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PLoS One. 2012; 7(10): e47668.
Published online 2012 Oct 17. doi:  10.1371/journal.pone.0047668
PMCID: PMC3474718

Activation of Fms-Like Tyrosine Kinase 3 Signaling Enhances Survivin Expression in a Mouse Model of Rheumatoid Arthritis

Serge Nataf, Editor


Survivin is known as an inhibitor of apoptosis and a positive regulator of cell division. We have recently identified survivin as a predictor of joint destruction in patients with rheumatoid arthritis (RA). Flt3 ligand (Flt3L) is expressed in the inflamed joints and has adjuvant properties in arthritis. Studies on 90 RA patients (median age 60.5 years [range, 24–87], disease duration 10.5 years [range, 0–35]) show a strong positive association between the levels of survivin and Flt3L in blood. Here, we present experimental evidence connecting survivin and Flt3L signaling. Treatment of BALB/c mice with Flt3L led to an increase of survivin in the bone marrow and in splenic dendritic cells. Flt3L changed the profile of survivin splice variants, increasing transcription of the short survivin40 in the bone marrow. Treatment with an Flt3 inhibitor reduced total survivin expression in bone marrow and in the dendritic cell population in spleen. Inhibition of survivin transcription in mice, by shRNA lentiviral constructs, reduced the gene expression of Flt3L. We conclude that expression of survivin is a downstream event of Flt3 signaling, which serves as an essential mechanism supporting survival of leukocytes during their differentiation, and maturation of dendritic cells, in RA.


Survivin is an intracellular protein and a member of the inhibitor of apoptosis proteins (IAPs), with many functions in cytoprotection, cell division and cellular adaptation. It is encoded by the BIRC5 gene on the human chromosome 17q25, into a 142 amino acid, 16.5 kDa protein but can be extensively alternatively spliced into several variants and form homodimers and heterodimers with two different splice variants, or an IAP-IAP complex by pairing with X-linked IAP (XIAP) [1], [2]. Transcription of survivin is negatively regulated by p53 [3] and positively regulated by STAT3 [4] and TCF-4 [5].

Similar to human protein, full-length murine survivin (survivin140) contains a single BIR-domain, which is critical for its anti-apoptotic function [6], and a carboxy-terminal coiled-coil domain that links its function to the cell cycle [7]. Murine survivin121 contains a BIR-domain that makes it able to inhibit caspase activity but lacks the coiled-coil structure. Additionally, there is a splice variant that predicts a 40 aa residue protein (survivin40), which lacks both the BIR- and a coiled-coil regions. The differential expression of these forms of survivin is believed to affect the balance between cell proliferation and programmed cell death [8].

Survivin has only limited expression in adult tissues, but is overexpressed in tumors and is therefore regarded as a cancer gene. Survivin is expressed in a cell-cycle dependent manner with a peak at G2/M. Together with Aurora B, borealin and INCENP, survivin forms the chromosomal passenger complex, which is recruited to chromosomes by the phosphorylation by histones which is recognized by the BIR domain of survivin. In anaphase, the chromosomal passenger complex relocalizes to form the mitotic spindle and stimulate cytokinesis. The requirement of survivin during fetal development has been demonstrated by lethality of knockout embryos [1].

Survivin is also expressed independently of cell cycle progression and is linked to the inhibition of apoptosis [3]. The pool of survivin with apoptotic inhibiting properties seems to be localized to the mitochondria [1], [9], and is released into the cytoplasm in response to death stimuli. Survivin inhibits apoptosis in complex with hepatitis B X interacting protein [10] or XIAP, perhaps by separating Smac/Diablo from XIAP, thus enabling caspase degradation [1]. There is an emerging role for survivin in normal adult CD34+ hematopoetic stem cells [11], [12] and in the development, maturation and survival of immune cells, for example in T cells [13][16] and neutrophils [17]. It is upregulated in response to stimulation with hematopoetic cytokines and growth factors [18][20].

Expression of survivin in malignancies is associated with unfavorable outcome [21], [22] and resistance to cytotoxic treatment [23][25]. In the context of rheumatoid arthritis (RA), extracellular survivin is a marker of poor prognosis. A prospective study on 651 patients at the early stage of RA with the mean disease duration of 6 month showed that high serum levels of survivin were predictive for severe cause of RA, characterized by persistent joint inflammation and progressive joint destructions [26]. The proportion of survivin-positive patients may vary from 20–30% in the group of established and treated RA patients [27] to 60% in the population of early RA patients [26]. Successful anti-rheumatic treatment may reduce serum levels of survivin, while survivin-positive patients accumulate among the patients who do not respond to anti-rheumatic treatment [26][28]. A growing number of publications [26], [27], [29][31] support the idea that survivin has a role in progression of RA. We have previously shown that survivin has a key function in the regulation of invasive properties of fibroblasts in the inflamed rheumatic joint, and that intracellular survivin is essential for urokinase expression and for the up-regulation of urokinase receptor [32]. Also, serum survivin modifies surface pattern of leukocyte adhesion molecules [33].

Fms-like tyrosine kinase 3 (Flt3) is a receptor tyrosine kinase class III, a class that also includes c-KIT, PDGFRα/β and c-FMS receptors. It is expressed on hematopoietic stem cells and promotes differentiation, maturation and survival of lymphoid progenitors in the bone marrow [34]. Flt3 is essential for the development of antigen presenting cells, such as B cells and dendritic cells (DC) [35][37]. Mutations in the Flt3 receptor, leading to its constant activation, are frequently found in acute myeloid leukemia (AML) [38]. It has been shown that bone marrow cells expressing Flt3 with internal tandem duplication mutations which keeps Flt3 signaling constantly active, have an increased survivin expression [39], [40] and this is associated with development of resistance to Flt3 inhibition [39].

