Role of LRP-1 in cancer cell migration in 3-dimensional collagen matrix

ABSTRACT

The low-density lipoprotein receptor-related protein-1 (LRP-1) is a member of Low Density Lipoprotein Receptor (LDLR) family, which is ubiquitously expressed and which is described as a multifunctional endocytic receptor which mediates the clearance of various extracellular matrix molecules including serine proteinases, proteinase-inhibitor complexes, and matricellular proteins. Several studies showed that high LRP-1 expression promotes breast cancer cell invasiveness, and LRP-1 invalidation leads to cell motility abrogation in both tumor and non-tumor cells. Furthermore, our group has reported that LRP-1 silencing prevents the invasion of a follicular thyroid carcinoma despite increased pericellular proteolytic activities from MMP2 and uPA using a 2D-cell culture model. As the use of 3D culture systems is becoming more and more popular due to their promise as enhanced models of tissue physiology, the aim of the present work is to characterize for the first time how the 3D collagen type I matrix may impact the ability of LRP-1 to regulate the migratory properties of thyroid carcinoma using as a model FTC-133 cells. Our results show that inhibition of LRP-1 activity or expression leads to morphological changes affecting cell-matrix interactions, reorganizations of the actin-cytoskeleton especially by inhibiting FAK activation and increasing RhoA activity and MLC-2 phosphorylation, thus preventing cell migration. Taken together, our results suggest that LRP-1 silencing leads to a decrease of cell migratory capacity in a 3D configuration.

Introduction

The low-density lipoprotein receptor-related protein-1 (LRP-1) is a member of low density lipoprotein receptor (LDLR) family, which is ubiquitously expressed in a variety of organs including adipose tissue, liver and brain.⁸ It is composed of a 515 kDa extracellular ligand-binding subunit (α-chain) that contains 4 clusters of ligand binding domains linked non-covalently to a 85 kDa transmembrane subunit encompassing a short cytoplasmic tail (β-chain).^14,26 Initially, LRP-1 was identified as a receptor playing an active role in the lipid metabolism, and then as a receptor of activated α2-macroglobulin.⁵³ Subsequent work has revealed that this receptor is a large endocytic receptor mediating the clearance of various extracellular matrix molecules including serine proteinases, proteinase-inhibitor complexes, and matricellular proteins such as thrombospondins.^21,26,57 Firstly considered to act only as a scavenger receptor, numerous evidence indicate that LRP-1 may mediate intracellular signaling^4,28,54 and modulate the activity of other transmembrane receptors such as tyrosine kinase receptors and integrins.⁵ Although several works have described its involvement in tumorigenesis, the precise role of LRP-1 remains controversial and the potential underlying mechanisms need to be clarified. Several studies have reported that low expression of LRP-1 is closely related to aggressiveness of tumor cells derived from various tissues such as human endometrial carcinoma,¹⁶ thyroid cancer,⁵¹ breast and prostate cancer.³¹ However, other studies showed that high LRP-1 expression promotes breast cancer cell invasiveness, and LRP-1 neutralization leads to cell motility abrogation in both tumor and non-tumor cells.⁵² Furthermore, our group has reported that LRP-1 silencing prevents the invasion of a follicular thyroid carcinoma despite increased pericellular proteolytic activities from MMP2 and uPA.¹² In this previous work, we established that LRP-1 may coordinate the adhesion and de-adhesion balance of malignant cells to support tumor progression by regulating the amount and distribution of focal contact proteins, such as FAK, paxillin and talin, and thus by contributing to the control of integrin activation and adhesion complex turnover.¹¹ LRP-1 has also been shown to regulate the internalization of CD44 in follicular thyroid carcinoma, a receptor known to control the adhesion dynamics of cancer cells.⁴⁵ Moreover, in schwann cells, LRP-1 expression has been shown to regulate their migration by inhibiting RhoA and activating Rac1.³⁸ Taken together, these results demonstrate that the role of LRP-1 in tumor cell migration and invasion is highly complex and likely depends on the tumor cell type and the composition and arrangement of the microenvironment. Previous studies indeed demonstrated that the extracellular matrix composition and organization are crucial to determine the endocytic and signaling functions of LRP-1.^55,58

