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Iron overload-induced calcium signals modulate mitochondrial fragmentation in HT-22 hippocampal neuron cells
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1098-1136(199606)17:2<83::aid-glia1>3.0.co;2-7openalex-snapshot
Relationship of iron to oligondendrocytes and myelination
inferredcites →https://doi.org/10.1002/biof.80openalex-snapshot
Iron in neuronal function and dysfunction
inferredcites →https://doi.org/10.1007/s00018-010-0435-2openalex-snapshot
Mitochondrial dynamics in cell death and neurodegeneration
inferredcites →https://doi.org/10.1007/s00018-013-1509-8openalex-snapshot
Iron deposits in the chronically inflamed central nervous system and contributes to neurodegeneration
inferredcites →https://doi.org/10.1007/s12035-013-8514-7openalex-snapshot
Cannabidiol Normalizes Caspase 3, Synaptophysin, and Mitochondrial Fission Protein DNM1L Expression Levels in Rats with Brain Iron Overload: Implications for Neuroprotection
inferredcites →https://doi.org/10.1016/0006-8993(94)90334-4openalex-snapshot
Protein kinase C activation inhibits glutamate-induced cytotoxicity in a neuronal cell line
inferredcites →https://doi.org/10.1016/j.cardiores.2006.02.019openalex-snapshot
Redox regulation of cardiac calcium channels and transporters
inferredcites →https://doi.org/10.1016/j.ceca.2010.12.002openalex-snapshot
Elevated intracellular calcium causes distinct mitochondrial remodelling and calcineurin-dependent fission in astrocytes
inferredcites →https://doi.org/10.1016/j.cjca.2015.10.012openalex-snapshot
Effects of Iron Overload on Cardiac Calcium Regulation: Translational Insights Into Mechanisms and Management of a Global Epidemic
inferredcites →https://doi.org/10.1016/j.neuro.2010.11.006openalex-snapshot
Iron overload triggers redox-sensitive signals in human IMR-32 neuroblastoma cells
inferredcites →https://doi.org/10.1016/j.tox.2015.08.009openalex-snapshot
Iron overload triggers mitochondrial fragmentation via calcineurin-sensitive signals in HT-22 hippocampal neuron cells
inferredcites →https://doi.org/10.1016/s0005-2728(98)00114-5openalex-snapshot
Mitochondrial dysfunction in neurodegenerative diseases
inferredcites →https://doi.org/10.1016/s0887-8994(01)00260-0openalex-snapshot
Systemic iron metabolism: a review and implications for brain iron metabolism
inferredcites →https://doi.org/10.1016/s0887-8994(01)00303-4openalex-snapshot
Iron and iron management proteins in neurobiology
inferredcites →https://doi.org/10.1016/s0962-8924(00)01803-1openalex-snapshot
Mitochondria as the central control point of apoptosis
inferredcites →https://doi.org/10.1016/s1534-5807(01)00055-7openalex-snapshot
The Role of Dynamin-Related Protein 1, a Mediator of Mitochondrial Fission, in Apoptosis
inferredcites →https://doi.org/10.1038/jcbfm.2008.93openalex-snapshot
Comparative Neuroprotective Effects of Cyclosporin a and NIM811, a Nonimmunosuppressive Cyclosporin a Analog, following Traumatic Brain Injury
inferredcites →https://doi.org/10.1038/nrn1434openalex-snapshot
Oxidative stress in neurodegeneration: cause or consequence?
