- Open Access
Kainic acid-induced microglial activation is attenuated in aged interleukin-18 deficient mice
© Zhang et al; licensee BioMed Central Ltd. 2010
- Received: 30 July 2009
- Accepted: 14 April 2010
- Published: 14 April 2010
Previously, we found that interleukin (IL)-18 deficiency aggravates kainic acid (KA)-induced hippocampal neurodegeneration in young C57BL/6 mice due to an over-compensation by IL-12. Additionally, IL-18 participates in fundamental inflammatory processes that increase during aging. In the present study, we were interested in the role of IL-18 in KA-induced neurodegeneration in aged female C57BL/6 mice.
Fifteen aged female IL-18 knockout (KO) and 15 age-matched wild-type (WT) mice (18 to 19 months old) were treated with KA at a dose of 25 mg/kg body weight intranasally. Seizure activities and behavioral changes were rated using a 6-point scoring system and open-field test, respectively. Seven days after KA treatment, degenerating neurons were detected by Nissl's method and Fluoro-Jade B staining; and microglial activation was analyzed by immunohistochemistry and flow cytometry.
Aged female IL-18 KO and WT mice showed similar responses to treatment with KA as demonstrated by comparable seizure activities, behavioral changes and neuronal cell death. However, aged female IL-18 KO mice failed to exhibit the strong microglial activation shown in WT mice. Interestingly, even though the number of activated microglia was less in KA-treated IL-18 KO mice than in KA-treated WT mice, the proportion of microglia that expressed the cytokines tumor necrosis factor (TNF)-α, IL-6 and IL-10 was higher in KA-treated IL-18 KO mice.
Deficiency of IL-18 attenuates microglial activation after KA-induced excitotoxicity in aged brain, while the net effects of IL-18 deficiency are balanced by the enhancement of other cytokines, such as TNF-α, IL-6 and IL-10.
- Glial Fibrillary Acidic Protein
- Microglial Activation
- Kainic Acid
- Kainic Acid Treatment
- Kainic Acid Administration
Administration of kainic acid (KA), an analog of the excitotoxin glutamate, to rodents results in neuronal death and seizures , which provides a well-characterized model for studies of human neurodegenerative diseases [2–4]. Synthesis and release of cytokines and other inflammatory factors by glial cells influence the survival and repair of hippocampal neurons after injury [5, 6].
Interleukin (IL)-18, first isolated as interferon-γ inducing factor , is related to the IL-1 family by mechanism of origin, receptor structure, and signal transduction pathways utilized . IL-18 serves as a link between innate and adaptive immune responses, through mechanisms such as stimulating the expression of adhesion molecules, inducing the production of chemokines (IL-8) and cytokines (tumor necrosis factor and IL-6), stimulating the activity of NK cells, stimulating the expression of Fas ligand on T and NK cells and the cytotoxic activity of CD8+ effector T cells, stimulating Th1 responses in combination with IL-12, stimulating Th2 responses in combination with IL-2, and stimulating Th17 responses in combination with IL-23 . IL-18 and IL-18 receptor (IL-18R) mRNA have been detected in brain tissue from adult rats and in cultured astrocytes and microglia [10, 11]. However, the effects of IL-18 in neurodegeneration are complicated. Our previous study showed that young (six to eight weeks old) IL-18 knockout (KO) mice were more sensitive to KA administration than wild-type (WT) animals with normal expression of IL-18, although exogenous IL-18 administration could aggravate KA-induced neurodegeneration .
We also found that aged female mice were more susceptible to KA-induced excitotoxicity than male mice, which resembles the situation for humans . It has also been suggested that IL-18 participates in fundamental inflammatory processes that increase during aging . In the present study, we therefore aimed to investigate the role of IL-18 in KA-induced neurodegeneration in aged female C57BL/6 mice. Our results demonstrate that deficiency of IL-18 attenuates microglial activation after KA-induced excitotoxicity in aged brain.
