- Research article
- Open Access
- Open Peer Review
Functional p53 is required for rapid restoration of daunorubicin-induced lesions of the spleen
© Herfindal et al.; licensee BioMed Central Ltd. 2013
- Received: 27 February 2013
- Accepted: 8 July 2013
- Published: 11 July 2013
The tumour suppressor and transcription factor p53 is a major determinant of the therapeutic response to anthracyclines. In healthy tissue, p53 is also considered pivotal for side effects of anthracycline treatment such as lesions in haematopoietic tissues like the spleen. We used a Trp53null mouse to explore the significance of p53 in anthracycline (daunorubicin) induced lesions in the spleen.
Mice with wild type or deleted Trp53 were treated with the daunorubicin (DNR) for three consecutive days. Spleens were collected at various time points after treatment, and examined for signs of chemotherapy-related lesions by microscopic analysis of haematoxylin-eosin or tunel-stained paraffin sections. Expression of death-inducing proteins was analysed by immunoblotting. Changes between Trp53 wild type and null mice were compared by t-tests.
Signs of cell death (pyknotic nuclei and tunel-positive cells) in the white pulp of the spleen occurred earlier following DNR exposure in wt-mice compared to Trp53-null mice. While the spleen of wt-mice recovered to normal morphology, the spleen of the Trp53-null animals still had lesions with large necrotic areas and disorganised histologic appearance eight days after treatment. Immunoblotting showed that only Trp53-wt mice had significant increase in p21 after DNR treatment. However, both wt and null mice had elevated p63 levels following DNR exposure.
p53 protects against severe and enduring cellular damage of the spleen parenchyma after DNR treatment, and initial DNR-induced apoptosis is not predictive of tissue lesions in the spleen. Our data indicate that p53 induction following DNR treatment serves to protect rather than to destroy normal tissue.
Numerous studies have demonstrated that the efficiency of DNA-damaging drugs in cancer therapy is dependent on the cellular status of the tumour suppressor factor p53[1–4]. The p53 pathway is often inactivated in human cancers, and deletions and mutations in p53 are associated with progressive and more aggressive disease, and with poor prognosis and anthracycline resistance in several types of cancer [1, 4–6]. In line with these results, there has been an increased focus on developing new drugs aiming to restore p53 activity in tumours [7–12]. However, the effect of p53 activation by drugs such as the anthracyclines on healthy tissue has to be considered in this respect, as induction of cell death and tissue damage in healthy tissue is an unwanted and severe side-effect of the anthracyclines.
It is known that anthracyclines cause lesions in haematopoietic tissues . We therefore addressed the role of p53 in the toxic activity of the anthracycline daunorubicin (DNR) in the spleen, and compared the effect of DNR on the spleen in C57Bl/6 wild type (wt) and C57Bl6 Trp53-null mice. DNR induced more rapid cell death and loss of spleen weight in wild type (wt) compared to Trp53-null mice. However, whereas the Trp53-null mice had severe lesions of the spleen at day 4 after treatment, there was spleen structure recovery in Trp53-wt animals. Our data points to p53 as a protective factor in chemotherapy-induced normal tissue damage.
The Trp53-null mouse was generated by Jacks et al. , and was provided by Prof. Lozano, MD Anderson Cancer Center, Houston, TX, USA. Trp53-wt and null mice (C57BL/6) were generated by litter-mate inbreeding. Genotypes of weaned mice were determined by PCR analysis of DNA from an ear biopsy .
The mice used were male, and age matched. DNR (Sanofi-Aventis, Lysaker, Norway,) was administered intravenously (10 mg/kg) through the tail vein for three consecutive days. Control animals received relevant vehicle. Health status and weight of the mice were monitored daily. The mice experiments were approved by the Norwegian Animal Research Authority and conducted according to the European Convention for the Protection of Vertebrates Used for Scientific Purposes.
Preparation and analysis of histological specimens
Spleens were excised from euthanized mice and washed in ice-cold PBS. Formalin-fixed tissues were embedded in paraffin, cut into 2-μm-thick sections and stained with haematoxylin and eosin (H&E). Terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end-labelling (TUNEL staining, In situ Cell Death Detection Kit, POD, Roche) was used for in situ staining of apoptotic DNA fragmentation. Pyknotic nuclei and cells containing lipofuscin-like pigments were assessed by microscopy of H&E-stained paraffin sections. The number of pyknotic nuclei in all the white pulp areas was counted and then divided by the number of white pulp regions.
The spleens were cut with scissors and cell suspensions were prepared by crushing the tissue pieces between two glass slides in PBS. Cell suspensions were filtered through a nylon cell strainer (40 μm), washed in PBS by centrifugation (160 × g, 6 min) and re-suspended at 0.5 × 106 cells/ml in RPMI-1640 (Sigma-Aldrich Inc, St. Louis, MO) supplemented with 10% FCS (Gibco, Grant Island, NY). Cell death was assessed by flow cytometry after AlexaFluor 647-AnnexinV (Molecular Probes, Eugene, OR) and propidium iodide (PI) labelling. At least 30 000 non-gated live cell events were collected for each sample on an AccuriC6 cytometer (Ann Arbor, MI). Cells positive for AnnexinV alone or together with PI were counted as dead (apoptotic or necrotic). Untreated cells had less than 15% spontaneous cell death, and this was subtracted from the data on anthracycline-treated cells.
The data was compared by one-way analysis of variance (ANOVA) using IBM SPSS Statistics for Mac (version 19.0; IBM Corp.: Armonk, NY, 2010).
