CCL2 modulates cytokine production in cultured mouse astrocytes
© Semple et al; licensee BioMed Central Ltd. 2010
Received: 4 June 2010
Accepted: 14 October 2010
Published: 14 October 2010
The chemokine CCL2 (also known as monocyte chemoattractant protein-1, or MCP-1) is upregulated in patients and rodent models of traumatic brain injury (TBI), contributing to post-traumatic neuroinflammation and degeneration by directing the infiltration of blood-derived macrophages into the injured brain. Our laboratory has previously reported that Ccl2-/- mice show reduced macrophage accumulation and tissue damage, corresponding to improved motor recovery, following experimental TBI. Surprisingly, Ccl2-deficient mice also exhibited delayed but exacerbated secretion of key proinflammatory cytokines in the injured cortex. Thus we sought to further characterise CCL2's potential ability to modulate immunoactivation of astrocytes in vitro.
Primary astrocytes were isolated from neonatal wild-type and Ccl2-deficient mice. Established astrocyte cultures were stimulated with various concentrations of lipopolysaccharide (LPS) and interleukin (IL)-1β for up to 24 hours. Separate experiments involved pre-incubation with mouse recombinant (r)CCL2 prior to IL-1β stimulation in wild-type cells. Following stimulation, cytokine secretion was measured in culture supernatant by immunoassays, whilst cytokine gene expression was quantified by real-time reverse transcriptase polymerase chain reaction.
LPS (0.1-100 μg/ml; 8 h) induced the significantly greater secretion of five key cytokines and chemokines in Ccl2-/- astrocytes compared to wild-type cells. Consistently, IL-6 mRNA levels were 2-fold higher in Ccl2-deficient cells. IL-1β (10 and 50 ng/ml; 2-24 h) also resulted in exacerbated IL-6 production from Ccl2-/- cultures. Despite this, treatment of wild-type cultures with rCCL2 alone (50-500 ng/ml) did not induce cytokine/chemokine production by astrocytes. However, pre-incubation of wild-type astrocytes with rCCL2 (250 ng/ml, 12 h) prior to stimulation with IL-1β (10 ng/ml, 8 h) significantly reduced IL-6 protein and gene expression.
Our data indicate that astrocytes are likely responsible for the exacerbated cytokine response seen in vivo post-injury in the absence of CCL2. Furthermore, evidence that CCL2 inhibits cytokine production by astrocytes following IL-1β stimulation, suggests a novel, immunomodulatory role for this chemokine in acute neuroinflammation. Further investigation is required to determine the physiological relevance of this phenomenon, which may have implications for therapeutics targeting CCL2-mediated leukocyte infiltration following TBI.
Cerebral inflammation involving the release of soluble mediators, infiltration of peripheral immune cells and activation of resident glial cells, is one of the key pathophysiological processes contributing to secondary degeneration following focal traumatic brain injury (TBI). The chemokine CCL2 (also known as macrophage chemoattractant protein-1, or MCP-1) is well recognised for its potent ability to mediate macrophage recruitment and migration to sites of inflammation [1, 2]. In the brain, CCL2 production is rapidly induced by a range of diverse inflammatory conditions, and is associated with the infiltration of blood-derived macrophages and activation of microglia [3, 4]. Transgenic mice over-expressing Ccl2 in the central nervous system (CNS) exhibit a robust accumulation of macrophages in the brain [5, 6], whereas mice deficient in the Ccl2 gene show reduced leukocyte infiltration after TBI, spinal cord injury and stroke [7–9]. Detection of elevated CCL2 in the serum and cerebrospinal fluid of severe TBI patients [9, 10] corroborates a central role for this chemokine in post-traumatic neuroinflammation.
