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Treatment with AMD3100 attenuates the microglial response and improves outcome after experimental stroke
Journal of Neuroinflammation volume 12, Article number: 24 (2015)
Recovery of lost neurological function after stroke is limited and dependent on multiple mechanisms including inflammatory processes. Selective pharmacological modulation of inflammation might be a promising approach to improve stroke outcome.
We used 1,1′-[1,4-phenylenebis(methylene)]bis[1,4,8,11-tetraazacyclotetradecane] (AMD3100), an antagonist to the C-X-C chemokine receptor type 4 (CXCR4) and potential allosteric agonist to CXCR7, administered to mice twice daily from day 2 after induction of photothrombosis (PT). In addition to functional outcome, the dynamics of post-stroke microglia response were monitored in vivo by 2-photon-laser-microscopy in heterozygous transgenic CX3CR1-green fluorescent protein (GFP) mice (CX3CR1GFP/+) and complemented with analyses for fractalkine (FKN) and pro-inflammatory cytokines.
We found a significantly enhanced recovery and modified microglia activation without affecting infarct size in mice treated with AMD3100 after PT. AMD3100 treatment significantly reduced the number of microglia in the peri-infarct area accompanied by stabilization of soma size and ramified cell morphology. Within the ischemic infarct core of AMD3100 treated wild-type mice we obtained significantly reduced levels of the endogenous CX3CR1 ligand FKN and the pro-inflammatory cytokines interleukin (IL)-1β and IL-6. Interestingly, in CX3CR1-deficient mice (homozygous transgenic CX3CR1-GFP mice) subjected to PT, the levels of FKN were significantly lower compared to their wild-type littermates. Moreover, AMD3100 treatment did not induce any relevant changes of cytokine levels in CX3CR1 deficient mice.
After AMD3100 treatment, attenuation of microglia activation contributes to enhanced recovery of lost neurological function in experimental stroke possibly due to a depression of FKN levels in the brain. We further hypothesize that this mechanism is dependent on a functional receptor CX3CR1.
After ischemic stroke, the brain may regain lost neurological function to a limited extent by compensation and relearning [1,2]. The definite outcome can be improved by established rehabilitation regimes and might be enhanced by supportive pharmacological treatments.
Parallel and partially opposite processes contribute to restoration of brain function after stroke. The interaction of multiple mechanisms including neuronal plasticity, astrogliosis, cell genesis, angiogenesis and inflammation are important for the clinical development. Interestingly, anti-inflammatory treatment significantly contributes to functional recovery; examples are the specific blockade of chemokines or pro-inflammatory molecules and their receptors. We have shown that modulation of the C-X-C chemokine receptor type 4/C-X-C chemokine receptor type 7 (CXCR4/CXCR7) pathway significantly improves functional outcome and is associated with a reduction of T-helper cells in the ischemic hemisphere . Also, treatment with specific recombinant T cell receptor ligands  has been shown to improve recovery after stroke.
Selective modulation of microglia function could be a promising strategy that has been addressed in several experimental studies [5-7]. Recent investigations suggest that the C-X-C chemokine ligand 12 (CXCL12)/CXCR4/CXCR7 and the fractalkine (FKN)/CX3CR1 pathways are instrumental in the regulation of microglia . CXCL12 stimulates the release of FKN, a chemokine that, in the brain, is mainly expressed by neurons [9,10] and exists in a membrane-bound and a soluble form [11-13]. While membranous FKN is involved in mechanisms of cell adhesion, the soluble form acts as a chemoattractant . The sole receptor for FKN is CX3C chemokine receptor 1 (CX3CR1) and is expressed on different immune cell populations including microglia [9,14-16]. Initial studies have demonstrated that the FKN/CX3CR1 pathway is instrumental in chemotaxis of microglia [8,9], leukocyte trafficking and microglia/macrophage recruitment . In in vitro assays, FKN showed neuroprotective properties by activation of neuronal cell survival pathways , and FKN also led to an increase of microglia survival .
After stroke, FKN expression increases in the necrotic infarct core within the first hours followed by an upregulation in the peri-infarct area within the first week after onset of the insult. CX3CR1-positive cells can be detected in the ischemic tissue from 24 hours and are strongly upregulated with a peak at day 7 after stroke . CX3CR1-deficient mice subjected to transient middle cerebral artery occlusion (MCAO) showed smaller lesions compared to heterozygote and wild-type littermates accompanied by reduced levels of pro-inflammatory cytokines . Results have been confirmed showing that the administration of FKN to wild-type mice resulted in smaller infarcts, but administration of FKN to FKN-deficient mice resulted in bigger infarcts in a model of permanent MCAO. Moreover, application of FKN to microglia cell cultures resulted in reduced phagocytosis . Summarizing these findings, administration of FKN but also CX3CR1 deficiency seems to be beneficial in the acute phase after stroke. However, the role of this pathway during the first weeks after stroke has not been investigated.
