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Centre for Medical Parasitology, Department of Clinical Microbiology, Copenhagen University Hospital (Rigshospitalet), and the Department of International Health, Immunology and Microbiology, University of Copenhagen, Copenhagen, DenmarkVascular Immunology Unit, Discipline of Pathology, Bosch Institute and School of Medical Sciences, Sydney Medical School, University of Sydney, New South Wales, Australia
Vascular Immunology Unit, Discipline of Pathology, Bosch Institute and School of Medical Sciences, Sydney Medical School, University of Sydney, New South Wales, Australia
Molecular Immunopathology Unit, Bosch Institute and School of Medical Sciences, Sydney Medical School, University of Sydney, New South Wales, Australia
Centre for Medical Parasitology, Department of Clinical Microbiology, Copenhagen University Hospital (Rigshospitalet), and the Department of International Health, Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark
Vascular Immunology Unit, Discipline of Pathology, Bosch Institute and School of Medical Sciences, Sydney Medical School, University of Sydney, New South Wales, Australia
Cerebral malaria (CM) is associated with high mortality and risk of sequelae, and development of adjunct therapies is hampered by limited knowledge of its pathogenesis. To assess the role of cerebral hypoxia, we used two experimental models of CM, Plasmodium berghei ANKA in CBA and C57BL/6 mice, and two models of malaria without neurologic signs, P. berghei K173 in CBA mice and P. berghei ANKA in BALB/c mice. Hypoxia was demonstrated in brain sections using intravenous pimonidazole and staining with hypoxia-inducible factor-1α–specific antibody. Cytopathic hypoxia was studied using poly (ADP-ribose) polymerase-1 (PARP-1) gene knockout mice. The effect of erythropoietin, an oxygen-sensitive cytokine that mediates protection against CM, on cerebral hypoxia was studied in C57BL/6 mice. Numerous hypoxic foci of neurons and glial cells were observed in mice with CM. Substantially fewer and smaller foci were observed in mice without CM, and hypoxia seemed to be confined to neuronal cell somas. PARP-1–deficient mice were not protected against CM, which argues against a role for cytopathic hypoxia. Erythropoietin therapy reversed the development of CM and substantially reduced the degree of neural hypoxia. These findings demonstrate cerebral hypoxia in malaria, strongly associated with cerebral dysfunction and a possible target for adjunctive therapy.
Cerebral malaria (CM) is the most serious complication of Plasmodium falciparum infection. Impaired cerebral microcirculation owing to sequestering of parasitized erythrocytes, platelets, and leukocytes is believed to be a major contributor to pathogenesis.
further direct evidence is needed to clarify the relative importance of the various consequences of impaired microcirculation. Thus, it is essential to quantify the extent of hypoxia in CM in situ and to study the association between hypoxia and clinical outcome.
Oxygen is a prerequisite for normal mammalian cellular function, and quick adaptations of the transcriptome occur to reduce hypoxia-associated tissue damage. During hypoxia, the transcription factor hypoxia-inducible factor (HIF)−1α is rapidly up-regulated,
Even in the presence of oxygen, cellular respiration can be severely impaired because of lack of reductants. This finding is important in conditions such as sepsis, and a key enzyme in this process is poly (ADP-ribose) polymerase-1 (PARP-1), which depletes cellular stores of NAD and NADH, thereby disrupting the intracellular redox state.
There is substantial indirect evidence of cerebral hypoperfusion in CM in humans. Noninvasive imaging of retinal and rectal vessels in patients with CM clearly demonstrates hypoperfusion and occlusion of the microcirculation,
Impaired microcirculation and tissue oxygenation in human cerebral malaria: a single photon emission computed tomography and near-infrared spectroscopy study.
including increased intracranial pressure and a significant decrease in cerebral blood flow, which progressively deteriorates as the clinical condition becomes aggravated.
Recently, in the Plasmodium berghei ANKA (PbA) mouse model of CM, intravital microscopy demonstrated cells plugging cerebral vessels, leading to markedly decreased cerebral blood flow.
Murine cerebral malaria is associated with a vasospasm-like microcirculatory dysfunction, and survival upon rescue treatment is markedly increased by nimodipine.
Murine cerebral malaria is associated with a vasospasm-like microcirculatory dysfunction, and survival upon rescue treatment is markedly increased by nimodipine.
The present study provided a direct measurement of the extent of hypoxia in murine CM and investigated the extent to which hypoxia may be related to the clinical course of the infection. Detecting hypoxic foci in affected tissue is possible through retro-orbital injection of pimonidazole HCl in vivo. Pimonidazole acts as a probe specific for hypoxia because at pO2 <10 mm Hg, it is reduced to a reactive intermediate that binds covalently to molecules containing a –SH group, including proteins, and can be detected by a specific monoclonal antibody.
Thus, the hypothesis that cerebral hypoperfusion in experimental CM is associated with hypoxia can be directly tested. We assessed the extent of hypoxia and subsequent HIF-1α response in CM and non-CM using several murine models and neuroprotective treatment. Furthermore, the possible role of cytopathic hypoxia was tested as a driving force for CM progression in PARP-1 gene knockout (PARP-1−/−) mice.