We recently identified an altered profile of cortical cytokine production in Ccl2-deficient mice subjected to a closed head injury model of focal TBI. Peak levels of interleukin (IL)-1α, IL-1β, IL-6, granulocyte-colony stimulating factor (G-CSF), IL-12(p40), CCL3 and CXCL1 were delayed and significantly exacerbated in Ccl2-/- mice compared to wild-type mice acutely post-injury, whilst the production of other inflammatory mediators including CCL5, interferon-gamma (IFNγ) and IL-2 had reduced production in chemokine-deficient animals . These findings appear paradoxical to the delayed neuroprotection shown in Ccl2-/- mice, which had reduced macrophage accumulation and tissue damage associated with improved functional recovery over 4 weeks post-injury. We hypothesise that the altered cytokine network in the brains of Ccl2-/- mice after injury may indicate a previously unrecognised role for CCL2 as a modulator of acute CNS inflammation. Based on astrocytes being the main source of chemokines including CCL2 [11–14], it is conceivable that CCL2 may exert immunomodulatory effects on this cell type.
In the current study, we aimed to elucidate whether CCL2 regulates immune processes by investigating cytokine production from Ccl2-/- astrocytes compared to wild-type cells in response to inflammatory stimuli in vitro. We demonstrate that primary Ccl2-/- astrocyte cultures secrete exacerbated levels of chemokines and cytokines such as interleukin (IL)-6 compared to wild-type cells in response to lipopolysaccharide (LPS) and IL-1β stimulation. Furthermore, production of IL-6 induced by IL-1β in wild-type astrocytes was suppressed by prior incubation with exogenous CCL2. These results indicate a likely immunomodulatory role for CCL2 in astrocytic cytokine production. In combination with other recently identified functions of this chemokine in neurotransmission [15, 16] and neuronal cell survival [17–19], these findings indicate that future application of therapeutics targeting CCL2-mediated leukocyte infiltration following TBI may have tangential effects in the injured brain.
Animals and reagents
The experimental procedure was approved by the Alfred Medical Research and Education Precinct (AMREP) Animal Centre, Melbourne, Australia. Ccl2-/- mice (B6.129S4-Ccl2tm1Rol/J) on a C57Bl/6 background were obtained from Jackson Laboratory (Maine, USA) and a breeding colony established at AMREP. C57Bl/6 mice were used as wild-type controls. Unless otherwise stated, all reagents were obtained from Invitrogen Laboratories, Carlsbad, CA or Sigma Aldrich, St Louis, MO.
Isolation of primary mouse astrocytes
Primary astrocyte cultures were obtained from newborn (0-2 day old) mice as previously described [20, 21]. Following isolation of cortices and removal of the meninges, dissociated cells were suspended in Dulbecco's Modified Eagle's Media (DMEM) containing 10% fetal bovine serum (FBS) and 0.25% gentamycin, and plated on 75 cm2 flasks pre-coated with 0.1 mg/ml poly-L-lysine. Cultures were maintained for 7 days to generate a confluent glial culture.
Prior to trypsinisation, contaminating microglial cells were separated by vigorous mechanical agitation and removed by subsequent washing in Hank's Balanced Salt Solution (HBSS). Astrocytic monolayers were then dislodged from flasks by trypsinisation (0.25% trypsin in HBSS and 1 mM EDTA). Cells were seeded in either 24-well plates (1 × 105 cells/well) or 75 cm2 flasks (5 × 105 cells/flask) and grown for 7-9 days until confluent prior to stimulation. Culture purity was determined by double-labelling immunohistochemistry for GFAP (1:1000; DAKO, Glostrup, Denmark) and CD11b (1:150; BD Pharminogen, San Diego, CA) to identify astrocytes (>95%) and microglia (<5%), respectively. The lack of Ccl2 mRNA amplified by quantitative PCR confirmed the absence of Ccl2 in gene-deficient cultures.
