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Calcium Dynamics Mediated by the Endoplasmic/Sarcoplasmic Reticulum and Related Diseases

The flow of intracellular calcium (Ca(2+)) is critical for the activation and regulation of important biological events that are required in living organisms. As the major Ca(2+) repositories inside the cell, the endoplasmic reticulum (ER) and the sarcoplasmic reticulum (SR) of muscle cells are cent...

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Autores principales: Reddish, Florence N., Miller, Cassandra L., Gorkhali, Rakshya, Yang, Jenny J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454937/
https://www.ncbi.nlm.nih.gov/pubmed/28489021
http://dx.doi.org/10.3390/ijms18051024
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author Reddish, Florence N.
Miller, Cassandra L.
Gorkhali, Rakshya
Yang, Jenny J.
author_facet Reddish, Florence N.
Miller, Cassandra L.
Gorkhali, Rakshya
Yang, Jenny J.
author_sort Reddish, Florence N.
collection PubMed
description The flow of intracellular calcium (Ca(2+)) is critical for the activation and regulation of important biological events that are required in living organisms. As the major Ca(2+) repositories inside the cell, the endoplasmic reticulum (ER) and the sarcoplasmic reticulum (SR) of muscle cells are central in maintaining and amplifying the intracellular Ca(2+) signal. The morphology of these organelles, along with the distribution of key calcium-binding proteins (CaBPs), regulatory proteins, pumps, and receptors fundamentally impact the local and global differences in Ca(2+) release kinetics. In this review, we will discuss the structural and morphological differences between the ER and SR and how they influence localized Ca(2+) release, related diseases, and the need for targeted genetically encoded calcium indicators (GECIs) to study these events.
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spelling pubmed-54549372017-06-08 Calcium Dynamics Mediated by the Endoplasmic/Sarcoplasmic Reticulum and Related Diseases Reddish, Florence N. Miller, Cassandra L. Gorkhali, Rakshya Yang, Jenny J. Int J Mol Sci Review The flow of intracellular calcium (Ca(2+)) is critical for the activation and regulation of important biological events that are required in living organisms. As the major Ca(2+) repositories inside the cell, the endoplasmic reticulum (ER) and the sarcoplasmic reticulum (SR) of muscle cells are central in maintaining and amplifying the intracellular Ca(2+) signal. The morphology of these organelles, along with the distribution of key calcium-binding proteins (CaBPs), regulatory proteins, pumps, and receptors fundamentally impact the local and global differences in Ca(2+) release kinetics. In this review, we will discuss the structural and morphological differences between the ER and SR and how they influence localized Ca(2+) release, related diseases, and the need for targeted genetically encoded calcium indicators (GECIs) to study these events. MDPI 2017-05-10 /pmc/articles/PMC5454937/ /pubmed/28489021 http://dx.doi.org/10.3390/ijms18051024 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Reddish, Florence N.
Miller, Cassandra L.
Gorkhali, Rakshya
Yang, Jenny J.
Calcium Dynamics Mediated by the Endoplasmic/Sarcoplasmic Reticulum and Related Diseases
title Calcium Dynamics Mediated by the Endoplasmic/Sarcoplasmic Reticulum and Related Diseases
title_full Calcium Dynamics Mediated by the Endoplasmic/Sarcoplasmic Reticulum and Related Diseases
title_fullStr Calcium Dynamics Mediated by the Endoplasmic/Sarcoplasmic Reticulum and Related Diseases
title_full_unstemmed Calcium Dynamics Mediated by the Endoplasmic/Sarcoplasmic Reticulum and Related Diseases
title_short Calcium Dynamics Mediated by the Endoplasmic/Sarcoplasmic Reticulum and Related Diseases
title_sort calcium dynamics mediated by the endoplasmic/sarcoplasmic reticulum and related diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454937/
https://www.ncbi.nlm.nih.gov/pubmed/28489021
http://dx.doi.org/10.3390/ijms18051024
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