The mechanism of chemotherapy-induced gastrointestinal (GI) syndrome (CIGIS) is still controversial, and it is unclear whether chemotherapy induces intestinal stem cell (ISC) apoptosis. β-Arrestins are regulators and mediators of G protein-coupled receptor signaling in cell apoptosis, division and growth. In this study, we aimed to investigate whether chemotherapy induces ISC apoptosis to contribute to mucositis in CIGIS and whether β-arrestin1 (β-arr1) is involved in this apoptosis. Different chemotherapeutic agents were used to generate a CIGIS model. Lgr5-EGFP-IRES-creERT2+/− knock-in mice were used as a CIGIS model to investigate ISC apoptosis. β-arr1 knockout mice were used to determine whether β-arr1 is involved in the apoptosis in CIGIS. Intestinal histology was performed, the ISC apoptosis was analyzed and the mucosal barrier was examined. The effects of β-arr1 in apoptosis were investigated in the samples from humans and mice as well as in cell lines. Here, we demonstrate that chemotherapy induced intestinal mucositis by promoting crypt cell apoptosis, especially in Lgr5+ stem cells and Paneth cells but not in goblet cells, epithelial cells or vascular endothelial cells. Furthermore, β-arr1 deficiency exacerbated the Lgr5+ stem cell apoptosis, but not Paneth cell apoptosis, in CIGIS. In addition, the data showed that β-arr1 reduced the chemotherapy-induced Lgr5+ stem cell apoptosis by inhibiting endoplasmic reticulum stress-mediated mitochondrial apoptotic signaling. Our study indicates that β-arr1 inhibits chemotherapy-induced ISC apoptosis to alleviate intestinal mucositis in CIGIS.
Gastrointestinal (GI) toxicity is the main limitation in chemotherapy and results in damage to the small intestine and complications that are known as GI syndrome.1 However, the cellular targets and underlying mechanisms of chemotherapy-induced GI syndrome (CIGIS) are still very controversial. Some believe that damage to the endothelial cells induces mucosal ischemia, which results in epithelial dysfunction.2 Others proposed that the decrease in goblet cells alters mucin secretion and intestinal flora, which leads to intestinal mucositis.3 Different chemotherapy agents have been shown to target particular cell positions within the crypt hierarchy. Recent studies demonstrated that progenitor cell apoptosis was induced by chemotherapeutic drugs.4 A study by our group found that chemotherapy increased intestinal crypt cell apoptosis and inhibited proliferation.5 However, no studies have explained the relationship between intestinal stem cells (ISCs) and CIGIS. Increasing evidence has indicated that the crypt base columnar (CBC) cells that express leucine-rich repeat-containing G protein-coupled receptor 5 (Lgr5) are ISCs.6, 7 Nevertheless, because these long slender CBC cells are in close proximity to Paneth cells, which are much more visually prominent, and because there were no unique markers for CBC cells until the Lgr5 knock-in mouse model was developed,8 it is still unclear whether the CBC cells are involved in CIGIS. In this study, we found that Lgr5+ CBC cells undergo apoptosis after chemotherapy.
Several signaling pathways have been shown to regulate chemotherapy-induced apoptosis in the crypt cells, including the p53 pathway, which was identified in our recent study.5 β-arrestin1 (β-arr1) was originally classified as a G protein-coupled receptor (GPCR) but was later shown to have much broader and more versatile roles. β-arr1 is involved in maintaining cellular homeostasis9 and has an important role in the pathogenesis of various diseases, including sepsis,10 cerebral ischemia11 and asthma.12 Based on a previous study, β-arr1 facilitated Akt-mediated activation of MDM2 (human murine double minute 2, the E3 ligase for p53) and also promoted MDM2 binding to, and degradation of, p53 by acting as a molecular scaffold.13 Based on these results, we hypothesized that inhibition of β-arr1 may aggravate chemotherapy-induced apoptosis via activation of p53. The activation of p53 then induces p53-dependent endoplasmic reticulum (ER) stress, which promotes cell apoptosis and inhibits the stemness of stem cells.14 Moreover, a recent report suggested that induction of ER stress decreases stem cells via differentiation, resulting in a loss of stem cells in the intestinal crypts.15 Here, our results show that a decrease in stem cells after chemotherapy may be linked to ER stress.
