Distinct modulation of microglial amyloid β phagocytosis and migration by neuropeptidesi
© Fleisher-Berkovich et al. 2010
Received: 16 August 2010
Accepted: 11 October 2010
Published: 11 October 2010
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© Fleisher-Berkovich et al. 2010
Received: 16 August 2010
Accepted: 11 October 2010
Published: 11 October 2010
Microglial activation plays an integral role in the development and course of neurodegeneration. Although neuropeptides such as bradykinin (BK), somatostatin (SST), and endothelin (ET) are known to be important mediators of inflammation in the periphery, evidence of a similar function in brain is scarce. Using immunocytochemistry, we demonstrate the expression of receptors for BK (B1, B2 subtypes), ET (ETA, ETB subtypes) and SST (SST 2, 3, 4 subtypes) in primary microglia and microglial cell lines. Exposure of BV2 and N9, as well as primary microglial cells to BK or SST increased Aβ uptake in a concentration-dependent manner, whereas endothelin decreased Aβ uptake. This was caused by increased phagocytosis of Aβ since the rate of intracellular Aβ degradation remained unaffected. All neuropeptides increased chemotactic activity of microglia. In addition, BK reduced Aβ-induced expression of proinflammatory genes including iNOS and COX-2. ET decreased the Aβ-induced expression of monocyte chemoattractant protein 1 and interleukin-6. These results suggest that neuropeptides play an important role in chemotaxis and Aβ clearance and modulate the brain's response to neuroinflammatory processes.
Besides the well described pathological hallmarks, the deposition of the amyloid β peptide (Aβ) in fibrillar plaques and neurofibrillar tangles of tau protein, neuroinflammation has a prominent role during Alzheimer disease (AD) . This is expressed by activated microglia and reactive astrocytes localized to amyloid plaques, and the release of biochemical markers, like cytokines, chemokines and nitric oxide, that are found to be increased in the brains of patients with AD. Microglia, the main immune effector of the brain, are able to migrate to sites of Aβ deposition and to eliminate Aβ by phagocytosis upon activation by multiple receptors amongst the toll-like receptors (TLR2, TLR4), scavenger receptor A and CD36.
It is known that certain neuropeptides decline during aging before the onset of AD [3, 4]. Neuropeptides belong to a family of signalling molecules released by neurons acting on cell surface receptors. Their role in inflammation has been widely studied in peripheral tissues [5, 6], but their particular function on glial cells has not been studied in detail so far. There is growing evidence that neuropeptides are able to alter neurodegenerative processes during AD [7–10]. Strikingly, brain regions like the hippocampus and the cortex that are affected early during AD, are also the regions where neuropeptides like bradykinin and somatostatin, as well as their receptors, are prominently present [11–13].
Somatostains are cyclic peptides that are widely expressed throughout the brain where they act as neuromodulators . Five G protein-coupled somatostatin receptors have been described (SSTR1-5), which are expressed in distinct yet overlapping patterns within the brain . Of note, two of them, SSTR2 and SSTR4, are expressed in the hippocampus and cortex . In AD, elimination of SST from the cortex and hippocampus is correlated to reduced cognitive function and memory impairment [10, 17]. In addition, SSTRs show marked depletion in the AD brain [18–20].
Bradykinin (BK) is a short-lived nonapeptide generated from the kininogen precursors that is upregulated after lesions in the CNS . Because of its attenuating effect on the secretion of pro-inflammatory cytokines from microglia BK has anti-inflammatory and thereby neuroprotective properties . Like somatostatin, bradykinin binds to G protein-coupled receptor at the cell surface. Two subtypes of bradykinin receptor, B1 and B2, have been characterized so far. The expression of B2 bradykinin receptors has been confirmed in the brain stem, basal nuclei and cerebral cortex, whereas B1 bradykinin receptors are present in the entorhinal cortex, dentate gyrus, and pyramidal neurons of the hippocampus. Besides neurons and astrocytes, primary microglia have been shown to express BK receptors .
Another prominent neuropeptide system in the brain is the endothelin (ET) system. Endothelins are 21 amino acid long cyclic peptides. Currently there are three described isoforms (endothelin 1-3), that derive from precursor proteins by proteolytic processing . They signal through two major receptor subtypes known as ETA and ETB receptors belonging to the superfamily of G-protein coupled receptor . ET-1, ET-3 as well as ET receptors are expressed in glial and neuronal cells . During AD it has been observed that endothelin-1 levels are decreased in the cerebrospinal fluid of AD patients  and its expression has been found to be elevated in frontal and occipital cortex in AD .
