Integrin αDβ2 influences cerebral edema, leukocyte accumulation and neurologic outcomes in experimental severe malaria

Malaria is an infectious disease of major worldwide clinical importance that causes a variety of severe, or complicated, syndromes including cerebral malaria, which is often fatal. Leukocyte integrins are essential for host defense but also mediate physiologic responses of the innate and adaptive immune systems. We previously showed that targeted deletion of the αD subunit (αD-/-) of the αDβ2 integrin, which is expressed on key leukocyte subsets in mice and humans, leads to absent expression of the integrin heterodimer on murine macrophages and reduces mortality in mice infected with Plasmodium berghei ANKA (P. berghei ANKA). To further identify mechanisms involved in the protective effect of αD deletion in this model of severe malaria we examined wild type C57BL/6 (WT) and αD-/- mice after P. berghei ANKA infection and found that vessel plugging and leukocyte infiltration were significantly decreased in the brains of αD-/- animals. Intravital microscopy demonstrated decreased rolling and adhesion of leukocytes in cerebral vessels of αD-/- mice. Flow cytometry analysis showed decreased T-lymphocyte accumulation in the brains of infected αD-/- animals. Evans blue dye exclusion assays demonstrated significantly less dye extravasation in the brains of αD-/- mice, indicating preserved blood-brain barrier integrity. WT mice that were salvaged from P. berghei ANKA infection by treatment with chloroquine had impaired aversive memory, which was not observed in αD-/- mice. We conclude that deletion of integrin αDβ2 alters the natural course of experimental severe malaria, demonstrating previously unrecognized activities of a key leukocyte integrin in immune-inflammatory responses that mediate cerebral involvement.

α D β 2 alters the natural course of experimental severe malaria, demonstrating previously unrecognized activities of a key leukocyte integrin in immune-inflammatory responses that mediate cerebral involvement.

Introduction
Malaria remains the world's most important parasitic disease and causes a spectrum of clinical involvement [1,2]. In a minority of patients severe, or complicated malaria a constellation of syndromes with systemic manifestations and injury to critical organs are developed [2]. The most feared of these syndromes is cerebral malaria (CM), a serious and often fatal encephalopathy that is usually caused by in humans by Plasmodium falciparum. CM is most common in children in endemic regions, although nonimmune or semi-immune adults can also develop cerebral involvement [2,3]. CM is lethal in 15-20% of individuals affected, and patients who survive may have debilitating long-term neurocognitive dysfunction [3][4][5]. Nevertheless, the biologic features that underly CM and other manifestations of severe malaria have not been adequately investigated or characterized.
Obstruction of cerebral vessels resulting from adhesion of infected red blood cells (iRBC) to the vascular endothelium is thought to be a central mechanism in CM [2,3]. Sequestration of iRBC and their cytoadherence to the vascular endothelium are mediated by a variety of receptors including CD36, thrombospondin, VCAM-1, E-selectin, and endothelial protein C receptor [6][7][8][9][10][11][12]. Leukocytes and platelets sequestered in the microvasculature are also part of this vaso obstructive process [13][14][15][16][17][18]. Thus, CM is an inflammatory vasculopathy. In addition to vascular obstruction, CM is accompanied by an excessive production and release of inflammatory mediators. Among these mediators, TNF, IL-1β, MCP-1, and IFN-γ have been demonstrated to influence endothelial cell receptors, increasing iRBC cytoadherence and sequestration and promoting localization of activated leucocytes in the brains of infected animals in experimental models of severe malaria [19][20][21][22][23].
The leukocyte integrins are essential for host defense and mediate innate and adaptive immune responses via cell-cell and cell-extracellular matrix interactions that depend on specific ligand recognition. Binding of target ligands by leukocyte integrins not only tethers leukocytes to other cells and matrix but also delivers outside-in signals to intracellular pathways [24]. Adhesive interactions may play key roles in the pathophysiology of cerebral malaria, and leukocyte integrin activity is reported to be altered by malaria pigment [25][26][27][28][29]. Neverthelss, little is known about integrin expression and function in clinical or experimental malaria and the contributions of leukocytic integrins to severe complications of malarial infection.
We previously demonstrated that targeted deletion of α D results in non-expression of the integrinα D β 2 , reduces mortality in an experimental model of severe malaria infection by Plasmodium berghei ANKA (P. berghei ANKA) that includes profound cerebral involvement, [37]. Part of the survival advantage appears to be due to reduction in acute lung injury, which also occurs in P. berghei ANKA infection [38,43]. We now report that integrin α D β 2 mediates events in the pathogenesis of cerebral involvement in this surrogate model of severe malaria, and that genetic deletion of α D dramatically ameliorates neurological manifestations and outcomes.

