Matches in SemOpenAlex for { <https://semopenalex.org/work/W39815190> ?p ?o ?g. }
Showing items 1 to 81 of
81
with 100 items per page.
- W39815190 abstract "Calcium (Ca2+) is an indispensable intracellular second messenger, essential for cellular life and death. Given the duality of the Ca2+ signal, intracellular Ca2+ levels must be tightly regulated to ensure Ca2+ homeostasis is maintained. Indeed, dysregulation of Ca2+ handling and homeostasis has been associated with a number of different disease states. The cellular arsenal for controlling intracellular Ca2+ includes a multitude of Ca2+ transport proteins, including the plasmalemmal and secretory pathway Ca2+ ATPases (the PMCAs, and SPCAs, respectively). Multiple isoforms of each exist, many of which have different tissue distributions and regulate diverse physiological functions. Secretory pathway Ca2+ ATPase 2 (SPCA2) was first characterised in 2005, and, as such, is the most recently identified Ca2+ ATPase. To date, only a small number of functional studies have been reported on SPCA2, however, a physiological role in secretory cells has been proposed for this novel enzyme. The mammary gland is a unique secretory organ in many ways, but when it comes to Ca2+ regulation and homeostasis it is especially so; during lactation the mammary epithelial cell must transport large quantities of Ca2+ in a unidirectional fashion, concurrent to maintaining a low intracellular Ca2+ concentration. Specific isoforms of plasmalemmal and secretory pathway Ca2+ ATPases are associated with lactation, and indeed with the supply of Ca2+ ions for the enrichment of milk. The recently identified SPCA2 has a number of characteristics suggestive of a role in lactation. This thesis reports the results of an investigation of the hypotheses that SPCAs, in particular the recently identified and less widely expressed SPCA2, are important in mammary gland development, and that different isoforms of plasmalemmal and secretory pathway Ca2+ ATPases have different Plasmalemmal and Secretory Pathway Ca2+ ATPases in the Mammary Gland vii localisations during lactation. The expression of both SPCA1 and SPCA2 in mammary glands isolated from virgin, pregnant, lactating and involuting mice was assessed; a more pronounced increase in SPCA2 mRNA was observed during lactation compared to SPCA1, suggesting that SPCA2 is the predominant SPCA isoform associated with the lactating phenotype. Immunolocalisation studies indicate that different plasmalemmal (PMCA1, PMCA2) and secretory pathway (SPCA1, SPCA2) Ca2+ ATPases have different localisations in the lactating mammary gland in vivo, and in a three-dimensional mammary gland culture model, suggesting different functional roles for these different Ca2+ ATPases during lactation. It is not uncommon for ion transporters, which are up-regulated in lactation to be similarly over-expressed in breast cancer. In addition, there is accumulating evidence to suggest that alterations in cellular Ca2+ signalling and homeostasis are associated with cancer. Indeed certain Ca2+ transport proteins are associated with tumorigenicity and have been identified as possible targets for anti¬cancer therapies. This thesis also reports the results of an investigation of the hypothesis that SPCAs, particularly SPCA2, are important in breast cancer. SPCA1 and SPCA2 mRNA levels were assessed in a bank of breast cancer derived and normal human breast epithelial cell lines and human clinical breast cancer samples. A pronounced increase in SPCA2 mRNA was observed in the breast cancer derived cell lines compared to the normal cell lines, and also in the clinical tumour samples compared to surrounding normal tissue, suggesting that up-regulated SPCA2 is associated with breast cancer. Given that SPCA2 was only identified in 2005, there is a paucity of published studies investigating SPCA2 function. Indeed, there have only been four published reports to date specifically characterising this novel Ca2+ ATPase, coming from only three research laboratories. This thesis reports the results of an investigation, which has attempted to further characterise SPCA2 function viii Plasmalemmal and Secretory Pathway Ca2+ ATPases in the Mammary Gland through gene over-expression and knock-down studies. Collectively, the results presented in this thesis suggest that SPCA2 is not involved in global Ca2+ regulation and proposes that SPCA2 may have a highly specialised role within the cell, which may be associated with Golgi function. In summary, the results presented in this thesis are the first to implicate SPCA2 in a physiological process, and in a disease state, and highlight the importance of this novel enzyme in the mammary gland. They also demonstrate that different isoforms of plasmalemmal and secretory pathway Ca2+ ATPases have different cellular localisations during lactation in the mammary gland, which may suggest different functional roles for these Ca2+ ATPases during this physiological process. In addition, the work presented in this thesis has attempted to characterise the recently identified Ca2+ ATPase, SPCA2, and collectively suggests that SPCA2 is not involved in global Ca2+ regulation, but rather, propose a highly specific physiological role for this novel enzyme within the cell." @default.
