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Lead increases lipopolysaccharide-induced liver injury through tumor necrosis factor-[alpha] overexpression by monocytes/macrophages: role of protein kinase C and p42/44 mitogen-activated protein kinase.

Although lead and lipopolysaccharide (LPS), both important environmental pollutants, activate cells through different receptors and participate in distinct upstream signaling pathways, Pb increases the amount of LPS-induced tumor necrosis factor-[alpha] (TNF-[alpha]). We examined the cells responsible for the excess production of Pb-increased LPS-induced TNF-[alpha] and liver injury, and the roles of protein kiuase C (PKC) and p42/44 mitogen-activated protein kinase (MAPK) in the induction of TNF-[alpha]. Peritoneal injection of Pb alone (100 [micro]mol/kg) or a low dose of LPS (5 mg/kg) did not affect serum TNF-[alpha] or liver functions in A/J mice. In contrast, coexposure to these noneffective doses of Pb plus LPS (Pb+LPS) strongly induced TNF-[alpha] expression and resulted in profound liver injury. Direct inhibition of TNF-[alpha] or functional inactivation of monocytes/macrophages significantly decreased the level of Pb+LPS-induced serum TNF-[alpha] and concurrently ameliorated liver injury. Pb+LPS coexposure stimulated the phosphorylation of p42/44 MAPK and the expression of TNF-[alpha] in [CD14.sup.+] cells of cultured mouse whole blood, peritoneal macrophages, and RAW264.7 cells. Moreover, blocking PKC or MAPK effectively reduced Pb+LPS-induced TNF-[alpha] expression and liver injury. In summary, monocytes/macrophages were the cells primarily responsible for producing, through the PKC/MAPK pathway, the excess Pb-increased/LPS-induced TNF-[alpha] that caused liver injury. Key words: lead, lipopolysaccharide, liver injury, monocytes/macrophage, p42/44 mitogen-activated protein kinase, protein kinase C, tumor necrosis factor-[alpha]. doi:10.1289/ehp.8550 available via[Online 10 November 2005]


Tumor necrosis factor-[alpha] (TNF-[alpha]) regulates a variety of biologic functions, including organ development, immune homeostasis, and malignance. The body subtly regulates the expression kinetics and dose of TNF-[alpha] to ensure its proper effect because TNF-[alpha] has opposite biologic effects in different circumstances (Aggarwal 2003; Pfeffer 2003). On the one hand, TNF-[alpha] is essential for the host in tissue repair and in protective immune responses against infection. On the other hand, inadequate TNF-[alpha] may have detrimental consequences in sepsis, tumor formation, and autoimmune diseases. Regulating the expression of TNF-[alpha] has been an important subject in managing acute inflammatory diseases that include bacterial sepsis (Spooner et al. 1992). Recent studies on chronic neuronal disease revealed a new feature of inflammation: a transient spike of TNF-[alpha] expression (i.e., a large amount that peaks after 1.5 hr and disappears after 3 hr) may induce neuronal degeneration resembling the delayed and progressive nature of the symptoms in patients with Parkinson's disease (Gao et al. 2002). These findings indicate that the extent of TNF-[alpha] expression during a disease determines not only severity and survival rate but also delayed disease sequelae.