In this study, β-arr1 reduced the chemotherapy-induced Lgr5+ stem cell apoptosis by inhibiting ER stress-mediated mitochondrial apoptotic signaling to alleviate intestinal mucositis in CIGIS.
Chemotherapy-induced intestinal injury and mucositis
Our study showed that intestinal crypt cells underwent apoptosis in chemotherapy patients with CIGIS but not in non-chemotherapy patients (Figure 1). To elucidate the pathogenesis of crypt apoptosis, we established animal models with intraperitoneal (i.p.) injections of 5-fluorouracil (5-FU) at a dose of 75 mg/kg/day every 24 h for 1, 3, 5 and 7 days. CIGIS worsened with increasing total dose of 5-FU. Histological evaluation revealed that 5-FU treatment resulted in significant intestinal mucosal injury (Figure 2a). Meanwhile, a mild switch in the apoptotic area was observed with prolonged 5-FU treatment (Figure 2a). The dynamic changes in apoptotic cells should be addressed in further studies. The small intestinal villus height decreased, and crypt depth was reduced after 5-FU treatment for 5 days compared with vehicle-treated mice (Figures 2b and c). Following 5-FU treatment, the apoptosis in the intestinal mucosa gradually increased (Figures 2a and d), and the proliferation of the intestinal crypt cells was gradually inhibited (Figures 2a and e). As a result, the intestinal permeability was significantly higher, and bacterial translocation evidently increased (Figure 2f), which are the characteristics of intestinal mucositis.16 Furthermore, we observed that apoptosis was centered in the bottom of the crypts, especially positions 3–6 of the crypts, where the apoptotic index ranged from 25 to 50% (Figures 2g and h).
Chemotherapy-induced ISC and Paneth cell apoptosis
To investigate apoptotic target cells in CIGIS, TUNEL staining was used to identify apoptosis, and several distinct cell markers, including periodic acid–Schiff (PAS), cytokeratin, CD34 and MMP7, were used to assess different types of cells in the crypts. Double immunostaining showed that apoptosis of goblet cells (PSA positive), epithelial cells (cytokeratin positive) and vascular endothelial cells (CD34 positive) was rarely observed after chemotherapy (Figures 3a and d). However, apoptosis of Paneth cells (MMP7 positive) was induced (Figure 3d). After 5-FU treatment for 5 days, an average of 21 apoptotic Paneth cells in every 100 crypts was observed, which was substantially increased compared with 5-FU treatment for 0 days (Figure 3d). To examine the response of stem cells following 5-FU treatment, Lgr5 knock-in mice were used to evaluate ISC apoptosis. Lineage tracing indicated that Lgr5-expressing cells at the base of the crypt can function as stem cells for all four epithelial lineages.8 Our data revealed that Lgr5+ stem cells were notably reduced after 5-FU treatment for 5 days (Figure 3e). Double immunostaining confirmed that 5-FU-induced apoptosis led to a reduction in Lgr5+ stem cells (Figures 3f and g). These results show that 5-FU induces marked apoptosis in both Paneth cells and Lgr5+ stem cells.
To elucidate the effects of chemotherapy in CIGIS, other two classical chemotherapeutic agents (cisplatin (Cis) and doxorubicin (Dox)) were used in the study. The results showed that, similar to 5-FU, apoptosis was also observed in the bottom of the crypts after Cis and Dox treatment for 5 days, and apoptosis was predominantly observed in Lgr5+ stem cells (Figures 3h and i). The apoptotic index confirmed that apoptosis of Lgr5+ stem cells was substantially increased in chemotherapy-induced CIGIS (Figure 3j). Taken together, the results strongly suggest that apoptosis of Lgr5+ stem cell contributes to CIGIS.
