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Nuclear Factor– B Is Activated in Intestinal Mucosa During Endotoxemia
Timothy A. Pritts, MD;
M. Ryan Moon, MD;
Josef E. Fischer, MD;
Andrew L. Salzman, MD;
Per-Olof Hasselgren, MD
Arch Surg. 1998;133:1311-1315.
ABSTRACT
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Background The transcription factor nuclear factor– B (NF-B) regulates a large number of genes involved in the inflammatory response to critical illness. The intestinal mucosa plays an active role in the inflammatory and metabolic response to sepsis and endotoxemia, but it is not known if NF-B is activated in the mucosa during these conditions.
Objective To test the hypothesis that endotoxemia in mice activates NF-B in intestinal mucosa.
Methods Mice were injected subcutaneously with lipopolysaccharide, 12.5 mg/kg, or a corresponding volume of saline. At various intervals following injection, jejunal mucosa was harvested and nuclear and cytoplasmic fractions were prepared. The nuclear fractions were analyzed by electrophoretic mobility shift assay for NF-B activation and by Western blot analysis for the NF-B subunits p50 and p65. Cytoplasmic fractions were analyzed by Western blotting for the NF-B inhibitory proteins IB- and IB- .
Results Electrophoretic mobility shift assay showed that NF-B was activated in jejunal mucosa 1 hour after injection of lipopolysaccharide and persisted for at least 4 hours. The NF-B subunits p50 and p65 were present in nuclear fractions of mucosa from endotoxemic mice at the corresponding time points. Cytoplasmic levels of the inhibitory proteins IB- and IB- decreased during endotoxemia, and the proteins were nearly absent 60 minutes after injection of lipopolysaccharide.
Conclusions The results suggest that IB is degraded and NF-B is activated in intestinal mucosa during endotoxemia. The findings support the concept that the intestinal mucosa is an important component of the inflammatory response to sepsis and endotoxemia.
INTRODUCTION
THERE IS increasing evidence that the intestinal mucosa plays an important role in the inflammatory and metabolic response to sepsis, endotoxemia, and other critical illness.1 In recent studies from our and other laboratories, the local mucosal production of the proinflammatory cytokines tumor necrosis factor,2 interleukin (IL)-1,3 and IL-64 was increased in endotoxemic and septic mice. In other studies, we found that sepsis and endotoxemia were associated with mucosal synthesis of the acute-phase proteins complement component C3 and serum amyloid A.5 The genes for several proinflammatory cytokines and acute-phase proteins are regulated by the transcription factor nuclear factor–B (NF-B), but it is not known whether NF-B is activated in intestinal mucosa during sepsis and endotoxemia.
Nuclear factor–B is a dimer consisting of various subunits, most commonly p50 and p65, and is normally sequestered in an inactive form in the cytoplasm by the inhibitory factor IB (for review, see Baldwin6). After appropriate stimuli, IB is phosphorylated, ubiquitinated, degraded by the 26S proteasome, and dissociated from NF-B. Several species of IB have been described, including IB- and IB-.7 After dissociation of IB from NF-B, the activated transcription factor translocates to the nucleus, where it binds to DNA and up-regulates gene transcription.
Although there is evidence that NF-B may be activated by different stimuli in cultured enterocytes,8 the participation of NF-B in the inflammatory response in intestinal mucosa in vivo is not known. The present experiments were designed to test the hypothesis that endotoxemia results in activation of NF-B in intestinal mucosa measuring mucosal levels of IB and NF-B activation in the jejunum of endotoxemic mice. We found that endotoxemia was associated with degradation of mucosal IB- and IB- and increased DNA binding activity of NF-B.
MATERIALS AND METHODS
EXPERIMENTAL ANIMALS
Male A/J mice weighing 18 to 23 g (Jackson Laboratory, Bar Harbor, Maine) were housed in a room with a temperature of 25°C and with a 12-hour light-dark cycle for 1 week before experiments. Endotoxemia was induced by the subcutaneous injection of lipopolysaccharide (LPS), 12.5 mg/kg (Escherichia coli endotoxin 0111:B4, Calbiochem Co, La Jolla, Calif) dissolved in 0.5 mL of sterile saline. Control mice were injected with the same volume of sterile saline. The mice had free access to drinking water throughout the experiments, but food was withheld after LPS or saline injection to avoid the influence of any difference in food intake between the groups of mice on mucosal responses. The dose and route of LPS administration used were based on a recent study in which mucosal IL-6 production was increased in endotoxemic mice.4 The animals were cared for in accordance with the National Research Council's Guide for the Care and Use of Laboratory Animals. The experiments were approved by the Institutional Animal Care and Use Committee at the University of Cincinnati, Cincinnati, Ohio.
