Inklusion und Digitalisierung in einer Beratungsstelle für Trans*Personen während der Covid-19 Pandemie

Aufgrund der Covid-19 Pandemie und der damit einhergehenden Kontaktbeschränkungen blieben Beratungsstellen ab März 2020 geschlossen. Diese Schließungen trafen die LSBTIQ*-Community und insbesondere die Trans* Community besonders, da transidente Personen eine besonders vulnerable Gruppe darstellen und ein kommunikativer Austausch in Präsenz unabdingbar für die erfolgreiche Bewältigung des Trans*Weges ist. Dieser Artikel fokussiert sich auf eine Gruppe in Sachsen und befasst sich mit ihren Herausforderungen und Erfahrungen, die mit den von der Beratungsstelle organisierten und online stattfindenden Gruppendiskussionen einhergehen. Die folgenden Ergebnisse stammen aus einer Onlineumfrage, die über die Onlineplattform „Discord“ mit einer Trans*Gruppe durch-geführt wurde sowie einer anschließenden Teilnehmenden Beobachtung. Ziel war es, in Erfahrung zu bringen, ob und in welcher Weise die virtuell stattfindenden Beratungen und Gruppenangebote der Beratungsstelle transidente Personen bei der Bewältigung von Ängsten und Problemen unterstützen konnten. Wir zeigen, wie die Gruppe mit dem Wegfall der persönlichen Beratungen und Diskussions-runden umgegangen ist und wie sich dies auf ihren Alltag auswirkte. Außerdem erfolgt eine Reflexion über technische Herausforderungen und Möglichkeiten und Grenzen sexuelle und geschlechtliche Diversität online zu besprechen. Durch einen direkten Vergleich zwischen den Online-Beratungserfahrungen während der Covid-19 Pandemie und den Offline-Beratungserfahrungen vor Covid-19, wird ebenfalls diskutiert, inwiefern die digitalisierte Beratung eine Alternative oder gar Verbesserung bietet, LSBTIQ*-Personen mehr Sicherheit und Möglichkeiten auf ihren Trans*Weg zu verschaffen oder ob persönliche Beratungen sowie peer-to-peer Gruppenangebote in Präsenz weiterhin unabdingbar bleiben.Because of the COVID-19 pandemic and the necessary contact restrictions, German counselling services closed in March 2020. These closures particularly affected the LGBTIQ* community, specifically the trans* community since trans* people are a particularly vulnerable group who require (in-person) counselling and communication with peers to successfully embark on their trans* journey. This article focuses on a group of trans* persons based in Saxony and explores their challenges and experiences with online counselling facilitated by a counselling service for people identifying as LGBTIQ*. The results were obtained from an online survey with a group of trans* people via the platform "Discord" and a subsequent session of participatory observation. We wanted to find out how and to what extent online counselling and group sessions facilitated by the resource centre could support trans* people in overcoming fears and problems. We highlight how the group members handled the cancellation of in-person counselling and group sessions and how this affected their daily life. Further, we reflect on challenges inherent in the audiovisual format, as well as the role of digital audiovisual media as a converging mirror towards online inclusive discourse and mediation. Comparing the Covid-19 online experience with previous live discussions, we analyse whether online counselling provides more security and better ways to facilitate their trans* experience, or if, on the contrary, in-person services provide better support

Redox Proteomic Analysis Reveals Oxidative Modifications of Proteins by Increased Levels of Intracellular Reactive Oxygen Species During Hypoxia Adaptation of Aspergillus fumigatus

We thank Silke Steinbach, Till Kindel, and Michael Cyrulies for their excellent technical assistance. Work of T.K., O.K. and A.A.B was supported by the Deutsche Forschungsge-meinschaft within the Collaborative Research Center TR124 FungiNet (project A1 and Z2).The work of E.S. was supported by the International Leibniz Research School for Microbial and Biomolecular Interactions (ILRS)and by the Medical Research Council Centre for Medical Mycology at the University of Aberdeen (MR/N006364/1).We thank Matthew Blango and Falk Hillmann for the critical reading of the manuscript.Peer reviewedPostprin

LSD1 modulates the non-canonical integrin β3 signaling pathway in non-small cell lung carcinoma cells

The epigenetic writer lysine-specific demethylase 1 (LSD1) is aberrantly upregulated in many cancer types and its overexpression correlates with poor survival and tumor progression. In this study, we analysed LSD1 function in non-small cell lung cancer adenocarcinomas. Expression profiling of 182 cases of lung adenocarcinoma proved a significant correlation of LSD1 overexpression with lung adenocarcinoma progression and metastasis. KRAS-mutated lung cancer cell clones were stably silenced for LSD1 expression. RNA-seq and comprehensive pathway analysis revealed, that genes related to a recently described non-canonical integrin β3 pathway, were significantly downregulated by LSD1 silencing. Hence, invasion and self-renewal capabilities were strongly decreased. Notably, this novel defined LSD1/integrin β3 axis, was also detected in human lung adenocarcinoma specimens. Furthermore, the linkage of LSD1 to an altered expression pattern of lung-lineage specific transcription factors and genes, which are involved in alveolar epithelial differentiation, was demonstrated. Thus, our findings point to a LSD1-integrin β3 axis, conferring attributes of invasiveness and tumor progression to lung adenocarcinoma