β-arr1 deficiency aggravated chemotherapy-induced intestinal crypt cells apoptosis
After chemotherapy, β-arr1 in the intestinal mucosa was significantly downregulated in patients (Figure 4a). Thus, to verify the role of β-arr1 in CIGIS, β-arr1 wild-type (WT) and knockout (KO) mice were used. Intestinal mucosal β-arr1 expression was significantly reduced by 5-FU treatment, and β-arr1 deficiency evidently enhanced cleaved caspase-3 expression compared with WT mice (Figures 4b and c). Furthermore, TUNEL staining and immunofluorescence staining of active caspase-3 confirmed that the apoptosis in β-arr1 KO mice was notably increased following 5-FU treatment (Figures 4d–f). The apoptosis was principally located at the bottom of the crypts, especially positions 3–5 of the crypts, and β-arr1 deficiency markedly increased the apoptosis in positions 2–4 of the crypts (Figure 4g). In addition, β-arr1 deficiency aggravated the inhibition of crypt cell proliferation, and the proliferative index was lower in the β-arr1 KO mice than the β-arr1 WT mice (Figures 4h and i).
β-arr1 deficiency increased chemotherapy-induced ISC apoptosis
To confirm that post-chemotherapy intestinal crypt apoptosis occurs in the stem cells, we crossed β-arr1+/− mice to Lgr5-cre+/− mice, and obtained β-arr1+/+/Lgr5-cre+/− mice and β-arr1−/−/Lgr5-cre+/− mice. TUNEL and EGFP (Lgr5) co-staining showed that apoptosis in Lgr5+ stem cells was induced, and the apoptosis of Lgr5+ stem cells was notably increased in β-arr1−/−/Lgr5-cre+/− mice compared with the β-arr1+/+/Lgr5-cre+/− mice at 5 days after 5-FU treatment (Figures 5a and b). However, the apoptotic signal of Lgr5+ stem cells was low at 0 days of 5-FU treatment (data not shown).
In addition to Lgr5+ stem cells, the apoptosis of Paneth cells was also observed after 5-FU treatment for 5 days (Figure 3d). To investigate the effects of Paneth cells in CIGIS, Paneth cells were labeled by MMP7 using immunohistochemical staining, and the results showed that although chemotherapy induced apoptosis of the Paneth cells, β-arr1 deficiency did not reduce the number of Paneth cells after 5-FU treatment for 5 days compared with WT mice (Figures 5c and d). To investigate the effect of goblet cells in CIGIS, goblet cells were labeled by PAS staining, and the results also showed that β-arr1 deficiency did not affect the number of goblet cells after 5-FU treatment for 5 days compared with WT mice (Figures 5e and f).
Deletion of β-arr1 enhanced intestinal injury, permeability, bacterial translocation, and reduced mortality in mice after 5-FU treatment
To explore the effects of β-arr1 in CIGIS, the morphological changes in the intestinal mucosa were observed in both β-arr1 WT mice and KO mice following 5-FU treatment. Progressive reductions in the height of the villus and the depth of the crypt were found in both β-arr1 WT and β-arr1 KO mice; however, the reductions were more severe in β-arr1 KO mice than in β-arr1 WT mice (Figure 6a). After 5 days of 5-FU treatment, the villus height was significantly smaller, and the crypt depth was also notably reduced in β-arr1 KO mice compared with WT mice (Figures 6b and c). In addition, the intestinal permeability was assessed by measuring the systemic plasma concentration of diamine oxidase (DAO), and the data showed that the intestinal permeability was significantly increased in β-arr1 KO mice compared with WT mice (Figure 6d) after 5-FU stimulation. In addition, the intestinal bacterial translocation was evaluated by examining endotoxin levels in the blood, and the data showed that the endotoxin level was doubled in β-arr1 KO mice compared with WT mice (Figure 6e). These data indicate that deletion of β-arr1 enhanced chemotherapy-induced intestinal injury and intestinal bacterial translocation. Furthermore, the intestinal function, the intestinal morphology and the survival rate were analyzed in mice administered 5-FU at a dose of 50 mg/kg/day i.p. Body weight, diarrhea and survival of mice were assessed once a day and recorded. The data showed that diarrhea and body weight loss significantly increased in β-arr1 KO mice compared with WT mice (Figures 6f and g). Moreover, the mice were killed after 5 days of 5-FU injection to observe the well-formed stool in the colon, and a large number of well-formed stool were observed in WT mice but not in β-arr1 KO mice (Figure 6h). The survival rate of the WT mice was significantly higher than that of the β-arr1 KO mice following 5-FU treatment (Figure 6i). Our data suggest that β-arr1 has an important protective role in chemotherapy-induced CIGIS.
