The DOI matches its Crossref record; 148 of the 149 references it cites were found in a registry or an index.
Inflammasomes in the CNS
Abstract
Microglia and macrophages in the CNS contain multimolecular complexes termed inflammasomes. Inflammasomes function as intracellular sensors for infectious agents as well as for host-derived danger signals that are associated with neurological diseases, including meningitis, stroke and Alzheimer's disease. Assembly of an inflammasome activates caspase 1 and, subsequently, the proteolysis and release of the cytokines interleukin-1β and interleukin-18, as well as pyroptotic cell death. Since the discovery of inflammasomes in 2002, there has been burgeoning recognition of their complexities and functions. Here, we review the current understanding of the functions of different inflammasomes in the CNS and their roles in neurological diseases.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“several inflammasomes have been characterized in microglia including NLRP1, NLRP3, and NLRC4 (Walsh et al, 2014).”
From Danger Signals and Inflammasomes: Stress-Evoked Sterile Inflammation in Mood Disorders (2017) · cites this paper as Walsh et al, 2014
In the citing paper
“The NLRP3 inflammasome has been the most studied inflammasome in the CNS (Walsh et al, 2014)”
From Danger Signals and Inflammasomes: Stress-Evoked Sterile Inflammation in Mood Disorders (2017) · cites this paper as Walsh et al, 2014
Citations
Cites
Martinon, F., Burns, K., & Tschopp, J. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00599-3 · Cited by 6,066
A role for mitochondria in nlrp3 inflammasome activation
Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602
Gout-associated uric acid crystals activate the NALP3 inflammasome
Martinon, F., Pétrilli, V., Mayor, A., Tardivel, A., & Tschopp, J. (2006) · Nature · doi:10.1038/nature04516 · Cited by 5,326
Mechanisms underlying inflammation in neurodegeneration
Glass, C. K., Saijo, K., Winner, B., Marchetto, M. C., & Gage, F. H. (2010) · Cell · doi:10.1016/j.cell.2010.02.016 · Cited by 3,580
Pyroptosis: host cell death and inflammation
Bergsbaken, T., Fink, S. L., & Cookson, B. T. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2070 · Cited by 3,288
Bauernfeind, F. G., Horvath, G. L., Stutz, A., Alnemri, E. S., MacDonald, K. L., Speert, D. P., Fernandes‐Alnemri, T., Wu, J., Monks, B. G., Fitzgerald, K. A., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901363 · Cited by 3,087
Cryopyrin activates the inflammasome in response to toxins and ATP
Mariathasan, S., Weiss, D. S., Newton, K., McBride, J., O'Rourke, K., Roose-Girma, M., Lee, W. P., Weinrauch, Y., Monack, D. M., & Dixit, V. M. (2006) · Nature · doi:10.1038/nature04515 · Cited by 3,080
Hornung, V., Bauernfeind, F., Halle, A., Samstad, E. O., Kono, H., Rock, K. L., Fitzgerald, K. A., & Latz, E. (2008) · Nature Immunology · doi:10.1038/ni.1631 · Cited by 3,065
Nakahira, K., Haspel, J. A., Rathinam, V. A. K., Lee, S.-J., Dolinay, T., Lam, H. C., Englert, J. A., Rabinovitch, M., Cernadas, M., Kim, H. P., et al. (2011) · Nature Immunology · doi:10.1038/ni.1980 · Cited by 3,049
NLRP3 is activated in Alzheimer’s disease and contributes to pathology in APP/PS1 mice
Heneka, M. T., Kummer, M. P., Stutz, A., Delekate, A., Schwartz, S., Vieira-Saecker, A., Griep, A., Axt, D., Remus, A., Tzeng, T.-C., et al. (2013) · Nature · doi:10.1038/nature11729 · Cited by 2,898
Flagged first, then by citations
1 of the 149 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 401–500 of 641
Cabantous, S., Poudiougou, B., Bergon, A., Barry, A., Oumar, A. A., Traore, A. M., Chevillard, C., Doumbo, O. K., Dessein, A. J. J., & Marquet, S. (2020) · Mediators of Inflammation · doi:10.1155/2020/3280689 · Cited by 17
Ducza, L., Szűcs, P., Hegedűs, K., Bakk, E., Gajtkó, A., Wéber, I., & Holló, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111408 · Cited by 17
“, in neurons and in the glial cells of the nervous system) [38].”