Based on our previous studies demonstrating that antagonism of CXCR4 by 1,1′-[1,4-phenylenebis(methylene)]bis[1,4,8,11-tetraazacyclotetradecane] (AMD3100) enhanced functional recovery after experimental stroke  we hypothesized that specific CXCR4 antagonism could be a therapeutic target to affect the FKN/CX3CR1 pathway and to modulate microglia function after stroke, to finally improve long-term outcome after permanent focal ischemia.
The microglial response and recovery of neurological function were observed in parallel until 14 days after ischemic stroke (Figure 1). Neurological function was assessed in wild-type male C57BL/6 N-mice (28 to 35 g, aged 12 to 16 weeks, purchased from Charles River, Sulzfeld, Germany) using a newly assembled neuroscore with a maximum score of 22 points (Table 1) consisting of paw placement, whisker-reflex and tail suspension, as well as a combination of the foot-fault test  and the ladder-rung test . The animals were trained at least three times in climbing the ladder before recording the neurological status prior to stroke. Animals were excluded from the study if the full score was not achieved before photothrombosis (PT) (neuroscore <22 points) or if only insufficient neurological deficits were observed at day 1 after PT (neuroscore >11 points). Permanent cerebral ischemia was induced by PT. Mice were treated with either AMD3100 or saline vehicle (vh) from day 2 to day 14, administered intraperitoneally twice daily (every 12 hours, 0.5 mg/kg body weight). Neurological deficits were assessed on days 1, 2, 7 and 14. Mice were randomized (every other animal was allocated to the same treatment group) and the studies were performed in a blinded fashion to the investigator who performed surgeries and behavioral tests. Microglial response was monitored in vivo by 2-photon-laser-microscopy (2PLSM) through a thinned skull-window before stroke, and at days 3, 7 and 14 (Figure 1). On day 14, animals were sacrificed and endpoint analysis was carried out by immunohistochemistry.
All animal experiments were approved by the Malmö/Lund ethical committee. Animals were housed in a controlled environment with a 12:12 hour light cycle beginning at 07:00 with room temperature maintained at 22°C and with ad libitum access to food and water. For surgery and 2PLSM the animals were anesthetized by inhalation of isoflurane (isoflurane in N2O/O2 - 0.3:0.7, 4% for induction, 1.8% for maintenance) and local anesthesia (bupivacain 0.25 mg/ml). During anesthesia, the body temperature was monitored by a rectal thermistor probe (Linton Instrumentation, Norfolk, UK) connected to a heating pad maintaining body temperature at 36.7°C.
For behavioral analysis, 60 male C57BL/6 mice (28 to 35 g, aged 12 to 16 weeks; Charles River, Sulzfeld, Germany) were purchased. Five out of 60 animals died and nine animals had to be excluded from the study (see below for exclusion criteria). From the 46 remaining animals, 13 mice were treated with AMD3100 after PT (PT/AMD3100), 14 mice were treated with saline after PT (PT/vh), 9 mice were treated with AMD3100 after sham surgery (sham/AMD3100) and 10 mice were treated with saline after sham surgery (sham/vh).
To visualize microglia in vivo, 30 male transgenic C57/Bl6 mice that carried GFP under the control of the CX3CR1 promotor underwent 2PLSM (aged 30 to 40 weeks, weighing 25 to 35 g, own breeding; breeding pairs were purchased from The Jackson Laboratory; B6.129P(Cg)-Ptprca Cx3cr1tm1Litt/LittJ) . To ensure the presence of CX3CR1 and to visualize microglia we only used mice heterozygous for CX3CR1 (CX3CR1GFP/+). It is of note that in addition to brain resident microglia other immune cells express CX3CR1 and, therefore, are positive for GFP. Hence, based on previous studies it can be assumed that the majority of cells are microglia investigated in the ischemic territory after PT [24,25]. Four out of these 30 mice had to be excluded due to traumatic injury or lethal anesthesia. The remaining 26 mice were randomized into the following treatment groups: PT/AMD3100, n = 10; PT/vh, n = 8; sham/AMD3100, n = 4; and sham/vh, n = 4. Three AMD3100-treated and one vehicle-treated animal could not be imaged on day 3, but were imaged at the time points before PT, and day 7 and day 14 after PT.
