle/Saale, Germany
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Abstract |
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Relaxin and the relaxin-like INSL3 have been shown to activate cAMP-dependent signaling pathways by binding to either LGR7 or LGR8.8-12 We recently demonstrated the expression and regulation of INSL3 and LGR8 transcripts in human thyroid carcinoma cell lines, identifying hyper- and neoplastic human thyrocytes as a new source and target of the actions of INSL3 and a novel INSL3 splice variant.8,13
Although still primarily undefined, relaxin appears to have oncogenic potential in various organs and tissues, including the human thyroid.14-17 Relaxin affects proliferation and differentiation of MCF-7 human carcinoma cells in a concentration-dependent manner18 and can modify the extracellular matrix by affecting the expression of matrix metalloproteinases (MMPs), which potentially contribute to relaxin’s role as a migration-promoting peptide in mammary carcinoma cells of different species,15 including humans.19
In the present study, we have for the first time revealed novel roles for RLN2 in human thyroid carcinoma cells. We identified neoplastic thyroid tissues as a source of RLN2 and LGR7, implicating an active RLN2-LGR7 signaling system in human thyroid carcinoma. Enhanced metabolic activity, anchorage-independent growth, and increased migratory and elastinolytic activity were among the phenotypes observed with stable transfectants of the human follicular thyroid carcinoma cell lines, FTC-133 and FTC-238, which overexpress and secrete bioactive proRLN2. Finally, relaxin up-regulated the production and secretion of cath-L and cath-D, identifying this insulin-like peptide hormone as a novel modulator of the oncogenic potential of human thyroid carcinoma cells.
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Materials and Methods |
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TopAbstractMaterials and MethodsResultsDiscussionReferences |
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A total of 59 thyroid tissues, including 10 goiter tissues, 9 Graves’ disease tissues, and 14 papillary thyroid carcinomas (PTCs), 12 follicular thyroid carcinomas (FTCs), and 14 undifferentiated thyroid carcinomas (UTCs), were collected from patients at the Department of Surgery, University of Halle, by surgical resection for clinical indications (Table 1)
. This study was approved by the ethical committee of the Martin Luther University, Faculty of Medicine, and all patients gave written consent. Tissues were fixed in formalin and embedded in paraffin and cryopreserved in liquid nitrogen. The human thyroid papillary carcinoma cell line BC-PAP; the follicular carcinoma cell lines FTC-133, FTC-236, FTC-238; and the anaplastic carcinoma cell lines Hth74, C643, UTC-8305, and UTC-8505 were propagated in Dulbecco’s minimal essential medium (DMEM)/Ham’s F12 (Biochrom, Berlin, Germany) supplemented with 10% fetal calf serum (FCS) in a 5% CO2 atmosphere at 37°C. Medium was changed every second day, and cells were routinely passaged every 3 to 5 days.
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Total RNA was extracted from the human thyroid cell lines and tissues for RT-PCR analysis using the Trizol reagent (Life Technologies, Karlsruhe, Germany) and RNeasy extraction kit (Qiagen, Hilden, Germany), respectively, according to the manufacturers’ protocols. The amount of isolated total RNA was determined by spectrophotometry at 260 and 280 nm.20
One µg of total RNA was used for first-strand cDNA synthesis using the Superscript reverse transcriptase kit and 500 ng/ml of oligo d(T) primer (both Life Technologies). Total RNA was also isolated from the human follicular thyroid carcinoma cell lines. For the amplification of RLN2 prorelaxin and the partial coding sequence of human LGR7 relaxin receptor, specific intron-spanning oligonucleotide primers (Table 2)
were used to preclude any genomic DNA amplification. Before semiquantitative RT-PCR analysis with the Bio 1D software (LTF, Wasserburg, Germany), cDNA samples were adjusted to equal 18S RNA input. RT-PCR reactions were performed in a 25-µl solution containing 2 µl of cDNA, 2.5 µl of 10x Advantage2 polymerase mix buffer, 10 nmol/L of dNTP, 20 pmol of each primer (Table 2)
, and 2 U TaqDNA-polymerase (Life Technologies). PCR cycles consisted of an initial denaturation for 5 minutes at 95°C, followed by 35 cycles of denaturation at 95°C for 45 seconds, annealing for 45 seconds (for temperatures see Table 2
), elongation for 1.5 minutes at 72°C, and a final extension cycle for 10 minutes at 72°C. PCR products were separated on a 1% low-melting point agarose gel. For sequence analysis, amplicons were purified by Magic column extraction, cloned into the pGEM-T vector (both Promega, Heidelberg, Germany), and sequenced in both directions using the PRISM dye Deoxy Terminator cycle sequencing kit (Perkin-Elmer, Foster City, CA) and T7 or SP6 sequencing primers.
