Extracellular proteolysis by matrix metalloproteinase-9 drives dendritic spine enlargement and long-term potentiation coordinately

How Matrix Metalloproteinases Regulate Cell Behavior

Sternlicht, M. D., & Werb, Z. (2001) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.17.1.463 · Cited by 3,959

Structural basis of long-term potentiation in single dendritic spines

Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,483

Learning induces long-term potentiation in the hippocampus

Whitlock, J. R., Heynen, A. J., Shuler, M. G., & Bear, M. F. (2006) · Science · doi:10.1126/science.1128134 · Cited by 1,913

Morphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity

Yuste, R., & Bonhoeffer, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1071 · Cited by 1,269

Induction of Cell Migration by Matrix Metalloprotease-2 Cleavage of Laminin-5

Giannelli, G., Falk-Marzillier, J., Schiraldi, O., Stetler-Stevenson, W. G., & Quaranta, V. (1997) · Science · doi:10.1126/science.277.5323.225 · Cited by 1,221

A Requirement for the Intercellular Messenger Nitric Oxide in Long-Term Potentiation

Schuman, E. M., & Madison, D. V. (1991) · Science · doi:10.1126/science.1720572 · Cited by 1,135

Regulation of distinct AMPA receptor phosphorylation sites during bidirectional synaptic plasticity

Lee, H.-K., Barbarosie, M., Kameyama, K., Bear, M. F., & Huganir, R. L. (2000) · Nature · doi:10.1038/35016089 · Cited by 1,116

Subunit-Specific Rules Governing AMPA Receptor Trafficking to Synapses in Hippocampal Pyramidal Neurons

Shi, S.-H., Hayashi, Y., Esteban, J. A., & Malinow, R. (2001) · Cell · doi:10.1016/s0092-8674(01)00321-x · Cited by 1,094

Patterned stimulation at the theta frequency is optimal for the induction of hippocampal long-term potentiation

Larson, J., Wong, D., & Lynch, G. (1986) · Brain Research · doi:10.1016/0006-8993(86)90579-2 · Cited by 1,037

Shrinkage of dendritic spines associated with long-term depression of hippocampal synapses

Zhou, Q., Homma, K. J., & Poo, M.-M. (2004) · Neuron · doi:10.1016/j.neuron.2004.11.011 · Cited by 1,025

Modafinil treatment prevents REM sleep deprivation-induced brain function impairment by increasing MMP-9 expression

He, B., Peng, H., Zhao, Y., Zhou, H. D., & Zhao, Z. (2011) · Brain Research · doi:10.1016/j.brainres.2011.09.002 · Cited by 19

DP-b99 Modulates Matrix Metalloproteinase Activity and Neuronal Plasticity

Yeghiazaryan, M., Rutkowska-Włodarczyk, I., Konopka, A., Wilczynski, G. M., Melikyan, A., Korkotian, E., Kaczmarek, L., & Figiel, I. (2014) · PLoS ONE · doi:10.1371/journal.pone.0099789 · Cited by 19

Nonneuronal contributions to synaptic function

Hodebourg, R., Scofield, M. D., Kalivas, P. W., & Kuhn, B. N. (2025) · Neuron · doi:10.1016/j.neuron.2025.04.004 · Cited by 19

BDNF-driven synaptic plasticity requires autocrine matrix metalloproteinase–9 activity

Legutko, D., Bijoch, Ł., Olszak, G., Kuźniewska, B., Kalita, K. B., Yasuda, R., Kaczmarek, L., & Michaluk, P. (2025) · Science Advances · doi:10.1126/sciadv.adx2369 · Cited by 22

Glutaminase and MMP-9 Downregulation in Cortex and Hippocampus of LPA1 Receptor Null Mice Correlate with Altered Dendritic Spine Plasticity

