Sirtuin-6 Preserves R-spondin-1 Expression and increases Resistance of intestinal Epithelium to injury in Mice
Sirtuin-6 (Sirt6) is a critical epigenetic regulator, but its function in the gut is unknown. Here, we studied the role of intestinal epithelial Sirt6 in colitis-associated intestinal epithelial injury. We found that Sirt6, which is predominantly expressed in epithelial cells in intestinal crypts, is decreased in colitis in both mice and humans. Colitis-derived inflammatory mediators including interferon-γ and reactive oxygen species strongly inhibited Sirt6 protein expression in young adult mouse colonocyte (YAMC) cells. The susceptibility of the cells to injurious insults was increased after knockdown of Sirt6 expression. In contrast, YAMC cells with Sirt6 overexpression exhibited more resistance to injurious insult. Furthermore, intestinal epithelial-specific Sirt6 (Sirt6IEC-KO) knockout mice exhibited greater susceptibility to dextran sulfate sodium (DSS)-induced colitis. RNA sequencing transcriptome analysis revealed that inflammatory mediators such as tumor necrosis factor (TNF)-α suppressed expression of R-spondin-1 (Rspo1, a critical growth factor for intestinal epithelial cells) in Sirt6-silenced YAMC cells in vitro. In addition, lipopolysaccharide was found to inhibit colonic Rspo1 expression in Sirt6IEC-KO mice but not their control littermates. Furthermore, Sirt6IEC-KO mice with DSS-induced colitis also exhibited in a significant decrease in Rspo1 expression in colons. In vitro, knockdown of Rspo1 attenuated the effect of ectopic expression of Sirt6 on protection of YAMC cells against cell death challenges. In conclusion, Sirt6 plays an important role in protecting intestinal epithelial cells against inflammatory injury in a mechanism associated with preserving Rspo1 levels in the cells.
Inflammatory bowel disease (IBD) is an idiopathic disorder affecting approximately 1.5 million Americans and others worldwide (1,2). The incidence of IBD seems to be increasing in many regions of the world (2,3). Crypt epithelial cell damage associated with colonic inflammation is a distinctive pathological hallmark of IBD (4). However, prevention and treatment of IBD remain a challenge, as the pathogenesis of the disease is unknown (5). Therefore, there is a strong rationale for exploring novel therapeutic targets that can be applied to strengthen epithelial cells against injurious insults for management of patients with IBD.
The sirtuins are a family of proteins that mainly function as nicotinamide adenine dinucleotide-dependent deacetylases (6). In mammals, there are seven sirtuin proteins, Sirt1 to Sirt7 (6). Among them, Sirt1 and Sirt6 are the most well-characterized, with functions associated with inflammation. Sirt1 is a cytosolic protein with nuclear translocation ability. Previous studies have shown that Sirt1 plays a role in regulation of inflammatory signals in the gut (7,8). In contrast, Sirt6 is a nuclear and chromatin-bound protein that emerges as an important epigenetic regulator controlling a number of metabolic and survival processes in cells (9). Recently, Kanfi et al. reported that mice overexpressing Sirt6 have increased longevity (10). Sirt6 knockout mice were found to die within one month after birth due to numerous abnormalities, including profound lymphopenia, loss of subcutaneous fat, lordokyphosis and severe metabolic defects (11). Evidence suggests that Sirt6 has both proinflammatory and antiinflammatory roles, depending on the context and cell type involved (9). Currently, the exact role of Sirt6 in intestinal epithelial cells remains unknown, and how it is affected during intestinal inflammation has not been explored.
In this study, our objectives were to evaluate the function of Sirt6 in intestinal epithelial cells and to determine the link between Sirt6 and colitis-associated intestinal epithelial injury using both in vivo and in vitro approaches. To this end, we first studied whether colitis development was associated with alterations in colonic Sirt6 expression in mice and humans. Then, using mice with intestinal epithelial cells deficient in the Sirt6 gene, we assessed the role of epithelial cell Sirt6 in dextran sulfate sodium (DSS)-induced intestinal injury. Furthermore, we confirmed the direct role of Sirt6 in intestinal epithelial cells in vitro in response to specific injurious insults using gain- and loss-of-function approaches. Finally, we explored downstream molecules mediating the protective effects of Sirt6 on intestinal epithelial cell damage induced by inflammation using gene silencing and RNA sequencing (RNA-seq) technology. We found that Sirt6 plays an important role in maintaining intestinal epithelial cell resistance to injurious insult via a mechanism involving R-spondin-1 (Rspo1) protein, a critical epithelial mitogen that stimulates intestinal crypt cell growth in inflammation. This study may open a new avenue for the development of therapeutic targets to maintain intestinal epithelial integrity in colitis in the future.