inferredcites →https://doi.org/10.1038/nrn1537openalex-snapshot
Iron, brain ageing and neurodegenerative disorders
inferredcites →https://doi.org/10.1038/nrn2417openalex-snapshot
Mitochondrial fragmentation in neurodegeneration
inferredcites →https://doi.org/10.1038/sj.embor.7401062openalex-snapshot
Reversible phosphorylation of Drp1 by cyclic AMP‐dependent protein kinase and calcineurin regulates mitochondrial fission and cell death
inferredcites →https://doi.org/10.1042/bst0161043openalex-snapshot
Effects of trifluoperazine and compounds W-7 and W-13 on chicken gizzard calpain II
inferredcites →https://doi.org/10.1046/j.1471-4159.2003.01794.xopenalex-snapshot
Cyclosporin A prevents calpain activation despite increased intracellular calcium concentrations, as well as translocation of apoptosis‐inducing factor, cytochrome c and caspase‐3 activation in neurons exposed to transient hypoglycemia
inferredcites →https://doi.org/10.1073/pnas.0808249105openalex-snapshot
Dephosphorylation by calcineurin regulates translocation of Drp1 to mitochondria
inferredcites →https://doi.org/10.1073/pnas.76.12.6270openalex-snapshot
Calcineurin: a calcium- and calmodulin-binding protein of the nervous system.
inferredcites →https://doi.org/10.1074/jbc.m110.213785openalex-snapshot
Iron Mediates N-Methyl-d-aspartate Receptor-dependent Stimulation of Calcium-induced Pathways and Hippocampal Synaptic Plasticity
inferredcites →https://doi.org/10.1074/jbc.m113.459677openalex-snapshot
A Calcineurin Docking Motif (LXVP) in Dynamin-related Protein 1 Contributes to Mitochondrial Fragmentation and Ischemic Neuronal Injury
inferredcites →https://doi.org/10.1074/jbc.m309767200openalex-snapshot
Critical Role of Calpain-mediated Cleavage of Calcineurin in Excitotoxic Neurodegeneration
inferredcites →https://doi.org/10.1074/jbc.m806235200openalex-snapshot
Mitochondrial DNA Damage in Iron Overload
inferredcites →https://doi.org/10.1083/jcb.201511036openalex-snapshot
Metabolic regulation of mitochondrial dynamics
inferredcites →https://doi.org/10.1089/ars.2010.3284openalex-snapshot
High-Glucose Stimulation Increases Reactive Oxygen Species Production Through the Calcium and Mitogen-Activated Protein Kinase-Mediated Activation of Mitochondrial Fission
inferredcites →https://doi.org/10.1111/jnc.12361openalex-snapshot
Mitochondrial dynamics modulate the expression of pro‐inflammatory mediators in microglial cells
inferredcites →https://doi.org/10.1159/000065701openalex-snapshot
Brain Iron Metabolism and Neurodegenerative Disorders
inferredcites →https://doi.org/10.1186/1755-8794-2-2openalex-snapshot
Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases
inferredcites →https://doi.org/10.1242/jcs.139394openalex-snapshot
Mitochondrial fission is required for cardiomyocyte hypertrophy via a Ca2+-calcineurin signalling pathway
inferredcites →https://doi.org/10.1253/circj.cj-12-1516openalex-snapshot
Thromboxane A2 Mediates Iron-Overload Cardiomyopathy in Mice Through Calcineurin-Nuclear Factor of Activated T Cells Signaling Pathway
inferredcites →https://doi.org/10.12688/f1000research.7431.1openalex-snapshot
Metals and Neurodegeneration
inferredcites →https://doi.org/10.18926/amo/32905openalex-snapshot
Calpain-calcineurin signaling in the pathogenesis of calcium-dependent disorder.