Flt3 ligand (Flt3L) is expressed by many cell types, and is present in a soluble intracellular form, and in a membrane bound form [41]. Flt3L has recently been outlined within a panel of preclinical biomarkers of predictive value for the development of RA [42]. We have recently shown that Flt3L is elevated in RA patients and that Flt3L has adjuvant properties when injected into the joint, facilitating development of arthritis in experimental settings [43]. Blockade of Flt3 signaling using a synthetic Flt3 inhibitor alleviates signs of synovitis and cartilage destruction in antigen-induced model of arthritis [44].

Since expression of the Flt3 receptor and survivin in adults is present in hematopoietic stem cells, we address the question whether Flt3L signaling could actually be linked to survivin in rheumatoid arthritis. We further tested the pathological significance of this relation using in vivo treatment with Flt3L and evaluated the possibility of targeting this pathway with an Flt3 inhibitor and lentiviral shRNA knockdown of survivin.


Higher Levels of Flt3 Ligand in Survivin Positive Rheumatoid Arthritis Patients

Survivin levels in the blood of 104 healthy controls (male n = 16, female n = 88, mean age 52.4 years [range 18–67]) were measured by ELISA. The evaluation of the results showed a non-Gaussian distribution of survivin levels in the studied group. The 95% confidence interval was calculated which indicated that the levels of survivin above 450 pg/ml was present in less than 5% of healthy individuals. Thus, the patients with serum or synovial fluid levels of survivin above 450 pg/ml represented the survivin-positive group (n = 29) and the remaining were survivin-negative (n = 61, Table 1). In the present material, 32% of the RA patients were survivin-positive. This is in agreement with our previous reports [27]. As expected, survivin-positive RA patients were significantly more often RF-positive (p = 0.0006) and a majority of the survivin positive patients had erosive joint disease (p = 0.003). The comparison between the groups revealed significantly higher levels of Flt3L in the blood of the survivin-positive RA patients compared to survivin-negative (pg/ml: 110 [range 30–3320] vs 70 [range 10–230], p = 0.003, Fig. 1A). This was also the case for synovial fluid (pg/ml: 200 [range 40–2000] vs 150 [range 30–930], p = 0.055), although not statistically significant (Fig. 1A). There was no significant difference in the levels of acute-phase reactants (e.g., C-reactive protein, serum amyloid A protein levels, IL-6 levels) between the survivin-positive and survivin-negative groups (Table 1).

Figure 1
Treatment with Flt3 ligand increases expression of surviving.
Table 1
Clinical characteristics of patients with rheumatoid arthritis.

Survivin Expression is Upregulated in Mouse Bone Marrow Following Treatment with Flt3 Ligand

To elucidate a causative relation behind the observed association between survivin and Flt3L levels in RA patients, arthritic mice were challenged with Flt3L. Two independent experiments were performed containing 15 Flt3L-treated mice and 19 PBS-treated controls. After 14 days of Flt3L treatment, survivin levels in bone marrow cell lysates were increased compared to the PBS treated group (pg/ml: 472.5±193.4 vs 286.5±48.9, p = 0.01, Fig. 1B). At day 28, the number of survivin+ cells in bone marrow of Flt3L treated mice was higher compared to PBS treated controls (28.1±6.3% vs 21.9±4.3%, p = 0.02, Fig. 1B). Additionally, Flt3L-treated mice tended to have somewhat higher survivin concentration per cell, measured as the intensity of intracellular staining (gMFI: 336±54 vs 288±29, n.s.). The intensity of survivin staining was higher in the Flt3+ cells compared to the Flt3− cell population (p = 0.003). Flt3L treatment tended to upregulate survivin expression in both Flt3+ and Flt3− cell populations (Fig. 1C).

Despite the similar size of survivin+ population in bone marrow and spleen, survivin gene expression in spleen was 4 times lower compared to bone marrow (p = 0.002, Fig. 2A, PBS). Flt3L treatment of arthritic mice did not affect total survivin levels in the spleen, since the percentage of survivin+ spleen cells was similar in the Flt3L treated group and the control group (20.3±5.3% vs. 19.5±6.3%). High intensity of survivin expression was attributed to the MHCII+CD11chi dendritic cell population in the spleen (Fig. 1D). Flt3L treatment increased the proportion of survivin+ cells within the MHCII+CD11chi population (73.9±6.2% vs 66.0±4.2%, p = 0.005, Fig. 1E). When cultured in vitro, splenocytes of Flt3L-treated mice (n = 7) secreted significantly higher levels of survivin compared to splenocytes of PBS-treated controls (n = 7) (pg/ml: 32.6±7.7 vs 24.3±6.2, p = 0.04), but Flt3L treatment did not increase serum levels of survivin (pg/ml: 1772±2503 vs 1190±1335).

Figure 2
The effect of Flt3L-treatment of BALB/c mice on the expression profile of the survivin splice variants.