β-arr1 reduced the chemotherapy-induced intestinal apoptosis by inhibiting ER stress-mediated mitochondrial apoptotic signaling
The apoptotic pathways have been linked to ER stress in recent studies.17 Thus, we determined whether ER stress has a key role in chemotherapy-induced intestinal apoptosis. The drugs 5-FU, Cis and Dox were administered to the mice, and both GRP78 and cleaved caspase-12 showed increased activation in β-arr1 KO mice compared with WT mice (Figure 7a). Immunohistochemistry (IHC) staining confirmed that GRP78 and cleaved caspase-12 showed higher expression in β-arr1 KO mice, especially in the intestinal crypts (Figures 7b and c). To further study the effect of β-arr1 in chemotherapy-induced intestinal apoptosis, a β-arr1 plasmid was transfected into HCT116 cells. Western blot analysis verified that β-arr1 overexpression downregulated the expression of GRP78 and inhibited the activation of caspase-12, caspase-9 and caspase-3 in 5-FU-induced apoptosis (Figure 7d). After cells were subjected to 5-FU for 12 h, β-arr1-overexpressing cells showed lower levels of apoptosis, and a drastic difference in apoptotic index was observed between β-arr1-transfected cells and vector-transfected cells (Figures 7e and f). These results revealed that β-arr1 alleviates intestinal apoptosis by downregulating ER stress after chemotherapy. In addition, 5-FU suppressed cytosolic accumulation of Bax and promoted mitochondrial cytochrome c release, which triggered mitochondrial apoptotic signaling. However, β-arr1 overexpression repressed cytochrome c release and inhibited 5-FU-induced mitochondrial apoptotic signaling (Figure 7g).
β-arr1 knockdown promoted chemotherapy-induced cell apoptosis via ER stress signaling
To confirm the protective effects of β-arr1 in CIGIS, we knocked down β-arr1 expression using small interfering RNA (siRNA) in the HCT116 cell line (Figure 8a). Twelve hours after 5-FU administration, β-arr1 siRNA markedly suppressed cell proliferation (Figures 8b and c) and induced cell apoptosis (Figures 8d and e) in vitro. Furthermore, consistent with the results in vivo, 5-FU increased GRP78, cleaved caspase-12, cleaved caspase-8 and cleaved caspase-3, which indicated the activation of ER stress, and knockdown of β-arr1 further upregulated ER stress signaling following treatment with 5-FU (Figure 8f).
Finally, we examined intestinal mucosa changes and the signal pathways of CIGIS in humans. Accordingly, the intestinal mucositis, the apoptosis in the crypt and the activation of ER stress were also observed among chemotherapy patients (Figures 8g and h) following inhibition of β-arr1 after chemotherapy (Figure 4a). Our data indicated that β-arr1 inhibited chemotherapy-induced intestinal apoptosis via inhibiting ER stress signaling.
Despite the broad general knowledge regarding intestinal mucositis following cytotoxic damage,18, 19 there have been few direct assessments of the behavior of ISCs during chemotherapy. The potential impact on the crypt stem cells after chemotherapy has remained elusive.