16 hours prior to stimulation, cultures were washed in HBSS and cultured with low-serum medium (DMEM containing 1% FBS). Astrocytes were then stimulated with either LPS (from Escherichia coli 0111:B4 γ-irradiated; 0.1-100 μg/ml), mouse recombinant (r) IL-1β (<1 EU/μg endotoxin; Peprotech, Rocky Hill, NJ; 0.1-50 ng/ml) or rCCL2 (R&D Systems, Minneapolis, MN; 50-500 ng/ml) in low-serum (1%) DMEM. LPS and IL-1β in particular have been shown to induce cytokine production by cultured astrocytes across a wide range of concentrations, from 1 ng/ml to 1 mg/ml LPS [21–30] and between 0.1 - 100 ng/ml IL-1β [31–35]. In some experiments, cultures were pre-treated with rCCL2 (250 ng/ml) for 12 h, before the addition of LPS or IL-1β for a further 8 h. This experimental design was based on one previously used to demonstrate the regulation of macrophage cytokine production by the chemokine fractalkine . Three separate cultures were stimulated, such that data represents the mean of three independent experiments. Parallel astrocyte cultures were incubated in medium alone as unstimulated controls. After stimulation (2 - 48 h) supernatant was collected, centrifuged (1000 rpm, 10 min at 4°C) and stored at -20°C until analysis, whilst cells were washed in HBSS and scrapped for collection, then centrifuged prior to storage of cell pellets at -80°C.
Measurement of cytokine production in culture supernatants
Commercially-available mouse multiplex kits (LINCOplex; Millipore, Billerica, MA) were used to quantify the production of the cytokines IL-6 and TNF, as well as the chemokines CXCL1, CCL3 and CCL5, in culture supernatants following stimulation with LPS. These five inflammatory mediators are all reportedly produced by mouse, rat and human astrocytes, in response to a variety of stimuli including mechanical injury and pro-inflammatory cytokines. Mouse IL-6 secreted in response to IL-1β stimulation was measured using Quantikine Immunoassays (R&D Systems; lower detection limit <1.6 pg/ml).
Quantification of gene expression by real-time reverse transcriptase polymerase chain reaction (qPCR)
RNA was extracted and isolated from astrocyte cells using the Purelink RNA Mini Kit (Invitrogen), including on-column DNase treatment, as per the manufacturers' instructions. RNA concentration and purity was determined using a Nanodrop1000 spectrophotometer (Thermo Fisher Scientific), with an absorbance ratio at 260 and 280 nm of >1.9 considered as highly pure RNA. One microgram of each sample was reverse transcribed into complementary-strand DNA (cDNA) using SuperScript™ III reverse transcriptase and oligo d(T)20 as the primer according to the manufacturers' protocol (Invitrogen). Quantitative PCR (qPCR) was performed using the TaqMan Universal master mix (Applied Biosystems, Foster City, CA) and TaqMan® gene expression assay for mouse IL-6 (Mm01210733_m1, Applied Biosystems). Samples were assayed in triplicate on a 384 well plate using the 7900 Fast Real-Time PCR system (Applied Biosystems).
The widely-accepted comparative Ct (threshold cycle) method was used to perform relative quantification of qPCR results . An arithmetic formula (fold difference = 2-ΔΔCt) was used to calculate the relative mRNA expression of stimulated cultures compared to unstimulated controls, after normalisation to levels of the housekeeping control gene, glyceraldehyde-3-phosphate dehydrogenase (GAPDH; Mm99999915_g1). Data are thus expressed as fold change compared to unstimulated wild-type cells.
Statistical analysis was performed using Sigma Stat 2.03 software (SPSS Inc., Chicago, IL). Data shown represent means ± standard error of the mean (SEM) from at least three independent experiments. Two-way Analysis of Variance (ANOVA) tests were used to evaluate cytokine production across time or different stimulus concentrations, with overall significance for factors of strain and time/concentration reported as such. Tukey's test was employed for post-hoc comparisons between and within individual factors (indicated on figures by * and #), whilst differences between two factors (e.g. gene expression in LPS-stimulated wild-type and Ccl2-/- cells) were analysed by t-tests. When necessary, non-parametric data was normalised by transformation by natural log (ln) prior to statistical analysis. Statistical significance was considered at the 5% level (p < 0.05).