Peñalver, A., Campos-Sandoval, J. A., Blanco, E., Cardona, C., Castilla, L., Martín‐Rufián, M., Estivill‐Torrús, G., Sanchez-Varo, R. M., Alonso, F. J., Pérez‐Hernández, M., et al. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00278 · Cited by 18

Matrix Metalloproteinase 9 Displays a Particular Time Response to Acute Stress: Variation in Its Levels and Activity Distribution in Rat Hippocampus

Aguayo, F. I., Pacheco, A., García‐Rojo, G., Pizarro-Bäuerle, J., Doberti, A. V., Tejos‐Bravo, M., García-Pérez, M. A., Rojas, P. S., & Fiedler, J. L. (2018) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.7b00387 · Cited by 18

Synaptic loss and retention of different classic cadherins with LTP‐associated synaptic structural remodeling in vivo

Huntley, G. W., Elste, A. M., Patil, S. B., Bozdagi, O., Benson, D. L., & Steward, O. (2010) · Hippocampus · doi:10.1002/hipo.20859 · Cited by 20

Cofilin Activation Is Temporally Associated with the Cessation of Growth in the Developing Hippocampus

Lauterborn, J. C., Kramár, E. A., Rice, J. D., Babayan, A. H., Cox, C. D., Karsten, C. A., Gall, C. M., & LYNCH, G. S. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw088 · Cited by 17

Destroy the old to build the new: Activity-dependent lysosomal exocytosis in neurons

Ibata, K., & Yuzaki, M. (2021) · Neuroscience Research · doi:10.1016/j.neures.2021.03.011 · Cited by 18

Matrix Metalloproteinase Dependent Cleavage of Cell Adhesion Molecules in the Pathogenesis of CNS Dysfunction with HIV and Methamphetamine

Conant, K. E., Seung Taik, L. I. M., Randall, B., & Maguire‐Zeiss, K. A. (2012) · Current HIV Research · doi:10.2174/157016212802138733 · Cited by 17

New approaches for solving old problems in neuronal protein trafficking

Bourke, A. M., Bowen, A. B., & Kennedy, M. J. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.04.004 · Cited by 17

Immunoexpression of gelatinase (MMP-2 and MMP-9) in the seminal vesicles and ventral prostate of Libyan jird (Meriones libycus) during the seasonal cycle of reproduction.

Belhocine, M., Gernigon-Spychalowicz, T., Jacob, M. P., Benazzoug, Y., & Exbrayat, J.-M. (2010) · PubMed · doi:10.14670/hh-25.619 · Cited by 17

Changes in brain white matter structure are associated with urine proteins in urologic chronic pelvic pain syndrome (UCPPS): A MAPP Network study

Woodworth, D. C., Dagher, A. M., Curatolo, A. S., Sachdev, M., Ashe-McNalley, C., Naliboff, B. D., Labus, J. S., Landis, J. R., Kutch, J. J., Mayer, E. A., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0206807 · Cited by 16

Propofol impairs spatial memory consolidation and prevents learning-induced increase in hippocampal matrix metalloproteinase-9 levels in rat

Zhang, J. J., Zhang, X., & Jiang, W. (2013) · Neuroreport · doi:10.1097/wnr.0b013e328364fe69 · Cited by 16

Spike Timing-Dependent Plasticity in the Mouse Barrel Cortex Is Strongly Modulated by Sensory Learning and Depends on Activity of Matrix Metalloproteinase 9

Lebida, K., & Mozrzymas, J. W. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0174-y · Cited by 16

Effects of Sodium Valproate Combined with Lamotrigine on Quality of Life and Serum Inflammatory Factors in Patients with Poststroke Secondary Epilepsy

Tao, S., Sun, J., Hao, F., Tang, W., Li, X., Guo, D. L., & Liu, X. (2020) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2020.104644 · Cited by 15

Experience‐dependent brain plasticity after stroke: effect of ibuprofen and poststroke delay

Jablonka, J., Kossut, M. M., Witte, O. W., & Liguz‐Lecznar, M. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08174.x · Cited by 15