Since there are multiple indications that suggest an important role for neuropeptides in inflammation in general and in particular during the chronic inflammatory processes of AD, we investigated the impact of these signaling molecules on inflammatory core functions of microglial cells.
Primary microglial murine cell cultures were prepared as previously described in detail (Hanisch et al., 2004). Briefly, mixed neuronal cultures were prepared from newborn mice and cultured in DMEM supplemented with 10% FCS and 100 U ml-1 penicillin/streptomycin. Microglial cells were harvested by shake-off after 10-14 days of primary cultivation. Primary rat microglial cultures were obtained from the whole brain of newborn Wistar rats at 0-24 h of age. Mixed glial cells were cultured in High glucose (4.5 mg/ml) DMEM, supplemented with 10% FCS, 0.2 mM L-glutamine, 0.1 mg/ml streptomycin, and 0.2 U/ml penicillin was used as the culture medium. After 12 days, to isolate microglia, cells were shaken at 200 rpm for 1 h. The medium containing detached microglia was collected and the isolated microglia were reseeded and allowed to settle for 24 h . BV2 and N9 cell lines were mantained in IMDM supplemented with 5% FCS and 100 U ml-1 penicillin/streptomycin.
Microglial phagocytosis of aggregated FAM-labeled Aβ1-42 (FAM-Aβ) (Anaspec) was measured by plate based assay after incubation of Aβ at 37°C for three days. Cells were plated at 50000 cells in 100 μl in black 96 well plates. After 1 h Aβ was added to a final concentration of 500 nM and incubated for up to 4 h. Finally, the Aβ-containing medium was removed and extracellular Aβ was quenched with 100 μl 0.2% trypan blue in PBS pH 4.4 for 1 min. After aspiration fluorescence was measured at 485 nm excitation/535 nm emission using a Infinite 200 reader (Tecan). To normalize for cell numbers 100 μl 50 μg/ml Hoechst Dye 33342 in PBS was added, incubated for 30 min and the fluorescence measured at 360 nm excitation/465 nm emission. Additionally, microglial Aβ phagocytosis was verified by confocal microscopy. Confocal microscopy was performed using a BX61 microscope equipped with a disc spinning unit (Olympus).
Transwell 96 well permeable supports, containing 8 μm pore size polyester membrane, were used. Medium containing 10-9- 10-7 M bradykinin (BK), endothelin-1 (ET) or somatostatin (SST) was added to the lower chamber, whereas cells, (106 cells/ml), were added to the top chamber and incubated for 3 h at 37°C. Cells that passed through the membrane were harvested from the lower part of the membrane using trypsin, and stained with calcein AM dye. The stained trypsinized cells were transferred to a black plate and read in a plate reader at 485 nm excitation, 520 nm emission.
Cells were fixed in 4% paraformaldehyd at room temperature, washed twice with 100 mM HEPES pH 7, incubated in 1 μg/ml FC-block (Calbiochem), permeabilized with 0,1% Tx-100 in PBS for 10 min and non specific binding was blocked with 10% goat serum in PBS for 2 h. Sample were incubated overnight with first antibody in blocking solution, washed three times with PBS and the secondary antibody was added for 1 h in 10% goat serum/PBS. Finally the cells were washed three times in PBS, once in water and mounted with Immomount (Thermo) containing 5 μg/ml Hoechst 33342. Confocal microscopy was performed using BX61 equipped with a disc spinning unit (Olympus). Images were deconvoluted using the next neighbor algorithm (Cell^P, Olympus)
BV2 and N9 cells were incubated in a black 96-well plate (50,000 cells per well) and incubated for 15 h with bradykinin, endothelin or somatostatin. Then, FAM-labelled Aβ was added. After 30 min, all media were removed, cells mildly washed with warmed medium and subsequently fresh medium added for the indicated time points (0, 1, 2, 3 or 4 h). At each time-point media were removed and replaced by 0.2% trypan blue solution for 1 min in room temperature. Fluorescence detection of FAM-labelled Aβ1-42 was performed as described above. In order to confirm that cells were plated equally, cells were stained with Hoechst 33342.
