Introduction
Microglia are considered to be central nervous system (CNS)-resident professional macrophages. They perform homoeostatic activity and mediate the innate defense system in the normal CNS. However, localized activation of microglia has been implicated in the pathogenesis of several neurodegenerative disorders, such as Parkinson’s disease (PD), Alzheimer’s disease (AD) and multiple sclerosis [
1].
In the CNS, microglia can be activated directly by products of microorganisms, environmental toxicants, and protein aggregates like β-amyloid (Aβ) or indirectly after neurodegeneration is induced [
2,
3]. Once microglia are activated in neurodegenerating microenvironment, they have macrophage-like capabilities, including phagocytosis and production of inflammatory cytokine [
4]. Activated microglia can phagocytose fibrillar Aβ (fAβ) or dead cells from the CNS and can secrete different neurotrophic factors for neuronal survival. However, once activated, they eventually become more detrimental by releasing proinflammatory molecules (nitric oxide (NO) and TNF-α), thus causing secondary damage to neurons and the surrounding cellular environment [
5]. Therefore, activation of microglia has become a hallmark of neurodegeneration. It has been debated whether neuroinflammation is an underling cause or a resulting condition in neurodegenerative diseases.
Abundant proinflammatory cytokines and oxygen radicals are presented in AD and PD brains. In PD brains, the highest density of microglia can be found in the substantia nigra (SN). They are not only highly activated but are also highly clustered around dystrophic dopamine neurons, and neuromelanin pigment taken up from degenerated dopaminergic nerve cells is characteristically observed in SN phagocytes [
3]. However, the resident microglia always fail to trigger an effective phagocytic response to clear Aβ deposits during AD progression [
6]. Although it is indisputable that microglia-mediated neuroinflammation plays a key role in the pathogenesis of neurodegenerative diseases, the relationships between neurotoxicity and phagocytic function of the activated microglia remain unclear.
Toll-like receptors (TLRs) are a class of conserved receptors that serve as an important link between innate and adaptive immunity. Microglia possess a number of TLRs, which play an important role in microglial activation in the brain of individuals with PD and AD. Recent studies indicated that peripheral lipopolysaccharide (LPS) injection caused microglia-related over-expression of TLR2 in aged mice [
7], and that fAβ peptides activate microglia via TLR2 signaling pathway [
8]. Other results show that the levels of TLR4 messenger RNA (mRNA) are upregulated in APP transgenic mice [
9], and that the upregulation of cytokines is TLR4 dependent in an AD mouse model [
10]. Targeting TLRs may be an important step to attenuate microglial activation in the CNS during AD or PD pathology.
Low-level laser therapy (LLLT) can modulate a broad-spectrum of cellular processes ranging from proliferation to apoptosis. It has been reported that the effects of laser irradiation on cell proliferation or inhibition are related to light fluence [
11,
12]. This phenomenon of photobiomodulation has also been widely applied in the treatment of skeletal muscle regeneration [
13], wound healing [
14], and skin wound care [
15]. Studies have shown that Aβ-induced cell apoptosis was significantly diminished with light irradiation [
16]. Furthermore, it has been demonstrated that LLLT has preventive effects on Aβ
25-35-induced cell apoptosis, in which LLLT promoted YAP cytoplasmic translocation and inhibited Aβ(25–35)-induced YAP nuclear translocation [
17].
Src kinases, non-receptor tyrosine kinases, are activated by oxidative events [
18]. They are critically involved in fundamental cellular processes, including cell proliferation, migration and phagocytosis [
19]. Recently, Han
et al. observed that CD11b negatively regulated TLR-triggered inflammatory responses in macrophage by increasing Cbl-b-mediated degradation of MyD88 and TRIF, which depended on Src-Syk activation [
20]. The involvement of LLLT-induced Src activation at relatively high laser doses in cells has been identified [
21]. Since microglia can be beneficial by phagocytosing Aβ or harmful by secretion of neurotoxins, we hypothesized that Src may be involved in microglial functional regulation under LLLT. Thus, the effect of LLLT on microglia functions needs to be clarified in developing strategies to slow or prevent the progression of AD or other inflammation-mediated neurodegenerative diseases.