Materials and Methods
C57BL/6J mice, Villin-Cre transgenic mice and Sirt6 conditionally mutated (Sirt6Co/Co) mice were obtained from Jackson Laboratories (Bar Harbor, ME, USA). The Villin-Cre transgenic mice express Cre recombinase specifically in intestinal epithelium (12), whereas the Sirt6Co/Co mice possess loxP sites flanking exons 2–3 of the Sirt6 gene, as previously described (13). Intestinal epithelium-specific Sirt6 knockout mice (Sirt6Co/Co, Villin-Cre or Sirt6IEC-KO mice) were generated by intercrossingSirt6Co/Comice with Villin-Cre mice. Mouse genotypes were confirmed using polymerase chain reaction (PCR)-based protocols provided by Jackson Laboratories. Co-housed littermates carrying the LoxP-flanked alleles but not expressing Cre recombinase were used as controls for Sirt6IEC-KO mice. All mice were housed in a specific pathogen-free animal facility at the Stanley Manne Children’s Research Institute. Animal husbandry was provided by trained technicians and veterinarians. All the animal experimental procedures were conducted in accordance with the National Institutes of Health guidelines and were approved by the Institutional Animal Care and Use Committee of Northwestern University.
Induction of Colitis
Colitis was induced in mice using our previously published protocol (14). Briefly, mice (male, 8–10 wks old) fed a normal diet were given ad libitum access to 3.5% DSS (m.w. 36,000–50,000; MP Biomedicals, Solon, OH, USA) to drink for up to 1 wk. Control mice were given regular drinking water. During experiments, mice were weighed and stools were tested for occult blood on a daily basis. The disease activity index of clinical colitis was calculated using our well-established scoring system, as previously described (14). At the end of time points indicated, mice were euthanized by CO2 inhalation. Colons and blood were collected. Blood was processed for isolation of plasma by centrifugation at 1,000g for 10 min at 4°C. Plasma samples and colonic tissues were stored at −80°C until used. In some experiments, whole colon tissues were processed for histological analysis, as described below.
Histology and Microscopic Examination
The fresh colonic tissues were fixed in 10% neutral buffered formalin and processed for routine histology as described before (15). Hematoxylin and eosin stained sections (5 µm) were examined under a light microscope using a scoring system in a blinded manner (14). Briefly, three independent parameter scores were measured: severity of inflammation (0 to 3: none, slight, moderate, severe); depth of injury (0 to 3: none, mucosal, mucosal and submucosal, transmural); and crypt damage (0 to 4: none, basal one-third damaged, basal two-thirds damaged, only surface epithelium intact, entire crypt and epithelium lost). Then, percent involvement of the colon tissues was estimated. Each parameter score was multiplied by the percentage of tissue involved and totals were added together to obtain a histopathology score.
Deparaffinized slides were processed for immunofluorescent staining using a method modified from our previously published protocol (16). Specifically, deparaffinized slides were hydrated through series alcohol, incubated in 10 mM sodium citrate buffer (pH 6.0) at 95–100°C for 15 min for antigen retrieval, and gradually cooled to room temperature for 45 min. Then, slides were treated with 10% goat serum (Vector Labs, Burlingame, CA, USA) for 1 h at room temperature to block nonspecific binding sites in tissues. Thereafter, slides were stained with rabbit monoclonal antibody against Sirt6 (1:50, CST, Danvers, MA, USA) at 4°C overnight. The negative control slides were stained with naïve rabbit IgG (R&D, Minneapolis, MN, USA). After washing with phosphate buffered saline (PBS), slides were incubated with goat anti-rabbit IgG antibody labeled with Alexa Fluor 488 (1:250; Thermo Fisher Scientific, Waltham, MA, USA) for 90 min at 37°C in the dark. Finally, slides were washed with PBS and mounted using mounting solution containing DAPI (Vector Labs). Slides were examined under an upright fluorescence microscope (model MD R; Leica Microsystems) using appropriate filters. Images were acquired with a digital camera (Qlmaging Retiga 4000R), transferred to an Apple iMac computer, analyzed by Openlab image analysis software and assembled with Adobe Photoshop CS5 software.