BV2 cells were seeded onto a 6-well plate at a concentration of 2 × 106 cells per well and incubated in full medium for one hour. Then, medium was replaced by serum-free medium (SFM) in the absence or presence of the respective neuropeptide. After 15 h incubation, the cells were added with SFM or Aβ1-42 (at final concentration of 0.5 μM) and incubated for additional 4 h. After removal of SFM, cells were lysed in lysis buffer (20 mM Tris-Hcl pH 7.5, 0.5 mM EDTA, 0.5% Triton X-100 and 5 μM sodium vanadate) in the presence of protease inhibitors. Protein concentration was determined by bicinchoninic acid (BCA) assay kit (Thermo). Cell lysates were separated in 7.5% SDS-PAGE and blotted onto a nitrocellulose membrane (Biorad). Membranes were blocked for 90 min with 4% BSA and incubated overnight at 4°C with anti-NEP antibody (1:4000) (Abcam) or anti-IDE antibody (1:4000) (Calbiochem). After washing membranes were incubated for 90 min with the HRP-conjugated secondary antibody. Immunoreactivity was detected using enhanced chemiluminescence (Millipore) solution followed by exposure to X-ray film (Fuji medical X-ray film, FujiFilm). Semi-quantitative analysis was carried out using a computerized image analysis system (EZ Quant - Gel 2.2, EZQuant Biology Software Solutions). Protein load was normalized detecting β-actin (1:4000, Sigma).
Total RNA was prepared from the cells using RNeasy mini kit (Qiagen) and reversed transcribed (RT) into complementary DNA using high capacity cDNA reverse transcription kit (Applied Biosystems) according to the manufacturer's instructions. Real time qPCR was performed on a StepOnePlus Real-Time PCR System (Applied Biosystems) using TaqMan gene expression assay (Applied Biosystems). PCR was carried out in 20 μl with 1 μl of the RT product corresponding to 40 ng of total RNA, 0.2 μM of each primer and 10 μl of the master mix with the following temperature profile: 95°C for 10 min and 40 cycles of 95°C for 15 s and 60°C for 1 min. Amplification specificity was verified by melting curve analysis. mRNA expression values were normalized to the level of GAPDH expression. For primer details see Table 1.
The immunohistochemical and densitometric data and were analyzed by 1-way, 2-way ANOVA and Tukey's's post hoc test (GraphPad Prism 5 or SPSS 17).
Microglial cells represent the brain's innate immune system and are actively involved in maintaining parenchymal homeostasis through active tissue scanning and removal of debris by phagocytosis . In neurodegenerative diseases, activation of microglia leads to an alteration of these physiological functions, which in turn may contribute to disease progression and neuronal death. Next to cytokines and chemokines, neurotransmitters including norepinephrine, glutamate and acetylcholine can modulate the inflammatory action of microglia and influence their functions [26, 27]. Thus, neuronal activity and release of these factors may determine the activation status and finally the conditions whether microglia turn towards a beneficial or detrimental phenotype. In AD, various neurotransmitter systems are compromised and may thereby impair microglial functions in response to Aβ deposition including phagocytosis and migration . Impaired microglial phagocytosis of Aβ, however, may directly contribute to disease progression and neuronal dysfunction.
The presence of neuropeptide receptors on microglia suggests that these factors may be actively involved in the regulation of microglial functions [22, 29, 30]. After confirming the expression of bradykinin, endothelin and somatostatin receptors on primary murine microglia as well as on the microglial cell lines, the capacity of microglia to phagocyte fibrillar Aβ after preincubation with increasing concentrations of either one of the respective neuropeptides was studied. Of note, the overall levels of the peptides are low in the normal rodent and human brain. In particular, the basal levels of endothelins have been found to be 0.37 × 10-9 M in human cerebrospinal fluid , but undergo a massive upregulation upon brain injury [32, 33]. Further, the release of somatostatin from incubated rat hypothalamus has been determined to be 3 × 10-9 M . Finally, the exact levels of brain bradykinin are unknown. Nevertheless, the literature is unanimous in that bradykinin, used at 10-7 M and higher, stimulates glial inflammation . We therefore used these peptides in the range from 10-9 to 10-7 M, corresponding to physiological as well as 10 to 100 fold increased concentrations.