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For stable transfection of FTC133 and FTC-238 with the pCMV-preproRLN2-IRES-EGFP15 or the pCMV-IRES-EGFP vector (Clontech, Heidelberg, Germany) we used the Lipofectamine 2000 kit according to the manufacturer’s protocol (Life Technologies). Both plasmids had been purified using the DNA Midi isolation kit (Qiagen). Stably transfected clones with the pCMV-preproRLN2-IRES-EGFP (FTC-133, 12 clones; FTC-238, 1 clone) and pCMV-IRES-EGFP vector (FTC-133, 9 clones; FTC-238, 3 clones), respectively, were selected, maintained in medium containing with 800 µg/ml geneticin (Life Technologies), and displayed bright EGFP production in fluorescence microscopy (Zeiss, Jena, Germany). Of those, three FTC-133- and one FTC-238-pCMV-preproRLN2-IRES-EGFP transfectants expressing relaxin transcripts (FTC-133-RLN2 and FTC-238-RLN2) and two clones each of FTC-133 and FTC-238 containing the pCMV-IRES-EGFP vector (FTC-133-EGFP and FTC-238-EGFP) were used in this study. In all assays performed, similar responses were obtained for all RLN2 transfectants when compared with EGFP controls. A medium change was performed every 2 to 3 days and transfectants were passaged every 3 to 5 days using accutase (PAA Laboratories GmbH, Linz, Austria). Before experimentation, cells were seeded at the desired cell densities either in 25-cm2 flasks or in 6-, 24-, or 96-well plates on the day of experimentation (Techno Plastic Products AG, Trasadingen, Switzerland).
Small Interfering (si) RNA
The day before transfection FTC-133 cells were seeded at 104 cells/well on a six-well plate. Cells were washed three times in phosphate-buffered saline (PBS) before transfection with nonsilencing- or LGR7-siRNA (Qiagen). The nonsilencing siRNA (siNC) conjugated to Alexa Fluor 555 with no sequence similarity to human gene sequences was used as a control (1027099: 5'-AATTCTCCGAACGTGTCACGT-3'). The following LGR7-siRNA target sequences were used: a single LGR7-siRNA at a final concentration of 300 nmol/L 5'-CTGCAGTTACCTGCTTTGGAA-3' (exon 15) and a combination of two human LGR7-siRNAs at a concentration of 50 nmol/L each 5'-GCTCCAGACCTTGGCAAAGAC-3' (exon 4) and 5'-TACTAGATAGGAATTGAGTCTC GTTGATT-3' (exon 20) were found to be optimal. The Lipofectamine 2000 kit (Life Technologies) was used for transfecting the siRNA constructs. After 24 hours the transfection medium was replaced with normal medium. The level of LGR7 mRNA suppression was highest at 72 hours after transfection. Total RNA was isolated and the level of LGR7 mRNA was determined by semiquantitative RT-PCR as described above. All siRNA experiments for RT-PCR, cAMP, and motility assays were performed in triplicates of three independent samples (see below).
Enzyme-Linked Immunosorbent Assay (ELISA)- and Fluorometric-Based Assays
Relaxin ELISA
Transfectants were seeded at 5 x 104 cells/well of a six-well plate and cultured in 1 ml of culture medium for 24 hours in a humidified CO2 incubator. Secreted relaxin in conditioned medium (200 µl) was determined by ELISA according to the manufacturer’s instructions (Immunodiagnostic, Bensheim, Germany). The color reaction was determined at 450 nm with an ELISA reader (SLT Labinstruments GmbH, Crailsheim, Germany).
cAMP Assay
Intracellular cAMP levels were determined in FTC-133-RLN2, clone 10, at 1 x 104 cells/well cultured for 24 hours in 96-well plates. Cells were preincubated with 3-isobutyl-1-methyl-xanthine (IBMX; Sigma, Munich, Germany) at 1 mmol/L for 2 hours at 37°C in a water-saturated CO2-incubator. The medium was replaced with 1 ml of 1) fresh medium containing 10 µmol/L forskolin as a positive control (Merck Biosciences, Bad Soden, Germany); 2) supernatants from one FTC-133-EGFP clone as negative control; 3) supernatants from FTC-133-RLN2 clones 4, 10, 11. Supernatants (200 µl) had been collected from six-well plate cultures of FTC-133-EGFP and FTC-133-RLN2, clones (8 x 104 cells/well) after 24 hours of culture and centrifuged at 3000 x g for 30 minutes to remove remaining cells. FTC-133-RLN2 clone 10 cells (1 x 104 cells/well) were incubated with these media/supernatants, all containing 1 mmol/L IBMX, for 1 hour at 37°C in a water-saturated CO2 incubator. Cells were harvested, washed, and lysed with cAMP extraction buffer and cAMP levels were detected with the colorimetric cAMP Biotrak enzyme immunoassay (Amersham, Freiburg, Germany). The reaction was stopped in 1 mol/L H2SO4 and the product was measured at 450 nm in a microplate reader (SLT).
BrdU Assay
A colorimetric BrdU cell proliferation ELISA (Roche Diagnostics, Mannheim, Germany) was used according to the manufacturer’s instructions. Briefly, on the day of assay, 20 µl of BrdU labeling solution were added to each well of a 96-well plate, except for negative controls that received no BrdU. Cells were incubated for 2 hours at 37°C in a water-saturated CO2 incubator. The assay was performed with 0.25, 0.5, and 1 x 104 stable transfectants/100 µl medium. Thereafter, plates were drained, air-dried for 20 minutes, and blocked with 200 µl/well of ELISA blocking reagent (Roche) for 30 minutes at room temperature. After decanting, 100 µl of BrdU antiserum was added to each well and dishes were incubated for 30 minutes at room temperature. Plates were drained, washed, and incubated with 100 µl/well of substrate solution for 10 minutes at room temperature. Finally, 25 µl of 1 mol/L H2SO4 were added to each well, incubated for 1 minute on a shaker at 300 rpm, and absorbance was measured within 5 minutes at 370 nm in an ELISA reader (SLT).
