MicroRNAs: New Regulators of Toll-Like Receptor Signalling Pathways

MicroRNAs: Target Recognition and Regulatory Functions

Bartel, D. P. (2009) · Cell · doi:10.1016/j.cell.2009.01.002 · Cited by 20,068

Untitled work

(2008) · doi:10.1038/nrg2290 · Cited by 5,199

NF-κB-dependent induction of microRNA miR-146, an inhibitor targeted to signaling proteins of innate immune responses

Taganov, K. D., Boldin, M. P., Chang, K.-J., & Baltimore, D. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605298103 · Cited by 4,317

Cellular and Molecular Immunology

Abbas, A. K., Lichtman, A. H., & Pillai, S. S. (1994) · Cited by 3,571

Regulation of mRNA Translation and Stability by microRNAs

Fabian, M. R., Sonenberg, N., & Filipowicz, W. (2010) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-060308-103103 · Cited by 3,214

MicroRNA-155 is induced during the macrophage inflammatory response

O'Connell, R. M., Taganov, K. D., Boldin, M. P., Cheng, G., & Baltimore, D. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610731104 · Cited by 1,866

Identification of Virus-Encoded MicroRNAs

Pfeffer, S., Zavolan, M., Grässer, F., Chien, M.-C., Russo, J., Ju, J.-Y., John, B., Enright, A., Marks, D., Sander, C., et al. (2004) · Science · doi:10.1126/science.1096781 · Cited by 1,708

Signaling in innate immunity and inflammation

Newton, K., & Dixit, V. M. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a006049 · Cited by 1,513

Regulation of the Germinal Center Response by MicroRNA-155

Thai, T., Calado, D. P., Casola, S. S., Ansel, K. M., Xiao, C., Xue, Y., Murphy, A. J., Frendewey, D. A., Valenzuela, D. M., Kutok, J. L., et al. (2007) · Science · doi:10.1126/science.1141229 · Cited by 1,477

MicroRNAs bind to Toll-like receptors to induce prometastatic inflammatory response

Fabbri, M., Paone, A., Calore, F., Galli, R., Gaudio, E., Santhanam, R., Lovat, F., Fadda, P., Mao, C., Nuovo, G. J., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1209414109 · Cited by 1,434

Transition from inflammation to proliferation: a critical step during wound healing

Landén, N. X., Li, D., & Ståhle, M. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2268-0 · Cited by 1,980

LPS-preconditioned mesenchymal stromal cells modify macrophage polarization for resolution of chronic inflammation via exosome-shuttled let-7b

Ti, D., Hao, H., Tong, C., Liu, J., Dong, L., Zheng, J., Zhao, Y., Liu, H., Fu, X., & Han, W. (2015) · Journal of Translational Medicine · doi:10.1186/s12967-015-0642-6 · Cited by 664

Toll-like receptors activation, signaling, and targeting: an overview

El-Zayat, S. R., Sibaii, H., & Mannaa, F. A. E. (2019) · Bulletin of the National Research Centre/Bulletin of the National Research Center · doi:10.1186/s42269-019-0227-2 · Cited by 603

Regulating IRFs in IFN Driven Disease

Jefferies, C. A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00325 · Cited by 364

Inhibition of Toll-Like Receptor Signaling as a Promising Therapy for Inflammatory Diseases: A Journey from Molecular to Nano Therapeutics

Gao, W., Xiong, Y., Li, Q., & Yang, H. Y. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00508 · Cited by 372

Advances in the role of STAT3 in macrophage polarization

Xia, T., Zhang, M., Lei, W., Yang, R., Fu, S.-P., Fan, Z., Yang, Y., & Zhang, T. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1160719 · Cited by 306

MicroRNAs: new players in IBD

Kalla, R., Ventham, N. T., Kennedy, N. A., Quintana, J. F., Nimmo, E. R., Buck, A. H., & Satsangi, J. (2014) · Gut · doi:10.1136/gutjnl-2014-307891 · Cited by 281