For protein analysis by Western blot, wild-type (n = 10), CX3CR1GFP/+ (n = 10) and CX3CR1GFP/GFP mice (n = 10) were subjected to PT and treated with AMD3100 (0.5 mg/kg twice daily) or vehicle for 5 days starting on day 2 after stroke. On day 6 after PT, FKN levels were determined in the infarct core. Tissue from these animals was also used for analysis of cytokine levels.
PT was carried out as described previously [26,27]. Briefly, anesthetized animals were placed into a stereotactic frame. After shaving, a sagittal skin incision was made on the scalp, subcutaneous connective tissue was removed and the skullbone was dried. Five minutes after intraperitoneal injection of the photosensitizer dye Rose Bengal (0.1 mL at 10 mg/mL; Sigma-Aldrich, Taufkirchen, Germany; Lot#MKBH0535V, the right hemisphere was illuminated with a cold light source (Schott KL 1500 LCD, intensity: 3050 K/4D) through a round aperture measuring 2.5 mm in diameter (equal to an illumination area of 4.909 mm2) for 20 minutes (coordinates related to Bregma: +1.5 mm lateral and +0.5 anterior). Thereafter, the scalp incision was sutured and the mice were transferred to their home cage to recover.
For 2PLSM, PT was induced in CX3CR1GFP/+ transgenic mice. The lesion was located rostral and adjacent to the thinned skull window (for details see below) at the approximate coordinates of 1.5 mm lateral and 0.5 anterior related to bregma. CX3CR1GFP/+ transgenic animals were illuminated at a light intensity of 3050 K/4E for 15 minutes through a 1.5 mm round aperture (equal to an illumination area of 1.767 mm2). Among the CX3CR1GFP/+ animals undergoing 2PLSM, 2 out of 10 AMD3100 treated (PT/AMD3100) animals and four out of eight vehicle-treated animals (PT/vh) received PT under the conditions 2.5 mm/3050 K/4D/20 minutes. Compared to the parameters in mice with a lesion size of 1.5 mm these PT settings did not affect values for soma size and cell number in the specific region of interest.
2PLSM was performed in accordance with Yang and collegues . Briefly, after placing the anesthetized animal onto a custom-made plate, a sagittal skin incision from eye to ear level was made and all connective tissue was removed from the skull to attach a custom-made blade to the dry bone (3 M Vetbond-glue, No. 1469SB) so that the head of the animal could be firmly adjusted to a skull-holder on the plate . Using a dental drill and microsurgical blades a thinned window measuring approximately 1.5 × 1.5 mm with a remaining bone thickness of about 20 μm was prepared. The animal was then transferred to the microscope stage and a drop of MilliQ water was placed onto the skull window. After optimization of imaging conditions, 2PLSM imaging was performed in Z-stack planes of 424.9 × 424.9 μm (x/y/z, 0.83 μm/pixel, unless stated otherwise) down to a subdural depth of 75 to 150 μm by a multiphoton Zeiss LSM 7MP upright laser scanning microscope using a W-Plan Apochromat 20_/1.0 DIC Vis-IR water immersion objective (×20, Carl Zeiss, Jena, Germany) controlled by ZEN 2010 imaging software (Carl Zeiss) (Figure 2). GFP was excited by a Mai Tai DeepSee Ti:Sapphire pulsed laser (Spectra-Physics, Irvine, CA, USA) tuned to 875 nm . Further computerized analysis followed ex vivo with ImageJ (1.43u, NIH, Washington, USA) and Adobe Photoshop (CS5 extended 12.04x64, Adobe, USA).
We studied number and soma size of GFP+ cells (CX3CR1+) in the entire area under the thinned skull window and defined a region “A” located adjacent to the infarct core and a region “B” most distant from the infarct core (Figure 2). Microglia were counted and their soma sizes determined at Otsu-threshold [29,30] within regions of interest represented by z-stacks measuring 424.9 × 424.9 × 75 μm (x/y/z) located in either A or B. To eliminate microglia activation caused by any experimental procedures (for example, preparing the skull window or laser stimulation) respective results obtained in sham-operated mice were subtracted from those found in mice subjected to PT. In addition, we defined a value “C” represented by the equation C(dx) = (A(dx) − A(pre)) − (B(dx) − B(pre)) where the increase in number in cells from before infarct induction (pre) to a day x (dx) in region B was subtracted from the respective value in region A. By combined use of sham corrections and this algorithm we gained precise information about the stroke-induced changes in number of microglial cells.