Our study showed that chemotherapy induces small intestinal crypt cell apoptosis in humans and mice, specifically in Lgr5+ stem cells. This is consistent with our recent results using radiotherapy.20 Lgr5+ stem cell apoptosis was observed after exposure to three different chemotherapeutic drugs, 5-FU, Cis and Dox. Interestingly, Paneth cells also underwent apoptosis in this study. As Paneth cells are considered long-lived cells in the crypt,21 the mechanism underlying their apoptosis during CIGIS is still unclear and requires further study. Paneth cells constitute the niche for Lgr5+ stem cells in intestinal crypts and provide growth factor signals, such as epidermal growth factor (EGF), WNT3, and the NOTCH ligands DLL1 and DLL4.22 Genetic depletion of Paneth cells with Sox9 ablation led to Olfm4+ CBC stem cell loss.22 These cells are likely the major regulators of stem cell abundance through direct physical contact with the stem cells.7 Therefore, it is conceivable that the apoptosis of Paneth cells may lead to the decrease in Lgr5+ stem cells and the marked villus and crypt shrinkage, as well as the attenuation of proliferation. However, a recent study contradicted this possibility.23 After intestinal injury, Paneth cells were not required for intestinal regeneration, whereas Lgr5+ stem cells were indispensable.23 Thus, Lgr5+ stem cells have a primary role in CIGIS.
In addition to the small intestine, Lgr5+ stem cells have also been found in the hair follicles,24, 25 the stomach,26 the colon,8 colon cancer27, 28, 29 and rectal cancer.29 Thus, the behavior of these stem cells following chemotherapy may be similar in these tissues and contribute to the study of the chemotherapy-related side effects, including alopecia, vomiting and anorexia. This model may be used to investigate the curative effects of chemotherapy in GI malignancies by monitoring the Lgr5+ oncogenic stem cells.
Our previous study suggested that p53-mediated intestinal crypt cell apoptosis contributes to chemotherapy-induced intestinal mucosal injury.5 However, the upstream and downstream molecules in this apoptotic signaling pathway are still unknown. β-arr1, a GPCR, has enormous potential as a new therapeutic target in many diseases.30 Meanwhile, increasing evidence has indicated that β-arr1 mediated the activation of Mdm2 and subsequent degradation of p53;13, 31 thus, β-arr1 may affect CIGIS. Our recent study indicated an essential role for the GPCR pathway in the regulation of ER stress-mediated apoptosis.6 In this study, chemotherapy-induced intestinal apoptosis was increased at the bottom of the intestinal crypts in β-arr1 KO mice, with activation of ER stress signaling. The results strongly indicated that β-arr1 serves as a linker between the GPCR and ER stress pathways. Lgr5+ stem cells have been reported to differentiate into different types of intestinal mucosal cells and are indispensable for intestinal regeneration.6, 23, 32 According to our study, the apoptosis after 5-FU treatment was predominantly found at positions 2–4 of the crypts in β-arr1 KO mice, which is where Lgr5 is localized.6 Using double immunostaining, we also verified that Lgr5+ stem cells were more vulnerable to apoptosis in KO mice following chemotherapy. ER stress was associated with differentiation,33 and the degree of stem cell activity was affected by ER stress signaling.7 The Lgr5+ stem cells are highly sensitive to ER stress.15 All these data support our findings that chemotherapy suppressed β-arr1 to activate ER stress, and the ER stress induced Lgr5+ stem cell apoptosis, which resulted in CIGIS. The replacement and regeneration of Lgr5+ stem cell after chemotherapy and the role of β-arr1 and ER stress in these processes will be further studied.