At different time points up to 4 hours after injection of saline or LPS, animals were anesthetized with pentobarbital sodium (40 mg/kg intraperitoneally), and the abdomen was opened through a midline incision. The jejunum was excised, flushed with ice-cold saline, and opened along the antimesenteric border. This procedure was done on an ice-cold board. The intestinal mucosa was harvested by scraping with a microscope slide, and the samples were immediately frozen in liquid nitrogen and stored at -80°C until analysis. The jejunum was studied because in previous reports we found that the response to sepsis and endotoxemia with regard to mucosal protein synthesis,9 IL-6 production,10 and acute-phase protein synthesis5 was more pronounced in the jejunum than in other parts of the gastrointestinal tract. Because in a recent study NF-B was activated in liver of endotoxemic mice,11 in an initial experiment, the left lobe of the liver was excised in addition to the jejunum to compare the response to endotoxemia in the 2 tissues.
PREPARATION OF NUCLEAR AND CYTOPLASMIC FRACTIONS
Nuclear and cytoplasmic fractions were prepared as described elsewhere12 with minor modifications. All steps were carried out on ice. Tissue samples were homogenized (Power Gen 700, Fischer Scientific, Indianapolis, Ind) in 1 mL of ice-cold buffer A (10-mmol/L HEPES, pH 7.9; 1.5-mmol/L magnesium chloride; 10-mmol/L potassium chloride; 1-mmol/L dithiothreitol; and 1-mmol/L phenylmethylsulfonylfluoride) and allowed to incubate on ice for 10 minutes. The samples were then centrifuged at 850g for 10 minutes at 4°C. The supernatants were discarded, and the pellets were resuspended in 400 µL of buffer A with 0.1% Triton X-100 (Sigma, St Louis, Mo), incubated for 10 minutes on ice, and centrifuged as above. The supernatant was removed and saved as the cytoplasmic fraction. The pellet was resuspended in 750 µL of buffer A, centrifuged as above, and resuspended in 200 µL of a buffer consisting of 20-mmol/L HEPES, pH 7.9, 25% glycerol (vol/vol), 420-mmol/L sodium chloride, 1.5-mmol/L magnesium chloride, and 0.2-mmol/L EDTA. After incubation for 30 minutes on ice, the nuclear fraction was recovered by centrifugation at 20,000g for 15 minutes at 4°C. The nuclear and cytoplasmic fractions were assayed for protein concentration by means of an assay kit (Bio-Rad Laboratories, Hercules, Calif) and stored at -8°C until further analysis.
ELECTROPHORETIC MOBILITY SHIFT ASSAY (EDTA)
Nuclear factor–B gel shift oligonucleotide 5‘ AGT TGA GGG GAC TTT CCC AGG C 3‘ (Santa Cruz Laboratories, Santa Cruz, Calif) was end labeled with phosphorus 32  –adenosine triphosphate with the use of polynucleotide kinase T4 (Gibco BRL, Grand Island, NY). End-labeled probe was purified from unincorporated (32P) –adenosine triphosphate by means of a purification column (Bio-Rad Laboratories) and recovered in Tris-EDTA buffer, pH 7.4. Aliquots of the nuclear fractions (7.5 µg of protein) were incubated in buffer containing 12% glycerol (vol/vol); 12-mmol/L HEPES, pH 7.9; 4-mmol/L Tris hydrochloride, pH 7.9; 1-mmol/L EDTA; 1-mmol/L dithiothreitol; 25-mmol/L potassium chloride; 5-mmol/L magnesium chloride; 0.04-µg/µL poly (d[I-C]) (Boehringer Mannheim, Indianapolis); and Tris-EDTA. Labeled probe was added and the samples were incubated for 10 minutes on ice. Where indicated in the "Results" section, an excess of unlabeled NF-B consensus DNA (20 ng) was added for competition reactions. For supershift reactions, 2 µL of antibody to one of the NF-B subunits p50, p52, or p65 (Santa Cruz Laboratories) was added 1 hour before addition of the radiolabeled probe. Samples were then subjected to electrophoretic separation on a nondenaturing 5% polyacrylamide gel at 30 mA with Tris borate EDTA buffer (0.45-mol/L Tris borate, 0.001-mol/L EDTA, pH 8.3). Blots were dried at 80°C for 1 hour and analyzed by exposure to radiographic film (X-Omat AR; Eastman-Kodak, Rochester, NY).