BackgroundWang, D., Zhang, L., He, D., Zhang, Y., Bao, J., Gao, W., Cheng, W., Zhu, C., Jin, H., Zhang, W., et al. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.154998 · Cited by 17
Anti-neuroinflammatory constituents from the fungus Penicillium purpurogenum MHZ 111
Sun, J., Zhu, Z., Song, Y., Ren, Y., Dong, D., Zheng, J., Liu, T., Zhao, Y., Tu, P., & Li, J. (2016) · Natural Product Research · doi:10.1080/14786419.2016.1207075 · Cited by 17
“Increasing evidence indicate that activated microglia are involved in various neuroinflammatory pathology, resulting in progressive neurodegenerative disorders (Walsh et al. 2014; Yuste et al. 2015).”
BackgroundA Protective Role for Interleukin-1 Signaling during Mouse Adenovirus Type 1-Induced Encephalitis
de Castro-Jorge, L. A., Pretto, C. D., Smith, A., Foreman, O., Carnahan, K. E., & Spindler, K. R. (2016) · Journal of Virology · doi:10.1128/jvi.02106-16 · Cited by 17
“For IL-1 to be in its active form, it needs two signals (13).”
BackgroundNeuroinflammation as a therapeutic target in neurodegenerative diseases
Gordon, R., & Woodruff, T. M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805120-7.00003-8 · Cited by 19
Mazaheri-Tehrani, E., Mohraz, M., Nasi, M., Chester, J., Gaetano, A. D., Tartaro, D. L., SeyedAlinaghi, S., Gholami, M., Biasi, S. D., Gibellini, L., et al. (2020) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/qai.0000000000002588 · Cited by 17
Kim, J. H., Park, J. H., Eisenhut, M., Yu, J., & Shin, J. I. (2016) · Medical Hypotheses · doi:10.1016/j.mehy.2016.05.018 · Cited by 18
“The basic components of this complex are sensor molecules such as the nucleotidebinding and oligomerization domain-like receptors (NLRs) and absent-in-melanoma 2 (AIM2), which can recognize pathogen-associated or danger-associated molecular patterns and the effector molecule procaspase-1 [4].”
BackgroundInfluentialAluminum as a CNS and Immune System Toxin Across the Life Span
Shaw, C. A. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-1370-7_4 · Cited by 17
Zhou, Y., Zhao, D., Yue, R., Khan, S. H., Shah, S. Z. A., Yin, X., Yang, L., Zhang, Z., & Zhou, X. (2015) · Antonie van Leeuwenhoek · doi:10.1007/s10482-015-0475-6 · Cited by 17
“NLRP3 inflammasome activation requires two signals: a priming signal that upregulates the expression of pro-IL-1b and NLRP3 through the nuclear factor-jB (NF-jB) pathway, and a second signal to form an activation platform for caspase-1 (Walsh et al. 2014).”
BackgroundChilders, G. M., Perry, C. A., Blachut, B., Martin, N. P., Bortner, C. D., Sieber, S. O., Li, J., Fessler, M. B., & Harry, G. J. (2021) · Environmental Health Perspectives · doi:10.1289/ehp8314 · Cited by 16
“…and related diseases that cause excessive IL-1b activation and with a loss of immune regulation in common pathologies, such as cancer, cardiometabolic disease, neurological disorders, and diabetes (Dinarello 2011; Franchi et al. 2009; Kaneko et al. 2019; Swanson et al. 2019; Walsh et al. 2014).”