A bout of treadmill exercise increases matrix metalloproteinase-9 activity in the rat hippocampus

Nishijima, T., Kawakami, M., & Kita, I. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.03.063 · Cited by 15

Resveratrol differentially affects MMP‐9 release from neurons and glia; implications for therapeutic efficacy

Amontree, M., Nelson, M., Stefansson, L., Pak, D. T. S., Maguire-Zeiss, K., Turner, R., & Conant, K. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16031 · Cited by 13

Matrix metalloproteinase inhibition counteracts impairment of cortical experience‐dependent plasticity after photothrombotic stroke

Cybulska-Kłosowicz, A., Liguz‐Lecznar, M., Nowicka, D., Ziemka‐Nałęcz, M., Kossut, M. M., & Skangiel-Kramska, J. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07713.x · Cited by 14

Chronic Intermittent Ethanol Exposure Induces Upregulation of Matrix Metalloproteinase-9 in the Rat Medial Prefrontal Cortex and Hippocampus

Yin, L., Li, F., Li, J., Yang, X., Xie, X., Xue, L., Li, Y., & Zhang, C. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02783-8 · Cited by 14

Manipulation of Extracellular Matrix Remodeling and Neurite Extension by Mouse Embryonic Stem Cells Using IKVAV and LRE Peptide Tethering in Hyaluronic Acid Matrices

Perera, T. H., Howell, S., & Callahan, L. A. S. (2019) · Biomacromolecules · doi:10.1021/acs.biomac.9b00578 · Cited by 14

Effects of uridine administration on hippocampal matrix metalloproteinases and their endogenous inhibitors in REM sleep-deprived rats

Çakır, A., Öcalan, B., Aydin, B., Koç, C., Cansev, M., Süyen, G. G., & Kahveci, N. (2022) · Brain Research · doi:10.1016/j.brainres.2022.148039 · Cited by 13

BACE1 Translation: At the Crossroads Between Alzheimer’s Disease Neurodegeneration and Memory Consolidation

Guix, F. X., Sartório, C. L., & ILL‐Raga, G. (2019) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-180089 · Cited by 13

Matrix metalloproteinase-9 and -2 enhance the ligand sensitivity of photoreceptor cyclic nucleotide-gated channels

Meighan, P. C., Meighan, S. E., Rich, E. D., Brown, R. L., & Varnum, M. D. (2012) · Channels · doi:10.4161/chan.20904 · Cited by 13

Extracellular Matrix Recycling as a Novel Plasticity Mechanism With a Potential Role in Disease

Dankovich, T. M., & Rizzoli, S. O. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.854897 · Cited by 12

Astrocyte-Secreted Lcn2 Modulates Dendritic Spine Morphology

Doliwa, M., Kuźniewska, B., Nader, K., Reniewicz, P., Kaczmarek, L., Michaluk, P., & Kalita, K. B. (2025) · Cells · doi:10.3390/cells14030159 · Cited by 13

Serum matrix metalloproteinase-9 levels and severity of symptoms in boys with attention deficit hyperactivity disorder ADHD/hyperkinetic disorder HKD

Kądziela-Olech, H., Cichocki, P., Chwiesko, J., Konstantynowicz, J., & Braszko, J. J. (2014) · European Child & Adolescent Psychiatry · doi:10.1007/s00787-014-0533-z · Cited by 12

Extracellular Vesicle-Associated Moonlighting Proteins: Heat Shock Proteins and Metalloproteinases

Eguchi, T., & Taha, E. A. (2020) · Heat shock proteins · doi:10.1007/7515_2020_25 · Cited by 10

MMP-9 Serum Levels in Schizophrenic Patients during Treatment Augmentation with Sarcosine (Results of the PULSAR Study)

Strzelecki, D., Kałużyńska, O., Szyburska, J., & Wysokiński, A. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17071075 · Cited by 12