WESTERN BLOT ANALYSIS
Aliquots of the nuclear or cytoplasmic fractions containing 25 µg of protein were boiled in equal volumes of loading buffer (125-mmol/L Tris hydrochloride, pH 6.8; 4% sodium dodecyl sulfate; 20% glycerol; and 10% 2-mercaptoethanol) for 3 minutes, and then separated by electrophoresis on an 8% to 16% Tris-glycine gradient gel (Novex, San Diego, Calif). A protein ladder (See-Blue Standard, Novex) was included as a molecular weight marker. The proteins were then transferred to nitrocellulose membranes by means of a transfer apparatus (Xcell II Blot Module, Novex). The membranes were blocked with 10% nonfat dried milk in Tris-buffered saline, pH 7.6, containing 0.05% polyoxyethylene sorbitan monolaurate (Tween-20, Bio-Rad Laboratories) for 1 hour and then incubated with a polyclonal rabbit antimouse antibody to IB-, IB-, p50, or p65 (Santa Cruz Laboratories) for 45 minutes. After washing twice in Tris-buffered saline containing 0.05% Tween-20, the blots were incubated with a peroxidase-conjugated goat anti–rabbit IgG secondary antibody for 15 minutes. The blots were washed in Tris-buffered saline containing 0.05% Tween-20 for 5 minutes 3 times, then in Tris-buffered saline for 5 minutes, incubated in enhanced chemiluminescence reagents (Amersham Life Sciences, Buckingham, England), and exposed on radiographic film (Eastman-Kodak).
RESULTS
In an initial experiment, electrophoretic mobility shift assay (EMSA) was performed on liver tissue and jejunal mucosa 1 hour after injection of saline or LPS. Similar to a recent report,11 endotoxemia resulted in NF-B activation in the liver (Figure 1). Nuclear factor–B DNA binding activity was seen 1 hour after LPS injection in jejunal mucosa as well. Whereas no NF-B activation was seen in the liver of saline-injected control mice, there was evidence of NF-B activation in jejunal mucosa from both control and endotoxemic mice. In multiple experiments (n=10), there was always a clear increase in NF-B activation in jejunal mucosa 1 hour after injection of LPS as compared with saline-injected animals. When excess unlabeled oligonucleotide was added, the NF-B band disappeared (last lane in Figure 1), indicating that the complex seen reflected NF-B binding activity.
We next examined NF-B activation in jejunal mucosa at different time points after injection of saline or LPS. The results from that experiment showed evidence of maximal NF-B activation 1 hour after injection of LPS, with a decline in binding activity during the next 3 hours (Figure 2). No increase in NF-B binding activity was seen earlier than 1 hour after induction of endotoxemia.
To investigate the composition of the DNA-binding complex, supershift analysis was performed. A supershift was seen after incubation with antibody to the NF-B subunit p50 (Figure 3). Little or no supershift was noted when antibodies to p52 and p65 were used. The greatest supershift was seen when antibodies to p50 and p65 were used together. These results suggest that the activated NF-B complex was composed primarily of p50 subunits.
When Western blot analysis of the nuclear fraction of jejunal mucosa was performed, results showed that p50 and p65 appeared at high concentrations in this fraction 1 hour after injection of LPS and thereafter declined during the next 3 hours (Figure 4). This result is consistent with translocation of both p50 and p65 to the nucleus in endotoxemic mice.
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Figure 4. Western blot analysis of the nuclear fraction of jejunal mucosa at different time points after injection of saline or lipopolysaccharide (LPS) in mice. Antibodies against p50 (top) and p65 (bottom) were used in these Western blots.
