Published online May 14, 2021. doi: 10.3748/wjg.v27.i18.2141
Peer-review started: December 26, 2020
First decision: January 29, 2021
Revised: February 6, 2021
Accepted: March 29, 2021
Article in press: March 29, 2021
Published online: May 14, 2021
Previous reports have suggested that the p38 mitogen-activated protein kinase signaling pathway is involved in the development of severe acute pancreatitis (SAP)-related acute lung injury (ALI). Inhibition of p38 by SB203580 blocked the inflammatory responses in SAP-ALI. However, the precise mechanism associated with p38 is unclear, particularly in pulmonary microvascular endothelial cell (PMVEC) injury.
To determine its role in the tumor necrosis factor-alpha (TNF-α)-induced inflammation and apoptosis of PMVECs in vitro. We then conducted in vivo experiments to confirm the effect of SB203580-mediated p38 inhibition on SAP-ALI.
In vitro, PMVEC were transfected with mitogen-activated protein kinase kinase 6 (Glu), which constitutively activates p38, and then stimulated with TNF-α. Flow cytometry and western blotting were performed to detect the cell apoptosis and inflammatory cytokine levels, respectively. In vivo, SAP-ALI was induced by 5% sodium taurocholate and three different doses of SB203580 (2.5, 5.0 or 10.0 mg/kg) were intraperitoneally injected prior to SAP induction. SAP-ALI was assessed by performing pulmonary histopathology assays, measuring myeloperoxidase activity, conducting arterial blood gas analyses and measuring TNF-α, interleukin (IL)-1β and IL-6 levels. Lung microvascular permeability was measured by determining bronchoalveolar lavage fluid protein concentration, Evans blue extravasation and ultrastructural changes in PMVECs. The apoptotic death of pulmonary cells was confirmed by performing a terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling analysis and examining the Bcl2, Bax, Bim and cle-caspase3 levels. The proteins levels of P-p38, NFκB, IκB, P-signal transducer and activator of transcription-3, nuclear factor erythroid 2-related factor 2, HO-1 and Myd88 were detected in the lungs to further evaluate the potential mechanism underlying the protective effect of SB203580.
In vitro, mitogen-activated protein kinase (Glu) transfection resulted in higher apoptotic rates and cytokine (IL-1β and IL-6) levels in TNF-α-treated PMVECs. In vivo, SB2035080 attenuated lung histopathological injury, decreased inflammatory activity (TNF-α, IL-1β, IL-6 and myeloperoxidase) and preserved pulmonary function. Furthermore, SB203580 significantly reversed changes in the bronchoalveolar lavage fluid protein concentration, Evans blue accumulation, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling-positive cell numbers, apoptosis-related proteins (cle-caspase3, Bim and Bax) and endothelial microstructure. Moreover, SB203580 significantly reduced the pulmonary P-p38, NFκB, P-signal transducer and activator of transcription-3 and Myd88 levels but increased the IκB and HO-1 levels.
p38 inhibition may protect against SAP-ALI by alleviating inflammation and the apoptotic death of PMVECs.
Core Tip: We explored the role of the p38 mitogen-activated protein kinase pathway in the tumor necrosis factor-alpha-induced inflammation and apoptosis of pulmonary microvascular endothelial cells in vitro and verified the effect of SB203580-mediated p38 inhibition on severe acute pancreatitis-related acute lung injury in rats. p38 mitogen-activated protein kinase overactivation promoted tumor necrosis factor-alpha-induced inflammatory cytokine expression and pulmonary microvascular endothelial cell apoptosis in vitro. SB203580 improved severe acute pancreatitis-related acute lung injury by downregulating P-p38, NFκB, P-SATA3 and Myd88 and upregulating IκB and HO-1, which alleviated inflammation and apoptotic cell death in rats.
