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Kupffer cells promote lead nitrate-induced hepatocyte apoptosis via oxidative stress

Comparative Hepatology volume 2, Article number: 8 (2003) Cite this article

Abstract

Background

Apoptosis and its modulation are crucial factors for the maintenance of liver health, allowing hepatocytes to die without provoking a potential harmful inflammatory response through a tightly controlled and regulated process. Since Kupffer cells play a key role in the maintenance of liver function, the aim of this study was to verify whether Kupffer cells are involved in the induction of liver apoptosis after i.v. injection of Pb(NO3)2 likely by secretion mechanisms.

Results

The in vivo hepatic apoptosis, induced by Pb(NO3)2 was prevented by a pre-treatment with gadolinium chloride (GdCl3), a Kupffer cells toxicant, that suppresses Kupffer cell activity and reduces to a half the apoptotic rate. In addition, in vivo Pb(NO3)2 administration deprives hepatocytes of reduced glutathione, whereas the loss of this important oxidation-preventing agent is considerably mitigated or abolished by pre-treatment with GdCl3. However, incubation of isolated hepatocytes and Kupffer cells and HepG2 cells with Pb(NO3)2 for 24 hours induced necrotic but not apoptotic cells. Apoptosis of hepatocytes and HepG2 cells was observed only after the addition of conditioned medium obtained from Kupffer cells cultured for 24 hours with Pb(NO3)2, thus indicating the secretion of soluble mediators of apoptosis by Kupffer cells. Apoptosis in the HepG2 cells was observed upon 24-hours incubation of HepG2 cells with 1 mM buthionine sulfoximine, a glutathione depleting agent, thus showing that there is an oxidative apoptogenic pathway in HepG2 cells.

Conclusion

Pb(NO3)2 has, at most, a direct necrotic (but not apoptogenic) effect on hepatocytes and HepG2 cells, giving a clue about the regulatory role of Kupffer cells in the induction of liver apoptosis after a single Pb(NO3)2 injection without pre-treatment with GdCl3, probably via secreting soluble factors that trigger oxidative stress in target cells.

Background

Every cell contains the making of its own demise, and apoptosis is the genetically programmed housekeeping mechanism by which the organism maintains health and homeostasis – ridding itself of aging, infected, damaged, mutated or excessive cells. Apoptosis is a normal physiological response to a lack of survival signals or to specific "suicidal signals" from the cytoplasm or from the intercellular environment, always leading to programmed pathways with well-defined biochemical and morphological features [1–4]. The cytoplasm of a cell undergoing apoptosis shrinks without membrane rupture, plasma and nuclear membranes develop bubble-like blebs, chromatin condenses and migrates to nuclear membrane and undergoes internucleosomal cleavage; finally, the cell contents are packed into membrane-bounded bodies (with organelles still functioning) to be ingested by neighbour counterparts (during the apoptotic process, epitopes appear on plasma membrane marking the cell as a phagocytic target). For this reason there is no cellular leakage and no inflammation [5, 6].

It has emerged from studies of apoptosis that the liver is a privileged system. In fact, although under normal conditions apoptosis occurs at a negligible rate in the liver (1–5 apoptotic hepatocytes/ 10 000 hepatocytes) [7, 8], this organ is constantly exposed to a variety of potentially apoptogenic, immune, inflammatory, and metabolic stimuli. Liver apoptosis has been observed under physiological, pathological, and experimental conditions [3]. Hepatocyte loss throughout apoptosis has been observed during physiological liver cell renewal; furthermore, liver regression during starvation is accompanied by an enhanced rate of apoptosis [9]. Beside this, apoptosis is responsible for cellular depletion after the "overshoot" of cell regeneration following partial hepatectomy or the withdrawal of liver hyperplasia-inducing treatments like Pb(NO3)2 [10–12]. Apoptosis of hepatocytes is also induced by a large number of toxic compounds and sometimes precedes the onset of necrosis or coexists with it [3].

Lining the walls of the liver sinusoids, Kupffer cells are in close contact with the blood stream; in contrast, the only contact that hepatocytes have with the plasma is in the space of Disse, beyond the "sinusoidal barrier". The Kupffer cells, together with other sinusoidal cells, play a key role in the maintenance of liver function, under both physiological and pathological circumstances. The major functions of Kupffer cells include phagocytosis of foreign particles, removal of endotoxins and other noxious substances, and modulation of the immune response [13].