Fifteen aged female IL-18 KO and 15 age-matched C57BL/6 WT mice (18 to 19 months old) were used in the present study. The mice were purchased from the Jackson Laboratory (Bar Harbor, ME, USA) at age of 2 months and kept at the animal facilities of Karolinska University Hospital, Huddinge, Sweden until the designed ages for experiments. All mice were housed on a 12 h light-dark schedule with water and food available ad libitum. The KA-induced excitotoxic model in mice was approved by the South Stockholm Research Animal Ethics Committee, Huddinge County Court, Stockholm, Sweden. All efforts were made to minimize the number of animals used and their sufferings.
KA administration and assessment of seizure activity
Mice were partially anesthetized with Isoflurane (Abbott Laboratories, Kent, UK) and held on their backs by hand. KA, (Opika-1, Ocean Produce International, Shelburne, Nova Scotia, Canada) dissolved in saline, (10 mg/1.3 ml) was slowly and gently dropped by micropipette into the nostrils of the mice at a dose of 25 mg/kg body weight as described previously . Four IL-18 KO mice and 5 WT mice were administrated with physiological saline as control. Mice were observed by two different examiners continuously for 5 hours to record the onset and extent of seizure activity. Seizures were rated according to the criteria described by Ben-Ari  with modifications: 0, normal; 1, immobilization; 2, rearing and falling; 3, seizure for less than 1 h; 4, seizure for 1-3 h; 5, seizure for more than 3 h; and 6, death.
Open-field test with zone monitoring
Open-field activity was measured one day before and six days after KA administration in 8 IL-18 KO mice and 7 WT mice. The open field test was used to measure exploratory behaviour and spontaneous motor activity of the animals. The apparatus consisted of four identical Plexiglas boxes (34 × 34 × 18 cm) with a lower and a higher row of infrared sensitive photocells connected to a computer that registered the interruptions of these cells which corresponded to the horizontal and vertical activities of the animals inside of the arena. Light bulbs (25 W) provided the illumination for each arena. Four mice were tested simultaneously, one per arena. At the beginning each mouse was placed into the center of open-field arena and its movement was recorded every 5 min during 60 min. The overall locomotion and the number of times the animal lifted its fore paws and stood on its back feet (rearing) were analyzed. All tests were carried out between the hours of 9:00 and 15:00.
All mice were anesthetized with sodium pentobarbital and transcardially perfused with phosphate-buffered saline (PBS) seven days after the administration of KA. The left hemisphere of each brain was fixed in 4% paraformaldehyde and kept in 10% sucrose until being frozen, and the right hippocampus was dissociated and put into Krebs-Ringer buffer (KRB) solution [120 mM NaCl, 5 mM KCl, 1.2 mM KH2PO4, 25 mM NaHCO3, 14 mM D-glucose, 2.5 mM MgSO4, 0.3% bovine serum albumin (BSA)] for isolation and flow cytometric analysis of microglia. Coronal sections (12-μm slices) from -1.15, - 1.94 and - 2.80 mm, respectively, relative to the bregma were prepared according to the information in Franklin's brain atlas . Sections were stained by Nissl's method and Fluoro-Jade B (FJB) (Histo-Chemo, Inc., Jefferson, AR) staining to evaluate degenerating neurons. FJB is an anionic fluorescein derivative useful for the histological staining of neurons undergoing degeneration. For assessment of severity and extent of neurodegeneration in the hippocampus after Nissl's staining, sections were scored using a semiquantitative grading system: 0, normal; 1, slight shrinkage of neurons (1 - 4% pyknotic neurons in area CA3); 2, moderate shrinkage of neurons (5 - 15% pyknotic neurons in area CA3); 3, severe shrinkage of neurons (more than 15% pyknotic neurons in area CA3); 4, slight loss of neurons (5 - 10% neuron loss in area CA3); 5, moderate loss of neurons (11 - 40% neuron loss in area CA3); and 6, severe loss of neurons (more than 40% neuron loss in area CA3). Using a blinded protocol, two different examiners duplicated the counting.