Materials and Methods
Mice, Parasites, and Infection
Female, 7-week-old, CBA mice (Animal Resources Centre, Canning Vale, Western Australia) were housed under standard conditions with ad libitum access to pellet food and water. After 1 week of acclimatization, mice were divided into three groups of seven mice each and were injected i.p. with either isotonic saline solution (noninfected control mice), 2 × 106P. berghei K173 (PbK)–infected erythrocytes (non-CM) or 106 PbA-infected erythrocytes (CM), as previously described.
Correlation between enhanced vascular permeability, up-regulation of cellular adhesion molecules and monocyte adhesion to the endothelium in the retina during the development of fatal murine cerebral malaria.
Age-matched BALB/c mice, housed under similar conditions, received 106 PbA-infected erythrocytes and served as another non-CM control group. Comparisons were made on days 7 and 8 after infection, at which time peripheral parasitemia was similarly low (mean, 4.8% to 10.4%) in all groups, thereby ruling out any confounding factors caused by global hypoxia secondary to anemia. Mice were observed daily for the appearance of CM-associated neurologic signs. Parasitemia was measured during infection by counting at least 500 erythrocytes in thin blood smears.
Female, 5-week-old, C57BL/6 mice (Taconic Europe A/S, Ejby, Denmark) were divided into four groups of five mice each. Two groups were infected i.p. with 104 PbA-infected erythrocytes transferred from one in vivo passage as previously described,
and two groups received a similar volume (200 μL) of isotonic saline solution i.p. On days 4 through 7 after infection, infected and noninfected mice received either 5000 U/kg recombinant human EPO (Eprex; Janssen-Cilag Pty., Ltd., Schaffhausen, Switzerland) or 200 μL sterile isotonic saline solution. Mice were observed daily for neurologic signs, and parasitemia was measured using flow cytometry.
In-depth validation of acridine orange staining for flow cytometric parasite and reticulocyte enumeration in an experimental model using Plasmodium berghei.
were provided by Dr. Nicolas Gleichenhaus (Nice, France). Eight female and 4 male PARP-1−/− mice were included in the study and were compared with 10 female and 9 male age-matched (31 to 43 weeks) C57BL/6 wild-type (WT) mice. Knockout and WT mice were infected with 106 PbA-infected erythrocytes. The described experimental setups enabled us to address whether hypoxia occurred in two CM models (PbA-infected CBA and C57BL/6 mice), two non-CM models (PbA-infected BALB/c mice and high-dosage PbK-infected CBA mice), and cytopathic hypoxia (PARP-1−/− mice). Survival was assessed twice daily.
All experiments complied with Australian, Danish, and European guidelines for animal research and were approved by the respective national or state boards for animal studies.
Tissue Processing
For detection of hypoxia at a comparable time point, all mice were euthanized in an experiment when susceptible mice exhibited clinical signs of CM. All PbA-infected CBA
mice demonstrated signs of CM at days 7 and 8 after infection, respectively, and most of these mice had entered the terminal phase of murine CM. Signs of CM included ruffled fur, loss of coordination, fitting, ataxia, coma, and body temperature lower than 32°C. Body temperature lower than 32°C was considered a proxy for a terminal outcome of the infection, as previously described.
On the day of euthanasia, mice were first briefly anesthetized using isoflurane (Baxter Healthcare Corp., Deerfield, IL). Packed cell volume was measured in PbK-infected mice after high-speed centrifugation of blood collected in capillary tubes. During anesthesia, mice were injected i.v. retro-orbitally with 80 mg/kg pimonidazole HCl (Hypoxyprobe-1 kit; HPI, Inc., Burlington, MA) and 15 mg/kg Hoechst 33342 (Catalog No. H3570; Invitrogen Corp., Carlsbad, CA) diluted in PBS (total volume, 300 μL), the latter to validate the success of the i.v. injection. Mice were allowed to recover, and the solution was left circulating for 30 minutes before euthanasia via cervical dislocation under deep isoflurane anesthesia. The brain was removed quickly, split sagittally, and immersion-fixed in formalin for 24 hours at room temperature before transfer to 70% (v/v) ethanol. Tissue was paraffin-embedded automatically using a Histokinette (Shandon, Inc., Pittsburgh, PA) and cut into 5-μm thin sagittal sections and 30-μm thick sections for Z-stacks.