Cytokine production was exacerbated in LPS-stimulated Ccl2-/- astrocytes
In general, the cytokines IL-6 and TNF (figure 1a and 1b) were differentially stimulated in Ccl2-/- astrocytes across the range of LPS concentrations (0.1 - 100 μg), with exacerbated production compared to wild-type cells. For IL-6, no differences were noted between the strains at 0.1 μg/ml LPS, whereas from 1-100 μg/ml, whilst IL-6 production by wild-type cells reached a plateau, production by Ccl2-/- astrocytes increased dose-dependently (p < 0.01; 2-way ANOVA effect of strain). TNF secretion showed a similar pattern, with Ccl2-/- astrocytes showing significantly greater cytokine production from 0.1 μg/ml LPS onwards (p < 0.001; 2-way ANOVA effect of strain). In addition, production of the neutrophil chemoattractant CXCL1 (figure 1c) and two macrophage chemokines CCL3 and CCL5 (figure 1d and 1e) was significantly elevated in Ccl2-/- astrocytes (p < 0.01; 2-way ANOVA effect of strain), with the later being particularly exacerbated in gene-deficient cells at higher LPS concentrations of 10 and 100 μg/ml (p < 0.001; post-hoc). CCL5 was secreted at notably lower levels (~ 5-15 pg/ml) compared to CCL3 and CXCL1 (~ 100-400 pg/ml) in cell supernatant, however its concentration was consistently enhanced in Ccl2-/- compared to wild-type astrocytes ((p < 0.01; 2-way ANOVA effect of strain).
Importantly, whilst cytokine and chemokine production was induced in wild-type cells by LPS treatment, this effect appeared to plateau from 0.1 μg/ml LPS, after which increasing concentrations of the stimulus did not augment mediator secretion further. In contrast, Ccl2-/- astrocytes exhibited an increasing dose-dependent response, with the maximal LPS concentration used (100 μg/ml) inducing the greatest secretion of all five mediators (p < 0.001, 2-way ANOVA effect of concentration).
IL-6 production by IL-1β-stimulated Ccl2-/- astrocytes is concentration-dependent
To further investigate this incongruity, wild-type and Ccl2-/- astrocyte cultures were treated with IL-1β at 1, 10 or 50 ng/ml and compared across a time course of 2 - 24 h. IL-1β at 1 ng/ml simulated low levels of IL-6 by astrocytes from both strains (< 7 pg/ml in wild-type cultures and < 2 pg/ml in Ccl2-/- cultures), with IL-6 secretion being consistently higher (~2-8 pg/ml) in wild-type astrocytes compared to Ccl2-/- cells (<2 pg/ml; p < 0.001; 2-way ANOVA effect of strain), which was evident at all time points from 2 h onwards (p < 0.001; post-hoc) (figure 3b). In contrast, using a higher concentration of IL-1β (10 ng/ml) induced a greater production of IL-6 compared to 1 ng/ml stimulation in both strains. IL-6 secretion was increased in wild-type astrocytes at 4 h compared to 2 h, however, little additional secretion was seen with an increased length of exposure (4-24 h) (figure 3c). On the contrary, IL-6 induction in Ccl2-/- astrocytes was more robust across the time course, with production exacerbated above levels in wild-type astrocytes steadily increasing over time to a maximum after 24 h stimulation (p < 0.001; post-hoc).
Similarly, stimulation with IL-1β at 50 ng/ml induced a further enhanced response from Ccl2-/- astrocytes compared to wild-type (2-way ANOVA effect of strain). This was evident as early as 2 h (6.32 ± 0.57 pg/ml; p < 0.01, post-hoc) and maintained across the time course, with IL-6 secretion peaking in Ccl2-/- astrocytes at 24 h (33.74 ± 2.24 pg/ml) (figure 3d). Interestingly, differences between the strains were less pronounced at 50 ng/ml compared to IL-6 production induced by IL-1β at 10 ng/ml.
In summary, the enhanced production of IL-6 in Ccl2-/- astrocytes following IL-1β stimulation was dependent on the concentration of the stimulus, but independent of the length of exposure time.
Exogenous CCL2 does not induce cytokine release in astrocytes
Given the differential production of cytokines in the absence of CCL2, we postulated that treatment with the exogenous recombinant chemokine may modulate cytokine secretion.