Infarct size measurement
Brains from perfusion-fixed animals were cut into coronal sections with a thickness of 30 μm and stained for neuronal nuclei (NeuN; procedure described in the immunohistochemistry paragraph). The noninjured portion of the ipsilateral and contralateral hemisphere were encircled and the indirect infarct volume was calculated by integration of areas from serial sections (1 mm) of each brain as described previously .
Brain sections (30 μm in thickness) were rinsed in phosphate-buffered saline (PBS). Endogenous peroxidase activity was quenched by washing the sections in a solution of PBS with 3% H2O2 and 10% methanol for 15 minutes. After subsequent rinsing in PBS, blocking was achieved by incubation in a solution containing 5% normal donkey serum (NDS) in 0.25% Triton X-100 in PBS (Tx/PBS) for 1 hour. Thereafter, sections were incubated with a mouse anti-neuronal Nuclei (NeuN) antibody (diluted at 1:1000, Merck Millipore, Billerica, MA, USA) or a rabbit anti-CXCR4 antibody (diluted at 1:200; Abcam, Cambridge, UK) at 4°C in 5% NDS in Tx/PBS overnight. The next day, sections were rinsed in 1% NDS in Tx/PBS followed by incubation with respective biotinylated secondary antibodies in 2% NDS in Tx/PBS at room temperature for 90 minutes. Sections were washed with Tx/PBS and incubated with avidin-biotin-complex (ABC; Vector Laboratories, Burlingame, CA, USA) for 1 hour. Following this incubation, the sections were rinsed in PBS. The ABC reaction was visualized using NiDAB (Dabsafe, Saveen Werner AB, Limhamn, Sweden) with the addition of NiCl2 and a mixture of 3% H2O2 in H2O. Thereafter, sections were rinsed in PBS, mounted on glass slides, dried overnight, dehydrated, treated with xylene and then cover-slipped with Pertex (Histolab AB, Västra Frölunda, Sweden).
Brain sections (thickness 30 μm) from 4% paraformaldehyde-perfused animals were used. After blocking in 5% NDS in Tx/PBS for 60 minutes, sections were incubated with primary antibody in Tx/PBS in 5% NDS at 4°C overnight. The following antibodies were used: rat anti-cluster of differentiation 68 (CD68; diluted at 1:200; AbD Serotec, Düsseldorf, Germany), rabbit anti-CXCR4 (diluted at 1:200; Abcam), mouse anti-CD45 (diluted at 1:25; AbD Serotec) and rabbit anti-ionized calcium binding adaptor molecule 1 (Iba1; diluted 1:2000; Wako Chemicals, Neuss, Germany). The next day, the sections were rinsed with 1% NDS in Tx/PBS three times for 10 minutes. All the following steps were performed in the dark in order to preserve the fluorophores conjugated to the secondary antibodies. Sections were incubated with secondary antibodies in 2% NDS in Tx/PBS for 90 minutes at room temperature and rinsed in PBS three times for 10 minutes. Finally, the sections were rinsed in PBS and mounted on supercharged glass slides, allowed to dry, cover-slipped using PVA-DABCO and analyzed using LSM 510 confocal microscopy (Carl Zeiss).
Proteins were extracted from brain tissue as described earlier . Proteins were separated on a 10% SDS polyacrylamide gel and were transferred onto polyvinyldifluoride membranes. Unspecific protein binding sites were blocked in blocking buffer containing 20 mM Tris, 136 mM NaCl, pH 7.6, 0.1% Tween 20 and 5% nonfat dry milk. FKN was detected by a rabbit anti-FKN antibody (Torrey Pines Biolabs, Secaucus, NJ, USA; dilution 1:1000). After overnight incubation at 4°C, signals were obtained by binding of a secondary anti-rabbit horse radish peroxidase-linked antibody (1:50000; Sigma-Aldrich, Deisenhofen, Germany) and visualized by exposing the membrane to a charge-coupled device camera (LAS1000, Fujifilm, Tokyo, Japan) using a chemiluminescence kit (Merck Millipore, Billerica, MA, USA). Membranes were stripped and reprobed for β-actin (Sigma-Aldrich), and diluted 1:50,000. After densitometric analysis using Image J software, FKN levels were calculated as a percentage of β-actin expression.
Measurement of cytokines
Tissue samples from the ischemic core were collected as described previously . Cytokine levels were measured from brain tissue homogenates by a multiplex immunoassay kit according to the manufacturer’s instructions using a SECTOR Imager 6000 reader (Mesoscale, Gaithersburg, MD, USA).