This study was designed to confirm whether Kupffer cells are involved in liver apoptosis induction after acute intoxication by Pb(NO3)2 and to assess any secretion mechanisms that may be implied, by investigating the real effect of Pb(NO3)2 on hepatocytes and Kupffer cells. It is worth noting that hepatocyte apoptosis is a tightly controlled process, regulated via several mechanisms including an oxidative mechanism that may account for the main apoptotic signalling pathway [14–17]. In fact, the concentration of glutathione – the most abundant antioxidant in the cell, found in reduced, GSH, and oxidized, GSSG, redox forms – decreases upon induction of apoptosis [18].

It is well known that modulation of the apoptotic process in the liver (together with the efficient elimination of apoptotic bodies) relies mainly on Kupffer cells and is thought to be regulated by their secretion of certain cytokines and growth factors [19–21]. In addition to this, previous experimental results have already shown that the apoptotic index of hepatocytes isolated using a perfused rat liver model after treatment with Pb(NO3)2 for 1, 3, or 5 days increases with time; in contrast, co-administration with gadolinium chloride (GdCl3), a selective Kupffer cell toxicant that suppresses their activity [22], reduces the apoptotic rate [23], suggesting a key role for liver macrophages in this process.

Results

In vivo administration of Pb(NO3)2, GdCl3, GdCl3 plus Pb(NO3)2, Pb(C2H3O2)2 or KNO3

In situ experiments

Pb(NO3)2 administration led to time-related modifications of liver structure (hyperplasia-apoptosis), which were totally or partially abolished by pre-treatment with GdCl3 (i.v. injected 24 hours but not 2 or 4 hours before Pb(NO3)2) (Fig. 1). GdCl3 administered the same day as Pb(NO3)2, reduced the hepatocyte apoptosis only moderately, but, when administered 24 hours before Pb(NO3)2, the apoptotic index was cut by half. Morphological data are confirmed by TUNEL assay; very few TUNEL positive cells were observed in livers of animals injected with 24 hours GdCl3 pre-treatment to Pb(NO3)2 administration (Fig. 1d). A single GdCl3injection induced low rate apoptosis as well as same modifications of liver structure. In particular, an influx of monocytes, a decreased number of Kupffer cells and a minimal uptake activity for the remaining liver macrophages was observed. Liver repopulation of Kupffer cells and re-establishment of active phagocytosis was observed two days later. The time-course of GdCl3-induced Kupffer cell depletion and repopulation, (monitored by measuring colloidal carbon uptake by liver macrophages), is shown in Figure 2.

Figure 1
figure 1

Light micrographs of rat liver sections, (a, b) haematoxylin eosin staining and (c, d) apoptotic detection by TUNEL staining, from (a, c) animals 5 days after a single Pb(NO3)2 injection and animals 5 (b) and 3 (d) days after Pb(NO3)2 injection 24 hours GdCl3pre-treated. (a) Apoptotic hepatocytes (arrows) show round shape, condensation of chromatin and cell shrinkage. One fragmented apoptotic hepatocytes (arrowhead). (b) The GdCl3 pre-treatment reduces the hepatocytes apoptosis. In (d), the number of TUNEL-positive nuclei (arrows) in hepatic parenchyma is much lower than 5 days after a single Pb(NO3)2 injection (c, arrows). Bar = 10 ÎĽm.

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Figure 2
figure 2

Light micrographs of rat liver sections (a,c) from control animals and (b,d) three days after a single GdCl3 injection; (a, b) toluidine blue staining and (c, d) unstained sections of livers of GdCl3-treated rats. In normal livers large Kupffer cells, lining liver sinusoids are indicated by arrows(a) or evidenced by the colloidal carbon particles uptaken by Kupffer cells (c) (arrowheads); b) three days after GdCl3 administration; the majority of large Kupffer cells disappeared from liver and (d) the phagocytic activity is depressed as the scarce internalization of carbon shows (arrowhead). The asterisk (b) indicates a hepatocyte in mitosis. Bar = 10 ÎĽm.

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Parallel experiments were carried out by injecting animals with Pb(C2H3O2)2 or KNO3 to seek whether the apoptotic liver induction was peculiar to Pb(NO3)2-treated animals. Neither Pb(C2H3O2)2 nor KNO3 induced apoptosis or mitosis in liver cells, even at longer observation times; conversely, extensive necrosis of hepatic parenchyma was observed five days after KNO3 injection.

Flow cytometry of isolated hepatocytes

In order to quantify the morphological data above described, flow cytometry analysis of isolated hepatocytes was performed (Tables 1, 2). The use of flow cytometry allowed us the simultaneous analysis of each sample for necrosis, apoptosis and for cell cycle (from which it is possible to have the percentage of cells synthesizing DNA). Isolated hepatocytes were obtained for each treatment by using well established enzymatic isolation procedure; cell viability in the isolated hepatocytes was always higher than 90% in each preparation from both normal untreated animals and treated animals.