One of the limitations of in vitro studies is that they were performed on conventional tissue culture substrate, a situation that does not take into account the tumor cell microenvironment in which tumor cells exert in vivo complex molecular and cellular interactions especially through the extracellular matrix (ECM). Tumor cells exist within a dynamic tridimensional (3D) matrix which is not completely reproduced by standard in vitro cell culture techniques. Several recent works showed clearly that cells can sense chemical composition of the ECM and its physical properties such as dimensionality, stiffness, and architecture.¹³ Bidimensional (2D) plastic or ECM coating and 3D matrices, as scaffolds for cell growth, supply the cell with very different biochemical and mechanical environments. In 2D conditions cell surface interact with a solid substrate or ECM coating via their basal surface. However, cells growing in 3D matrix exhibit adapted cell-surface mechano-transducers and ECM adhesion proteins.^10,25 Setting in culture of cells in 2D versus 3D platforms results in significant modifications in cell growth,^6,22 migration,^3,39,46 morphology^2,62 and gene expression.^22,36 The use of in vitro 3D collagen matrix to mimic in vivo cellular environment becomes increasingly popular and improves our understanding of cell growth, survival, migration, and cell-ECM interactions that may occur in vivo under physiological and pathological conditions.¹³

Several studies have thus reported a positive contribution of LRP-1 to migration and invasion events in various cell types,^7,8,37 including malignant tumor cells.^12,15 In the present study, we characterized for the first time how the 3D collagen type I matrix may impact the ability of LRP-1 to regulate the migratory properties of thyroid carcinoma.

Results

LRP-1 supports thyroid carcinoma cell migration in 3D collagen matrix

To demonstrate the involvement of LRP-1 in tumor cell migration in a 3D environment, 2 different strategies were used: treatment with RAP (Receptor Associated Protein) to inhibit LRP-1 activity⁶⁰ and LRP-1 silencing. The recombinant protein RAP was purified on a nickel-agarose column and controlled after SDS-PAGE by Coomassie blue staining and immunoblotting (Fig. 1A). LRP-1 silencing was conducted by using previously validated short interfering sequence.¹² A clonal cell line that stably overexpresses a specific short hairpin RNA for LRP-1 (shLRP-1) was selected, and a control cell line was established after transfection with pSuppressorNeo carrying a non-silencing sequence (shCTRL). The expression of LRP-1 was analyzed by both real-time PCR (Fig. 1B) and western-blotting (Fig. 1C). Transfection with shCTRL had no effect on the LRP-1 expression level compared to wild type cells (data not shown).¹² At the opposite, stable transfection of FTC-133 cells by the LRP-1-specific shRNA plasmid resulted in a 70 % down regulation of the expression of LRP-1 at the mRNA and the protein levels (Fig. 1B and 1C).

Figure 1.

Validation of LRP-1-silencing efficiency and purification of human recombinant RAP. (A) Purified recombinant RAP was assessed by SDS-PAGE followed by CBS and immunoblotting using anti-RAP antibody (IB). (B) Total RNAs were purified from FTC-133 cells transfected with non-silencing shRNA (shCTRL) or shRNA targeting LRP-1 (shLRP-1). The transcriptional level of LRP-1 was assessed by reverse transcription followed by a real-time PCR. β-actin primers were used as a normalization control. Graph represents the relative LRP-1 expression in percent. *, P< 0.05 (C) Whole-cell extracts from each clonal cell were subjected to immunoblot analysis under non-reducing conditions with anti-LRP-1 α-chain (8G1) and β-chain (5A6) antibodies. β-actin antibody was used for normalization.