To ascertain this hypothesis, wild-type cultures were incubated with mouse rCCL2 for 12 h with a range of concentrations (50, 100, 250 and 500 ng/ml), and the production of IL-6, TNF, CXCL1, CCL3 and CCL5 was measured in the collected supernatant. Even at the highest concentration of rCCL2, production of TNF, CXCL1, CCL3 and CCL5 were below detectable levels (reported as 0.9, 1.2, 2.8 and 0.7 pg/ml respectively). IL-6 concentrations were barely detectable in unstimulated cultures, and increasing concentrations of rCCL2 had no additional effect on IL-6 secretion (p = 0.700; one-way ANOVA; data not shown). Similarly, IL-6 production from Ccl2-/- astrocytes following rCCL2 treatment was negligible (<0.2 pg/ml; data not shown).
rCCL2 reduces IL-1β induction of IL-6 production and expression
IL-6 gene expression was next measured by qPCR in wild-type cells collected post-stimulation (figure 4b). As for supernatant measurements, cultures were incubated for 12 h with either media only or rCCL2 (250 ng/ml), before the addition of IL-1β (10 ng/ml; 8 h). 10 ng/ml of IL-1β was chosen for investigation, as it was the concentration at which we observed the greatest effect of rCCL2 inhibition (figure 4a). Consistent with protein production, the levels of IL-6 mRNA were consistently low in unstimulated cells regardless of pre-incubation with either media alone or rCCL2. Also consistent with the protein data, IL-1β stimulation robustly increased IL-6 expression by ~ 50 fold compared to levels in unstimulated cells (p < 0.001; 2-way ANOVA). In contrast, rCCL2 pre-treatment significantly inhibited IL-6 mRNA levels in response to IL-1β by 44% compared to pre-treatment with media alone (p < 0.05), corresponding with the reduced IL-6 protein detected under the same conditions.
Investigations into inflammatory neuropathologies such as multiple sclerosis and stroke have demonstrated neuroprotection resulting either from interference with the Ccl2 gene, by administration of neutralising anti-CCL2 antibodies, or targeting the CCR2 receptor [7, 42–44]. Besides the chemotactic ability of CCL2 to drive the migration of monocytic cells into the brain, recent evidence has shown that CCL2 also has alternative neuroactive properties in the CNS [17–19, 45]. Furthermore, research by our group and others have reported alterations in the inflammatory cytokine response and tissue damage in Ccl2-deficient mice after TBI or stroke, prior to the onset of leukocyte infiltration [7, 9]. The purpose of our current study was thus to investigate whether CCL2 can influence astrocyte-specific cytokine secretion following an immune challenge in vitro.
The production of the cytokine IL-6 and chemokines CXCL1 and CCL3 was significantly exacerbated in the supernatant of Ccl2-/- astrocytes following stimulation with LPS, corresponding to the delayed and enhanced secretion detected in the injured mouse brain . TNF, whose production was elevated in the brains of Ccl2-/- mice across a time course of 2-24 h after experimental TBI, was also elevated in LPS-stimulated Ccl2-/- astrocytes in vitro. Differences in cytokine protein levels in wild-type and Ccl2-/- astrocyte cultures are likely due to variations in gene expression, as we also detected an enhanced elevation of IL-6 mRNA levels in Ccl2-/- astrocytes compared to wild-type cells.
Interestingly, the macrophage chemoattractant CCL5 was produced at lower levels in the brains of Ccl2-/- mice compared to wild-type after TBI, however, gene-deficient astrocytes had a profile of exacerbated CCL5 production. Particularly considering the low concentration of CCL5 detected in culture supernatant following LPS stimulation compared to the other cytokines measured, it is possible that this chemokine may be primarily produced during neuroinflammation by other CNS cells such as microglia, as has been previously suggested [35, 46, 47].
