Decreased catalytic function with altered sumoylation of DNA topoisomerase I in the nuclei of scleroderma fibroblasts
© Zhou et al.; licensee BioMed Central Ltd. 2011
Received: 12 November 2010
Accepted: 9 August 2011
Published: 9 August 2011
Sumoylation is involved in nucleolus-nucleoplasm transport of DNA topoisomerase I (topo I), which may associate with changes of cellular and topo I functions. Skin fibroblasts of patients with systemic sclerosis (SSc) exhibit profibrotic cellular changes. The aims of this study were to examine the catalytic function and sumoylation of topo I in the nuclei of SSc fibroblasts, a major cell type involved in the fibrotic process.
Eleven pairs of fibroblast strains obtained from nonlesional skin biopsies of SSc patients and age/sex/ethnicity-matched normal controls were examined for catalytic function of nuclear topo I. Immunoprecipitation (IP)-Western blots were used to examine sumoylation of fibroblast topo I. Real-time quantitative RT-PCR was used to measure transcript levels of SUMO1 and COL1A2 in the fibroblasts.
Topo I in nuclear extracts of SSc fibroblasts generally showed a significantly lower efficiency than that of normal fibroblasts in relaxing equivalent amounts of supercoiled DNA. Increased sumoylation of topo I was clearly observed in 7 of 11 SSc fibroblast strains. Inhibition of SUMO1 with SUMO1 siRNA improved the catalytic efficiency of topo I in the SSc fibroblasts. In contrast, sumoylation of recombinant topo I proteins reduced their catalytic function.
The catalytic function of topo I was decreased in SSc fibroblasts, to which increased sumoylation of topo I may contribute.
Systemic sclerosis (SSc) is a human multi-system fibrotic disease with high morbidity and mortality but the etiology is largely unknown and the pathogenesis has yet to be clearly elucidated. Cutaneous fibrosis is a common clinical presentation and, based on the extent of skin involvement, SSc is classified into limited and diffuse cutaneous forms. The latter subset is characterized by more rapid progression of skin and visceral involvement, as well as poorer prognosis [1, 2]. Skin fibroblasts obtained from SSc patients have been found to be profibrotic and to synthesize excessive amounts of ECM proteins, which contribute to tissue fibrosis . It is believed that a possible defect in regulation of biological functions is present in SSc fibroblasts.
The majority of SSc patients (95%) have autoantibodies against various nuclear, nucleolar and cytoplasmic proteins, which include non-specific antinuclear antibodies (ANA) and a number of disease specific autoantibodies. Anti-DNA topoisomerase I (topo I) autoantibody is one of the disease-specific autoantibodies, and it occurs in 15 to 25% of patients [4–6]. A causal contribution of anti-topo I to the SSc phenotype is still unclear. There is no direct evidence indicating pathogenic roles of the antibodies. On the other hand, there is a strong association between anti-topo I autoantibody and the diffuse cutaneous form of SSc [5, 6]. Levels of anti-topo I autoantibodies have been reported to correlate with disease severity and activity in SSc, and the lack of these antibodies conveys a better outcome in SSc . In addition to anti-topo I, other SSc specific autoantibodies include those directed against centromeric proteins (ACA) that are associated with limited cutaneous disease, RNA polymerases (I, II and III) (ARA) and fibrillarin that are associated most often with diffuse skin involvement .
Topo I is a monomeric 100 kD nuclear protein that catalyzes the breaking and joining of DNA strands prior to transcription [9, 10], and is associated with transcription, DNA replication and chromatin condensation. Topo I translocates between the nucleolus and the nucleoplasm, but is enriched in the nucleolus where there is a high level of transcription and replication of the ribosomal DNA [9, 10]. Sumoylation is a post-translational modification, in which the substrates covalently attach the small ubiquitin-like modifier (SUMO) to lysine residues. Sumoylation is an important mechanism in regulating functions of target proteins and has been associated with the pathogenesis of autoimmune and inflammatory diseases, such as type I diabetes mellitus and rheumatoid arthritis [11, 12]. Sumoylation of topo I was reported to facilitate its movement between the nucleolus and the nucleoplasm [13, 14].