Immunohistochemistry
Sections were cleaned of paraffin and rehydrated according to standard procedures. Heat-induced epitope retrieval was performed by boiling sections in citrate buffer (pH 6) in a microwave oven. Endogenous peroxidase activity was quenched via incubation in 0.5% (w/v) H2O2 (diluted from 30% H2O2; Sigma-Aldrich Corp., St. Louis, MO) dissolved in Tris-buffered saline solution with 0.5% (v/v) Tween-20 (Merck KGaA, Darmstadt, Germany). Nonspecific binding was blocked using serum-free protein block (Catalog No. X0909; Dako A/S, Glostrup, Denmark). Primary antibodies used included mouse anti-pimonidazole (50× dilution; HPI, Inc.) and mouse anti–HIF-1α (600× dilution; Catalog No. ab1; Abcam, Inc., Cambridge, MA). Primary antibodies were diluted in 10% (v/v) goat serum (In Vitro A/S, Fredensborg, Denmark) and incubated overnight at 4°C. Primary antibodies were detected using a biotinylated goat anti-mouse secondary antibody (200× dilution; Catalog No. B8774; Sigma-Aldrich Corp.). Biotinylated antibody was labeled using an avidin-biotin-peroxidase complex according to the manufacturer's recommendations (Vectastain ABC kit; Catalog No. PK4000; Vector Laboratories, Inc., Burlingame, CA) and was visualized using 3,3-diaminobenzidine tetrahydrochloride tablets (Kem-En-Tec Diagnostics A/S, Taastrup, Denmark) dissolved in Tris-buffered saline solution–0.5% Tween 20 with 0.015% H2O2 (Sigma-Aldrich Corp.). Sections were counterstained using Mayer's hematoxylin (VWR International ApS, Herlev, Denmark) before mounting. Chromogenically stained samples were visualized using an Imager.Z1 microscope fitted with an AxioCam MRc5 Camera (Carl Zeiss MicroImaging GmbH, Göttingen, Germany).
To assess the co-localization of pimonidazole reactivity with a specific cell type, anti-pimonidazole was co-incubated overnight with rabbit anti-glial fibrillary acidic protein (250× dilution; Catalog No. Z334; Dako A/S) for co-localization with astroglia. The primary antibodies were detected using goat anti-mouse IgG–Alexa 568 (1000× dilution; Catalog No. A11031; Invitrogen Corp.) and goat anti-rabbit IgG–Alexa 488 (1000× dilution; Catalog No. A11034; Invitrogen Corp.). For neuronal co-localization, the anti-pimonidazole was first incubated alone overnight, detected using goat anti-mouse IgG–Alexa, and incubated for 40 minutes at room temperature with mouse anti-neuronal nuclei–Alexa 488 (100× dilution; Catalog No. MAB377X; Chemicon, Milipore Corp., Billerica, MA). For labeling of vessels, a fluorescein isothiocyanate–conjugated tomato lectin (100× dilution; Catalog No. FL-1171; Vector Laboratories, Inc.) was incubated simultaneously with the primary antibody. Nuclei were labeled using DAPI (20,000× dilution; Catalog No. D1306; Invitrogen Corp.).
Low-magnification fluorescence microscopy was performed using an Olympus IX-71 equipped with an F-view CCD camera (Olympus Corp., Tokyo, Japan) illuminated with a mercury burner. Confocal immunofluorescence microscopy was performed using a Nikon TE 2000E Eclipse with 60× numerical aperture 1.4 Apoplan oil immersion objective lens (Nikon Instruments, Inc., Melville, NY), with gain adjusted for each laser (408 nm, 450/35; 488 nm, 515/30; and 543 nm, 605/75). Optical sectioning was performed in 600-nm increments. Standard negative control staining, without any primary antibody, was performed simultaneously for each primary antibody.
Quantification of Immunopositive Cells
All slides were randomized, blinded, and assessed using digital image analysis by one individual (C.H.). The degree of hypoxia was assessed by thresholding the staining intensity for pimonidazole-labeled areas in various parts of the brain including the olfactory lobe, cortex, corpus callosum, hippocampus, thalamus, hypothalamus, cerebellum, midbrain, pons, and medulla. Photographs were taken at identical settings using an RGB filter at 200× magnification with 2 × 2 mosaic function to increase the area sampled (area per micrograph, 1.456 mm2). If the region did not fill the entire frame (eg, when tissue boundaries and ventricles were included), these areas were cropped using ImageJ software (version 1.43I; National Institutes of Health, Bethesda, MD). The segmentation plug-in (ImageJ) was used to perform color-based thresholding on the brownish diaminobenzidine precipitation. Thresholding of the images was performed by sampling tissue with positive staining repeatedly in various areas and sections. From these randomly chosen areas, it was possible to set hue (stop), saturation (pass), and brightness (pass), which convincingly differentiated intensely stained tissue from unstained tissue and artifacts. The filtered image was converted to eight-bit gray scale and thresholded in a manner similar to that previously described.
The number of HIF-1α–positive cells was assessed from a total of at least 16 (range, 16 to 21) micrographs per sagittal section from random parts of the brain. All images were obtained at 200× magnification with deformation on the x axis 2000 μm and on the y axis 2000 μm [A(sample) = 4 mm2] using a motorized stage (piezodrive; Märzhäuser Wetzlar GmbH & Co. KG, Wetzlar, Germany). The area of the field of vision [A(frame)] was 0.364 mm2, yielding a sampling fraction of A(sample)/A(frame) of approximately 11. The number of cells was calculated from N = ΣQ− × A(sample)/A(frame) × corners in tissue/(micrographs sampled × 4), where N is the total number and ΣQ− is the counted number (modified from Andersen et al.
