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Toll-like receptor signaling in amyotrophic lateral sclerosis spinal cord tissue
Abstract
Increasing evidence indicates that inflammatory responses could play a critical role in the pathogenesis of motor neuron injury in amyotrophic lateral sclerosis (ALS). Recent findings have underlined the role of Toll-like receptors (TLRs) and the receptor for advanced glycation endproducts (RAGE) in the regulation of both innate and adaptive immunity in different pathologies associated with neuroinflammation. In the present study we investigated the expression and cellular distribution of TLR2, TLR4, RAGE and their endogenous ligand high mobility group box 1 (HMGB1) in the spinal cord of control (n=6) and sporadic ALS (n=12) patients. The immunohistochemical analysis of TLR2, TLR4 and RAGE showed increased expression in reactive glial cells in both gray (ventral horn) and white matter of ALS spinal cord. TLR2 was predominantly detected in cells of the microglia/macrophage lineage, whereas the TLR4 and RAGE was strongly expressed in astrocytes. Real-time quantitative PCR analysis confirmed the increased expression of both TLR2 and TLR4 and HMGB1 mRNA level in ALS patients. In ALS spinal cord, HMGB1 signal is increased in the cytoplasm of reactive glia, indicating a possible release of this molecule from glial cells. Our findings show increased expression of TLR2, TLR4, RAGE and HMGB1 in reactive glia in human ALS spinal cord, suggesting activation of the TLR/RAGE signaling pathways. The activation of these pathways may contribute to the progression of inflammation, resulting in motor neuron injury. In this context, future studies, using animal models, will be important to achieve a better understanding of these signaling pathways in ALS in view of the development of new therapeutic strategies.
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“The levels of RAGE and its ligands (e.g., AGEs) were increased in the spinal cord and cerebrospinal fluid (CSF) of ALS patients.299,341”
From Role of neuroinflammation in neurodegeneration development (2023) · cites this paper as [299]
In the citing paper
“An analysis of post-mortem tissue from sporadic ALS patients showed a increased TLR4 expression in the spinal cord,299”
From Role of neuroinflammation in neurodegeneration development (2023) · cites this paper as [299]
Citations
Cites
El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis
Brooks, B. R., Miller, R. G., Swash, M., & Munsat, T. L. (2000) · Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders · doi:10.1080/146608200300079536 · Cited by 5,433
Release of chromatin protein HMGB1 by necrotic cells triggers inflammation
Scaffidi, P., Misteli, T., & Bianchi, M. E. (2002) · Nature · doi:10.1038/nature00858 · Cited by 4,221
Assumption-free analysis of quantitative real-time polymerase chain reaction (PCR) data
Ramakers, C. R. B., Ruijter, J. M., Deprez, R. H. L., & Moorman, A. F. M. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(02)01423-4 · Cited by 3,740
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
Kwiatkowski, T. J., Bosco, D. A., LeClerc, A. L., Tamrazian, E., Vanderburg, C. R., Russ, C., Davis, A., Gilchrist, J. M., Kasarskis, E. J., Munsat, T. L., et al. (2009) · Science · doi:10.1126/science.1166066 · Cited by 2,624
HMGB1 and RAGE in Inflammation and Cancer
Sims, G. P., Rowe, D. C., Rietdijk, S. T., Herbst, R., & Coyle, A. J. (2010) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132603 · Cited by 1,436
Molecular biology of amyotrophic lateral sclerosis: insights from genetics
Pasinelli, P., & Brown, R. H. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1971 · Cited by 1,107
Broad Expression of Toll-Like Receptors in the Human Central Nervous System
Bsibsi, M., Ravid, R., Gveric, D. O., & van Noort, J. M. (2002) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/61.11.1013 · Cited by 1,000