We first investigated whether shRNA-mediated inhibition of LRP-1 expression altered migration of FTC-133 cells into 3-D collagen gels. The migration speed of individual cells cultured within collagen type I matrix has been determined by quantifying their migration speed and 3D trajectories using computer-assisted videomicroscopy. To this end, FTC-133 cells were seeded into a type-I collagen matrix and individual cells were examined for their migrating potential during the first 6 h (Fig. 2A, left panel) or after 18h (Fig. 2A, right panel). From one hand, migration of shLRP-1 overexpressing cells was diminished 2.8 fold after 18h whereas there is no modification of the migration rate during the six first hours of culture. On the other hand, RAP treatment decreased cell migration speed of FTC-133 cells by 2 fold regardless of the observed migration times. Indeed, the length of trajectory of FTC-133 cells is more than twice as high as the length of trajectory of RAP-treated cells during the six first hours of culture and after 18h (Fig. 2B). Furthermore, the distance traveled by LRP-1-silenced cells is 2.9 times lower than for control cells between 18 h and 24 h.

Figure 2.

Thyroid carcinoma cell migration on 3D collagen matrix is drastically altered by LRP-1 blockade or silencing. FTC-133 cells were cultured for 24 h within 3D collagen I matrix, and then were tracked by time-lapse videomicroscopy. (A) Cell migration speed (µm/h) was assessed during the first 6 h and the last 6 h of culture and data represent the average of 3 independent experiments (at least 25 cells were tracked per experiment). Error bars represent SEM. ***, P < 0.001 significant difference. (B) Distance of migration covered by cells during the first 6 h and the last 6 h. Data represent the average of 3 independent experiments (at least 25 cells tracked per experiment). (C) Quantitative analysis of 3D FTC-133 cell trajectories during the last 6 h of culture. Each color corresponds to a distinct cell.

Using live-cell microscopy, we measured the individual cell trajectory length inside collagen matrix. Migration of the cells embedded in the collagen was evaluated by tracing cell movements projected into the x–y-z plane. Trajectories of cells expressing or not LRP-1 revealed significant distinct patterns (Fig. 2C). Wild-type FTC-133 actively migrated through the collagen matrix whereas LRP-1-silenced cells exhibited circular trajectories around their starting point. Similar data were obtained under RAP treatment and are together in accordance with the inhibition of cell migration speed and observed traveled distance in Figure 2A and 2B.

LRP-1 promotes cell elongation in 3D collagen matrix

To determine whether cell spreading could be LRP-1 dependent, wild-type FTC-133 cells treated or not with RAP, and both control and LRP-1-silenced carcinoma cells were seeded inside collagen matrix for different time periods before analysis of spreading (Fig. 3A). After 60 min, wild-type and control cells were spread and begun to exhibit thin projections as shown by arrows in Figure 3A. Several distinct protrusions and filopodiae consistent with migratory activity were detected after 240 min in control cells. In striking contrast, LRP-1-silenced cells displayed overspread morphology with membrane ruffles and failed to extend filopodiae. To support this observation, the number of cells exhibiting a rounded form was quantified. As expected, the number of rounded cells was increased by 2.7 and 8.1-fold under RAP treatment and LRP-1 silencing, respectively (Fig. 3B). Additionally, quantitative analysis by measurement of length-width ratio confirmed that cell elongation was reduced by about 40% under RAP treatment or LRP-1-silencing, as shown in Figure 3C. Altogether, these results demonstrate that unlike fast-invading carcinoma control cells, inhibition of LRP-1 activity or expression leads to major morphological changes affecting cell-matrix interactions.

Figure 3.

LRP-1 blockade or silencing impacts the FTC-133 carcinoma cell morphology on 3D collagen matrix. (A) Cells were seeded within 3D type I collagen matrix. Typical morphology of cells cultured within 3D matrix was obtained by phase contrast microscopy. Arrows show examples of nascent thin projections. Bar: 100 μm. (B) Percentage of round cell was calculated by using 30 isolated cells (180 min after seeding) for each condition in 3 independent experiments. ***, P < 0.001. (C) Ratio (length/width) was calculated using Image J software by using 20 isolated cells (60 min and 180 min after seeding) for each condition in 3 independent experiments. ***, P < 0.001.

