Clusters of activated microglia in normal-appearing white matter show signs of innate immune activation
Journal of Neuroinflammation volume 9, Article number: 156 (2012)
In brain tissues from multiple sclerosis (MS) patients, clusters of activated HLA-DR-expressing microglia, also referred to as preactive lesions, are located throughout the normal-appearing white matter. The aim of this study was to gain more insight into the frequency, distribution and cellular architecture of preactive lesions using a large cohort of well-characterized MS brain samples.
Here, we document the frequency of preactive lesions and their association with distinct white matter lesions in a cohort of 21 MS patients. Immunohistochemistry was used to gain further insight into the cellular and molecular composition of preactive lesions.
Preactive lesions were observed in a majority of MS patients (67%) irrespective of disease duration, gender or subtype of disease. Microglial clusters were predominantly observed in the vicinity of active demyelinating lesions and are not associated with T cell infiltrates, axonal alterations, activated astrocytes or blood–brain barrier disruption. Microglia in preactive lesions consistently express interleukin-10 and TNF-α, but not interleukin-4, whereas matrix metalloproteases-2 and −9 are virtually absent in microglial nodules. Interestingly, key subunits of the free-radical-generating enzyme NADPH oxidase-2 were abundantly expressed in microglial clusters.
The high frequency of preactive lesions suggests that it is unlikely that most of them will progress into full-blown demyelinating lesions. Preactive lesions are not associated with blood–brain barrier disruption, suggesting that an intrinsic trigger of innate immune activation, rather than extrinsic factors crossing a damaged blood–brain barrier, induces the formation of clusters of activated microglia.
Multiple sclerosis (MS) is a chronic, progressive, inflammatory, demyelinating and neurodegenerative disease of the central nervous system (CNS). Examination of brain tissue of individuals with MS reveals focal lesions throughout the white matter and extensive demyelination in the cerebral cortex of chronic MS patients . Common pathological features of MS white matter lesions include blood–brain barrier leakage, inflammatory infiltrates consisting of lymphocytes and macrophages, destruction of myelin sheaths and oligodendrocyte loss, axonal damage and loss, and glial scar formation [2–4]. In particular monocyte-derived macrophages and resident microglia contribute to MS lesion formation as they phagocytose myelin, leading to extensive myelin damage and oligodendrocyte dysfunction . Importantly, during inflammation, activated microglia and infiltrated macrophages secrete various inflammatory mediators, including cytokines, chemokines, nitric oxide and reactive oxygen species (ROS), which all contribute to disease progression [5–7]. On the other hand it has been demonstrated that activated microglia and macrophages also exert beneficial effects by inducing remyelination, neuronal regeneration and repair [6, 8, 9]. Nonetheless, the initial trigger and molecular mechanisms underlying the pathogenesis of MS remain enigmatic.
Classification of MS lesions is usually based on standard histopathological staining for inflammatory cells and myelin proteins . Active MS lesions are characterized by myelin loss and abundant phagocytic macrophages and microglia, which in some cases contain myelin degradation products. In time, these inflammatory lesions might transform into chronic active lesions with a hypocellular demyelinated gliotic center and a hypercellular rim containing myelin-laden macrophages and microglia. However, post-mortem material from patients with established MS mostly contain chronic inactive lesions, which are characterized by extensive astrogliosis in the absence of infiltrated immune cells and microglial activation. In some cases, remyelination is observed, indicating that intrinsic control of inflammation and repair does occur in the MS brain .