- W39815190 created "2016-06-24" @default.
- W39815190 creator A5009899535 @default.
- W39815190 date "2007-11-01" @default.
- W39815190 modified "2023-09-27" @default.
- W39815190 title "Plasmalemmal and Secretory Pathway Calcium ATPases in the Mammary Gland" @default.
- W39815190 hasPublicationYear "2007" @default.
- W39815190 type Work @default.
- W39815190 sameAs 39815190 @default.
- W39815190 citedByCount "0" @default.
- W39815190 crossrefType "journal-article" @default.
- W39815190 hasAuthorship W39815190A5009899535 @default.
- W39815190 hasConcept C104317684 @default.
- W39815190 hasConcept C119062480 @default.
- W39815190 hasConcept C158617107 @default.
- W39815190 hasConcept C163235415 @default.
- W39815190 hasConcept C178790620 @default.
- W39815190 hasConcept C181080969 @default.
- W39815190 hasConcept C181199279 @default.
- W39815190 hasConcept C185592680 @default.
- W39815190 hasConcept C201571599 @default.
- W39815190 hasConcept C23265538 @default.
- W39815190 hasConcept C49039625 @default.
- W39815190 hasConcept C51705589 @default.
- W39815190 hasConcept C519063684 @default.
- W39815190 hasConcept C53345823 @default.
- W39815190 hasConcept C55493867 @default.
- W39815190 hasConcept C63645605 @default.
- W39815190 hasConcept C6492254 @default.
- W39815190 hasConcept C79879829 @default.
- W39815190 hasConcept C86803240 @default.
- W39815190 hasConcept C87975464 @default.
- W39815190 hasConcept C95444343 @default.
- W39815190 hasConceptScore W39815190C104317684 @default.
- W39815190 hasConceptScore W39815190C119062480 @default.
- W39815190 hasConceptScore W39815190C158617107 @default.
- W39815190 hasConceptScore W39815190C163235415 @default.
- W39815190 hasConceptScore W39815190C178790620 @default.
- W39815190 hasConceptScore W39815190C181080969 @default.
- W39815190 hasConceptScore W39815190C181199279 @default.
- W39815190 hasConceptScore W39815190C185592680 @default.
- W39815190 hasConceptScore W39815190C201571599 @default.
- W39815190 hasConceptScore W39815190C23265538 @default.
- W39815190 hasConceptScore W39815190C49039625 @default.
- W39815190 hasConceptScore W39815190C51705589 @default.
- W39815190 hasConceptScore W39815190C519063684 @default.
- W39815190 hasConceptScore W39815190C53345823 @default.
- W39815190 hasConceptScore W39815190C55493867 @default.
- W39815190 hasConceptScore W39815190C63645605 @default.
- W39815190 hasConceptScore W39815190C6492254 @default.
- W39815190 hasConceptScore W39815190C79879829 @default.
- W39815190 hasConceptScore W39815190C86803240 @default.
- W39815190 hasConceptScore W39815190C87975464 @default.
- W39815190 hasConceptScore W39815190C95444343 @default.
- W39815190 hasLocation W398151901 @default.
- W39815190 hasOpenAccess W39815190 @default.
- W39815190 hasPrimaryLocation W398151901 @default.
- W39815190 hasRelatedWork W1581121842 @default.
- W39815190 hasRelatedWork W1943758270 @default.
- W39815190 hasRelatedWork W1976396638 @default.
- W39815190 hasRelatedWork W1983166456 @default.
- W39815190 hasRelatedWork W1984181658 @default.
- W39815190 hasRelatedWork W1988021631 @default.
- W39815190 hasRelatedWork W2003848758 @default.
- W39815190 hasRelatedWork W2021844822 @default.
- W39815190 hasRelatedWork W2031878500 @default.
- W39815190 hasRelatedWork W2087404419 @default.
- W39815190 hasRelatedWork W2093041672 @default.
- W39815190 hasRelatedWork W2098679983 @default.
- W39815190 hasRelatedWork W2101973675 @default.
- W39815190 hasRelatedWork W2118170088 @default.
- W39815190 hasRelatedWork W2140624006 @default.
- W39815190 hasRelatedWork W2416406364 @default.
- W39815190 hasRelatedWork W2507299671 @default.
- W39815190 hasRelatedWork W2607636199 @default.
- W39815190 hasRelatedWork W26230513 @default.
- W39815190 hasRelatedWork W3004688614 @default.
- W39815190 isParatext "false" @default.
- W39815190 isRetracted "false" @default.
- W39815190 magId "39815190" @default.
- W39815190 workType "article" @default.