All studies were performed in accordance with protocols approved by the Human Research Ethics Committee at Peking Union Medical College Hospital, Beijing, China. In this study, we recruited 15 patients with ulcerative colitis (UC) who required diagnostic colonoscopy and 17 healthy individuals undergoing colonoscopy for colorectal cancer screening at the Department of Gastroenterology at Peking Union Medical College Hospital. Under diagnostic colonoscopy procedures, two colonic biopsies were taken from sites showing active mucosal inflammation in the sigmoid colon in patients with UC. Comparable noninflamed sites of colonic mucosa in individuals who were not subsequently diagnosed with inflammatory injury in their colons were used as controls. Immediately after biopsy, a portion of samples was processed for routine histology and pathologic assessment, and the rest was immersed in RNAlater solution (Thermo Fisher Scientific) and stored at -80° for RNA extraction and quantitative reverse transcription (RT)-PCR.
Conditionally immortalized young adult mouse colonocyte (YAMC) and HT-29 cell lines were used. YAMC cells (passage 7–15) were used according to the protocol described by Whitehead et al. (17). Briefly, the cells were maintained in RPMI 1640 medium (Thermo Fisher Scientific) containing 5% heat-inactivated fetal bovine serum (Thermo Fisher Scientific), 5 U/mL mouse interferon-γ (IFN-γ; PeproTech, Rocky Hill, NJ, USA), 100 unit/mL penicillin, 100 µg/mL streptomycin (Thermo Fisher Scientific), 5 µg/mL insulin, 5 µg/mL transferrin and 5 ng/mL selenous acid (#354351; BD Biosciences, San Jose, CA, USA) at 33°C as permissive conditions in a water-saturated atmosphere incubator with 5% CO2 (18). Before experiments, the medium was replaced with one without IFN-γ and the cells were moved to 37°C (a nonpermissive temperature) for 24 h to allow them to differentiate. Then, cells were continuously cultured under nonpermissive conditions (IFN-γ-free and 37°C) for the duration of the experiment. HT-29 cells (a human intestinal epithelial cell line derived from colonic adenocarcinoma) were purchased from American Type Culture Collection (ATCC, Rockville, MD, USA) and cultured in a water-saturated atmosphere with 5% CO2 at 37°C. HT-29 cells (passages 20–35 after receipt from ATCC) were maintained in Dulbecco’s Modified Eagle Minimum Essential Medium (Thermo Fisher Scientific) containing 100 unit/mL penicillin, 100 µg/mL streptomycin and 10% heat-inactivated fetal bovine serum.
Preparation of Plasmid Constructs
A PCR fragment encoding the full open reading frame of Sirt6 was generated from mouse mRNA by RT-PCR and processed for DNA sequencing. The sequence data were compared against the National Center for Biotechnology Information database using BLAST. The mouse Sirt6 coding DNA sequence with no mutations and mismatches was inserted into XhoI and NheI sites of pIRES2-zsGreen1 expression plasmid using a standard molecular cloning protocol of our lab (19). The construct was sequenced to verify the correct orientation and sequence of the insert and was named pIRES2-zsGreen1-mSirt6.
YAMC cells were seeded onto 6-well plates at densities ranging from 1.5 to 3 × 105 cells per well and cultured with complete medium at 33°C overnight. On the second day, the cells were transfected with plasmid DNA (2 µg/well) or nucleic acids of siRNAs (50 nM) by using lipofectamine 2000 (Thermo Fisher Scientific) according to the manufacturer’s protocol. After 24 h, the medium was replaced with interferon-γ-free culture medium. Cells were then cultured at 37°C for an additional 24 h and processed for experiments or harvested for molecular biology studies. siRNAs of Sirt6, Rspo1 or their controls with unrelated sequences were purchased from Origene (Rockville, MD, USA).