The goal of this study was to determine whether there is abnormal function, distribution and/or sumoylation of topo I in fibroblasts obtained from SSc patients that might associate with the presence of anti-nuclear and -nucleolar autoantibodies.
Material and methods
Dermal fibroblast cultures
Nonlesional skin biopsies (3 mm punch biopsies) were obtained from the upper arms of 11 SSc patients with disease of less than five years duration and 11 age- and gender-matched normal controls. All SSc patients fulfilled American College of Rheumatology criteria for SSc , and were positive for ANA. Two patients were positive for anti-topo I, four for ACA, two for ARA and one for anti-fibrillarin. Six patients had a diffused form of SSc, and five had limited SSc. Normal controls were undergoing dermatologic surgery and had no identified history of autoimmune diseases. All subjects provided informed consent and the study was approved by the Committee for the Protection of Human Subjects at The University of Texas Health Science Center at Houston.
Each skin sample was transported in Dulbecco's Modified Essential Media (DMEM) with 10% fetal calf serum (FCS) supplemented with penicillin and streptomycin for processing the same day. The tissue samples were washed in 70% ethanol, PBS and DMEM supplemented with 10% FCS. Cultured fibroblast cell strains were established by mincing tissues and placing them into 60 mm culture dishes secured by glass coverslips. The primary cultures were maintained in DMEM with 10% FCS and supplemented with penicillin and streptomycin. The early passage (< 5 passages) fibroblast strains were plated at a density of 2.5 × 105 cells in 35 mm plates and grown for assays accordingly.
Catalytic function of topo I in SSc fibroblasts
Nuclear proteins were extracted from equal amounts of the cultured fibroblast cells by using nuclear extract kits (Active Motif, Carlsbad, CA, USA). The Topoisomerase I Assay kit (TopoGEN Inc., Port Orange, FL, USA) was used for measuring the catalytic function of topo I. Briefly, supercoiled DNA substrate (0.25 μg) (TopoGen, Inc.) was reacted with nuclear proteins containing topo I at serial dilutions. After 30-minute incubations at 37°C, the reaction was terminated with stop buffer (5% Sarkosyl, 0.125% bromophenol blue and 25% glycerol). The reaction mixtures were loaded and electrophoretically separated on a 1% agarose gel, and then stained with ethidium bromide. The catalytic activity of topo I was determined by measuring the intensity of the supercoiled DNA bands after reactions with a serial dilution of topo I in the nuclear extract of fibroblasts. A Bio-imaging system (Gene Genius, Syngene, Frederick, MD, USA) was used to scan the bands in agarose gel. The Gene Snap software (Syngene) was used to quantify the intensity of the bands. A total of 11 pairs of SSc and control fibroblast strains were examined with this assay.
SSc and normal fibroblasts were grown in culture media as described above. After 7, 14 and 18 days, the cells were washed with PBS and fixed with 100% methanol at 4°C for two minutes. The cells were washed with PBS again, and incubated with serum from SSc patients (evenly pooled from four SSc patients) who had positive anti-topo I autoantibodies, or monoclonal antibodies of mouse anti-human topo I or mouse anti-human SUMO 1. This was followed by incubation with green fluorescent protein (GFP) tagged secondary antibodies (rabbit anti-human IgG antibodies and anti-mouse antibodies). Nuclei were visualized by counterstaining DNA with 4',6-diamidino-2-phenylindole (DAPI) (Vector Laboratory Inc., Burlingame, CA, USA). The images of fibroblasts with fluorescence labeled proteins were acquired using fluorescence microscopy (Nikon Eclipse TE2000-4., Melville, NY. USA).