Table 1 Time-course of necrosis, apoptosis and DNA synthesis in hepatocytes isolated from control, Pb(NO3)2-treated, and co-administered GdCl3 plus Pb(NO3)2 rats.*
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Table 2 Percentage of necrosis and apoptosis in hepatocytes isolated from control, KNO3, GdCl3 and Pb(C2H3O2)2 treated animals.*
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Apoptotic rates and DNA synthesis were significantly affected at 3 and 5 days after the Pb(NO3)2 injection on isolated hepatocytes (Table 1). Pre-administration of GdCl3 reduced the apoptotic rate to a half when administered the day before but not the same day of Pb(NO3)2 injection. A low apoptotic rate was induced five days after a single GdCl3 injection compared to a single Pb(NO3)2 injection, while an apoptotic rate similar to controls was measured one day after a single GdCl3 injection (Table 2). GdCl3, Pb(C2H3O2)2, and KNO3 were toxic (i.e. induction of necrosis) for liver cells at different extent (Table 2). Neither Pb(C2H3O2)2 nor KNO3 induced apoptosis or mitosis in liver cells, even at longer observation times; conversely, i.v. injection of KNO3 gave rise to extensive necrosis of parenchymal cells, mostly five days after the injection (45%), probably due to the increased levels of K (Table 2).

GSH activity in hepatocytes isolated from rats treated with Pb(NO3)2, GdCl3 or GdC3 plus Pb(NO3)2

To verify whether an oxidative mechanism is involved in liver apoptotic signalling after acute Pb(NO3)2 intoxication, the activity of both the reduced and oxidized forms of glutathione (GSH and GSSG, respectively) was measured in isolated hepatocytes. The results showed a direct relationship between apoptogenic treatment and reduction in GSH activity (Table 3). In fact, the highest apoptotic rate – i.e., 5 days of treatment with Pb(NO3)2 – corresponds to the highest levels of GSH depletion, accompanied by a drop in total enzymatic activity with respect to controls. In detail, the intracellular hepatocyte content of GSH (16.05 nmol/mg of total protein) was depleted to 3.20 nmol/mg of total protein at 3 days after Pb(NO3)2 injection, and was drastically reduced at 15 days after the injection (i.e., 2.74 nmol/mg of protein, corresponding approximately to a 75% drop with respect to controls) (Table 3). Experimental conditions corresponding to the lowest apoptotic rates – controls, GdCl3 and 1 day Pb(NO3)2 – were, on the contrary, related to the highest concentrations of GSH or the highest levels of total enzymatic activity (Table 3).

Table 3 GSH/GSSG levels in hepatocytes after in vivo treatment with Pb(NO3)2, GdCl3 or with 24 hours pretreatment of GdCl3 before exposure to Pb(NO3)2.*
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The loss of GSH due to Pb(NO3)2 intoxication was remarkably mitigated or abolished when GdCl3 was administered 24 hours (but not 2 or 4 hours) before Pb(NO3)2 injection (again when Kupffer cells are depleted) (Table 3).

Apoptotic rates and GSH activity in hepatocytes isolated from rats treated with Pb(NO3)2, GdCl3 or GdCl3 plus Pb(NO3)2in the presence or absence of pre-treatment with 2 mM BSO

To establish a possible cause-effect relationship between the intracellular levels of GSH in hepatocytes and hepatic apoptosis, rats were treated with 2 mM BSO (a GSH depleting agent that inhibits the synthesis of this important radical scavenging compound within 24 hours) for 1, 2 or 3 weeks before injection with Pb(NO3)2, GdCl3 or both (Table 4). Treatment with BSO reduced GSH content by about 72% compared to untreated animals. When rats were injected, at the end of BSO administration, with Pb(NO3)2, GdCl3 or GdCl3 24 hours before Pb(NO3)2, an overall increase in the liver apoptotic rate was measured when compared to animals in which the synthesis of GSH was not inhibited (data not shown).

Table 4 Hepatic GSH levels after treatment with Pb(NO3)2, GdCl3 or with 24 hours pretreatment of GdCl3 before exposure to Pb(NO3)2 .*
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Summary of in vivo experiments

To sum up, from in vivo experiments it may be concluded that: i) Pb(NO3)2 but not Pb(C2H3O2)2 or KNO3 induces hepatocyte apoptosis; ii) KNO3 causes extensive necrosis of hepatocytes; iii) pre-treatment with GdCl3 reduced modifications described for a single injection of Pb(NO3)2, when given 24 hours previously; iv) i.v. injection of Pb(NO3)2 deprived hepatocytes of GSH, whereas 24 hours GdCl3 pre-treatment remarkably mitigated or abolished this loss; v) there is a possible cause-effect relationship between the intracellular levels of GSH in hepatocytes and hepatic apoptosis.