Total RNA was isolated from tissues and cultured cells using Trizol solution (Thermo Fisher Scientific), as recommended by the manufacturer. To avoid contamination by DSS, which has been reported to inhibit the activity of both polymerase and reverse transcriptase (20), RNA extracted from colons of DSS-treated mice were further purified using a lithium chloride method previously described by Viennois et al. (20). The concentration of RNA was determined by absorbance at 260 nm, and the purity was checked by the 260:280 nm ratio (between 1.8 and 2.0) using an ultraviolet spectrophotometer.
Quantitative Real-Time RT-PCR
Sequence of qRT-PCR primers
Protein Extraction and Western Blot
Total proteins were isolated from tissues and cells using our previously described protocol (22). The protein concentrations were measured using a Pierce BCA protein assay kit (Thermo Fisher Scientific), following the protocol provided by the manufacturer. Then, proteins (10 µg/sample) were mixed with 2 × Laemmli sample buffer (Bio-Rad) and boiled for 5 min for denaturing. The denatured total proteins were resolved on 4–20% TGX precast sodium dodecyl sulfate polyacrylamide gel electrophoresis gels (Bio-Rad) and transferred onto polyvinylidene difluoride membranes (Bio-Rad) as previously described (22). The membranes containing sample proteins were used for immunodetection of Sirt6 or Rspo1 proteins. Briefly, blots preincubated with PBS containing 5% nonfat dry milk (Bio-Rad) were incubated with primary Ab against Sirt6 (1:1000, CST) or Rspo1 (1:200, LsBio, Seattle, WA, USA) with gentle shaking at 4°C overnight. After incubation, blots were washed three times with PBS containing 0.1% Tween 20, and then incubated with 5% nonfat dry milk containing 1/6000 diluted horseradish peroxide-conjugated goat anti-rabbit antibody (Jackson ImmunoResearch, West Grove, PA, USA) for 2 h at room temperature. After additional washing with PBS containing 0.1% Tween 20, immune complexes on the blot were developed with an ECL kit (Thermo Fisher Scientific) and visualized by Bio-Rad ChemiDoc MP System (Bio-Rad). Images were analyzed with Imaging Lab 4.1 software (Bio-Rad). For detection of housekeeping gene expression, blots were stripped and reprobed with a horseradish peroxide-conjugated mouse mAb against β-actin (1:50,000, clone AC-15, Sigma-Aldrich, St. Louis, MO, USA) followed by development with the ECL kit, scanning and analyzing as described above.
induction of Cell Death and Assessment of Cell Viability
It has been shown that development of IBD is associated with numerous types of intestinal epithelial cell death, such as apoptosis, necroptosis and DNA damage related to cell injury (23,24). Thus, we executed models of cell death induced by various cell death inducers: methyl methanesulfonate (MMS, a DNA-damaging reagent), H2O2 (oxidative damage), TNF-α plus cycloheximide (apoptotic challenge) and TNF-α plus z-VAD-fmk (necroptosis stimulation) using YAMC cells. Briefly, cells were subjected to transfection with siSirt6/siControl, pSirt6/pVector or siRspo1/siControl using the protocol described above. After 24 h, the transfected cells were reseeded in 96-well, white-walled, clear-bottomed plates at 1.5 × 104 density per well and cultured with IFN-γ-free medium at 37°C for 24 h, followed by treatment with adequate cell-death-inducer cocktails: MMS (2 mM), H2O2 (400 µM), TNF-α (20 ng/mL) + cycloheximide (5 µg/mL) and TNF-α (20 ng/mL) + z-VAD-fmk (20 µM). All cell-death-inducer cocktails were prepared in IFN-γ-free medium. For MMS treatment, cells were challenged with MMS for 1 h, followed by culture with MMS-free medium for an additional 24 h. For other treatment regimens, cells were treated with adequate cell-death-inducer cocktails for 24 h. At the end of treatments, cell viability was assessed using CellTiter-Glo Assay Kit (Promega, Madison, WI, USA), following the manufacturer’s protocol.