CIGIS symptoms were much more severe in the β-arr1 KO mice than those in the WT mice. The β-arr1 gene increased survival in the CIGIS model, suggesting that β-arr1 effectively prevented CIGIS. These results provide a rationale to target β-arr1 in CIGIS for therapeutic purposes. Several factors, including EGF,34 insulin-like growth factor-1 (IGF-1)35 and R-spondin1,36, 37 have been shown to protect mice from chemotherapy-induced mucositis. EGF and IGF-1 are directly regulated by β-arr1. Thus far, no direct relationship between R-spondin1 and β-arr1 has been reported, but researchers found that R-spondin1 protected mice from chemotherapy-induced mucositis through the Wnt/beta-catenin pathway, and β-arrestin is a required component of Wnt/beta-catenin signaling in vitro and in vivo.38, 39, 40, 41 Thus, it is possible that β-arr1 affects R-spondin1 to mediate CIGIS protection. To date, the therapeutic potential of β-arrestin-based agents has been widely investigated,9, 42, 43, 44 but they have not been tested with intestinal disorders or CIGIS. Based on our results, we speculate that induction of β-arr1 expression (β-arr1-agonist) will be a potential therapy for CIGIS.
Materials and Methods
Human biopsy samples
Small intestinal biopsies were obtained from three cancer patients (two gastric cancers and one periampullary cancer) without small intestinal tumors who had received chemotherapy in the previous 2 weeks and manifested lower alimentary tract symptoms. Three patients were pooled in the chemotherapy group; two of them received the FOLFOX4 regimen, which included 5-FU, calcium folinate and oxaliplatin, and another was only administered oxaliplatin. The control group samples were obtained from three patients (one gastric cancer, one pancreatic cancer and one intestinal obstruction) without small intestinal disease who did not receive chemotherapy. During the operation, a sample from the small intestine (2–3 cm) was collected. All samples were acquired from The Third Affiliated Hospital of Sun Yat-sen University and Sun Yat-sen University Cancer Center. The acquisition of the tissue samples was approved by the Research Ethics Committee of The Third Affiliated Hospital of Sun Yat-Sen University. Written informed consent was obtained from each patient before inclusion in the study.
Mouse genotyping and modeling
The C57BL/6 J mice, β-arrestin-1+/− heterozygous mice with a C57B/L6 background (obtained from Dr. Robert J Lefkowitz, Duke University Medical Center, Durham, NC, USA), and Lgr5-EGFP-IRES-creERT2+/− knock-in mice (Jackson Laboratory, Bar Harbor, ME, USA) were housed in the Sun Yat-sen University Vaccine Research Center. β-arr1 WT and KO littermates were generated by breeding heterozygous mice. Lgr5-EGFP-IRES-creERT2+/− knock-in littermates were generated by breeding Lgr5-EGFP-IRES-creERT2+/+ and Lgr5-EGFP-IRES-creERT2+/− mice. β-arr1+/− mice were crossed with Lgr5-cre+/− mice, and β-arr1+/−/Lgr5-cre+/− mice were generated. Furthermore, male and female β-arr1+/−/Lgr5-cre+/− mice were bred to generate β-arr1+/+/Lgr5-cre+/− and β-arr1−/−/Lgr5-cre+/− mice.
The β-arr1 mice were genotyped by real-time polymerase chain reaction (PCR) analysis using genomic DNA extracted from tail snips. β-arr1 mutant primers are as follows: forward primer, 5′-CCTAGTGCTGGGATTACAAG-3′, and reverse primer, 5′-CATAGCCTGAAGAACGAGAT-3′ (obtained from Dr. Robert J Lefkowitz). The Lgr5-EGFP-IRES-creERT2 mice were genotyped by PCR using genomic DNA extracted from tail snips. The WT reverse primer, 5′-ATACCCCATCCCTTTTGAGC-3′, and the mutant reverse primer, 5′-GAACTTCAGGGTCAGCTTGC-3′, were used. Sex-matched, 8- to 10-week-old mice (20–25 g) were used for all experiments with 8–10 mice in each group. CIGIS models were induced by i.p. injection of 5-FU (Sigma, St. Louis, MO, USA) at a dose of 75 mg/kg/day for 1, 3, 5 or 7 days. In addition, CIGIS models were also induced by i.p. injection of Cis (Sigma) at 5 mg/kg/day for 5 days and Dox (Sigma) at 6 mg/kg/day for 3 days.