Flt3L Changes the Profile of Survivin Splice Variants in Bone Marrow

Gene expression analysis showed an increase in the overall transcription of survivin in the bone marrow of Flt3L-treated mice (n = 6) compared to PBS treated controls (n = 6) (Fig. 2A). This increase was not seen in spleen. Moreover, survivin gene expression in spleen was lower compared to the expression in the bone marrow (p = 0.002, Fig. 2A). Further analysis of different splice variants of survivin (Fig. 2C) was done on spleen and bone marrow samples. Flt3L treatment increased transcription of the short survivin40 variant in bone marrow, while no increase in the transcription of the full-length variant survivin140 could be detected (Fig. 2D). Since it was hard to design specific primers for the survivin121 transcript, a primer pair localized in the exon 1 and exon 2 was used. These primers were able to detect survivin140 and survivin121 transcripts, but not survivin40 transcript. The transcription of survivin140 and survivin121 variants was similar in Flt3L treated and in PBS treated mice. Western blot showed the dominating expression of survivin140 in spleen and survivin140 and survivin121 in bone marrow samples (Fig. 2B).

Survivin Expression in the Bone Marrow is Dependent on Flt3 Receptor Activity

We hypothesized that blockade of Flt3 receptor would affect survivin production in the bone marrow. Survivin was measured in arthritic mice treated with the Flt3 inhibitor SU11248 (sunitinib) in 3 independent experiments containing totally 24 sunitinib-treated mice and 25 control mice treated with citric acid. On day 28, a reduction of total survivin levels was observed in bone marrow lysates of sunitinib treated mice compared to the citric acid treated controls (pg/ml: 1796±388 vs. 2590±1107, p = 0.049, Fig. 3A). Sunitinib significantly reduced the number of survivin+ cells in mouse bone marrow (46.8±4.2% vs 59.3±6.8%, p = 0.0007), and the intensity of intracellular survivin staining (p = 0.002, Fig. 3C). This reduction of survivin expression could be seen mainly on Flt3− cells (p = 0.003, Fig. 3B).

Figure 3
Survivin levels in bone marrow and spleen of BALB/c AIA mice after Flt3 inhibition in vivo.

To assess whether sunitinib suppressed the expression of survivin in secondary lymphoid organs, we analyzed survivin levels in the spleen. The total survivin levels in the spleen were not reduced following sunitinib treatment (Fig. 3C), however a significant reduction of survivin expression in the MHCII+CD11chi dendritic cell population was identified (gMFI: 2684±607 vs 2179±207, p = 0.02). The number of survivin+ dendritic cells was also reduced with sunitinib treatment (58.1±5.3 vs 67.6±11.5%, p = 0.05, Fig. 1E). In spleen, Flt3 inhibition resulted in a reduction of CD11c+ cell population (p = 0.02, Table 2). The latter observation was in consistence with our previous findings on the inhibitory effect of sunitinib on the development of dendritic cells [44].

Table 2
Percentage of major leukocyte populations in bone marrow and spleen of sunitinib treated mice.

Survivin shRNA Reduces Flt3 Ligand Expression in the Spleen

Finally, we studied if Flt3/Flt3L system was changed by survivin inhibition. BALB/c mice received lentiviral constructs, containing a sequence coding for shRNA targeting survivin gene transcripts (n = 8), or the same lentiviral construct containing a non-targeting shRNA sequence (n = 9), by a single intra-articular injection. On day 28, the efficacy of survivin inhibition was confirmed on the transcription level by qPCR and on the protein level by flow cytometry. shRNA successfully reduced the total population of survivin+ cells by 35% (17.1±5.2 vs 26.4±3.4, p = 0.002), and the intensity of survivin expression in the spleen (gMFI: 582±95 vs 789±61, p<0.0001, Fig. 4A). The gene transcription of survivin in spleen tissue and bone marrow was not significantly changed (Fig. 4A and data not shown). Inhibition of survivin led to a reduction in Flt3L transcription in the spleen (0.85±0.12 vs 1.01±0.12, p = 0.04, Fig. 4B), and to a reduction of survivin+ MHCII+CD11chi dendritic cells (40.8±9.1 vs 52.5±3.4, p = 0.006, Fig. 4C).

Figure 4
In vivo downregulation of survivin using shRNA in BALB/c mice.


High levels of survivin and Flt3L in blood and synovial fluid of patients with rheumatoid arthritis are implied in the pathogenesis of joint inflammation [26], [27], [43]. Additionally, a tight clinical association observed between these parameters with respect to joint destruction and effect of anti-rheumatic treatment [28] prompted us to study common biological processes linking high expression of survivin and Flt3L in RA patients. The analysis of a cohort of RA patients with the established joint disease showed a clear association of high Flt3L levels with high levels of survivin in blood. Neither Flt3L nor survivin was a consequence of inflammation, measured by CRP, WBC count, serum amyloid A protein and IL6. Due to the cross-sectional nature of the study, one can see a clear difference in the frequency of radiologic erosions, which is a sign of severe disease, in the survivin positive group compared to the survivin negative group. The survivin-positive group contains higher proportion of patients treated with immunosuppressive anti-rheumatic drugs compared to the survivin-negative group. High levels of survivin characterize patients with therapy resistant cause of RA, suggesting that many patients responding to anti-rheumatic treatment convert from survivin-positive to survivin-negative. The results from the patient material show an association between Flt3L and survivin in RA, suggesting the existence of a mutual mechanism regulating levels of these proteins. Similarity of the groups with respect to disease duration, age, levels of C-reactive protein and white blood cell count further support this argument.