LRP-1 induces FAK activation and MLC-2 inhibition in 3D collagen matrix

Focal adhesion kinase (FAK) is a cytoplasmic tyrosine kinase which is widely expressed and located in integrin-mediated focal adhesions that regulates integrin signaling. FAK can be rapidly activated by a variety of mechanical stimuli and plays an important role in control of cell adhesion and migration making it a major mechanosensitive kinase.^41,44 Previous results obtained by Dedieu et al. (2008) established that LRP-1 is required for FAK association with focal contacts and reported that FAK activation is reduced in cells lacking LRP-1.¹² To determine whether FAK activation could be differentially regulated by LRP-1 in 3D collagen environment, we analyzed FAK phosphorylation on tyrosine 397 (p397-FAK) in control cells, RAP-treated cells or LRP-1 silenced cells seeded inside collagen matrix (Fig. 4A). Western-blotting of cell lysates demonstrated 36% and 84% decrease in p397-FAK expression when cells were treated with RAP for 3 h and 24 h, respectively. FAK phosphorylation was similarly decreased in LRP-1-deficient cells by 28% and 40% after 3 h and 24 h after seeding, respectively.

Figure 4.

FAK and MLC-2 Phosphorylation and Rho activation are LRP-1 dependent in 3D matrix. Wild-type FTC-133 (treated with or without RAP) and clonal cells (shCTRL and shLRP-1) were seeded in 3D collagen matrix for 3 h and 24 h. Whole-cell extracts were subjected to Western-blot analysis to evaluate the level of FAK activation (A) and the phosphorylation of MLC-2 (B). The respective phosphorylation rates of FAK (A) and MLC-2 (B) were determined as intensity ratios of phospho-protein to corresponding pan-protein and expressed in relative units +/− SD, with a value of 100% ascribed to wild-type cells (right panels). GAPDH antibody was used as a loading control. (C) Cell lysates were incubated with GST-RBD beads. The bound RhoA was detected with a monoclonal anti-RhoA antibody (Top). The relative amount of total RhoA in the cell lysates were assessed by using a monoclonal antibody against RhoA (Bottom). Quantitative analysis of the GTP-RhoA associated with RBD beads was obtained by densitometry. The amount of RhoA bound to RBD was normalized to the RhoA content of cell extracts. *, P<0.05; ***, P < 0.001.

Mesenchymal-type movement in 3D matrix is known to be driven by GTPase Rac pathway which activates WASP-family verprolin-homologous protein 2 (WAVE2) to shift cell movement from amoeboid to mesenchymal form through decreasing actinomyosin contractility and inhibiting the RhoA GTPase.⁴⁹ To address this point, we assessed the impact of silencing LRP-1 expression or RAP treatment in FTC-133 cells on RhoA activation in cells seeded in 3D collagen matrix (Fig. 4B). Interestingly, both RAP treatment and down-regulation of LRP-1 expression induce an increase of the formation of active GTP-bound RhoA by 72% and 88%, respectively and as compared to corresponding controls. One of the major downstream effector of RhoA is the serine/threonine RhoA-associated kinase ROCK which phosphorylates MLC-2 at serine 19.²³ To confirm whether RhoA is inhibited by LRP-1 in our experimental model, we analyzed phosphorylated MLC-2 level in control cells, RAP-treated cells or LRP-1 silenced cells seeded in 3D collagen matrix. Whereas RAP treatment appears to moderately and transiently influence the phosphorylation of MLC-2, LRP-1 silencing leads to an increase in the amount of phosphorylated-MLC-2 by 27% and 49% after 3 h and 24 h incubation respectively (Fig. 4C).