In this study, we investigated the effects of LLLT on LPS-activated microglia-induced neurotoxicity using microglia-like BV-2 cells and neuron-like neuroblastoma SH-SY5Y cells. We also examined the phagocytic effects of microglia and the interaction between microglial phagocytosis and neuroinflammation during LLLT. Our results suggested that LLLT could induce Src activation for neuroprotection by attenuating microglia-mediated inflammation and by enhancing microglial phagocytic activity.
Materials and methods
Chemicals and plasmids
The following reagents were used: LPS purified from Salmonella typhimurium (Sigma-Aldrich, St. Louis, MO, USA) to stimulate microglia; wortmannin and LY290042 (Sigma-Aldrich) to inhibit phosphatidylinositol 3-kinase (PI3K); API-2 (Sigma-Aldrich) to inhibit Akt; SMT ((C2H6N2S)2·H2SO4) (Sigma-Aldrich) to inhibit iNOS; PTIO (Beyotime Biotech., Haimen, Jiangsu, China) to scavenge NO; FITC-phalloidin (Sigma-Aldrich) to stain F-actin; latex beads (Sigma-Aldrich) to detect microglial phagocytosis; and propidium iodide (PI), CFSE, PKH26 and PKH67 (Sigma-Aldrich) to stain cells. Dual Luciferase Reporter Gene Assay kits were purchased from Beyotime Biotechnology and Nuclear/Cytosol Fractionation Kits were purchased from Biovision (Cambridge BioScience, Cambridge, U.K.).
The following antibodies were used: rabbit anti-MyD88, rabbit anti-GAPDH, rat-anti-Histone 3, rabbit anti-iNOS, and rat anti-β-actin. All were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Antibodies specific for phosphorylated Syk Y519/520, Src Y416, FAK Y397, FAK Y861, Akt ser473, and Akt Thr308 were all purchased from Cell Signaling Technology (Beverly, MS, USA). Rabbit anti-Akt, mouse anti-FAK and rabbit anti-Rac1 antibody were obtained from Santa Cruz Biotechnology.
In addition, we used jetPEI™-macrophage transfecting reagent (Invitrogen, Carlsbad, CA, USA) to transfect plasmid DNA into cells and the cells were examined 36 to 48 h after transfection. The plasmid of pRaichu-Rac1 was kindly supplied by Dr. Michiyuki Matsuda. Rac1Q61L, Rac1T17N and wt Rac1 were purchased from Upstate Biotechnology (Lake Placid, NY, USA). Dr. Dianne Cox kindly provided the shRNA Syk and scramble shRNA. GFP-FRNK was a gift from Dr. Thomas Parsons. Dr. X. Shen (Institute of Biophysics, Chinese Academy of Sciences) kindly provided the pNF-κB-Luc. Dr. David A. Geller kindly provided the iNOS-Luc, and the pRL-TK was purchased from Promega (Mannheim, Germany).
Cell culture
Murine microglia-like cell line BV-2 was maintained in Dulbecco’s modified Eagle’s medium (DMEM) with 15% heat-inactivated fetal calf serum (FCS), penicillin (100 units/ml), and streptomycin (100 μg/ml) in 5% CO2, 95% air at 37°C in a humidified incubator. To generate activated microglia, we stimulated cells LPS alone (100 ng/ml) or with different concentrations of inhibitors before LLLT treatment.
Primary microglia were isolated from postnatal day 1 to day 2 mouse brains (C57BL/6 J), as described previously [
22]. Cells were cultured in DMEM/F12, with 20% fetal bovine serum (FBS), penicillin (100 units/ml), and streptomycin (100 μg/ml) in 5% CO
2, 95% air at 37°C in a humidified incubator. Astrocytes were separated from the microglial cultures using a mild trypsinization protocol described by Saura
et al.[
23].