The in vivo lipopolysaccharide (LPS)-induced model of liver damage of mice, used to determine TNF-[alpha]--mediated organ failure, is both sensitive and convenient. LPS, a component of the outer membrane of gram-negative bacteria, plays a major role in inducing septic shock and is a potent inducer of TNF-[alpha] in vivo and in vitro (Goldfeld et al. 1990; Ulich et al. 1991). The binding of LPS to CD14/LPS-binding protein and Toll-like receptor-4 triggers multiple signal cascades that activate nuclear factor-[kappa]B and p42/44 mitogen-activated protein kinase (MAPK) and lead to the expression of proinflammatory cytokines, including TNF-[alpha] (Triantafilou and Triantafilou 2002). LPS causes liver injury at high doses (Kosai et al. 1999) but a modest, noninjurious inflammation at low doses (Ganey and Roth 2001) in several animal models. High-dose LPS-induced liver injury is partly attributed to excess TNF-[alpha] production (Hewett et al. 1993). TNF-[alpha]-associated signal transduction has been well characterized. TNF-[alpha] might trigger apoptosis in hepatocytes by signaling through the Fas-associated death-domain protein of the TNF receptor that activates caspases (Leist et al. 1996; Schuchmann et al. 2003). Blocking TNF production or trimming the signaling pathway using caspase-inhibitors reduces TNF-[alpha]--mediated liver injury (Kunstle et al. 1997). In addition, LPS induces apoptosis in macrophages through TNF-[alpha] (Comalada et al. 2003). Convincing evidence shows that metal pollutants in the living environment may modulate the effects of LPS. Among them, lead, an important industrial pollutant, not only altered the immune response (Luster et al. 1978) but also increased the mortality of an LPS challenge or bacterial infections in several animal studies (Dentener et al. 1989; Selye et al. 1966). Thus, the influence of environmental factors on TNF-[alpha] production is a significant issue.

Several pieces of evidence (Liu et al. 2001) suggest that Pb might act on calcium channels to alter intracellular calcium homeostasis in bone cells (Pounds 1984; Rosen and Pounds 1989; Schanne et al. 1989) and neuronal cells (Goldstein 1993; Pounds 1984; Rosen and Pounds 1989; Schanne et al. 1989). Although the cellular target of Pb is still elusive, exposure to Pb activates protein kinase C (PKC) in several types of cells, such as astrocytes and neuronal cells in the brain (Costa 1998; Markovac and Goldstein 1988). We previously (Cheng et al. 2004) demonstrated that Pb stimulates PKC to activate p42/44 MAPK, which results in the expression of TNF-[alpha] in glial cells. Although LPS and Pb trigger intracellular signals by different routes, Pb increases LPS-induced TNF-[alpha] production (Liu et al. 2005). Coexpesure to Pb plus LPS also induces TNF-[alpha] expression through PKC and p42/44 MAPK, causing liver injury in rats (Cheng and Liu 2005). In this study, we measured the liver injury in mice as the biologic end point for exploring the mechanism of Pb-increased/LPS-induced TNF-[alpha] expression. Thus, the aims of this study were to identify the cells in the blood responsible for TNF-[alpha] release and to reveal the role of PKC and p42/44 MAPK in the induction of TNF-[alpha] during coexposure to Pb plus LPS.

Materials and Methods

Chemicals. We obtained LPS (derived from Escherichia coli, serotype 055:B5), TNF-[alpha] inhibitor pentoxifylline (PTX), and macrophage cytotoxic agent Gd[Cl.sub.3-6][H.sub.2]O (gadolinium chloride hexahydrate) from Sigma Chemical (St. Louis, MO, USA). Lead acetate was purchased from Merck (Darmstadt, Germany). PKC inhibitor chelerythrine chloride ([C.sub.21][H.sub.18]N[O.sub.4]Cl) was obtained from Calbiochem (Bad Soden, Germany), and p42/44 MAPK inhibitor U0126 was purchased from Promega (Madison, WI, USA).

Cells and animals. Peritoneal macrophages were isolated by flushing the peritoneal cavity of A/J mice with 10 mL of sterile ice-cold phosphate buffer. Peritoneal lavage fluid was centrifuged at 200g, and pelleted cells were resuspended in Dulbecco's modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum (FBS), penicillin, and streptomycin (100 U/mL). Cells were then seeded at 2 x [10.sup.5]/well in a 96-well plate, incubated at 37[degrees]C for 4 hr, and washed with phosphate-buffered saline (PBS) to remove unattached cells. Attached cells, taken as macrophages and confirmed with F4/80 stain, were used for sequential experiments. RAW264.7 cells, a mouse macrophage cell line (American Type Culture Collection, Rockville, MD, USA), were cultured in DMEM supplemented with 10% FBS. A/J mice weighing 20-25 g were obtained from and housed in the laboratory animal center of our institution. Animals were housed individually in a room with a 12/12-hr light/dark cycle and central air-conditioning (25[degrees]C, 70% humidity), and were fed with standard food ad libitum. The animal experiment procedures were reviewed and implemented through the Institutional Animal Care and Use Committee process of National Cheng Kung University.