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Nuclear factor–B is usually activated by the degradation and dissociation of IB from NF-B.13 Western blot analysis showed that IB- and IB- levels in the cytoplasmic fraction of jejunal mucosa decreased in endotoxemic mice; the inhibitory proteins were almost not detectable at 1 hour after injection of LPS but reappeared at 2 hours (Figure 5). Notably, the changes in concentrations over time were almost identical for IB- and IB-. These results are consistent with degradation of the inhibitory proteins in intestinal mucosa during endotoxemia followed by a relatively rapid resynthesis of the proteins, similar to changes in IB levels in other tissues after stimulus.14-15
COMMENT
In the present study, endotoxemia in mice resulted in disappearance of IB and activation of NF-B in jejunal mucosa. Results from the experiments in which supershift assay and Western blot analysis of the nuclear fraction were performed suggest that the activated NF-B consisted primarily of p50 subunits, but that p65 subunits were present as well. This is the first report of NF-B activation in intestinal mucosa in vivo during endotoxemia. The results lend further support to the concept that the intestinal mucosa participates in the inflammatory response to endotoxemia.
In recent studies from our and other laboratories, the local production of tumor necrosis factor,2 IL-1,3 IL-6,4 and the acute-phase proteins C3 and serum amyloid A5 was increased in intestinal mucosa during sepsis and endotoxemia. Nuclear factor–B activates the genes for several proinflammatory cytokines and acute-phase proteins (for review, see Baldwin6). It may therefore be speculated that the results observed in the present study reflect a role of NF-B in the transcriptional regulation of mucosal cytokines and acute-phase protein synthesis. Further experiments will be needed, however, to clarify the relationship between NF-B activation and the synthesis of proinflammatory cytokines and acute-phase proteins in the intestinal mucosa.
The result of up-regulated NF-B activity in the liver 1 hour after injection of LPS was similar to a recent report11 and suggests that NF-B is activated in multiple organs and tissues during endotoxemia. The liver is an important production site for proinflammatory cytokines and acute-phase proteins during sepsis and endotoxemia, and the genes for these inflammatory products may be regulated by NF-B in the liver as well.
The classic form of NF-B is a p50/65 dimer. Besides p50/65, NF-B may consist of homodimers and heterodimers of these and other subunits.7 In the present study, supershift analysis suggested that the NF-B binding complex consisted mainly of p50 subunits. However, Western blotting indicated that p65 translocated to the nuclear fraction as well. These apparently conflicting results may reflect a greater abundance of p50 than p65 in the nuclear fraction, or a greater sensitivity of Western blotting than of supershift analysis to detect proteins present in the nuclear fraction.
Several members of the IB family have been described, including IB-, IB-, IB-, IB- , and IB- .16 The best-known IB molecules are IB- and IB-. IB- is usually degraded rapidly after stimulus, whereas IB- degradation is delayed and more protracted and has been suggested to account for a more prolonged inflammatory response.17 The finding in the present study that IB- and IB- degradation (ie, disappearance) showed similar time courses was surprising and may indicate that the breakdown of these molecules is regulated differently in different cell types and tissues. In a recent study, IB- degradation occurred more than an hour later than the degradation of IB- in liver tissue during endotoxemia.14
It should be noted that in the present study EMSA was performed on whole mucosa, and it is not known in which cell type(s) NF-B activation took place. In recent studies from our8 and other18 laboratories, evidence was found that NF-B is activated after stimulus in cultured enterocytes. Thus, it is possible that the present results at least in part reflected NF-B activation in enterocytes, although other mucosal cells may have participated in the response as well.
Jejunal mucosa was studied in the present report because we found previously that this segment of the gastrointestinal tract is particularly sensitive to the effects of sepsis and endotoxemia with respect to the production of IL-6,10 total proteins,19 and acute-phase proteins.5 It will be important in future experiments to test whether sepsis and endotoxemia result in NF-B activation in other parts of the gastrointestinal tract as well.
The intracellular pathways involved in NF-B activation in intestinal mucosa are not known from the present study. In a recent report we found that NF-B activation in cultured human enterocytes required serine protease activity but not tyrosine kinase activity or oxygen radicals.20 This was different from several other cell types in which these mechanisms were involved in NF-B activation.21-22 Thus, NF-B activation may be regulated by different intracellular mechanisms in different cell types and tissues. The intracellular signaling pathways involved in the regulation of NF-B activation in intestinal mucosa will be an important area for future research considering the potential consequences of mucosal NF-B activation during sepsis, endotoxemia, and perhaps other conditions as well.