Mice and parasites
C57BL/6 wild type (α D +/+ ) and α D β 2 -deficient (α D -/-) mice [37] weighing 20-25g, littermate, were obtained from the Oswaldo Cruz Foundation breeding unit and used throughout the study. The animals were kept at constant temperature (25˚C) with free access to food and water in a room with a 12-h light/dark cycle.
Plasmodium berghei ANKA (P. berghei ANKA) was maintained and provided by Dr. Leonardo de Moura Carvalho from Laboratório de Malária, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, RJ, Brazil), and used as the infective parasite. The blood stage forms of the parasites were stored in liquid nitrogen after in vivo passages in C57BL/6 mice according to the protocol described elsewhere [27]. Mice were infected intraperitoneally (i.p.) with 10 5 parasitized red blood cells and parasitemia was determined by direct light microscopy at different time points.
For cognitive impairment studies, the animals were inoculated intraperitoneally (i.p.) with 10 6 parasitized red blood cells, inoculum that was provided in order to standardize clinical and behavioural signs of CM at day 6 post-infection, allowing intervention with antimalarial drugs.

Ethics statement
The Animal Welfare Committee of the Oswaldo Cruz Institute approved the experiments in these studies under license number P-0528-08. The procedures described in this study were in accordance with the local guidelines and guidelines published in the National Institutes of Health Guide for the Care and Use of Laboratory Animals. The study is reported in accordance with the ARRIVE guidelines for reporting experiments involving animals.

Brain edema
The permeability of the blood-brain barrier was determined at 7 days post infection (dpi) by intravenous injection of Evans blue dye 2% (w/v) solution in phosphate-buffered saline (PBS). One hour later the animals were sacrificed with terminal anesthesia by isoflurane and the vasculature was intracardiacaly perfused with 20 mL phosphate-buffered saline (PBS) using a peristaltic pump system. Brain tissue was placed in 3 mL of formamide at 56˚C overnight to extract the Evans blue dye. The supernatant was read in a spectrophotometer at 620 nm [44].

Isolation of brain leukocytes
Leukocytes were isolated from mouse brains as described [45]. Briefly, at 7 dpi, P. berghei ANKA-infected mice were sacrificed and by intracardiacaly perfused with phosphate-buffered saline (PBS) for 5 min using a peristaltic pump system to remove both circulating and nonadherent RBC and leukocytes. Brains were collected and placed in a 50 mL tube containing ice-cold PBS, 0,05% collagenase D (Sigma-Aldrich) and 2U/mL DNase I (Sigma-Aldrich). The brain was cut in small pieces and passed through a 70 mm cell strainer placed in a 10 cm Petri dish containing 10 mL of iced-cold PBS. The material was centrifuge for 10 mim at 390 g, resuspended in 20 mL of 1x PBS plus 30% Percoll, overlaid onto 70% Percoll and centrifuged at 390g for 20 min at room temperature. The cells were collected from the interface and washed twice with PBS before counting in Neubauer chambers and labeled for flow cytometry.

Immunolabeling and flow cytometry
Cells were stained with appropriate dilutions of the following fluorochrome-labeled monoclonal antibodies (mAbs): PE-Cy5 anti-mouse CD8a (Ly-2 -clone 5-6.7) and FITC anti CD4 (L3T4 clone RM4-5) and then washed with PBS, fixed and analyzed by flow cytometry in a FACScalibur device (Becton Dickinson, USA). All reagents were purchased from Pharmingen/Becton-Dickinson (USA). Analyses were performed using CellQuest software. Cells were identified by their size (forward light scatter) and granularity (side light scatter) as previously described [46].

