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Article: The endoplasmic reticulum and junctional membrane communication during calcium signaling

TitleThe endoplasmic reticulum and junctional membrane communication during calcium signaling
Authors
KeywordsCalcium
Cyclic ADP-ribose
Endoplasmic reticulum
Inositol trisphosphate
NAADP
Organelle
Issue Date2013
Citation
Biochimica et Biophysica Acta - Molecular Cell Research, 2013, v. 1833, n. 11, p. 2542-2559 How to Cite?
AbstractThe endoplasmic reticulum is a major organelle in all eukaryotic cells which performs multiple functions including protein and lipid synthesis and sorting, drug metabolism, and Ca2+ storage and release. The endoplasmic reticulum, and its specialized muscle counterpart the sarcoplasmic reticulum, is the largest and most extensive of Ca2+ storage organelle in eukaryotic cells, often occupying in excess of 10% of the cell volume. There are three major components of Ca2+ storage organelles which mediate their major functions: Ca2+ uptake, mediated by pumps and exchangers; storage enhanced by luminal Ca2+ binding proteins, and Ca2+ mobilization mediated by specific ion channels. Ca2+ mobilization from the endoplasmic reticulum plays a central role in Ca2+ signaling. Through Ca2+ release channels in its membrane, the pervading and plastic structure of the endoplasmic reticulum allows Ca2+ release to be rapidly targeted to specific cytoplasmic sites across the whole cell. That several endoplasmic reticulum Ca2+ release channels are also activated by Ca2+ itself, contributes to endoplasmic reticulum membrane excitability which is the principal basis for generating spatio-temporal complex cellular Ca2+ signals, allowing specific processes to be regulated by this universal messenger. In addition, the endoplasmic reticulum forms discrete junctions with the plasma membrane and membranes of organelles such as mitochondria and lysosomes, forming nanodomains at their interfaces that play critical roles in Ca2+ signaling during key cellular processes such as cellular bioenergetics, apoptosis and autophagy. At these junctions key Ca2+ transport and regulatory processes come into play, and a recurring theme in this review is the often tortuous paths in identifying these mechanisms unequivocally. This article is part of a Special Issue entitled: Functional and structural diversity of endoplasmic reticulum. © 2013 Elsevier B.V.
Persistent Identifierhttp://hdl.handle.net/10722/343126
ISSN
2023 Impact Factor: 4.6
2023 SCImago Journal Rankings: 1.500

 

DC FieldValueLanguage
dc.contributor.authorLam, Andy K.M.-
dc.contributor.authorGalione, Antony-
dc.date.accessioned2024-05-10T09:05:39Z-
dc.date.available2024-05-10T09:05:39Z-
dc.date.issued2013-
dc.identifier.citationBiochimica et Biophysica Acta - Molecular Cell Research, 2013, v. 1833, n. 11, p. 2542-2559-
dc.identifier.issn0167-4889-
dc.identifier.urihttp://hdl.handle.net/10722/343126-
dc.description.abstractThe endoplasmic reticulum is a major organelle in all eukaryotic cells which performs multiple functions including protein and lipid synthesis and sorting, drug metabolism, and Ca2+ storage and release. The endoplasmic reticulum, and its specialized muscle counterpart the sarcoplasmic reticulum, is the largest and most extensive of Ca2+ storage organelle in eukaryotic cells, often occupying in excess of 10% of the cell volume. There are three major components of Ca2+ storage organelles which mediate their major functions: Ca2+ uptake, mediated by pumps and exchangers; storage enhanced by luminal Ca2+ binding proteins, and Ca2+ mobilization mediated by specific ion channels. Ca2+ mobilization from the endoplasmic reticulum plays a central role in Ca2+ signaling. Through Ca2+ release channels in its membrane, the pervading and plastic structure of the endoplasmic reticulum allows Ca2+ release to be rapidly targeted to specific cytoplasmic sites across the whole cell. That several endoplasmic reticulum Ca2+ release channels are also activated by Ca2+ itself, contributes to endoplasmic reticulum membrane excitability which is the principal basis for generating spatio-temporal complex cellular Ca2+ signals, allowing specific processes to be regulated by this universal messenger. In addition, the endoplasmic reticulum forms discrete junctions with the plasma membrane and membranes of organelles such as mitochondria and lysosomes, forming nanodomains at their interfaces that play critical roles in Ca2+ signaling during key cellular processes such as cellular bioenergetics, apoptosis and autophagy. At these junctions key Ca2+ transport and regulatory processes come into play, and a recurring theme in this review is the often tortuous paths in identifying these mechanisms unequivocally. This article is part of a Special Issue entitled: Functional and structural diversity of endoplasmic reticulum. © 2013 Elsevier B.V.-
dc.languageeng-
dc.relation.ispartofBiochimica et Biophysica Acta - Molecular Cell Research-
dc.subjectCalcium-
dc.subjectCyclic ADP-ribose-
dc.subjectEndoplasmic reticulum-
dc.subjectInositol trisphosphate-
dc.subjectNAADP-
dc.subjectOrganelle-
dc.titleThe endoplasmic reticulum and junctional membrane communication during calcium signaling-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.bbamcr.2013.06.004-
dc.identifier.pmid23770047-
dc.identifier.scopuseid_2-s2.0-84880577375-
dc.identifier.volume1833-
dc.identifier.issue11-
dc.identifier.spage2542-
dc.identifier.epage2559-
dc.identifier.eissn1879-2596-

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