Cell Cytotoxicity (MTT) Assay
The cytotoxicity Easy-for-You assay kit (Biomedica, Wien, Austria) was performed in 96-well plates according to the manufacturer’s instructions. Stable transfectants were plated in 200 µl of medium at 0.25, 0.5, and 1 x 104 cells/well and grown overnight in a CO2 incubator. On addition of chromophorous substrate (20 µl) for 2 hours, NADH2-dependent colored formazan salt formation was monitored hourly for 4 hours at 450 nm using an ELISA reader (SLT).
Luminometric ATP Assay
Stable transfectants plated in 96-well plates at a density of 0.25, 0.5, and 1 x 104 cells/well in 100 µl of medium were allowed to grow overnight at 37°C in a CO2 incubator. Wells devoid of cells served as blank. Substrate (100 µl) was added to each well (CellTiter-Glo Luminescent; Promega) and incubated on a shaker and on the benchtop for 2 minutes and 10 minutes at room temperature, respectively. Luminescence was measured with a Sirius luminometer (Berthold Detection Systems GmbH, Pforzheim, Germany).
Soft Agar Assay
Two-layered soft agar assays were performed in six-well plates. The bottom layer of agar (1.5 ml per well) consisted of 5 ml of 3% agar (Roth, Karlsruhe, Germany) in sterile water, 3 ml of FCS (Biochrom), 45 µl of geneticin (50 mg/ml, Life Technologies), 300 µl of a 1:1000 dilution of amphotericin B (stock, 250 µg/ml), and 900 µl of a 1:1000 dilution of gentamicin (stock, 10 mg/ml; all from Sigma) added to 30 ml with Ham’s F12 medium. Once solidified at room temperature for 10 minutes, 20,000, 50,000, or 100,000 cells of FTC-133-RLN2 and FTC-133-EGFP were mixed into 1 ml of upper agar layer prepared from a stock consisting of 1.6 ml of 3% agar, 10% FCS, 22.5 µl of geneticin (50 mg/ml), 150 µl (1:1000 dilution) of amphotericin B (250 µg/ml), 450 µl (1:1000 dilution) of gentamicin (10 mg/ml) in 15 ml of culture medium. This cell suspension was carefully layered on top of the bottom layer and once this top agar layer had solidified 1 ml of the culture medium was carefully added and changed once a week. After 4 to 6 weeks, cell colonies in the agar were colored overnight at 37°C in a 5% CO2 atmosphere with 200 µl of iodo-tetrazolium chloride in vivo stain (Sigma). Colored cell colonies were examined by bright-field microscopy (Zeiss).
Motility and Migration Assays
Cellular motility and migration were evaluated in 24-well Transwell chambers (Costar, Bodenheim, Germany). The upper and lower culture compartments were separated by polycarbonate filters with 8-µm pore size. For migration assays, the upper site of the filters (upper chamber) was coated with 50 µg/ml of human elastin (Sigma) before seeding cells. To investigate the effect of recombinant human RLN2 (generously provided by Dr. Laura Parry, University of Melbourne, Melbourne, Australia) on the motility of untransfected thyroid carcinoma cells, FTC-133 or FTC-238 were plated at 1 x 104 cells/well in Ham’s F12 medium with or without 10% FCS and incubated for 24 hours in a 5% CO2 atmosphere at 37°C in the absence or presence of human RLN2 at 100 ng/ml or 500 ng/ml added to the wells (lower chamber). To investigate a similar autocrine/paracrine effect of relaxin secreted by the transfectants, RLN2 and EGFP clones were seeded onto the filter at 1 x 104 cells/well and placed in the well harboring 5 x 104 of either RLN2 or EGFP transfectants (lower chamber). Control experiments were performed to determine the specificity of RLN2-mediated signaling on the motility of FTC-133 and FTC-238 tumor cells seeded on the filter: 1) recombinant RLN2 (500 ng/ml) was heat-inactivated for 10 minutes at 90°C before incubation with the cells; 2) supernatant collected from FTC-133-RLN2, clone 10, grown to confluency in a six-well was diluted 1:1, 1:2, and 1:4 with normal culture medium (v/v) before incubation with FTC-133 on the filter; 3) FTC-133 and FTC-238 were transfected with specific LGR7 siRNA constructs and motility was determined in the presence or absence of recombinant RLN2 at 100 or 500 ng/ml). After a 16-hour incubation period, cells remaining on top of the filter were wiped off with cotton swabs and those transfectants that had traversed the membrane pores to the lower surface of the membrane were washed with chilled PBS, incubated for 5 minutes in 1:1 PBS/methanol (Merck, Darmstadt, Germany) and 15 minutes in methanol before staining with 0.1% toluidine blue (Merck) in 2.5% sodium carbonate (Roth). Migrated cells were counted by light microscopy (Zeiss) in four separate high-power fields per filter.