Blood collection and biochemistry study. The blood of mice was collected from the inferior vena cava under ethyl ether anesthesia, drawn using venipuncture into serum separation tubes, allowed to clot for 10 min at room temperature, and then centrifuged (1,000g, 10 min, 4[degrees]C). Serum samples were stored at 70[degrees]C. To determine the serum concentrations of aspartate aminotransferase (AST) and alanine aminotransferase (ALT), serum was spotted to slides (Fuji Dri-Chem; Fujifilm, Kanagawa, Japan) and evaluated using a slide analyzer (Fuji Dri-Chem 3500S; Fujifilm).

Preparation of mouse whole-blood and cytokine assays. Induction of TNF-[alpha] in mouse whole blood was performed as described previously (Mullarkey et al. 2003). Briefly, Pb and LPS were added to heparinized whole blood obtained from A/J mice (100 [micro]L/well). After 2 hr incubation at 37[degrees]C in a 5% C[O.sub.2] atmosphere, the blood was centrifuged at 1,000g for 10 min at 4[degrees]C. TNF-[alpha] in conditioned medium was determined using enzyme-linked immunosorbent assay (ELISA) (R&D Systems, Minneapolis, MN, USA), measuring absorbance at 450 nm and extrapolating from a standard curve with a sensitivity limit of 32.5 pg/mL.

Flow cytometric analysis. To identify the TNF-[alpha]-secreting cells, Pb or LPS was added to whole blood with monensin (eBioscience, San Diego, CA, USA). Red blood cells were lysed using hypotonic shock, and leukocytes were subjected to surface CD14 labeling using phycoerythrin-conjugated CD14 antibody (eBioscience). Cells were fixed and permeabilized using a commercial kit (Cytofix/ Cytoperm; PharMingen, San Diego, CA, USA) and stained for intracellular TNF-[alpha] using fluorescein isothiocyanate (FITC)-conjugated rat anti-mouse TNF-[alpha] Ab (PharMingen). To analyze the phosphorylation status of p42/44 MAPK in peritoneal macrophages, exudate cells were fixed using 2% formaldehyde; they were then resuspended in methanol at a concentration of 90%. Cells were incubated with the primary phospho-p42/44 MAPK antibody (New England Biolabs, Beverly, MA, USA) for 30 min at room temperature. After being washed in PBS containing 0.5% FBS, secondary antibody hybridization was carried out using goat anti-rabbit IgG (Alexa Fluor 488; Molecular Probes, Eugene, OR, USA). Macrophage-specific marker F4/80 was first stained with biotin-conjugated anti-F4/80 antibody and then with phycoerythrin-conjugated streptavidin secondary antibody (eBioscience). Flow cytometric analysis was then performed (FACSCalibur; Becton Dickinson, San Jose, CA, USA). Data were analyzed using the CellQuest (BD Biosciences, San Jose, CA, USA) and WinMDI 2.8 software packages (University of Massachusetts, Amherst, MA, USA).