- Citation: Zhang XX, Wang HY, Yang XF, Lin ZQ, Shi N, Chen CJ, Yao LB, Yang XM, Guo J, Xia Q, Xue P. Alleviation of acute pancreatitis-associated lung injury by inhibiting the p38 mitogen-activated protein kinase pathway in pulmonary microvascular endothelial cells. World J Gastroenterol 2021; 27(18): 2141-2159
- URL: https://www.wjgnet.com/1007-9327/full/v27/i18/2141.htm
- DOI: https://dx.doi.org/10.3748/wjg.v27.i18.2141
Acute pancreatitis (AP), a common gastrointestinal disease, ranges from a self-limiting disease to a severe condition with high mortality. The overall mortality rate is approximately 2%[1], while the mortality rate of severe AP (SAP) with distant organ dysfunction increases to 37%-50%[2]. To date, the pathogenesis of SAP has not been completely clarified, and no specific pharmacological therapies for SAP or its associated organ failure are available. The management of AP is mainly limited to supportive care. The lung is the most vulnerable organ in patients with SAP. Acute lung injury (ALI) or its more severe form, acute respiratory distress syndrome, is reported to occur in 10%-25% of patients with AP and accounts for up to 60% of AP-associated deaths[3,4]. Therefore, the identification of an effective therapy for AP-associated ALI is still urgently needed to decrease AP mortality.
ALI secondary to SAP is clinically and histologically indistinguishable from other indirect (sepsis, trauma or burns) or direct (e.g., toxins or infection) insults to the lungs[5]. ALI is characterized by disruption of the alveolar capillary barrier, which increases endothelial and epithelial permeability, decreases lung compliance and impairs gas exchange[6]. Multiple biological processes are involved in the mechanisms of endothelial permeability, such as cytoskeletal rearrangements, assembly/ disassembly of cell junctions and survival/death[7-9]. Pulmonary microvascular endothelial cells (PMVECs) line the interior of blood vessels and are an essential part of the blood and tissue microenvironment. They are major actors responding to insults related to ALI[10,11]. PMVECs are the main targets of humoral and cellular mediators during injury[12] and actively produce proinflammatory cytokines, increase the levels of adhesion molecules and secrete prothrombotic substances, promoting injury by transforming to a prothrombotic and proinflamma
p38 mitogen-activated protein kinase (p38 MAPK), a member of the serine/ threonine kinase family, is ubiquitously expressed. It plays an important role in diverse processes including endocytosis, gene transcription, cell proliferation, cytokine production, apoptosis and cytoskeletal redistribution[8]. Therefore, unsurprisingly, p38 MAPK is involved in many cascades that result in the development of mild AP with limited pancreatic injury to SAP with ALI. In an experimental AP model, p38 MAPK activation was observed in the lungs as early as 2 h after model establish
Rat PMVECs were obtained from the BeNa Culture Collection (338210, Beijing, China). Cells were identified according to staining with rat anti–factor VIII and binding of FITC-labeled lectin (Sigma, United States)[17]. The cells were cultured in DMEM (Thermo Fisher, United States) supplemented with 100 mL/L fetal bovine serum (BI, Australia), 50 U/mL penicillin and 50 µg/mL streptomycin (Thermo Fisher, United States). PMVECs were maintained at 37 °C in a humidified atmosphere with 950 mL/L O2 and 50 mL/L CO2.
The MAPK pathway is comprised of three sequential dual-specificity kinases, and MAPK kinase (MKK) 6 is highly selective for p38 activation. Overexpression of activated MKK 6 (Glu) constitutively activates p38 MAPK[18,19]. Lentiviruses carrying either no inserted sequence (null) or the MKK 6 (Glu) gene were constructed by Wuhan PeptBio company limited China. PMVECs were infected with the lentivirus at a multiplicity of infection of 10 in the presence of 5 μg/mL polybrene (Sigma, United States). After lentivirus infection, MKK 6 (Glu)-overexpressing cells and control cells were obtained via puromycin (2 μg/mL) screening and analyzed using western blotting. When the cells reached 70%–80% confluence, they were treated with TNF-α (20 ng/mL) for the indicated times and then used for the subsequent analyses.
PMVEC apoptosis was assessed using an Annexin V-FITC/PI kit (4A Biotech, China). Briefly, PMVECs were detached using trypsin, washed with cold PBS, pelleted and resuspended in binding buffer. Then, 10 μL of Annexin V was added, and they were incubated for 5 min in the dark. After mixing with 5 μL of propidium iodide, the cells were analyzed using a flow cytometer (BD Biosciences, United States).