). The number of corners in tissue divided by the number of micrographs times 4 was used as a correction factor, taking into account that tissue may not completely cover the area of sampled micrographs. It was noted whether the HIF-1α–positive cells were endothelial cells, neurons, glial cells, or cells in circulation on the basis of morphologic characteristics. Flat cells lining vessels were termed endothelial cells; cells with large round nuclei were termed neurons; smaller ovoid, flat, or round nuclei were termed glial cells; and nucleated cells trapped inside the vessels were leukocytes.
Statistical Analysis
Groupwise comparisons were performed using one-way analysis of variance and post hoc tests (Welch test) for parametric data. Kruskal-Wallis and appropriate post hoc tests were used for non-parametric data. Survival analyses were performed using a log rank test. All statistical analyses were performed using R for Windows (version 2.10.1; http://www.r-project.org). P < 0.05 was considered statistically significant.
Results
Experimental Models and Outcome
Use of different inbred mouse strains and murine parasite lines enabled comparison of animals with and without CM. Parasitemia progressively increased in all experiments, although to a different extent (repeated-measures analysis of variance, P = 0.001; Figure 1). However, terminal parasitemia was not significantly different between the groups (analysis of variance, P = 0.061; Figure 1). Clinical manifestations of CM were observed only in PbA-infected CBA mice and C57BL/6 mice. CBA mice died on day 7 after infection, with low parasitemia, whereas C57BL/6 died on day 8 after infection, with notably higher parasitemia (mean ± SD, 5.1% ± 1.9 versus 10.4% ± 4.7; P = 0.0289). PbK-infected CBA mice demonstrated parasitemia comparable to that in C57BL/6 mice (8.8% ± 5.4; P = 0.58) but exhibited no signs of CM. Packed cell volume in PbK-infected mice was 0.35 ± 0.04. In PARP−/− and WT mice, parasitemia at the time of death was similar: 6.4% ± 0.70 versus 6.3% ± 1.2 (Welch test, P = 0.83) and comparable to that in moribund C57BL/6 mice euthanized at day 8 in other experiments (Welch test, P = 0.12 and P = 0.13).
Figure 1Parasitemia in experimental groups. The parasitemia was calculated from Diff-Quick–stained thin blood smears at days 5, 6, and 7 after infection in CBA mice and at flow cytometry in C57BL/6 mice. The number of mice in the two infections in CBA mice was 7 at each time point, and 5 in the C57BL/6-infected mice. Data are from two separate experiments.
Pimonidazole HCl was injected i.v. to detect hypoxic areas. Few areas and cells seemed to be hypoxic in noninfected mice (Figure 2, A and D). In non-CM, ie, in PbK-infected CBA mice (Figure 2, B and E) and in PbA-infected BALB/c mice (data not shown), some cells stained positive for hypoxia. The cells were scattered and non-uniformly distributed. In both CM models, ie, PbA-infected CBA and C57BL/6 mice, the number of positive cells was visibly higher, and cells were often grouped in multicellular foci. Moreover, in CM mice, the intensely labeled cells often were surrounded by areas of low-intensity intercellular and intracellular staining (Figure 2, C, F, and I, and Figure 3). Staining was also localized perivascularly (Figure 2, C and F; see also Supplemental Video S1 at http://ajp.amjpathol.org). The degree of hypoxia was assessed from binary masked chromogenic images from different areas of the brain in a sagittal view covering the entire brain (Figure 4, D–G). A groupwise comparison revealed highly significant differences (Kruskal-Wallis test, P < 0.001; Figure 2J), and CM mice demonstrated an approximately fivefold higher degree of pimonidazole reactivity than did non-CM mice. Post hoc tests revealed that noninfected and PbA-infected mice, in particular, differed in level of hypoxia (P < 0.001). Non–CM PbK-infected mice also demonstrated significantly more staining than did noninfected mice (P = 0.013), although significantly less than PbA mice (P = 0.0028). In C57BL/6 mice infected with PbA (CM) (Figure 3, saline solution–treated PbA), the staining pattern and intensity were similar to those in PbA-infected CBA mice despite less parasitemia, and these mice demonstrated significantly more staining than did noninfected mice (Wilcoxon test, P < 0.001; Figure 3D).