Statistical analysis was performed using Excel® (Microsoft Excel® for Mac 2011, 14.3.6) and SPSS-Statistics® (IBM, Version21, IBM Svenska, Stockholm, Sweden). Results from behavioral testings were evaluated by the Mann–Whitney U-test (significance level 0.05, confidence interval 0.95). Quantity of cells, soma sizes and Western blot results were evaluated by Students t test (significance level 0.05, confidence interval 0.95). Cytokine levels were analyzed by one-way analysis of variance. Post-hoc multiple comparisons were performed as stated in the figure legends and P < 0.05 was considered significant.
Treatment with AMD3100 improves functional outcome after photothrombosis in mice without affecting infarct size
After permanent focal ischemia induced by PT in wild-type C57BL/6 mice and treatment either with saline or AMD3100, neurological function was assessed by a composite neuroscore before and on day 1, 2, 7 and 14 after PT (Table 1). We observed a significant improvement of the neuroscore in AMD3100-treated mice compared to vehicle-treated animals during the second week after PT (vh 2.3%, AMD3100 18.2%, Mann–Whitney U-test P = 0.004; Figure 3A). Over the whole observation period of 14 days, AMD3100-treated animals finally recovered significantly better than vh-treated animals (vh 18.2%, AMD3100 27.3%, Mann–Whitney U-test P = 0.008; Figure 3B). Treatment with AMD3100 did not affect behavior in sham-operated mice (data not shown). Importantly, analysis of infarct volumes did not show a significant difference between the treatment groups (vh, 5.35 ± 0.81; AMD3100, 5.56 ± 0.65; Student’s t test P = 0.85; Figure 4A).
Treatment with AMD3100 reduces soma size and number of microglia cells in CX3CR1GFP/+ mice after photothrombosis
PT caused an intensive accumulation of GFP+ microglial cells in CX3CR1GFP/+ mice (Figure 4B). Treatment with AMD3100 strongly attenuated this inflammatory response in the ischemic territory. 2PLSM was carried out to characterize the dynamics during activation of microglial cells in the ischemic territory. We used heterozygous CX3CR1GFP/+ mice with one allele for GFP and one functional CX3CR1 allele. To evaluate the stroke-induced microglial response we studied the number and morphology of GFP+ cells accumulating in the peri-infarct area (Figures 2 and 5A-D). By calculating cell numbers within the defined regions A and B we found a significantly lower number of GFP+ cells in the proximal peri-infarct area of AMD3100- compared to vehicle-treated animals at days 3, 7 and 14 after PT (Figure 5A-C). Interestingly, this occurred already 1 day after initiating AMD3100 treatment. No changes in the number of cells have been observed within the treatment groups during the observation period of 14 days. Hence, soma sizes were significantly decreased from day 7 onwards in vehicle-treated mice (Figure 5C).
In addition, we observed a clear morphological change of the microglial cells in AMD3100-treated animals, in particular during the early phase after stroke (Figure 5D). At day 3, the microglial somas in vehicle-treated mice more than doubled their size compared to baseline measurements before stroke (increase of soma size: 119.
4%) (Figure 5C, D). Soma sizes of microglia in AMD3100-treated mice only increased by 13.2% (Figure 5C, D). At later time points soma sizes were similar, there was no significant difference in the increase of soma size detectable among the treatment groups. Together, our results suggest that treatment with AMD3100 significantly modifies activation of microglia in the peri-infarct area after PT in mice within 24 hours after the first drug administration.
Green fluorescent protein-positive cells in CX3CR1GFP/+ mice reveal microglia/macrophage-specific immunohistochemical properties of phagocytosing cells
To further analyze the phenotype of CX3CR1+ green fluorescent cells in CX3CR1GFP/+ mice, we performed immunohistochemistry in the animals that had been sacrificed after 2PLSM-experiments at d14 after stroke. As shown in Figures 4B and 6, accumulation of GFP+ cells was observed in the infarct core and the peri-infarct area. The majority of cells also were found positive for Iba1, a marker for activated microglia/macrophages  (Figure 6). The distribution of cells in the infarct core was not homogenous, but mostly appeared in a typical amoeboid morphology indicative for phagocytosing cells. For further characterization, co-stainings were performed with CD68, a marker for phagocytosis, and CD45, a marker for peripheral immune cells infiltrating the ischemic territory (Figure 6). GFP+ cells were positive for CD68 and CD45 in the infarct core and adjacent peri-infarct area. Some of the cells co-expressed CD68 and CD45. Together, our data show the accumulation of microglia/macrophages in the ischemic territory.