Altogether, our results clearly indicate that LRP-1 silencing or inhibition of LRP-1 mediated-endocytosis induce reorganizations of the actin-cytoskeleton especially by inhibiting FAK activation and increasing MLC-2 phosphorylation, thus preventing cell migration in a 3D environment.

Discussion

Several works have shown recently that cells can sense chemical composition of the extracellular matrix and its physical properties such as dimensionality, stiffness, and architecture. The use of in vitro 3D collagen matrix to mimic in vivo cellular environments becomes increasingly popular and improves our understanding of cell growth, survival, migration, and cell-ECM interactions that occur in vivo under physiologically normal and diseased conditions.⁹ For this reason, we proposed to study the impact of extracellular matrix on the role of LRP-1 in FTC-133 cells by using a complex cellular system such as 3D culture systems. Our data show the pro-migratory effect of LRP-1 receptor in 3D culture. In fact, inhibition of the LRP-1 function or its silencing induce a decrease in cell migration speed by suppressing cell protrusion and by regulating FAK and MLC-2 phosphorylation. The discrepancies in results observed with RAP treatment and shLRP-1 transfected cells could be explained by the 2 methods used to invalidate LRP-1. Indeed, a treatment by RAP does not modify LRP-1 expression in cell membrane, endocytosis kinetic and intracellular signaling pathways associated with this last mechanism, whereas downregulation of LRP-1 by shLRP-1 induces a strong decrease of LRP-1 expression at the cell membrane and then subsequent modifications of the membrane proteome (including sometimes middle or long-term changes), concomitantly with drastic modifications of intracellular signaling associated with LRP-1 co-receptors). To our knowledge, this is the first study to show that LRP-1 silencing leads to a decrease of cell migratory capacity in a 3D configuration.

Cell migration is dependent of physical and extracellular modulators which include: confinement, determined by pore-size through which the cell migrates; geometry defined by ECM alignment and dimensionality (2D vs. 3D); and stiffness depending on the composition, flexibility, density and cross-link status of ECM components.^32,33,61 To mimic in vivo microenvironment, we proposed to use a representative model which is 3D gel of type I collagen. Type I collagen is the most abundant collagen of extracellular matrix in the human body and represents a pre-intravasation microenvironment.⁵⁰ Previous data from our group^17,40 have shown that the 3D collagen gel prepared here at physiological concentration⁴⁷ is close to the 3D fibrous nature of a mesenchymal stroma because of a highly fibrillar organization. Furthermore, our native fibrillar collagen is prepared without pepsinization and presents intact telopeptides, which correspond to the flanking regions of the molecules and permit to form intra- and intermolecular cross-links that promote the staggering and the resilience of fibrillar collagen.²⁹

Morphology of FTC-133 carcinomas cultured in 3D matrix appears different from that of cells cultured on rigid 2D substrate. Indeed, FTC-133 cells on plastic or substrate-coated support were broader and more flattened and exhibit most of the time prominent lamellae and retraction fibers at the rear of the cell.⁴⁵ In collagen 3D matrix, wild-type FTC-133 cells displayed a spindle-shaped, elongated, or stellate phenotype with thinner and longer protrusions and dendritic extensions at the migration front, which is rather in favor of a mesenchymal migration mode.⁵⁶ LRP-1 silencing or RAP treatment induce morphological changes, especially by maintaining carcinoma cells in a rounded morphology. The cells are then characterized by an increase in circularity, a decrease in elongation and a higher fraction of rounded cells. Interestingly, a similar phenotype was obtained in 2D culture as LRP-1-silenced cells displayed overspread morphology and failed to extend membrane extension onto gelatin.¹² Thus, LRP-1 expression in tumor cells may be, at least in part, responsible for mesenchymal phenotype acquisition.