The present study was performed in accordance with the guidelines of the Guide for the Care and Use of Laboratory Animals (Institute of Laboratory Animal Resources, Commission on Life Sciences, National Research Council. Washington, DC: National Academy Press, 1996.); it was approved by the Institutional Animal Care and Use Committee of our university (South China Normal University, Guangzhou, China). The human neuroblastoma cell line SH-SY5Y was cultured in DMEM containing 10% heat-inactivated FBS, penicillin (100 units/ml), and streptomycin (100 μg/ml) in 5% CO2, 95% air at 37°C in a humidified incubator.
LLLT treatment
The experiment was conducted as described in our previous work [
24]. After 36 to 48 h of serum starved with 0.5% FBS, the microglial cells were irradiated with He-Ne laser (632.8 nm, 64.6 mW/cm
2, HN-1000), (Laser Technology Application Research Institute Co., Ltd., Guangzhou, China) for 0.8, 1.33, 2.66, 5.32, 6.66, or 13.33 min in the dark, with the corresponding fluences of 3, 5, 10, 20, 25, and 50 J/cm
2 respectively.
Transient transfection and luciferase activity
Transient transfection of cells was performed using jetPEI™-macrophage transfecting reagent according to manufacturer’s instructions (Polyplus-transfection, Strasbourg, France). For luciferase activity assay, microglial cells in a 48-well plate (5 × 104 cells/well) were incubated with plasmids containing 0.3 μg of pNF-κB or iNOS reporter luciferase plasmid. We used pRL-TK as an internal control of transfection efficiency. To correct for differences in transfection efficiency, each group of cells was transfected with 30 ng of pRL-TK and incubated overnight. The ratio of luciferase activity to pRL-TK activity in each sample served as a measure of normalized luciferase activity. Forty-eight hours after co-transfection, the cells were incubated with 100 ng/ml LPS for 12 h, and then cells were treated with LLLT and cultured for another 6 h. Cell extracts were prepared for determination of luciferase activity using Dual Luciferase Reporter Gene Assay Kit according to the manufacturer’s instructions. Luciferase assays were performed on a 96-well plate reader (Tecan Infinite M200, Tecan Group Ltd, Mannedorf, Switzerland) for 20 s. Results are expressed as the ratio of luciferase to pRL-TK (mean ± SEM).
Confocal laser scanning microscopy (LSM)
Fluorescent emission from FITC was monitored confocally using a commercial laser scanning microscope (LSM 510/ConfoCor2) combination system (Zeiss, Jena, Germany) equipped with a Plan-Neofluar 40×/1.3 NA Oil DIC objective. FITC fluorescence was excited at 488 nm with the Ar-Ion laser (reflected by a beam splitter HFT 488 nm), and the fluorescence emission was recorded through a 500 to 530 nm IR band-pass filter. For intracellular measurements, the desired measurement position was chosen in the LSM image. To quantify the results, the average emission intensities from desired measurement positions were processed with Zeiss Rel3.2 image processing software (Zeiss, Jena, Germany).
Nitric oxide measurement
Nitric Oxide (NO) production in microglia was detected with the fluorescent probe DAF-FM DA. DAF-FM DA is a cell permeable fluorescent probe for the detection of NO. It can passively diffuse across cellular membranes; once inside cells, it is deacetylated by intracellular esterases to become DAF-FM [
25]. DAF-FM is essentially non-fluorescent until it reacts with NO. With excitation/emission maxima of 495/515 nm, the fluorescent intensity and images of DAF-FM can be detected by a 96-well plate reader and by confocal laser microscopy, respectively.