We further assessed the expression of CXCR4 to find out more about the target cells of AMD3100. In addition to neocortical neurons, CXCR4-positive cells were detected in the ischemic territory (Figure 7). Co-staining of CXCR4 with GFP demonstrates their expression in microglia/macrophages in this region supporting previous studies (Figure 7) . These results illustrate that the majority of GFP+ cells accumulating in and around the infarct display microglia/macrophage properties and that these cells might be susceptible for the treatment with AMD3100.
Reduction of fractalkine levels depends on functional CX3CR1 in the subacute post-stroke phase
FKN is the endogenous ligand for CX3CR1 and it has been shown that activation of the CXCL12/CXCR4 pathway induces the release of FKN by increased activity of the protease ADAM10/17 . To test if CXCR4 antagonism affects FKN after PT, wild-type (n = 8), heterozygote (CX3CR1GFP/+) (n = 8) and CX3CR1-deficient (CX3CR1GFP/GFP) mice (n = 8) were subjected to PT and treated with AMD3100 (0.5 mg/kg twice daily) or vehicle for a total of 5 days. On day 6 after PT, FKN levels were determined in the infarct core by Western blotting. Three specific bands have been identified (Figure 8). While the 95 kDa band corresponds to the released soluble form of FKN, the origin of the 55 kDa and 78 kDa bands have not been unraveled yet. FKN levels found in wild-type animals were decreased in animals treated with AMD3100 compared to mice treated with vehicle. In particular, soluble FKN (95 kDa FKN; vh, 3.51 ± 0.5; AMD3100, 1.87 ± 0.14 arbitrary units (AU)) and the 55 kDa FKN (vh, 1.15 ± 0.22; AMD3100, 0.42 ± 0.04 AU) signal were significantly reduced in AMD3100-treated animals (Figure 8A).
Interestingly, vehicle-treated CX3CR1-deficient mice showed lower FKN levels compared to their wild-type littermates, and treatment did not significantly affect the levels of any of the three forms of FKN (Figure 8B). In addition, the levels of FKN did not differ when comparing mice of both genotypes treated with AMD3100 (data not shown). CX3CR1GFP/+ mice showed a less prominent reduction compared to wild-type animals of the 78 kDa FKN (vh, 2.03 ± 0.16; AMD3100, 1.37 ± 0.13 AU) and the 95 kDa FKN form (vh, 1.92 ± 0.13; AMD3100, 1.45 ± 0.04 AU) while the 55 kDa form (vh, 1.91 ± 0.17; AMD3100, 1.54 ± 0.05 AU) remained unaffected. These results show that treatment with AMD3100 significantly affects the release of FKN in the infarct core, and that the release is dependent on a functional receptor, CX3CR1.
Treatment with AMD3100 reduced the level of pro-inflammatory cytokines in CX3CR1 wild-type mice after photothrombosis
Levels of pro-inflammatory cytokines were measured in order to study inflammation in the ischemic territory of CX3CR1 wild-type and CX3CR1-deficient mice subjected to PT. As shown in Figure 9, reduced levels of interleukin (IL)-1β) and IL-6 were found in CX3CR1 wild-type mice treated with AMD3100 (0.5 mg/kg) for a total of 5 days (study III) compared to vehicle-treated animals. Interestingly, the levels of IL-12p70, interferon-gamma, IL-2, CXCL1 and IL-5 were also lower in AMD3100-treated mice (data not shown); however, differences did not reach statistical significance. In contrast, treatment with AMD3100 did not affect the levels of cytokines in CX3CR1-deficient mice, whereas levels of IL-12p70 were significantly increased compared to vehicle-treated mice (Figure 9). Based on these experiments, we conclude that a functional CX3CR1 receptor is essential to achieve anti-inflammatory effects mediated by AMD3100 treatment.
The present investigation demonstrates that treatment with the CXCR4 antagonist AMD3100 in mice subjected to permanent focal ischemia enhances long-term recovery of lost neurological function. Moreover, our data show a correlation between the improved outcome after stroke and a reduced microglial response during the first 14 days. Importantly, treatment did not interfere with the acute tissue response involving cell death mechanisms and the early activation of microglia observed during the first hours after stroke. In addition, we provide the first in vivo evidence that levels of FKN, the endogenous ligand for CX3CR1, in the ischemic territory are affected by inhibition of the CXCL12/CXCR4 pathway.