The Anti-Inflammatory Properties of Phytochemicals and Their Effects on Epigenetic Mechanisms Involved in TLR4/NF-κB-Mediated Inflammation

Saleh, H. A., Yousef, M. H., & Abdelnaser, A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.606069 · Cited by 269

Circulating microRNAs as Potential Biomarkers of Infectious Disease

Correia, C. N., Nalpas, N., McLoughlin, K. E., Browne, J. A., Gordon, S. V., MacHugh, D. E., & Shaughnessy, R. G. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00118 · Cited by 245

Toll-like receptors and chronic inflammation in rheumatic diseases: new developments

Joosten, L. A. B., Abdollahi‐Roodsaz, S., Dinarello, C. A., O'Neill, L. A. J., & Netea, M. G. (2016) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2016.61 · Cited by 208

Human urine-derived stem cells protect against renal ischemia/reperfusion injury in a rat model via exosomal miR-146a-5p which targets IRAK1

Li, X., Liao, J., Su, X., Li, W., Bi, Z., Wang, J., Su, Q., Huang, H., Wei, Y., Gao, Y., et al. (2020) · Theranostics · doi:10.7150/thno.42153 · Cited by 194

Neuroinflammatory targets and treatments for epilepsy validated in experimental models

Aronica, E., Bauer, S., Bozzi, Y., Caleo, M., Dingledine, R. J., Gorter, J. A., Henshall, D. C., Kaufer, D., Koh, S., Löscher, W., et al. (2017) · Epilepsia · doi:10.1111/epi.13783 · Cited by 194

Kupffer Cells

Slevin, E., Baiocchi, L., Wu, N., Ekser, B., Sato, K., Lin, E. P.-Y., Ceci, L., Chen, L., Ramos‐Lorenzo, S., Xu, W., et al. (2020) · American Journal Of Pathology · doi:10.1016/j.ajpath.2020.08.014 · Cited by 173

Exploring New Inflammatory Biomarkers and Pathways during LPS-Induced M1 Polarization

Cunha, C., Gomes, C., Vaz, A. R., & Brites, D. (2016) · Mediators of Inflammation · doi:10.1155/2016/6986175 · Cited by 153

NLRP3 Inflammasome at the Interface of Inflammation, Endothelial Dysfunction, and Type 2 Diabetes

Góra, I. M., Ciechanowska, A., & Ładyżyński, P. (2021) · Cells · doi:10.3390/cells10020314 · Cited by 159

Comprehensive Molecular Profiles of Functionally Effective MSC-Derived Extracellular Vesicles in Immunomodulation

Kim, H., Lee, M. J., Bae, E., Ryu, J. S., Kaur, G., Kim, H. J., Kim, J. Y., Barreda, H., Jung, S. Y., Choi, J. M., et al. (2020) · Molecular Therapy · doi:10.1016/j.ymthe.2020.04.020 · Cited by 149

Toll-like receptor-guided therapeutic intervention of human cancers: molecular and immunological perspectives

Mukherjee, S., Patra, R., Behzadi, P., Masotti, A., Paolini, A., & Sarshar, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1244345 · Cited by 158

Activation of TLR2 and TLR6 by Dengue NS1 Protein and Its Implications in the Immunopathogenesis of Dengue Virus Infection

Chen, J., Ng, M. L., & Chu, J. J. H. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005053 · Cited by 134

MicroRNA let-7 and viral infections: focus on mechanisms of action

Letafati, A., Najafi, S., Mottahedi, M., Karimzadeh, M., Shahini, A., Garousi, S., Abbasi‐Kolli, M., Nahand, J. S., Zadeh, S. S. T., Hamblin, M. R., et al. (2022) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-022-00317-9 · Cited by 137

Evolutionary Parasitology

Schmid‐Hempel, P. (2021) · doi:10.1093/oso/9780198832140.001.0001 · Cited by 137

Regulation of Endotoxin Tolerance and Compensatory Anti-inflammatory Response Syndrome by Non-coding RNAs