Brain extracts and cytokine measurements
Excised brain tissues (0.1 g) were placed in 1 mL of homogenization buffer and macerated. The homogenates were subsequently frozen in liquid nitrogen. Prior to cytokine assay, samples were thawed and centrifuged at 6000 g for 20 min at 4˚C and the supernatants were collected and used for cytokine measurements. Cytokines were analyzed using Luminex technology on the BioPlex system (Bio-Rad) using a mouse multiplex cytokine kit and assay protocols according to the manufacturer's instructions (Upstate Biotechnology). Data analyses were performed with the Bio-Plex Manager software.

Quantitative RT-PCR
Extraction of total RNA from brain and spleen was performed using TRIzol 1 (Invitrogen-Carlsbad, CA, USA), according to the manufacturer's instructions. After extraction, RNA concentration and quality were determined using a NanoDrop 2000 spectrophotometer (Thermo Scientific-Waltham, MA, USA). One microgram of total RNA was reverse-transcribed to single-strand cDNA using the SuperScript First-Stand (Invitrogen-Carlsbad, CA, USA). α D transcripts in the cDNA pool obtained from the reverse transcriptase reaction were quantified by real-time quantitative fluorogenic PCR. TaqMan Universal PCR Master Mix (Applied Biosystems-Foster City, CA, USA) was used to quantify gene expression according to the manufacturer's instructions. RNA expression levels were calculated using the Data Assist Software v.3, and normalized against the expression levels of the housekeeping gene hypoxanthine guanine phosphoribosyl transferase (HPRT) [37]. The primers used were as follows: α D (TaqManmurine-Mm01159115_m1) and HPRT (TaqMan-murine-Mm01545399_m1).

Intravital microscopy
Intravital microscopy was performed in infected and non-infected mice of both genotypes. Animals were anaesthetised with an intraperitoneal mixture of ketamine (150 mg/kg; Laboratório Cristália, Itapira, SP, Brazil) and xylazine (10 mg/kg; Rompun 1 ; Bayer, São Paulo, SP, Brazil). The tail vein was cannulated for the intravenous administration of fluorescent tracers and additional anesthesia. The core temperature was monitored with a rectal probe and maintained at 37˚C with a homoeothermic blanket system (Harvard Apparatus, Cambridge, UK). Intravital microscopy was performed as previously described [47]. Briefly, animals were fixed in a stereotaxic frame, the left parietal bone was exposed by a midline skin incision; a cranial window overlying the right parietal bone was created with a high-speed drill (Beltec, and the dura mater and the arachnoid membranes were excised and withdrawn to expose the cerebral microcirculation. The cranial window was suffused with artificial cerebrospinal fluid (in mmol: NaCl, 132; KCl, 2.95; CaCl2, 1.71; MgCl2, 0.64; NaHCO3, 24.6; dextrose, 3.71; and urea, 6.7; at 37˚C, pH 7.4). During this procedure, the core temperature was maintained at 37 C with the homoeothermic blanket system (Harvard Apparatus, Cambridge, UK). Rhodamine 6G (0.3 mg/kg; Sigma, St. Louis, MO, USA) was injected via the tail vein cannula. The animals were then placed under an upright fixed-stage intravital microscope equipped with a mercury lamp (Olympus BX51/WI, NY, USA) coupled to a CCD digital video camera system (Optronics, TKY, Japan). Olympus 20X objectives were used in the experiments and produced total magnifications of 200X.
In order to evaluate leukocyte-endothelial interactions in post-capillary venules, rhodamine 6G-labeled leukocytes were visualized with a fluorescent light source (epi-illumination at 510-560 nm using a 590 nm emission filter). Rolling leukocytes were defined as white cells moving at a velocity less than that of erythrocytes and expressed as number of cells/min). Leukocytes were considered to be adherent to the venular wall (100 μm of length) if they remained stationary for at least 30 seconds.