For subsequent experiments we focused specifically on astrocyte production of IL-6, as this multi-functional cytokine is central to CNS inflammation and degeneration following TBI [40, 41], and is secreted in vitro in response to mechanical injury and exposure to inflammatory cytokines [22, 26, 29, 31, 48, 49]. Consistent with the LPS-stimulated phenotype, a similarly enhanced response by Ccl2-/- astrocytes was evident following stimulation with the pro-inflammatory cytokine IL-1β at both 10 and 50 ng/ml. Interestingly, this characteristic exacerbated response was not evident in Ccl2-/- astrocytes at a lower concentration of IL-1β (1 ng/ml), when wild-type cells produced a higher level of IL-6. This finding may reflect what we observed in vivo, where secretion of IL-6 was similar in wild-type and Ccl2-/- mice early after injury (2-4 h) before a delayed and enhanced response in Ccl2-/- mice occurred at 12 h, corresponding to the time of maximal IL-1β in the lesioned cortex .
There have been several other studies suggesting that Ccl2-deficiency deregulates inflammatory cytokine synthesis in the CNS, primarily restricted to in vivo rodent models. Contrary to our findings, Hughes and colleagues (2006) reported that IL-6 and IL-1β were significantly reduced in the brains of Ccl2-/- mice after induction of ischaemic stroke . Similarly, lower levels of IL-1β and TNF were induced in Ccl2-/- mice compared to wild-type after a striatal injection of LPS . A third study also using LPS as the stimulus found that peripheral administration resulted in elevated IL-1β and TNF levels in serum of Ccl2-/- mice, whereas cytokine production in the brain was attenuated . It is worth noting that all three of these studies considered only one time point (6 h) after stroke or LPS stimulation. Since we have shown here that alterations in cytokine production resulting from Ccl2-deficiency are time and concentration-dependent both in vivo and in vitro, it is possible that these studies do not comprehensively reflect the overall neuroinflammatory response specific to this strain. Importantly, our current work is the first to examine Ccl2-deficient anomalies in cytokine production or synthesis in depth by using an in vitro system of astrocyte activation.
Previous studies have suggested that the early and robust upregulation of CCL2 in neuropathologies such as TBI may indicate a central role for this chemokine in initiating the cytokine response . Given that cytokine production in the brain coincides with CCL2 upregulation and most often precedes evidence of microglial activation or macrophage infiltration from the periphery, it is unlikely that the influence of CCL2 on acute cytokine production is dependent on the chemoattraction of leukocytes and subsequent secretion from these cells . Furthermore, investigation of the macrophage and microglial marker F4/80 in the brains of Ccl2-/- mice early after injury or disease onset has failed to detect any difference from wild-type mice, suggesting that the contribution of CCL2 to acute neuropathology may be independent to its classic actions as a chemokine [7, 50, 52]. Given that incubation of cultured astrocytes with rCCL2 alone does not induce production of IL-6, TNF, CXCL1, CCL3 or CCL5 above levels in unstimulated cells, it is also unlikely that CCL2 directly stimulates cytokine production from astrocytes.
Alternatively, based on our findings of exacerbated cytokine production in the brains of injured Ccl2-deficient mice and immune-challenged Ccl2-deficient astrocytes, we hypothesised that CCL2 may act during early immunoactivation in an inhibitory manner. Interestingly, CCL2 has recently been proposed to protect neurons from cell death induced by N-methyl-D-aspartate, glutamate, β-amyloid and human immunodeficiency virus-mediated Tat toxicity [17–19]. Further prompting our own investigations into alternative properties of CCL2, Rankine and colleagues (2006) previously showed that co-administration of LPS and rCCL2 into the mouse brain did not have a synergistic pro-inflammatory effect as they had hypothesised - instead, the addition of rCCL2 in combination with LPS resulted in a non-significant trend towards reduced IL-6 production.
Also relevant to our findings, Zisman and colleagues showed that treatment with anti-CCL2 antibodies prior to an intraperitoneal LPS challenge increased plasma TNF and IL-12 levels, whilst administration of rCCL2 reduced pro-inflammatory cytokine production by 20-35% . Similarly, in cultured astrocytes we have demonstrated that pre-exposure to rCCL2 was sufficient to reduce the IL-1β-stimulated production of IL-6 in culture supernatant. Furthermore, this inhibitory effect was also evident at a transcriptional level, as the increase in IL-6 mRNA expression induced by IL-1β stimulation was significantly lower in rCCL2-treated cultures. To our knowledge, this is the first in vitro evidence that CCL2 can act on astrocytes in an immunomodulatory manner to down-regulate cytokine expression and production.