Total RNA was extracted from YAMC cells using RNeasy Micro Kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions. RNA integrity and quantity were assessed using Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA). PolyA-enriched RNA was purified from total RNA using paramagnetic oligo-dT beads, fragmented and used for constructing cDNA libraries with NEBNext Ultra RNA Library Prep Kit for Illumina following the manufacturer’s protocol (NEB, Ipswich, MA, USA). Libraries were amplified, followed by removing primers prior to sequencing. These libraries were sequenced on Illumina HiSeq 2500 generating 100 bp paired end reads (Peking Jabrehoo Med Tech Co., Beijing, China). After sequencing, raw reads were cleaned by removing adaptor sequences, empty reads and low-quality sequences. The reads that passed filtering were aligned to reference sequences of the mouse transcriptome (Ensembl release 75) using the Bowtie version 1.0.1 alignment tool. Read counts were normalized using edgeR, and reads per kilobase per million mapped reads values were calculated as the number of counted reads per 1000 mapped and counted bases per geometric mean of normalized read counts per million. Fold change ratio between the two groups was calculated by reads per kilobase per million mapped reads, and an absolute value of log2 ratio ≥ 0.415 was used as a threshold to judge the difference of gene expression. Heatmaps of differentially expressed genes were generated by the GENE-E visualization and analysis platform. Gene ontology term analysis was performed using Gene Set Enrichment Analysis software (25,26) and visualized by the REViGO tool (27).
Measurement of Myeloperoxidase Activity
Briefly, colon tissues were homogenized in 250 µL myeloperoxidase (MPO) assay buffer and centrifuged at 13000g for 10 min at 4°C to remove insoluble material. The supernatants were processed for measurement of MPO activity using an MPO Colorimetric Activity Assay Kit (Sigma-Aldrich), following the manufacturer’s protocol. MPO activity was normalized by the protein loading in each sample and reported as unit/gm protein.
Cytokine and Chemokine Measurements
Plasma cytokine/chemokine measurements were made using Meso Scale Diagnostics (MSD, Gaithersburg, MD, USA) multiplex array technology. Briefly, cytokines and chemokines were measured using a mouse-specific 96-well multispot plate of V-PLEX Plus Proinflammatory Panel 1 Kit (MSD), which included five markers: IL-1β, IL-6, IL-10, TNF-α and KC. The assay was performed according to the manufacturer’s instructions. A total volume of 50 µL diluted (1:2.5) sample was used in each well. The assay was run in duplicate for each sample. Plate readings were performed on a SECTOR Imager 2400 instrument (MSD). Raw data were analyzed using MSD Discovery Workbench software (version 4.0). The curves were fitted using a 4PL fit with 1/y2 weighting according to the manufacturer’s instructions, and concentrations were determined from the standard curves.
All experiments were performed at least twice. Statistical analysis was performed with Graphpad Prism 6 software. Reported data are the mean ± standard error of the mean, and statistical significance was assessed with either the Student t test or one-way analysis of variance followed by Fisher’s least significant difference post hoc test. P < 0.05 was considered significant.
Web Deposition of Data
Data in this study have been deposited in the Gene Expression Omnibus site (https://doi.org/www.ncbi.nlm.nih.gov/geo), accession number GSE89620.
Sirt6 is Highly Expressed in Mouse Intestines and Predominantly Localized to Intestinal Epithelial Cells in the Crypt Compartment
Colitis is Associated with Downregulation of Colonic Sirt6 Expression in Mice and Humans
IFN-γ Attenuates Sirt6 Protein Expression in Colonic Epithelial Cells
Sirt6 Plays a Role in Maintaining the Resistance of Intestinal Epithelial Cells to Cell Death Challenges
In addition, when Sirt6 was overexpressed by transfection with pIRES2-zsGreen1-mSirt6, an expression plasmid construct containing the full open reading frame of mouse Sirt6 cDNA (Figure 4C), YAMC cells were markedly resistant to cell death induced by DNA damage, superoxides, apoptotic stimulation and necroptosis signals (Figure 4D). Taken together, our data suggest that Sirt6 renders intestinal epithelial cells resistant to cell death insults.