The protein concentration of nuclear extracts from cultured fibroblasts was measured using the standard curve in a TECAN spectrophotometer (Tecan Group Ltd., Switzerland, 8708 Mannedorf). Equal amounts of protein from each sample were subjected to SDS-polyacrylamide gel electrophoresis. Resolved proteins were transferred onto nitrocellulose membranes and incubated with 1:1,000 diluted primary antibodies including mouse anti-human topo I (ImmunoVision, Springdale, AR, USA), anti-human SUMO1 (ABGENT, San Diego, CA, USA) and anti-collagen type I, individually. The secondary antibody was a peroxidase-conjugated anti-mouse IgG (Amersham, Piscataway, NJ, USA). Specific proteins were detected by chemiluminescence using an Enhanced Chemiluminescence (ECL) system (Amersham). The intensity of the bands was quantified using ImageQuant software (Molecular Dynamics, Sunnyvale, CA, USA).
Immunoprecipitation (IP) Western blotting
Approximately 3.5 × 107 fibroblast cells of each subject were harvested by trypsinizing the adherent cells and washed twice with 25 ml ice-cold PBS containing phosphatase inhibitors. Cell pellets were then gently resuspended by 2 ml hypotonic buffer and nuclear extracts prepared and measured for protein concentration by a spectrophotometer as described above. Equal amounts of protein (500 ug) from each sample were subjected to immunoprecipitation (IP) with mouse anti-SUMO-1(GMP1, Invitrogen, Carlsbad, CA, USA) using nuclear complex co-IP kit (Active Motif, Carlsbad, CA), and then subjected to SDS-polyacrylamide gel electrophoresis. Resolved proteins were transferred onto nitrocellulose membranes and incubated with primary antibodies of mouse anti-human topo I (ImmunoVision) diluted to 1:1,000. The secondary antibody was a horseradish peroxidase-conjugated anti-mouse IgG (eBioscience, San Diego, CA, USA). Specific proteins were detected by chemiluminescence using Supersignal West Pico stable peroxide solution (Thermo Scientific, Rockford, IL, USA). The intensity of the bands was quantified using ImageQuant software (Molecular Dynamics).
Inhibition of SUMO1 with siRNA transfection in fibroblasts
SUMO1 siRNAs were purchased from Invitrogen. Three SSc fibroblast strains that showed stronger sumoylation of topo I and weaker catalytic topo I function were used for transfection of SUMO1 siRNA. Briefly, the fibroblasts were grown at a density of 1.5 × 105 cells in 25-cm2 flasks until confluency. The DMEM culture medium in each culture flask was replaced with Opti_MEM 1 (Invitrogen) without FCS. The fibroblasts were transfected with SUMO siRNA using Lipofectamine RNAiMAX (Invitrogen) at a concentration of 15 ug/ml. A fluorescein-labeled non-silencing control siRNA (Qiagen, Valencia, CA, USA) was used for detection of transfection efficiency. After 24 hours, the culture medium was replaced with normal DMEM. The fibroblasts were examined for gene and protein expression, as well as topo I catalytic function after 48- or 72-hour transfection.
Sumoylation assay of topo I
A mixture containing recombinant topo I protein (TopoGEN Inc.), SUMO-1 protein (Active Motif), activating enzyme E1/conjugating enzyme E2 (Active Motif) and sumoylation buffer (15 mM ATP, 25 mM MgCl2 and 250 mM Tris-HCl) was incubated at 30°C for three hours. A mutant SUMO-1 protein (Active Motif) lacking sumoylation function was used as a negative control. The reaction was stopped with 5 mM EDTA and the recombinant human topo I with and without sumoylation were examined by Western blotting and topo I catalytic assays. The experiments were performed in triplicate.