Protein lysates were prepared from excised spleens, snap-frozen in liquid N2 and stored at -80°C. Tissue was grinded with a pestle and lysed in RIPA buffer supplemented with Complete mini protease inhibitor (Roche Diagnostics, Mannheim, Germany). The relative protein concentration was determined by Bradford and adjusted by Coomassie staining, and immunoblotting was as described . Primary antibodies were from Santa Cruz Biotechology (Santa Cruz, CA, USA; p21, p63, Bax), and Imgenex (San Diego, CA, USA; p73) and secondary alkaline-phosphatase-conjugated antibody (a-3687 and a-3562) were from Sigma. CDP-Star substrate was from Tropix (Bedford, MA, USA). Chemiluminescence was detected using a Luminescent Image Analyser Apparatus (LAS 3000, FujiFilm, Tokyo, Japan) and Image Gauge Software (FujiFilm, Tokyo, Japan).
We next studied the in vivo effect of DNR treatment on the intact spleen in wt and Trp53-null mice. A typical therapy regime for AML patients consists of multiple 1–3 hour infusions of DNR during 3–6 days . To study how p53 is involved in the drug-induced damage and recovery of the spleen, we administered DNR (10 mg/kg) i.v. to the mice every day for three days. Whereas spleen weight reduction was evident two days after onset of DNR-treatment in wt-mice (Figure 1B), in the Trp53-null mice reduced spleen weight was not observed until about five to six days after onset of treatment (Figure 1C). Also, weight reduction was more prominent in the wt mice compared to Trp53-null animals. A p53-dependent decrease in spleen mass has similarly been reported by others after ionising radiation . Two weeks after treatment, there was an increase in spleen weight in both wt- and Trp53-null mice treated with DNR (Figure 1B,C; right plot).
However, when we studied spleens from 3 Trp53-wt and 4 -null mice 4 days after the last DNR injection, we found pyknotic nuclei and gross pathological lesions in histological sections in both red and white pulp of the spleen only in the Trp53-null mice (Figure 2B). At this time, the wt mice had established normal spleen morphology with little or no signs of cell death (Figure 2B). Thus a late wave of p53-independent cell death seems to appear in the spleen of the Trp53-null mice. This later wave of cell death coincides with decreased spleen weight (Figure 1C).
We also found signs of DNR-induced cell death in the red pulp of the wt-mice. An increasing number of cells containing lipofuscin-like pigments were detected 4 hours after the last DNR injection (Figure 2C). Elevated levels of lipofuscin-like pigments have been found in the spleen of mice subjected to ionising radiation , and could be due to accumulation of non-degradable debris in for instance macrophages . The number of cells positive for lipofuscin-like pigments decreased during the next 20 hours (Figure 2C), as was seen for pyknosis and TUNEL-positive cells (Figure 2A). Interestingly, Trp53-null mice had high numbers of cells containing lipofuscin-like pigments both in the red pulp (Figure 2C) and in the white pulps (not shown), and treatment with DNR did not increase the number of cells containing lipofuscin-like pigments (Figure 2C). This suggests that natural turnover of cells in the spleen of Trp53-null mice leave degradation products such as lipofuscin-like pigments.
Four hours after completed DNR treatment we also detected a 4–5 fold increase in the number of mature and maturing polymorphonuclear cells in the red pulp both in Trp53-wt and null mice (Figure 2D). Stem cells and progenitors have been reported to migrate between bone marrow and spleen after induction of haematopoietic cell stress . This migration could be a response to bone marrow deprivation after DNR treatment, and indicate that the spleen red pulp partly replaces haematopoietic functions after extensive DNR treatment.
p63 is, together with p73, shown to be crucial for p53-meidated cell death after DNA damage , and can increase Bax expression and sensitise cells to apoptotic stimuli . We found that p63 and to some degree Bax was elevated in spleens from wt-mice at 24 and 48 hours after DNR treatment (Figure 3), the same time points where there was an increase in apoptotic nuclei and lipofuscin-like pigments (Figure 2A and C). We did not find any change in the expression of p73 neither in Trp53-wt nor null mice (data not shown). The Trp53-null mice had a prolonged increase of p63 and Bax, which lasted until 96 hours after termination of DNR treatment (Figure 3). This coincides with the late wave of p53-independent cell death that appeared in the spleen of the Trp53-null mice. It thus appears that in addition to lack of early p21-mediated cell cycle arrest (eventually resulting in mitotic catastrophe), the late massive cell death seen in the spleen of Trp53-null mice (Figure 2B, right panel), but not in Trp53-wt mice (Figure 2B, left panel) could also be mediated by up-regulation of p63 and Bax in the absence of p53.
This report indicates an anthracycline-induced early p53-dependent cell death in the spleen. In the Trp53-wt mice, the spleen appeared to recover after DNR treatment with no histopathological signs of cell death or tissue deterioration present four days after end of treatment. However, Trp53-null mice suffered from large lesions in the spleen parenchyma corresponding to a later induction of p53-independent cell death. These findings have clinical implications for therapy aiming to restore p53-dependent cell death pathways in cancer cells with non-functional p53. The efficacy of this therapy approach is debated , and the response apparently varies between drugs . We show here that restoration of p53 activity does not damage the anthracycline-sensitive spleen, but may rather serve to protect this during intensive chemotherapy.
This work was supported by the Norwegian Cancer Society, Lillemor Grobsoks Legat for Cancer Research and Norwegian Western Regional Health Authorities. The authors wish to thank Ing. Nina Lied Larsen for TUNEL staining, Ing. Wenche Eilifsen and Line Wergeland for animal maintenance. Flow cytometry was at Flow Cytometry Core Facility, University of Bergen, and histological sectioning and staining was performed at the Gade Institute and the Molecular Imaging Center (Fuge, Norwegian Research Council), University of Bergen.
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- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/13/341/prepub
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