Extracellular matrix: a new player in memory maintenance and psychiatric disorders

Bach, D. R., Brown, S. A., Kleim, B., & Tyagarajan, S. K. (2019) · Swiss Medical Weekly · doi:10.4414/smw.2019.20060 · Cited by 11

CCR5 deficiency normalizes TIMP levels, working memory, and gamma oscillation power in APOE4 targeted replacement mice

Greco, G. A., Rock, M. B., Amontree, M., Lanfranco, M. F., Korthas, H. T., Hong, S. H., Turner, R. S., Rebeck, G. W., & Conant, K. E. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106057 · Cited by 11

Cotransplantation of NSCs and ethyl stearate promotes synaptic plasticity in PD rats by Drd1/ERK/AP-1 signaling pathway

Yi, L., Ma, H., Yang, X., Qi, Z., Zhong, J., Ye, S., Li, X., Chen, D., Li, C., & Li, C. (2023) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2023.117292 · Cited by 11

Targeted therapy of cognitive deficits in fragile X syndrome

Puścian, A., Winiarski, M., Borowska, J., Łęski, S., Górkiewicz, T., Chaturvedi, M., Nowicka, K., Wołyniak, M., Chmielewska, J. J., Nikolaev, T., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01527-5 · Cited by 11

The tetrapartite synapse in neuropsychiatric disorders: Matrix metalloproteinases (MMPs) as promising targets for treatment and rational drug design

Filho, A. J. M. C., Mottin, M., Lós, D. B., Andrade, C. H., & Macêdo, D. S. (2022) · Biochimie · doi:10.1016/j.biochi.2022.07.015 · Cited by 11

Biophysical Modeling of Actin-Mediated Structural Plasticity Reveals Mechanical Adaptation in Dendritic Spines

Bonilla-Quintana, M., & Rangamani, P. (2024) · eNeuro · doi:10.1523/eneuro.0497-23.2024 · Cited by 11

Dopamine increases NMDA ‐stimulated calcium flux in striatopallidal neurons through a matrix metalloproteinase‐dependent mechanism

Li, Y., Partridge, J. G., Berger, C., Sepulveda‐Rodriguez, A., Vicini, S., & Conant, K. E. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13146 · Cited by 11

Od c-Fos do MMP-9 w kontroli plastyczności synaptycznej zdrowego i chorego umysłu, spojrzenie osobiste

Kaczmarek, L. (2018) · Postępy Biochemii · doi:10.18388/pb.2018_119 · Cited by 11

Chronic Monocular Deprivation Reveals MMP9-Dependent and -Independent Aspects of Murine Visual System Plasticity

Murase, S., Robertson, S., Lantz, C. L., Liu, J., Winkowski, D. E., & Quinlan, E. M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052438 · Cited by 10

Effect of the Matrix Metalloproteinase Inhibitor Doxycycline on Human Trace Fear Memory

Wehrli, J. M., Xia, Y., Offenhammer, B., Kleim, B., Müller, D., & Bach, D. R. (2023) · eNeuro · doi:10.1523/eneuro.0243-22.2023 · Cited by 9

Contributions of site- and sex-specific LTPs to everyday memory

Gall, C. M., Le, A. A., & LYNCH, G. S. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0223 · Cited by 10

Extracellular matrix molecules, their receptors, and extracellular proteases as synaptic plasticity modulators

Mukhina, I. V., Александровна, К. С., & Dityatev, A. E. (2012) · Neurochemical Journal · doi:10.1134/s1819712412020055 · Cited by 8

MMP-9 in Control of Synaptic Plasticity: a Subjective Account

Kaczmarek, L. (2016) · Russian Agency for Digital Standardization · doi:10.20388/omp2016.002.0027 · Cited by 9

Intracellular signaling and perception of neuronal scaffold through integrins and their adapter proteins

Wehrle‐Haller, B., & Bastmeyer, M. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63486-3.00018-9 · Cited by 9