Quantitative reverse-transcriptase-polymerase chain reaction (RT-PCR) for measurement of SUMO1 expression, as well as COL1A2 expression after SUMO1 siRNA transfection
The primers and probes of SUMO1, COL1A2, 18S and GAPDH were obtained from Applied Biosystems (Assays-on-Demand product line; Foster City, CA, USA). Total RNA from each sample was extracted from the cultured fibroblasts described above using a total RNA kit from OMEGA Biotek (Norcross, GA, USA) after treatment with DNase I. Complementary DNA (cDNA) was synthesized using SuperScript II reverse transcriptase (Invitrogen). Synthesized cDNAs were mixed with primer/probe of SUMO1 or COL1A2 in 2 × TaqMan universal PCR buffer and then assayed on an ABI Prism 7900 Sequence Detector System (Applied Biosystems). Each sample was assayed in triplicate. The data were analyzed with SDS2.2 (ABI). The amount of each transcript was normalized with 18S and GAPDH levels.
Measurement of autoantibodies
Patients' sera were tested for antinuclear antibodies by indirect immunofluorescence (IIF) using HEp-2 cells as antigen substrate and fluorescent goat anti-human IgG as a secondary antibody (Antibodies Inc., Davis, CA, USA). Anti-topo I antibodies were detected by passive immunodiffusion kits that employed calf thymus extracts as the antigen source (INOVA Diagnostics, San Diego, CA, USA), anti-RNA polymerase III antibodies were detected by ELISA using commercial kits (MBL, Nagoya, Japan). Anti-centromere antibodies were determined visually by their distinctive IIF patterns on HEp-2 cells. Anti-fibrillarin antibodies were detected by immunoprecipitation as described previously .
Reduced catalytic function of topo I in SSc fibroblasts
Altered localization of topo I in SSc fibroblasts
Altered sumoylation of topo I in SSc fibroblasts
Inhibition of SUMO1 in SSc fibroblasts increased catalytic function of topo I
Sumoylation of recombinant topo I decreased its catalytic function
A novel finding of these studies is the observation that human SSc fibroblasts have a decreased catalytic function of topo I. Human topo I plays an important role in DNA metabolic processes, such as transcription and replication, in which it releases topological stress in DNA chains [9, 10]. Topo I is generally localized in the nucleolus where a high level of transcription and replication of ribosomal DNA occurs. In response to inhibitory factors to topo I, such as camptothecin, UV irradiation and transcription inhibitors, topo I molecules were usually relocated from the nucleolus to the nucleoplasm due to mechanisms that are not clearly understood. [17–19]. Interestingly, SSc fibroblasts examined herein showed enhanced staining of topo I in the nucleoplasm, which suggests a relocation of topo I, and also supports a reduced function of topo I-associated DNA metabolic processes.
The cytoplasmic staining of topo I observed in some SSc fibroblasts was mainly detected by anti-topo I positive serum from SSc patients and was different from that found using anti-topo I monoclonal antibodies. Considering that the polyclonal human sera may contain mainly a variety of autoantibodies that have non-specific and antigen specific cross-reactions to cytoplasmic proteins is a possible explanation. With respect to possible cross-reactions, it is interesting that mitochondrial topo I has high amino acid homology to nuclear topo I. On the other hand, it is also possible that the cytoplasmic staining of topo I may represent ubiquitinated topo I molecules being processed by cytoplasmic proteasomes. It is worth noting that the topo I autoantigenic component, a 70 kD polypeptide, has been reported to be exported via ectocytosis in SSc fibroblasts , and anti-topo I autoantibodies of SSc patients have been shown to bind to SSc fibroblasts .
