Publication:
Localization and quantification of endoplasmic reticulum Ca(2+)-ATPase isoform transcripts

cris.lastimport.scopus2025-05-06T22:06:15Z
cris.virtual.departmentInternal Medicineen_US
cris.virtual.departmentInternal Medicine-NTUHen_US
cris.virtual.orcid0000-0002-3339-1509en_US
cris.virtualsource.department09021acc-cf4a-48d7-a773-e5e2ac837c7e
cris.virtualsource.department09021acc-cf4a-48d7-a773-e5e2ac837c7e
cris.virtualsource.orcid09021acc-cf4a-48d7-a773-e5e2ac837c7e
dc.contributor.authorKWAN-DUN WUen_US
dc.contributor.authorLee, W Sen_US
dc.contributor.authorWey, Jen_US
dc.contributor.authorBungard, Den_US
dc.contributor.authorLytton, Jen_US
dc.date.accessioned2023-06-02T02:52:15Z
dc.date.available2023-06-02T02:52:15Z
dc.date.issued1995-09
dc.description.abstractThe Ca(2+)-adenosinetriphosphatase pump of the sarcoplasmic or endoplasmic reticulum (SERCA) plays a critical role in Ca2+ signaling and homeostasis in all cells and is encoded by a family of homologous and alternatively spliced genes. To understand more clearly the role the different isoforms play in cell physiology, we have undertaken a quantitative and qualitative assessment of the tissue distribution of transcripts encoding each SERCA isoform. SERCA1 expression is restricted to fast-twitch striated muscles, SERCA2a to cardiac and slow-twitch striated muscles, whereas SERCA2b is ubiquitously expressed. SERCA3 is expressed most abundantly in large and small intestine, thymus, and cerebellum and at lower levels in spleen, lymph node, and lung. In situ hybridization analyses revealed SERCA3 transcripts in cells of the intestinal crypt, the thymic cortex, and Purkinje cells in cerebellum. In addition, SERCA3 was expressed abundantly in isolated rat spleen lymphocytes, in various murine lymphoid cell lines, and in primary cultured microvascular endothelial cells. This analysis demonstrates that SERCA3 is expressed selectively in cells in which Ca2+ signaling plays a critical and sensitive role in regulating physiological processes.en_US
dc.identifier.doi10.1152/ajpcell.1995.269.3.C775
dc.identifier.issn0002-9513
dc.identifier.pmid7573409
dc.identifier.scopus2-s2.0-0028855203
dc.identifier.urihttps://scholars.lib.ntu.edu.tw/handle/123456789/631734
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/0028855203
dc.language.isoenen_US
dc.relation.ispartofThe American journal of physiologyen_US
dc.relation.journalissue3 Pt 1en_US
dc.relation.journalvolume269en_US
dc.relation.pageendC784en_US
dc.subjectin situ hybridization | quantitative Northern blotting | sarcoplasmic or endoplasmic reticulum calcium-adenosinetriphosphatase isoformsen_US
dc.titleLocalization and quantification of endoplasmic reticulum Ca(2+)-ATPase isoform transcriptsen_US
dc.typejournal articleen
dspace.entity.typePublication

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