AMD3100 enhances recovery of lost neurological function after photothrombosis
In line with previous investigations showing an improved outcome after AMD3100 treatment in mice subjected to permanent MCAO  and rats subjected to transient MCAO  we observed better neurological scores in mice subjected to PT treated with AMD3100 for a total of 12 days starting on day 2 after stroke. In contrast to previous studies performed in rats, AMD3100 treatment had no immediate effect on recovery. Differences have not been observed until the second week after stroke onset. This might be due to various mechanisms of recovery dependent on the experimental model (permanent versus transient model) and species, including specific pharmacokinetics in mice and rats. In addition, several studies have demonstrated that application of CXCL12 (stromal cell line derived factor 1, SDF1) exerts beneficial effects on cellular repair mechanism recovery and, especially, the proliferation of neuronal progenitor cells and their migration to the site of injury [35,36]. Hampered CXCL12/CXCR4 signaling by AMD3100 downregulates the migration of neuroblasts at the site of ischemic injury 4 weeks after stroke . In these studies, however, functional outcome after administration of the CXCR4 antagonist AMD3100 has not been assessed. We have shown that administration of AMD3100 during the first days after stroke conveys anti-inflammatory actions . The migration of neuronal progenitor cells from stem cell niches towards the ischemic lesion is relevant for stroke recovery; however, during the early period after stroke and due to multiple ongoing processes, the inhibition of detrimental inflammatory processes prevails and is of prime significance to regain function.
Microglia activation is downregulated by blockade of CXCL12 actions
Our study supports the idea that downregulation of the FKN/CX3CR1 pathway diminishes detrimental actions of post-stroke inflammation. Similar results were observed in the acute phase after transient MCAO showing that CX3CR1 deficiency reduced ischemic damage and CX3CR1-deficient mice displayed a stroke-protective inflammatory milieu during the first 72 hours after stroke [19,38].
The interaction between microglia, neurons and other surrounding cells after stroke is mainly accomplished by molecular cues such as the release of danger-associated molecule patterns and, more specifically, cytokines/chemokines . Among others, the CXCL12/CXCR4 and the FKN/CX3CR1 pathways have been implicated in the activation of immune cells in the post-ischemic brain [12,13,17]. Earlier studies demonstrated an involvement of the FKN/CX3CR1 pathway in cell adhesion and chemoattraction of monocytes but also microglia in vitro [8,40]. In addition, it has been shown that the application of FKN to microglia cultures reduces their phagocytotic activity . It has therefore been suggested that the activation of CX3CR1 by released FKN is involved in the regulation of microglia to remain in a ramified phenotype with potential neuroprotective properties [20,41]. AMD3100 specifically blocks the actions of CXCL12 and thus inhibits the neuronal and glial release of FKN [13,42]. Consequently, an excessive inflammatory response would be expected. According to our observations, however, this is not the case. Also others demonstrated that AMD3100 attenuated the post-stroke inflammatory response during the early phase after transient MCAO in mice and reduced brain edema, which was accompanied by an improved functional outcome . A reduction of inflammation has also been observed in a rat transient MCAO model when treatment was initialized on day 2 after stroke onset . In the present study we observed a lower cell number, a stabilization of morphology of microglia accompanied by reduced levels of pro-inflammatory cytokines indicating that AMD3100 treatment mitigates the post-stroke stimulation of microglial cells. In AMD3100-treated mice, microglia hardly showed any signs of swelling in the early post-stroke phase, and microglia accumulation or proliferation was reduced during the whole observation period of 14 days, possibly due to an initial inhibition of phenotype transformation. Based on previous studies, the majority of GFP-positive cells studied here are microglia cells. However, cells cannot be distinguished from invading macrophages based on the presentation of antigens.
Our results also indicate the necessity of a specific time window to achieve beneficial effects by treatment with AMD3100. To summarize, our data imply that both pathways (CXCL12/CXCR4 and FKN/CX3CR1) specifically impact on the activation of microglia and putative intercellular crosstalks. Specifically, we demonstrated that the blockade of CXCL12 actions at the CXCR4 reduced FKN levels, which could be responsible for the observed attenuated microglia activation. It has also been shown that AMD3100 acts as an allosteric agonist on the receptor CXCR7 . Based on our results, we conclude that the effects at CXCR4 are not abrogated by potential binding of AMD3100 to CXCR7. However, we cannot exclude that AMD3100 bound to CXCR7 exerts functions contributing to recovery of function after stroke.
Phenotype of GFP+ cells in the ischemic territory of CX3CR1GFP/+ mice
Investigation of the phenotype of GFP+ immune cells in the ischemic territory showed that 14 days after induction of PT, GFP+/CD68+ microglia/macrophages accumulated predominantly in the ischemic infarct core. Only a small population of cells was positive for CD45, indicating also the presence of blood-derived leukocytes. Together with an amoeboid morphology these cells most likely represented phagocytes. Co-localization of GFP+ cells with Iba1 further supports the idea that these cells were in an activated state as demonstrated previously . Within the infarct core, micrographs also show CD68+ cells lacking GFP. A conceivable explanation of this finding could be the existence of different CD68-expressing immune cell populations that may downregulate the expression of GFP driven by the CX3CR1 promotor. Further research is needed to explain this phenomenon.