Histological analysis
Brain tissues were fixed in 10% phosphate-buffered formalin, processed and embedded in paraffin. Sections were cut 5 μm and stained with hematoxylin & eosin, and examined under a light microscope by a blinded pathologist.

Neurobehavioral parameters
CM was defined by clinical evaluation of neurobehavioral parameters based on a multifactorial SHIRPA protocol as described previously [48][49][50]. CM was identified by the observation of eighteen clinical signs, and to each alteration was given grade one. Above foursigns, including piloerection, curved trunk, alterations in gait, seizures, limb paralysis, coma, respiratory rate, skin color alterations, heart rate, lacrimation, palpebral closure, decreased grip strength, limb, abdominal and body tone and body temperature alterations it was considered clinical CM, that was confirmed by histological evaluation [27].

Step-down inhibitory avoidance test
The step-down inhibitory avoidance test was performed as we previously described [27]. Animals that were positive for evidence for CM by SHIRPA testing were treated with oral chloroquine (25 mg/kg b.w.) [48], started six days after infection and continued for seven days. Fifteen days post-infection, animals were subjected to behavioral tests. In the training phase, animals were placed on a platform and their latency to step down on the grid with all four paws was measured with an automatic device. Immediately upon stepping down on the grid the animals received a 0.6 mA, 3.0-second foot shock. A retention test trial was performed 1.5 and 24 h after training and the time the animals spent on the platform was recorded.

Statistics
Statistical analysis was carried out using the GraphPad Prism software (San Diego, CA, USA). P values were calculated using an unpaired Ordinary one-way ANOVA test when result from more than two groups were analyzed among each other, the post test used was the bonferroni's multiple comparison test. P values were generated using an unpaired T-test when result from only two groups were analyzed. Results are expressed as means ± SEM (median (IQR)). The level of significance was set at P� 0.05.

Plasmodium berghei ANKA infection increases the expression of α D mRNA transcripts in brain tissue
P. berghei ANKA infection in mice is a standard model of experimental cerebral malaria and reproduces most aspects of the human pathology [20,51,52]. CM development can be observed to day 6 to 12 post-infection. Accodantly [53,54], mice that have survived so on presented severe anemia. Once our main interest was the role of α D β 2 integrin, we performed our analysis at day 7 and 10 post-infection. To investigate if P. berghei ANKA infection modulates α D subunit expression in the brains of infected mice, we examined α D mRNA by real time PCR in brain samples from infected and control animals compared to levels detected in the spleen, where there is high constitutive of integrin α D β 2 on macrophage subpopulations [37]. Real time PCR analysis of uninfected animals demonstrated a low level of the α D transcript in the brain, consistent with absence of cerebral α D β 2 by immunohistochemical analysis under basal conditions [37]. Expression of the α D transcript in the brain increased dramatically at 7 and 10 days after infection with P. berghei ANKA (Fig 1). Integrin α D β 2 deficiency alters the abundance of inflammatory mediators in the brain during experimental CM The production of inflammatory mediators in the brain is thought to be a critical determinant of CM pathophysiology and neurologic outcomes in severe malaria [21,22,55,56]. We previously found that α D β 2 deficiency alters the patterns of systemic and lung cytokines and chemokines during P. berghei ANKA infection, leading to a delay in mortality, but without triggering alteration in parasitemia when compared to infected wild animals (S1A and S1B Fig) [37, 38]. Therefore, we measured cytokine and chemokine levels in brain tissue using specific Luminex assays and found increased accumulation of IL-6 (Fig 2A), KC (Fig 2B), IL-17 (Fig 2C), MCP-1 (Fig 2D), IFN-g ( Fig 2E) and TNF-α ( Fig 2F) in infected α D +/+ mice as compared to uninfected controls. In contrast, brain cytokine levels in infected α D -/mice were modestly increased when compared to uninfected controls, and cytokines values were significantly decreased in comparison to levels in infected α D +/+ mice (Fig 2A-2F). These results indicate that regulation of cytokine production and accumulation in the brain is directly or indirectly influenced by α D β 2 in P. berghei ANKA infection.