Immunohistochemistry of brain sections
Frozen hippocampal sections were prepared as described for histopathological analysis. After washes with Tris buffer, the sections were blocked by "protein block" (DAKO, Glostrup, Denmark) at room temperature for 30 min. Subsequently, they were exposed to rat antibodies to CD11b (1:100, Serotec, Oxford, UK) and rabbit antibodies to glial fibrillary acidic protein (GFAP) (1:2000; DAKO), respectively, followed by staining with the avidin-biotin technique (Vectastain Elite Kit, Vector Labs, Burlingame, CA, USA). Peroxidase-substrate solution DAB (Sigma-Aldrich, Stockholm, Sweden) was added until the desired intensity of yellow color developed. Omission of primary antibodies served as negative control. Slides were observed using a Nikon Eclipse E800-U microscope (Nikon, Japan). Positive immunostaining of cells was rated using a semiquantitative scale - baseline staining (·), mild response (+), moderate response (+ +), intense response (+ + +) - by two observers, independently. Criteria for each scale followed the description by Colburn et al .
Isolation and flow cytometric analysis of microglia
As mentioned above, seven days after KA treatment, the right hippocampus of each brain was collected and put into KRB solution for isolation and flow cytometric analysis of microglia. The hippocampi were dissected and dissociated by pipetting. Next, after trypsinization at 37°C for 15 min, fetal bovine serum (10%, final concentration) was added to inactivate trypsin activity. The tissues were then dissociated with repeated pipetting in KRB solution containing DNase I (Sigma-Aldrich). Cell suspensions were passed through a 70-μm pore-size strainer and spun down. The cell pellets were resuspended in 30% Percoll in PBS and centrifuged at 500 × g for 20 min. The resulting pellets were resuspended, passed through a 40-μm pore-size strainer, collected, and stained for flow cytometry.
Microglia-enriched cell suspensions were washed with PBS containing 1% BSA (BSA/PBS), permeabilized, fixed and incubated with the following antibodies: APC-labeled rat anti-mouse CD11b (Caltag, Burlingame, CA, USA), either PerCP-labeled rat anti-mouse CD45 (Serotec), RPE-labeled mouse anti-mouse major histocompatibility complex (MHC)-II I-Ak (Serotec) and FITC-labeled rat anti-mouse tumor necrosis factor-α (TNF-α) (Becton Dickinson Biosciences, San José, CA, USA), or RPE-labeled rat anti-mouse IL-6 (BD Pharmingen, San Diego, CA, USA) and FITC-labeled rat anti-mouse IL-10 (Pharmingen). FITC-, RPE-, PerCP (Serotec), and APC-(Caltag) labeled rat IgG were used as isotype controls to set the gates. Cell size, granularity, and fluorescence intensity were measured using FACScalibur flow cytometer (Becton Dickinson). A minimum of 5 × 103 cells were analyzed with CellQuest software (Becton Dickinson). Microglia from all four groups (WT mice with or without KA treatment, and IL-18 KO mice with or without KA treatment) were collected and analyzed on the same day with the same cytometer settings.
Data presentation and statistics
The Mann-Whitney U test was used to analyze the clinical, histopathological and immunohistochemical data, and one-factor analysis of variance (ANOVA) was used to analyze flow cytometric and behavioral results. Data are presented as mean ± SD. P < 0.05 was considered as significant in all tests. Graphics and calculations were performed using GraphPad PRISM version 5.0 (GraphPad, USA), and SPSS Version 15.0 (SPSS Inc, USA).
IL-18 deficiency does not affect KA-induced seizure activity in aged female mice
Survey of seizure activity in mice after KA treatment.
Seizure Activity Variables
KO (n = 11)
WT (n = 10)
Tonic/clonic twitching without seizures
Seizures < 1 h
Seizures 1-3 h
Seizures > 3 h
Death due to seizures
Clinical scores (Medians with percentiles)
IL-18 deficiency does not influence KA-induced behavioral changes in aged female mice
Aged female IL-18 KO mice and WT mice show similar KA-induced hippocampal neurodegeneration
KA-induced hippocampal astrogliosis is not changed by IL-18 deficiency in aged female mice
IL-18 deficiency attenuates KA-induced microglial activation in aged female mice
By flow cytometry, microglia of hippocampi were identified as a homogeneous population of CD11b positive cells with low/moderate CD45 staining (CD11b+/CD45low/moderate cells, Fig. 4E). The possible macrophage contamination was excluded by deletion of the high CD45 staining cells. Similar to the findings of immunohistochemistry the number of activated microglia (MHC-II positive cells) in WT mice was significantly higher than in the IL-18 KO mice 7 days after KA treatment (Fig. 4F). Before KA treatment, there was no difference in the numbers of MHC-II positive cells between the two groups.