CIGIS assessment and survival rate
Mice were weighed once daily after beginning the 5-FU treatment. Five days later, mice were killed, and the colon was harvested. The number of well-formed stools was recorded. Similarly, animal well-being was assessed daily after the 5-FU (50 mg/kg/day) treatment, and the incidence and severity of diarrhea were scored. Scores were recorded as 0, 1, 2 or 3, where 0 is normal stool consistency, 1 is loose stools, 2 is overt diarrhea and 3 is liquid feces with severe perianal/tail soilage (extreme diarrhea).45
Cells culture, transfection and induction of apoptosis
HCT116 cell lines were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA) and were routinely cultured in McCoy’s 5A medium supplemented with 10% fetal bovine serum, 30 U/ml penicillin, and 30 mg/ml streptomycin at 37 °C under 5% CO2. HCT116 cells were transfected with a GFP-β-arr1 plasmid (kindly provided by Professor Pei G, Shanghai Institutes for Biological Sciences) using Lipofectamine 2000 (Invitrogen, Carlsbad, NM, USA). To assess chemotherapy-induced apoptosis, cells were incubated in culture medium containing 0, 10 or 100 μg/ml 5-FU for 12 h. Cells were harvested and lysed in ice-cold sample buffer. Samples were stored for western blotting or fixed for microscopic assessment of apoptosis.
Small interfering RNA
HCT116 cells were cultured in six-well plates. For β-arr1 siRNA treatment, cells were transfected with 20 μM β-arr1 siRNA (Santa Cruz Biotechnology, Santa Cruz, CA, USA). Three β-arr1 siRNA sequences targeting the coding region of β-arr1 mRNA were purchased, siRNA-1 (5′-GUCACCAACAACACCAACATT-3′), siRNA-2 (5′-GGGUCCUGUACAAUCUCAUTT-3′) and siRNA-3 (5′-CUGUACAUGUUUGGUUAAUTT-3′). The most effective sequence was selected. After incubation for 24 h, transfection medium was replaced by regular culture medium before 5-FU administration. A siRNA directed against glyceraldehyde-3-phosphate dehydrogenase provided in the kit was used as a control. After these cells had grown to a density of 90%, 10 μg/ml of 5-FU was added for 12 h.
Sample collection and preparation
Immediately after the animals were killed, the entire small intestine was carefully isolated and placed on ice. The 5 cm segments (duodenum) were removed. The rest of the intestine was rinsed thoroughly with ice-cold physiological saline as previously described.46
Intestinal permeability and bacterial translocation
Inferior vena cava blood from the control group and the treatment group was collected. Blood DAO (mg/ml) and endotoxin (Eμ/ml) levels were determined with an ELISA kit (Roche, Basel, Switzerland) to estimate intestinal permeability and bacterial translocation, respectively. ELISA was performed according to the manufacturer’s instructions.
Histological analysis and TUNEL staining
Formalin-fixed tissues were embedded in paraffin and sectioned. The 4 μm sections were stained by hematoxylin and eosin (H&E). TUNEL staining was performed using the ApopTag kit (Roche) according to the manufacturer’s instructions. The apoptotic index (%) was determined by dividing the number of apoptotic cells by the total number of cells in the epithelium of at least 20 randomly selected villi and crypts.
Sections were dewaxed in xylene and rehydrated through a graded series of alcohols. Sections were oxidized in 1% periodic acid at room temperature for 20 min and rinsed in distilled water. Sections were treated for 30 min in Schiff’s reagent (Sigma) and washed for 7 min in running water. Slides were counter-stained with methyl green, dehydrated and mounted.