Cerebral edema and leukocyte plugging of microvessels are significantly decreased in α D β 2 -deficient mice
The histology of cerebral malaria is characterized by brain edema, partial or complete occlusion of brain microvessels due to accumulation of host blood cells, micro-hemorrhages and, in some cases, necrosis of the surrounding parenchyma [5,14,57,58]. To assess the status of the blood-brain barrier (BBB) and cerebral edema during P. berghei ANKA infection, α D +/+ and α D -/mice were infused with Evans blue dye and brain vascular barrier permeability was examined by quantification of dye extravasation in the brain tissue. We observed a reduction of dye extravasation in α D -/mice as compared to α D +/+ animals (Fig 3A and 3B) on day 7 post-infection, a time point at which clinical scoring also indicated amelioration of neurological signs of experimental CM in α D -/mice ( Fig 3C).
Neurologic signs that herald onset of experimental CM are generally accompanied by the sequestration of leukocytes and infected erythrocytes in the cerebral vasculature [20,27,48]. Histological analysis of brain sections obtained seven days post-infection from infected α D +/+ mice revealed accumulation of leukocytes in brain microvessels, and inflammatory interstitial infiltrates in the parenchyma (Fig 4C and 4D). In contrast, these features were not detected in samples from uninfected α D +/+ or α D -/mice (Fig 4A and 4B, respectively) or in brain tissue from infected α D -/animals (Fig 4E and 4F). Thus, preservation of BBB integrity in infected α D -/mice (Fig 3) was associated with a decrease in sequestration of inflammatory cells in brain microvessels and with improved clinical scores.

Integrin α D β 2 deficiency alters leukocyte accumulation in brain microvessels in experimental CM
To evaluate contribution of integrin α D β 2 to leukocyte-endothelial interactions in the cerebral microcirculation in P. berghei ANKA, we examined post-capillary venules displayed through a cranial window by intravital microscopy. At 6 days post-infection, we observed a significant increase (p < 0.05) in rolling ( Fig 5A) and adherent leukocytes (Fig 5B and 5C) in α D +/+ mice when compared to uninfected α D +/+ or α D -/animals. Rolling and intravascular adhesion of leukocytes in brain vessels of P. berghei ANKA-infected mice was also detected in another report, and the number of adherent intravascular leukocytes increased as neurologic involvement progressed [59]. Rolling and adhesion were significantly reduced in infected α D -/mice  when compared to infected α D +/+ animals (Fig 5A, 5B and 5C). Venular plugging with leukocytes was detected in α D +/+ but not α D -/mice (Fig 4D and 4F). Microvascular obstruction may result in dysregulated cerebral blood distribution and hemodynamics in clinical [2] and experimental [22] CM.

Integrin α D β 2 deficiency reduces CD4 + and CD8 + T lymphocytes accumulation in the brain during experimental CM
T-lymphocyte accumulation and activity contribute to development of experimental CM [20,22,59]. Therefore, we performed flow cytometric analyses of brain cell suspensions from α D +/+ and α D -/mice at post-infection day 7. As shown in Fig 6A, there was a significant increase in the total number of mononuclear cells accumulating in the brains of α D +/+ infected mice, consistent with previous reports [22 , 59]. The increase in the number of accumulated mononuclear cells was dramatically attenuated in α D -/mice and did not reach statistical significance as compared to uninfected controls ( Fig 6A). The number of both CD4 + and CD8 + T cells was increased in the brains of infected α D +/+ mice (Fig 6B and 6C). As in analysis of total mononuclear cells (Fig 6A), brain CD4 + and CD8 + T cell accumulation was substantially reduced in infected α D -/mice. These data indicate that T-lymphocyte accumulation in the brain, a key event in experimental CM pathogenesis [20], may be directly dependent on the expression of integrin α D β 2 during P. berghei ANKA infection.