In vitroexperiments

Apoptosis in hepatocytes and HepG2 cultures in presence of Pb(NO3)2, Pb(C2H3O2)2, KNO3 or conditioned medium collected from Kupffer cells incubated with Pb(NO3)2

Necrosis and apoptosis were evaluated at fixed time intervals (6, 8, 16, 24, 48 hours) by light microscopy in cultures of hepatocytes and Kupffer cells isolated from normal rats and incubated up to 48 hours with 10 mM Pb(NO3)2 (Table 5). More than 95% of Kupffer cells died within 24 hours of incubation with Pb(NO3)2, and only cell debris were found in the culture wells at 48 hours. Within 24 hours of culture in the presence of Pb(NO3)2 some necrotic hepatocytes were observed, whereas almost all hepatocytes were necrotic at 48 hours. Similar results were found for hepatocytes incubated with KNO3. 80% necrotic hepatocytes were observed at 24 hours of incubation with Pb(C2H3O2)2. Apoptosis was never detected after incubation with Pb(NO3)2, Pb(C2H3O2)2 or KNO3 for up to 48 hours, but it was observed only after incubation with conditioned medium (CM) of Kupffer cells cultured for 24 hours in presence of Pb(NO3)2; values ranged from about 35% at 24 hours to about 48% at 48 hours of incubation (Fig. 3 and Table 5). Necrosis was never observed in such condition. Figure 3 shows many apoptotic hepatocytes detaching from culture dishes.

Table 5 Evaluation of apoptosis versus necrosis in hepatocyte cultures incubated with 10 mM Pb(NO3)2, Pb(C2H3O2)2 or KNO3 and with CM from Kupffer cells.*
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Figure 3
figure 3

Nomarsky light microscopy of rat hepatocyte cultures. Cells were incubated with Pb(NO3)2 (10 mM) or with conditioned medium (CM) from Kupffer cells incubated for 24 hours with Pb(NO3)2 (a) control hepatocytes (b) 24 hours incubation with Pb(NO3)2. Apoptotic hepatocytes are not present. (c) Apoptotic cells (arrows) are present when incubated with CM from Kupffer cells incubated for 24 hours with Pb(NO3)2. (d-e) Hepatocytes pre-incubated with 1 mM BSO for 24 hours, and subsequently incubated for 24 hours (d) or 48 hours (e) with Pb(NO3)2. Deprivation of GHS leads to apoptosis also upon incubation with Pb(NO3)2. Arrows indicate apoptotic hepatocytes that are characterized by shrinkage in volume, round shape, very condensed cytoplasm and dark nucleus. Bar = 10 ÎĽm.

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Extremely low apoptotic rates and high necrotic rates (especially for cells cultured with Pb(NO3)2) were measured for HepG2 cells incubated with Pb(NO3)2, Pb(C2H3O2)2 or KNO3 for up to 24 hours. Apoptosis was detected upon incubation with Kupffer cells CM (Table 6 and Fig. 4). CM collected from control Kupffer cells, or cells cultured for 24 hours with KNO3, was unable to induce apoptosis in HepG2 cells.

Table 6 Evaluation of apoptosis versus necrosis in HepG2 cultures incubated with 10 mM Pb(NO3)2, Pb(C2H3O3)2 or KNO3 and with conditioned medium from Kupffer cells incubated with10 mM Pb(NO3)2 for 24 hours.*
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Figure 4
figure 4

Light micrographs of Hep G2 cells.(a) control untreated cells. (b) HepG2 cells were incubated for 24 hours with conditioned medium from Kupffer cells incubated 24 hours with Pb(NO3)2. Apoptotic cells are indicated by arrows. They appear with modified shape, i.e., elongated or pear-like, and the nucleus is more stained. Haematoxylin-eosin staining. Bar = 10 ÎĽm.

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Apoptotic rates and GSH activity in HepG2 cells after treatment with1 mM BSO

The cause-effect relationship between intracellular levels of GSH and the apoptotic rate was also investigated in HepG2 cells. When Pb(NO3)2 or KNO3 administration in HepG2 cells for 6, 8, 16 or 24 hours was preceded by 24 hours pre-treatment with BSO (1 mM final concentration), a higher apoptotic rate than in control cells (in which GSH synthesis had not been blocked by BSO) was observed (Table 7). The apoptotic rates in the presence of BSO were not significant, whereas the necrotic index rose considerably – values of around 40% at longer incubation times with Pb(NO3)2 and KNO3 in GSH-deprived cells (Table 7).

