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Calpain-Specific Proteolysis in Primate Retina: Contribution of Calpains in Cell Death

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Drusen in the Optic Nerve Head

inferredcites →https://doi.org/10.1001/archopht.1997.01100160201010openalex-snapshot

TUNEL-Positive Ganglion Cells in Human Primary Open-angle Glaucoma

inferredcites →https://doi.org/10.1002/(sici)1097-4547(19990301)55:5<643::aid-jnr11>3.0.co;2-vopenalex-snapshot

Species differences in fodrin proteolysis in the ischemic brain

inferredcites →https://doi.org/10.1002/jnr.20827openalex-snapshot

Presence of calpain‐induced proteolysis in retinal degeneration and dysfunction in a rat model of acute ocular hypertension

inferredcites →https://doi.org/10.1006/abbi.1995.1284openalex-snapshot

Casein Zymography: A Method to Study μ-Calpain, M-Calpain, and Their Inhibitory Agents

inferredcites →https://doi.org/10.1006/exer.1996.0220openalex-snapshot

Loss of Cytoskeletal Proteins and Lens Cell Opacification in the Selenite Cataract Model

inferredcites →https://doi.org/10.1006/exer.1998.0686openalex-snapshot

Decreased Sensitivity of Lens-Specific Calpain Lp82 to Calpastatin Inhibitor

inferredcites →https://doi.org/10.1007/bf02815181openalex-snapshot

Dual response of calpain to rat brain postdecapitative ischemia

inferredcites →https://doi.org/10.1016/j.brainres.2005.05.048openalex-snapshot

Proteolysis of neuronal cytoskeletal proteins by calpain contributes to rat retinal cell death induced by hypoxia

inferredcites →https://doi.org/10.1016/j.exer.2006.02.014openalex-snapshot

Low activity by the calpain system in primate lenses causes resistance to calcium-induced proteolysis

inferredcites →https://doi.org/10.1016/j.neuroscience.2006.05.060openalex-snapshot

Amelioration of retinal degeneration and proteolysis in acute ocular hypertensive rats by calpain inhibitor ((1S)-1-((((1S)-1-benzyl-3-cyclopropylamino-2,3-di-oxopropyl)amino)carbonyl)-3-methylbutyl)carbamic acid 5-methoxy-3-oxapentyl ester

inferredcites →https://doi.org/10.1016/s0006-8993(97)01414-5openalex-snapshot

Temporal ordering of pathogenic events following transient global ischemia

inferredcites →https://doi.org/10.1016/s0008-4182(02)80113-2openalex-snapshot

Membrane conductance of Müller glial cells in proliferative diabetic retinopathy

inferredcites →https://doi.org/10.1016/s0021-9258(18)67679-3openalex-snapshot

Isolation and sequence analyses of cDNA clones for the large subunits of two isozymes of rabbit calcium-dependent protease.

inferredcites →https://doi.org/10.1016/s0021-9258(19)74593-1openalex-snapshot

Spatial resolution of fodrin proteolysis in postischemic brain.

inferredcites →https://doi.org/10.1016/s0167-4781(01)00212-3openalex-snapshot

Different expression patterns for ubiquitous calpains and Capn3 splice variants in monkey ocular tissues

inferredcites →https://doi.org/10.1016/s1096-4959(01)00489-4openalex-snapshot

Involvement of calpain in hypoxia-induced damage in rat retina in vitro

inferredcites →https://doi.org/10.1021/jm0201924openalex-snapshot

Structure−Activity Relationship Study and Drug Profile ofN-(4-Fluorophenylsulfonyl)- l -valyl- l -leucinal (SJA6017) as a Potent Calpain Inhibitor

inferredcites →https://doi.org/10.1042/bj2230047openalex-snapshot

Calpain and calpastatin in porcine retina. Identification and action on microtubule-associated proteins

inferredcites →https://doi.org/10.1042/bj3190683openalex-snapshot

Non-erythroid α-spectrin breakdown by calpain and interleukin 1 β-converting-enzyme-like protease(s) in apoptotic cells: contributory roles of both protease families in neuronal apoptosis

inferredcites →https://doi.org/10.1042/bj3280721openalex-snapshot

Structure and physiological function of calpains

inferredcites →https://doi.org/10.1046/j.1471-4159.1998.70062526.xopenalex-snapshot

Postischemic Reperfusion Induces α‐Fodrin Proteolysis by m‐Calpain in the Synaptosome and Nucleus in Rat Brain

inferredcites →https://doi.org/10.1074/jbc.272.40.24876openalex-snapshot

Distinct Substrate Specificities and Functional Roles for the 78- and 76-kDa Forms of μ-Calpain in Human Platelets

inferredcites →https://doi.org/10.1076/0271-3683(200007)2111-zft571openalex-snapshot

Involvement of calpain isoforms in ischemia-reperfusion injury in rat retina

inferredcites →https://doi.org/10.1076/0271-3683(200009)2131-rft710openalex-snapshot