Vergadi, E., Vaporidi, K., & Tsatsanis, C. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02705 · Cited by 124

Toll-Like Receptor Function in Acute Wounds

Chen, L., & DiPietro, L. A. (2017) · Advances in Wound Care · doi:10.1089/wound.2017.0734 · Cited by 121

Acupuncture Attenuates Inflammation in Microglia of Vascular Dementia Rats by Inhibiting miR-93-Mediated TLR4/MyD88/NF-κB Signaling Pathway

Wang, L., Yang, J., Lin, L.-T., Huang, J., Wang, X., Su, X.-T., Cao, Y., Fisher, M., & Liu, C. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/8253904 · Cited by 117

Potential Roles of Exosomal MicroRNAs as Diagnostic Biomarkers and Therapeutic Application in Alzheimer’s Disease

Chen, J.-J., Zhao, B., Zhao, J., & Li, S. (2017) · Neural Plasticity · doi:10.1155/2017/7027380 · Cited by 93

Modulation of endothelial function by Toll like receptors

Salvador, B., Arranz, A., Francisco, S., Córdoba, L., Punzón, C., Llamas, M. Á., & Fresno, M. (2016) · Pharmacological Research · doi:10.1016/j.phrs.2016.03.038 · Cited by 107

miRNA regulation of innate immunity

Momen‐Heravi, F., & Bala, S. (2018) · Journal of Leukocyte Biology · doi:10.1002/jlb.3mir1117-459r · Cited by 105

Toll-Like Receptors and Prostate Cancer

Zhao, S., Zhang, Y., Zhang, Q., Wang, F., & Zhang, D. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00352 · Cited by 103

Collaborative Action of Toll-Like and Nod-Like Receptors as Modulators of the Inflammatory Response to Pathogenic Bacteria

Oviedo-Boyso, J., Bravo-Patiño, A., & Baizabal-Aguirre, V. M. (2014) · Mediators of Inflammation · doi:10.1155/2014/432785 · Cited by 101

MicroRNA-3570 Modulates the NF-κB Pathway in Teleost Fish by Targeting MyD88

Chu, Q., Sun, Y., Cui, J., & Xu, T. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1602064 · Cited by 92

Interplay Between Exosomes, microRNAs and Toll-Like Receptors in Brain Disorders

Paschon, V., Takada, S. H., Ikebara, J. M., de Sousa, É., Raeisossadati, R., Ulrich, H., & Kihara, A. H. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9142-1 · Cited by 95

Effect of age on pro-inflammatory miRNAs contained in mesenchymal stem cell-derived extracellular vesicles

Fafián‐Labora, J., Lesende‐Rodriguez, I., Fernández‐Pernas, P., Sangiao‐Alvarellos, S., Monserrat, L., Arntz, O. J., van de Loo, F. A. J., Mateos, J., & Arufe, M. C. (2017) · Scientific Reports · doi:10.1038/srep43923 · Cited by 92

Downregulated Glia Interplay and Increased miRNA-155 as Promising Markers to Track ALS at an Early Stage

Cunha, C., Santos, C., Gomes, C., Fernandes, A. M. A., Correia, A. M., Sebastião, A. M., Vaz, A. R., & Brites, D. M. T. O. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0631-2 · Cited by 88

Mice with miR-146a deficiency develop severe gouty arthritis via dysregulation of TRAF 6, IRAK 1 and NALP3 inflammasome

Zhang, Q., Qing, Y., Yin, C., Zhou, L., Liu, X., Mi, Q., & Zhou, J. (2018) · Arthritis Research & Therapy · doi:10.1186/s13075-018-1546-7 · Cited by 81

Maternal aryl hydrocarbon receptor activation protects newborns against necrotizing enterocolitis

Lü, P., Yamaguchi, Y., Fulton, W. B., Wang, S., Zhou, Q., Jia, H., Kovler, M. L., Salazar, A. G., Sampah, M. E., Prindle, T., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21356-4 · Cited by 79