Our clinical observations were further extended in the experimental setting, where the requirement of Flt3/Flt3L signaling for expression of survivin in vivo was assessed. Survivin levels were increased following treatment with recombinant Flt3L and they were decreased with Flt3 receptor blockade. This proves that survivin production in the bone marrow is dependent on Flt3 signaling and makes Flt3L a major trigger of survivin transcription and expression in leukocytes. Interestingly, we showed the existence of a negative regulation loop where the low expression of survivin in spleen (induced by shRNA) resulted in the low levels of Flt3L in spleen. In the joints of RA patients, the elevated levels of Flt3L could originate from immune cells or fibroblast-like stromal cells in the synovium, by an inflammation caused shedding of the membrane bound form [45] or as a response to lack of antigen presenting cells. It is for example known that the human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency is associated with elevated levels of Flt3L in humans [37] and the same is true in mice following Flt3 inhibition [44], [46].

Flt3/Flt3L signaling is important for the maturation of hematopoietic cells [34]. Here, we show that Flt3L induces survivin production in the Flt3+ progenitors in bone marrow, and in dendritic MHCII+CD11chi cells in spleen. Survivin is increased after Flt3L treatment also in the Flt3− population in the bone marrow, suggesting that survivin is induced in Flt3 positive hematopoietic progenitors and remains upregulated after internalization of activated Flt3. Thus, survivin expression induced by Flt3L is associated with differentiation of cells rather than cell proliferation. Our findings are in agreement with previous reports on the induction of survivin production in CD34+ stem cells [20] prior to their differentiation.

Spleen is a maturation site for the peripheral dendritic cells and the process has recently been shown to be dependent on Flt3 expression [47], [48]. In our study, a reduction of the intracellular pool of survivin by inhibition of Flt3 led to a pronounced reduction of CD11c+ population of dendritic cells in the spleen. The obvious effect of Flt3L treatment/Flt3 inhibition on survivin levels in the MHCII+CD11chi population in the spleen further supports a strong relationship between the induction of survivin and DC development. We have previously shown that inhibition of Flt3 receptor reduces the DC population in spleen [44]. In RA patients, we have seen that high levels of extracellular survivin are associated with an increased number of circulating CD11c+ survivin expressing cells in blood [33]. Our present results suggest that modulation of survivin levels is an essential mechanism regulating homeostasis of peripheral dendritic cells.

Interestingly, studies on the Flt3L-induced expressions of different survivin-transcripts revealed an effect on the short survivin40-transcript in bone marrow. This variant lacks both the BIR-domain, essential for the interaction with caspases and for the anti-apoptotic effects of survivin [6], as well as the coiled coil-domain required for the formation of chromosomal passenger complex [7]. As survivin40 retains the N-terminal domain, it has been believed to bind other survivin variants [8], and to modulate their function by preventing homodimerization and facilitating interaction through the BIR- and coiled-coil domains. However, we could not detect survivin40 on protein level with western blot, as this has been shown earlier by another group [8] and might either indicate that this transcript is not translated or that the antibodies used are not able to detect the survivin40. The increase in survivin protein after Flt3L treatment can either be a result of an increased survivin40-expression or of a decrease in survivin140- or survivin121- turnover. In spleen, high survivin expression is seen within the MHCII+CD11chi population. This population represents a small part of the total amount of spleen cells and verification of survivin changes requires cell sorting prior to the RNA analyses.

In conclusion, our findings indicate that expression of survivin is a downstream event of Flt3L signaling, which serves as an essential mechanism supporting survival of hematopoietic cells during their differentiation and maturation of antigen presenting cells in bone marrow and spleen during arthritis.

Materials and Methods

Ethics Statement

The study involving human participants (S441-01) was approved by the Ethics Committee of Sahlgrenska University Hospital. All studies were conducted in compliance with the Declaration of Helsinki, and all patients gave written informed consent to participate in the study. All animal experiments (Protocol Numbers: 176-2008, 328-2008) were approved by the Ethical Committee on Animal Experiments in Gothenburg.


Synovial fluid and serum samples were obtained from 90 patients with RA attending the Rheumatology Clinic at Sahlgrenska University Hospital, Göteborg, Sweden, for acute joint effusion. All the patients met the diagnostic criteria for RA suggested by the American College of Rheumatology (ACR) [49]. The presence of bone erosions, defined as the loss of cortical definition at the joint, was recorded in proximal interphalangeal, metacarpophalangeal, carpus, wrist and metatarsophalangeal joints using recent radiographs of hands and feet. The presence of one erosion was sufficient to fulfill the requirement of an erosive disease. The presence of rheumatoid factor of any of the immunoglobulin isotypes was considered positive. Clinical characteristics of the patients are presented in Table 1. Blood from 104 healthy blood donors (male n = 16, female n = 88, mean age 52,4 years [range 18–67]) was used to calculate normal levels of survivin.

Collection and Preparation of Samples

Synovial fluid was obtained by arthrocentesis, aseptically aspirated and transmitted into sodium citrate (0.129 mol/l; pH 7.4) containing tubes. In most cases synovial fluid was obtained from knee joints. Synovial fluid samples were aliquoted and frozen in −70°C immediately after joint injections. Blood samples were centrifuged at 1000 rpm and serum was aliquoted and stored at -70°C.

Laboratory Measures of Disease Activity

Serum levels of C-reactive protein (CRP) were measured by standard nephelometry, with established normal range 0–5 mg/ml. Serum amyloid A protein (SAA) levels were detected by an ELISA (Biosource, Camarillo, CA). White blood cell (WBC) counts in blood and synovial fluid samples were obtained with a microcell counter F300 (Sysmex, Toa, Japan). Levels of IL-6 were measured as described previously [43], and rheumatoid factor (RF) were measured using standard laboratory techniques at Sahlgrenska University Hospital, Göteborg, Sweden.