Expression of TNF-α, IL-6 and IL-10 is increased in IL-18 KO mice after KA treatment
In the present study, we investigated the role of IL-18 in the pathogenesis of KA-induced excitotoxic neurodegeneration in the aged situation by using IL-18-deficient aged (18 to 19 months old) mice and age-matched WT mice. The study was motivated by the fact that most common neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease are typically diseases of higher ages and by the hypothesis that findings of KA-induced neurodegeneration of young individuals may deviate from findings in older subjects. Since previously we also found that aged female C57BL/6 mice were more sensitive to KA treatment than aged male mice , we performed this study on female animals.
Our results show that IL-18 deficiency does not influence susceptibility to KA-induced injury in aged female mice, since KA-induced seizures, behavioral changes and histopathological changes including astrogliosis were similar in IL-18 KO mice and WT controls. However, we found also that aged IL-18-deficient mice show lower microglial activation in response to KA than do WT mice as demonstrated by lower numbers of CD11b-positive and MHC-II-positive cells. On the other hand, in these activated microglia the percentages of TNF-α-, IL-6- and IL-10-positive cells were significantly higher in IL-18 KO mice than in WT mice. These results are in contrast to our previous findings in KA-induced excitotoxic neurodegeneration of IL-18-deficient young mice . Young (6 to 8 weeks old) IL-18 KO mice were more sensitive to KA administration than age-matched animals with normal expression of IL-18. In that situation we concluded that excitotoxic injury in IL-18 deficient mice might be due to overcompensation by other microglia-derived, disease-promoting factors, of which IL-12 is one candidate. Our present finding that aged IL-18 KO mice display similar susceptibility to KA treatment as WT mice might be due to the balancing influence of other microglia-derived cytokines such as TNF-α, IL-6 and IL-10.
However, we also found in young animals that exogenous IL-18 administration could aggravate KA-induced neurodegeneration, when high doses of IL-18 are applied . A recent study of Jeon and co-workers gave hints in the same direction by showing that levels of IL-18 and its receptor in hippocampal homogenates increased from day 1 post-KA onward . Other researchers have found that lower IL-18 concentrations are associated with improved activities of daily living in 65- to 80-year-old men, suggesting that IL-18 might play an active role in age-related functional impairment . Moreover, increased hippocampal concentrations of the proinflammatory cytokines IL-1α, IL-18 and IFN-γ are accompanied by deficits in long-term potentiation in older rats . The imbalance between pro-inflammatory and anti-inflammatory cytokines in the aged brain significantly contributes to age-related deficits in synaptic function .
Upon neuronal injury, microglia, as the main effector cells of the immune system in the CNS, acquire changes in morphology and expression of surface antigens and soluble molecules . In the present study, lower KA-induced microglial activation in the hippocampi of aged IL-18 KO mice was found compared with WT as detected by immunohistochemistry and flow cytometry. This finding is in agreement with studies of Sugama and co-workers, who found that stress-induced microglial activation is reduced in IL-18 KO mice . IL-18 null mice also show diminished microglial activation and reduced dopaminergic neuron loss following acute 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine treatment . Interestingly, even though the number of activated microglia is smaller in KA-treated IL-18 KO mice than in KA-treated WT mice, the proportion of microglia cells that express the cytokines TNF-α, IL-6 and IL-10 is higher in the KA-treated IL-18 KO mice, which may account for the similar neuropathological and clinical outcome of the IL-18-deficient, aged mice.
This study demonstrates that deficiency of IL-18 attenuates microglial activation in KA-induced excitotoxicity in aged brain, while the net effects of IL-18 are balanced by other cytokines, such as TNF-α, IL-6 and IL-10. IL-18 may participate in KA-induced hippocampal neurodegeneration in young animals, but IL-18 does not seem to represent a key cytokine in this process in aged individuals.