MicroRNA 181b‐3p and its target importin α5 regulate toll‐like receptor 4 signaling in Kupffer cells and liver injury in mice in response to ethanol

Saikia, P., Bellos, D., McMullen, M. R., Pollard, K. A., de la Motte, C., & Nagy, L. E. (2017) · Hepatology · doi:10.1002/hep.29144 · Cited by 81

Inducible microRNA-214 contributes to the suppression of NF-κB-mediated inflammatory response via targeting myd88 gene in fish

Chu, Q., Sun, Y., Cui, J., & Xu, T. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.777078 · Cited by 80

Aberrant Expression of Intracellular let-7e, miR-146a, and miR-155 Correlates with Severity of Depression in Patients with Major Depressive Disorder and Is Ameliorated after Antidepressant Treatment

Hung, Y.-Y., Wu, M., Tsai, M.-C., Huang, Y., & Kang, H. (2019) · Cells · doi:10.3390/cells8070647 · Cited by 81

Anti-Inflammatory Effect of Exercise Mediated by Toll-Like Receptor Regulation in Innate Immune Cells – A Review

Collao, N., Rada, I., Francaux, M., Deldicque, L., & Zbinden‐Foncea, H. (2019) · International Reviews of Immunology · doi:10.1080/08830185.2019.1682569 · Cited by 79

Toll-Like Receptor-4 Signaling Drives Persistent Fibroblast Activation and Prevents Fibrosis Resolution in Scleroderma

Bhattacharyya, S., Midwood, K. S., Yin, H. H., & Varga, J. (2017) · Advances in Wound Care · doi:10.1089/wound.2017.0732 · Cited by 75

Bacterial Infection Drives the Expression Dynamics of microRNAs and Their isomiRs

Siddle, K. J., Tailleux, L., Deschamps, M., Loh, Y. E., Deluen, C., Gicquel, B., Antoniewski, C., Barreiro, L. B., Farinelli, L., & Quintana‐Murci, L. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005064 · Cited by 75

Mechanistic Actions of microRNAs in Diabetic Wound Healing

Petkovic, M., Sørensen, A. E., Leal, E. C., Carvalho, E., & Dalgaard, L. T. (2020) · Cells · doi:10.3390/cells9102228 · Cited by 74

Visfatin Promotes IL-6 and TNF-α Production in Human Synovial Fibroblasts by Repressing miR-199a-5p through ERK, p38 and JNK Signaling Pathways

Wu, M., Tsai, C., Huang, Y., Fong, Y., & Tang, C. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19010190 · Cited by 72

Staphylococcus aureus: an underestimated factor in the pathogenesis of atopic dermatitis?

Blicharz, L., Rudnicka, L., & Samochocki, Z. (2019) · Advances in Dermatology and Allergology · doi:10.5114/ada.2019.82821 · Cited by 70

The Inducible microRNA-21 Negatively Modulates the Inflammatory Response in Teleost Fish via Targeting IRAK4

Chu, Q., Yan, X., Liu, L., & Xu, T. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01623 · Cited by 70

MicroRNA regulation of Toll-like receptor signaling pathways in teleost fish

Zhou, Z., Lin, Z., Pang, X., Shan, P., & Wang, J. (2018) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2018.01.036 · Cited by 68

Exposure to environmentally relevant concentrations of deltamethrin renders the Chinese rare minnow (Gobiocypris rarus) vulnerable to Pseudomonas fluorescens infection

Zhang, L., Hong, X., Zhao, X., Yan, S., Ma, X., & Zha, J. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.136943 · Cited by 68

TLR4 signaling in the development of colitis-associated cancer and its possible interplay with microRNA-155

Guo, J., Liao, M., & Wang, J. (2021) · Cell Communication and Signaling · doi:10.1186/s12964-021-00771-6 · Cited by 66

Expression of microRNAs miR21, miR146a, and miR155 in tuberous sclerosis complex cortical tubers and their regulation in human astrocytes and SEGA‐derived cell cultures

van Scheppingen, J., Iyer, A. M., Prabowo, A. S., Mühlebner, A., Anink, J. J., Scholl, T., Feucht, M., Jansen, F. E., Spliet, W. G., Krsek, P., et al. (2016) · Glia · doi:10.1002/glia.22983 · Cited by 60