This change in shape could arise from the decrease of cell/matrix adhesion and could suggest that along with loss of traction the amoeboid-like cells may have greater difficulty to migrate in absence of LRP-1 and thus results in a decrease in the cell migration speed. Indeed, previous results obtained in 2D have shown that LRP-1 may coordinate the adhesion-deadhesion balance in malignant cells to support tumor progression.¹¹ We have previously provided molecular knowledge on LRP-1 roles in multiple cancer-related events. Indeed, LRP-1 silencing prevents thyroid carcinoma cell invasiveness despite a major increase in pericellular proteolytic activities. This suggests that LRP-1 promotes cell invasion by subtly controlling the adhesive properties and the actin network structure. In addition, LRP-1 promotes cell invasion through ERK and JNK MAPK pathways to regulate focal adhesion disassembly to support invasion.^11,34,45 By controlling focal adhesions components and the turn-over of the cytoskeleton organization proteins and integrins, Dedieu and collaborators described LRP-1 as a crucial actor of the epithelial-mesenchymal transition.¹² In addition, signaling induced by urokinase-type plasminogen activator (uPA)-urokinase receptor (uPAR) is another migration- and invasion-related pathway regulated by LRP-1 that can enhance cell invasion and migration.^1,19,59 Furthermore, Hu et al. have described in a previous work that LRP-1 is involved in the β1-integrin recruitment and the subsequent activation of the β1-integrin-linked kinase (ILK).²⁷ The focal adhesion protein kinase, ILK, is known to consolidate the integrin/cytoskeleton connections., LRP-1 could play a key role in regulating the actin polymerization and cytoskeleton dynamics during retraction of migrating cells by controlling ILK activity.⁶³ Furthermore, in rounded amoeboid movement, cells move with high levels of actomyosin contractility driven by Rho-Rho kinase (ROCK) signaling.^48,49 ROCK decreases myosin phosphatase activity, increasing phosphorylation of MLC-2 and activity of myosin II,³⁰ as suggested by our data.

Although most studies have suggested that rounded-amoeboid cancer cells do not require MMPs to invade, a recent work demonstrated that rounded amoeboid melanoma cells secrete higher levels of several MMPs, including collagenase MMP-13 and gelatinase MMP-9 to invade through type I collagen.⁴² Moreover, Orgaz and collaborators showed that MMP-9 promotes rounded-amoeboid 3D migration using a non-catalytic mechanism through regulation of actomyosin contractility via CD44 receptor ⁴² LRP-1 was previously reported to bind with high affinity to MMP-9 and to mediate its cellular catabolism.²⁴ Besides, both LRP-1 silencing and RAP treatment led to accumulation of CD44 at the tumor cell surface in our thyroid carcinoma environment.⁴⁵ We therefore believe that the residual migratory activity observed in our study under LRP-1 silencing or blocking, could be attributed to amoeboid movement.

Materials and methods

Cell line

The human FTC-133 cell line was derived from a lymph node metastasis of a follicular thyroid carcinoma.²⁰ This cell line was obtained from the European Collection of Cell Cultures, ECACC. Cells were cultured in Dulbecco's Modified Eagle Medium-Ham's F12 (DMEM:F12, Invitrogen, Cergy Pontoise, France) supplemented with 10% fetal bovine serum (FBS) and was maintained at 37˚C in a humidified 5% CO₂ atmosphere. Generation of 2 clonal cell lines that stably overexpress a non-silencing sequence (shCTRL) or a specific short hairpin RNA (shRNA) for LRP-1 (shLRP-1) was described previously.¹¹ Cells were routinely passaged at preconfluency until 15 subcultures using 0.05% trypsin, 0.53 mM EDTA (Invitrogen) and screened for the presence of mycoplasma using PCR methods.