BackgroundFranklin, M. E., Bennett, C., Arboite, M., Álvarez-Ciara, A., Corrales, N., Verdelus, J., Dietrich, W. D., Keane, R. W., Vaccari, J. P. D. R., & Prasad, A. (2023) · Biomaterials · doi:10.1016/j.biomaterials.2023.122102 · Cited by 17
Inflammasomes in stroke: a triggering role for acid‐sensing ion channels
Vats, K., Sarmah, D., Kaur, H., Wanve, M., Kalia, K., Borah, A., Dave, K. R., Yavagal, D. R., & Bhattacharya, P. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13852 · Cited by 16
Miller, A. D., & Zachary, J. F. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-35775-3.00014-x · Cited by 16
Inflammasome activation and assembly in Huntington’s disease
Furlam, T. D. O., Roque, I. G., da Silva, E. W. M., Vianna, P. P., Valadão, P. A. C., Guatimosim, C., Teixeira, A. L., & de Miranda, A. S. (2022) · Molecular Immunology · doi:10.1016/j.molimm.2022.09.002 · Cited by 16
Kuwahara‐Otani, S., Maeda, S., Kobayashi, K., Minato, Y., Tanaka, K., Yamanishi, K., Hata, M., Li, W., Hayakawa, T., Noguchi, K., et al. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.03.051 · Cited by 16
di Michele, F., Talamo, A., Niolu, C., & Siracusano, A. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200406090051 · Cited by 16
Samadianzakaria, A., Abdolmaleki, Z., & Faedmaleki, F. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.10.002 · Cited by 15
Kaur, B., Biby, S., Namme, J. N., More, S., Xu, Y., & Zhang, S. (2024) · Advances in pharmacology · doi:10.1016/bs.apha.2024.10.004 · Cited by 15
Li, D., Liu, S., Lu, X., Gong, Z., Wang, H., Xia, X., Lu, F., Jiang, J., Zhang, Y., Xu, G., et al. (2024) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70130 · Cited by 15
Pacheco, A. D. O. L., Vicentini, G., Matteucci, K. C., Rosa‐Ribeiro, R., Weinlich, R., & Bortoluci, K. R. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.4ab1118-416rr · Cited by 16
Yuan, G., Chen, B., Meng, Y., Lu, J., Shi, X., Hu, A., Hu, Y., & Wang, D. (2021) · Molecular Medicine Reports · doi:10.3892/mmr.2021.12378 · Cited by 15
Pereira, A. C., Madeira, N. G. G. F., Morais, S., Macedo, A., Cruz, M. T., & Pereira, C. (2022) · Cells · doi:10.3390/cells11030433 · Cited by 16
An Update On Medical Treatment for Intracerebral Hemorrhage
Li, X., Feng, D., & Chen, G. (2018) · Translational Stroke Research · doi:10.1007/s12975-018-0664-5 · Cited by 15
Pyroptosis in Spinal Cord Injury: Implications for Pathogenesis and Therapeutic Approaches
Gu, G., Yu, H., Zou, H., Kou, W., Zhang, P., Gu, G., Lu, J., Shi, W., Chu, P., Zhang, Y., et al. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2906210 · Cited by 14
ADAM8 Activates NLRP3 Inflammasome to Promote Cerebral Ischemia-Reperfusion Injury
Lu, H., Meng, Y., Han, X., & Zhang, W. (2021) · Journal of Healthcare Engineering · doi:10.1155/2021/3097432 · Cited by 14
“1e innate immunity is closely related to inflammatory processes and predominate in various viral and bacterial infections [10].”
BackgroundRetractedTherapeutic potential of baicalein against neurodegenerative diseases: An updated review
Siddiqui, N., Talib, M., Tripathi, P. N., Kumar, A., & Sharma, A. K. (2024) · Health Sciences Review · doi:10.1016/j.hsr.2024.100172 · Cited by 15
Zhang, Y., Li, S., Hou, L., Wu, M., Liu, J., Wang, R., Wang, Q., & Zhao, J. (2023) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2023.116497 · Cited by 15
Wang, W., Pang, C., Zhang, J., Peng, L., Zhang, X., Shi, L., & Zhang, H. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1266315 · Cited by 14
Shiraishi, Y., Kimura, A., Kimura, H. J., Ohmori, T., Takahashi, M., & Takeshita, K. (2020) · Journal of Orthopaedic Science · doi:10.1016/j.jos.2020.04.006 · Cited by 14
Inflammasome Signaling Regulates the Microbial–Neuroimmune Axis and Visceral Pain in Mice
Aguilera, M., Rossini, V., Hickey, A., Simnica, D., Grady, F., Felice, V. D., Moloney, A., Pawley, L. C., Fanning, A., McCarthy, L., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158336 · Cited by 13
Zhao, J., Chen, C., Ge, L., Jiang, Z., Hu, Z., & Yin, L. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1386780 · Cited by 13
Therapeutic Targets in Innate Immunity to Tackle Alzheimer’s Disease
Serradas, M. L., Ding, Y., Martorell, P., Kulińska, I., & Castro‐Gomez, S. (2024) · Cells · doi:10.3390/cells13171426 · Cited by 16
“The NLRP1 downstream pathway stands as the sole exception to the conventional activation of NLRPs, as it, along with the NLRCs, does not require the adapter to interact with pro-caspase 1 [154,156,157].”