LPS Tolerance Inhibits Cellular Respiration and Induces Global Changes in the Macrophage Secretome

Gillen, J., Ondee, T., Gurusamy, D., Issara-Amphorn, J., Manes, N. P., Yoon, S. H., Leelahavanichkul, A., & Nita‐Lazar, A. (2021) · Biomolecules · doi:10.3390/biom11020164 · Cited by 59

MicroRNAs: Novel Players in the Dialogue between Pancreatic Islets and Immune System in Autoimmune Diabetes

Ventriglia, G., Nigi, L., Sebastiani, G., & Dotta, F. (2015) · BioMed Research International · doi:10.1155/2015/749734 · Cited by 58

miR-192 targeting IL-1RI regulates the immune response in miiuy croaker after pathogen infection in vitro and in vivo

Chu, Q., & Xu, T. (2016) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2016.05.007 · Cited by 58

MicroRNA-148 as a negative regulator of the common TLR adaptor mediates inflammatory response in teleost fish

Chu, Q., Gao, Y., Bi, D., & Xu, T. (2017) · Scientific Reports · doi:10.1038/s41598-017-04354-9 · Cited by 56

MicroRNA regulation of Toll‐like receptor, RIG‐I‐like receptor and Nod‐like receptor pathways in teleost fish

Chu, Q., & Xu, T. (2020) · Reviews in Aquaculture · doi:10.1111/raq.12428 · Cited by 56

Specific and selective induction of miR-124 in immune cells by the quinoline ABX464: a transformative therapy for inflammatory diseases

Tazi, J., Begon‐Pescia, C., Campos, N., Apolit, C., Garcel, A., & Scherrer, D. (2020) · Drug Discovery Today · doi:10.1016/j.drudis.2020.12.019 · Cited by 53

miR-146a is essential for lipopolysaccharide (LPS)-induced cross-tolerance against kidney ischemia/reperfusion injury in mice

Dai, Y., Jia, P., Fang, Y., Liu, H., Jiao, X., He, C., & Ding, X. (2016) · Scientific Reports · doi:10.1038/srep27091 · Cited by 55

Curcumin primed exosomes reverses LPS‐induced pro‐inflammatory gene expression in buffalo granulosa cells

Vashisht, M., Rani, P., SUNITA, S., Onteru, S. K., & Singh, D. (2017) · Journal of Cellular Biochemistry · doi:10.1002/jcb.26309 · Cited by 52

Recent findings regarding let-7 in immunity

Jiang, S. (2018) · Cancer Letters · doi:10.1016/j.canlet.2018.07.027 · Cited by 51

Deep sequencing and miRNA profiles in alcohol-induced neuroinflammation and the TLR4 response in mice cerebral cortex

Ureña‐Peralta, J. R., Alfonso‐Loeches, S., Cuesta-Diaz, C. M., Garcia‐García, F., & Guerri, C. (2018) · Scientific Reports · doi:10.1038/s41598-018-34277-y · Cited by 50

Association of MiR-146a Expression and Type 2 Diabetes Mellitus: A Meta-Analysis.

Alipoor, B., Ghaedi, H., Meshkani, R., Torkamandi, S., Saffari, S., Iranpour, M., & Omrani, M. D. (2017) · Europe PMC (PubMed Central) · doi:10.22088/acadpub.bums.6.3.156 · Cited by 48

Circulating plasma microRNAs dysregulation and metabolic endotoxemia induced by a high-fat high-saturated diet

Quintanilha, B. J., Ferreira, L. R. P., Ferreira, F. M., Cunha‐Neto, E., Sampaio, G. R., & Rogero, M. M. (2019) · Clinical Nutrition · doi:10.1016/j.clnu.2019.02.042 · Cited by 52