Immunohistochemistry and Evaluation
Human paraffin-embedded serial 3-µm thyroid tissue sections (Table 2)
were dewaxed and rehydrated in PBS plus 0.1% Tween 20 (PBST). Sections were treated with proteinase K (30 µg/ml; both Sigma) for 30 minutes at 37°C and 3% H2O2 in methanol for 25 minutes at room temperature to inactivate endogenous peroxidase activity. Sections were washed in PBST and nonspecific binding sites were blocked with 10% goat serum in PBST (blocking buffer) for 1 hour at room temperature. Detection of immunoreactive RLN2 in the human thyroid tissue sections was performed with two previously characterized rabbit polyclonal antibodies against RLN2. One polyclonal antiserum against RLN2 was from Immunodiagnostik (Bensheim, Germany)21
and was diluted 1:300 in blocking buffer overnight at 4°C. Serial sections were also immunostained with the R6 rabbit anti-porcine relaxin antiserum (generously provided by Prof. Bernhard Steinetz, Nelson Institute of Environmental Medicine, New York University Medical Center, Tuxedo, NY) at a dilution of 1:800 in blocking buffer at 4°C overnight. Nonimmune rabbit serum (1:300) served as control. As a secondary antibody, horseradish peroxidase-conjugated goat anti-rabbit was used at a dilution of 1:500 for 1 hour at room temperature. After washing in PBST, detection was performed with filtered diaminobenzidine solution for 10 minutes and immunostained sections were counterstained with hematoxylin. Immunoreactive relaxin receptor LGR7 in human thyroid tissues was detected with a previously characterized rabbit polyclonal antiserum against human LGR7 (generously provided by Prof. Aaron Hsueh, Dept. of Obstetrics and Gynecology, Stanford University, Stanford, CA) used at 1:800 in blocking buffer.8
All immunostained tissue sections (two sections per patient) were evaluated by two independent reviewers blinded to the histological diagnosis. Planimetric measurement of immunostained tissues was performed semiquantitatively using the Axioplan light microscope and the Zeiss KS300 software (Zeiss). The percentage of immunostained tissue areas per total section area (100%) was classified into four groups: 0 to 10% negative; 10 to 40% low; 40 to 80% moderate; 
80% high.
Immunofluorescence and Confocal Laser-Scanning Microscopy
For immunofluorescent detection of cathepsin-D (cath-D), cathepsin-L (cath-L), mannose-6-phosphate receptors (M-6-PR), and the lysosomal marker CD63, transfectants were plated on sterile glass slides at 2 x 104 cells/ml and incubated in a humidified atmosphere at 5% CO2 for 2 to 3 days before fixation of cells with 4% formaldehyde. Sections were incubated overnight at 4°C with previously characterized primary rabbit polyclonal antiserum to human cath-D22 diluted at 1:500 and mouse monoclonal antibodies (mAbs) specific for human procath-L (2D4) and all three cath-L forms (procath-L, single-chain, and heavy chain of cath-L; 33/1)23,24 at 1:100 each, respectively, in blocking solution (2% bovine serum albumin, 0.05% saponin in PBS; Sigma). Cells were washed with PBST and incubated with 10% goat or donkey antiserum for 30 minutes before a 1-hour incubation with the secondary rhodamine-conjugated goat anti-rabbit antiserum (1:400; Dianova, Hamburg, Germany) or rhodamine-conjugated donkey anti-mouse antiserum (1:100; Jackson ImmunoResearch, West Grove, PA), respectively. Immunofluorescent localization of mannose-6-phosphate receptors (M6PR type I+II; Abcam, Cambridge, UK) and lysosomal marker CD63 (Sigma) was performed with mAbs diluted at 1:200 and 1:1000 in blocking buffer (for M6PR containing 0.05% saponin; Sigma), respectively. After blocking nonspecific binding sites with 10% donkey serum, the secondary rhodamine-conjugated donkey anti-mouse antiserum (1:100; Jackson ImmunoResearch) was used for visualization. In all cases, nuclear Hoechst stain (1:100; Sigma) was used, and labeled cells were embedded in Fluoroguard anti-fade reagent (Bio-Rad, Munich, Germany) before fluorescence microscopy or confocal laser-scanning microscopy (KLSM-410; both Zeiss).