BackgroundPei, Y., Cheng, F., Li, W., Yu, Q., Ma, C., Zou, Y., Xu, T., Liu, S., Zhang, S., & Wang, Q. (2021) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2021.11.003 · Cited by 14
Zhao, Y., Zhu, T., Li, H., Zhao, J., & Li, X. (2019) · Clinical Interventions in Aging · doi:10.2147/cia.s223595 · Cited by 13
“39 It has been demonstrated that ischemia-like conditions can increase the level of NLRP inflammasomes and IL-1β.41 Fann et al41 showed that the NLRP1 and NLRP3 inflammasomes play a major role in neuronal cell death and sensorimotor impairment following stroke.”
BackgroundInfluentialAL-Ayadhi, L. Y., Abualnaja, A. A., AlZarroug, A., Alharbi, T., Alhowikan, A. M., Halepoto, D. M., & Al-Mazidi, S. H. (2023) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s408554 · Cited by 12
“The inherent immunity is intimately associated with inflammatory routes and leads to numerous bacterial and viral infections.(17) Researchers have reported several inflammasomes, which play a significant role in the manifestation and progress of different major diseases such as ischemic Parkinson’s disease and stroke.”
BackgroundMahmoudian, M., Lorigooini, Z., Rahimi‐Madiseh, M., Shabani, S., & Amini-Khoei, H. (2024) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-024-03143-2 · Cited by 12
“The change in cytokine profile in ASD patients implies a role of the immune system in the pathophysiology of this disorder (Walsh et al. 2014).”
Zhang, M.-J., Zhou, Y., Wang, X., Xue, C., ., Y. P., Guo, L., Gao, C., Li, J., & Zhang, L. (2016) · Meta Gene · doi:10.1016/j.mgene.2016.06.006 · Cited by 12
“In the central nervous system, microglia, astrocytes and neurons can express receptors for IL-18 and thereby participate in local inflammation associated with many neurological diseases including meningitis, stroke and Alzheimer's disease (Walsh et al., 2014).”
BackgroundNanoparticle-based Caspase Sensors
Maysinger, D., & Hutter, E. (2015) · Nanomedicine · doi:10.2217/nnm.14.158 · Cited by 12
In�vivo effects of the NLRP1/NLRP3 inflammasome pathway on latent respiratory virus infection
Li, Y., Wei, X., Ji, S., Gui, S., & Zhang, S. (2018) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2018.3521 · Cited by 13
Reimers, D., Vallejo-Muñoz, M., Casarejos, M. J., Jiménez‐Escrig, A., Gonzalo‐Gobernado, R., & Bazán, E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22168697 · Cited by 12
“The anti-phagocytic effect of ASC is associated withthe activation of IF, where the molecule recruits procaspase-1, generating active caspase-1 [4,11,13].”
BackgroundYu, X., Yu, C., & He, W. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.952211 · Cited by 15
“NLRP3 inflammasome is associated with numerous CNS disorders, from sterile acute brain injuries to chronic neurodegenerative diseases (Walsh et al., 2014).”
BackgroundSater, A. A. A., & Philpott, D. J. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-374279-7.10020-7 · Cited by 12
Johnson, A. M., Ou, Z.-Y. A., Gordon, R., & Saminathan, H. (2021) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2021.106113 · Cited by 11
Hong, Z., Cheng, J., Ye, Y., Chen, X., & Zhang, F. (2022) · World Neurosurgery · doi:10.1016/j.wneu.2022.08.139 · Cited by 11
Microglial autophagy in cerebrovascular diseases
Chen, M., Zhang, H., Chu, Y., Tang, Y., Pang, X., Qin, C., & Tian, D. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1023679 · Cited by 11
Marín‐Aguilar, F., Ruı́z-Cabello, J., & Cordero, M. D. (2018) · Experientia supplementum · doi:10.1007/978-3-319-89390-7_13 · Cited by 12
Ischemic, Traumatic and Neurodegenerative Brain Inflammatory Changes
Dugue, R., & Barone, F. C. (2016) · Future Neurology · doi:10.2217/fnl.16.5 · Cited by 11
Li, K., Yang, T., Chen, F., Lou, C., Chen, Y., Chen, Z., Lin, Y., Sun, X., Liu, G., Xie, C., et al. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.09.056 · Cited by 11
Tyagi, M., Naik, U. P., Tyagi, K., Sharma, M., Kaushal, G., Bhushan, A., Bukrinsky, M., & Tyagi, P. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27052192 · Cited by 15
“Another emerging contributor is ART-induced mitochondrial and lysosomal dysfunction, which can activate inflammasomes such as NLRP3 and AIM2, thereby sustaining glial activation [192,193].”