Maroso, M., Balosso, S., Ravizza, T., Liu, J., Aronica, E., Iyer, A. M., Rossetti, C., Molteni, M., Casalgrandi, M., Manfredi, A. A., et al. (2010) · Nature Medicine · doi:10.1038/nm.2127 · Cited by 842
Self-citationRamasamy, R., Vannucci, S. J., Yan, S. S. D., Herold, K., Yan, S. F., & Schmidt, A. M. (2005) · Glycobiology · doi:10.1093/glycob/cwi053 · Cited by 834
Inflammatory processes in Alzheimer's disease
Heneka, M. T., & O'Banion, M. K. (2007) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.11.017 · Cited by 782
High‐mobility group box 1 (HMGB1) protein at the crossroads between innate and adaptive immunity
Bianchi, M. E., & Manfredi, A. A. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2007.00574.x · Cited by 600
Kim, J.-B., Choi, J., Yu, Y., Nam, K., Piao, C.-S., Kim, S.-W., Lee, M., Han, P., Park, J. S., & Lee, J.-K. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3815-05.2006 · Cited by 580
Henkel-Tigges, J., Engelhardt, J., Siklós, L., Simpson, E. P., Kim, S. H., Pan, T., Goodman, J. C., Siddique, T., Beers, D. R., & Appel, S. H. (2003) · Annals of Neurology · doi:10.1002/ana.10805 · Cited by 576
Inflammatory processes in Alzheimer's disease
McGeer, E. G., & McGeer, P. L. (2003) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(03)00124-6 · Cited by 475
Inflammatory processes in amyotrophic lateral sclerosis
McGeer, P. L., & McGeer, E. G. (2002) · Muscle & Nerve · doi:10.1002/mus.10191 · Cited by 470
Bianchi, M. E. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.1008585 · Cited by 419
Cultured astrocytes express toll‐like receptors for bacterial products
Bowman, C. C., Rasley, A., Tranguch, S. L., & Marriott, I. (2003) · Glia · doi:10.1002/glia.10256 · Cited by 395
Toll‐like receptors in central nervous system glial inflammation and homeostasis
Kielian, T. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20767 · Cited by 373
Differential activation of astrocytes by innate and adaptive immune stimuli
Carpentier, P. A., Begolka, W. S., Olson, J. K., Elhofy, A., Karpus, W. J., & Miller, S. D. (2004) · Glia · doi:10.1002/glia.20117 · Cited by 368
Hreggvidsdottir, H. S., Östberg, T., Wähämaa, H., Schierbeck, H., Aveberger, A.-C., Klevenvall, L., Palmblad, K., Ottosson, L., Andersson, U., & Harris, H. E. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.0908548 · Cited by 289
Extracellular mutant SOD1 induces microglial‐mediated motoneuron injury
Zhao, W., Beers, D. R., Henkel, J. S., Zhang, W., Urushitani, M., Julien, J., & Appel, S. H. (2010) · Glia · doi:10.1002/glia.20919 · Cited by 288
The IL-1β system in epilepsy-associated malformations of cortical development
Ravizza, T., Boer, K., Redeker, S., Spliet, W. G. M., van Rijen, P. C., Troost, D., Vezzani, A., & Aronica, E. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.06.003 · Cited by 268
Self-citationtRNA splicing endonuclease mutations cause pontocerebellar hypoplasia
Budde, B. S., Namavar, Y., Barth, P. G., Poll‐The, B. T., Nürnberg, G., Becker, C., van Ruissen, F., Weterman, M. A. J., Fluiter, K., Beek, E. T. T., et al. (2008) · Nature Genetics · doi:10.1038/ng.204 · Cited by 262
Self-citationPreferential expression and function of Toll-like receptor 3 in human astrocytes
Farina, C., Krumbholz, M., Giese, T., Hartmann, G., Aloisi, F., & Meinl, E. (2004) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2004.09.009 · Cited by 256
Sasaki, N., Toki, S., Chowei, H., Saito, T., Nakano, N., Hayashi, Y., Takeuchi, M., & Makita, Z. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03075-4 · Cited by 253
The role of Toll-like receptors in chronic inflammation
Drexler, S. K., & Foxwell, B. M. J. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.10.009 · Cited by 250
Screening of innate immune receptors in neurodegenerative diseases: A similar pattern