Western Blot Analysis
For the detection of relaxin, cellular proteins of stable RLN2 and EGFP transfectants as well as untransfected FTC-133 and FTC-238 cells were extracted in RIPA buffer [1% Nonidet P-40, 0.1% sodium dodecyl sulfate (SDS) in PBS] with the addition of protease inhibitor cocktail (all from Sigma). Protein concentrations were determined by Bradford assay (Bio-Rad). Extracted proteins (40 µg) were separated under nonreducing conditions on a 15% SDS gel and blotted at 330 mA for 35 minutes onto Hybond-ECL nitrocellulose membranes (Amersham, Freiburg, Germany). Nonspecific binding sites were blocked for 1.5 hours in blocking buffer [1% milk, 5% bovine serum albumin in PBS containing 0.1% Tween 20 (PBST)]. Membranes were incubated with the rabbit polyclonal R6 antiserum against relaxin diluted 1:2500 in blocking solution overnight at 4°C, then washed in PBST and incubated with the secondary goat anti-rabbit at 1:20,000 in blocking buffer for 1 hour at room temperature before immunodetection with the ECL kit (Amersham). For the detection of cathepsins, cells were isolated in 2x extraction buffer under reducing conditions [125 mmol/L Tris-HCl, pH 6.8, 4% SDS, 20% glycerol, 10% mercaptoethanol (ME); 2% bromophenol blue; all reagents from Sigma]. Supernatants containing secreted cathepsins were collected from a confluent cell layer cultured in medium plus 2.5% FCS after 72 hours and centrifuged at 4000 x g for 30 minutes at 4°C to pellet remaining cells. Equal volumes of the supernatants and 2x extraction buffer were mixed and protein extracts of both cellular and soluble fractions (40 µl each) were separated on a reducing 12% SDS-polyacrylamide gel electrophoresis. After protein transfer and blocking of nonspecific binding sites for 2 hours with 5% skimmed milk in PBST, membranes were incubated overnight at 4°C with the rabbit polyclonal antibodies to cath-D (1:7500),22 cath-B (both 1:500), and cath-H (1:10,000) and mAbs to cath-K (1:200), cath-V (1:500). Also, we used the two mAbs specific for procath-L (2D4 at 1:500) and all three cath-L forms (33/1 at 1:500),23,24 respectively. Secondary horseradish peroxidase-conjugated goat anti-rabbit and rabbit anti-mouse Igs were used at 1:20,000 for 1 hour at room temperature, respectively. Membranes were washed and immunoreactive proteins were visualized with the ECL kit (Amersham). In all cases, ß-actin was used to determine equal protein loading. Membranes were incubated in stripping solution (2% SDS, 125 mmol/L Tris-HCl, pH 8.0, 0.7% ME), blocked and incubated at 1:20,000 in blocking buffer for 1 hour each with a mAb to human ß-actin (Sigma) and the secondary goat anti-mouse, respectively, before immunodetection with the ECL kit (Amersham).
Statistical Analysis
Statistical analysis was performed with the SPSS software package (SPSS GmbH, Munich, Germany). Student’s t-test and one-way analysis of variance were used. All experiments were performed at least in triplicates and were expressed as mean ± SEM with P values of P < 0.05 considered as statistically significant.
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Results |
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TopAbstractMaterials and MethodsResultsDiscussionReferences |
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RT-PCR analysis of the human thyroid tissues investigated (Table 1)
revealed the expression of RLN2 and LGR7. RLN2 transcripts were detected in 12 of 14 (86%) papillary thyroid carcinoma (PTC), 10 of 12 (83%) follicular thyroid carcinoma (FTC), and 13 of 14 (93%) undifferentiated thyroid carcinoma (UTC) tissues, respectively (Table 1)
. LGR7 transcripts were demonstrated in 12 of 14 (86%) PTC and in 100% of FTC and UTC tissues tested (data not shown). Goiter and Graves’ disease tissues investigated did not express RLN2 transcripts. Goiter and Graves’ disease tissues and thyroid tissue sections with the primary antiserum omitted were also devoid of RLN2 immunostaining (Figure 1, A, C, E, and G)
. Similar to the RT-PCR data, immunoreactive RLN2 was exclusively detected in the human PTC, FTC, and UTC investigated (Figure 1, B, D, and F
; Table 1
). Independent of pTNM classification, the presence of immunostained RLN2 was moderate in PTC/FTC and moderate to high in UTC. Similar results for the immunodetection of RLN2 in serial tissue sections were obtained with either the R6 antiserum or the anti-RLN2 serum from Immundiagnostik21
(data shown for the latter relaxin antiserum).
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and Graves’ disease. Moderate to high immunoreactive LGR7 was detected in all human thyroid carcinoma tissues investigated (Figure 1, J, L, and N)
. Thyroid tissue sections with the primary antiserum omitted were devoid of specific LGR7 immunostaining (Figure 1, I, K, M, and O)
. Stable Transfectants of Human Thyroid Carcinoma Cells Produce Bioactive Relaxin
Human thyroid carcinoma cell lines were investigated for transcriptional gene activity of RLN2 and LGR7 (Figure 2, A–C)
. All follicular thyroid carcinoma cell lines, FTC-133, FTC-236, and FTC-238, and the anaplastic, undifferentiated thyroid carcinoma cell lines Hth74, UTC-8305, UTC-8505, and C643 weakly expressed transcripts encoding RLN2 when 2 µl of cDNA were used in the PCR reaction (Figure 2C)
. These cell lines also expressed LGR7 transcripts at low levels (data not shown). FTC-133 expressed LGR7 transcripts. However, endogenous RLN2 expression was only detected at higher cDNA concentration (2 µl/tube) in each PCR reaction (Figure 2C)
, but was not detectable when 1 µl of cDNA was used in the PCR reaction (Figure 2A)
. We chose FTC-133 and FTC-238 for stable transfection with the pCMV-preproRLN2-IRES-EGFP construct. The FTC-133-RLN2 stable transfectants overexpressed relaxin transcripts as determined by RT-PCR analysis (Figure 2A)
. Western blot analysis revealed a single specific immunoreactive band at 
18 kd corresponding to proRLN2 relaxin, which was very weak in EGFP clones (Figure 3A)
. The amounts of relaxin secreted by the FTC-133-RLN2 transfectants (580 to 1050 pg/ml) was maximally 95-fold that of corresponding EGFP controls that produced small levels of immunoreactive relaxin as calculated with a relaxin standard in an RLN2 ELISA (Figure 3B)
. Similar results were obtained for FTC-238-RLN2 stable transfectant that produced 70-fold higher levels of relaxin (730 pg/ml) as compared to corresponding EGFP controls with low levels of relaxin (data not shown).
