9
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      Extracellular polyphosphate signals through Ras and Akt to primeDictyostelium discoideumcells for development

      , , ,
      Journal of Cell Science
      The Company of Biologists

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          <p id="d9641612e186">Linear chains of five to hundreds of phosphates called polyphosphate are found in organisms ranging from bacteria to humans, but their function is poorly understood. In <i>Dictyostelium discoideum</i>, polyphosphate is used as a secreted signal that inhibits cytokinesis in an autocrine negative feedback loop. To elucidate how cells respond to this unusual signal, we undertook a proteomic analysis of cells treated with physiological levels of polyphosphate and observed that polyphosphate causes cells to decrease levels of actin cytoskeleton proteins, possibly explaining how polyphosphate inhibits cytokinesis. Polyphosphate also causes proteasome protein levels to decrease, and in both <i>Dictyostelium</i> and human leukemia cells, decreases proteasome activity and cell proliferation. Polyphosphate also induces <i>Dictyostelium</i> cells to begin development by increasing expression of the cell–cell adhesion molecule CsA (also known as CsaA) and causing aggregation, and this effect, as well as the inhibition of proteasome activity, is mediated by Ras and Akt proteins. Surprisingly, Ras and Akt do not affect the ability of polyphosphate to inhibit proliferation, suggesting that a branching pathway mediates the effects of polyphosphate, with one branch affecting proliferation, and the other branch affecting development. </p><p class="first" id="d9641612e198"> <b>Summary:</b> Polyphosphate is present in all eukaryotes, but little is known about its function. Here, we describe how <i>Dictyostelium</i> uses polyphosphate as a signal to initiate development. </p>

          Related collections

          Most cited references49

          • Record: found
          • Abstract: found
          • Article: not found

          Ten years of protein kinase B signalling: a hard Akt to follow.

          It is ten years since the publication of three papers describing the cloning of a new proto-oncogene serine/threonine kinase termed protein kinase B (PKB)/Akt. Key roles for this protein kinase in cellular processes such as glucose metabolism, cell proliferation, apoptosis, transcription and cell migration are now well established. The explosion of publications involving PKB/Akt in the past three years emphasizes the high level of current interest in this signalling molecule. This review focuses on tracing the characterization of this kinase, through the elucidation of its mechanism of regulation, to its role in regulating physiological and pathophysiological processes, to our current understanding of the biology of PKB/Akt, and prospects for the future.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Regulation of proteasome activity in health and disease.

            The ubiquitin-proteasome system (UPS) is the primary selective degradation system in the nuclei and cytoplasm of eukaryotic cells, required for the turnover of myriad soluble proteins. The hundreds of factors that comprise the UPS include an enzymatic cascade that tags proteins for degradation via the covalent attachment of a poly-ubiquitin chain, and a large multimeric enzyme that degrades ubiquitinated proteins, the proteasome. Protein degradation by the UPS regulates many pathways and is a crucial component of the cellular proteostasis network. Dysfunction of the ubiquitination machinery or the proteolytic activity of the proteasome is associated with numerous human diseases. In this review we discuss the contributions of the proteasome to human pathology, describe mechanisms that regulate the proteolytic capacity of the proteasome, and discuss strategies to modulate proteasome function as a therapeutic approach to ameliorate diseases associated with altered UPS function. This article is part of a Special Issue entitled: Ubiquitin-Proteasome System. Guest Editors: Thomas Sommer and Dieter H. Wolf. © 2013 Elsevier B.V. All rights reserved.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Advances in protein kinase B signalling: AKTion on multiple fronts.

                Bookmark

                Author and article information

                Journal
                Journal of Cell Science
                J Cell Sci
                The Company of Biologists
                0021-9533
                1477-9137
                July 15 2017
                July 15 2017
                July 15 2017
                June 05 2017
                : 130
                : 14
                : 2394-2404
                Article
                10.1242/jcs.203372
                5536921
                28584190
                7272da27-d3c4-4f47-a598-87aae4038a78
                © 2017

                http://www.biologists.com/user-licence-1-1/

                History

                Comments

                Comment on this article