Adult male Sprague-Dawley rats (n = 25, 210-230 g) were purchased from the Experimental Animal Center of Sichuan University (Chengdu, China). The animals were housed at 22-25 °C on a 12 h day-night cycle and fed standard rodent chow and tap water ad libitum for 1 wk of acclimation. The animal experiments performed in this study were conducted in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals. The protocol was designed to minimize pain or discomfort to the animals and approved by the Animal Ethics Committee of West China Hospital of Sichuan University.
After fasting for 12 h, the SAP model was established by biliary-pancreatic duct injection of 50 g/L sodium taurocholate (Sigma, United States, 1 mL/kg) using a micropump at a speed of 0.2 mL/min[20]. In the sham group, the rats received the same volume of saline instead of sodium taurocholate. All rats received a saline injection subcutaneously to compensate for fluid loss during the surgery (20 mL/kg body weight). The rats were randomly divided into the SO group, SAP group and SAP + SB203580 group. The SAP + SB203580 group was further divided into low-dose (SB2.5 group), middle-dose (SB5 group) and high-dose (SB10 group) subgroups according to the dose of SB203580 (2.5 mg/kg, 5.0 mg/kg and 10.0 mg/kg, respectively, n = 5). SB203580 (Selleck, United States) was intraperitoneally administered before model establishment. The rats were sacrificed 12 h after model induction, and samples were harvested rapidly for subsequent analysis.
At the end of the experiment, arterial blood samples were collected by cardiac puncture. A blood gas analysis was performed to detect the partial pressure of oxygen (PaO2) and oxygen saturation (SaO2, Cobas b 123 Analyzer, Roche, Switzerland).
After opening the chest, the right lung was ligated. Bronchoalveolar lavage fluid (BALF) was collected through slow and careful lavage of the left lung with 2 mL of 4 °C PBS. Then, the fluid was centrifuged at 500 g for 5 min. The supernatant was collected and stored at -80 °C until the analyses of the protein concentration and cytokine levels.
The pancreas and lung were fixed with 40 g/L formaldehyde for 24 h. The tissues were then embedded in paraffin, and continuously sliced at a 5 mm thickness for staining with hematoxylin and eosin. The pancreatic and pulmonary histological assessment was performed and scored by two pathologists using a microscope at 200 × magnification[21,22]. For the assessment of the apoptosis of lung tissue, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining was performed with a commercially available In Situ Cell Death Detection Kit (Roche, Mannheim, Germany) according to the manufacturer’s instructions.
Concentrations of TNF-α, interleukin (IL)-1β and IL-6 in the serum and BALF were evaluated using ELISA kits according to the manufacturer’s instructions (R and D Systems, United States). The BALF protein concentration was determined using a BCA kit (Thermo, United States).
Evans blue extravasation was used to quantify the capillary permeability in the lungs. A 10 g/L Evans Blue solution (20 mg/kg, Sigma-Aldrich, United States) was injected into the tail vein 1 h before exsanguination. PBS was used to flush the remaining Evans blue from the pulmonary vascular system. After the complete removal of blood, the left lung was removed, weighed, homogenized in formamide and incubated at 37 °C for 24 h. Finally, the supernatant was quantified spectrophotometrically at 620 nm.
Pulmonary myeloperoxidase (MPO) activity was measured using the method described by Dawra et al[23]. Briefly, lung tissue was homogenized in phosphate buffer (100 mmol/L, pH 7.4) at 4 °C and centrifuged to pellet the tissues. The samples were then resuspended in phosphate buffer (100 mmol/L, pH 5.4) containing protease inhibitors, 5 g/L hexadecyl trimethyl ammonium bromide and 10 mmol/L EDTA and subjected to three rapid freeze-thaw cycles. The suspension was sonicated and centrifuged to obtain the supernatant. Twenty microliters of the supernatant were incubated with 200 μL of phosphate buffer (pH 5.4) containing 5 g/L hexadecyl trimethyl ammonium bromide and 2 mmol/L 3,3,5,5-tetramethylbenzidine for 3 min at room temperature followed by the addition of 50 μL H2O2. The difference in the absorbance of this assay solution between 0 min and 3 min was measured at 655 nm at 37 °C with a microplate reader (BMG LABTECH, Germany). MPO activity was calculated from a human MPO standard curve, normalized to the protein concentration and reported as mU/mg protein.