Purification of recombinant RAP

Histidine-tagged RAP was expressed in Escherichia coli BL21 pLysS (Promega, Charbonnières-les-Bains, France) using the pT7H6FX-RAP construct kindly provided by M. S. Nielsen (Department of Medical Biochemistry, University of Aarhus, Denmark). Purification of recombinant RAP was performed by gravity-flow chromatography using a nickel-charged resin (Ni-nitrilotriacetic acid [NTA]- agarose from Qiagen, Courtaboeuf, France) and then controlled after SDS-PAGE by Coomassie blue staining (CBS) and immunoblotting. The LRP-1 binding capacity was confirmed using a BIAcore X system (BIAcore AB, Uppsala, Sweden), as previously reported (Selvais et al., 2009)

3D culture

Acid-extracted, non-pepsinized collagen type I from rat tail tendons was prepared as described by Garnotel et al.¹⁸ Lyophilized collagen was dissolved in a sterile 18 mM acetic acid solution at a concentration of 3 mg/ml.

For 3D cell culture, 5 × 10⁴ FTC-133 cells were resuspended in 100 μl fetal bovine serum and mixed with a solution containing 100 μl DMEM:F12 10X, 100 μl NaHCO₃ 0.26 M, 100 μl H₂O, 90 μl NaOH 0.1 M, 10 μl glutamine 200 mM and 500 μl collagen 3 mg/ml. This solution was deposited in 24-well plates (1 ml/well). After polymerization at 37°C during 10 min, gels were recovered by 1 ml DMEM:F12 10% foetal bovine serum (FBS) and 3D cultures were maintained at 37˚C in a humidified 5% CO₂ atmosphere. For RAP treatment, RAP was added at 500 nM both in the culture medium and in the collagen gel

3D cell migration quantification and cell morphology

3D cultures, prepared as described above, were seeded in 24-well plates (1 ml/well). Cell motility was analyzed by time-lapse videomicroscopy using an inverted microscope Axiovert 200 M (Zeiss, Le Pecq, France) equipped with a small transparent environmental chamber Climabox (Zeiss) with 5% (v/v) CO₂ in air at 37°C. The microscope was driven by the Metamorph software (Roper Scientific, Evry, France) and images were recorded with a charge-coupled device camera CoolsnapHQ (Roper scientific). Cell speed was quantified (μm/h) for each individual non-mitotic cell using an interactive tracking method as previously described.⁴⁰ The length/width ratio was calculated using ImageJ, as follows: length was scored as the longest distance between any 2 points of the cells; width was scored as the secondary axis of the best fit ellipse of the circled cells. This factor estimates the degree of variance from a circle. A value of 1.00 is a perfect circle.⁴³

RNA isolation, reverse transcription, and real-time PCR

Total RNAs were isolated and purified with an Extract-All kit (Eurobio Laboratories, Courtaboeuf, France). Reverse transcription (RT) and real-time PCR were performed with Verso SYBR 2-Step QRT Rox kit (AB-4113/A) and Absolute QPCR SYBR green Rox (AB-1162/B), respectively (Thermo Fisher Scientific). Quantitative PCR was carried out on a Chromo4 real-time detector (Bio-Rad Laboratories, Marne-la-Vallée, France), and β-actin was used for normalization. Primers for LRP-1¹² and β-actin³⁴ were previously described. All primers were synthesized by Eurogentec France (Angers, France). Results shown are representative of 3 independent experiments.

Expression and purification of recombinant proteins in bacteria

GST-tagged fusion proteins of the Rho-binding domain (RBD) of Rhotekin were expressed using the bacterial expression vector pGEX4T1 in the BL21DE3 strain of Escherichia coli and purified. We thank Dr. Dario Diviani (Department of Pharmacology and Toxicology, Lausanne, Switzerland) for the gift of the bacterial expression vector pGEX4T1. To induce Expression of fusion proteins was induced with 1 mM IPTG in exponentially growing bacterial cultures incubated 24 h at 16°C. After centrifugation. bacteria were lysed in buffer A (20 mM Tris, pH 7.4/100 mM NaCl/5 mM MgCl2/1% (wt/vol) Triton X-100/1 mM benzamidine/2 mg/ml leupeptin/2 mg/ml pepstatin), sonicated, and centrifuged at 38,000 ´ g for 30 min at 4°C. Supernatants were then incubated with glutathione Sepharose beads (Pharmacia) for 2 h at 4°C, the resin was washed 5 times with 10 bed volumes of buffer A and used immediately for the Rhotekin RBD pulldown assay.