Zhang, C., Yang, R., Hao, X., Geng, Z., & Wang, Z. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.114055 · Cited by 10
Wang, J., Wang, Y., Steffani, M., Stöß, C., Ankerst, D. P., Friess, H., Hüser, N., & Hartmann, D. (2022) · Cancers · doi:10.3390/cancers14020447 · Cited by 10
“However, excessively activated pyroptosis aggravated inflammatory response, resulted in liver damage, and even induced the development of liver fibrosis and liver cancer [16].”
BackgroundOxyhemoglobin and Cerebral Blood Flow Transients Detect Infarction in Rat Focal Brain Ischemia
Lückl, J., Baker, W. B., Boda, K., Emri, M., Yodh, A. G., & Greenberg, J. H. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.11.028 · Cited by 9
“, 2015), stimulates microglial cells and inflammasome formation, and activates cytokine gene expression (Jander et al., 2001; Walsh et al., 2014).”
BackgroundDong, Z., Peng, Q., Pan, K., Lin, W., & Wang, Y. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03931-x · Cited by 10
Ox-inflammasome involvement in neuroinflammation
Vallese, A., Cordone, V., Pecorelli, A., & Valacchi, G. (2023) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2023.07.010 · Cited by 13
Ketelauri, P., Scharov, K., von Gall, C., & Johann, S. (2023) · Cells · doi:10.3390/cells12141836 · Cited by 9
“The NOD-like receptor family, including NLRP1, NLRP3, and NLRC4, and absent in melanoma 2 (AIM2) containing a HIN200 and pyrin domain are among the most studied inflammasomes [34,35].”
BackgroundWang, B., Cao, X., Lin, J., Qian, Q., Yu, L., & Qian, Q. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.108683 · Cited by 10
RetractedHuang, R., Hou, L., Ruan, Z., Zhang, D., Sun, W., & Wang, Q. (2020) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2020.109232 · Cited by 10
Edye, M. E., Walker, L. E., Sills, G. J., Allan, S. M., & Brough, D. (2014) · Inflammasome · doi:10.2478/infl-2014-0004 · Cited by 11
“Additionally, neutralisation of the inflammasome adapter protein ASC has been shown to be protective in mouse models of acute sterile brain injury (traumatic brain injury and spinal cord injury) [8] and therefore may provide an additional target for anti-inflammatory AEDs.”
BackgroundLu, Y., Zhang, Z., Chen, H., Wang, M., Mao, W., Hu, J., Zuo, D., Lv, B., Wu, W.-F., Qi, S., et al. (2023) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10590 · Cited by 9
“36,37,44 However, we do not deny that other types of cells also exist in pyrop-tosis and their role in the progression of AIS is still worthy of further study.”
BackgroundHan, X., Fu, X., Guo, W., Liu, Y., Sun, J., Wang, T., & Yang, W. (2024) · Inflammation · doi:10.1007/s10753-024-02190-4 · Cited by 10
“NLRP2 and NLRP3 are expressed in astrocytes [22, 23].”
Zhao, H., Liu, L.-M., Lu, X., Quinonez, A. T., Roberts, R., Zhai, T.-Y., & Liang, C. (2024) · Hearing Research · doi:10.1016/j.heares.2025.109319 · Cited by 9
Exploring the Role of NLRP3 in Neurodegeneration: Cutting‐Edge Therapeutic Strategies and Inhibitors
Mustafa, M. A., Bansal, P., Pallavi, M., Panigrahi, R., Nathiya, D., Kumar, S., Al-Hasnaawei, S., Chauhan, A. S., & Singla, S. (2025) · Developmental Neurobiology · doi:10.1002/dneu.22982 · Cited by 12
“…of danger: pathogen-associated molecular patterns (PAMPs) from infectious agents and damage-associated molecular patterns (DAMPs), which arise from internal cellular stress such as misfolded proteins, peptide aggregates, or misplaced genetic material (Walsh et al. 2014; Singhal et al. 2014).”