Figure 2Fluorescent representations of pimonidazole binding in uninfected (A), PbK-infected (B), and PbA-infected (C) CBA mice. Images are representative of results from the noninfected mice in each group at day 7 after infection. DAPI labels nuclei blue, and antibodies detecting pimonidazole adducts emit light in the red spectrum. The area framed by the white box is enlarged in the upper right corner in C. Chromogenic representations of pimonidazole binding in uninfected (D), PbK-infected (E), and PbA-infected (F) mice. The framed area in E is shown at higher magnification in G, and for F, the areas are magnified in H and I. Staining shows positively labeled cells (G and H) and cells surrounded by smears of labeling (I). In I, distinct cells can be observed, including an astrocyte-like cell (white arrow) and a neuron-like cell (black arrow). Scale bars: 200 μm (A–C, but not inserts); 100 μm (D–F); 25 μm (G–I). Quantification of staining is represented for selected regions in boxplots. J: All areas/total demonstrated a significant increase in PbA-infected mice (P < 0.001) and PbK-infected mice (P = 0.013) compared with noninfected mice. PbA-infected mice demonstrated significantly higher levels of hypoxia than did PbK-infected mice (P = 0.0028). K: In the corpus callosum, PbA-infected mice demonstrated significantly more hypoxia than did noninfected mice (P = 0.024), and likewise in the midbrain (L) (P = 0.021) and pons (M) (P = 0.0082). Values are given as normalized to noninfected mice. The boxplots show the median as a line, interquartile hinges, and the whiskers encompass values 1.5× from the interquartile range (Tukey test). Open circles indicate outliers. *0.05 > P > 0.01, **0.01 > P > 0.001, ***P < 0.001 using the Wilcoxon rank test.
Figure 3A: EPO treatment reduces the risk of CM, which can be assessed by measuring body temperature. Quantifications of the overall distribution of pimonidazole adducts are depicted in a boxplot (D) expressed relative to saline solution–treated noninfected mice. PbA-infected mice demonstrated a significantly higher level of hypoxia than did EPO-treated infected mice (P = 0.015) and noninfected mice (P < 0.001). Boxplots show the median as a line, interquartile hinges, and whiskers encompass values 1.5× from the interquartile range (Tukey test). Circles indicate outliers. *0.05 > P > 0.01, ***P < 0.001 using the Wilcoxon rank test. Representative micrographs depict pimonidazole staining in saline solution–treated nonfected (B), EPO-treated noninfected (C), saline solution–treated PbA-infected (E), and EPO-treated PbA-infected (F) mice. Black arrow indicates a cell with neuron-like structure. White arrow indicates a glial-like cell. Scale bars: 100 μm.
Figure 4Approaches to assessment of tissue hypoxia. A: Tissue was cut in sagittal sections. B: For HIF-1α, the fractionator principle was applied, only counting cells in a predetermined fraction of the tissue. C: Each micrograph was assessed for HIF-1α expression, and the cellular subset was noted. V indicates the vessel lumen, and nucleated cells trapped intravascularly were noted for being HIF-1α–positive, if observed. Asterisk indicates a glial cell, arrowhead denotes an endothelial cell, and arrow indicates a neuron. D: For pimonidazole reactivity, a multifocal staining pattern was observed in CM mice. To assess the degree of hypoxia in each region of interest (E), the image was color thresholded (F) and converted to a binary image (G).
From this generalized approach, we proceeded to assess whether the differences were restricted to particular brain regions. A significant difference in pimonidazole binding was observed in the corpus callosum (Figure 2K; Kruskal-Wallis test, P = 0.028; noninfected versus PbA, P = 0.024), the medulla (data not shown; P = 0.048), the midbrain (Figure 2L; P = 0.032; noninfected versus PbA, P = 0.021), the pons (Figure 2M; P = 0.011; noninfected versus PbA, P = 0.0082), and the olfactory lobe (data not shown; P = 0.041). In contrast, no significant difference was observed in the cerebellum (P = 0.35), the cortex (P = 0.31), the hippocampus (P = 0.66), the hypothalamus (P = 0.48), or the thalamus (P = 0.80). The staining was regional within each individual infected mouse; thus, one mouse did not necessarily demonstrate pronounced staining in the pons, medulla, and olfactory lobe. The low-intensity staining was specific inasmuch as it was observed only in CM mice. This staining pattern was similar in fluorescent and chromogenic detection and, thus, could not be ascribed to endogenous biotin, peroxidase activity, or autofluorescence. Thus, it reflected hypoxia, albeit at a slightly lower grade than that observed in some single large cells. The detection and assessment of cerebral hypoxia was demonstrated to be reproducible in independent experiments.
Cellular Localization of Pimonidazole Reactivity Using Fluorescent Labeling
To try to identify the cell types affected by hypoxia, we performed double staining for neurons and astrocytes, respectively, together with pimonidazole. As noted in the representative micrographs, pimonidazole staining using fluorescence was detectable in neurons but was not visible in astrocytes (Figure 5, A and B, respectively). This staining pattern was compared with the observed cell architecture at chromogenic staining (Figures 2 and 3). In both of these figures, positively staining single cells with astrocyte-like architecture are visible, whereas they were not visible on fluorescent images. Thus, chromogenic staining seems to be more sensitive than fluorescent labeling for detection of hypoxia under our experimental conditions. In PbK-infected mice without CM, only a few neurons were positive for hypoxia (Figure 2G).
Figure 5Double immunofluorescence of pimonidazole (HP) binding and neurons (NeuN) (A) and astrocytes (GFAP) (B) at day 7 after infection. NeuN labels neuronal nuclei and the perinuclear area. Arrows denote pronounced co-localization of areas in which both neurons and pimonidazole are present. When staining for astrocytes, co-localization is not observed. Scale bars: 25 μm.