The expression of CXCR4 in the post-ischemic brain confirms a target for AMD3100 treatment after ischemic injury. CXCR4+ cells in the infarct core and adjacent peri-infarct area displayed a round-shaped morphology and have been identified as immune cells previously . Other CXCR4+ cells observed throughout the brain could be identified as neurons [3,44].
Relevance of fractalkine for immune cell activation and inflammation after stroke
Several studies have examined the role of FKN after experimental stroke, with conflicting results. Here we demonstrate a significant decrease of FKN levels in the ischemic infarct core of wild-type mice treated with AMD3100 for 5 days. Thus, antagonism of CXCR4 reduces the release of FKN after stroke, which confirms earlier published data . Importantly, immunofluorescence analysis showed CXCR4 expression on immune cells and neuron-like cells in the post-ischemic brain indicating that both cell types are susceptible for AMD3100 treatment and may release FKN.
In mice deficient for CX3CR1, FKN levels were lower than those obtained in wild-type littermates. A possible explanation might be a positive feedback loop between glia and neurons regulating FKN shedding. Moreover, treatment with AMD3100 did not affect the already reduced levels of FKN in CX3CR1-deficient mice subjected to PT. We therefore propose that a functional receptor, CX3CR1, is necessary for FKN modulation through CXCR4 antagonism.
It also has been shown that in CX3CR1-deficient mice there might be a lower production of pro-inflammatory cytokines, leading to a protective inflammatory milieu in stroke with smaller lesions [19,45]. However, one has to consider that smaller infarct sizes per se may result in lower levels of pro-inflammatory molecules. In the present study we could not find any differences concerning the levels of pro-inflammatory cytokines in the infarct core after PT in wild-type compared to CX3CR1-deficient mice. On the other hand, our results indicate that anti-inflammatory effects caused by AMD3100 treatment require a functional CX3CR1 since the drug was ineffective in deficient mice.
We demonstrate that reduced endogenous FKN levels and reduced levels of pro-inflammatory cytokines are accompanied by an enhanced recovery of lost neurological function. This is in contrast to studies showing that FKN significantly reduced brain damage after permanent focal ischemia . Discrepancies might be explained by differences in the study designs. While the present project investigated the role of endogenous FKN, recombinant FKN was administered to mice shortly before induction of stroke in the previous study and infarct volumes have been studied at an earlier time point after stroke . Nevertheless, it could be speculated that an increase of FKN in the early phase after stroke has different effects on inflammatory cascades and cell death mechanisms than at later stages. Acutely after stroke there are more brain resident CX3CR1+ microglial cells present in the ischemic territory that are responsive to FKN. Several days later, the tissue milieu in the ischemic territory changes, with accumulation of different subsets of CX3CR1-expressing immune cells [23,46].
Our study shows that treatment with the CXCR4 antagonist AMD3100 significantly enhanced long-term recovery of lost neurological function after permanent focal ischemia. Treatment with AMD3100 inhibited the activation of microglia in the proximal peri-infarct area most likely due to reduced levels of FKN during the first week after stroke. Results support the idea that specific CXCR4 antagonism might be exploited in future approaches to improve rehabilitative treatment in stroke patients.
C-X-C chemokine ligand
C-X-C chemokine receptor
Green fluorescent protein
Middle cerebral artery occlusion
Normal donkey serum
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This study was supported by the Swedish Research Council (grant 2011–2684 and grant 2011–2652), the EU 7th work program through the European Stroke Network (grant No. 201024), the Hans-Christian and Alice Wachtmeister Foundation, the Swedish Brain Fund, the Thorsten och Elsa Segerfalk stiftelse, the European-Neurological-Society-Fellowship 2012, the Stiftung-Felgenhauer and the Crafoord Foundation.
The authors declare that they have no competing interests.
HLW carried out the in vivo experiments and wrote the manuscript. GvdM, ARA and KR performed Western blots and immunohistochemistry experiments. TW participated in the design of the study and revised the manuscript. KR conceived the study and revised the manuscript. All authors read and approved the final manuscript.
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Walter, H.L., van der Maten, G., Antunes, A.R. et al. Treatment with AMD3100 attenuates the microglial response and improves outcome after experimental stroke. J Neuroinflammation 12, 24 (2015). https://doi.org/10.1186/s12974-014-0232-1
- Chemokine receptor
- Stroke recovery