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• W2003280203 abstract "Intracellular calcium signals activated by growth factors in endothelial cells during angiogenesis regulate cytosolic and nuclear events involved in survival, proliferation and motility. Among the intracellular messengers released upon proangiogenic stimulation, arachidonic acid (AA) and its metabolites play a key role, and their effects are strictly related to calcium homeostasis. In human breast tumor-derived endothelial cells (B-TECs) AA stimulates proliferation and tubulogenesis in a calcium-dependent way. Here, to characterize the proteins whose expression is regulated by AA-induced calcium entry, we used a proteomic approach (two-dimensional gel electrophoresis and matrix-assisted laser desorption ionization mass spectrometry, 2-DE and MALDI-MS) and we compared the proteomes of B-TECs stimulated with AA in presence or in absence of calcium entry (with addition to the culture medium of the calcium chelator EGTA, which completely prevents calcium fluxes throughout the plasma membrane). We found that six proteins increased their levels of expression, all higher when AA-induced calcium entry was abolished. These proteins have been identified by mass spectrometry and database search, and their potential roles in AA-stimulated pathway and in angiogenesis are discussed." @default.
• W2003280203 created "2016-06-24" @default.
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• W2003280203 date "2009-09-22" @default.
• W2003280203 modified "2023-10-16" @default.
• W2003280203 title "Arachidonic acid and calcium signals in human breast tumor-derived endothelial cells: a proteomic study" @default.
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• W2003280203 doi "https://doi.org/10.1080/10799890903208039" @default.
• W2003280203 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19769547" @default.
• W2003280203 hasPublicationYear "2009" @default.
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