- Open Access
Chlorotyrosine protein adducts are reliable biomarkers of neutrophil-induced cytotoxicity in vivo
© Gujral et al; licensee BioMed Central Ltd 2004
- Published: 14 January 2004
A limitation for investigating the pathophysiological role of neutrophils in vivo is the lack of a reliable biomarker for neutrophil cytotoxicity in the liver. Therefore, we investigated if immunohistochemical detection of chlorotyrosine protein adducts can be used as a specific footprint for generation of neutrophil-derived hypochlorous acid in vivo.
C3Heb/FeJ mice were treated with 100 micrograms/kg endotoxin (ET) alone or in combination with 700 mg/kg galactosamine (Gal/ET). Some animals received additionally two doses of 10 mg/kg of the pancaspase inhibitor Z-VAD-fmk. An antibody against chlorotyrosine was used for the immunohistochemical analysis.
At 6 h after Gal/ET, hepatocellular apoptosis was evident without increase in plasma ALT activities. Neutrophils accumulated in sinusoids but there was no evidence for chlorotyrosine staining. At 7 h after Gal/ET, about 54% of the sequestered neutrophils had extravasated, there was extensive necrosis and increased plasma ALT activities. Extensive immunostaining for chlorotyrosine, mainly colocalized with neutrophils, could be observed. Treatment with Z-VAD-fmk eliminated apoptosis, necrosis and the increase in plasma ALT values. Neutrophil extravasation was prevented but the overall number of neutrophils in the liver was unchanged. Chlorotyrosine staining was absent in these samples. After ET alone (7 h), sinusoidal neutrophil accumulation was similar to Gal/ET treatment but there was no apoptosis, neutrophil extravasation, ALT release or chlorotyrosine staining.
Chlorotyrosine staining in liver samples correlated well with evidence of neutrophil-induced liver injury in the endotoxemia model. These results indicate that assessment of chlorotyrosine protein adduct formation by immunohistochemistry could be a useful marker of neutrophil-induced liver cell injury in vivo.
- Liver Section
- Alcoholic Hepatitis
- Hypochlorous Acid
- Liver Cell Injury
- Hepatocellular Apoptosis
Neutrophils are involved in the pathophysiology of hepatic ischemia-reperfusion injury, endotoxin- and sepsis-induced liver failure, alcoholic hepatitis, and certain drug toxicities . Prerequisite for neutrophil cytotoxicity is the accumulation in sinusoids, extravasation and the adherence to the parenchymal cells . Neutrophils cause cell injury by generation of reactive oxygen species and protease release [3–6]. A limitation for investigating the pathophysiological role of neutrophils in vivo is the lack of a reliable biomarker for neutrophil cytotoxicity in the liver. Neutrophils generate superoxide with NADPH oxidase. They also release myeloperoxidase at the same time and, therefore, form hypochlorous acid as a major oxidant . Hypochlorous acid is a potent chlorinating agent which can cause the formation of chlorotyrosine protein adducts . Antibodies can be generated to detect chlorotyrosine in the tissue [8, 9]. However, this approach has never been validated in models of neutrophil-induced liver injury in vivo. Therefore, we investigated if immunohistochemical detection of chlorotyrosine protein adducts can be used as a specific footprint for generation of neutrophil-derived hypochlorous acid in vivo. To test this hypothesis, we used the well-characterized model of galactosamine/endotoxin (Gal/ET)-induced liver injury, where neutrophil cytotoxicity aggravates the initial apoptotic injury , by a reactive oxygen-dependent mechanism .
Neutrophil extravasation, liver injury and chlorotyrosine adduct formation during murine endotoxemia.