Candida albicans Induces Cross-Kingdom miRNA Trafficking in Human Monocytes To Promote Fungal Growth

Halder, L. D., Babych, S., Palme, D. I., Mansouri-Ghahnavieh, E., Ivanov, L., Ashonibare, V. J., Langenhorst, D., Prusty, B. K., Rambach, G., Wich, M., et al. (2022) · mBio · doi:10.1128/mbio.03563-21 · Cited by 48

Emerging roles of microRNAs in the regulation of Toll-like receptor (TLR)-signaling

Banerjee, S. (2020) · Frontiers in bioscience · doi:10.2741/4917 · Cited by 47

Hyaluronic acid 35 normalizes TLR4 signaling in Kupffer cells from ethanol-fed rats via regulation of microRNA291b and its target Tollip

Saikia, P., Roychowdhury, S., Bellos, D., Pollard, K. A., McMullen, M. R., McCullough, R. L., McCullough, A. J., Gholam, P. M., de la Motte, C., & Nagy, L. E. (2017) · Scientific Reports · doi:10.1038/s41598-017-15760-4 · Cited by 46

miRNA-133 augments coelomocyte phagocytosis in bacteria-challenged Apostichopus japonicus via targeting the TLR component of IRAK-1 in vitro and in vivo

Meng, L., Zhang, P., Li, C., Lv, Z., Zhang, W., & Jin, C.-H. (2015) · Scientific Reports · doi:10.1038/srep12608 · Cited by 45

Leptin Induces Oncostatin M Production in Osteoblasts by Downregulating miR-93 through the Akt Signaling Pathway

Yang, W., Tsai, C., Fong, Y., Huang, Y., Wang, S.-J., Chang, Y.-S., & Tang, C. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms150915778 · Cited by 45

Aberrant MicroRNAomics in Pulmonary Complications: Implications in Lung Health and Diseases

Dutta, R. K., Chinnapaiyan, S., & Unwalla, H. J. (2019) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2019.09.007 · Cited by 45

Altered MicroRNA Expression Is Responsible for the Pro‐Osteogenic Phenotype of Interstitial Cells in Calcified Human Aortic Valves

Song, R., Fullerton, D. A., Ao, L., Zhao, K., Reece, T. B., Cleveland, J. C., & Meng, X. (2017) · Journal of the American Heart Association · doi:10.1161/jaha.116.005364 · Cited by 45

A Review of Macrophage MicroRNAs’ Role in Human Asthma

Feketea, G. M., Bocșan, I. C., Popescu, C., Găman, M., Stanciu, L. A., & Zdrenghea, M. (2019) · Cells · doi:10.3390/cells8050420 · Cited by 46

Down-regulation of miR-144 elicits proinflammatory cytokine production by targeting toll-like receptor 2 in nonalcoholic steatohepatitis of high-fat-diet-induced metabolic syndrome E3 rats

Li, D., Wang, X., Lan, X., Li, Y., Liu, L., Yi, J., Li, J., Sun, Q., Wang, Y., Li, H., et al. (2014) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2014.12.007 · Cited by 41

Impact of Polyunsaturated Fatty Acids on miRNA Profiles of Monocytes/Macrophages and Endothelial Cells—A Pilot Study

Roessler, C., Kuhlmann, K., Hellwing, C., Leimert, A., & Schumann, J. E. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18020284 · Cited by 41

Innate and adaptive immune response in stroke: Focus on epigenetic regulation

Picascia, A., Grimaldi, V., Iannone, C., Soricelli, A., & Claudio Napoli, A. (2015) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2015.10.013 · Cited by 40

MicroRNAs associated with inflammation in shoulder tendinopathy and glenohumeral arthritis

Thankam, F. G., Boosani, C. S., Dilisio, M. F., & Agrawal, D. K. (2017) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-017-3097-7 · Cited by 40

The rs2910164 variant is associated with reduced miR-146a expression but not cytokine levels in patients with type 2 diabetes