SIRT1, MMP-9 and TIMP-1 levels in children with specific learning disorder

Işık, C. M., Çiçek, A. U., Özbek, D. Ü., & Bakır, S. (2022) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2022.06.015 · Cited by 8

The role of integrin beta in schizophrenia: a preliminary exploration

He, B., Wang, Y., Li, H., & Huang, Y. (2022) · CNS Spectrums · doi:10.1017/s1092852922001080 · Cited by 8

Inhibition of Matrix Metalloproteinase 9 Activity Promotes Synaptogenesis in the Hippocampus

Salamian, A., Legutko, D., Nowicka, K., Badyra, B., Kaźmierska, P., Caban, B., Kowalczyk, T., Kaczmarek, L., & Beroun, A. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab050 · Cited by 7

The cell adhesion protein dystroglycan affects the structural remodeling of dendritic spines

Figiel, I., Bączyńska, E., Wójtowicz, T., Magnowska, M., Buszka, A., Bijata, M., & Włodarczyk, J. (2022) · Scientific Reports · doi:10.1038/s41598-022-06462-7 · Cited by 9

Extracellular matrix metalloproteinase-9 (MMP-9) is required in female mice for 17β-estradiol enhancement of hippocampal memory consolidation

Gross, K. S., Lincoln, C. M., Anderson, M. M., Geiger, G. E., & Frick, K. M. (2022) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2022.105773 · Cited by 13

Personality traits and the R668Q polymorphism located in the MMP-9 gene

Suchankova, P., Pettersson, R., Nordenström, K., Holm, G., & Ekman, A. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.11.026 · Cited by 9

Metaloproteinaza macierzy pozakomórkowej 9 i epileptogeneza â kluczowa rola enzymu i strategie zmierzające do zapobiegania rozwojowi choroby

Khomiak, D., & Kaczmarek, L. (2018) · Postępy Biochemii · doi:10.18388/pb.2018_134 · Cited by 8

Osteopontin and Integrin Mediated Modulation of Post-Synapses in HIV Envelope Glycoprotein Exposed Hippocampal Neurons

Mahmud, F. J., Boucher, T., Liang, S., & Brown, A. M. (2020) · Brain Sciences · doi:10.3390/brainsci10060346 · Cited by 8

Selenium deficiency impedes maturation of parvalbumin interneurons, perineuronal nets, and neural network activity

Sasuclark, A. R., Watanabe, M., Roshto, K., Kilonzo, V. W., Zhang, Y., & Pitts, M. W. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103548 · Cited by 8

MMP-2/9 inhibition modulates sharp wave abundance, inhibitory proteoglycan sulfation, and fear memory in juvenile zebrafish: relevance to affective disorders

Blanco, I., Deasy, S., Amontree, M., Gabriel, M., Caccavano, A., Vicini, S., Glasgow, E. F., & Conant, K. E. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03007-y · Cited by 7

Dynamics of biomarkers across the stages of traumatic spinal cord injury-implications for neural plasticity and repair

Begenisic, T., Pavese, C., Aiachini, B., Nardone, A., & Rossi, D. (2021) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-211169 · Cited by 7

Functional Polymorphism of MMP9 and BDNF as Potential Biomarker of Auditory Neuroplasticity in Prelingual Deafness Treatment With Cochlear Implantation—A Retrospective Cohort Analysis

Matusiak, M., Oziębło, D., Obrycka, A., Ołdak, M., Kaczmarek, L., Skarzynski, P. H., & Skarżyńśki, H. (2021) · Trends in Hearing · doi:10.1177/23312165211002140 · Cited by 7

Functional changes in piriform cortex pyramidal neurons in the chronic methamphetamine-treated rat

Hori, N., Kadota, T., & Akaike, N. (2015) · General Physiology and Biophysics · doi:10.4149/gpb_2014024 · Cited by 7