Western blot analysis. RAW264.7 cells were cultured in 0.01% FBS/DMEM for 30 min and sequentially stimulated with Pb (10 [micro]M), LPS (1 ng/mL), Pb (10 [micro]M) plus LPS (Pb+LPS) (1 ng/mL), or saline (control). After stimulation, cells were washed with cold PBS and then solubilized with ice-cold buffer containing 25 mM HEPES (pH 7.5), 300 mM NaCl, 1.5 mM Mg[Cl.sub.2], 0.2 mM EDTA, 0.1% Triton X-100, 20 mM [beta]-glycerophosphate, 0.1 mM sodium orthovanadate, 0.5 mM dithiothreitol, 100 [micro]g/mL phenylmethylsulfonyl fluoride, and 2 [micro]g/mL leupeptin. Approximately 10-30 lag of protein was separated using electrophoresis in a 10% sodium dodecyl sulfate-polyacrylamide gel. After electrophoresis, the protein was electro-transferred onto polyvinylidene fluoride membranes (NEN Life Science Products, Inc., Boston, MA, USA). Membranes were probed with antibodies specific for phospho-p42/44 MAPK or p42/44 MAPK (New England Biolabs). After being probed with a horseradish peroxidase--conjugated secondary antibody, protein signals were visualized using enhanced chemiluminescence reagents (Amersham, Arlington Heights, IL, USA) combined with Kodak X-ML film exposure (Eastman-Kodak, Rochester, NY, USA).

Histology. Liver tissue obtained from mice was fixed in 3.7% buffered formalin and embedded in paraffin. Sections (5 [micro]m) were routinely stained with hematoxylin and eosin Y stain.

Statistical analysis. Data are expressed as mean [+ or -] SE. We used one-way or two-way analysis of variance and Student's t-test. Statistical significance was set at p < 0.05.


Expression of TNF-[alpha] and liver injury in mice after coexposure to Pb plus LPS. We evaluated the role of TNF-[alpha] in Pb-increased LPS-induced liver injury. A/J mice were intraperitoneally given Pb (100 [micro]mol/kg) (Shinozuka et al. 1996), LPS (5 mg/kg) (Ohta and Sitkovsky 2001), Pb+LPS (Pb, 100 [micro]mol/kg; LPS, 5 mg/kg), or saline (control). Blood was collected 1.5 hr later to determine serum TNF-[alpha] (Figure 1A) and 24 hr later to measure the levels of AST (Figure 1B) and ALT (Figure 1C) that indicate liver injury. Histologic examination of the liver was performed 24 hr post-treatment (Figure 2). Serum TNF-[alpha] was not detected in mice that received saline or Pb alone. Mice challenged with LPS alone showed a small amount of serum TNF-[alpha] (< 250 pg/mL) and a slight increase in AST (300 U/L) and ALT (30 U/L). However, we observed few histologic changes indicating hepatocellular damage in mice that received saline (Figure 2A), Pb alone (Figure 2B), or LPS alone (Figure 2C). Pb significantly increased LPS-induced TNF-[alpha] production in mice treated with Pb+LPS. The induction of serum TNF-[alpha] by LPS was drastically increased by Pb that reached around 2,000 pg/mL in 1.5 hr. Concurrently, the mean levels of AST and ALT were significantly elevated in the Pb+LPS group to 720 U/L and 600 U/L, respectively. In addition, Pb+LPS-treated mice showed multiple profoundly necrotic areas in the liver (Figure 2D).


To establish a causal relationship between TNF-[alpha] and liver injury, we used PTX, a potent inhibitor of TNF transcription in vivo (Lechner et al. 1993), to suppress the production of TNF-[alpha]. Mice that had been given PTX (100 mg/kg) 1 hr before Pb+LPS treatment had lower serum TNF-[alpha] than did those that had not been given PTX (Figure 3A). Along with a decrease in TNF-[alpha] induction, the Pb+LPS-stimulated AST (Figure 3B) and ALT levels (Figure 3C) were also markedly attenuated by PTX. Moreover, PTX significantly decreased the number of necrotic hepatocellular lesions in Pb+LPS-treated mice (Figure 2H).