Table 7 Apoptotic indices in HepG2 cells incubated with 10 mM Pb(NO3)2 or KNO3 after 24 hours incubation with BSO 1 mM.*
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Summary of in vitroexperiments

In conclusion, from the in vitro experiments it derives that Pb(NO3)2 showed a direct necrotic but not apoptogenic effect on hepatocytes and HepG2 cells. In fact, apoptosis was observed only when these cells had been incubated with the CM collected from Kupffer cells previously cultured with Pb(NO3)2 for 24 hours. There is also for HepG2 cells a possible cause-effect relationship between intracellular levels of GSH and apoptosis.

Discussion

When administered to rats, Pb(NO3)2 induces liver hyperplasia within three days, whereas the subsequent regression from hyperplasia is due to the onset of apoptosis [11]. As a result of the administration of Pb(NO3)2, hepatocytes lose their contacts with the neighbouring cells and become roundish (entering the early stages of their death programme) and apoptotic cells appear in the sinusoidal lumen [12].

When the administration of Pb(NO3)2 coincides with the depletion of Kupffer cells (i.e., when it is combined with GdCl3 pre-treatment, a Kupffer cells toxicant, known to suppresses Kupffer cell activity), a decrease in the apoptotic rates is observed with respect to five day-treatment with Pb(NO3)2, which usually correlates with the highest apoptotic rates. However, it is worth noting that modifications induced by a single injection of Pb(NO3)2 were reduced only when GdCl3 was administered 24 hours (i.e., the time coinciding with the highest Kupffer cell depletion) but not 2 or 4 hours before Pb(NO3)2 treatment. The reason why there was liver protection from apoptosis when GdCl3 was given 24 hours before, but not the same day as Pb(NO3)2, could be found in the absence of a consistent number of Kupffer cells and, as a consequence, of the soluble molecules released by them on Pb(NO3)2 injection. Moreover, GdCl3 is responsible not only for Kupffer cells depletion, but also for inhibiting their phagocytic activity [22, 24]. Since Kupffer cells play a key role in the liver phagocytic activity (included the phagocytosis of apoptotic cells) [25, 26] and in the related signalling pathways, GdCl3 administration might cause fewer signals to be released, leading consequently to a decreased apoptotic rate [22]. In addition, the data indicating that, the morphological modifications of liver parenchyma observed for 2 or 4 hours GdCl3 pre-treatment were similar to those described for a single injection of Pb(NO3)2, further support the role of Kupffer cells in Pb(NO3)2-induced liver changes. On the other hand, the possible compensation for the absence of resident macrophages due to monocytic liver infiltration, will happen slighter late, i.e. at three days after GdCl3 administration [24]. All together these data are in favour of the fact that, the apoptogenic effect of Pb(NO3)2 on hepatocytes may be mediated by Kupffer cells and allowed us to verify the hypothesis that the apoptogenic action of Kupffer cells could be exerted by releasing factors and/or cytokines. likely in synergy with [27]. In addition, Kupffer cells may induce hepatic apoptosis in synergy with other cells (i.e., endothelial cells), that can in turn, directly or indirectly stimulate hepatocytes to apoptosis. Kupffer cell death signals could also be combined with signals released by endothelial cells or by other non-parenchymal liver cells. It is worth noting that endothelial liver cells show the highest resistance to in vivo Pb(NO3)2 injection, whereas Kupffer cells undergo apoptosis within 24 hours from the injection [27]. It has been increasingly recognized that, under normal and pathological conditions, many hepatocyte functions are regulated by substances released by neighbouring non-parenchymal cells [28]. In fact, many mediators performing multiple paracrine and autocrine actions are secreted into the blood flow or the intercellular spaces.