Mice deficient in integrin α D β 2 are protected from CM-induced cognitive impairment
CM is associated with long-term cognitive impairment in humans [2,4,[60][61][62][63]. Cognitive dysfunction also occurs in animal models [27,48]. Therefore we asked if the altered leukocyte and cytokine responses we detected in infected α D β 2 -deficient mice influence this delayed outcome. We performed experiments in which α D +/+ and α D -/mice were rescued from experimental CM by treatment with chloroquine initiated after the first clinical signs of CM were detected by the modified SHIRPA score test (Fig 3C), as we have previously described [48]. At days 15 and 16 after infection, surviving animals were examined using an step-down inhibitory avoidance test to assess aversive memory performance. In agreement with our previous observations [27,48] there was a defect in short and long term aversive memory in infected wildtype mice rescued from CM by chloroquine treatment (Fig 7A and 7B). In contrast, short and long term aversive memory were preserved in integrin α D β 2 -deficient animals, and were similar to responses detected in uninfected mice (Fig 7A and 7B).

Discussion
Severe malaria, a group of complications with organ-specific and systemic manifestations that can result in multiorgan failure, presents differently in children and adults and is commonly caused by P. falciparum [2,52,64,65]. Among the major clinical complications of severe malaria CM, is most frequent and lethal in children but occurs in all age groups and is a major cause of morbidity and mortality in plasmodial infection [64,66,67]. Biologic features of both the parasite and the host influence the severity of malarial infection [1,66,67]. An evolving perception is that differential host responses to malaria infection contribute to dysregulated application of the SHIRPA protocol in control (CT) in infected α D +/+ and α D -/as described in Materials and Methods. Significance was evaluated by ANOVA followed by bonferroni's multiple comparison test and #P � 0.05 compared to the respective control group; � P � 0.05 compared to α D +/+ infected mice.
https://doi.org/10.1371/journal.pone.0224610.g003   [1,14,52,[64][65][66][67]. Animal models have been important in generating concepts regarding the pathogenesis and natural history of severe malaria and its specific organ involvement [20,68,69]. In this study we utilized a murine model that has features of severe human malaria and has been studied extensively as a surrogate for clinical CMinfection of mice of susceptible genotype with the murine malaria parasite P. berghei ANKAto provide additional evidence that innate host effector systems contribute to cerebral involvement and to both life-threatening and chronic CNS complications.
We found that targeted deletion of the α D polypeptide integrin subunit, yielding absence of the integrin α D β 2 heterodimer on leukocyte subsets [37], resulted in decreased brain chemokine and cytokine levels, preserved cerebral vascular barrier integrity, blunted intravascular leukocyte accumulation, and decreased numbers of T lymphocytes in brain tissue. Each of these variables is thought to be central in the pathogenesis of severe malaria [14,20,65] and is associated with brain inflammation and injury in experimental CM [20,52,68,69]. Consistent with these results, we also found that cognitive function was relatively preserved in integrin α D β 2 "knockout" mice compared to wild type controls when they were rescued by anti-malarial treatment at the onset of signs of neurologic involvement and later studied. These findings in rescued animals indicate that integrin α D β 2 influences key events that alter brain function in experimental CM. Our observations are the first to demonstrate that α D β 2 is an inflammatory effector molecule in CNS infection caused by malaria parasites or other pathogens. It was previously reported that blocking antibodies against α D reduced neutrophil and macrophage numbers and improved cognition and other functional outcomes in experimental traumatic brain injury in rats [70,71], suggesting that α D β 2 has broad effector activities in both sterile and infectious CNS inflammation. Decreased brain chemokine and cytokine levels in infected α D -/mice in part mechanistically accounts for preserved blood-brain barrier integrity and reduced vascular and parenchymal inflammation [14,20,57]. Disrupted blood brain barrier integrity is a cardinal feature of clinical and experimental CM [2,22,64,67,72]. Endothelial responses to TNF, which was reduced in the brains of infected α D -/mice (Fig 2), may be particularly important in differentially influencing vascular barrier integrity and other features of severe versus