Dolls/puppets as soulmates – biographical traces of dolls/puppets in art, literature, work and performance

https://dedo.ub.uni-siegen.deDie vorliegende vierte Ausgabe der Zeitschrift denkste: puppe / just a bit of: doll (de:do), ein multidisziplinäres Online-Journal für Mensch-Puppen-Diskurse, greift den Themenschwerpunkt Puppen als Seelenverwandte – biographische Spuren von Puppen in Kunst, Literatur, Werk und Darstellung auf. Es geht um die Frage nach Wirkungen früher Puppenerfahrungen in der späteren künstlerischen Arbeit und damit nach den möglichen (biographischen) Wurzeln und Zusammenhängen von Puppenmotiv und Puppen-Narrativen im künstlerisch-literarischen Werk. Puppenbezüge in Werk- und Schaffensprozessen können frühe Erfahrungen biographischer Brüche und Verletzungen transformieren bzw. sie künstlerisch produktiv integrieren, sie können aber auch Ausdruck für Kontinuität und Intensivierung früher Prägungen und Vorlieben sein. In den vorliegenden Beiträgen geht es um puppenbezogene künstlerische Ausdrucksformen, die als Beiträge hier formal unterschiedlich aufbereitet werden: als wissenschaftsbasierter Text, Selbstbericht, Miszelle, Rezension, Interview und: Kunstwerk. Untersucht und thematisiert werden Puppen-Sammlungen, die Herstellung besonderer Puppen, literarische Puppentexte, Inszenierungen und Bilder. Außerdem wurden weitere Beiträge einbezogen, die Puppen als Varianten „künstlicher Menschen“ in unterschiedlichsten Themenbezügen behandeln. In vielen Beiträgen deutet sich an, dass die Affinität zum „Phänomen Puppe“ in seinen verschiedenen künstlerischen Umsetzungsformen auf biographisch geprägte Spuren verweist: als Ausdrucks- und Darstellungsmittel steht die Puppe somit auch für etwas Besonderes der Menschen, die sich künstlerisch auf sie beziehen und mit ihr interagieren und „spielen“.This fourth issue of denkste: puppe / just a bit of: doll (de:do), a multidisciplinary online journal for human-doll discourses, takes up the thematic focus on dolls/puppets as soulmates – biographical traces of dolls/puppets in art, literature, work and performance. It is about the impact of early doll experiences in later artistic work and thus about the possible (biographical) roots and connections of doll motifs and doll narratives in artistic-literary work. Doll/puppet references in work and creative processes can transform early experiences of biographical breaks and harm or integrate them in an artistically productive way, but they can also be an expression of continuity and intensification of early experience and preferences. The present contributions deal with doll/puppet-related artistic forms of expression, which are formally presented in different ways: as science-based text, self-report, miscellaneous, review, interview and: work of art. Doll/puppet collections, the making of particular puppets, literary puppet texts, performances and images are examined and addressed. In addition, further contributions were included, which deal with dolls as variants of "artificial humans" in the most diverse thematic contexts. Most of the contributions indicate that the affinity to the “phenomenon of the doll” in its various artistic forms of realization refers to biographically shaped traces: as a means of expression and representation the doll thus also stands for something special about the human beings who refer to it artistically and interact and "play" with it

Nature's lessons in design: nanomachines to scaffold, remodel and shape membrane compartments.

Compartmentalisation of cellular processes is fundamental to regulation of metabolism in Eukaryotic organisms and is primarily provided by membrane-bound organelles. These organelles are dynamic structures whose membrane barriers are continually shaped, remodelled and scaffolded by a rich variety of highly sophisticated protein complexes. Towards the goal of bottom-up assembly of compartmentalised protocells in synthetic biology, we believe it will be important to harness and reconstitute the membrane shaping and sculpting characteristics of natural cells. We review different in vitro membrane models and how biophysical investigations of minimal systems combined with appropriate theoretical modelling have been used to gain new insights into the intricate mechanisms of these membrane nanomachines, paying particular attention to proteins involved in membrane fusion, fission and cytoskeletal scaffolding processes. We argue that minimal machineries need to be developed and optimised for employment in artificial protocell systems rather than the complex environs of a living organism. Thus, well-characterised minimal components might be predictably combined into functional, compartmentalised protocellular materials that can be engineered for wide-ranging applications

Amyloid β-Oligomers Inhibit the Nuclear Ca²⁺ Signals and the Neuroprotective Gene Expression Induced by Gabazine in Hippocampal Neurons

Hippocampal neuronal activity generates dendritic and somatic Ca2+ signals, which, depending on stimulus intensity, rapidly propagate to the nucleus and induce the expression of transcription factors and genes with crucial roles in cognitive functions. Soluble amyloid-beta oligomers (AβOs), the main synaptotoxins engaged in the pathogenesis of Alzheimer’s disease, generate aberrant Ca2+ signals in primary hippocampal neurons, increase their oxidative tone and disrupt structural plasticity. Here, we explored the effects of sub-lethal AβOs concentrations on activity-generated nuclear Ca2+ signals and on the Ca2+-dependent expression of neuroprotective genes. To induce neuronal activity, neuron-enriched primary hippocampal cultures were treated with the GABAA receptor blocker gabazine (GBZ), and nuclear Ca2+ signals were measured in AβOs-treated or control neurons transfected with a genetically encoded nuclear Ca2+ sensor. Incubation (6 h) with AβOs significantly reduced the nuclear Ca2+ signals and the enhanced phosphorylation of cyclic AMP response element-binding protein (CREB) induced by GBZ. Likewise, incubation (6 h) with AβOs significantly reduced the GBZ-induced increases in the mRNA levels of neuronal Per-Arnt-Sim domain protein 4 (Npas4), brain-derived neurotrophic factor (BDNF), ryanodine receptor type-2 (RyR2), and the antioxidant enzyme NADPH-quinone oxidoreductase (Nqo1). Based on these findings we propose that AβOs, by inhibiting the generation of activity-induced nuclear Ca2+ signals, disrupt key neuroprotective gene expression pathways required for hippocampal-dependent learning and memory processes

The Analysis of the Editing Defects in the dyw2 Mutant Provides New Clues for the Prediction of RNA Targets of Arabidopsis E+-Class PPR Proteins

C to U editing is one of the post-transcriptional steps which are required for the proper expression of chloroplast and mitochondrial genes in plants. It depends on several proteins acting together which include the PLS-class pentatricopeptide repeat proteins (PPR). DYW2 was recently shown to be required for the editing of many sites in both organelles. In particular almost all the sites associated with the E+ subfamily of PPR proteins are depending on DYW2, suggesting that DYW2 is required for the function of E+-type PPR proteins. Here we strengthened this link by identifying 16 major editing sites controlled by 3 PPR proteins: OTP90, a DYW-type PPR and PGN and MEF37, 2 E+-type PPR proteins. A re-analysis of the DYW2 editotype showed that the 49 sites known to be associated with the 18 characterized E+-type PPR proteins all depend on DYW2. Considering only the 288 DYW2-dependent editing sites as potential E+-type PPR sites, instead of the 795 known editing sites, improves the performances of binding predictions systems based on the PPR code for E+-type PPR proteins. However, it does not compensate for poor binding predictions