Intestinal Epithelial Cell-specific Knockout of Sirt6 increases Susceptibility to DSS-induced Colitis in Mice
In this study, we first investigated the physiological impact of downregulation of Sirt6 expression in the intestinal epithelium of mice using a tissue-specific knockout approach. Sirt6Co/Comice (a mouse line harboring a loxP-flanked Sirt6 allele ) were crossed with Vil-Cre mice to establish the Sirt6Co/Co; Vil-Cre+/− (ie, Sirt6IEC-KO) mouse line. Genotyping analysis of tail biopsy samples revealed that Sirt6IEC-KO mice were characterized as heterozygous for Vil-Cre transgene and homozygous for floxed Sirt6 allele (Supplementary Figure S2A). Using Western blot, we found that Sirt6IEC-KO mice lacked Sirt6 protein expression in an intestinal tissue-specific manner (Supplementary Figure S2B). The Sirt6IEC-KO mice were fertile and healthy. Their body weights were indistinguishable from those of their control littermates (Supplementary Figure S2C). Histological examination showed that Sirt6IEC-KO mice did not display any phenotypical abnormalities in their intestines (Supplementary Figure S2D). Together, the data suggest that Sirt6 expression is not essential for orchestrating morphogenesis and maintaining integrity in intestinal epithelial cells under a normal physiological state.
Sirt6 Plays an Important Role in Sustaining R-spondin-1 Expression in Intestinal Epithelial Cells under Inflammation
In the present study, we investigated the role of intestinal epithelial Sirt6 in gut injury and inflammation. Our findings show that Sirt6 is expressed by intestinal epithelial cells, predominantly in crypt cells. We demonstrated that colitis is associated with decreased levels of intestinal Sirt6. Inflammatory mediators, including IFN-γ and reactive oxygen species, directly inhibited Sirt6 expression in intestinal epithelial cells. Mice deficient in Sirt6 in intestinal epithelial cells are prone to DSS-induced colonic mucosal injury, suggesting that inflammation-induced impairment of Sirt6 expression in intestines contributes to the pathogenesis of colitis. Furthermore, we found for the first time that Sirt6 is critical in maintaining levels of Rspo1 in intestinal epithelial cells under inflammatory conditions. Since Rspo1 is an important trophic factor for intestinal epithelial cell growth (35,36), our data strongly suggest the notion that Sirt6 plays a central role in protecting against colitis-associated intestinal epithelial cell injury via preservation of Rspo1.
Emerging studies have shown that Sirt6 is a key regulator of genome stability, glucose homeostasis, metabolism and inflammation (9). It governs diverse cellular functions, such as transcription, telomere integrity and DNA repair (9). Mouse pups with whole-body Sirt6 deficiency exhibit postnatal growth retardation and eventually die at about 4 wks after birth, highlighting the importance of Sirt6 for growth and survival (11). Furthermore, a distinctive phenotype of colitis with prominent epithelial sloughing was previously found in weaning Sirt6-null mice (11), suggesting that Sirt6 is required in remodeling tissue architecture as intestinal mucosa grow and mature during postnatal development. However, we did not find a significant effect of intestinal epithelial deletion of Sirt6 on intestinal morphology in mice, implying that Sirt6 in intestinal epithelial cells is not an essential protein for intestinal development and homeostasis in normal physiological states.
Evidence suggests that Sirt6 expression is inhibited in numerous pathological conditions associated with inflammation. For example, decreased Sirt6 expression in fetal membranes occurs in preterm labor (37). Balestrieri et al. found that Sirt6 protein expression is downregulated in diabetic atherosclerotic lesions (38). A previous study identified that H2O2 treatment results in marked reduction of Sirt6 in endothelial cells (39). Consistent with these previous findings, our data indicate that mucosal Sirt6 protein expression is decreased in colitis. Furthermore, we found that not only H2O2, but also IFN-γ is a strong inhibitor of Sirt6 expression in intestinal epithelial cells. In addition, our study shows that deletion of Sirt6 in intestinal epithelial cells exacerbates DSS-induced colitis, strongly supporting the notion that inflammation-induced downregulation of intestinal epithelial Sirt6 directly impacts intestinal mucosal integrity during colitis development.