Lysates from PMVECs or lung tissues were extracted with RIPA lysis buffer (Abcam, United Kingdom) supplemented with protease inhibitors (Roche, Germany). The total protein concentration was quantified using a BCA kit (Thermo, United States). The same amounts of protein were separated on 10% or 12% SDS-PAGE gels and transferred to a polyvinylidene fluoride membrane. Membranes were blocked with 50 g/L nonfat milk for 2 h at room temperature and subsequently incubated with the following primary antibodies overnight at 4 °C: P-p38 (1:2000), NFκB (1:1000), IκB (1:1000), cleaved caspase-3 (cle-casp3, 1:1000), P-signal transducer and activator of transcription-3 (P-STAT3, 1:1000), myeloid differentiation factor 88 (Myd88, 1:1000), nuclear factor erythroid 2-related factor 2 (Nrf2, 1:1000), Bax (1:1000) and Bim (1:1000) from CST, United States; IL-1β (1:1000), heme oxygenase-1 (HO-1, 1:1000) and Bcl2 (1:1000) from Abcam, United States; and TNF-α (1:1000), IL-6 (1:1000) and β-actin (1:1000) from Proteintech, China. After rinsing with Tris-buffered saline containing Tween 20 (10 min, × 3), the membranes were incubated with a secondary goat anti-rabbit (1:5000, Proteintech, China) or a goat anti-mouse IgG-HRP antibody (1:10000, Proteintech, China) for 1-2 h at room temperature. Finally, after washing, the membranes were imaged using a chemiluminescence detection system (Bio-Rad, United States) and analyzed with Image Lab software.
A 2 mm3 peripheral specimen was fixed with 25 mL/L glutaraldehyde for 2 h and then washed with 0.1 mol/L phosphate buffer (PH 7.4, 10 min × 3). After fixing the samples with 10 mL/L osmium tetroxide for 2 h, the specimens were dehydrated through a graded series of ethanol solutions and acetone and embedded in Epon 812 (Sigma, United States). Ultrathin sections were cut with an ultramicrotome (Leica, Germany). Finally, the sections were stained with uranyl acetate and lead citrate and examined using a JEM-1230 transmission electron microscope (JEOL, Japan).
All statistical tests were performed using SPSS 20.0 (SPSS, United States) by a biomedical statistician. Data are presented as the mean ± SE for continuous variables or frequencies and percentages for categorical variables. Data were analyzed using one-way analysis of variance or the Kruskal-Wallis test. A P value of < 0.05 was considered statistically significant.
We overexpressed a constitutively activated MKK6 (Glu) in PMVECs, which was confirmed to over activate p38 MAPK (Figure 1A). Then, the cells were incubated in the absence or presence of TNF-α. Flow cytometry analysis showed TNF-α induced apoptosis in both null and MKK (Glu) cells. Compared with the null groups, the apoptotic rate was significantly higher in the MKK (Glu) group treated with TNF-α (Figure 1B and 1C). Meanwhile, the levels of inflammatory cytokines (IL-6 and IL-1β) were also significantly upregulated in the MKK (Glu) cells (Figure 1D and 1E).
Representative images of hematoxylin and eosin staining of the pancreas were shown in Figure 2A. Except for slight pancreatic edema, no obvious changes indicative of AP were observed in sham-operated animals. Sodium taurocholate induced typical histopathological changes associated with AP, including diffuse edema, marked neutrophil infiltration, intrapancreatic hemorrhage and acinar cell necrosis. The histopathological scores were all significantly increased (Figure 2B-F). All three tested doses of SB203580 (2.5, 5.0 and 10.0 mg/kg) alleviated injury to the pancreatic tissues (all P < 0.05). We explored the difference in the therapeutic effect among the three different doses; compared to the SB2.5 group, 10.0 mg/kg SB203580 further significantly decreased the histopathological inflammatory infiltration, necrosis and total scores (Figure 2B, 2D and 2F).