The in vitro and in vivo data, excluding completely a direct apoptogenic effect of Pb(NO3)2 on hepatocytes, support what above discussed. In fact, a single intravenous injection of Pb(C2H3O2)2 or KNO3 cannot determine neither hepatic apoptosis or hyperplasia – two metabolic modifications specifically induced after Pb(NO3)2 injection [10] – thus ruling out a direct apoptogenic action of Pb or nitrates on hepatocytes. Again, apoptosis was never observed when hepatocytes or HepG2 cells were cultured with Pb(NO3)2, Pb(C2H3O2)2 or KNO3, but only when they had been incubated with the CM collected from Kupffer cells previously cultured with Pb(NO3)2 for 24 hours. In fact, after 24 hours Pb(NO3)2 incubation, necrotic but not apoptotic hepatocytes and HepG2 cells were observed; in contrast, incubation with the conditioned medium collected from Kupffer cells pre-cultured with Pb(NO3)2 for 24 hours was responsible for apoptosis, but not necrosis. Therefore, both in vitro and in vivo experimental results obtained under these conditions suggest that apoptosis of hepatocytes after acute intoxication with Pb(NO3)2 is indirectly induced by soluble factors released by Kupffer cells that probably act in synergy with the secreted products of endothelial sinusoidal cells. These results are in agreement with those showing that Pb stimulates intercellular signalling between hepatocytes and Kupffer cells [29]. However, what induces Kupffer cells to release soluble mediators upon Pb(NO3)2 injection remains unknown at the moment, and Kupffer cell-derived factors still lack identification. The release of Pb/lipopolysacharide induced by TNF-alpha (produced by Kupffer cells on hepatocytes or hepatoma cell lines) has been reported [29], in agreement with the extensive studies of the apoptogenic activity of TNF-alpha. Studies reporting Kupffer cell activity against liver metastasis by induction of Fas and Fas ligand expression on malignant glioma cells [30], or to sensitive colon cancer cells to Fas-mediated apoptosis in cirrhotic rat livers [31] further support the beneficial effects of communication between Kupffer cells and parenchymal cells.

Although the mechanism by which Kupffer cells promote hepatocyte apoptosis has not been clarified, a clue to the role of soluble factors released by liver macrophages that trigger oxidative apoptotic pathways in target cells (i.e., hepatocytes) is given by the dramatic drop in intracellular GSH activity in hepatocytes isolated from rats treated for five days with Pb(NO3)2 (i.e., after the treatment leading to the highest apoptotic rate) with respect to control levels.

In fact, the loss of GSH under those conditions is considerably mitigated or abolished when GdCl3 is administered to rats 24 hours before Pb(NO3)2 (Pb(NO3)2 acts when Kupffer cells are depleted). These data are in agreement with those indicating that the intensity of oxidative stress exhibited by post-ischaemic lobes is closely linked to Kupffer cell activity [32]. Moreover, the same trend is observed when rats are previously fed with 2 mM BSO for 2 or 3 weeks.

In hepatocytes, like some other cells, upon oxidative stress, GSSG may either recycle to GSH or exit from cells, leading to overall glutathione depletion [33]. Cells deprived of GSH are much more prone to undergo oxidative stress since their redox balance is altered and, therefore, their ability to get rid of reactive oxygen species originated from cellular metabolism is compromised [34]. Thus, an oxidative mechanism may be a point of convergence of many different apoptogenic stimuli (i.e., H2O2, tumour necrosis factor, cycloheximide and natural killer cells, all eliciting oxidative stress) into a main signalling pathway [16, 32, 33, 35]. It is well known that NO mediates Kupffer cell-induced reduction of mitochondrial energization in syngenic hepatoma cells [20]. In fact, oxidative apoptotic pathways include damage to mitochondria and changes in mitochondrial permeability transition, which may result in necrosis from ATP depletion or caspase-dependent apoptosis (if ATP depletion does not occur fully). Moreover, the product of the antiapoptotic oncogene bcl-2 works throughout a radical-scavenging mechanism even in cells lacking bcl-2 [36, 37]. It is worth noting that glutathione depletion can either decrease or increase death-receptor-mediated apoptosis. However, the duration of glutathione depletion before death-receptor stimulation is critical; prolonged, but not acute, glutathione depletion promotes apoptosis in mice [38, 39].

Our hypothesis indicating the crucial and pre-eminent role of Kupffer cells in the onset of liver apoptosis after Pb(NO3)2 injection is summarized in Fig. 5. In vivo Pb(NO3)2 injection induces Kupffer cells to release factors that can act directly on hepatocytes or indirectly throughout stimulation of other cells (i.e., endothelial liver cells) inducing the death programme in hepatocytes, probably throughout oxidative stress. GdCl3 can block the Pb(NO3)2-induced cascade by destroying Kupffer cells, and in turn, can modify extracellular concentration of molecules released by macrophages (most probably cytokines), which are able to induce depletion of intracellular GSH levels and oxidative apoptotic signalling in hepatocytes.