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. Supernatants derived from the FTC-133-RLN2 clones 4, 10, and 11 caused a weak but specific increase in intracellular cAMP in FTC-133 clone 10 that was used as responder cell line in this assay (Figure 4)
. The increase in cAMP levels was highest with supernatant from a 24-hour culture of FTC-133-RLN2, clone 10, and this clone also showed the strongest production of relaxin in the RLN2-ELISA (Figure 3B)
. FTC-133-RLN2 transfectants displayed enhanced metabolic activity and enhanced mitochondrial activity reflected by the increased formation of NADH2-dependent formazan salt in the MTT cell viability assays (Figure 5A)
and elevated intracellular ATP levels (Figure 5B)
. Suppression of LGR7 expression by LGR7 siRNA treatment of FTC-133 abolished the enhanced MTT response on incubation with recombinant RLN2 (data not shown). Overexpression of RLN2 failed to result in a significant increase in cell proliferation as determined by nonradioactive BrdU proliferation assays (Figure 5C)
. FTC-238-RLN2 clones did not display altered MTT or ATP values as compared to FTC-238-EGFP controls (data not shown). This may indicate cell-type-specific RLN2-induced and LGR7-mediated metabolic changes among human follicular thyroid carcinoma cells.
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Soft agar assays were performed with FTC-133-RLN2 and FTC-133-EGFP transfectants. Relaxin significantly enhanced the numbers of colonies (maximum eightfold) during anchorage-independent growth of FTC-133-RLN2 clones as compared to FTC-133-EGFP controls (Figure 6A)
. FTC-133-RLN2 transfectants (Figure 6B)
generated smaller-sized colonies when compared to EGFP controls (Figure 6C)
. RLN2 significantly enhanced the motility of human thyroid carcinoma cells as determined in filter-based motility assays using recombinant RLN2 and RLN2 secreted by the stable transfectants. The motility-promoting action of RLN2 was unaffected by FCS. The paracrine actions of recombinant RLN2 caused a significant concentration-dependent increase in the motility of FTC-133 (Figure 7A)
and FTC-238 cells (data not shown). In addition, RLN2 transfectants of both FTC-133 (Figure 7B)
and FTC-238 (Figure 7C)
plated onto the filter displayed enhanced cellular motility as compared to corresponding EGFP controls. When the FTC-133-RLN2 transfectants were also present in the lower chamber an additive autocrine/paracrine effect of RLN2 on the motility was observed for all RLN2-transfectants seeded on top of the filter as depicted for FTC-133-RLN2 clone 10 (Figure 7B)
. In addition, secreted relaxin from the FTC-133-RLN2 transfectants in the lower chambers also resulted in an increased number of FTC-133-EGFP clones to traverse the filter from the upper chamber (Figure 7B)
. To determine the ability of FTC-133-RLN2 clones to actively penetrate an extracellular matrix, we performed migration assays using filters coated with elastin. FTC-133-RLN2 transfectants displayed a 4.5-fold increased rate of migration through an elastin matrix as compared to EGFP control cells indicating a novel role for relaxin in enhancing the elastinolytic activity of human thyroid carcinoma cells (Figure 7D)
. This relaxin-mediated increased elastinolytic activity was also shown for FTC-238 carcinoma cells exposed to human recombinant RLN2 and for FTC-238-RLN2 transfectants resulting in increased migration through elastin matrices (Figure 7E)
.
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The specificity of RLN2-induced enhanced migration of human thyroid carcinoma cells was demonstrated by heat inactivation or dilution of RLN2 ligand. Heat-inactivated RLN2 was unable to enhance the motility of thyroid carcinoma cells (Figure 8A
; black columns). Also, RLN2-mediated enhanced motility of FTC-133 was concentration-dependent as demonstrated by the inability of higher dilutions of supernatants from a relaxin-secreting FTC-133-RLN2 transfectant (clone 10) to increase the motility of FTC-133 (Figure 8A
; gray columns). An intact LGR7 receptor signaling system was identified as a pathway for the specific RLN2-mediated promigratory action in human thyroid carcinoma cells. Specific siRNA-LGR7 treatment was used to suppress LGR7 signaling. We used a single siRNA construct targeting exon 15 of the human LGR7 mRNA that effectively decreased the relative amount of LGR7 transcripts by half in FTC-133 cells as determined by semiquantitative RT-PCR (Figure 8B)
. Suppression of LGR7 transcript levels in FTC-133 was associated with a significant reduction in cAMP response (Figure 8C)
and decreased tumor cell motility (Figure 8D)
, effectively rendering these human thyroid carcinoma cells nonresponsive to RLN2. To exclude a nonspecific inhibitory effect of the single siRNA construct used at 300 nmol/L, we used a set of two additional LGR7 siRNAs at 50 nmol/L each (total 100 nmol/L), targeting sequences located in exons 4 and 20 of LGR7. We observed a significant reduction in the motility of FTC-133 and FTC-238 on treatment with 100 or 500 ng/ml of relaxin respectively (data not shown). Thus, the RLN2-LGR7 ligand-receptor signaling system is an important novel mediator of thyroid carcinoma invasiveness.