To date, the use of MRI-guided tissue sampling has significantly increased the yield of MS lesions in autopsy specimens. Particularly, lesions that are macroscopically invisible, including preactive lesions, are now commonly observed. In 2001, de Groot and colleagues described the occurrence of preactive lesions for the first time and speculated that this lesion type might represent one of the earliest stages of MS lesion development . Preactive lesions are observed throughout the normal-appearing white matter and are characterized by clustering of activated microglia as demonstrated by enhanced expression of HLA-DR in the absence of overt demyelination. Many recent reports suggest that microglial activation represents an early stage of tissue damage, which precedes the formation of demyelinating lesions [2, 13–16]. Although most histopathological studies have focused on active and chronic inactive lesions, remarkably little is known about the occurrence and cellular composition of preactive lesions . The aim of this study was to gain more insight in the frequency, distribution and cellular architecture of preactive lesions using a large cohort of well-characterized MS brain samples.
Brain tissue samples were obtained from the Netherlands Brain Bank (coordinator Dr. Huitinga, Amsterdam, The Netherlands). The Netherlands Brain Bank received permission to perform autopsies for the use of tissue and for access to medical records for research purposes from the Ethical Committee of the VU University Medical Center, Amsterdam, The Netherlands. All patients and controls, or their next of kin, had given informed consent for autopsy and use of brain tissue for research purposes. Relevant clinical information was retrieved from the medical records and is summarized in Table 1. A total of 213 paraffin-embedded tissue blocks from 21 MS patients (female-to-male ratio: 7:14; average age 59 years; average post-mortem delay 8 h) and 6 white matter blocks from 6 donors (female-to-male ratio: 4/2; average age 71; average post-mortem delay 7 h) without neurological disease were selected. Normal-appearing white matter (NAWM) and white matter lesion samples were selected on the basis of post-mortem MRI.
Formalin-fixed, paraffin-embedded tissue was sectioned at 5 μm and stained for proteolipid protein (PLP), HLA-DR (clone LN3) and CD68 as described previously . Sections were deparaffinized in xylene and rehydrated through graded alcohol into distilled water. Endogenous peroxidase activity was quenched by incubating the slides in 0.3% hydrogen peroxide in methanol. For HLA-DR detection, slides were rinsed with distilled water and transferred to citric acid. Heat-induced antigen retrieval was performed using microwave irradiation for 5 min on the high setting and for 10 min on the medium setting. Slides were then cooled to room temperature and rinsed in phosphate-buffered saline (PBS). Serial sections were incubated overnight with anti-HLA-DR, anti-CD68 or PLP. Then, slides were incubated with EnVision Kit horseradish peroxidase-labeled anti-mouse/rabbit (DAKO) for 30 min at room temperature and finally diaminobenzidine tetrachloride. Between incubation steps, sections were thoroughly washed with PBS. After a short rinse in tap water, sections were incubated with hematoxylin for 1 min and extensively washed with tap water for 10 min. Finally, sections were dehydrated with ethanol followed by xylol and mounted with Entellan (Merck, Darmstadt, Germany). All antibodies were diluted in PBS containing 0.1% bovine serum albumin (Boehringer-Mannheim), which also served as a negative control. For the detection of NADPH oxidase-2 subunits gp91phox, p22phox and p47phox, we used cryosections and use the same Envision protocol as described above.
For double staining of amyloid precursor protein (APP) or CD3 with HLA-DR, sections were first stained for HLA-DR and labeled with DAB. Subsequently, APP and CD3 were detected with the alkaline phosphatase method. For double immunostaining for HLA-DR and FITC-labeled fibrinogen, claudin-5, glial fibrillary acidic protein (GFAP), neurofilament (NF), matrix metalloproteinase-2 (MMP2) and −9 (MMP9), tumor necrosis factor-α (TNF-α), interleukin-4 (IL4) and −10 (IL10), we used cryosections of snap-frozen brain tissue blocks (n = 10) from five MS patients (2 blocks per patient) with several preactive lesions (cases 8, 9, 12, 13 and 20). Cryosections (5 μm) were air-dried and fixed in acetone for 10 min and preincubated for 30 min with 20% goat serum, and subsequently incubated overnight at 4 °C with specific primary antibodies. Next, sections were incubated with either Alexa-546 or −594-labeled secondary antibodies (1:400; Molecular Probes) for 1 h at room temperature. Between the incubation steps, sections were thoroughly washed with PBS. After washing, slides were covered with Vectashield (Vector Laboratories) supplemented with 0.4% DAPI to stain nuclei. Microscopic analysis was performed with a Leica DM 6000 (Leica Microsystems, Heidelberg, Germany). Additional information on the antibodies used in this study is summarized in Table 2.