Western blot analysis
Expressions of proteins were quantified by western blot analysis. After individual incubations, cell proteins were extracted in lysis buffer (50 mM Tris–HCl pH 8.0, 150 mM NaCl, 1% TritonX-100, 100 μg/ml PMSF) supplemented with protease inhibitor cocktail set I for 60 min on ice. After centrifugation (4°C, 12,000 rpm, 20 min), the resulting lysates were resolved on 8% SDS-PAGE Bis-Tris gels (30 mg/lane; Invitrogen, Life Technologies, Grand Island, NY, USA) and transferred to nitrocellulose membranes (Millipore, Bedford, MA, USA). The membranes were blocked in TBST (10 mM Tris–HCl, pH 7.4, 150 mM NaCl, 0.1% Tween-20) containing 5% non-fat milk and then incubated with a designated primary antibody and a secondary antibody. The signals were detected with an ODYSSEY™ Infrared Imaging System (Li-Cor, Lincoln, NE, USA). The intensity of the western blot signals was quantitated using ImageJ software (NIH, Bethesda, MD, USA), and the densitometry analyses are presented as the ratio of protein/β-actin protein, and are compared with controls and normalized to 1.
Rac1 activity assay
We measured Rac1 activity in LLLT treated microglial cell lysate using Rac1 Activation Assay Kit (Upstate Biotechnology, Lake Placid, NY, USA) according to the manufacturer’s instructions.
Microglia cytotoxicity assay
Cytotoxicity of microglial cells was assessed using a Transwell™ cell-culture system or a coincubation system. In the Transwell™ cell-culture system, 5 × 106 microglial cells in 1 ml medium were added to the upper chamber of 6-well Transwell™ plates with 0.4-μm pores (Costar, Corning Inc., NY, USA), and cells were incubated with 100 ng/ml LPS for 10 h at 37°C. After being washed with PBS, target SH-SY5Y cells were resuspended at 1 × 106 cells/mL and labeled with 1 mM carboxyfluorescein diacetate succinimidyl ester (CFSE) (Molecular Probes Europe, Leiden, The Netherlands) for 8 min at 37°C. The labeling reaction was quenched by the addition of cold DMEM containing 10% FBS. After washing with PBS, the CFSE-labeled target cells in 1.5 ml medium were added to the lower chamber of Transwell™ plates. When microglia were exposed to light, we took the upper chamber in a new 6-well plate for LLLT. Immediately thereafter, the 6-well plate was replaced by the lower Transwell™ chamber with SH-SY5Y cells to microglial cells at a ratio of 1:8 at 37°C in a humidified atmosphere of 5% CO2. By using this procedure, we prevented the direct impact of LLLT on the neuronal cells. In co-culture conditions, microglial cells were treated with LLLT. After 24 h incubation, cells in the lower chamber were harvested, propidium iodide (PI) was added to stain dead cells, and all samples were directly analyzed by fluorescence-activated cell sorting (FACS). Target cells killed by microglial cells were represented by the cell population showing double-positive staining for CFSE and PI.
In a coincubation system, 5 × 106 PKH26 (red)-labeled microglial cells with 100 ng/ml LPS in 1 ml medium were added to the 6-well plate. After 10 h incubation, the cells were treated with LLLT. Then 1 × 106 PKH67 (green)-labeled SH-SY5Y cells in 1.5 ml medium were added to the treated microglial cells. After 24 h coincubation, mix-cultured cells were harvested and PI was added to stain dead cells. All samples were analyzed by FACS. Target cells killed by microglial cells were represented by the cell population showing double-positive staining for PKH67 and PI/PKH26. Based on the evidence that phagocytes engulf dead cell corpses but not living cells, the dead PKH67-labled SH-SY5Y cells phagocytosed by PKH26-labled microglia can also be represented by the cell population showing double-positive staining for PKH67 and PKH26/PI.
Phagocytosis assay
Microglial cells were collected and 1 × 105 cells were cultured in 35 mm glass-bottomed dishes overnight. The cells were incubated in the presence or absence of the inhibitors, and then subjected to LLLT treatment. The fluorescent microspheres, as a marker of phagocytosis, were added to the treated cells at indicated time points after having been washed in PBS containing 0.1% BSA. Cells were then fixed with 4% paraformaldehyde, and three random fields of cells (>100 cells) were counted under a confocal microscope.