Antigen Induced Arthritis using Methylated Bovine Serum Albumin (mBSA)

Female Balb/c mice were purchased from the Charles River Laboratory (Germany) and housed at the animal facility at the Department of Rheumatology & Inflammation Research, under standard conditions of temperature and light, and fed laboratory chow and water ad libitum. Mice (10 weeks old) were immunized with subcutaneous injection of mBSA (200 µg/mouse, Sigma-Aldrich) dissolved in PBS and mixed with IFA (Sigma-Aldrich) at day 0, followed by booster with mBSA (100 µg/mouse) at the tail root at day 7. Arthritis was induced by a single intra-articular injection of mBSA (30 µg/mouse) in PBS given at day 21. Mice were sacrificed on day 10 or 28. Samples of serum, bone marrow and spleen were collected for further analysis.

In Vivo Treatment with Flt3 Ligand and Flt3 Inhibitor

Arthritic mice were treated with a daily intraperitoneal injection of recombinant Flt3L, in the dose of 1.5µg/mouse, starting 4 days prior to first immunization. Flt3L was purchased from Creative BioMart (Shirley, NY) or purified from Sp2.0 hybridoma transfected with Flt3L gene [43]. Control mice were treated with PBS injection or a control cell line supernatant purified with the same procedure. Flt3 receptor was inhibited using sunitinib (SU11248, Pfizer). Treatment was given by gavage (day 7–28, 40 mg/kg mouse), and the control group was treated with the same volume of citrate buffer as previously described [44]. Specificity of sunitinib for Flt3 inhibition in our model has been previously shown [44].

Knockdown of Survivin using Lentiviral Vector

Lentiviral construct, encoding short hairpin (sh)RNA targeting survivin with the sequence CCGGCAAAGACTACCCGTCAGTCAACTCGAGTTGACTGACGGGTAGTCTTTGTTTTTG (TRCN0000054616, Sigma-Aldrich), were selected after in vitro evaluation. Lentiviral particles were given by a single intra-articular injection at immunization day 0 (107 transduction particles/knee, n = 8). The control group received the same amount of lentiviral particles with non-targeting scrambled sequence (n = 9). Downregulation of survivin was confirmed in bone marrow and spleen.

Cell Preparation and Cell Culture

Bone marrow cells from femur and tibia were flushed with PBS. Single cell suspensions from spleens were prepared by mechanically disruption of tissues through a 70 µm cell strainer. Erythrocytes were lysed in NH4Cl solution (0.83%, pH 7.29). Leukocyte pellet was resuspended in Iscoves complete medium (10% FBS, 4 mM L-glutamine, 50 µM β-mercaptoethanol, 50 µg/ml gentamycin sulphate ) or FACS buffer (PBS, 10% FBS, 0.09% NaN3, 0.5 mM EDTA). Freshly prepared mouse spleen cells were plated on 96-well plate at 2×105 cells/well in Iscoves complete medium. Supernatants were collected after 48 hours. Cell lysates were prepared by freezing the cells in −20°C overnight in 6 M urea.

Determination of Survivin and Flt3 Ligand Levels

Survivin and Flt3L protein levels in plasma, synovial fluid, supernatant and lysates were determined by ELISA (DYC647E, DY308, DY427, R&D Systems). Plasma and synovial fluid samples were tested in parallel ELISA plates, in dilution 1∶10, lysates 1∶3 and supernatant 1∶2 in PBS-BSA. The obtained absorbance values were compared to serial dilution of the recombinant proteins and presented as pg/mL. For intracellular staining of survivin, cells were permeabilized with Cytofix/Cytoperm™ Fixation/Permeabilization Solution Kit (BD Pharmingen™) and stained with anti-Survivin antibody (IC6472P, clone 91630, R&D Systems) or with isotype-matched IgG (IC002P, clone 11711, R&D systems).

Flow Cytometry

2×106 cells were plated on a 96-well plate, washed with FACS buffer and pelleted (4 min, 1200 rpm, 4°C). Cells were pre-incubated with Fc-block (BD Biosciences) for 30 minutes at 4°C and stained at 4°C for surface markers. Flt3 expression was detected using a biotinylated anti-mouse CD135 antibody (A2F10, Biolegend) followed by a Streptavidin-APC incubation (BD Biosciences). Then the following antibodies against surface markers were used; CD3-APC-eFluor® 780 (17A2), MHC-II-eFluor® 450 (M5/114.15.2), (eBioscience), Gr-1-PerCp (RB6-8C5), CD11b-PerCp (M1/70) (Biolegend), B220-FITC (RA3-6B2), CD11b-V450 (M1/70), CD11c-APC (HL3), B220-V500 (RA3-6B2) (BD Biosciences). Following staining, cells were washed, resuspended in FACS buffer, and collected in FACSCanto II equipped with FACSDiva software (BD Biosciences). Data were analyzed using the FlowJo software (Tree Star Inc., Ashland, OR). The gating of the cells was based on the isotype control values as well as fluorochrome minus one (FMO) settings when needed. Data is shown as percentage or geometric mean fluorescence intensity (gMFI), calculated in FlowJo and compared to data acquired on the same run.