Increased Level of HIF-1α Expression in PbA-Infected Mice
Similar to pimonidazole reactivity, the level of HIF-1α was significantly increased in infected mice (Figure 6). However, the staining pattern for HIF-1α was different from that for pimonidazole binding. It was more common to find single or small groups of HIF-1α–positive cells in the same area (Figure 6, A–C). Clusters of positive cells were also detected, but only in PbA-infected mice (Figure 6, D–F). There was a significant difference between the groups in the number of endothelial cells that stained positive for HIF-1α (Figure 6G; analysis of variance, P = 0.031). The number of HIF-1α–positive endothelial cells in PbA-infected mice was larger; however, there was only borderline significance when compared with noninfected mice (Welch test, P = 0.05), and no difference when compared with PbK-infected mice (Welch test, P = 0.069). There were no statistically significant differences between the number of HIF-1α–positive glial cells (Figure 6J; analysis of variance, P = 0.31), neurons (Figure 6I; analysis of variance, P = 0.45), or intravascular cells in the various groups (Figure 6; analysis of variance, P = 0.62). Primarily glial cells with astrocyte-like architecture, but also microglial-like cells were HIF-1α–positive. Clusters of HIF-1α–positive cells (Figure 6, D–F) were observed only in PbA-infected mice.
Figure 6Representative images of HIF-1α staining in noninfected (A), PbK-infected (B), and PbA-infected (C) mice. Diverse expression in several cell types was observed in patches (D), and pronounced perivascular labeling of neurons was demonstrated in PbA mice (E and F). F: Nuclei are blue, vessels are green, and HIF-1α–positive cells are red. Scale bars: 100 μm (A–C); 50 μm (D–F). Quantifications are visualized in stripcharts for each quantitative trait: G: Endothelial cells. H: Intravascular staining. I: Neurons. J: Glial cells. Horizontal bar indicates the mean, and vertical bars indicate SD. *0.05 > P > 0.01 using the Wilcoxon rank test.
To assess whether cytopathic hypoxia was essential for development of murine CM, PbA infection in PARP-1−/− knockout mice was compared with that in C57BL/6 WT mice. There was no statistically significant difference in survival between PARP-1−/− and WT mice (P = 0.15) (Figure 7), and the infection was clinically indistinguishable in WT and knockout mice. Both knockout and WT moribund mice exhibited signs of CM, and most died on days 7 to 9 after infection.
Figure 7Survival curves of WT and PARP knockout mice. Most mice of both genotypes died of CM at days 7 to 9 after infection. PARP−/− mice were not protected (P = 0.15), although the onset of symptoms seemed to be delayed by approximately 1 day in the PARP knockout genotype. Data for PARP−/− mice are indicated by the filled line and circles, and for PARP WT mice by the dashed line and squares.
EPO Therapy Improves Survival and Decreases Hypoxia
To assess whether ameliorative treatment with EPO also reduced cerebral hypoxia, we included four groups of mice: those with or without PbA infection and those with or without EPO therapy. Similar to findings of previous studies,
EPO therapy significantly improved survival (analysis of variance, P = 0.01; Figure 3A) and reversed the clinical symptoms of CM. EPO therapy reduced tissue hypoxia (Figure 3) in comparison with saline solution–treated mice with CM (Kruskal-Wallis test, P < 0.001; Figure 3, B–F). Post hoc tests revealed no statistically significant difference between the two uninfected groups (P = 0.80; Figure 3, B and C), whereas infected saline solution–treated mice (Figure 3E) demonstrated significantly more staining than did noninfected mice (P < 0.001) and infected EPO-treated mice (P = 0.015; Figure 3F). PbA-infected EPO-treated mice did not differ significantly from the noninfected groups in the amount of pimonidazole staining (P = 0.54 for both groups).
Discussion
The present study directly demonstrates the presence of multifocal areas of cerebral hypoxia in two murine models of CM. To our knowledge, this is the first study of its kind and provides strong direct evidence that tissue hypoxia is present in CM. A distinct staining pattern was observed, with marked hypoxia in neuronal somas and widespread low-grade intercellular and intracellular hypoxia. The staining pattern was unrelated to peripheral parasitemia but was closely related to cerebral manifestations. Single cells with astrocyte-like architecture also were hypoxic. This diffuse staining pattern is in accordance with findings of previously published articles on the use of pimonidazole HCl as a probe for hypoxic tissue.
Murine cerebral malaria is associated with a vasospasm-like microcirculatory dysfunction, and survival upon rescue treatment is markedly increased by nimodipine.
Correlation between enhanced vascular permeability, up-regulation of cellular adhesion molecules and monocyte adhesion to the endothelium in the retina during the development of fatal murine cerebral malaria.