Number of Extravasated Neutrophils (per 10 HPF)
Plasma ALT Activities (U/L)
Chlorotyrosine Staining (Intensity)
0 – 0
64 – 16
0 – 0
Gal/ET 6 h
23 – 3
41 – 9
15 – 2*
Gal/ET 6 h + ZVAD
6 – 2
18 – 13
2 – 1#
Gal/ET 7 h
186 – 30*,$
1252 – 369*,$
45 – 2*,$
Gal/ET 7 h + ZVAD
19 – 5#
10 – 3#
3 – 1#
Gal/ET treatment causes caspase activation and hepatocellular apoptosis . To confirm this, hepatic caspase-3 activities were measured using a synthetic fluorogenic caspase-3 substrate, Ac-DEVD-MCA. Compared to controls, caspase-3 activities increased by 365-fold and 600-fold at 6 h and 7 h, respectively. Hepatocellular apoptosis was quantified, using morphological criteria, in liver sections stained with the terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay, and expressed as a percentage of the total cells evaluated [11, 12]. Apoptotic cells were rare in control livers (<0.1%). After Gal/ET treatment, hepatocellular apoptosis increased to 13% at 6 h and 19% at 7 h.
If parenchymal cell apoptosis is prevented by various caspase inhibitors  or by injection of endotoxin without galactosamine , transmigration of neutrophils does not occur and any injury is eliminated. Therefore, in order to investigate the effect of a pancaspase inhibitor on neutrophil-induced cytotoxicity and chlorotyrosine adduct formation, animals were treated with Z-VAD-fmk in addition to Gal/ET. Z-VAD reduced the hepatic caspase-3 activities to baseline and the hepatocellular apoptosis at 6 and 7 h by 90%. It also reduced the number of extravasated neutrophils in the tissue and liver cell injury (plasma ALT and necrosis) at 7 h, by 90% (Table 1). This was accompanied by reduced immunostaining for chlorotyrosine adducts inside the hepatocytes. Only mild positive staining was observed in the sinusoids around the neutrophils. However, the pancaspase inhibitor did not affect the total number of neutrophils accumulated in the livers at both time points, i.e., 6 h and 7 h after Gal/ET.
These data show that the formation of chlorotyrosine protein adducts closely follows the extravasation of neutrophils (Gal/ET 7 h). Protein adduct formation also correlated well with the dramatic increase in the plasma ALT levels and liver cell necrosis as indicators for cytotoxicity of neutrophils. These findings are consistent with the hypothesis that the activated neutrophils generated hypochlorous acid. In contrast, no adducts were formed during the early phase of the apoptotic injury, i.e., when 90% of the neutrophils in the liver remained inactive in the sinusoids (Gal/ET 6 h). Likewise, no protein adducts were formed when the neutrophils were primed but not fully activated (ET 7 h), or when the chemotactic signal for neutrophil extravasation was removed by elimination of the apoptotic cell injury (Gal/ET 7 h + ZVAD). Neutrophils can mediate tissue injury either through reactive oxygen species or the release of proteases [3–6]. In this regard, our study further supports the role of reactive oxygen species, and hypochlorous acid in particular, in neutrophil-induced cytotoxicity in vivo.
Chlorotyrosine-protein adducts are formed in the liver during murine endotoxemia, a well-established model of neutrophil-induced liver injury in vivo. These adducts can be easily and reliably detected through immunohistochemistry and, thus, can serve as a valuable biomarker for neutrophil-induced cytotoxicity.
Male C3Heb/FeJ mice (Jackson Laboratories, Bar Harbor, ME) were treated i.p. with 100 micrograms/kg Salmonella abortus equi endotoxin (ET) alone or in combination with 700 mg/kg galactosamine (Gal/ET; Sigma Chemical Co., St. Louis, MO). Animals were sacrificed 6 or 7 h after treatment. Some animals received additionally two 10 mg/kg doses of the pancaspase inhibitor Z-VAD-fmk (Enzyme Systems Products, Dublin, CA) at 3 and 4.5 h after Gal/ET. An antibody against chlorotyrosine was generated by standard procedures and used for the immunohistochemical analysis . The following parameters were measured as previously described: caspase-3 activity , DNA strand breaks with terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL staining) [11, 12], neutrophil localization (anti-Gr1 immunostaining), plasma ALT activities , imunohistochemistry for chlorotyrosine adducts, and histological assessment of necrosis in liver sections stained with H&E [11, 12].