uncomplicated malaria phenotypes [1,64]. Other proinflammatory cytokines including IFNγ, which was also reduced in brain tissue from P. berghei ANKA-infected α D -/animals (Fig 2), are implicated as well [20,65]. In previous investigations we found that integrin α D β 2 regulates in vivo systemic [37] and pulmonary [38] chemokine and cytokine levels and that engagement of α D β 2 on human monocytes induces outside-in signals to chemokine and citokynes expression pathways [36]. Thus, interruption of cytokine and chemokine expression in α D -/mice provide a mechanism for amelioration of inflammatory vasculopathy in P. berghei ANKA-infection animals. Intravascular leukocyte sequestration reflects cerebrovascular endothelial signaling and circulating leukocyte activation, and is a major feature of experimental malaria [22,57,59,64]. Monocytes, lymphocytes, and platelets are sequestered in brain microvessels and post-capillary venules in mice with cerebral involvement, reflecting key cell-cell interactions [20,57,73].   Reduced accumulation of intravascular leukocytes in cerebral microvessels of α D -/mice infected with P. berghei ANKA- (Fig 5) was one of the most striking findings in our study. Circulating leukocyte numbers are similar in α D -/and wild type animals [37], suggesting that the decreased cerebrovascular leukocyte sequestration in infected knockout mice was due to altered leukocyte adhesion and cellular interactions. Integrin α D β 2 mediates adhesion of murine macrophages and cell lines in static assays [37, 74,75] and intravascular arrest and retention of macrophages in experimental atherogenesis [39]. Our observations in this study demonstrate for the first time that integrin α D β 2 influences intravascular leukocyte adhesion and accumulation in experimental CM. These events potentially include adhesion of α D β 2positive leukocytes to inflamed endothelium, activated platelets, iRBC, and/or other leukocytes [22,31,33,59], and remain to be dissected. Our preliminary observations suggest that α D β 2 expression is induced on circulating monocytes [36] which sequester in cerebral microvessels and mediate critical intercellular interactions in experimental CM caused by P. berghei ANKA infection [59]. Our observation that α D β 2 influences brain CD4 + and CD8 + T cell recruitment in P. berghei ANKA infection (Fig 6) is one of the most significant findings from our experiments, given the critical contributions of T lymphocytes, particularly CD8 + T cells, to the pathogenesis of experimental CM [20,59,68]. CD4 + and CD8 + T cells sequester in brain blood vessels in P. berghei ANKA-infected mice [20,22,59], and likely were among the rolling and adherent leukocytes that we observed in infected wild type animals. Nevertheless, although integrin α D β 2 is present on subsets of human T lymphocytes [36,76], it was not detected on lymphocytes from mice of several genetic backgrounds under basal uninflamed conditions [36,77]. It is possible that α D β 2 is induced on T cells in P. berghei ANKA infection as the related integrin, α L β 2 (LFA-1), is reported to be [78]. If so, α D β 2 may directly mediate adhesion and intravascular accumulation of CD4 + and CD8 + T cells in infected animals, events that are abrogated in α D β 2 -deficient mice. Alternatively, an indirect mechanism may be involved. Reciprocal interactions between monocytes and T lymphocytes are reported to influence T cell recruitment to the brain in a complex fashion in P. berghei ANKA infection [59]. Thus, critical signaling events between α D β2 -positive monocytes and T cells lacking this integrin heterodimer may occur, and may be interrupted in α D β 2 -deficient mice. Futher studies will be required to resolve this issue.
Integrins on leukocytes, and on other relevant cells such as platelets, have intricate activities in inflammation and infection [31,33,73]. This report demonstrates that integrin α D β 2 is a functionally important effector in inflammatory events central to experimental CM, including increased blood brain barrier permeability, CD4 + and CD8 + T lymphocyte accumulation in the brain, and late cognitive impairment in survivors. Blunting of acute brain injury in α D β 2deficient mice likely contributes to the early survival advantage of α D −/− animals in lethal systemic P. berghei ANKA infection [37], as suggested by improved clinical scores in this study (Fig 3C). Dissecting the roles of leukocyte integrins in CM and other manifestations of severe malaria will provide new insights into the innate and adaptive immune fabric of host responses to Plasmodio, and increased understanding of cell-and organ-specific events in malarial inflammation.
Supporting information S1 Fig. Deletion