Protein Preparation and Western Blotting

Total protein was prepared from cells and tissue by homogenization and sonication in the presence of protease inhibitors (Complete Mini, Roche Diagnostics GmbH, Mannheim, Germany). Protein concentrations were measured using the BCA Protein Assay kit (Pierce, Rockford, IL) according to the manufacturer’s protocol. Proteins were separated on SDS-PAGE 4–12% Bis-Tris gels (NuPAGE, Invitrogen), and transferred to PVDF membranes (NuPAGE, Invitrogen). Membranes were blocked with 5% non-fat milk and incubated with rabbit-anti-survivin antibodies (840471, R&D systems) at 4°C over night. Detection was performed with peroxidase conjugated anti-rabbit secondary antibody (NA934VS, GE Healthcare) and ECL Prime™ Western Blotting Reagents (GE Healthcare). Chemiluminescent signals were visualized by the Chemidoc equipment and Quantity-One software (BioRad Laboratories).

Gene Expression Analysis

Total RNA from spleen tissue and bone marrow cells was extracted using the RNeasy Mini Kit (Qiagen, Valencia, CA) according to the manufacturer’s instructions. Concentration and quality of the RNA was evaluated with NanoDrop spectrophotometer (Thermo Scientific, USA) and Experion (BioRad Laboratories). 400 ng RNA was used for cDNA synthesis using RT2 First Strand Kit (SABiosciences, Qiagen). Real-time amplification was performed with RT2 SYBR® Green qPCR Mastermix (SABioscences, Qiagen) using a ViiA™ 7 Real-Time PCR System (Applied Biosystems) according to the manufacturer’s instructions. A negative control (no template) reaction was also performed for each primer pair tested. A melting curve for each PCR was performed between 60 and 95°C to ensure that only a single product had been amplified. For Flt3 and Flt3L PCR Assays from SABiosciences (Qiagen) were used (sequences available upon request). Primers used for quantification of survivin expression were designed using Primer3 [50], uniqueness checked using the In silico PCR feature of the UCSC Genome Browser, and NetPrimer (PremierBiosoft) was used to check for secondary structures. Primers were ordered from Sigma-Aldrich, and are noted in table 3. Expression levels of the genes were normalized to the two reference genes, Gapdh and Ppia (TATAA, Sweden, sequences available upon request). Primer concentration used was 0.5 µM. The results were expressed as the fold change compared with the expression level in the control cells with the ddCq-method.

Table 3
Primers for real time PCR.

Statistical Analysis

Patient data was expressed as mean (±SD) and analyzed with GraphPad Prism, version 5.0 for Mac (GraphPad, San Diego, CA). The patient material was stratified by the level of survivin, and the difference between the groups regarding Flt3L levels, age, rheumatoid factor, disease duration, presence of erosions, CRP, and WBC count in blood and synovial fluid, was calculated using the Mann-Whitney test or Chi-Square test for categorical data. Experimental data was also analyzed using GraphPad Prism, expressed as mean with SD and significance regarding differences between groups was calculated using the Mann-Whitney test. The two-tailed tests were used and for the statistical evaluation of the results p values <0.05 was considered significant.

Funding Statement

This work was funded by grants from the Medical Society of Göteborg, the Swedish Association against Rheumatism, the King Gustaf V:s 80-year Foundation, the Commission of European Union (HEALTH-F2-2010-261460), the Swedish Research Council, IngaBritt and Arne Lundberg Foundation, Professor Nanna Swartz Foundation, Torsten Söderberg Foundation, AME Wolff Foundation, Rune and Ulla Amlövs Trust, the Swedish Research Agency for Innovation Systems (VINNOVA), the Swedish Foundation for Strategic Research, the Pharmacist Hedberg’s Foundation, Magnus Bergwall Foundation, the University of Göteborg, the Family Thölen and Kristlers Foundation, the Regional agreement on medical training and clinical research between the Western Götaland county council and the University of Göteborg (LUA/ALF). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.