Alipoor, B., Ghaedi, H., Meshkani, R., Omrani, M. D., Sharifi, Z., & Golmohammadi, T. (2017) · Journal of Endocrinological Investigation · doi:10.1007/s40618-017-0766-z · Cited by 40

MiR-146a down-regulates inflammatory response by targeting TLR3 and TRAF6 in Coxsackievirus B infection

Fei, Y., Chaulagain, A., Wang, T., Chen, Y., Liu, J., Yi, M., Wang, Y., Huang, Y., Lin, L., Chen, S., et al. (2019) · RNA · doi:10.1261/rna.071985.119 · Cited by 40

Differential expression and clinical significance of three inflammation-related microRNAs in gangliogliomas

Prabowo, A. S., van Scheppingen, J., Iyer, A. M., Anink, J. J., Spliet, W. G. M., van Rijen, P. C., Meeteren, A. Y. N. S., & Aronica, E. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0315-7 · Cited by 38

miR-200a-3p regulates TLR1 expression in bacterial challenged miiuy croaker

Wang, Y., Xu, G., Han, J., & Xu, T. (2016) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2016.06.004 · Cited by 37

Resolvin D2 decreases TLR4 expression to mediate resolution in human monocytes

Croasdell, A., Sime, P. J., & Phipps, R. P. (2016) · The FASEB Journal · doi:10.1096/fj.201600375r · Cited by 36

Interleukin-8, CXCL1, and MicroRNA miR-146a Responses to Probiotic Escherichia coli Nissle 1917 and Enteropathogenic E. coli in Human Intestinal Epithelial T84 and Monocytic THP-1 Cells after Apical or Basolateral Infection

Sabharwal, H., Cichon, C., Ölschläger, T., Sonnenborn, U., & Schmidt, M. A. (2016) · Infection and Immunity · doi:10.1128/iai.00402-16 · Cited by 36

MicroRNAs in shaping the resolution phase of inflammation

Naqvi, R. A., Gupta, M., George, A., & Naqvi, A. R. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.03.019 · Cited by 35

Epigenetic Biomarkers for Human Sepsis and Septic Shock: Insights from Immunosuppression

Beltrán-García, J., Osca-Verdegal, R., Mateo, C. R., Carbonell, N., Ferreres, J., Rodríguez, M. D. P., Mulet, S., García-López, E., Pallardó, F. V., & García‐Giménez, J. L. (2020) · Epigenomics · doi:10.2217/epi-2019-0329 · Cited by 36

Implication of miR-126 and miR-139-5p in Plasmacytoid Dendritic Cell Dysregulation in Systemic Sclerosis

Chouri, E., Wang, M., Hillen, M. R., Angiolilli, C., Silva‐Cardoso, S. C., Wichers, C. G. K., van der Kroef, M., Bekker, C. P. J., Cossu, M., van Bon, L., et al. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10030491 · Cited by 34

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Fuso, A., Iyer, A. M., van Scheppingen, J., Maccarrone, M., Scholl, T., Hainfellner, J. A., Feucht, M., Jansen, F. E., Spliet, W. G. M., Kršek, P., et al. (2016) · Journal of Molecular Neuroscience · doi:10.1007/s12031-016-0750-7 · Cited by 32

Molecular profiling of regulatory T cells in pulmonary sarcoidosis

Kachamakova‐Trojanowska, N., Jaźwa, A., Szade, K., Kasper, Ł., Soja, J., Andrychiewicz, A., Jakieła, B., Plutecka, H., Sanak, M., Józkowicz, A., et al. (2018) · Journal of Autoimmunity · doi:10.1016/j.jaut.2018.07.012 · Cited by 32

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Yang, Q., Zhang, Q., Qing, Y., Zhou, L., Mi, Q., & Zhou, J. (2018) · Arthritis Research & Therapy · doi:10.1186/s13075-018-1550-y · Cited by 32

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Kim, J., Ha, S., Son, M., Kim, D., Kim, M., Kim, B., Kim, D., Chung, H. Y., & Chung, K. W. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01234-w · Cited by 31

