Literature DB >> 31646530

Readily Releasable Stores of Calcium in Neuronal Endolysosomes: Physiological and Pathophysiological Relevance.

Koffi L Lakpa1, Peter W Halcrow1, Xuesong Chen1, Jonathan D Geiger2.   

Abstract

Neurons are long-lived post-mitotic cells that possess an elaborate system of endosomes and lysosomes (endolysosomes) for protein quality control. Relatively recently, endolysosomes were recognized to contain high concentrations (400-600 μM) of readily releasable calcium. The release of calcium from this acidic organelle store contributes to calcium-dependent processes of fundamental physiological importance to neurons including neurotransmitter release, membrane excitability, neurite outgrowth, synaptic remodeling, and cell viability. Pathologically, disturbances of endolysosome structure and/or function have been noted in a variety of neurodegenerative disorders including Alzheimer's disease (AD) and HIV-1 associated neurocognitive disorder (HAND). And, dysregulation of intracellular calcium has been implicated in the neuropathogenesis of these same neurological disorders. Thus, it is important to better understand mechanisms by which calcium is released from endolysosomes as well as the consequences of such release to inter-organellar signaling, physiological functions of neurons, and possible pathological consequences. In doing so, a path forward towards new therapeutic modalities might be facilitated.

Entities:  

Keywords:  Alzheimer’s disease; Calcium; Endolysosomes; Endosomes; HIV-1 associated neurocognitive disorder; Lysosomes; N-type calcium channels; Neurodegenerative diseases; Neurons; Store-operated calcium entry

Mesh:

Substances:

Year:  2020        PMID: 31646530      PMCID: PMC7047846          DOI: 10.1007/978-3-030-12457-1_27

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  5 in total

1.  Heterogeneity of ferrous iron-containing endolysosomes and effects of endolysosome iron on endolysosome numbers, sizes, and localization patterns.

Authors:  Peter W Halcrow; Nirmal Kumar; Zahra Afghah; Jalyn P Fischer; Nabab Khan; Xuesong Chen; Olimpia Meucci; Jonathan D Geiger
Journal:  J Neurochem       Date:  2022-02-23       Impact factor: 5.546

2.  A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl-/H+-Exchanger, Causes Early-Onset Neurodegeneration.

Authors:  Maya M Polovitskaya; Carlo Barbini; Diego Martinelli; Frederike L Harms; F Sessions Cole; Paolo Calligari; Gianfranco Bocchinfuso; Lorenzo Stella; Andrea Ciolfi; Marcello Niceta; Teresa Rizza; Marwan Shinawi; Kathleen Sisco; Jessika Johannsen; Jonas Denecke; Rosalba Carrozzo; Daniel J Wegner; Kerstin Kutsche; Marco Tartaglia; Thomas J Jentsch
Journal:  Am J Hum Genet       Date:  2020-11-19       Impact factor: 11.025

Review 3.  Lysosomal Stress Response (LSR): Physiological Importance and Pathological Relevance.

Authors:  Koffi L Lakpa; Nabab Khan; Zahra Afghah; Xuesong Chen; Jonathan D Geiger
Journal:  J Neuroimmune Pharmacol       Date:  2021-03-22       Impact factor: 4.147

Review 4.  Neurodegeneration Upon Dysfunction of Endosomal/Lysosomal CLC Chloride Transporters.

Authors:  Shroddha Bose; Hailan He; Tobias Stauber
Journal:  Front Cell Dev Biol       Date:  2021-02-23

5.  SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction.

Authors:  Lara Marrone; Paolo M Marchi; Christopher P Webster; Raffaele Marroccella; Ian Coldicott; Steven Reynolds; João Alves-Cruzeiro; Zih-Liang Yang; Adrian Higginbottom; Mukhran Khundadze; Pamela J Shaw; Christian A Hübner; Matthew R Livesey; Mimoun Azzouz
Journal:  Hum Mol Genet       Date:  2022-08-23       Impact factor: 5.121

  5 in total

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