Phagocytic efficiency was determined by using the method of Pan
et al.[
26]. Briefly, the phagocytic efficiency was based on a weighted average of ingested microspheres per cell. The number of cells containing microspheres, the number of microspheres per cell, and the total number of cells were counted respectively. Phagocytic efficiency was calculated:
where Xn represents the number of cells containing n microspheres (n = 1, 2, 3, up to a maximum of 6 points for more than 5 microspheres ingested per cell).
Phalloidin staining
The treated cells were rinsed with PBS before being fixed in 3.7% formaldehyde and washed again in PBS. The cells were then incubated at room temperature with 0.1% Triton X-100 buffer for 5 min and washed again in PBS. FITC-phalloidin (1:50 diluted in PBS) was added to the cover slips and incubated at room temperature protected from light for 30 min. The cover slips were mounted on glass slides. The FITC-labeled phalloidin was viewed under a confocal microscope.
Quantitative measurement of F-actin
To assess the total F-actin content in microglial cells, microglia were treated with LPS for indicated time periods. The reaction was stopped by the addition of formaldehyde (3.7% final, V/V) for 15 min at room temperature. The fixed cells were then permeabilized with 10 mM imidazole, 40 mM KCl, 10 mM EGTA (ethylene glycol tetraacetic acid), 1 mM MgCl2, and 1% Triton X-100 at 4°C for 15 min. F-actin was then stained with FITC-phalloidin (Molecular Probes™, Life Technologies, Grand Lake, NY, USA) for 2 h at room temperature. After the cells were washed with PBS, F-actin-bound FITC-phalloidin was extracted with methanol. The extracts were centrifuged to remove any insoluble material, and relative fluorescence was measured using a 96-well plate reader with excitation and emission wavelengths set at 465 and 535 nm, respectively. The F-actin ratio was calculated as:
Statistical analysis
Data are from one representative experiment among at least three independent experiments and are expressed as the mean ± SEM. Significant differences between groups were compared using the one-way ANOVA procedure followed by Student’s t tests using SPSS software (SPSS Inc., Chicago, IL, USA) and the differences were considered statistically significant at P <0.05.
Discussion
In the present study, we found a regulatory role of LLLT for microglial functions. Our major findings showed that LLLT significantly reduced LPS-activated microglia-induced neuronal cell death. In LPS-activated microglia-like BV-2 cells, LLLT attenuated inflammation cytokine TNF-α, decreased the production of NO, down-regulated overexpression of iNOS, and caused MyD88 degradation. Another important observation was that microglial phagocytosis was improved after LLLT treatment, characterized by an increase in Rac1 activity, actin polymerization and the ability of the microbeads to phagocytize. Moreover, we found that LLLT could induce the enhancement of microglial phagocytic activity by a Src-dependent PI3K/Akt pathway. Understanding the mechanism and functional significance of LLLT-induced microglia-mediated phagocytosis and neuroinflammation may lead to new neurotherapies.
AD is known to be associated with neuroinflammation and activated microglia. Uncontrolled and excessive activation of microglia is capable of releasing various potentially cytotoxic molecules such as NO, oxygen radicals, and proinflammatory cytokines such as TNF-α, IL-1β, and IL-6 [
37,
38]. Chronic neuroinflammation induced by excessive production of these neurotoxic molecules plays an important role in the degenerative process of AD patients. LPS acts as a potent stimulator of microglia and has been used to study the inflammatory process in the pathogenesis of AD and anti-inflammatory therapy for AD treatment. Evidence from some rat models showed that microglia were activated immediately after LPS injection. Significant elevations of cluster differentiation marker CD45, glial fibrillary acidic protein (GFAP), scavenger receptor A (SRA), and Fcγ receptor mRNA were seen after 24 h [
39]. LPS-induced inflammation also exacerbates phospho-tau pathology in rTg4510 mice [
40].
TLRs play a key role in microglia-mediated neuroinflammation. Previous studies revealed that integrin CD11b could be activated by TLR-triggered inside-out signaling, and then negatively regulated TLR-induced inflammatory response by promoting degradation of their adaptors [
20]. Similar to the results of the present study, Mallard
et al. demonstrated that microglial MyD88 signaling played an important role in regulating acute neuronal toxicity and MyD88 deficiency attenuated release of microglial proinflammatory cytokines following LPS exposure [
41].