GABAAR α2-activated neuroimmune signal controls binge drinking and impulsivity through regulation of the CCL2/CX3CL1 balance

Aurelian, L., & Balan, I. S. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05220-4 · Cited by 31

Toll-like receptor-4 null mutation causes fetal loss and fetal growth restriction associated with impaired maternal immune tolerance in mice

Chan, H. Y., Moldenhauer, L. M., Groome, H. M., Schjenken, J. E., & Robertson, S. A. (2021) · Scientific Reports · doi:10.1038/s41598-021-95213-1 · Cited by 31

TNIP2 mediates GRβ-promoted inflammation and is associated with severity of major depressive disorder

Chiang, T.-I., Hung, Y.-Y., Wu, M., Huang, Y., & Kang, H. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.04.021 · Cited by 29

miR-200 modulates coelomocytes antibacterial activities and LPS priming via targeting Tollip in Apostichopus japonicus

Lv, Z., Li, C., Zhang, P., Wang, Z., Zhang, W., & Jin, C. (2015) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2015.04.014 · Cited by 29

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Zhang, J., Fu, S., Liu, Y., Liu, Y., & Wen-jun, W. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms160922438 · Cited by 27

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Ikehata, N., Takanashi, M., Satomi, T., Watanabe, M., Hasegawa, O., Kono, M., Enomoto, A., Chikazu, D., & Kuroda, M. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.12.098 · Cited by 29

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Armstrong, D. A., Dessaint, J. A., Ringelberg, C. S., Hazlett, H. F., Howard, L., Abdalla, M. A. K., Barnaby, R., Stanton, B. A., Cervinski, M. A., & Ashare, A. (2018) · Journal of Molecular Diagnostics · doi:10.1016/j.jmoldx.2018.04.003 · Cited by 27

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Piotto, C., Julier, Z., & Martino, M. M. (2018) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2018.00098 · Cited by 28

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Li, H., Di, G., Zhang, Y., Xue, R., Zhang, J., & Liang, J. (2019) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2019.11.010 · Cited by 27

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Zebardast, A., Tehrani, S. S., Latifi, T., & Sadeghi, F. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30297 · Cited by 27

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Dong, H., Gao, Q., Peng, X., Sun, Y., Han, T., Zhao, B., Liu, Y., Wang, C., Song, X., Wu, J., et al. (2017) · Frontiers in Veterinary Science · doi:10.3389/fvets.2017.00186 · Cited by 27

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Kronstadt, S. M., Pottash, A. E., Levy, D. H., Wang, S., Chao, W., & Jay, S. M. (2021) · Advanced Therapeutics · doi:10.1002/adtp.202000259 · Cited by 26

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Guillot‐Sestier, M., & Town, T. (2017) · Journal of Neural Transmission · doi:10.1007/s00702-017-1792-x · Cited by 26

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Vaz, A. R., Falcão, A. S., Scarpa, E., Semproni, C., & Brites, D. M. T. O. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.01012 · Cited by 28

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Rashidi, S., Mansouri, R., Ali‐Hassanzadeh, M., Ghani, E., Barazesh, A., Karimazar, M., Nguewa, P., & Silva, E. A. C. (2021) · Parasitology · doi:10.1017/s0031182021001177 · Cited by 25

Review Article MicroRNAs: New Regulators of Toll-Like Receptor Signalling Pathways

He, X., Jing, Z., & Cheng, G. (2016)

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Banerjee, S. (2020) · Frontiers in bioscience · doi:10.2741/4917 · Cited by 47

MicroRNAs: the fine-tuners of Toll-like receptor signalling

O'Neill, L. A. J., Sheedy, F. J., & McCoy, C. E. (2011) · Nature reviews. Immunology · doi:10.1038/nri2957 · Cited by 881

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Bayraktar, R., Bertilaccio, M. T. S., & Calin, G. A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01053 · Cited by 139

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Quinn, S. R., & O'Neill, L. A. (2011) · International Immunology · doi:10.1093/intimm/dxr034 · Cited by 314