inferredcites →https://doi.org/10.3233/jad-2010-100354openalex-snapshot
Mitochondrial Iron Metabolism and Its Role in Neurodegeneration
inferredcites →https://doi.org/10.3389/fnmol.2014.00013openalex-snapshot
Ryanodine receptor-mediated Ca2+ release underlies iron-induced mitochondrial fission and stimulates mitochondrial Ca2+ uptake in primary hippocampal neurons
inferredcites →https://doi.org/10.3389/fphar.2014.00038openalex-snapshot
The interplay between iron accumulation, mitochondrial dysfunction, and inflammation during the execution step of neurodegenerative disorders
inferredcites →https://doi.org/10.4061/2011/720658openalex-snapshot
Iron and Mechanisms of Neurotoxicity
inferredcites →https://doi.org/10.5115/acb.2014.47.2.91openalex-snapshot
FK506 reduces calpain-regulated calcineurin activity in both the cytoplasm and the nucleus
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Mitochondrial Dysfunction in Aging: Future Therapies and Precision Medicine Approaches
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Inhibition of calpain reduces cell apoptosis by suppressing mitochondrial fission in acute viral myocarditis
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Iron Deposition in Parkinson’s Disease: A Mini-Review
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The Ca2+-Regulated Enzymes Calpain and Calcineurin in Neurodegenerative Processes and Prospects for Neuroprotective Pharmacotherapy
inferred← citeshttps://doi.org/10.1007/s11064-019-02731-6openalex-snapshot
Dexmedetomidine Promotes SH-SY5Y Cell Resistance Against Impairment of Iron Overload by Inhibiting NF-κB Pathways
inferred← citeshttps://doi.org/10.1007/s11064-023-04006-7openalex-snapshot
Neuroprotective Effects of Ferrostatin and Necrostatin Against Entorhinal Amyloidopathy-Induced Electrophysiological Alterations Mediated by voltage-gated Ca2+ Channels in the Dentate Gyrus Granular Cells
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Exploring mitochondrial dynamics and localization under cellular stress: A comprehensive insight
inferred← citeshttps://doi.org/10.1007/s12264-019-00424-2openalex-snapshot
L-type Calcium Channels are Involved in Iron-induced Neurotoxicity in Primary Cultured Ventral Mesencephalon Neurons of Rats
inferred← citeshttps://doi.org/10.1007/s12640-019-00045-7openalex-snapshot
Effects of Al Exposure on Mitochondrial Dynamics in Rat Hippocampus
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Mitochondrial uncoupler BAM15 inhibits artery constriction and potently activates AMPK in vascular smooth muscle cells
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Restoration of metal homeostasis: a potential strategy against neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2017.01.015openalex-snapshot
Pathological consequences of MICU1 mutations on mitochondrial calcium signalling and bioenergetics
inferred← citeshttps://doi.org/10.1016/j.biocel.2018.06.005openalex-snapshot
Peroxiredoxin 5 prevents iron overload-induced neuronal death by inhibiting mitochondrial fragmentation and endoplasmic reticulum stress in mouse hippocampal HT-22 cells
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Mitochondrial dysfunction: A fatal blow in depression
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Link of impaired metal ion homeostasis to mitochondrial dysfunction in neurons
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A mitochondrial inside-out iron-calcium signal reveals drug targets for Parkinson’s disease
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The differential impact of iron on ferroptosis, oxidative stress, and inflammatory reaction in head-kidney macrophages of yellow catfish (Pelteobagrus fulvidraco) with and without ammonia stress
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Maternal exposure to deltamethrin during pregnancy and lactation impairs hippocampal learning and memory function of male offspring by ferroptosis
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Fluoride induces neutrophil extracellular traps and aggravates brain inflammation by disrupting neutrophil calcium homeostasis and causing ferroptosis
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Long-term iron exposure causes widespread molecular alterations associated with memory impairment in mice
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The calcium–iron connection in ferroptosis-mediated neuronal death
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Nature's answer to Ferroptosis: how bioactive compounds rewire oxidative stress circuits in cerebral ischemia
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Calcium signaling hypothesis: A non-negligible pathogenesis in Alzheimer’s disease
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Hemorphin LVV-H3 attenuates calcineurin activity and regulates cytokine levels in experimental Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.neuro.2021.11.003openalex-snapshot
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Rhodiola crenulata alleviates hypobaric hypoxia-induced brain injury by maintaining BBB integrity and balancing energy metabolism dysfunction
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inferred← citeshttps://doi.org/10.1038/s41420-026-03034-wopenalex-snapshot
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Inhibiting acid‐sensing ion channel exerts neuroprotective effects in experimental epilepsy via suppressing ferroptosis
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Nitrogen-doped graphene quantum dots induce ferroptosis through disrupting calcium homeostasis in microglia
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Additional file 1 of Nitrogen-doped graphene quantum dots induce ferroptosis through disrupting calcium homeostasis in microglia
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