Rhotekin Rho-binding domain (RBD) pulldown assay

FTC-133 cells were grown for 3 h in 3D culture. Gels were then digested by collagenase P at 1 mg/ml. After centrifugation, cells were lysed in Rho-binding domain (RBD) lysis buffer (50 mM Tris pH 7.2, 150 mM NaCl, 1% (w/v) Triton X-100, 30 mM MgCl2, 1 mM DTT, 10% glycerol, 1 mM benzamidine, 10 μg/ml leupeptin, 10 μg/ml aprotinin and 1 mM PMSF). After centrifugation at 38 000 g for 10 min at 4°C, lysates were incubated with 30 μg of RDB beads for 1 h at 4°C. Beads were then washed 3 times with RBD buffer without sodium deoxycholate, resuspended in SDS sample buffer and analyzed by SDS–PAGE.

Western-blotting

FTC-133 cells were grown for 3 h or 24 h in 3D culture. Gels were digested by collagenase P at 1 mg/ml. After centrifugation, cells were harvested in lysis buffer (50 mM Tris pH 7.2, 150 mM NaCl, 1% (w/v) Triton X-100, 30 mM MgCl2, 1 mM DTT, 10% glycerol, 1 mM PMSF supplemented with proteinase inhibitor cocktail from Sigma-Aldrich). Cell lysates were cleared by centrifugation at 21,000 x g for 10 min at 4 C. Proteins in total lysates were assayed before SDS-PAGE using the the Bradford method (Bio-Rad Laboratories, Marnes-la-Coquette, France). Protein aliquots were applied to a 10% SDS-PAGE. After transfer onto nitrocellulose membrane (Whatman GmbH, Dassel, Germany), blots were blocked overnight with 5% non-fat dry milk in Tris-buffered saline, 0.1% Tween 20 and then incubated overnight at 4°C with primary antibody: mouse monoclonal anti-LRP-1 α-chain (clone 8G1, 1:1000, Merck Biosciences), mouse monoclonal anti-LRP-1 β-chain (clone 5A6, 1:1000, Merck Biosciences), mouse monoclonal anti-RAP (clone 7F1, Merck), rabbit polyclonal anti-MLC-2 (Myosin Light Chain 2, 1:1000, Cell Signaling), rabbit polyclonal anti-(S19) phosphorylated-MLC-2 (1:1000, Cell signaling), mouse monoclonal antibodies raised against total FAK (1:5000, Millipore) or (Y397) phosphorylated-FAK (1:1000, Millipore), mouse monoclonal anti-RhoA (1:250, Santa Cruz), rabbit polyclonal anti-GAPDH (1:1000, Cell signaling). The membranes were then washed and incubated with secondary antibody for 1 h: Horseradish peroxidase-conjugated anti-rabbit or anti-mouse antibodies (1:10000, Cell Signaling Technology). Chemiluminescent detection was conducted using an ECL plus chemiluminescence kit from Amersham Biosciences. β-actin antibodies or GAPDH antibodies were used to ensure equal loading of the protein samples and for normalization. Immunoblots presented are representative of at least 3 separate experiments.

Statistical analysis

Results are expressed as means ± SD. The significance of differences between 2 groups was determined using Student's t-test. Statistical significance was set at p < 0.05.

Disclosure of potential conflicts of interest

No potential conflicts of interest were disclosed.

Acknowledgments

The authors acknowledge the technical assistance of Cathy Hachet and Laurence Van Gulick.

Funding

This work was supported by funding from the CNRS and by Université de Reims Champagne Ardenne.