Sirt6 is an enzyme that has ADP-ribosyltransferase activity (40,41) and histone deacetylase activity (42, 43, 44, 45). It influences chromatin structure and gene expression. Particularly, previous studies demonstrated that Sirt6 functions at chromatin to attenuate NF-κB-dependent transcription (46). On the other hand, Sirt6 was found to positively regulate TNF-α production at the post-transcriptional level in vitro (47). Thus, the effect of downregulation of Sirt6 in regulating the inflammatory response may be complicated in vivo. Indeed, our data show that knockout of Sirt6 in intestinal epithelial cells did not influence the cytokine profile in colitis (Supplementary Figure S4), while the Sirt6IEC-KO mice were more susceptible to DSS-induced colitis than their control littermates. This observation suggests that Sirt6 protects intestinal epithelial cells against inflammatory injury through a cytokine-independent mechanism. Using global RNA expression data obtained by RNA-seq transcriptome analysis, we found that knockdown of Sirt6 markedly alters gene expression in naïve intestinal epithelial cells. Furthermore, we found that the response to TNF-α challenge in Sirt6-silenced IECs differs from that in IECs with intact Sirt6 expression. Together, it appears that Sirt6 plays an important role in maintaining the homeostasis of gene expression in intestinal epithelial cells in both the normal physiological state and inflammation.
In addition, our finding that knocking down Sirt6 expression in intestinal epithelial cells decreases Rspo1 expression in inflammation is intriguing. Rspo1 is a trophic factor for intestinal epithelial cells (35,36). Previously, Zhao et al. (35) reported that Rspo1 is predominantly expressed in crypt Paneth cells and differentiated enterocytes along the intestinal villus epithelium, where Sirt6 is also expressed in the mouse gut. Wnt/β-catenin signaling plays an essential role in regulating gastrointestinal homeostasis. Rspo1 has been shown to stimulate intestinal epithelial cell proliferation and protect epithelial cells from constant exposure to toxins, inflammatory cytokines and reactive oxygen radicals by increasing β-catenin nuclear localization and subsequently turning on Wnt downstream target gene activation (35,48,49). Administration of recombinant Rspo1 was reported to strongly ameliorate colitis symptoms in several experimental colitis mouse models (35,48,50), suggesting that it has a protective role in the gut under inflammation. We show here that a decrease in Rspo1 expression is associated with an increase in sensitivity to various death inducers in Sirt6 knockdown cells. Sirt6IEC-KO mice exhibit a lack of ability to maintain Rspo1 expression in their intestines under inflammation, implying that an increase in susceptibility to inflammatory intestinal injury in Sirt6IEC-KO mice may be due to a lack of the protective factor Rspo1. Furthermore, we found that Rspo1 mediates the role of Sirt6 in the protection of intestinal epithelial cells against cell injury. Together, our data in combination with previous findings support the notion that the Sirt6-Rspo1 signal axis plays a role in the protection of intestinal epithelial cells against inflammatory injury.
In summary, our study reveals that expression of Sirt6 in intestinal epithelial cells is necessary for protection of the intestinal mucosa against colitis. We identified that intestinal inflammation causes downregulation of Sirt6 in the gut, which leads to increased susceptibility of intestinal epithelial cells to injury. In addition, we found Rspo1 to be regulated by Sirt6 in intestinal epithelial cells. Our data suggest that inflammation-induced downregulation of Sirt6 contributes to decreased Rspo1 expression in intestinal epithelial cells, thus leading to an increased susceptibility of the intestinal mucosa to injury under inflammatory conditions. These findings provide novel insights into both the pathogenesis of colitis and potential therapeutic targets for intestinal injury and inflammation.
The authors declare that they have no competing interests as defined by Molecular Medicine or other interests that might be perceived to influence the results and discussion reported in this paper.
This study was supported by National Institute of Diabetes and Digestive and Kidney Diseases grant R01DK064240 (XDT), National Institute of General Medical Sciences grant R01GM117628 (XDT), Eunice Kennedy Shriver National Institute of Child Health and Human Development grant R01HD060876 (IDP), US Department of Veterans Affairs Merit Award I01BX001690 (XDT), the Dorothy M and Edward E Burwell Professorship (XDT) and Ministry of Health of the People’s Republic of China Special Project grant 201002020 (JQ). The sponsors had no role in study design or collection, analysis or interpretation of the data.
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