1. Altieri DC (2010) Survivin and IAP proteins in cell-death mechanisms. Biochem J 430: 199–205 [PMC free article] [PubMed]
2. Noton EA, Colnaghi R, Tate S, Starck C, Carvalho A, et al. (2006) Molecular analysis of survivin isoforms: evidence that alternatively spliced variants do not play a role in mitosis. J Biol Chem 281: 1286–1295 [PubMed]
3. Xia F, Altieri DC (2006) Mitosis-independent survivin gene expression in vivo and regulation by p53. Cancer Res 66: 3392–3395 [PubMed]
4. Aoki Y, Feldman GM, Tosato G (2003) Inhibition of STAT3 signaling induces apoptosis and decreases survivin expression in primary effusion lymphoma. Blood 101: 1535–1542 [PubMed]
5. Kim PJ, Plescia J, Clevers H, Fearon ER, Altieri DC (2003) Survivin and molecular pathogenesis of colorectal cancer. Lancet 362: 205–209 [PubMed]
6. Takahashi R, Deveraux Q, Tamm I, Welsh K, Assa-Munt N, et al. (1998) A single BIR domain of XIAP sufficient for inhibiting caspases. J Biol Chem 273: 7787–7790 [PubMed]
7. Jeyaprakash AA, Klein UR, Lindner D, Ebert J, Nigg EA, et al. (2007) Structure of a Survivin-Borealin-INCENP core complex reveals how chromosomal passengers travel together. Cell 131: 271–285 [PubMed]
8. Conway EM, Pollefeyt S, Cornelissen J, DeBaere I, Steiner-Mosonyi M, et al. (2000) Three differentially expressed survivin cDNA variants encode proteins with distinct antiapoptotic functions. Blood 95: 1435–1442 [PubMed]
9. Kang BH, Xia F, Pop R, Dohi T, Socolovsky M, et al. (2011) Developmental Control of Apoptosis by the Immunophilin Aryl Hydrocarbon Receptor-interacting Protein (AIP) Involves Mitochondrial Import of the Survivin Protein. J Biol Chem 286: 16758–16767 [PMC free article] [PubMed]
10. Marusawa H, Matsuzawa S, Welsh K, Zou H, Armstrong R, et al. (2003) HBXIP functions as a cofactor of survivin in apoptosis suppression. EMBO J 22: 2729–2740 [PMC free article] [PubMed]
11. Leung CG, Xu Y, Mularski B, Liu H, Gurbuxani S, et al. (2007) Requirements for survivin in terminal differentiation of erythroid cells and maintenance of hematopoietic stem and progenitor cells. J Exp Med 204: 1603–1611 [PMC free article] [PubMed]
12. Li F, Cheng Q, Ling X, Stablewski A, Tang L, et al. (2010) Generation of a novel transgenic mouse model for bioluminescent monitoring of survivin gene activity in vivo at various pathophysiological processes: survivin expression overlaps with stem cell markers. Am J Pathol 176: 1629–1638 [PMC free article] [PubMed]
13. Xing Z, Conway EM, Kang C, Winoto A (2004) Essential role of survivin, an inhibitor of apoptosis protein, in T cell development, maturation, and homeostasis. J Exp Med 199: 69–80 [PMC free article] [PubMed]
14. Okada H, Bakal C, Shahinian A, Elia A, Wakeham A, et al. (2004) Survivin loss in thymocytes triggers p53-mediated growth arrest and p53-independent cell death. J Exp Med 199: 399–410 [PMC free article] [PubMed]
15. Song J, So T, Cheng M, Tang X, Croft M (2005) Sustained survivin expression from OX40 costimulatory signals drives T cell clonal expansion. Immunity 22: 621–631 [PubMed]
16. Kornacker M, Verneris MR, Kornacker B, Scheffold C, Negrin RS (2001) Survivin expression correlates with apoptosis resistance after lymphocyte activation and is found preferentially in memory T cells. Immunol Lett 76: 169–173 [PubMed]
17. Altznauer F, Martinelli S, Yousefi S, Thurig C, Schmid I, et al. (2004) Inflammation-associated cell cycle-independent block of apoptosis by survivin in terminally differentiated neutrophils. J Exp Med 199: 1343–1354 [PMC free article] [PubMed]
18. Fukuda S, Pelus LM (2001) Regulation of the inhibitor-of-apoptosis family member survivin in normal cord blood and bone marrow CD34(+) cells by hematopoietic growth factors: implication of survivin expression in normal hematopoiesis. Blood 98: 2091–2100 [PubMed]
19. Carter BZ, Milella M, Altieri DC, Andreeff M (2001) Cytokine-regulated expression of survivin in myeloid leukemia. Blood 97: 2784–2790 [PubMed]
20. Gu L, Chiang KY, Zhu N, Findley HW, Zhou M (2007) Contribution of STAT3 to the activation of survivin by GM-CSF in CD34+ cell lines. Exp Hematol 35: 957–966 [PubMed]
21. Williams NS, Gaynor RB, Scoggin S, Verma U, Gokaslan T, et al. (2003) Identification and validation of genes involved in the pathogenesis of colorectal cancer using cDNA microarrays and RNA interference. Clin Cancer Res 9: 931–946 [PubMed]
22. Kuttler F, Valnet-Rabier MB, Angonin R, Ferrand C, Deconinck E, et al. (2002) Relationship between expression of genes involved in cell cycle control and apoptosis in diffuse large B cell lymphoma: a preferential survivin-cyclin B link. Leukemia 16: 726–735 [PubMed]
23. Morgillo F, Woo JK, Kim ES, Hong WK, Lee HY (2006) Heterodimerization of insulin-like growth factor receptor/epidermal growth factor receptor and induction of survivin expression counteract the antitumor action of erlotinib. Cancer Res 66: 10100–10111 [PubMed]
24. Tran J, Master Z, Yu JL, Rak J, Dumont DJ, et al. (2002) A role for survivin in chemoresistance of endothelial cells mediated by VEGF. Proc Natl Acad Sci U S A 99: 4349–4354 [PMC free article] [PubMed]
25. Petrarca CR, Brunetto AT, Duval V, Brondani A, Carvalho GP, et al. (2011) Survivin as a predictive biomarker of complete pathologic response to neoadjuvant chemotherapy in patients with stage II and stage III breast cancer. Clin Breast Cancer 11: 129–134 [PubMed]