Expression of intron-containing HIV-1 RNA induces NLRP1 inflammasome activation in myeloid cells
Jalloh, S., Hughes, I. A., Akiyama, H., Gojanovich, A. D., Quiñones-Molina, A. A., Yang, M., Henderson, A. J., Mostoslavsky, G., & Gummuluru, S. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003320 · Cited by 9
“Additionally, overexpression of recombinant HIV-1 proteins such as gp120, viral protein R (Vpr), viral protein U (Vpu), and transactivator of transcription (Tat) can activate NLRP3 inflammasome and IL-1 β production in myeloid cells [22,45–51].”
Richter, F., Koulen, P., & Kaja, S. (2016) · Scientific Reports · doi:10.1038/srep23481 · Cited by 9
Blewett, N. H., Iben, J., Gaidamakov, S., & Maraia, R. J. (2017) · Molecular and Cellular Biology · doi:10.1128/mcb.00588-16 · Cited by 10
“Astrocytes and microglia are major immune effector cells in the CNS (82, 83).”
BackgroundInfluentialKaneko, N., Iwasaki, T., Ito, Y., Takeda, H., Sawasaki, T., Morikawa, S., Nakano, N., Kurata, M., & Masumoto, J. (2017) · Inflammation and Regeneration · doi:10.1186/s41232-017-0040-y · Cited by 9
“It has been reported to be activated by muramyl dipeptide (MDP), anthrax lethal toxins, and related to neuronal diseases [19].”
Wu, C., & Chen, B. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17030305 · Cited by 9
“The interactions between innate immune cells in the brain have also become better understood in recent years, prompting the realization that each of these cell types contributes to the development of inflammation in the brain [7].”
BackgroundEstrogen preconditioning: A promising strategy to reduce inflammation in the ischemic brain.
Vaccari, J. P. D. R., Bramlett, H. M., Pérez‐Pinzón, M. A., & Raval, A. P. (2019) · PubMed · Cited by 9
Sadier, N. S., Hazimeh, I. A., Khazaal, W., Sabouri, A. A. K. A., Almutary, A. G., Alnuqaydan, A. M., & Abbas, L. A. (2025) · Inflammopharmacology · doi:10.1007/s10787-025-01733-x · Cited by 9
“NLRP3 inhibitors, such as astragaloside IV, Hyperoside, MCC950, itaconate, and BSYZ, significantly decreased the expressions of NLRP3, ASC, cleaved caspase-1, and mature IL-1 in MPTP-induced mice in vivo (Wang et al. 2022; Huang et al. 2021; Mo et al. 2018; Sun et al. 2022; Yang et al. 2019).”
InfluentialLin, C., Chen, Z., Lin, Y., Yang, C., Shi, C., Lin, C.-M., Huang, T. H., Lu, J., Lu, K., & Yang, Y. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157571 · Cited by 8
“Various stimuli, including mitochondrial damage, ATP, K+ efflux, and Ca2+ influx from tissue damage, can trigger NLRP3 activation [9,10].”
Sevoflurane Promotes Neurodegeneration Through Inflammasome Formation in APP/PS1 Mice
Li, G., Wang, Y., Cao, F., Wang, D., Zhou, L., & Jin, Y. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.647136 · Cited by 8
“Activation of the immune system and inflammation play an essential role in cognitive impairment (Walsh et al., 2014).”
BackgroundGao, L., Sun, X., Pan, M.-B., Zhang, W., Zhu, D., Lu, Z., Wang, K., Dong, Y., & Guan, Y. (2023) · Brain Sciences · doi:10.3390/brainsci13060897 · Cited by 8
“Inflammasomes are large multimolecular complexes that function as intracellular sensors for infectious agents and host-derived danger signals that are associated with neurological diseases [5].”
BackgroundMicroglia in the pathogenesis of depression, insomnia and their comorbidity
Liu, F., Guo, D., Gao, T., Diao, M., & Han, Y. (2023) · Brain Behavior and Immunity Integrative · doi:10.1016/j.bbii.2023.100030 · Cited by 8
You, Y., An, D., Wan, Y., Zheng, B.-X., Dai, H., Zhang, S., Zhang, X., Wang, R., Shi, P. D., Jin, M., et al. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-05111-0 · Cited by 9
Xu, A., Huang, F., Chen, E., Zhang, Z., He, Y.-X., Yu, X., & He, G. (2024) · International Journal of Hyperthermia · doi:10.1080/02656736.2024.2382162 · Cited by 8
“Microglia are also considered the main cells in the CNS where pyroptosis occurs [14,15].”