- Jaeschke H: Reactive oxygen and mechanisms of inflammatory liver injury. J Gastroenterol Hepatol. 2000, 15: 718-724. 10.1046/j.1440-1746.2000.02207.x.View ArticlePubMedGoogle Scholar
- Chosay JG, Essani NA, Dunn CJ, Jaeschke H: Neutrophil margination and extravasation in sinusoids and venules of the liver during endotoxin-induced injury. Am J Physiol. 1997, 272: G1195-G1200.PubMedGoogle Scholar
- Jaeschke H, Ho Y-S, Fisher MA, Lawson JA, Farhood A: Glutathione peroxidase deficient mice are more susceptible to neutrophil-mediated hepatic parenchymal cell injury during endotoxemia: importance of an intracellular oxidant stress. Hepatology. 1999, 29: 443-450. 10.1002/hep.510290222.View ArticlePubMedGoogle Scholar
- Jaeschke H, Farhood A, Smith CW: Neutrophil-induced liver cell injury in endotoxin shock is a CD11b/CD18 – dependent mechanism. Am J Physiol. 1991, 261: G1051-G1056.PubMedGoogle Scholar
- Mavier P, Preaux A-M, Guigui B, Lescs MC, Zafrani ES, Dhumeaux D: In vitro toxicity of polymorphonuclear neutrophils to rat hepatocytes: Evidence for a proteinase-mediated mechanism. Hepatology. 1988, 8: 254-258. 10.1002/hep.1840080211.View ArticlePubMedGoogle Scholar
- Harbrecht BG, Billiar TR, Curran RD, Stadler J, Simmons RL: Hepatocyte injury by activated neutrophils in vitro is mediated by proteases. Ann Surg. 1993, 218: 120-128. 10.1097/00000658-199308000-00002.PubMed CentralView ArticlePubMedGoogle Scholar
- Domigan NM, Charlton TS, Duncan MW, Winterbourn CC, Kettle AJ: Chlorination of tyrosyl residues in peptides by myeloperoxidase and human neutrophils. J Biol Chem. 1995, 270: 16542-16548. 10.1074/jbc.270.28.16542.View ArticlePubMedGoogle Scholar
- Hazell LJ, Arnold L, Flowers D, Waeg G, Malle E, Stocker R: Presence of hypochlorite-modified proteins in human atherosclerotic lesions. J Clin Invest. 1996, 97: 1535-1544. 10.1172/JCI118576.PubMed CentralView ArticlePubMedGoogle Scholar
- Malle E, Woenckhaus C, Waeg G, Esterbauer H, Grone EF, Groene HJ: Immunological evidence of hypochlorite-modified proteins in human kidney. Am J Pathol. 1997, 150: 603-615.PubMed CentralPubMedGoogle Scholar
- Jaeschke H, Fisher MA, Lawson JA, Simmons CA, Farhood A, Jones DA: Activation of caspase-3 (CPP32)-like proteases is essential for TNF-alpha-induced hepatic parenchymal cell apoptosis and neutrophil-mediated necrosis in a murine endotoxin shock model. J Immunol. 1998, 160: 3480-3486.PubMedGoogle Scholar
- Gujral JS, Farhood A, Knight TR, Bajt ML, Jaeschke H: Mode of cell death after acetaminophen overdose in mice: apoptosis or oncotic necrosis?. Toxicol Sci. 2002, 67: 322-328. 10.1093/toxsci/67.2.322.View ArticlePubMedGoogle Scholar
- Gujral JS, Bucci TJ, Farhood A, Jaeschke H: Mechanism of cell death during hepatic ischemia-reperfusion in rats: Apoptosis or necrosis?. Hepatology. 2001, 33: 397-405. 10.1053/jhep.2001.22002.View ArticlePubMedGoogle Scholar
- Matthews AM, Roberts DW, Hinson JA, Pumford NR: Acetaminophen-induced hepatotoxicity. Analysis of total covalent binding vs. specific binding to cysteine. Drug Metab Dispos. 1996, 24: 1192-1196.PubMedGoogle Scholar
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