Neuroimmune regulation of the prefrontal cortex tetrapartite synapse

Liss, A., Siddiqi, M. T., Marsland, P., & Varodayan, F. P. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110335 · Cited by 8

Matrix Metalloproteinase 9 (MMP-9) in Learning and Memory

Knapska, E., & Kaczmarek, L. (2015) · Springer eBooks · doi:10.1007/978-3-319-24364-1_9 · Cited by 9

Effects of matrix metalloproteinase inhibitors on N-methyl-D-aspartate receptor and contribute to long-term potentiation in the anterior cingulate cortex of adult mice

Matsuura, T., Li, X., Chen, T., & Zhuo, M. (2019) · Molecular Pain · doi:10.1177/1744806919842958 · Cited by 6

Results from a Double-Blind, Randomized, Placebo-Controlled, Single-Dose, Crossover Trial of Lovastatin or Minocycline in Fragile X Syndrome

McKinney, W. S., Schmitt, L., Stefano, L. A. D., Ethridge, L. E., Norris, J. E., Horn, P. S., Dauterman, S., Rosselot, H., Pedapati, E. V., Reisinger, D. L., et al. (2024) · Journal of Child and Adolescent Psychopharmacology · doi:10.1089/cap.2024.0103 · Cited by 5

Morphology and MMP-9, AR and IGFR-1 responses of the seminal vesicle in TRAMP mice model

Pozzo, C. F. S. D., Kido, L. A., Montico, F., Gonçalves, M. P., & Cagnon, V. H. A. (2016) · Tissue and Cell · doi:10.1016/j.tice.2016.03.005 · Cited by 5

Cyclin Y, a novel actin-binding protein, regulates spine plasticity through the cofilin-actin pathway

Hwang, H., Hur, Y.-N., Sohn, H., Seo, J., Hong, J., Cho, E., Choi, Y., Lee, S., Song, S., Lee, A.-R., et al. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101915 · Cited by 5

Electrophysiology of Dendritic Spines: Information Processing, Dynamic Compartmentalization, and Synaptic Plasticity

Marafiga, J. R., & Calcagnotto, M. E. (2023) · Advances in neurobiology · doi:10.1007/978-3-031-36159-3_3 · Cited by 4

Synaptic Plasticity in the Hippocampus

Bliss, T., Collingridge, G. L., Cooke, S. F., Georgiou, J., & Morris, R. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0010 · Cited by 4

The Molecular Basis of Destabilization of Synapses as a Factor of Structural Plasticity

Kudryashova, I. V. (2019) · Neurochemical Journal · doi:10.1134/s1819712419010136 · Cited by 4

A Possible Link between Microglial Process Dysfunction and Neuropsychiatric Disorders

Hayashi, Y., Wu, Z., & Nakanishi, H. (2014) · Cited by 4

The impact of doxycycline on human contextual fear memory

Wehrli, J. M., Xia, Y., Abivardi, A., Kleim, B., & Bach, D. R. (2024) · Psychopharmacology · doi:10.1007/s00213-024-06540-w · Cited by 3

Degrading Epilepsy: The Role of Extracellular Proteases and the Extracellular Matrix

Wong, M. (2012) · Epiliepsy currents/Epilepsy currents · doi:10.5698/1535-7511-12.3.118 · Cited by 3

MMP-3 deficiency does not influence the length and number of CA1 dendrites of hippocampus of adult mice

Nowak, D., Groef, L. D., Moons, L., & Mozrzymas, J. W. (2018) · Acta Neurobiologiae Experimentalis · doi:10.21307/ane-2018-026 · Cited by 3

Dopamine Toxicity Induces ROS-Dependent Death of Murine Neuroblastoma Cells: Impact on the Interactions of Cofilin With UCHL1 and MMP9

Roy, T., Banerjee, R., Chatterjee, A., & Swarnakar, S. (2025) · Neurochemical Research · doi:10.1007/s11064-025-04362-6 · Cited by 2