Identification and characterization of a retina-specific calpain (Rt88) from rat

inferredcites →https://doi.org/10.1097/00005072-199607000-00010openalex-snapshot

Prolonged Calpain-mediated Spectrin Breakdown Occurs Regionally Following Experimental Brain Injury in the Rat

inferredcites →https://doi.org/10.1152/physrev.1991.71.3.813openalex-snapshot

Calcium-activated neutral protease (calpain) system: structure, function, and regulation.

inferredcites →https://doi.org/10.1161/01.str.26.10.1901openalex-snapshot

Three Distinct Phases of Fodrin Proteolysis Induced in Postischemic Hippocampus

inferredcites →https://doi.org/10.1515/bc.2004.054openalex-snapshot

Interaction of calpastatin with calpain: a review

inferredcites →https://doi.org/10.2337/diabetes.53.2007.s12openalex-snapshot

Structure, Activation, and Biology of Calpain

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4530990openalex-extracted

inferred← citeshttps://doi.org/10.1002/ibra.12097openalex-snapshot

Research progress of neonatal hypoxic‐ischemic encephalopathy in nonhuman primate models

inferred← citeshttps://doi.org/10.1002/med.21534openalex-snapshot

Involvement of calpain in the neuropathogenesis of Alzheimer’s disease

inferred← citeshttps://doi.org/10.1002/prca.200780094openalex-snapshot

Proteomics as a research tool in clinical and experimental ophthalmology

inferred← citeshttps://doi.org/10.1007/978-3-319-75402-4_36openalex-snapshot

Protein Carbonylation-Dependent Photoreceptor Cell Death Induced by N-Methyl-N-nitrosourea in Mice

inferred← citeshttps://doi.org/10.1016/j.arr.2022.101572openalex-snapshot

Restoring the oxidative balance in age-related diseases – An approach in glaucoma

inferred← citeshttps://doi.org/10.1016/j.bbadis.2010.08.008openalex-snapshot

Calpain inhibitors reduce retinal hypoxia in ischemic retinopathy by improving neovascular architecture and functional perfusion

inferred← citeshttps://doi.org/10.1016/j.bbadis.2017.03.021openalex-snapshot

Endothelial cell calpain as a critical modulator of angiogenesis

inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.02.087openalex-snapshot

Calpain-mediated Hsp70.1 cleavage in hippocampal CA1 neuronal death

inferred← citeshttps://doi.org/10.1016/j.celrep.2018.06.017openalex-snapshot

Rbfox Splicing Factors Maintain Skeletal Muscle Mass by Regulating Calpain3 and Proteostasis

inferred← citeshttps://doi.org/10.1016/j.ejphar.2013.10.073openalex-snapshot

Calcium channels and their blockers in intraocular pressure and glaucoma

inferred← citeshttps://doi.org/10.1016/j.exer.2015.06.006openalex-snapshot

Assessment of retinal ganglion cell damage in glaucomatous optic neuropathy: Axon transport, injury and soma loss

inferred← citeshttps://doi.org/10.1016/j.exer.2023.109653openalex-snapshot

A Simplified Protocol to Induce Hypoxia in a Standard Incubator: A Focus on Retinal Cells

inferred← citeshttps://doi.org/10.1016/j.jneumeth.2011.08.017openalex-snapshot

An in situ method for the examination of calcium-dependent proteolysis

inferred← citeshttps://doi.org/10.1016/j.jtcvs.2015.08.101openalex-snapshot

Calpain inhibition improves collateral-dependent perfusion in a hypercholesterolemic swine model of chronic myocardial ischemia

inferred← citeshttps://doi.org/10.1016/j.molmed.2022.05.007openalex-snapshot

Calpains as mechanistic drivers and therapeutic targets for ocular disease

inferred← citeshttps://doi.org/10.1016/j.nbd.2016.05.007openalex-snapshot

Calpain-1 and calpain-2 play opposite roles in retinal ganglion cell degeneration induced by retinal ischemia/reperfusion injury

inferred← citeshttps://doi.org/10.1016/j.neuro.2014.09.006openalex-snapshot

Associations among exposure to methylmercury, reduced Reelin expression, and gender in the cerebellum of developing mice

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2009.09.003openalex-snapshot

The role of lysosomal rupture in neuronal death

inferred← citeshttps://doi.org/10.1016/j.preteyeres.2010.09.002openalex-snapshot

Use of calcium channel blockers for glaucoma

inferred← citeshttps://doi.org/10.1016/j.survophthal.2007.12.006openalex-snapshot

The Role of Calcium-Activated Protease Calpain in Experimental Retinal Pathology

inferred← citeshttps://doi.org/10.1016/j.trsl.2020.10.003openalex-snapshot

The antidiabetic drug glibenclamide exerts direct retinal neuroprotection

inferred← citeshttps://doi.org/10.1038/cddis.2011.29openalex-snapshot

Calpain-mediated cleavage of Beclin-1 and autophagy deregulation following retinal ischemic injury in vivo

inferred← citeshttps://doi.org/10.1042/bj20120025openalex-snapshot

Peptidylarginine deiminase modulates the physiological roles of enolase via citrullination: links between altered multifunction of enolase and neurodegenerative diseases