Numbers of blocks containing different lesions types were counted separately for all patients included in the study and expressed as percentage. Pearson correlation testing was performed for respective groups. The frequency of preactive lesions relative to other white matter lesions was compared using one-way ANOVA followed by Tukey’s multiple comparison test.
Frequency and distribution of preactive lesions in MS brain tissue
To gain insight into the frequency of preactive lesions, we randomly selected a cohort of 21 MS patients from our database between 2006 and 2010. Of these 21 MS patients, a total of 213 tissue blocks were collected. Identification of lesions was based on immunohistochemical staining for microglia/macrophages (anti-HLA-DR) and proteolipid protein (PLP). From the total number of tissue blocks, we observed 24 blocks with active lesions with severe myelin loss and abundant phagocytic macrophages and microglia, 66 blocks with chronic active lesions with a demyelinated center and a border containing macrophages and microglia, and 28 blocks with chronic inactive lesions with few HLA-DR-positive inflammatory cells and extensive astrogliosis in 213 tissue samples derived from 21 MS cases (for patient details and lesion distribution, see Table 1). Preactive lesions, defined as circumscribed nodules of activated microglia (HLA-DR + and CD68+) in the absence of apparent myelin loss (Figure 1), were observed in 44 out of these 213 tissue blocks (21%) from 14 MS patients (67%) and absent in all white matter samples from non-neurological control patients. Occasionally, we observed preactive lesions that were surrounded by a halo devoid of HLA-DR-positive microglia, suggesting that microglia from this area had migrated towards the ‘center’ of the preactive lesion (Figure 1H). Preactive lesions were found in both male (9) and female (5) MS patients irrespective of MS subtype (Table 1). Notably, preactive lesions were observed in both patients with relatively short disease duration, e.g., cases 8 (14 years) and 17 (13 years), and patients with long disease duration, e.g., cases 3 (54 years) and 4 (40 years) (Table 1).
Next, we studied the association between preactive lesions and inflammatory white matter lesions. The occurrence of preactive lesions negatively correlates with the number of blocks containing no active lesions (Figure 2A; p = 0.0128), whereas the presence of preactive lesions weakly correlates with the number of blocks with active lesions (Figure 2B; p = 0.049). No significant correlation was found between the presence of preactive lesions and the number of chronic active lesion or chronic inactive lesion blocks (data not shown). Statistical analysis revealed that the occurrence of preactive lesions is not associated with the different types of white matter lesions within the same block, and preactive lesions were even detected in tissue sections of blocks lacking white matter lesions (Figure 2C). Taken together, our observations reveal that preactive lesions, characterized by clusters of activated microglia, can be observed in tissue blocks containing different stages of white matter lesions, but have a tendency to occur more frequently in the vicinity of active lesions. Moreover, preactive lesions are present in MS brain tissue samples regardless of gender, type of MS or disease duration.
Cellular composition of preactive lesions
To examine the cellular composition of preactive lesions, we performed double immunohistochemistry on ten tissue blocks from five cases with abundant preactive lesions (cases 8, 9, 12, 13 and 20) using markers for different CNS cells and typical pathological features of MS pathology. Since MS lesions are generally concentrated around inflamed venules and veins, we first analyzed the association between preactive lesions and the cerebrovasculature, and showed that preactive lesions are not evidently associated with blood vessels (Figure 3A). Moreover, markers for blood–brain barrier disruption, including the key tight junction molecule claudin-5 (Figure 3B) and fibrinogen (Figure 3C), a serum component that is commonly used as a marker for leaky vessels, revealed no marked changes in the blood–brain barrier integrity surrounding microglial clusters. Analysis of the expression of glial fibrillary acidic protein (Figure 3D) and neurofilaments (Figure 3E), common markers for astrocytes and axons, respectively, demonstrated no signs of astrogliosis or axonal changes in or surrounding preactive lesions. Intra-axonal amyloid precursor protein accumulation, indicative of acute axonal injury, was absent from preactive lesions (Figure 3F), but present in the rim of a chronic active MS lesions (Figure 3G). T cell infiltrates were not associated with preactive lesions (Figure 3H), but restricted to highly inflammatory areas (Figure 3I).