Figure 5
figure 5

Scheme of the role of Kupffer cells during Pb(NO3)2-induced hepatic apoptosis. Pb(NO3)2 particles induce, as an early event, Kupffer cells (KC) to secrete molecules (probably cytokines such as TNF alpha) which stimulate hepatocytes (HEP) to proliferate; the increased level of secreted molecules could initiate hepatocyte apoptosis. Activated Kupffer cells may release other molecules prompting endothelial cells (EC) to release additional cytokines, promoting apoptosis of hepatocytes. At the same time, EC can release cytokines that could promote hepatocyte apoptosis as well as activation of KC. As a late event, Pb(NO3)2 particles induce KC death. GdCl3 particles could inhibit the effects of Pb(NO3)2 by depleting Kupffer cells, likely by inducing apoptosis.

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Conclusions

Pb(NO3)2 has, at most, a direct necrotic (but not apoptogenic) effect on hepatocytes and HepG2 cells, giving a clue about the regulatory role of Kupffer cells in the induction of liver apoptosis after a single Pb(NO3)2 injection without pre-treatment with GdCl3, probably via secreting soluble factors that trigger oxidative stress in target cells.

Methods

In vivoexperiments

Adult male Wistar rats (weighing 200–250 g) were used. Animal husbandry was carried out as outlined in the "Guide for the Care and Use of Laboratory Animals" prepared by the National Academy of Sciences (NIH publication 86–23 revised 1985). Animals were fed standard laboratory food and water ad libitum. Pb(NO3)2 (Farmitalia, Milano, Italy) was i.v. injected at a concentration of 10 μM/110 g.b.w. GdCl3 (Aldrich Chem. Co., Brussel, Belgium) (0.75 mg/100 g.b.w.) was injected intravenously into tail veins 2, 4 or 24 hours before Pb(NO3)2 intravenous administration. Control animals were injected with saline solution or with 10 mM Pb(C2H3O2)2 or KNO3 (400 μl/100 g.b.w). The animals, anaesthetized with Farmotal (Farmitalia, Milano, Italia) (10 mg/100 g.b.w.), were sacrificed at 1, 3, 5 or 15 days after treatments.

a) Apoptosis determination

Hepatocytes were isolated by enzymatic perfusion [40]; non-viable cells, evaluated by trypan blue exclusion test, did not exceed 5% in any of the saline-injected animals. Apoptotic, mitotic and necrotic indices of hepatocytes were quantified by flow cytometry and checked by light microscopy on haematoxylin-eosin-stained hepatocytes.

An EPICSXL flow cytometer (Coulter Electronic Inc. Miami, FL, USA) with a 5-W argon laser having a 488-nm excitation wavelength was used. Hepatocytes were stained with propidium iodide (10 ÎĽg/ml) in phosphate-buffered saline containing 40 units/ml Rnase and 0.5% Tween 20. The 635-nm emission wavelength was monitored for propidium iodide emission. Histograms of relative DNA content were analysed using MultiCycle software (Phoenix Flow Systems, San Diego, CA, USA) to quantify the percentage of cells in each stage of the cell cycle. For each flow cytometry analysis at least 10 000 events were calculated.

b) Glutathione determination

The cellular content of glutathione was evaluated on in situ perfused livers, and on hepatocytes isolated from the livers of rats injected with Pb(NO3)2, GdCl3, GdCl3 + Pb(NO3)2, at 1, 3, 5 and 15 days after treatment. Freshly isolated hepatocytes, harvested by centrifugation at 200 g in a refrigerated centrifuge, were washed and suspended in phosphate-buffered saline. Cells were lysated by repeated cycles of freezing and thawing. Proteins were precipitated by adding sodium metaphosphoric acid (5% w/v). GSH and GSSG was measured in the clear supernatant obtained after centrifugation at 22 000 g for 15 minutes, by high-performance liquid chromatography [15]. Rat livers were perfused in situ with PBS to eliminate blood and snap frozen at -80°C before GSH determination as described for isolated cells. In each case, results are expressed as nmol of GSH/GSSG per mg of total proteins in the original cell extract. Proteins were determined by processing aliquots of cell lysates according to the method of Lowry et al. [41].