The histopathological changes in the pulmonary tissues were shown in Figure 3A. In SAP rats, lung damage was characterized by neutrophil infiltration, thickened alveolar walls, intra-alveolar hemorrhaging and alveolar collapse. The histopathological scores were also significantly increased (Figure 3B-D). These changes were accompanied by significantly increased IL-1 and TNF-α levels in the BALF and serum (Figure 4A-D) and pulmonary MPO activity (Figure 4E) and a decreased PaO2 (Figure 4F). There was no change of SO2 in the SAP rats (Figure 4G). At the same time, western blotting analysis also confirmed increased levels of inflammatory cytokines (IL-1, TNF-α, IL-6) in the SAP group compared with the sham group (Figure 4H-J). SB203580 treatment alleviated the histopathological injuries and scores, decreased the levels of inflammatory factors (IL-1, TNF-α, IL-6 and MPO) and preserved PaO2. Among the three doses tested, SB203580 at 10.0 mg/kg consistently and significantly reduced all histopathological and biochemical severity indices with the highest efficiency.
The permeability of the PMVECs was evaluated in vivo by measuring the BALF protein concentration and Evans blue accumulation in the lung tissue. Quantitative analysis showed a significant increase in these two parameters in SAP rats, which were suppressed by SB203580 cotreatment (Figure 5A and 5B). They further decreased after treatment with increasing SB203580 doses. The microstructure and integrity of the endothelium were evaluated using transmission electron microscopy. In the sham group, the lung tissues showed a normal capillary endothelium, as evidenced by an intact capillary basal membrane, dense endothelial cell-cell junctions and continuous and clear delineation between cells (Figure 5C). In the SAP group, capillary endothelial dissolution and rupture were noted. In addition, low electron density clouds with an irregular thickness indicating basal membrane edema, increased vacuolization, loose cellular junctions, swollen cellular organelles and nuclear degeneration were often observed. In contrast, the swelling and injury of endothelial cells were partially alleviated in lungs from SB203580-treated rats. After treatment with 10.0 mg/kg SB203580, no obvious rupture of endothelial cells or red cells extravasating from the vessels were observed.
TUNEL staining was used to examine cell death in lung tissues. Cell apoptosis in the lung tissues was assessed by the colocalization of TUNEL-green and DAPI-blue staining. A prominent increase in the number of positively stained cells was observed in the SAP group compared to the sham group, indicating a higher apoptotic rate (Figure 6A). Treatment of SAP rats with SB203580 significantly decreased the number of apoptotic cells, and the greatest inhibitory effect was observed in rats treated with 10.0 mg/kg SB203580. Proteins regulating the apoptotic signaling pathways were examined using western blotting to further confirm the cell death pathway. As shown in Figure 6B-E, although no change in the antiapoptotic protein Bcl2 was observed, the levels of the proapoptotic proteins Bax, Bim and cle-caspase3 were upregulated in the SAP group compared to the sham group. SB203580 treatment reversed the changes in the levels of these proteins in the SAP group in a dose-dependent manner.
Levels of the P-p38, NFκB, IκB, Nrf2, HO-1, P-SATA3 and Myd88 proteins were detected in the lungs for further evaluation of the protective mechanism of SB203580. Figure 7 showed increased levels of P-p38, NFκB, P-SATA3 and Myd88 but decreased levels of IκB, Nrf2 and HO-1 in the SAP group compared with the sham group. Intriguingly, SB203580 reversed the changes in the levels of these proteins, reducing P-p38, NFκB, P-SATA3 and Myd88 levels but increasing IκB and HO-1 levels compared with the SAP group. However, except for P-p38 and HO-1, the improvement of these parameters was not positively related to the dose of SB203580. In addition, SB203580 slightly increased the level of Nrf2, but the difference was not statistically significant (Figure 7E).
Although the mechanisms of ALI/acute respiratory distress syndrome following SAP have not been completely elucidated, an increasing number of studies have described PMVEC injury and dysfunction as prerequisites for ALI[24]. The PMVECs are activated, participate in host defenses and result in increased microvascular permeability and damaged lung function[8,25]. Regardless of the etiology, an exaggerated inflammatory response is widely accepted to play a vital role in the transition of AP into a systemic disease[26]. Various inflammatory mediators have been related to AP severity and they induce their own or other mediators’ secretion through a positive feedback mechanism, leading to amplification of the inflammatory cascade[27]. TNF-α was discovered to play a role in the early phase and cause the activation and injury of endothelial cells, functioning as a key promoter of the development of SAP-ALI[28]. In the present study, TNF-α was used to mimic SAP-related PMVEC injury in vitro.
p38 is activated by various insults, including cytokines, while the activation of p38 MAPK inevitably induces the expression of proinflammatory cytokines[29]. In our study, TNF-α induced higher levels of inflammatory cytokines (IL-1β and IL-6) in PMVECs with p38 overactivation (Figure 1D and 1E). These results further confirmed a positive role for the p38 MAPK signaling pathway in regulating cytokine expression.