Preactive lesions express distinct inflammatory mediators
To examine the phenotype of microglia in preactive lesions, we determined the expression of several key molecules known to be involved in MS pathology in the same tissue blocks used to study the cellular composition of preactive lesions. Interleukin-4 immunostaining was consistently observed in the cerebrovasculature and not associated with microglia (Figure 4A-C), whereas clusters of activated microglia markedly expressed interleukin-10 (Figure 4D-F). Matrix metalloproteinase-2 (Figure 4G-I) and −9 (Figure 4J-L) immunostaining, both involved in the breakdown of extracellular matrix, was virtually lacking in nodules of activated microglia, whereas TNF-α was clearly localized to microglia in preactive lesions (Figure 4M-O).
Increased microglial NADPH oxidase-2 immunostaining in preactive lesions
Recently, we demonstrated that various subunits of the ROS-generating enzyme NADPH oxidase-2 are clearly upregulated in activated microglia in active demyelinating and slowly expanding chronic MS lesions . Here, we analyzed the expression of three key NADPH oxidase-2 subunits, namely gp91phox, p22phox and p47phox, in the same tissue blocks as described above. Preactive lesions, defined as microglial clusters in NAWM [Figure 5A (PLP), B,C (HL-DRA)], were consistently labeled with antibodies directed against the NADPH oxidase-2 subunits, gp91phox (Figure 5D), p22phox (Figure 5E) and p47phox (Figure 5F) in consecutive sections.
Despite major advances in the development of novel MS therapeutics that significantly reduce the number of exacerbations, the etiology of this chronic and devastating disease still remains unclear. Most therapeutic approaches are effective in the initial inflammatory phase of the disease, but fail to limit the ongoing neurodegeneration. Consequently, the concept that MS is a purely immune-mediated, or indeed autoimmune-mediated disease, has been challenged . Despite these ideas and many comprehensive neuropathological studies, little is known about the initial trigger of focal MS lesions.
The NAWM represents an interesting region to search for clues that might trigger the formation of a demyelinating lesion . Several neuropathological, biochemical and imaging studies reveal alterations in the NAWM, including signs of oligodendrocyte stress, subtle myelin changes and axonal alterations [16, 21–25]. Perhaps the most prominent pathological feature in NAWM is the occurrence of widespread microglial activation and clustering . The detection of nodules of strongly positive HLA-DR-positive activated microglia in the absence of overt demyelination in NAWM of MS patients has led to the classification of so-called preactive lesions . Here, we examined the cellular composition and immune markers expressed in preactive MS lesions, and their relationship with focal demyelinated white matter lesions. Preactive lesions were frequently observed in 14 out of 21 MS patients (67%), which is in line with previous observations by De Groot and colleagues . The frequency of preactive lesions was higher, albeit weakly significantly, in regions in the vicinity of active lesions. Preactive lesions were observed in the majority of patients with established MS, suggesting that their occurrence is not restricted to the early phase of the disease, but that focal clusters of activated microglia continuously emerge regardless of disease duration. Since preactive lesions were frequently detected even in patients with long-standing disease, it is unlikely that all preactive lesions eventually progress into demyelinating lesions. Instead, these observations suggest that most of them are likely to spontaneously resolve over time without progressing into an active demyelinating stage.