This study was supported by grants from Swedish Medicine Association, Foundation Dementia, Gamla Tjänarinnor foundation, SADF (Insamlingsstiftelsen för Alzheimer-och Demensforskning) foundation and Gun och Bertil Stohnes foundation as well as funds from Swedish National Board of Health and Welfare.
- Pollard H, Charriaut-Marlangue C, Cantagrel S, Represa A, Robain O, Moreau J, Ben-Ari Y: Kainate-induced apoptotic cell death in hippocampal neurons. Neuroscience. 1994, 63: 7-18. 10.1016/0306-4522(94)90003-5.View ArticlePubMedGoogle Scholar
- Chen Z, Duan RS, Q HC, Wu Q, Mix E, Winblad B, Ljunggren HG, Zhu J: IL-12p35 deficiency alleviates kainic acid-induced hippocampal neurodegeneration in C57BL/6 mice. Neurobiol Dis. 2004, 17: 171-178. 10.1016/j.nbd.2004.07.018.View ArticlePubMedGoogle Scholar
- Chen Z, Duan RS, Quezada HC, Mix E, Nennesmo I, Adem A, Winblad B, Zhu J: Increased microglial activation and astrogliosis after intranasal administration of kainic acid in C57BL/6 mice. J Neurobiol. 2005, 62: 207-218. 10.1002/neu.20099.View ArticlePubMedGoogle Scholar
- Penkowa M, Florit S, Giralt M, Quintana A, Molinero A, Carrasco J, Hidalgo J: Metallothionein reduces central nervous system inflammation, neurodegeneration, and cell death following kainic acid-induced epileptic seizures. J Neurosci Res. 2005, 79: 522-534. 10.1002/jnr.20387.View ArticlePubMedGoogle Scholar
- Akiyama H, Tooyama I, Kondo H, Ikeda K, Kimura H, McGeer EG, McGeer PL: Early response of brain resident microglia to kainic acid-induced hippocampal lesions. Brain Res. 1994, 635: 257-268. 10.1016/0006-8993(94)91447-8.View ArticlePubMedGoogle Scholar
- Rizzi M, Perego C, Aliprandi M, Richichi C, Ravizza T, Colella D, Veliskova J, Moshe SL, De Simoni MG, Vezzani A: Glia activation and cytokine increase in rat hippocampus by kainic acid-induced status epilepticus during postnatal development. Neurobiol Dis. 2003, 14: 494-503. 10.1016/j.nbd.2003.08.001.View ArticlePubMedGoogle Scholar
- Okamura H, Tsutsi H, Komatsu T, Yutsudo M, Hakura A, Tanimoto T, Torigoe K, Okura T, Nukada Y, Hattori K, Akita K, Namba M, Tanabe F, Konishi K, Fukuda S, Kurimoto M: Cloning of a new cytokine that induces IFN-gamma production by T cells. Nature. 1995, 378: 88-91. 10.1038/378088a0.View ArticlePubMedGoogle Scholar
- Dinarello CA: IL-18: A TH1-inducing, proinflammatory cytokine and new member of the IL-1 family. J Allergy Clin Immunol. 1999, 103: 11-24. 10.1016/S0091-6749(99)70518-X.View ArticlePubMedGoogle Scholar
- Arend WP, Palmer G, Gabay C: IL-1, IL-18, and IL-33 families of cytokines. Immunol Rev. 2008, 223: 20-38. 10.1111/j.1600-065X.2008.00624.x.View ArticlePubMedGoogle Scholar
- Culhane AC, Hall MD, Rothwell NJ, Luheshi GN: Cloning of rat brain interleukin-18 cDNA. Mol Psychiatry. 1998, 3: 362-366. 10.1038/sj.mp.4000389.View ArticlePubMedGoogle Scholar
- Conti B, Park LC, Calingasan NY, Kim Y, Kim H, Bae Y, Gibson GE, Joh TH: Cultures of astrocytes and microglia express interleukin 18. Brain Res Mol Brain Res. 1999, 67: 46-52. 10.1016/S0169-328X(99)00034-0.View ArticlePubMedGoogle Scholar
- Zhang XM, Duan RS, Chen Z, Quezada HC, Mix E, Winblad B, Zhu J: IL-18 deficiency aggravates kainic acid-induced hippocampal neurodegeneration in C57BL/6 mice due to an overcompensation by IL-12. Exp Neurol. 2007, 205: 64-73. 10.1016/j.expneurol.2007.01.019.View ArticlePubMedGoogle Scholar