Sumoylation is an important post-translational modification. Previous studies have indicated that sumoylation of topo I facilitates translocation of topo I protein from the nucleolus to nucleoplasm [13, 14]. Increased sumoylation of topo I in certain SSc fibroblasts observed herein supports a potential mechanism that may drive the movement of topo I from the nucleolar compartments to the nucleoplasm where a degradation process may occur in proteasomes. To further investigate the association between altered sumoylation and topo I function in SSc fibroblasts, we inhibited the SUMO1 expression with sequence specific SUMO1 siRNA. Interestingly, SUMO1 inhibition was associated with a favorable improvement of the catalytic function of fibroblast topo I, suggesting that decreased topo I function observed in SSc fibroblasts may be a result of increased sumoylation. This possibility was consistent with the follow-up studies of sumoylation of recombinant human topo I that showed a reduction of catalytic function. However, sumoylation may not fully explain the reduction of topo I function in all SSc fibroblasts, especially in those fibroblasts which did not show the changes of sumoylation of topo I. These fibroblasts include two each from patients with ACA and with non-SSc specific ANAs. In contrast, the fibroblasts from all seven patients with either anti-topo I ARA or anti-fibrillarin showed hyper-sumoylation of topo I. All these three autoantibodies target primary nucleolar proteins. It is worth noting that the presence of any one of these autoantibodies in SSc patients is associated with the diffuse form of SSc and internal organ fibrosis , while the anti-centromere positive patients usually have a limited form of SSc with favorable clinical outcomes . Indeed, all SSc patients examined here with hypersumoylation of topo I presented as the diffuse form of SSc, except one, who was positive to ARA, but also clinically had lupus-like disease and anti-ribonucleoprotein (RNP) autoantibodies. All four SSc patients with unchanged sumoylation of topo I presented as the limited form of SSc at the time of skin biopsies. Therefore, sumoylaton of topo I in SSc fibroblasts appeared to be correlated with the status of skin fibrosis, which in some SSc patients changes over time. Recent studies of SSc genetics have indicated that different genetic susceptibility markers may determine the types of autoantibodies presenting in SSc patients [22, 23]. The characteristic patterns and specific genetic associations of SSc autoantibodies suggest that distinctive mechanisms contribute to different autoantibody-associated SSc subsets.
Topo I is an essential functional component of human cells. Previous reports indicated that knock out of the topo I gene was associated with death at an early stage of embryogenesis [24, 25]. Inactivation of the topo I gene in vitro was found to induce genomic instability with chromosomal aberrations . Inhibition of topo I function through camptothecin or topotecan (a camptothecin derivative) in human HEp-2 cells altered nuclear structure and function and targeted topo I for proteasomal degradation . Although, we do not know whether sumoylation of topo I in SSc fibroblasts contributes to any changes of specific antigen binding or autoantibody presentation in SSc patients, decreased catalytic function of topo I may alter the nuclear structure and function of the fibroblasts, which may influence other nuclear proteins including RNA pol III and fibrillarin. Of potential significance to our study, topotecan used therapeutically for cancer has been reported to induce SSc-like disease . Whether decreased catalytic function of topo I in SSc fibroblasts examined herein may result in any consequences associated with pathological changes in SSc is worthy of further investigations.
In summary, our studies of topo I in SSc fibroblasts indicate that topo I is functionally altered and is relocated to the nucleoplasm. In some fibroblasts, especially those obtained from skin biopsies of SSc patients who were positive for anti-topo I, anti-RNA polymerase III and anti-fibrillarin autoantibodies, these alterations were associated with increased sumoylation of topo I. In contrast, the fibroblasts of anti-centromere positive patients showed unchanged sumoylation of topo I. Inhibition of SUMO1 gene improved catalytic function of topo I in SSc fibroblasts. These observations may provide important insights into the nature of SSc fibroblasts that may contribute to pathological processes, induction of an autoimmune response to topo I, and/or disease development in SSc.
collagen type 1A2
Dulbecco's Modified Essential Media
fetal calf serum
green fluorescent protein
small ubiquitin-like modifier 1
- Topo I:
DNA topoisomerase I.
This study was supported by grants from the Department of the Army, Medical Research Acquisition Activity, grant number PR064803 to Zhou and the National Institutes of Health, grant number P50 AR054144 to Arnett.
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