TNF-[alpha] producing cells. We detected rare TNF-[[alpha].sup.+] cells in the liver using immunohisto-chemical staining (data not shown). We then checked blood cells using an in vitro whole-blood culture model. LPS (5 [micro]g/mL) increased the expression of mean TNF-[alpha] in whole-blood culture to 75 pg/mL (mean value) in 1.5 hr. Although Pb (1 [micro]M) itself did not induce detectable TNF-[alpha], it significantly increased the TNF-[alpha]-inducing effect of LPS, which then reached approximately 125 pg/mL (Figure 4A). Because [CD14.sup.+] macrophages/monocytes have been documented as a major source of TNF-[alpha] (Haziot et al. 1996), we analyzed the [CD14.sup.+] cells in the whole-blood culture after Pb+LPS coexposure. Using flow cytometric analysis, we determined whether [CD14.sup.+] cells were the primary TNF-[alpha]--secreting cells in blood. The cells were stained with phycoerythrin-anti-CD14 and FITC-anti-TNF-[alpha] after stimulation. TNF-[[alpha].sup.+]/[CD14.sup.+] cells (5.9%) were separated from single negative cells (Figure 4B, top right quadrant). Intracellular TNF-[alpha] stain showed that < 8% of the [CD14.sup.+] cells were in untreated or Pb-treated whole-blood culture. Approximately 12% of the [CD14.sup.+] cells in the LPS group were also TNF-[[alpha].sup.+]. Coexposure to Pb+LPS increased the number of TNF-[[alpha].sup.+] cells to about 20% of the [CD14.sup.+] cells (Figure 4C).


Macrophages/monocytes mediating Pb+LPS-induced liver injury. To confirm whether Pb+LPS-induced liver injury involves macrophages/monocytes, we inactivated macrophages/monocytes using GdCl3 (40 mg/kg) 24 hr before Pb+LPS treatment. Mouse peritoneal macrophages that received Gd[Cl.sub.3] were drastically reduced, and few cells expressed a high level of F4/80 (F4/[80.sup.high]), representing peritoneal macrophages in peritoneal exudate (data not shown). Gd[Cl.sub.3] decreased the level of serum TNF-[alpha] in mice that had received Pb+LPS (Figure 5A). In parallel with a reduction in TNF-[alpha], Gd[Cl.sub.3] markedly decreased serum AST (Figure 5B) and ALT (Figure 5C) measured 24 hr after Pb+LPS treatment. GdCl3 also reduced the number of hepatocellular lesions in mice that received Pb+LPS, as shown by reduced necrotic areas in the liver (Figure 2L).


The activation of p42/44 MAPK in peritoneal macrophages and RA W264. 7 cells treated with Pb+LPS. We examined whether Pb acted through the common PKC and p42/44 MAPK pathway to increase LPS-induced TNF-[alpha] expression in peritoneal macrophages and RAW264.7 cells. The endothelial cells around large vessels in the livers of mice treated with Pb+LPS showed phosphorylated p42/44 MAPK, but the hepatocytes did not (data not shown). We further characterized the phosphorylation status of p42/44 MAPK in peritoneal macrophages, which showed high F4/80 expression (Figure 6A). An increase in the phosphorylation of p42/44 MAPK in peritoneal macrophages was observed in the Pb+LPS group (Figure 6B, C). Similarly, Pb+LPS treatment induced phosphorylation of p42/44 MAPK in RAW264.7 cells (Figure 6D, E).


Effects of PKC and p42/44 MAPK inhibitors on TNF-[alpha] and liver injury in vivo. To evaluate the actions of PKC and p42/44 MAPK in vivo, mice were treated with either [C.sub.21][H.sub.18]N[O.sub.4]Cl (5 mg/kg) 30 min or U0126 (25 [micro]mol/kg) 10 min before being exposed to Pb, LPS, or Pb+LPS. Both [C.sub.21][H.sub.18]N[O.sub.4]Cl and U0126 effectively decreased the serum TNF-[alpha] induced by Pb+LPS (Figure 7A), as well as the AST and ALT levels elevated by Pb+LPS (Figure 7B, C). No obvious damage occurred in the livers of mice that had received [C.sub.21][H.sub.18]N[O.sub.4]Cl or U0126 alone (Figure 2M, Q). Both [C.sub.21][H.sub.18]N[O.sub.4]Cl and U0126 effectively attenuated the necrotic lesions developed in the livers of mice after Pb+LPS treatment (Figure 2P, T).