de França, J. S., de Sales-Neto, J. M., Carvalho, D. C. M., Lima, É. D. A., Olegário, T. R., Mendes, R. K. S., Lima-Júnior, C. G., Vasconcellos, M. L. A. A., & Rodrigues‐Mascarenhas, S. (2020) · Inflammation · doi:10.1007/s10753-020-01385-9 · Cited by 8
Reduced expression of inflammasome complex components in cluster headache
Şahin, E., Karaaslan, Z., Şanlı, E., Kahraman, Ö. T., Ulusoy, C. A., Orhan, E. K., Ekizoğlu, E., Küçükali, C. İ., Tüzün, E., & Baykan, B. B. (2022) · Headache The Journal of Head and Face Pain · doi:10.1111/head.14334 · Cited by 8
MacDowell, K. S., Martín‐Hernández, D., Ulecia-Morón, C., Bris, Á. G., Madrigal, J. L. M., García‐Bueno, B., & Caso, J. R. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.107217 · Cited by 8
Molecular Network of NLRP3 Inflammasome Activation- Responsive Genes in a Human Monocyte Cell Line
Kawana, N., Yamamoto, Y., Kino, Y., & Satoh, J. (2014) · Cited by 8
Bakr, N. M., Hashim, N. A., Awad, A., & Sarhan, A. E. M. (2017) · Egyptian Journal of Medical Human Genetics · doi:10.1016/j.ejmhg.2017.08.014 · Cited by 8
“nervous system (CNS), microglia, astrocytes and neurons can produce receptors for IL-18, which participated in local inflammation and related with many neurological diseases such as meningitis, Alzheimer’s disease and stroke [14].”
BackgroundAlbornoz, E. A., Amarilla, A. A., Modhiran, N., Parker, S. E., Li, X. X., Wijesundara, D. K., Zamora, A. C. P., McMillan, C. L. D., Liang, B., Peng, N. Y. G., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.11.475947 · Cited by 8
Liu, Y., Qin, K., Jiang, C., Gao, J., Hou, B., & Xie, A. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04373-4 · Cited by 7
Chiarini, A., Armato, U., Gui, L., Yin, M., Chang, S., & Prà, I. D. (2024) · Brain Research · doi:10.1016/j.brainres.2024.149283 · Cited by 7
“Among them, NLPR2 predominates, followed in decreasing order by NLRP3, NLRP4, and PYHIN AIM2 (absent in melanoma 2) (Minkiewicz et al., 2013; Walsh et al., 2014).”
Characterizing stroke-related cellular changes in the surviving neurons of mouse ischemic stroke
Ikegami, T., Sasaki, T., Shimbo, T., Kitayama, T., Yamamoto, Y., Ouchi, Y., Yamazaki, S., Sugiyama, S., Nishiyama, K., Gon, Y., et al. (2025) · Neurochemistry International · doi:10.1016/j.neuint.2025.106086 · Cited by 6
Melatonin Alters the miRNA Transcriptome of Inflammasome Activation in Murine Microglial Cells
Tarakcioglu, E., Tastan, B., Arioz, B. I., Tüfekçi, K. U., & Genç, Ş. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03674-1 · Cited by 7
Therapeutic targeting of neuroinflammation in methamphetamine use disorder
Jeffery, N., Mock, P. Y., Yang, K., Tham, C. L., Israf, D. A., Li, H., Wang, X., & Lam, K. W. (2024) · Future Medicinal Chemistry · doi:10.1080/17568919.2024.2447226 · Cited by 7
MicroRNAs as regulators of NLRP3 inflammasome activation in herpes simplex virus type 2 infection
Dass, D., Banerjee, A., More, A. N., & Mukherjee, A. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1602965 · Cited by 6
Blood–spinal cord barrier disruption after spinal cord injury: a time-dependent mechanistic review
Jiang, Z. G., Zhang, C., Zhao, Z., & Ning, B. (2026) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2026.1805529 · Cited by 6
“Importantly, it should be noted that inflammatory corpuscles have been observed in various types of neurons, including those found in spinal cord injury lesions (de Rivero Vaccari et al., 2012; de Rivero Vaccari et al., 2016; Tan et al., 2015; Walsh et al., 2014).”