In particular, the olfactory lobe and the brainstem were affected with hypoxia. The impaired microcirculation is of pathophysiologic relevance owing to impaired oxygen delivery. Even perivascularly, cerebral hypoxia was observed in terminally ill mice with CM. Optical sectioning (Video S1) demonstrated an example of one such area in which hypoxic cells in the brain parenchyma are adjacent to plugged vessels. The extent of cerebral hypoxia detected in CM mice likely causes impaired neuronal communication,
A low degree of hypoxia could also be demonstrated as scattered, single, hypoxic cells in non-CM models without clinically obvious neurologic impairment, which suggests that even in the absence of cerebral signs, malaria may affect neural tissue.
A close association was not observed between the hypoxic brain areas detected using pimonidazole binding and the areas that seemed to be hypoperfused in other studies that used magnetic resonance imaging.
One explanation for this could be that the frequent vasospasms observed in murine CM are localized primarily in the cerebral cortex, whereas smaller, yet more severe, focal occlusions in other parts of the brain may not be observed on magnetic resonance images.
Cerebral hypoxia is a serious condition that, if not reversed, will lead to severe brain injury. A compensatory increase in cerebral blood flow is the natural response to local hypoxia. This may be another reason why relatively crude measurements of perfusion have yielded conflicting results about blood flow in human CM. Transcranial Doppler ultrasound failed to demonstrate decreased blood flow in human CM
; however, the resolution of the technique may not be sufficient to detect localized foci of hypoperfusion and occlusion. Low resolution has also proved limiting in magnetic resonance imaging in patients with CM.
underscore the need to address strategies to reverse cerebral occlusion and hypoperfusion.
In non-CM mice, hypoxia was much less pronounced than in CM mice, and was confined to neuronal somas. This is most likely because tissue oxygenation is balanced between oxygen supply and metabolic rate. Thus, in conditions of slightly decreased oxygen supply, which is likely in non-CM mice with severe anemia,
Magnetic resonance spectroscopy reveals an impaired brain metabolic profile in mice resistant to cerebral malaria infected with Plasmodium berghei ANKA.
The hypoxia in non-CM mice could not be explained by reduced microcirculation because the PbK parasites used in the study do not sequester in the microvasculature.
When patients with malaria without CM were assessed for retinopathy, retinal whitening was detected, which suggests some degree of hypoperfusion and ischemia in uncomplicated malaria in humans.
During normoxia, HIF-1α is quickly degraded by ubiquitinylation in the cytosol, whereas hypoxic conditions facilitate the heterodimerization of HIF-1α and HIF-1β (constitutively expressed), nuclear translocation, and binding to the hypoxia-responsive elements on downstream targets.
Nuclear translocation was not obvious in the present study inasmuch as most staining was cytosolic. A high level of cytosolic HIF-1α expression points to increased stabilization of HIF-1α and limited nuclear translocation. A high level of cytosolic HIF-1α has been documented previously during hypoxic stimulation in vitro.
Detection of reactive oxygen species via endogenous oxidative pentose phosphate cycle activity in response to oxygen concentration: implications for the mechanism of HIF-1alpha stabilization under moderate hypoxia.
We assessed expression at one time point only, and HIF-1α might be translocated later. In addition to hypoxia, several mediators regulate HIF-1α expression, stabilization, and degradation. One of those is c-Jun N-terminal kinase-1, which increases stabilization in the cytosol.
In contrast to pimonidazole staining, which was primarily localized in neurons, the HIF-1α–positive cells were predominantly endothelial cells. This discrepancy most likely reflects the two different parameters detected by these markers. Pimonidazole reactivity solely reflects low oxygen tension, whereas HIF-1α demonstrates the acute cellular response to hypoxia and inflammation. Because HIF-1α expression is an important physiologic response to hypoxia, it may be speculated that the low levels of HIF-1α in tissues with pronounced hypoxia may represent an insufficient response that contributes to development of CM. If some degree of respiratory impairment in the neuronal mitochondria is assumed, this promotes prolyl hydroxylase-dependent degradation of HIF-1α stability,
which may negatively influence detection. Inasmuch as HIF-1α is also involved in a cellular response to inflammation, it is likely that this arm is most heavily affected in the endothelium lining the vessels with increased levels of inflammatory cytokines,
thereby sustaining a detectable response. The method described herein will enable this hypothesis to be addressed further in future studies.
In human brain tissue obtained postmortem, no HIF-1α expression was observed; however, HIF-2α was detected in the nuclei and cytoplasm in the vasculature and to a significantly larger extent in CM.
Induction of the vascular endothelial growth factor pathway in the brain of adults with fatal falciparum malaria is a non-specific response to severe disease.
Induction of the vascular endothelial growth factor pathway in the brain of adults with fatal falciparum malaria is a non-specific response to severe disease.
raised the possibility that local cerebral perfusion may compensate for occlusions caused by sequestering cells in the vascular beds; however, this is to some extent contradicted by the increased levels of HIF-2α, vascular endothelial growth factor, and DEC-1, all proteins induced by hypoxia. The failure to detect HIF-1α probably reflects the heterogeneity of the study population, and in particular the short half-life of HIF-1α, more than its unchanged expression.