PKC and p42/44 MAPK in the induction of TNF-[alpha] in peritoneal macrophages and RAW264.7 cells. Pb (10 [micro]M) significantly increased the expression of TNF-[alpha] induced by low doses of LPS (0.1 and 1 ng/mL) in mouse F4/[80.sup.high] peritoneal macrophages (Figure 8A). In addition, Pb increased the expression of TNF-[alpha] in RAW264.7 cells after treatment with 1 or 10 ng/mL LPS (Figure 8D). This Pb-induced increase is more obvious at 10 [micro]M than at 1 [micro]M.


Using MAPK and PKC inhibitors, we demonstrated that p42/44 MAPK and PKC were involved in the Pb+LPS-induced TNF-[alpha] expression of peritoneal macrophages and RAW264.7 cells. At doses between 7.5 and 30 [micro]M, U0126, a p42/44 MAPK inhibitor, significantly suppressed the Pb+LPS-induced expression of TNF-[alpha]. (Figure 8B, E). At a dose of 5 [micro]g/mL, [C.sub.21][H.sub.18]N[O.sub.4]Cl, a PKC inhibitor, also reduced Pb+LPS-associated TNF-[alpha] expression (Figure 8C, F).


Monocytes/macrophages are the primary secretors of TNF-[alpha] during inflammation and infection (Beutler and Cerami 1989). We demonstrated that the harmful effects of these cells triggered by LPS may become worse for the host in the presence of Pb, as reflected by severe liver injury. Inactivating the function of these phagocytic cells and blocking the signal pathways for TNF-[alpha] production effectively relieve the damage caused by environmental insults such as LPS and Pb.

Pb and low doses of LPS neither directly stimulated TNF-[[alpha].sup.+] production nor activated phosphorylation of MAPK in hepatocytes other than endothelial cells. Previous studies on the cellular source of TNF-[alpha] in animal exposed to Pb or LPS were not conclusive. Pb might increase the transcription of TNF-[alpha] mRNA in hepatocytes (Kubo et al. 1996), and LPS might stimulate liver Kupffer cells to release TNF-[alpha] (Suzuki et al. 1996; Tsukada et al. 2003). However, in a mixed culture of hepatocytes and Kupffer cells, Pb and LPS stimulated only a small increase in the production of TNF-[alpha] that did not cause obvious cell death in the cultured hepatocytes (Milosevic and Maier 2000; Zhang et al. 1996). In our animal model, serum TNF-[alpha] rapidly (within 1.5 hr) reached maximal levels after the Pb+LPS challenge. Moreover, cells releasing TNF-[alpha] after LPS stimulation in vivo have been identified as [CD14.sup.+] (Haziot et al. 1996; Perera et al. 1997), but Kupffer cells express little CD14 (Lichtman et al. 1998). We also found that the TNF-[alpha] induced by Pb+LPS was expressed primarily by [CD14.sup.+] cells in the whole-blood culture and in mouse F4/[80.sup.+] peritoneal macrophages, which indicates that the TNF-[alpha] was produced by cells outside the liver. The increase in TNF-[alpha] caused by Pb in the serum of LPS-treated mice was approximately 10-fold. However, the increase of TNF-[alpha] was only 2-fold in peritoneal macrophages. This indicates that other cells and mechanisms might contribute to the Pb-increased LPS-induced TNF-[alpha] production in vivo and need further investigation.