Much attention has been paid to therapeutic strategies aimed at controlling microglia-mediated neurotoxicity. LLLT is a non-thermal irradiation using light in visible to near infrared range which has been used clinically to accelerate wound healing and reduce pain and inflammation in a variety of pathologies [
42,
43]. Moreover, transcranial LLLT has shown good effects on treatment of stroke, traumatic brain injury, and neurodegenerative disease [
44]. Although in many pre-clinical and clinical studies the 810-nm NIR light has been used for nerve repairs [
45‐
47], the effects of laser irradiation with different wavelengths on microglial activation remain unclear. Studies had shown that the 632.8-nm laser had advantages over other wavelengths in treating neurological diseases [
48,
49]. Therefore, LLLT using the 632.8-nm laser may have high clinical relevance. Recently, it has been debated whether He-Ne laser light can activate a number of signaling pathways including MAPK/ERK, Src, Akt and RTK/PKCs signaling pathway [
11,
21,
24,
50].
We explored the role of Src activation involved in LPS-activated microglia after LLLT treatment. In our experiments, we demonstrated that LLLT triggered a significant activation of Src in LPS-activated BV-2 cells (Figure
1C). In addition, the activation of Syk triggered by LLLT was Src-dependent. LLLT-mediated Src/Syk activation could significantly decrease MyD88 and iNOS expression (Figure
2B). Blockade of Src activation or knockdown of Syk negatively affects neuronal survival under LLLT treatment (Figure
2A).
Excessive accumulation of NO has long been known to be toxic to neurons [
51]. Oxygen-free radicals such as superoxide can react with NO to form deadly intermediates such as peroxynitrite. Our results indicated that LLLT could efficiently reduce LPS-activated microglia-induced iNOS (Figures
1D and
2C) by downregulating TLR-triggered proinflammation (Figure
2D - I).
How does LLLT activate Src? One of the most plausible explanations is that LLLT activates Src through reactive oxygen species (ROS). LLLT has been demonstrated to increase the level of intracellular ROS generation [
52]. With LLLT treatment, light is absorbed by endogenous photosensitizers (porphyrins or cytochromes) that dominantly locate at plasma membrane, mitochondria or lysomes. The photosensitizers’ activation results in ROS (
1O
2, O
2
-, and H
2O
2) production [
53]. Intracellular oxidants could mediate the activation of Src [
54]. This hypothesis was also supported by our previous work [
21]. Although there may be many other contributors responsible for LLLT-mediated neuroprotective effect, our experimental results suggest that Src and Syk are primary participants in downregulation of TLRs-triggered neuroinflammatory signaling pathway (Figures
2 and
3).
The deposition of Aβ in the extracellular space of the brain plays an important role in microglial activation in AD. Although the role of microglia-mediated inflammation in the pathogenesis of AD is obvious, microglia have been reported to mediate the clearance of Aβ through receptor-mediated phagocytosis, which could delay the progression of AD.
Recent studies suggested that Aβ oligomers could induce a potent inflammatory response and subsequently disturb microglial phagocytosis and clearance of Aβ fibrils, thereby contributing to an initial neurodegenerative characteristic of AD [
26]. To address whether LLLT-mediated anti-inflammatory effects can improve microglial phagocytosis, we investigated the microglial phagocytic activity after LLLT treatment. Phagocytic activity of the LPS-activated microglia was markedly enhanced after LLLT treatment (Figures
3 and
6). Furthermore, LLLT could also activate the PI3K/Akt signal pathway (Figure
5), which was dependent on Src activation under LLLT treatment. Since phagocytosis is a Rac1-mediated actin-based process, our results demonstrated that not only the activity of Rac1 but also the F-actin accumulation were increased by PI3K/Akt after LLLT. A constitutively active form of Rac1 greatly increased F-actin polymerization, while a dominant negative form of Rac1 inhibited F-actin polymerization under LLLT treatment (Figure
5B). Thus, these results suggested that LLLT-induced Src activation could also improve microglial phagocytic activity by PI3K/Akt/Rac1 signal pathway.