Cachón-González, M. B., Zhao, C., Franklin, R. J. M., & Cox, T. M. (2022) · Human Molecular Genetics · doi:10.1093/hmg/ddac299 · Cited by 6
“An idea supported by the recent discovery that the canonical inflammasome Nlrp3 (nucleotide-binding leucine-rich repeat receptor family member pyrin-domain containing) is activated in diverse lysosomal disorders, Gaucher disease (30) and mucopolysaccharidosis type IIIA (MPSIIIA) (31), caused by defects in glucosylcera…”
BackgroundA Neuroprimer: Principles of Central Nervous System Immunity
Owens, G. P. (2017) · Seminars in Pediatric Neurology · doi:10.1016/j.spen.2017.08.004 · Cited by 8
Pathways Driving Neuroprogression in Depression: The Role of Immune Activation
Oriolo, G., Grande, I., Martín‐Santos, R., Vieta, E., & Carvalho, A. F. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811073-7.00010-6 · Cited by 6
Mammadova, N., Greenlee, M. H. W., Moore, S. J., Sakaguchi, D. S., & Greenlee, J. J. (2020) · American Journal Of Pathology · doi:10.1016/j.ajpath.2020.03.006 · Cited by 6
Caspase 1 activity influences juvenile Batten disease ( CLN 3) pathogenesis
Burkovetskaya, M. E., Bosch, M. E., Karpuk, N., Fallet, R. W., & Kielian, T. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14480 · Cited by 7
Synthesis of deuterium-labelled analogues of NLRP3 inflammasome inhibitor MCC950
Salla, M., Butler, M. S., Massey, N. L., Reid, J. C., Cooper, M. A., & Robertson, A. A. B. (2017) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2017.12.054 · Cited by 7
Myers, M. G., & Toal, C. B. (1995) · PubMed · Cited by 6
Tang, X., Zheng, N., Lin, Q., You, Y., Gong, Z., Zhuang, Y., Wu, J., Wang, Y., Huang, H., Ke, J., et al. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01922 · Cited by 6
“Current evidence suggests that pyroptosis is critically involved in several disorders of central nervous system diseases, including traumatic spinal cord injury, hemorrhagic stroke, and Alzheimer’s disease (Walsh et al., 2014; Mamik and Power, 2017; Chen et al., 2020).”
The pterocarpanquinone LQB 118 inhibits inflammation triggered by zymosan in vivo and in vitro
Lima, É. D. A., Silva, L. H. A. C., Carvalho, D. C. M., Netto, C. D., Costa, P. R. R., & Rodrigues‐Mascarenhas, S. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.106399 · Cited by 5
Yap, J. K. Y., Pickard, B. S., Gan, S. Y., & Chan, E. W. L. (2021) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2021.106014 · Cited by 6
“The roles of 82 inflammasomes, especially NLR family pyrin domain-containing 3 (NLRP3), in AD have 83 been widely implicated in glial cells, but not in neurons (Tan et al., 2013).”
MethodInfluentialElectroacupuncture alleviates cognitive dysfunction and neuronal pyroptosis in septic mice
Li, Y., Li, Z., He, F., Qin, C., Fan, R., Zhang, F., & Wang, B. (2022) · Acupuncture in Medicine · doi:10.1177/09645284221117847 · Cited by 5
Metadata
- Authors
- Walsh, J. G., Muruve, D. A., & Power, C.
- Affiliations
- University of Alberta (CA)
- University of Calgary (CA)
- Corresponding author
- Power, Christopher
- Venue
- Nature Reviews Neuroscience
- Published
- 2014-01-08
- Volume
- 15
- Issue
- 2
- Pages
- 84-97
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W1981649246
- Cited by
- 637
- References
- 149
- Citations by year
- 2026: 25 · 2025: 18 · 2024: 46 · 2023: 49 · 2022: 77 · 2021: 67 · 2020: 76 · 2019: 58 · 2018: 51 · 2017: 47 · 2016: 57 · 2015: 43 · 2014: 22
- FWCI
- 5.34
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- inflammasome, central nervous system, caspase-1, IL-1β, IL-18, pyroptosis, microglia, macrophages, neurological disorders, meningitis, stroke, Alzheimer's disease, innate immunity, damage-associated molecular patterns
- MeSH terms
- Animals, Central Nervous System, Humans, Macrophages, Nervous System Diseases, Neuroglia, Inflammasomes
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review