According to previous studies, p38 MAPK is involved in both survival and apoptosis pathways. It promotes anti- or proapoptotic effects in a cell type and stimulus-specific manner in endothelial cells. For example, one group reported that SB203580 inhibited p38 MAPK and then decreased the endothelial cell apoptosis stimulated by TNF-α and cycloheximide[30], while another group illustrated that SB203580 enhanced endothelial cell apoptosis triggered by TNF-α alone[31]. It was reported that endothelial cells are relatively resistant to TNF-α, which induce only modest or no cell damage[31,32]. Then, we chose to overexpress activated MKK 6 (Glu) to constitutively activate p38 MAPK in PMVECs. Flow cytometry analysis revealed apoptotic cell death in null PMVECs stimulated with TNF-α, and MKK 6 (Glu) transfection resulted in a significantly higher apoptotic rate (Figure 1B). This finding indicated that persistent activation of p38 MAPK promotes TNF-α-induced PMVEC apoptosis. However, SB203580 pretreatment conversely aggravated PMVEC injury in this study (data not shown) and did not alleviate cell apoptosis. This discrepancy may be attributed to the extent or duration of p38 MAPK activation[33]. Rapid and transient p38 activation modulates inhibitors of the apoptosis protein family to prevent TNF-α-induced apoptosis[31], while sustained activation leads to apoptosis through the phosphorylation and downregulation of Bcl-xL[30]. Therefore, SB203580 may exert a beneficial effect to maintain an appropriate level of p38 MAPK activity.
Many small-molecule inhibitors targeting p38 MAPK, such as SB203850, CNI-1493[34], SB202190[35], RWJ-67657[36] and UM101[37], have been tested in various cell injury or disease models. In AP, the p38 MAPK signaling pathway is involved not only in pancreatic acinar injury[20,38] but also in injury to distant organs (lung, liver, kidney, gut and placenta)[39-43]. SB203850 is a pyridinyl imidazole derivative that competes for ATP binding, and the inhibition of p38 MAPK has been shown to attenuate the severity of AP and its related distant organ injury[14,15,39,44]. In the present study, we treated SAP rats with SB203580 to investigate its protective effect on SAP-associated lung injury and the potential underlying mechanisms. As shown in Figure 2, SB203580 significantly alleviated pancreatic histopathological damage in SAP rats. Furthermore, it alleviated lung histopathological injuries (Figure 3), decreased the levels of inflammatory factors (IL-1β, TNF-α, IL-6 and MPO, Figure 4) and preserved PaO2, consistent with previous reports[14,15]. Based on these results, SB203580 effectively decreased the inflammatory response in rats with SAP-ALI. In addition, by analyzing three different doses of SB203580, we observed a dose-dependent improvement in the therapeutic effects, as 10.0 mg/kg was the most effective.
Although apoptosis is regarded as a protective mechanism, excessive apoptosis is harmful to the alveolar capillary membrane and pulmonary function. As the first-line responder to systemic injurious factor insults, damage to endothelial cells is detected earlier than damage to epithelial cells[45]. PMVEC damage results in lung injury, which in turn promotes the secretion of inflammatory mediators to destroy PMVECs in individuals with SAP[46]. In the present study, increased Evans blue extravasation and BALF protein concentrations revealed increased capillary permeability in SAP rats. Moreover, transmission electron microscopy analysis directly confirmed capillary endothelial dissolution and rupture in the lung (Figure 5). Finally, the results of the TUNEL and western blot analyses (Figure 6) suggested that an increased number of apoptotic cells was involved in the pathological process of SAP-ALI. However, SB203580 significantly reversed the changes in Evans blue accumulation, BALF protein concentration, TUNEL-positive cells, apoptosis-regulated proteins and endothelial microstructure, providing evidence for the underlying protective effects of p38 MAPK inhibitors on endothelial cell apoptosis.