Novel roles of microglia

Nakanishi, H. (2014) · Clinical and Experimental Neuroimmunology · doi:10.1111/cen3.12161 · Cited by 3

Transgenic Mice with Enhanced Cognition

Lee, Y. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-417042-1.00005-x · Cited by 1

Doxycycline diminishes the rewarding and psychomotor effects induced by morphine and cocaine

Sales, A. J., Gobira, P. H., Pedrazzi, J. F. C., Silveira, J. R., Bel, E. A. D., Gomes, F. V., & Guimarães, F. S. (2023) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2023.110870 · Cited by 2

How dendritic spines shape is determined by MMP-9 activity in FXS

Dziembowska, M. (2023) · International review of neurobiology · doi:10.1016/bs.irn.2023.10.001 · Cited by 2

Extracellular Remodeling by Lysosomes: An Inside-Out Mechanism of Spine Plasticity

Evans, P. R., & Yasuda, R. (2017) · Neuron · doi:10.1016/j.neuron.2016.12.025 · Cited by 2

Therapeutic approaches for the future treatment of Fragile X

Sastre, A., Campillo, N. E., Gil, C., & Martı́nez, A. (2015) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2015.01.003 · Cited by 2

Mapping Connectome in Mammalian Brain: A Novel Approach by Bioengineering Neuro-Glia specific Vectors

Ganguly, K., & Trigun, S. K. (2020) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2020.110244 · Cited by 2

Dendritic Spines

Müller, D., & Nikonenko, I. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397267-5.00145-x · Cited by 4

Metabotropic NMDA Receptor Signaling Contributes to Sex Differences in Synaptic Plasticity and Episodic MemoryPreprint

Le, A. A., Lauterborn, J. C., Jia, Y., Cox, C. D., LYNCH, G. S., & Gall, C. M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.26.577478 · Cited by 2

In Vivo Zymography: An Essential Activity Assay for Studying the Activity of Matrix Metalloproteinases in Specific Brain Cells

Hodebourg, R. (2025) · Methods in molecular biology · doi:10.1007/978-1-0716-4482-9_3 · Cited by 1

Main characteristics and biological effects of martix metalloproteinases in the nervous system

Stefovska, V. G. (2015) · Scripta Scientifica Medica · doi:10.14748/ssm.v47i1.1002 · Cited by 1

Microglia and synaptic reorganization: focus on the movement and functions of microglial processes

Hayashi, Y., & Nakanishi, H. (2013) · Folia Pharmacologica Japonica · doi:10.1254/fpj.142.231 · Cited by 1

The Role of the Brain Extracellular Matrix in Synaptic Plasticity After Brain Injuries (Review)

Dembitskaya, Y., Tyurikova, O., & Semyanov, A. V. (2016) · Современные технологии в медицине · doi:10.17691/stm2016.8.4.31 · Cited by 1

Spreading Depressions and Periinfarct Spreading Depolarizations in the Context of Cortical Plasticity

Sadowska, M., Mehlhorn, C., Średniawa, W., Szewczyk, Ł. M., Szlachcic, A., Urban, P., Winiarski, M. J., & Jablonka, J. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.10.032 · Cited by 1

Outcome of congenital deafness treatment by cochlear implantation – focus on functional polymorphism of MMP9 and BDNF genes

Matusiak, M., Oziębło, D., Ołdak, M., Obrycka, A., Kaczmarek, L., & Skarżyńśki, H. (2022) · Nowa Audiofonologia · doi:10.17431/10.2.1 · Cited by 1

Contribution of mechanical forces to structural synaptic plasticity: insights from 3D cellular motility mechanisms

Teodoro, R. O., Ramos, M. R., & Carvalho, L. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00498 · Cited by 1

Activity-Mediated Structural Plasticity of Dendritic Spines

Müller, D., Roo, M. D., & Nikonenko, I. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418675-0.00012-2 · Cited by 1

Neonatal Proinflammatory Stress and the Maturation of Intercellular Communication in the Hippocampus

Kudryashova, I. V., Stepanichev, M. Y., & Gulyaeva, N. V. (2020) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-020-00971-6 · Cited by 1

[Proteolytic cleavage of neuroligins and functions of their cleavage products].