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Cathepsins are lysosomal acid hydrolases, and some members possess elastinolytic activity.25
We investigated the production of six cathepsins (cath-B-, D, -H, -L, -K, -V) in cellular and secreted protein fractions of RLN2 and EGFP clones from FTC-133 and FTC-238. Western blot analysis revealed that all FTC-133 transfectants were devoid of immunoreactive cath-B, -H, -K, and -V but produced cath-D and elastinolytic cath-L immunoreactive forms. The mAb 2D4 specifically detected the proform (42 kd) as a cellular and secreted cath-L form (Figure 9A)
. Also, using mAb 33/1 the three known immunoreactive forms of cath-L resembling the proform (42 kd), single-chain (31 kd), and heavy chain (24 kd) of the two-chain cath-L were detected in cellular protein extracts (Figure 9B)
. FTC-133-RLN2 clones consistently displayed an up-regulation of the heavy chain cath-L (24 kd) in cellular extracts suggesting complete processing of cath-L in these clones. Procath-L (42 kd), single-chain (31 kd), and heavy chain cath-L immunoforms were also identified as a secretion product of FTC-133 transfectants with the amount of heavy chain cath-L secreted by FTC-133-RLN2 clones being consistently higher as compared to FTC-133-EGFP transfectants (Figure 9B)
. Immunoreactive 25-kd and 52-kd cath-D, resembling the heavy chain and proenzyme, were detected in cellular extracts of the FTC-133-RLN2 clones (Figure 9C)
. Production of procath-D (52 kd) was enhanced and that of cath-D heavy chain (25 kd) decreased as compared to EGFP controls. Procath-D was the only secreted cath-D form detected in all FTC-133-clones (Figure 9C)
. Similar changes in the production and secretion of cath-L (Figure 9D)
and cath-D forms (data not shown) were observed in FTC-238-RLN2 transfectants as compared to FTC-238-EGFP controls suggesting that these alterations are part of a common RLN2-mediated response in human thyroid carcinoma cells. The mAbs 2D4 and 33/1 used to immunolocalize human procath-L and all three forms, procath-L, single chain, and heavy chain form, respectively, gave similar results in RLN2 and EGFP transfectants of FTC-133 and FTC-238.
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and FTC-238 (data not shown) when compared with corresponding EGFP controls (Figure 10A)
or normal FTC-133 and FTC-238 (data not shown). mAb 33/1 revealed a similar perinuclear to polar cytosolic distribution of cath-L forms in RLN2 transfectants (Figure 10, E and F)
as compared to a diffuse cytoplasmatic cath-L immunostaining in EGFP clones (Figure 10D)
. Confocal laser-scanning microscopy confirmed the perinuclear immunolocalization of cath-L exclusively in RLN2 transfectants and revealed the presence of nuclear cath-L in both FTC-133-RLN2 and FTC-133-EGFP transfectants (Figure 10G)
. By contrast, no differences in the exclusively cytoplasmic distribution were observed with the polyclonal anti-cath-D antiserum for FTC-133-EGFP (Figure 10H)
and FTC-133-RLN2 transfectants (Figure 10I)
.
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similar to that observed for (pro)cath-L (Figure 10, B and C)
. By contrast, a diffuse cytosolic immunodistribution was observed in EGFP transfectants (Figure 10J)
. Lysosomal CD63 marker did not reveal differences in cellular distribution among transfectants as shown for one FTC-133-RLN2 clone (Figure 10L)
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Discussion |
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TopAbstractMaterials and MethodsResultsDiscussionReferences |
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Stable transfectants of the relaxin-responsive human follicular thyroid carcinoma cell lines FTC-133 and FTC-238 were used to analyze functional roles of RLN2 in human neoplastic thyrocytes. These transfectants produced a single proRLN2 immunoprotein indicating incomplete processing of RLN2 hormone in these thyroid carcinoma cells likely reflecting their limited capacity to process constitutively produced relaxin proform. Another explanation may be that human neoplastic thyrocytes generally have a limited capability to properly process relaxin-like members because we also detected proINSL3 as the main product in human thyroid carcinoma tissues.13 As shown in other cell models, proRLN2 was bioactive and specifically activated LGR7 receptors.15,27-29 Down-regulation of LGR7 gene expression with an LGR7 siRNA construct caused a statistically significant reduction in cAMP response on stimulation of cells with either recombinant RLN2 or RLN2-containing supernatants derived from FTC-133-RLN2 secreting transfectants demonstrating predominantly LGR7-mediated RLN2 signaling pathways in these thyroid carcinoma cells.
Among the specific relaxin-mediated effects was a novel role of RLN2 as modulator of metabolic activity causing enhanced mitochondrial activity and increased intracellular ATP production in the FTC-133-RLN2 clones. A protective role of relaxin in mitochondria was demonstrated in guinea pig cardiomyocytes exposed to hypoxic conditions, which was associated with an ability of relaxin to prevent mitochondrial membrane breakdown and sustain mitochondrial integrity under hypoxia.30 Similar to a recent report on relaxin in endometrial cancer,31 relaxin failed to act as a potent mitogen in thyroid carcinoma cells. Instead, increased cellular viability and enhanced tumor cell survival appeared to be important relaxin-mediated actions on neoplastic thyrocytes as reflected by the large number of disseminated small-sized colonies during anchorage-independent growth of the FTC-133-RLN2 transfectants.