Letiembre, M., Liu, Y., Walter, S., Hao, W., Pfander, T., Wrede, A., Schulz-Schaeffer, W., & Fassbender, K. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.08.018 · Cited by 228
Ince (1998) · doi:10.1046/j.1365-2990.1998.00108.x · Cited by 224
Pivotal Advance: HMGB1 expression in active lesions of human and experimental multiple sclerosis
Andersson, Å., Covacu, R., Sunnemark, D., Danilov, A. I., Bianco, A. D., Khademi, M., Wallström, E., Lobell, A., Brundin, L., Lassmann, H., et al. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.1207844 · Cited by 211
Piao, Y., Wakabayashi, K., Kakita, A., Yamada, M., Hayashi, S., Morita, T., Ikuta, F., Oyanagi, K., & Takahashi, H. (2003) · Brain Pathology · doi:10.1111/j.1750-3639.2003.tb00002.x · Cited by 210
Activation of toll-like receptor, RAGE and HMGB1 signalling in malformations of cortical development
Zurolo, E., Iyer, A., Maroso, M., Carbonell, C., Anink, J. J., Ravizza, T., Fluiter, K., Spliet, W. G. M., van Rijen, P. C., Vezzani, A., et al. (2011) · Brain · doi:10.1093/brain/awr032 · Cited by 207
Self-citationToll-Like Receptor 2 Signaling in Response to Brain Injury: An Innate Bridge to Neuroinflammation
Babcock, A. A., Wirenfeldt, M., Holm, T. H., Nielsen, H. H., Dissing‐Olesen, L., Toft‐Hansen, H., Millward, J. M., Landmann, R. M., Rivest, S., Finsen, B. R., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4937-05.2006 · Cited by 188
Toll-like Receptors in Defense and Damage of the Central Nervous System
Aravalli, R. N., Peterson, P. K., & Lokensgard, J. R. (2007) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-007-9071-5 · Cited by 173
Immunohistochemical characterization of the inflammatory infiltrate in amyotrophic lateral sclerosis
Troost, D., van den Oord, J. J., & de Jong, J. M. B. V. (1990) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1990.tb01276.x · Cited by 153
Self-citationInnate immunity in amyotrophic lateral sclerosis
Moisse, K., & Strong, M. J. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2006.03.001 · Cited by 144
Innate and adaptive immunity in amyotrophic lateral sclerosis: Evidence of complement activation
Sta, M., Sylva-Steenland, R. M. R., Casula, M., de Jong, J. M. B. V., Troost, D., Aronica, E., & Baas, F. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.01.002 · Cited by 143
Self-citationSite-Specific Blockade of RAGE-VdPrevents Amyloid-β Oligomer Neurotoxicity
Sturchler, E., Galichet, A., Weibel, M., Leclerc, E., & Heizmann, C. W. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4878-07.2008 · Cited by 136
Selective Proinflammatory Activation of Astrocytes by High-Mobility Group Box 1 Protein Signaling
Pedrazzi, M., Patrone, M., Passalacqua, M., Ranzato, E., Colamassaro, D., Sparatore, B., Pontremoli, S., & Melloni, E. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.12.8525 · Cited by 132
Aronica, E., Gorter, J. A., Jansen, G. H., Veelen, C. W. M. V., van Rijen, P. C., Ramkema, M., & Troost, D. (2003) · Epilepsia · doi:10.1046/j.1528-1157.2003.54802.x · Cited by 126
Self-citationPreventing Activation of Receptor for Advanced Glycation Endproducts in Alzheimers Disease
Lue, L.-F., Yan, S. D., Stern, D. F., & Walker, D. G. (2005) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1568007054038210 · Cited by 126
Liu, Y., Hao, W., Dawson, A., Liu, S., & Fassbender, K. C. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m804446200 · Cited by 119
Bianchi, M. E., & Manfredi, A. A. (2009) · Science · doi:10.1126/science.1172794 · Cited by 117
Toll‐like receptors in the brain and their potential roles in neuropathology
Crack, P. J., & Bray, P. (2007) · Immunology and Cell Biology · doi:10.1038/sj.icb.7100103 · Cited by 116
Kamei, Y., Inagaki, N., Nishizawa, M., Tsutsumi, O., Taketani, Y., & Inagaki, M. (1998) · Glia · doi:10.1002/(sici)1098-1136(199807)23:3 · Cited by 114
Expression and distribution of id helix‐loop‐helix proteins in human astrocytic tumors