GSH depletion experiments were performed by feeding normal rats with D.L-buthionine sulfoximine (2 mM BSO, Sigma Chem. Co., MI, USA) in order to block GSH synthesis for 1, 2, or 3 weeks, and then treated with Pb(NO3)2, GdCl3 + Pb(NO3)2 or GdCl3 for 1, 3, 5 or 15 days. Control groups drank only water or 2 mM BSO for 1, 2 or 3 weeks.

c)TdT-mediated dUTP-biotin nick end labelling (TUNEL)

Apoptotic cells were detected by TUNEL, based on the specific binding of terminal deoxynucleotidyl transferase (TdT) to 3-OH ends of DNA [42].

d) Uptake of colloidal carbon

A suspension of colloidal carbon was prepared by dialyzing 10–15 ml of Indian ink (Pelikan black #17) against distilled water for 48 hours using a dialyzing membrane with a 12 000–14 000 MW cut-off. The suspension was stored at 4°C for up to 30 days prior to use and diluted in Krebs-Henseleit buffer to a concentration of 2.4 mg/ml. To test the phagocytic capacity of Kupffer cells, the diluted solution was given i.v. (0.2 ml/250 g.b.w.) 30 minutes before killing the rats. Rats were sacrificed in groups of three respectively 1, 3, 5 and 7 days after GdCl3 administration.

In vitroexperiments

a) Experiments with isolated hepatocytes, HepG2 cells and Kupffer cells

Hepatocytes, isolated as described above, and Kupffer cells, isolated according to Dini [25] were cultured in RPMI-1640 supplemented with 10% fetal calf serum, 2 mM L-Glutamine, 100 I.U./ml penicillin and streptomycin in a controlled atmosphere (5% CO2) at 37°C. All the experiments with hepatocytes (plated on collagen-coated slides) and Kupffer cells at a density of 1 × 106 cells/ml in complete medium were performed 24 hours after plating. HepG2 cells were routinely trypsinized, plated on 7.5 × 105/25 cm2 flasks, and used for experiments 3 days after trypsinization at a density of 2 × 106/25 cm2 flasks.

Hepatocytes, HepG2 and Kupffer cells were incubated with Pb(NO3)2, Pb(C2H3O2)2, KNO3 (30 ÎĽl of 30 mg/10 ml solution in 3 ml of medium containing 3 Ă— 105 HepG2 cells or 1 Ă— 106 hepatocytes or Kupffer cells) for 4, 6, 8, and 24 hours. Conditioned media from untreated Kupffer cells and Kupffer cells cultured for 24 hours with Pb(NO3)2, Pb(C2H3O2)2 or KNO3 were diluted 1:2 in fresh medium containing 10% FCS and added to 24-hour-cultured hepatocytes or HepG2 cells. The apoptotic rate was evaluated by light microscopy on haematoxylin-eosin stained slides, counting at a magnification of 40 Ă— at least 300 cells in at least 10 randomly selected fields.

b) Glutathione determination

The relationship between intracellular GSH/GSSG rates and hepatic apoptosis was tested in HepG2 cells. Cells were pre-treated 24 hours beforehand with 1 mM BSO before 24 hours incubation with Pb(NO3)2 or KNO3. Controls were incubated with normal culture medium or with Pb(NO3)2or KNO3 for up to 24 hours. The apoptotic rate was evaluated by light microscopy on haematoxylin-eosin stained slides. GSH was determined as described above.

Statistical analysis

Statistical analyses were performed using Student's t-test for independent samples, and p values < 0.05 were considered significant. For data reported in Tables 1, 2, 4 and 7, normality was checked with the chi-squared goodness-of-fit test. For data reported in Tables 5 and 6, normality was checked with the Kolmogorov-Smirnov test. Homogeneity of variances was checked with both Bartlett and Cochran' tests. Data are presented as mean (standard deviation).

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Acknowledgements

This work was supported by grants from the MIUR. The authors thank Mr George Metcalf, University of Lecce, for his help in the linguistic revision of the manuscript.

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  1. Department of Science and Biological and Environmental Technologies, University of Lecce, via per Monteroni, Lecce, Italy

    Patrizia Pagliara, Emanuela C Carlà, Sonia Caforio, Alfonsina Chionna, Silvia Massa, Luigi Abbro & Luciana Dini

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Correspondence to Luciana Dini.

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Authors' Contributions

PP carried out the culture experiments and the high-performance liquid chromatography. ECC performed the TUNEL assays and the isolation of hepatocytes and Kupffer cells. SC carried out the isolation of hepatocytes and Kupffer cells and took care of the animal treatments. AC performed the culture experiments. SM participated in the writing of the manuscript. LA participated in the design of the study, drafted the manuscript and performed the flow cytometry. LD conceived the study and participated in its design and coordination. All the authors read and approved the final manuscript.

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Pagliara, P., CarlĂ , E.C., Caforio, S. et al. Kupffer cells promote lead nitrate-induced hepatocyte apoptosis via oxidative stress. Comp Hepatol 2, 8 (2003). https://doi.org/10.1186/1476-5926-2-8

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Comparative Hepatology

ISSN: 1476-5926