One limitation of this study is the relative simplicity of the culture system used. It must be noted that cultured primary astrocytes may respond quite differently in isolation compared to in vivo, where they may be influenced by interactions with adjacent endothelial cells, microglia and extracellular matrix components. However, the consistency between our findings in cultured astrocytes and the mouse cortex in vivo  supports the use of primary astrocyte cultures as an appropriate model system.
The mechanisms underlying a novel role for CCL2 in CNS cytokine production need to be further elucidated. Whilst CCL2 mediates immune cell chemotaxis by binding to the CCR2 receptor, the presence of CCR2 on astrocytes in the brain remains controversial [14, 54–57]. Quinones and colleagues recently found that CCL2 treatment in vitro can induce glial cell migration and inhibit the spontaneous apoptosis of mouse astrocytes in a dose-dependent manner. Whilst the latter pro-survival effect was shown to be dependent on signaling via CCR2, residual chemotaxis of Ccr2-/- astrocytes in response to CCL2 may indicate the presence of an alternative receptor for this chemokine on primary astrocytes . Whether CCR2 is the primary receptor involved in CCL2-modulation of cytokine production, and which intracellular pathways are responsible for the reduction in cytokine expression observed in IL-1β-stimulated astrocytes pre-exposed to rCCL2, remain unanswered. The use of specific neutralising antibodies, or the recently generated cell-conditional CCL2 knockout mice in which gene deletion is specific to either astrocytes or endothelial cells, may prove essential in answering these questions and eliminating potential confound resulting from global gene deficiency .
Lastly, the consequences of an altered cytokine environment in the presence or absence of CCL2 remain unclear. Of note, Ccl2-/- mice show long-term improvements in neurological recovery and reduced tissue damage following experimental TBI, despite the aberrations in early cytokine secretion . Given the acute nature of cytokine production in the injured brain, it is feasible that the aberrant, exacerbated cytokine profile seen in Ccl2-/- mice may contribute to early post-traumatic degeneration in this strain, which may compensate for the lack of CCL2 and contribute to early leukocyte infiltration. We hypothesise that CCL2 may have differential acute and long-term effects during neuropathology, as has been indicated for TNF [60, 61]. A deeper understanding of the consequences of CCL2 deletion in CNS inflammation and cytokine production may allow us to better tailor therapeutic approaches to the appropriate time post-injury. Thus further studies are necessary to elucidate the biological and physiological relevance of these findings.
In the current study we have employed an in vitro model of astrocyte activation to characterise the Ccl2-/- genotype-specific profile of cytokine and chemokine secretion as observed in the injured brains of Ccl2-/- mice. Our findings provide evidence that astrocytes are primarily responsible for exacerbated cytokine response in the absence of CCL2. Furthermore, we present data showing that rCCL2 can inhibit the astrocytic production of inflammatory cytokines in response to IL-1β stimulation. In light of these findings, we propose that CCL2 plays a novel, immunomodulatory role in the inflamed CNS by altering cytokine production in astrocytes, and that this effect is relative to the concentration of the stimulus present. This study highlights the complexity of chemokine - cytokine interactions in the CNS, and suggests that CCL2 may affect multiple cytokine pathways which could participate in neurodegenerative processes. Our data indicate that chemoattraction of immune cells is only one of the functions performed by CCL2 in the injured CNS, and that further investigation is required before targeting of this chemokine as a means of neuroprotection for neuropathologies in which CCL2 upregulation is a characteristic feature.
The authors declare that they have no competing interests.
Supported by the Victorian Neurotrauma Initiative, Australian Government (Australian Postgraduate Award for BD Semple), Transport Accident Commission and National Health and Medical Research Council.
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