A second line of evidence excluding hepatocytes as the source of TNF-[alpha] comes from studies of cell signaling. PKC and p42/44 MAPK are downstream signals of Pb stimulation in neurons (Olivi et al. 2003), bone-marrow-derived macrophages (Flohe et al. 2002), and glioma cells (Cheng et al. 2004), and they may regulate genes responding to Pb poisoning. Long-term exposure to Pb leads to PKC activation in rat livers; however, Pb also inhibited the activity of PKC[alpha] in a human hepatoma cell line (Liu et al. 1997; Tonner and Heiman 1997), and the inhibition was much more pronounced when Pb levels were high (Sun et al. 1999). Because circulating Pb will quickly deposit in the liver (Bornemann and Colburn 1985), we speculated (Cheng and Liu 2005) that a transient accumulation of Pb in the liver will suppress the activation of PKC and p42/44 MAPK in hepatocytes. Pb or LPS alone at the doses we used did not alter the phosphorylation of p42/44 MAPK in HepG2 cells (data not shown). In addition, in our animal model, we did not find phosphorylation of p42/44 MAPK in hepatocytes, further indicating that they were not induced to produce TNF-[alpha] in response to Pb exposure. In contrast to liver cells, coexposure to Pb+LPS significantly stimulated p42/44 MAPK phosphorylation in peritoneal macrophages; suppressing p42/44 MAPK phosphorylation or inhibiting PKC activity resulted in reduced TNF-[alpha] expression.

As mentioned above, both Pb and a high dose of LPS activated PKC and MAPK, which stimulated TNF-[alpha] expression (Cheng et al. 2004). In our study model, the synergistic effect of Pb+LPS was demonstrable: coexposing mice to Pb+LPS strongly induced TNF-[alpha] expression in peritoneal macrophages and in whole blood. In addition, significant interaction between the LPS-treatment factor and Pb-dose factor was indicated by dose-dependent TNF-[alpha] expression in different groups of RAW264.7 cells. Although Pb alone or LPS alone slightly increased the phosphorylation of MAPK in peritoneal macrophages, only coexposing them to Pb+LPS induced obvious p42/44 MAPK phosphorylation and TNF-[alpha] expression. Apparently, the minimal level of MAPK activation required to induce a large amount of TNF-[alpha] was higher than the levels of MAPK in cells after exposure to a single dose of Pb alone or LPS alone. After the signals initiated by Pb+LPS merged in the PKC and MAPK pathway, MAPK activation was sufficient for TNF-[alpha] production. That an otherwise insignificant effect of LPS in mice became vital after the mice had been co-exposed to Pb+LPS has implications for setting the maximal tolerable concentration for a particular pollutant. It seems that risk assessment based on a single-exposure experimental design does not truly reflect the hazard of an environmental pollutant to humans.

In conclusion, the PKC/MAPK pathway leading to TNF-[alpha] expression played a key role in Pb+LPS-induced liver injury in mice. Our results also indicate that immune cells are very sensitive to environmental pollution and emphasize the synergistic effect of multiple pollutants in disease progression. Specifically, monocytes/macrophages may serve as watchful janitors in response to Pb+LPS, even when it injures their host.

Received 30 July 2005; accepted 9 November 2005.


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Yu-Jung Cheng, (1,2) Bet-Chang Yang, (2,3) and Ming-Yie Liu (1,2)

(1) Department of Environmental and Occupational Health, (2) Institute of Basic Medical Sciences, and (3) Department of Microbiology and Immunology, National Cheng Kung University Medical College, Tainan, Taiwan

Address correspondence to B.-C. Yang, Department of Microbiology and Immunology, National Cheng Kung University Medical College, Tainan 70428, Taiwan. Telephone: 886-6-235-3535 Ext. 5637. Fax: 886-6-208-2705. E-mail:

We thank S.-T. Wang for comments on statistical analysis and B. Franke for editorial assistance.

This study was supported in part by grant NSC-94-2211-E-006-090 to M.-Y.L. (co-correspondence) and grant NSC-94-2314-B-006-050 to B.-C.Y. from the National Science Council, Taiwan.

The authors declare they have no competing financial interests.
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Title Annotation:Research
Author:Liu, Ming-Yie
Publication:Environmental Health Perspectives
Date:Apr 1, 2006
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