Because p38 MAPK is a proximal initiator of signal transduction, various substrates are directly or indirectly activated by p38 MAPK, permitting it to perform a wide range of functions[29,47]. The biological consequences of p38 MAPK inhibition are complicated by interactions with other signaling pathways. p38 MAPK was reported to have a dual function in regulating Nrf2/HO-1 signaling[48,49]. HO-1 possesses cytoprotective properties, including anti-inflammatory, antioxidant and antiapoptotic activities. NFκB, which is downstream of p38 MAPK, represses Nrf2 transcriptional activity[50,51], while HO-1 inhibits proinflammatory mediators through the inactivation of NFκB[52]. STAT3 is activated by p38 MAPK, transferring signals to the nucleus and regulating gene expression[53,54]. MyD88 is considered a classical proinflammatory and proapoptotic upstream signaling adaptor molecule of p38 MAPK[55]. While the mechanism underlying the effects of SB203580 must be further elucidated, the levels of these key proteins involved in inflammatory, oxidative and apoptotic signaling pathways were measured. In the present study, SB203580 treatment reversed the increased levels of P-p38, NFκB, P-STAT3 and Myd88 and decreased levels of IκB and HO-1 in the SAP group (Figure 7). Therefore, the protective effects of p38 inhibition via SB203580 were likely partially attributed to the inhibition of pulmonary proinflammatory and proapoptotic signaling pathways.
In conclusion, p38 MAPK overactivation promoted TNF-α-induced inflammatory cytokine expression and PMVEC apoptosis in vitro. The inhibition of p38 MAPK with SB203580 protected against SAP-ALI by alleviating inflammation and apoptotic cell death in rats. Therefore, SB203580 may alleviate SAP-ALI by inhibiting the proinflammatory and proapoptotic effects of the p38 MAPK pathway on PMVECs. These results suggest the possibility of applying p38 MAPK inhibitors as treatments for SAP-ALI in the clinical setting.
Acute lung injury (ALI) is the main reason for the high mortality of patients with severe acute pancreatitis (SAP). Injury and dysfunction of pulmonary microvascular endothelial cells (PMVEC) are considered prerequisites for ALI. The p38 mitogen-activated protein kinase (p38 MAPK) signaling pathway is involved in the development of SAP-related ALI. However, the precise mechanism by which p38 MAPK regulates PMVEC injury in SAP-related ALI is unclear.
To date, no specific pharmacological therapies for SAP associated ALI are available. Elucidating the mechanism of PMVEC injury regulated by p38 MAPK is expected to help identify new treatments for SAP-associated ALI.
To determine the role of p38 MAPK in the tumor necrosis factor-alpha-induced injury of PMVECs in vitro and to explore the effect of SB203580-mediated p38 inhibition on SAP-ALI in vivo.
In vitro, PMVECs were transfected with MAPK kinase 6 (Glu) and stimulated with tumor necrosis factor-alpha to detect cell apoptosis and inflammatory cytokine levels. In vivo, SAP-ALI rats were treated with three different doses of SB203580 (2.5, 5.0 or 10.0 mg/kg). Blood, bronchoalveolar lavage fluid and tissue samples were harvested to assess cytokine levels, blood gas analyses, histopathological changes, myeloperoxidase activity, bronchoalveolar protein concentration, Evans blue extravasa
In vitro, MAPK kinase (Glu) transfection resulted in higher apoptotic rates and cytokine levels in TNF-α-treated PMVECs. In vivo, SB2035080 attenuated lung histopathological injury, decreased inflammatory activity and preserved pulmonary function. Furthermore, SB203580 significantly reversed the microvascular permeability, the increase in the number of terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling-positive cells, the increased expression of apoptosis-related proteins and the endothelial microstructure changes. Moreover, SB203580 significantly reduced pulmonary P-p38, NFκB, P-SATA3 and Myd88 levels but increased the IκB and HO-1 levels.
p38 inhibition may protect against SAP-ALI by alleviating inflammation and the apoptotic death of PMVECs.
In this study, p38 MAPK overactivation promoted PMVEC injury in vitro, while p38 inhibition protected against SAP-ALI in vivo. These results suggest the potential of applying p38 MAPK inhibitors as treatments for SAP-ALI in the clinical setting.
Manuscript source: Unsolicited manuscript
Specialty type: Gastroenterology and hepatology
Country/Territory of origin: China
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