Vandeputte, D. A. A., Troost, D., Leenstra, S., Ijlst‐Keizers, H., Ramkema, M., Bosch, D. A., Baas, F., Das, N. K., & Aronica, E. (2002) · Glia · doi:10.1002/glia.10076 · Cited by 110
Self-citationToll-Like Receptor (TLR)2 and TLR4 Agonists Regulate CCR Expression in Human Monocytic Cells
Parker, L. C., Whyte, M. K. B., Vogel, S. N., Dower, S., & Sabroe, I. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.8.4977 · Cited by 99
Overmyer, M., Helisalmi, S., Soininen, H., Laakso, M., Riekkinen Sr., P., & Alafuzoff, I. (1999) · Acta Neuropathologica · doi:10.1007/s004010051002 · Cited by 91
Role of ERK map kinase and CRM1 in IL‐1β‐stimulated release of HMGB1 from cortical astrocytes
Hayakawa, K., Arai, K., & Lo, E. H. (2010) · Glia · doi:10.1002/glia.20982 · Cited by 71
Aronica, E., Leenstra, S., Jansen, G. H., Veelen, C. W. M. V., Yankaya, B., & Troost, D. (2001) · Acta Neuropathologica · doi:10.1007/s004010000296 · Cited by 61
Self-citationThe Role of Toll-like Receptors in Perinatal Brain Injury
Mallard, C. E., Wang, X., & Hagberg, H. (2009) · Clinics in Perinatology · doi:10.1016/j.clp.2009.07.009 · Cited by 56
Ma, L., & Nicholson, L. F. B. (2004) · Brain Research · doi:10.1016/j.brainres.2004.05.052 · Cited by 54
Coco, D. L., Veglianese, P., Allievi, E., & Bendotti, C. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.10.063 · Cited by 52
Leech giant glial cell: functional role in a simple nervous system
Deitmer, J. W., Rose, C. R., Munsch, T., Schmidt, J., Nett, W., Schneider, H.-P., & Lohr, C. (1999) · Glia · doi:10.1002/(sici)1098-1136(199912)28:3 · Cited by 43
Kleen, J. K., & Holmes, G. L. (2010) · Nature Medicine · doi:10.1038/nm0410-369 · Cited by 31
Mouri, F., Tsukada, J., Mizobe, T., Higashi, T., Yoshida, Y., Minami, Y., Izumi, H., Kominato, Y., Kohno, K., & Tanaka, Y. (2007) · European Journal Of Haematology · doi:10.1111/j.1600-0609.2007.00981.x · Cited by 28
Birth order and the genetics of amyotrophic lateral sclerosis
Vivekananda, U., Johnston, C. A., McKenna‐Yasek, D., Shaw, C. E., Leigh, P. N., Brown, R. H., & Al‐Chalabi, A. (2007) · Journal of Neurology · doi:10.1007/s00415-007-0709-2 · Cited by 9
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TLR4 and CD14 trafficking and its influence on LPS-induced pro-inflammatory signaling
Ciesielska, A., Matyjek, M., & Kwiatkowska, K. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03656-y · Cited by 1,420
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Metadata
- Authors
- Casula, M., Iyer, A. M., Spliet, W. G. M., Anink, J. J., Steentjes, K., Sta, M., Troost, D., & Aronica, E.
- Affiliations
- Amsterdam UMC Location University of Amsterdam (NL)
- University Medical Center Utrecht (NL)
- Corresponding author
- Aronica, E.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 2011-04
- Volume
- 179
- Pages
- 233-243
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W2069842601
- Cited by
- 200
- References
- 56
- Citations by year
- 2026: 7 · 2025: 7 · 2024: 13 · 2023: 8 · 2022: 15 · 2021: 16 · 2020: 9 · 2019: 8 · 2018: 21 · 2017: 28 · 2016: 11 · 2015: 19 · 2014: 13 · 2013: 13 · 2012: 10
- FWCI
- 7.72
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Pure Amsterdam UMC (submittedVersion)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Advanced Glycation End Products research
- Keywords
- amyotrophic lateral sclerosis, TLR2, TLR4, receptor for advanced glycation end products, high mobility group box 1, neuroinflammation, reactive glia, microglia/macrophages, astrocytes, motor neuron injury, spinal cord, ventral horn
- MeSH terms
- Receptor for Advanced Glycation End Products, Aged, Aged, 80 and over, Amyotrophic Lateral Sclerosis, Astrocytes, Female, Humans, Immunohistochemistry, Male, Middle Aged, Spinal Cord, Signal Transduction, In Situ Hybridization, Reverse Transcriptase Polymerase Chain Reaction, HMGB1 Protein, Toll-Like Receptor 2, Toll-Like Receptor 4
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