Microglia are innate immune cells of myeloid origin residing in the CNS and continuously screen their surroundings. They react rapidly to changes in their microenvironment, and can become morphologically and functionally activated by a variety of triggers. Activated microglia in MS brains can be detrimental by amplifying an inflammatory response by the production of cytokines, chemokines and free radicals, which might contribute to oligodendrocyte cell death, axonal injury and demyelination. Alternatively, activated microglia produce factors that are known to promote remyelination and stimulate neuroprotection. This study reveals that microglia in preactive lesions express TNF-α and IL-10, whereas preactive lesions were virtually devoid of IL-4, and MMP-2 and −9. TNF-α is a cytokine that exerts pleiotropic functions, and although it is usually considered as a proinflammatory mediator, it also activates cell survival pathways (reviewed in ). Thus, the presence of TNF-α, as well as IL-10, suggests attempts to regulate inflammation. We recently described enhanced NADP oxidase expression in activated microglia in active and chronic active MS lesions, indicating the important role of free radicals in demyelination and associated tissue injury . In the current study, we demonstrate that microglia in preactive lesions also show pronounced expression of key subunits of NADPH oxidase-2, indicating the assembly of a functional NADPH oxidase-2 complex. This strongly suggests that activated microglia in preactive lesions might be involved in the production of reactive oxygen species.
Although the white matter is highly vascularized, preactive lesions did not clearly localize to blood vessels and microvessels in close vicinity to preactive lesions showed no clear signs of tight junction alterations. In addition, we observed no extravascular deposition of the serum protein fibrinogen or infiltrated T cells, indicating the lack of blood–brain barrier disruption. The apparently intact blood–brain barrier in preactive lesions suggests that a yet-unknown intrinsic CNS trigger induces the microglial activation and clustering rather than a response to T cells or serum components that enter via a compromised blood–brain barrier. Potential pathogenic triggers of microglial activation and clustering in the NAWM might be axonal injury or oligodendrocyte stress. Microarray analysis has revealed that both anti-inflammatory as well as pro-inflammatory genes are consistently upregulated in NAWM, particularly in oligodendrocytes . In search for early molecular alterations in NAWM, Zeis and colleagues identified oxidative damage to oligodendrocytes, which was paralleled by an increase in the expression of genes known to be involved in antioxidant defense [23, 28]. In addition, we previously reported the presence of αB-crystallin-immunopositive oligodendrocytes in preactive lesions, indicative of oligodendrocyte stress . Importantly, neurofilament staining showed a normal expression pattern, and APP-positive axonal bulbs were not associated with preactive lesions, but restricted to areas with abundant inflammatory cells. Nonetheless, we cannot exclude the possibility that more subtle axonal alterations, such as changes in axonal ion transporters or mitochondrial dysfunction [30–33], lead to microglial activation and clustering.
Taken together, we showed that preactive lesions are detected in the majority of MS samples irrespective of gender, disease duration or subtype of disease. Given the high frequency of preactive lesions in our set of MS brain samples, it appears unlikely that most of them will progress into full-blown demyelinating lesions. The balance between proinflammatory signals, such as reactive oxygen species, and anti-apoptotic signals or anti-inflammatory signals, e.g., IL-10, may be the determining factor in lesion development. Although the number of preactive lesions was higher in areas surrounding inflammatory lesions, microglial clusters were not associated with T cell influx, axonal changes or activated astrocytes. Importantly, vessels in close proximity to preactive lesions showed no signs of blood–brain barrier disruption, suggesting that an intrinsic trigger of innate immune activation rather than extrinsic factors crossing a damaged blood–brain barrier induce the formation of clusters of activated microglia.
Bo L, Vedeler CA, Nyland HI, Trapp BD, Mørk SJ: Subpial demyelination in the cerebral cortex of multiple sclerosis patients. J Neuropathol Exp Neurol 2003, 62:723–732.