In recent in vitro experiments, we found that NF-B was activated in cultured human intestinal epithelial cells by IL-1.8 It remains to be determined whether IL-1 plays a similar role in intestinal mucosa in vivo.
AUTHOR INFORMATION
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Supported in part by grant 8510 from the Shriners of North America, Tampa, Fla (Dr Hasselgren) and grant 1R01HL59352-01 from the National Institutes of Health, Bethesda, Md (Dr Salzman). Dr Pritts was supported by training grant 1T32GM08478 from the National Institutes of Health. Dr Moon was supported by a research fellowship from the Surgical Infection Society (Zeneca ICI Fellowship Award).
Presented at the 18th Annual Meeting of the Surgical Infection Society, New York, NY, April 30, 1998.
Reprints: Per-Olof Hasselgren, MD, Department of Surgery, University of Cincinnati Medical Center, 231 Bethesda Ave, Mail Location 558, Cincinnati, OH 45267 (e-mail: hasselp{at}email.uc.edu).
Statement of Clinical Relevance
Sepsis continues to be a major cause of morbidity and mortality in surgical patients. Recent studies have shown that the intestinal mucosa plays an important role in the inflammatory response to sepsis and endotoxemia, producing both proinflammatory cytokines and certain acute-phase proteins. The regulatory mechanisms of this response are not well understood. The transcription factor NF-B regulates the transcription of the genes for a large number of inflammatory proteins. Previous studies in our laboratory have demonstrated that NF-B is activated by different inflammatory stimuli in cultured enterocytes in vitro, but the role of NF-B in the intestinal mucosa in vivo is not known. The present study provides evidence that NF-B is activated in the intestinal mucosa in vivo during endotoxemia. Understanding the role of NF-B in the inflammatory response in the intesinal mucosa during endotoxemia may eventually allow therapeutic manipulation of this response in the intestine.
From the Department of Surgery, University of Cincinnati (Drs Pritts, Moon, Fischer, and Hasselgren); Division of Critical Care, Children's Hospital Medical Center (Dr Salzman); and Shriners Hospital for Children (Drs Pritts, Moon, Fischer, and Hasselgren), Cincinnati, Ohio.
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Discussion
Mitchell Fink, MD, Boston, Mass: The results of these carefully performed experiments speak for themselves: NF-B is activated in jejunal mucosa following the injection of lipopolysaccharide in mice. The intestinal mucosa, however, is a complex tissue and consists of myriad cell types, including enterocytes, intraepithelial and subepithelial lymphocytes, intraepithelial and subepithelial lymphocytes of various subtypes, plasma cells, polymorphonuclear leukocytes, macrophages, mast cells, endothelial cells, and specialized antigen-processing, or M cells. Even among the enterocytes themselves are multiple subtypes, including primordial and pluripotent crypt cells, villus-absorptive enterocytes, goblet cells, Panneth cells, and enterochromaffin cells. Thus the obvious question to ask is, which mucosal cell populations is NF-B being activated in? Have the authors done any studies using eluted epithelial cells in an effort to narrow the field at least partially?
Finally, let's assume for the moment that endotoxin activates NF-B in enterocytes in vivo. What do the authors think the mechanism might be, since in vitro cultured enterocytes do not seem to respond to LPS even in the presence of serum? Does LPS activate some other cells, say macrophages in the lamina propria, triggering the production of interferon gamma and possibly other cytokines that in turn activate NF-B in enterocytes? Or is it possible that, unlike cultured, immortalized enterocytic cell lines, native enterocytes are actually responsive to LPS?
Dr Pritts: The intestinal mucosa is indeed a very complex tissue composed of many cell types. We have not yet examined which specific cell type (or types) are activated during endotoxemia in vivo. As you also noted, we have previously shown that NF-B can be activated in cultured enterocytes in vitro, and in other studies we have also used immunohistochemistry to show that the enterocytes produce IL-6 in vivo in the intestinal mucosa. We feel that this provides circumstantial evidence that NF-B may be activated in enterocytes in vivo, but we will need to address that in further studies.
You also asked about potential mechanisms of NF-B activation in the intestinal mucosa in vivo, pointing out that cultured enterocytes, at least under most conditions, do not appear to react to endotoxin directly in vitro. Further studies will be needed to address the mechanisms leading to in vivo NF-B activation in detail. It is our suspicion that IL-1 and TNF- may at least play a role.
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