Activating LGR7 signaling cascades, relaxin affected the migratory behavior of human neoplastic thyrocytes. Relaxin has previously been identified as a hormone promoting the motility of human and canine mammary carcinoma cell lines (human, MCF-7 and SK-BR3; canine, CF33.Mt)15,32 as well as noncarcinogenic bronchial epithelial cells and inflammatory cells infiltrating wounds.33,34 Here we demonstrate that both recombinant RLN2 and secreted proRLN2 profoundly accelerated the cellular motility of two human thyroid carcinoma cell lines (FTC-133 and FTC-238) and the corresponding RLN2 transfectants in an autocrine/paracrine LGR7-dependent manner. The ability to promote tumor cell motility appears to be characteristic for both relaxin members, relaxin and INSL3, because INSL3 can also act as a motility-enhancing factor on PC-3 human prostate carcinoma cells.35 MMPs and their tissue inhibitors of metalloproteinases (TIMPs) have been identified to potentially facilitate relaxin’s effects on cellular migration and ECM invasion.31,36-38 In human mammary carcinoma cells, relaxin was shown to affect the expression profile of specific MMPs32 and one report indicated a correlation between increased relaxin serum levels and metastases in human breast cancer patients.39 We demonstrated a strong correlation between relaxin-mediated induction of specific MMPs and degradation of extracellular matrix (ECM) components resulting in enhanced migration of canine mammary carcinoma cells.15 In the present study, we have identified the highly potent proteolytic lysosomal acid hydrolases of the cathepsin family as novel relaxin target enzymes in thyroid carcinoma cells and demonstrated a significantly increased elastinolytic activity of the FTC-133-RLN2 clones. Cathepsin proteases have been implicated in numerous pathologies, including inflammatory processes,40 Alzheimer’s disease,41,42 and metastasis of tumor cells.43-46 Both cathepsins, cath-D and cath-L, produced by all transfectants studied are reported to be active in human thyroid carcinoma tissues.46-48 The significant up-regulation in the production and secretion of cath-L forms in RLN2 transfectants correlated with an enhanced elastinolytic activity and the ability to invade elastin matrices. Known as a powerful protease promoting migration and basement membrane degradation by tumor cells,49-51 cath-L also confers to endothelial progenitor cells the proteolytic, promigratory capacity essential for neovascularization in vivo.52 Most apparent for procath-L, relaxin affected the cytosolic distribution of cath-L in RLN2 transfectants. The polar to perinuclear distribution of (pro)cath-L in these RLN2 clones as opposed to an even granular cytoplasmic distribution in the EGFP controls seem to reflect a specific relaxin-induced state of differentiation because our data clearly identified relaxin as a differentiation factor and not a mitogen for human thyroid carcinoma cells. Expression and subcellular distribution of cath-L was shown to be affected by the state of enterocytic differentiation of the human colon carcinoma cell line HT-29.53 Although the exact role for relaxin in this process is unclear, it may involve changes in the endosome to lysosome routing of mannose-6-phosphate-tagged cath-L because mannose-6-phosphate receptors54 displayed a cytoplasmic distribution similar to that detected for procath-L in the RLN2 transfectants. Interestingly, no change in the cytoplasmic distribution for cath-D was observed in the RLN2 transfectants suggesting a specific role for relaxin in cath-L containing vesicular trafficking.
In thyroid carcinoma tissues, cath-D concentrations are significantly higher and correlate with tumor size and stage.48 Relaxin transfectants had significantly increased levels of procath-D and, like in human breast cancer, procath-D was the major secreted glycoprotein in all RLN2 transfectants investigated. In contrast to human breast cancer, estrogens are not regarded as regulators of cath-D production in thyroid carcinoma tissues.47,48 Our finding of abundant production of relaxin in thyroid neoplasia implicates relaxin as a potential novel local regulator of procath-D production in human thyroid carcinoma. By up-regulating the production and secretion of (pro)cath-D and -L, relaxin may not only enhance the local proteolytic activity and tumor cell invasiveness but will also promote tumor angiogenic capacity and survival of human thyroid carcinoma cells.55-58
In summary, RLN2 and its receptor LGR7 are expressed in the majority of human thyroid carcinoma tissues and exert, in an autocrine/paracrine manner, enhanced tumor-promoting activity and invasiveness in neoplastic thyrocytes. These findings provide the rationale for future oncostatic strategies aimed at suppressing relaxin-mediated signal transduction pathways as a novel therapeutic approach in human thyroid cancer.
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Acknowledgements |
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Footnotes |
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Supported by the Deutsche Forschungsgemeinschaft (grants KL1249/5-1 and KL1249/5-2) and the Wilhelm Roux Program, Medical Faculty, Martin Luther University Halle-Wittenberg.
S.H.-K. and J.B. contributed equally to this study.
Accepted for publication April 13, 2006.
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TopAbstractMaterials and MethodsResultsDiscussionReferences |
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0.005). A statistically less significant (P 