Activation of the PI3K/Akt signaling pathway has been correlated with tumor metastasis and invasion [
55]. Indeed, PI3K is a key signaling molecular for integrin activation and regulation of actin reorganization [
56]. The nonreceptor tyrosine kinase FAK-Src complex can initiate a cascade of phosphorylation events to trigger multiple intracellular pathways, including MAPK/ERK and PI3K/Akt signaling [
57,
58]. In this study, using LPS-activated BV-2 cells, we found that LLLT-mediated anti-inflammatory effect did not require FAK. One of the most plausible explanations of the above results is that Syk activation does not require actin polymerization since it is unaffected by inhibitors such as cytochalasin D, whereas FAK activation requires actin polymerization [
59,
60]. Thus, activation of Syk, but not FAK, plays a key role in Src-mediated anti-inflammatory signal under LLLT. However, inhibition of FAK by transfecting BV-2 cells with FRNK, a naturally occurring inhibitor of FAK signaling, contributed to partial inhibition of microglia phagocytosis.
FAK translocation between cytosolic and membrane is highly regulated by many factors, including tyrosine phosphorylation and actin assembly [
61]. Since p85 was associated with FAK to further activate Akt by binding to tyrosine phosphorylated residue 397 of FAK [
62], this may explain why FAK could also be activated before actin polymerization and only had partial effects on Src-mediated microglial phagocytosis. Our results suggest that LLLT-induced phagocytic activity depends on Src-mediated PI3K/Akt signaling pathway, partially due to the phosphorylation of FAK.
Microglial activation is considered as a hallmark of AD. Alternatively, microglial activation is usually associated with marked increase in CD11b expression [
63]. Integrin CD11b/CD18 (macrophage antigen complex 1, MAC1, also known as complement receptor 3, CR3) is essential for the phagocytosis of multiple compounds and mediates the activation of phagocytes in response to a diverse set of stimuli [
64]. The MAC1 receptor is located on microglia, suggesting its role in neurodegeneration. In addition, previous reports indicated that MAC1 might be a key receptor for Aβ to activate microglia to produce extracellular superoxide, resulting in neurotoxicity [
65]. Conversely, others indicated that ROS was a key player in microglial activation in which ROS increased microglial expression of CD11b via NO [
66]. In fact, a recent study showed that activation of CD11b via inside-out signaling negatively regulated TLR-triggered proinflammatory response [
20].
It is important to note that the role of microglial activation in AD is still debated, and a simplistic view of microglia as solely beneficial or detrimental cells does not reflect the complexity of microglial function [
67]. Functionally, microglia react in diverse ways: they secrete inflammatory mediators, proteolytic enzymes or neurotrophic factors, and are also able to take up soluble and insoluble molecules. Hence, the ideal microglia-targeted AD treatment modalities should not only focus on microglial neurotoxic characteristics, but also on the phagocytic activity.
However, in this study, we used human neuroblastoma SH-SY5Y as the target neuronal cells to mimic responses of inflammation-mediated neurotoxicity. Given that microglia may have recognized markers of malignancy, our results need to be further confirmed using primary cortical neurons in the future studies.
Taken together, the current investigation demonstrates that LLLT can inhibit LPS-activated microglia-induced neurotoxicity and enhance its phagocytic activity through activation of non-receptor tyrosine kinase Src. Although cultured mouse microglia and its treatment with etiological reagents may not truly resemble microglia in the brain of patients, our results suggest that targeting Src may be an important step for the attenuation of microglial activation. Better understanding of the regulation mechanism of activated microglia may provide a therapeutic strategy to control the progression of neurodegenerative diseases.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
SS conceived the main idea of the study and performed the majority of the experiments and drafted the manuscript. FZ participated in the major experiments. SS and FZ analyzed the data. FZ and WRC contributed materials and reagents. FZ and WRC participated in its design and coordination and helped draft the manuscript. All authors reviewed and approved the final version of the manuscript.