26. Svensson B, Hafstrom I, Forslind K, Albertsson K, Tarkowski A, et al. (2010) Increased expression of proto-oncogene survivin predicts Joint destruction and persistent disease activity in early rheumatoid arthritis. Ann Med 42: 45–54 [PubMed]
27. Bokarewa M, Lindblad S, Bokarew D, Tarkowski A (2005) Balance between survivin, a key member of the apoptosis inhibitor family, and its specific antibodies determines erosivity in rheumatoid arthritis. Arthritis Res Ther 7: R349–358 [PMC free article] [PubMed]
28. Isgren A, Forslind K, Erlandsson M, Axelsson C, Andersson S, et al. (2012) High survivin levels predict poor clinical response to infliximab treatment in patients with rheumatoid arthritis. Semin Arthritis Rheum 41: 652–657 [PubMed]
29. Ahn JK, Oh JM, Lee J, Bae EK, Ahn KS, et al. (2010) Increased extracellular survivin in the synovial fluid of rheumatoid arthritis patients: fibroblast-like synoviocytes as a potential source of extracellular survivin. Inflammation 33: 381–388 [PubMed]
30. Dharmapatni AA, Smith MD, Findlay DM, Holding CA, Evdokiou A, et al. (2009) Elevated expression of caspase-3 inhibitors, survivin and xIAP correlates with low levels of apoptosis in active rheumatoid synovium. Arthritis Res Ther 11: R13. [PMC free article] [PubMed]
31. Smith MD, Weedon H, Papangelis V, Walker J, Roberts-Thomson PJ, et al. (2010) Apoptosis in the rheumatoid arthritis synovial membrane: modulation by disease-modifying anti-rheumatic drug treatment. Rheumatology (Oxford) 49: 862–875 [PubMed]
32. Baran M, Mollers LN, Andersson S, Jonsson IM, Ekwall AK, et al. (2009) Survivin is an essential mediator of arthritis interacting with urokinase signalling. J Cell Mol Med 13: 3797–3808 [PubMed]
33. Mera S, Magnusson M, Tarkowski A, Bokarewa M (2008) Extracellular survivin up-regulates adhesion molecules on the surface of leukocytes changing their reactivity pattern. J Leukoc Biol 83: 149–155 [PubMed]
34. Boyer SW, Schroeder AV, Smith-Berdan S, Forsberg EC (2011) All hematopoietic cells develop from hematopoietic stem cells through Flk2/Flt3-positive progenitor cells. Cell Stem Cell 9: 64–73 [PMC free article] [PubMed]
35. McKenna HJ, Stocking KL, Miller RE, Brasel K, De Smedt T, et al. (2000) Mice lacking flt3 ligand have deficient hematopoiesis affecting hematopoietic progenitor cells, dendritic cells, and natural killer cells. Blood 95: 3489–3497 [PubMed]
36. Mackarehtschian K, Hardin JD, Moore KA, Boast S, Goff SP, et al. (1995) Targeted disruption of the flk2/flt3 gene leads to deficiencies in primitive hematopoietic progenitors. Immunity 3: 147–161 [PubMed]
37. Bigley V, Haniffa M, Doulatov S, Wang XN, Dickinson R, et al. (2011) The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency. J Exp Med 208: 227–234 [PMC free article] [PubMed]
38. Small D (2006) FLT3 mutations: biology and treatment. Hematology Am Soc Hematol Educ Program: 178–184. [PubMed]
39. Zhou J, Bi C, Janakakumara JV, Liu SC, Chng WJ, et al. (2009) Enhanced activation of STAT pathways and overexpression of survivin confer resistance to FLT3 inhibitors and could be therapeutic targets in AML. Blood 113: 4052–4062 [PubMed]
40. Fukuda S, Singh P, Moh A, Abe M, Conway EM, et al. (2009) Survivin mediates aberrant hematopoietic progenitor cell proliferation and acute leukemia in mice induced by internal tandem duplication of Flt3. Blood 114: 394–403 [PMC free article] [PubMed]
41. Chklovskaia E, Nissen C, Landmann L, Rahner C, Pfister O, et al. (2001) Cell-surface trafficking and release of flt3 ligand from T lymphocytes is induced by common cytokine receptor gamma-chain signaling and inhibited by cyclosporin A. Blood. 97: 1027–1034 [PubMed]
42. Deane KD, O’Donnell CI, Hueber W, Majka DS, Lazar AA, et al. (2010) The number of elevated cytokines and chemokines in preclinical seropositive rheumatoid arthritis predicts time to diagnosis in an age-dependent manner. Arthritis Rheum 62: 3161–3172 [PMC free article] [PubMed]
43. Dehlin M, Bokarewa M, Rottapel R, Foster SJ, Magnusson M, et al. (2008) Intra-articular fms-like tyrosine kinase 3 ligand expression is a driving force in induction and progression of arthritis. PLoS One 3: e3633. [PMC free article] [PubMed]
44. Dehlin M, Andersson S, Erlandsson M, Brisslert M, Bokarewa M (2011) Inhibition of fms-like tyrosine kinase 3 alleviates experimental arthritis by reducing formation of dendritic cells and antigen presentation. J Leukoc Biol 90: 811–817 [PubMed]
45. Horiuchi K, Morioka H, Takaishi H, Akiyama H, Blobel CP, et al. (2009) Ectodomain shedding of FLT3 ligand is mediated by TNF-alpha converting enzyme. J Immunol 182: 7408–7414 [PMC free article] [PubMed]
46. Tussiwand R, Onai N, Mazzucchelli L, Manz MG (2005) Inhibition of natural type I IFN-producing and dendritic cell development by a small molecule receptor tyrosine kinase inhibitor with Flt3 affinity. J Immunol 175: 3674–3680 [PubMed]
47. Karsunky H, Merad M, Cozzio A, Weissman IL, Manz MG (2003) Flt3 ligand regulates dendritic cell development from Flt3+ lymphoid and myeloid-committed progenitors to Flt3+ dendritic cells in vivo. J Exp Med 198: 305–313 [PMC free article] [PubMed]
48. Schmid MA, Kingston D, Boddupalli S, Manz MG (2010) Instructive cytokine signals in dendritic cell lineage commitment. Immunol Rev 234: 32–44 [PubMed]
49. Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, et al. (1988) The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum 31: 315–324 [PubMed]
50. Rozen S, Skaletsky H (2000) Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol 132: 365–386 [PubMed]

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