Antibodies and immunostaining
Primary antibodies used for immunostaining included those for EGFP (Santa Cruz Biotechnology), MMP7 (R & D Systems, Minneapolis, MN, USA), cytokeratin (Leica, Solms, Germany), CD34 (Abcam, Cambridge, MA, USA), GRP78 (Enzo Life Sciences, Lausen, Switzerland), cleaved caspase-3, cleaved caspase-4, cleaved caspase-9, cleaved caspase-12, Cox IV (all from Cell Signaling Technology, Danvers, MA, USA); secondary antibodies included goat anti-mouse HRP (Santa Cruz Biotechnology), goat anti-rabbit HRP (Santa Cruz Biotechnology), donkey anti-goat HRP (Santa Cruz Biotechnology), chicken anti-rat AP (Santa Cruz Biotechnology), chicken anti-rabbit AP (Santa Cruz Biotechnology), chicken anti-mouse AP (Santa Cruz Biotechnology), goat anti-rabbit Alexa 488/594 (Invitrogen), rabbit anti-goat Alexa 594 (Invitrogen), chicken anti-rabbit Alexa 594 (Invitrogen) and chicken anti-mouse Alexa 594 (Invitrogen). Immunostaining was performed using these antibodies. The sections were counter-stained with hematoxylin or nuclear fast red (Vector, Burlingame, CA, USA). For double staining, EGFP, MMP7, cytokeratin, CD34 and PAS staining was performed following TUNEL staining or cleaved caspase-3 staining.
Antibodies and western blotting
Total protein was extracted, and mitochondrial and cytosolic fractions were analyzed by SDS-PAGE (Invitrogen) as previously described.47 The primary antibodies included those for p53 (Abcam), cleaved caspase-3 (Cell Signaling), Cox IV (Cell Signaling), Bax (Abcam), Bak (Abcam), cytochrome c (Santa Cruz Biotechnology), β-actin (Sigma) and β-arr1 (kindly provided by Dr. Robert J Lefkowitz, Duke University Medical Center). Appropriate horseradish peroxidase-conjugated secondary antibodies were used to detect the primary antibody/antigen complexes. ImageJ free software (http://imagej.nih.gov/ij/download.html) was used to quantify the results of western blotting.
Quantitative data are expressed as the mean±S.D. Data were analyzed by an unpaired t-test or ANOVA, in which multiple comparisons were performed using the method of least significant difference. The survival rate was analyzed by the log-rank test. Statistical significance was defined as a P-value <0.05.
We thank Professor Robert J Lefkowitz at Duke University for providing the ARRB1 heterozygous and ARRB2 heterozygous mice; Professor G Pei at the Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences for providing the ARRB1 and ARRB2 plasmids; and our doctors and research nurses for their assistance in collecting the tissue samples. This work was supported in part by Grants-in-Aid from the National Natural Science Foundation of China (U1501224, 81370511) (BW), the Major Projects Incubator Program of the National Key Basic Research Program of China (2012CB526700) (BW), the Research Fund for the Doctoral Program of Higher Education of China (2012171110081) (BW) and the International Cooperative Innovative Platform of Guangdong Province Universities and Colleges (gjhz1101) (BW).
Study concept and design (YZ, CX and BW); acquisition of data (YZ, CX, YY, ZL, ST, YY, JJ, HL, JC and BW); analysis and interpretation of data (YZ, CX, YY, ZL, ST, YY, JJ, HL, JC and BW); drafting of the manuscript (YZ and BW); critical revision of the manuscript for important intellectual content (YZ, CX, ZL, ST, YY and BW); statistical analysis (YZ, CX and BW); obtained funding (BW); technical or material support (JJ and HL); study supervision (BW).
Approval for this research was obtained from the Research Ethics Committee of The Third Affiliated Hospital of Sun Yat-Sen University.
Provenance and peer review
This paper was not commissioned, but externally peer reviewed.
Data sharing statement
Available data in this paper will be shared upon request to the corresponding author.
chemotherapy-induced GI syndrome
intestinal stem cells
crypt base columnar
small interfering RNA
epidermal growth factor
insulin-like growth factor-1
About this article
Veterinary Pathology (2019)