Consistent with this interpretation, HIF-2α is up-regulated for a considerably longer time during prolonged hypoxia and is not considered an acute marker of hypoxia.
which is a strongly hypoxia-regulated cytokine. In the present study, EPO therapy initiated before the onset of neurologic symptoms resulted in a significant decrease in cerebral hypoxia, which coincided with decreased signs of CM. Indeed, EPO reverted tissue hypoxia, as indicated by the pimonidazole technique, to the levels in noninfected mice. EPO is neuroprotective in both cerebral hypoxia and ischemia-reperfusion injury,
and, thus, seems to be a promising candidate for adjunctive treatment of CM, in particular with respect to hypoxia. Previous studies have documented that EPO dose-dependently reduces the mortality of murine CM.
Studies of endogenous EPO in human CM have yielded conflicting findings. Some authors have suggested that its local expression in the brain is unrelated to CM,
. Another and perhaps more important property of EPO in the context of CM is its stimulatory effect on nitric oxide secretion caused by endothelial nitric oxide synthase,
The role of nitric oxide in CM has been thoroughly evaluated, and decreased production has been suggested to be important in the pathogenesis of murine and human CM.
These pleiotropic effects of EPO likely contribute to the improved survival in complex ways. EPO seemed to decrease parasitemia, which might contribute to survival in these mice, although this remains to be established.
There was a tendency toward slightly delayed development of CM in PARP−/− mice; however, this was not significant. It has been hypothesized that cytopathic hypoxia has a significant contributory role in the pathogenesis of CM.
PARP-1 does not seem to be the driving force for murine CM.
The use of isoflurane as anesthetic also needs to be addressed. In several studies, isoflurane, compared with other anesthetic agents, maintained stable cerebral blood flow and high tissue oxygenation
The role of cerebral metabolism in determining the local cerebral blood flow effects of volatile anesthetics: evidence for persistent flow-metabolism coupling.
and, thus, does not cause false interpretations of tissue hypoxia. Indeed, the decrease in blood pressure and cerebral perfusion caused by the related anesthetic desflurane has been associated with increased brain oxygenation,
The role of cerebral metabolism in determining the local cerebral blood flow effects of volatile anesthetics: evidence for persistent flow-metabolism coupling.
Extracellular signal-regulated kinases trigger isoflurane preconditioning concomitant with upregulation of hypoxia-inducible factor-1alpha and vascular endothelial growth factor expression in rats.
Extracellular signal-regulated kinases trigger isoflurane preconditioning concomitant with upregulation of hypoxia-inducible factor-1alpha and vascular endothelial growth factor expression in rats.
as opposed to the brief duration in the present study. Thus, anesthesia likely is not the cause of the observed changes.
Pimonidazole-based detection of hypoxia is semiquantitative but has been shown to distinguish hypoxic areas as well as with use of a quantitative enzyme-linked immunosorbent assay–based approach.
Furthermore, IHC enabled us to obtain detailed information about the perivascular expression pattern and to pinpoint neuronal and perivascular hypoxia due to cerebral hypoperfusion. Considered together with the bulk of data on hypoperfusion in murine and human CM,
Murine cerebral malaria is associated with a vasospasm-like microcirculatory dysfunction, and survival upon rescue treatment is markedly increased by nimodipine.
this new approach seems appropriate for further mechanistic research. The results overall suggest that cerebral hypoperfusion leads to tissue hypoxia in murine CM and that this is likely a key event in development of acute cerebral disease.
Acknowledgments
We thank Nicolas Gleichenhaus (Université de Nice-Sophia Antipolis, France) for information about where to purchase PARP-1 knockout mice and Fatima El-Assaad for expertise during i.v. injections.
In this z stack (30 μm) neuron-like cells are stained positive for pimonidazole in spite of close proximity to a vessel. Pimonidazole binding is visualised in red, FITC-conjugated lectin binds to the endothelium and DAPI stains nuclei blue. The recording is made using a 60x objective as described in materials and methods.
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Detection of reactive oxygen species via endogenous oxidative pentose phosphate cycle activity in response to oxygen concentration: implications for the mechanism of HIF-1alpha stabilization under moderate hypoxia.
Induction of the vascular endothelial growth factor pathway in the brain of adults with fatal falciparum malaria is a non-specific response to severe disease.
The role of cerebral metabolism in determining the local cerebral blood flow effects of volatile anesthetics: evidence for persistent flow-metabolism coupling.
Extracellular signal-regulated kinases trigger isoflurane preconditioning concomitant with upregulation of hypoxia-inducible factor-1alpha and vascular endothelial growth factor expression in rats.
Supported by Aase og Einar Danielsen Fonden, Fonden til Lægevidenskabens Fremme, and the Australian National Health and Medical Research Council (NHMRC project grants 571014 and 512469). C.H. was funded by a grant from the Danish Council for Independent Research–Medical Sciences (FSS; grant 2112-04-0015).
C.H. and V.C. contributed equally to this work.
Supplemental material for this article can be found on http://ajp.amjpathol.org or at doi: 10.1016/j.ajpath.2011.06.027.
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