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Titolo/Abstract/Parole chiave

From cell signalling to cell death: endoplasmic reticulum-mitochondria calcium transfer and its remodelling for cancer cell survival

Bononi, Angela (2012) From cell signalling to cell death: endoplasmic reticulum-mitochondria calcium transfer and its remodelling for cancer cell survival. Tesi di Dottorato , Università degli studi di Ferrara.

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    Abstract

    The tight interplay between endoplasmic reticulum (ER) and mitochondria is a key determinant of cell function and survival through the control of intracellular calcium (Ca2+) signalling. The physical platform for the association between the ER and mitochondria is a domain of the ER called the “mitochondria-associated membranes” (MAMs). MAMs are crucial for highly efficient transmission of Ca2+ from the ER to mitochondria, thus controlling fundamental processes involved in energy production and also determining cell fate by triggering or preventing apoptosis. In particular, we show that: i) despite different roles in cell survival, all three isoforms of the outer mitochondrial membrane protein voltage-dependent anion channels (VDAC) are equivalent in allowing mitochondrial Ca2+ loading upon agonist stimulation, vice versa VDAC1, by selectively interacting with the inositol trisphosphate receptors (IP3Rs) - an interaction that is further strengthened by apoptotic stimuli - is preferentially involved in the transmission of the low-amplitude apoptotic Ca2+ signals to mitochondria, highlighting a non-redundant molecular route for transferring Ca2+ signals to mitochondria in apoptosis; ii) the promyelocytic leukemia (PML) tumor suppressor exerts its extranuclear proapoptotic action by its unexpected and fundamental role at MAMs, where PML was found in protein complexes with the type 3 IP3R, the protein kinase Akt and the phosphatase PP2a, which are essential for Akt- and PP2a-dependent modulation of IP3R phosphorylation and in turn for IP3R-mediated Ca2+ release from ER; iii) the PTEN (phosphatase and tensin homolog deleted on chromosome 10) tumor suppressor localizes at the ER and MAMs, and ER-localized PTEN is specifically involved in increasing both Ca2+ transfer from the ER to mitochondria and cell sensitivity to Ca2+-mediated apoptosis. The improved knowledge of the functioning of proteins involved in regulating Ca2+ signalling may reveal novel unexplored pharmacological targets, and help in treating cancer as well as other pathologies.

    Tipologia del documento:Tesi di Dottorato (Tesi di Dottorato)
    Data:14 Marzo 2012
    Relatore:Pinton, Paolo
    Coordinatore ciclo:Bernardi, Francesco
    Istituzione:Università degli studi di Ferrara
    Dottorato:XXIV Anno 2009 > BIOCHIMICA, BIOLOGIA MOLECOLARE E BIOTECNOLOGIE
    Struttura:Dipartimento > Biochimica e biologia molecolare
    Soggetti:Area 06 - Scienze mediche > MED/04 Patologia generale
    Parole chiave:calcio, calcium, mitocondri, mitochondria, reticolo endoplasmatico, endoplasmic reticulum, apaptosis, VDAC, PML, PTEN
    Depositato il:13 Feb 2013 14:54

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