inferred← citeshttps://doi.org/10.1080/02713683.2017.1383442openalex-snapshot

Neuroprotective effects of inhibitors of Acid-Sensing ion channels (ASICs) in optic nerve crush model in rodents

inferred← citeshttps://doi.org/10.1080/02713683.2018.1454478openalex-snapshot

Neuroprotective Effects of Psalmotoxin-1, an Acid-Sensing Ion Channel (ASIC) Inhibitor, in Ischemia Reperfusion in Mouse Eyes

inferred← citeshttps://doi.org/10.1093/jb/mvq009openalex-snapshot

Characteristic properties of endoplasmic reticulum membrane m-calpain, calpastatin and lumen m-calpain: a comparative study between membrane and lumen m-calpains

inferred← citeshttps://doi.org/10.1111/cns.12471openalex-snapshot

A role of Heat Shock Protein 70 in Photoreceptor Cell Death: Potential as a Novel Therapeutic Target in Retinal Degeneration

inferred← citeshttps://doi.org/10.1111/j.1471-4159.2011.07596.xopenalex-snapshot

Hsp70.1 and related lysosomal factors for necrotic neuronal death

inferred← citeshttps://doi.org/10.1111/jnc.12750openalex-snapshot

Heat shock protein 70 induction by valproic acid delays photoreceptor cell death by N‐methyl‐N‐nitrosourea in mice

inferred← citeshttps://doi.org/10.1124/jpet.109.156612openalex-snapshot

A Novel Calpain Inhibitor, ((1S)-1-((((1S)-1-Benzyl-3-cyclopropylamino-2,3-di-oxopropyl)amino)carbonyl)-3-methylbutyl)carbamic Acid 5-Methoxy-3-oxapentyl Ester (SNJ-1945), Reduces Murine Retinal Cell Death In Vitro and In Vivo

inferred← citeshttps://doi.org/10.1167/iovs.07-0287openalex-snapshot

A Key Role for Calpains in Retinal Ganglion Cell Death

inferred← citeshttps://doi.org/10.1167/iovs.11-7497openalex-snapshot

Calpain, Not Caspase, Is the Causative Protease for Hypoxic Damage in Cultured Monkey Retinal Cells

inferred← citeshttps://doi.org/10.1167/iovs.15-17360openalex-snapshot

Hypoxia Activates Calpains in the Nerve Fiber Layer of Monkey Retinal Explants

inferred← citeshttps://doi.org/10.1167/iovs.15-18680openalex-snapshot

Calpain-5 Expression in the Retina Localizes to Photoreceptor Synapses

inferred← citeshttps://doi.org/10.1167/iovs.61.13.13openalex-snapshot

Activation of Cytosolic Calpain, Not Caspase, Is Underlying Mechanism for Hypoxic RGC Damage in Human Retinal Explants

inferred← citeshttps://doi.org/10.1186/s13104-017-2927-8openalex-snapshot

Calpain-5 gene expression in the mouse eye and brain

inferred← citeshttps://doi.org/10.1254/fpj.146.321openalex-snapshot

A potential of novel therapeutic approach by heat shock protein 70 expression in retinitis pigmentosa

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Using Evolutionary Conserved Modules in Gene Networks as a Strategy to Leverage High Throughput Gene Expression Queries

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Protective Effects of Resveratrol in Experimental Retinal Detachment

inferred← citeshttps://doi.org/10.15226/2376-4589/2/2/00114openalex-snapshot

Why is Hippocampal CA1 Especially Vulnerable to Ischemia?

inferred← citeshttps://doi.org/10.2174/187152708784936644openalex-snapshot

Neuroprotection in Glaucoma Using Calpain-1 Inhibitors: Regional Differences in Calpain-1 Activity in the Trabecular Meshwork, Optic Nerve and Implications for Therapeutics

inferred← citeshttps://doi.org/10.3109/02713683.2013.845225openalex-snapshot

Calpain Protease Causes Hypoxia-Induced Proteolysis in Cultured Human Retina

inferred← citeshttps://doi.org/10.3389/fcvm.2023.1194402openalex-snapshot

Calpain: the regulatory point of myocardial ischemia-reperfusion injury

inferred← citeshttps://doi.org/10.3389/fmolb.2024.1378656openalex-snapshot

Cleavage of Hsp70.1 causes lysosomal cell death under stress conditions

inferred← citeshttps://doi.org/10.3389/fnins.2020.00760openalex-snapshot

Dystrophin Is Required for the Proper Timing in Retinal Histogenesis: A Thorough Investigation on the mdx Mouse Model of Duchenne Muscular Dystrophy

inferred← citeshttps://doi.org/10.3390/ijms18020334openalex-snapshot

Proteomic Analysis of Various Rat Ocular Tissues after Ischemia–Reperfusion Injury and Possible Relevance to Acute Glaucoma

inferred← citeshttps://doi.org/10.3390/life12050638openalex-snapshot

Retinal Glutamate Neurotransmission: From Physiology to Pathophysiological Mechanisms of Retinal Ganglion Cell Degeneration

inferred← citeshttps://doi.org/10.4103/1673-5374.245466openalex-snapshot

Basics on the use of acid-sensing ion channels’ inhibitors as therapeutics

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