- Zhang XM, Zhu SW, Duan RS, Mohammed AH, Winblad B, Zhu J: Gender differences in susceptibility to kainic acid-induced neurodegeneration in aged C57BL/6 mice. Neurotoxicology. 2008, 29: 406-412. 10.1016/j.neuro.2008.01.006.View ArticlePubMedGoogle Scholar
- Dinarello CA: Interleukin 1 and interleukin 18 as mediators of inflammation and the aging process. Am J Clin Nutr. 2006, 83: 447S-455S.PubMedGoogle Scholar
- Chen Z, Ljunggren HG, Bogdanovic N, Nennesmo I, Winblad B, Zhu J: Excitotoxic neurodegeneration induced by intranasal administration of kainic acid in C57BL/6 mice. Brain Res. 2002, 931: 135-145. 10.1016/S0006-8993(02)02268-0.View ArticlePubMedGoogle Scholar
- Ben-Ari Y: Limbic seizure and brain damage produced by kainic acid: mechanisms and relevance to human temporal lobe epilepsy. Neuroscience. 1985, 14: 375-403. 10.1016/0306-4522(85)90299-4.View ArticlePubMedGoogle Scholar
- Paxinos GP, Franklin KBJ: The Mouse Brain in Stereotaxic Coordinates. 1997, San Diego: Academic PressGoogle Scholar
- Colburn RW, DeLeo JA, Rickman AJ, Yeager MP, Kwon P, Hickey WF: Dissociation of microglial activation and neuropathic pain behaviors following peripheral nerve injury in the rat. J Neuroimmunol. 1997, 79: 163-175. 10.1016/S0165-5728(97)00119-7.View ArticlePubMedGoogle Scholar
- Jeon GS, Park SK, Park SW, Kim DW, Chung CK, Cho SS: Glial expression of interleukin-18 and its receptor after excitotoxic damage in the mouse hippocampus. Neurochem Res. 2008, 33: 179-184. 10.1007/s11064-007-9434-6.View ArticlePubMedGoogle Scholar
- Frayling TM, Rafiq S, Murray A, Hurst AJ, Weedon MN, Henley W, Bandinelli S, Corsi AM, Ferrucci L, Guralnik JM, Wallace RB, Melzer D: An interleukin-18 polymorphism is associated with reduced serum concentrations and better physical functioning in older people. J Gerontol A Biol Sci Med Sci. 2007, 62: 73-78.PubMed CentralView ArticlePubMedGoogle Scholar
- Griffin R, Nally R, Nolan Y, McCartney Y, Linden J, Lynch MA: The age-related attenuation in long-term potentiation is associated with microglial activation. J Neurochem. 2006, 99: 1263-1272. 10.1111/j.1471-4159.2006.04165.x.View ArticlePubMedGoogle Scholar
- Maher FO, Nolan Y, Lynch MA: Downregulation of IL-4-induced signalling in hippocampus contributes to deficits in LTP in the aged rat. Neurobiol Aging. 2005, 26: 717-728. 10.1016/j.neurobiolaging.2004.07.002.View ArticlePubMedGoogle Scholar
- Kreutzberg GW: Microglia: a sensor for pathological events in the CNS. Trends Neurosci. 1996, 19: 312-318. 10.1016/0166-2236(96)10049-7.View ArticlePubMedGoogle Scholar
- Sugama S, Fujita M, Hashimoto M, Conti B: Stress induced morphological microglial activation in the rodent brain: involvement of interleukin-18. Neuroscience. 2007, 146: 1388-1399. 10.1016/j.neuroscience.2007.02.043.View ArticlePubMedGoogle Scholar
- Sugama S, Wirz SA, Barr AM, Conti B, Bartfai T, Shibasaki T: Interleukin-18 null mice show diminished microglial activation and reduced dopaminergic neuron loss following acute 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine treatment. Neuroscience. 2004, 128: 451-458. 10.1016/j.neuroscience.2004.07.020.View ArticlePubMedGoogle Scholar
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