Yu, J., & Xu, J. (2020) · PubMed Central · doi:10.3785/j.issn.1008-9292.2020.08.11 · Cited by 1

Matrix metalloproteinase-9 (MMP-9) at the synapse : functions and targets

Michaluk, P. (2010) · Utrecht University Repository (Utrecht University) · Cited by 1

Minocycline—A Lesson From a Failure

Granzotto, A., & Sensi, S. L. (2020) · JAMA Neurology · doi:10.1001/jamaneurol.2020.1154 · Cited by 1

Recycling as a mechanism for extracellular matrix remodeling at the synapse

Dankovich, T. M. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8998 · Cited by 1

A multi-faceted analysis of synapses reveals the role of neuroligin-1 cleavage in presynaptic vesicle accumulation in the lateral amygdalaPreprint

Thomas, C. I., Anderson, J. R., Alexis, A., Guerrero‐Given, D., Chavez, A., McNabb, M. C., Ünal, B., Ehlers, M., Bolton, M. M., & Kamasawa, N. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.07.566075 · Cited by 1

The impact of doxycycline on human contextual fear memoryPreprint

Wehrli, J. M., Xia, Y., Abivardi, A., Kleim, B., & Bach, D. R. (2024) · doi:10.31234/osf.io/m5cyv · Cited by 1

Using the natural resistance of motor neuron subpopulations to identify therapeutic targets in amyotrophic lateral sclerosis

Spiller, K. J. (2014) · doi:10.7916/d8fn145w

Positive Modulation of AMPA Receptors as a Broad-Spectrum Strategy for Treating Neuropsychiatric Disorders

LYNCH, G. S., Lauterborn, J. C., & Gall, C. M. (2010) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0346-0241-9_5

Mecanismos neurobiológicos involucrados en la persistencia de la memoria de largo término: rol de C-fos en hipocampo y corteza retrosplenial

Katche, C. (2011) · Repositorio Digital Institucional de la Universidad de Buenos Aires (Universidad de Buenos Aires)

The development of bursting networks following chemical long term potentiation

Niedringhaus, M. S. (2012) · DigitalGeorgetown (Georgetown University Library)

IntegrinDynamicsProduceaDelayedStageofLong-Term PotentiationandMemoryConsolidation

Babayan, A. H., Kramár, E., Chen, L., Rex, C. S., & Lauterborn, J. C. (2012)

In vivo roles for matrix metalloproteinase-9 in mature hippocampal synaptic physiology and plasticity

Bozdagi, O., Nagy, V., Kwei, K. T., & Huntley, G. W. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00202.2007 · Cited by 182

Matrix metalloproteinases regulate the formation of dendritic spine head protrusions during chemically induced long-term potentiation. PLoS One 8: e63314

Szepesi, Z., Bijata, M., Ruszczycki, B., Kaczmarek, L., & Włodarczyk, J. (2013)

Matrix metalloproteinase-9 is required for hippocampal late-phase long-term potentiation and memory

Nagy, V., Bozdagi, O., Matynia, A., Balcerzyk, M., Okulski, P., Dzwonek, J., Costa, R. M., Silva, A. J., Kaczmarek, L., & Huntley, G. W. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4359-05.2006 · Cited by 499

MMP9: A novel function in synaptic plasticity

Dziembowska, M., & Włodarczyk, J. (2012) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2012.01.023 · Cited by 132

Matrix Metalloproteinases Regulate the Formation of Dendritic Spine Head Protrusions during Chemically Induced Long-Term Potentiation

Szepesi, Z., Bijata, M., Ruszczycki, B., Kaczmarek, L., & Włodarczyk, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063314 · Cited by 72