Barnett MH, Prineas JW: Relapsing and remitting multiple sclerosis: pathology of the newly forming lesion. Ann Neurol 2004, 5:458–468.
Amor S, Puentes F, Baker D, van der Valk P: Inflammation in neurodegenerative diseases. Immunology 2010, 129:154–169.
Lassmann H, Suchanek G, Ozawa K: Histopathology and the blood-cerebrospinal fluid barrier in multiple sclerosis. Ann Neurol 1994, 36:S42-S46.
Hendriks JJ, Teunissen CE, de Vries HE, Dijkstra CD: Macrophages and neurodegeneration. Brain Res Brain Res Rev 2005, 48:185–195.
Nataf S: Neuroinflammation responses and neurodegeneration in multiple sclerosis. Rev Neurol (Paris) 2009, 165:1023–1028.
Van Horssen J, Witte ME, Schreibelt G, de Vries HE: Radical changes in multiple sclerosis pathogenesis. Biochim Biophys Acta 2011, 1812:141–150.
Lassmann H, van Horssen J: The molecular basis of neurodegeneration in multiple sclerosis. FEBS Lett 2011, 23:3715–3723.
Gay FW, Drye TJ, Dick GW, Esiri MM: The application of multifactorial cluster analysis in the staging of plaques in early multiple sclerosis. Identification and characterization of the primary demyelinating lesion. Brain 1997, 120:1461–1483.
der Valk V, De Groot CJ: Staging of multiple sclerosis (MS) lesions: pathology of the time frame of MS. Neuropathol Appl Neurobiol 2000, 1:2–10.
Patrikios P, Stadelmann C, Kutzelnigg A, Rauschka H, Schmidbauer M, Laursen H, Sorensen PS, Brück W, Lucchinetti C, Lassmann H: Remyelination is extensive in a subset of multiple sclerosis patients. Brain 2006, 129:3165–3172.
De Groot CJ, Bergers E, Kamphorst W, Ravid R, Polman CH, Barkhof F, van der Valk P: Post-mortem MRI-guided sampling of multiple sclerosis brain lesions: increased yield of active demyelinating and (p)reactive lesions. Brain 2001, 124:1635–1645.
Linker R, Gold R, Luhder F: Function of neurotrophic factors beyond the nervous system: inflammation and autoimmune demyelination. Crit Rev Immunol 2009, 29:43–68.
Marik C, Felts PA, Bauer J, Lassmann H, Smith KJ: Lesion genesis in a subset of patients with multiple sclerosis: a role for innate immunity? Brain 1997, 130:2800–2815.
Van der Valk P, Amor S: Preactive lesions in multiple sclerosis. Curr Opin Neurol 2009, 3:207–213.
van Noort JM, van den Elsen PJ, van Horssen J, Geurts JJ, van der Valk P, Amor S: Preactive multiple sclerosis lesions offer novel clues for neuroprotective therapeutic strategies. CNS Neurol Disord Drug Targets 2011, 10:68–81.
Van Horssen J, Schreibelt G, Bo L, Montagne L, Drukarch B, van Muiswinkel F, de Vries HE: NAD(P)H:quinone oxidoreductase 1 expression in multiple sclerosis lesions. Free Radic Biol Med 2006, 41:311–317.
Verhoeven AJ, Bolscher BG, Meerhof LJ, van Zwieten R, Keijer J, Weening RS, Roos D: Characterization of two monoclonal antibodies against cytochrome b558 of human neutrophils. Blood 1989, 6:1686–1694.
Fischer MT, Sharma R, Lim JL, Haider L, Frischer JM, Mahad D, Bradl M, van Horssen J, Lassmann H: NADPH oxidase expression in active multiple sclerosis lesions in relation to oxidative tissue damage and mitochondrial injury. Brain 2012, 135:886–899.
Trapp BD, Nave KA: Multiple sclerosis: an immune or neurodegenerative disorder? Annu Rev Neurosci 2008, 31:247–269.