While bradykinin and somatostatin increased microglial Aβ phagocytosis in a concentration-dependent manner, endothelin showed the opposite action, suggesting a distinct regulation of Aβ uptake by neuropeptides. Importantly, none of the investigated peptides altered the intracellular degradation of Aβ thus confirming that the observed differences are solely due to increased uptake by microglia. While there is no previous information on the modulation of microglial phagocytosis by these substances, in general a positive regulation of phagocytosis by bradykinin had been reported in peripheral leucocytes after intravenous application of this neuropeptide in rabbits . In contrast, somatostatin had been found to suppress the phagocytic capacity of macrophages for Leishmania major parasites . Together, these data suggest that the neuropeptides do not generally up- or downregulate phagocytosis, but the later action strongly involves target-specific mechanisms.
Since somatostatin is reduced in AD brain and in CSF of AD patients [38, 39], one can speculate that this reduction contributes to Aβ deposition in the AD brain through impaired microglial phagocytosis along with the previously described negative influence on Aβ degradation by neprilysin . Likewise, the increase of endothelin expression observed in AD frontal and occipital cortex could compromise the effective clearance of the brain from Aβ by reducing microglial phagocytosis .
Interestingly, immunostimulation of microglia with bacterial lipopolysaccharide (LPS) almost completely abolished the regulatory effects of neuropeptides on microglial Aβ phagocytosis. Systemic bacterial infection has been reported to aggravate the clinical symptoms of AD patients , a phenomenon which may be explained by several mechanisms. However, extrapolating the findings of this study, it can be hypothesized that an additional immune challenge, in this case by LPS, leads to the reduction of beneficial microglial functions evoked neuropeptides such as bradykinin and somatostatin -even if those are decreased in AD brains as stated above, since the increased Aβ uptake observed in response to these neuropeptides is compromised by pre-exposure to LPS.
Since in the CNS migration of microglial towards inflammatory lesion sites plays an important role in resolving neuroinflammation and restoring local homeostasis, the effect of the three neuropeptides on migration were investigated. In contrast to the divergent effects on phagocytosis, all three neuropeptides collectively increased microglial migration. Bradykinin has been shown before to stimulate microglial migration in a concentration- and time-dependent manner and seems to involve the bradykinin 1 receptor , however no positive regulation on migration in general, but inhibition of Leishmania major promastigote-induced macrophage migration had been reported previously for somatostatin .
Once phagocyted, microglial cells are able to degrade Aβ fibrils . Several enzymatic systems have been described to be involved in this process, but the detailed mechanisms underlying phagolysosomal decomposition have not been elucidated. Both neprilysin (NEP) and insulin degrading enzyme (IDE) play the pivotal role for Aβ degradation in the brain . While NEP is presumably acting within a cell, IDE is also being secreted and involved in extracellular Aβ degradation . To test whether neuropeptides are also influencing the generation of these systems, in the absence or presence of Aβ, microglial expression of these enzymes was detected. In the case of Bradykinin there was a trend to increased levels of IDE, however this effect did not reach the level of statistical significance. Of note, the same neuropeptide increased microglial NEP levels, an effect that disappeared when cells were challenged with Aβ. The latter phenomenon suggests that Aβ has a negative regulatory function on NEP levels. The two other neuropeptides tested did not influence either NEP or IDE levels suggesting that this effect is specific for bradykinin. Since previous studies suggested an anti-inflammatory role of neuropeptides, in particular of bradykinin , we analyzed the regulation of inflammatory gene mRNA levels in response to Aβ stimulation and neuropeptide incubation. Under all conditions, incubation of microglial cells with Aβ strongly upregulated inflammatory gene transcription including tumor necrosis factor α, interleukin-1β, interleukin-6, inducible nitric oxide synthase (iNOS), monocyte chemoattractant protein-1, macrophage inflammatory protein-1α, cyclooxygenase-2, while cycloxygenase-1 was downregulated by the identical treatment. However, a significant decrease of inflammatory mRNA levels was only observed in N9 cells, where bradykinin decreased iNOS and in the BV2 cell line, where IL-6 and MCP-1 were negatively controlled by endothelin. It seems possible that the chosen time point have not allowed for the detection of stronger regulatory effects, however, it still suggests that the observed neuropeptide regulation of microglia function is a direct effect and not secondary to chemo- or cytokine regulation.
Together our data suggest that neuropeptides may be critically involved in the modulation and guidance of microglial functions relevant for AD. Since these neuropeptides are generated and secreted from neurons, the latter may be intimately involved in immune cell regulation and modification of the neuroinflammatory component of AD. Future studies are needed to unravel the intracellular signaling pathways involved and to verify these data in appropriate animal models.
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