Aboul-Enein F, Krssak M, Hoftberger R, Prayer D, Kristoferitsch W: Reduced NAA-levels in the NAWM of patients with MS is a feature of progression. A study with quantitative magnetic resonance spectroscopy at 3 Tesla. PLoS One 2010, 5:e11625.
Bjartmar C, Kinkel RP, Kidd G, Rudick RA, Trapp BD: Axonal loss in normal-appearing white matter in a patient with acute MS. Neurology 2001, 57:1248–1252.
Graumann U, Reynolds R, Steck AJ, Schaeren-Wiemers N: Molecular changes in normal appearing white matter in multiple sclerosis are characteristic of neuroprotective mechanisms against hypoxic insult. Brain Pathol 2003, 13:554–73.
Wheeler D, Bandaru VV, Calabresi PA, Nath A, Haughey NJ: A defect of sphingolipid metabolism modifies the properties of normal appearing white matter in multiple sclerosis. Brain 2008, 131:3092–3102.
Zeis T, Graumann U, Reynolds R, Schaeren-Wiemers N: Normal-appearing white matter in multiple sclerosis is in a subtle balance between inflammation and neuroprotection. Brain 2008, 131:288–303.
Allen IV, McQuaid S, Mirakhur M, Nevin G: Pathological abnormalities in the normal-appearing white matter in multiple sclerosis. Neurol Sci 2001, 22:141–144.
Caminero A, Comabella M, Montalban X: Tumor necrosis factor alpha (TNF-alpha), anti-TNF-alpha and demyelination revisited: an ongoing story. J Neuroimmunol 2011, 234:1–6.
Zeis T, Probst A, Steck AJ, Stadelmann C, Bruck W, Schaeren-Wiemers N: Molecular changes in white matter adjacent to an active demyelinating lesion in early multiple sclerosis. Brain Pathol 2009, 19:459–466.
Van Noort JM, Bsibsi M, Gerritsen WH, van der Valk P, Bajramovic JJ, Steinman L, Amor S: Alpha b-crystallin is a target for adaptive immune responses and a trigger of innate responses in preactive multiple sclerosis lesions. J Neuropathol Exp Neurol 2010, 7:694–703.
Witte ME, Bo L, Rodenburg RJ, Belien JA, Musters R, Hazes T, Wintjes LT, Smeitink JA, Geurts JJ, De Vries HE, van der Valk P, van Horssen J: Enhanced number and activity of mitochondria in multiple sclerosis lesions. J Pathol 2009, 2:193–204.
Mahad D, Ziabreva I, Lassmann H, Turnbull D: Mitochondrial defects in acute multiple sclerosis lesions. Brain 2008, 131:1722–1735.
Stirling DP, Stys PK: Mechanisms of axonal injury: internodal nanocomplexes and calcium deregulation. Trends Mol Med 2010, 16:160–170.
Witte ME, Geurts JJ, de Vries HE, van der Valk P, van Horssen J: Mitochondrial dysfunction: a potential link between neuroinflammation and neurodegeneration? Mitochondrion 2010, 5:411–418.
This work was supported by grants from the Dutch MS Research Foundation, The Netherlands, project nos. MS 08–657 and MS 05-358c (J. van Horssen), ENC Erasmus Mundus (S. Singh) and the DFG (M. Kipp).
The author(s) declare that they have no competing interests.
JvH and SS analyzed the data and wrote the manuscript. SvdP, JL, LP, WG and RPB carried out the immunohistochemical analyses. MK and MW participated in the design, analyzed the data and prepared the figures. E-JK, JG, HdV, PvdE and PvdV reviewed the manuscript and SA supervised the study. All authors read and approved the final manuscript.
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van Horssen, J., Singh, S., van der Pol, S. et al. Clusters of activated microglia in normal-appearing white matter show signs of innate immune activation. J Neuroinflammation 9, 156 (2012). https://doi.org/10.1186/1742-2094-9-156