Ceramides and Cell Signaling Molecules in Psoriatic Epidermis: Reduced Levels of Ceramides, PKC-α, and JNK

Ceramides are the main lipids in the stratum corneum and are generated during cellular stress and apoptosis by de novo synthesis or by the action of sphingomyelinase. In addition, they are lipid second messengers produced by sphingolipid metabolism and trigger important cell responses, including protein kinase C-alpha (PKC-α) activation and the stimulation of signal transduction pathways with apoptosis and stress-activated protein kinases (SAPK), such as c-jun N-terminal kinase (JNK). Thus, ceramides have anti-proliferative and apoptotic effects. This study measured the changes in the levels of epidermal ceramides and ceramide-related apoptotic signaling molecules in psoriasis patients. Samples from lesional and non-lesional epidermis were obtained from psoriasis patients. Total ceramides were fractionated using thin-layer chromatography, and the levels of PKC-α and JNK expression were measured using Western blot analysis with specific antibodies. The ceramide level was reduced significantly, and this was associated with the downregulation of apoptotic signaling molecules, such as PKC-α and JNK, in the lesional epidermis of psoriasis patients. These results suggest that the decreased level of ceramides downregulates the apoptotic pathway, leading to epidermal proliferation in psoriasis

An Inverse Relationship Between Ceramide Synthesis and Clinical Severity in Patients with Psoriasis

Ceramides play major roles in maintaining the epidermal barrier. It has been sus-pected that the depletion of ceramides, associated with disrupted barrier function in the epidermis, leads to the clinical manifestation of dryness and inflammation seen in patients with psoriasis. The aim of the present study was to determine the relation-ship between the level of ceramide synthesis in the epidermis and the clinical severity in patients with psoriasis. Samples from lesional and unlesional epidermis obtained from psoriasis patients were incubated with [14C]serine, an initiator of ceramide syn-thesis. otal ceramide was fractionated using high performance thin layer chromato-graphy, and the radioactivity was measured. The clinical severity of psoriasis was graded according to the psoriasis area and severity index scoring system. The level of ceramide synthesis in the lesional epidermis of patients was significantly lower than that in the unlesional epidermis and bore a negative correlation with the clinical severity of psoriasis. The present results suggest that the decreased level of ceramide synthesis in the epidermis contributes to the clinical severity of psoriasis

A Study on Altered Expression of Serine Palmitoyltransferase and Ceramidase in Psoriatic Skin Lesion

Ceramides are the main lipid component maintaining the lamellae structure of stratum corneum, as well as lipid second messengers for the regulation of cellular proliferation and/or apoptosis. In our previous study, psoriatic skin lesions showed marked decreased levels of ceramides and signaling molecules, specially protein kinase C-alpha (PKC-α) and c-jun N-terminal kinase (JNK) in proportion to the psoriasis area and severity index (PASI) scores, which suggested that the depletion of ceramide is responsible for epidermal hyperproliferation of psoriasis via downregulation of proapoptotic signal cascade such as PKC-α and JNK. In this study, we investigated the protein expression of serine palmitoyltransferase (SPT) and ceramidase, two major ceramide metabolizing enzymes, in both psoriatic epidermis and non-lesional epidermis. The expression of SPT, the ceramide generating enzyme in the de novo synthesis in psoriatic epidermis, was significantly less than that of the non-lesional epidermis, which was inversely correlated with PASI score. However, the expression of ceramidase, the degradative enzyme of ceramides, showed no significant difference between the lesional epidermis and the non-lesional epidermis of psoriatic patients. This might suggest that decreased expression of SPT protein is one of the important causative factors for decreased ceramide levels in psoriasis

Exclusive diffractive processes and the quark substructure of mesons

Exclusive diffractive processes on the nucleon are investigated within a model in which the quark-nucleon interaction is mediated by Pomeron exchange and the quark substructure of mesons is described within a framework based on the Dyson-Schwinger equations of QCD. The model quark-nucleon interaction has four parameters which are completely determined by high-energy $\pi N$ and $K N$ elastic scattering data. The model is then used to predict vector-meson electroproduction observables. The obtained $\rho$- and $\phi$-meson electroproduction cross sections are in excellent agreement with experimental data. The predicted $q^2$ dependence of $J/\psi$-meson electroproduction also agrees with experimental data. It is shown that confined-quark dynamics play a central role in determining the behavior of the diffractive, vector-meson electroproduction cross section. In particular, the onset of the asymptotic $1/q^4$ behavior of the cross section is determined by a momentum scale that is set by the current-quark masses of the quark and antiquark inside the vector meson. This is the origin of the striking differences between the $q^2$ dependence of $\rho$-, $\phi$- and $J/\psi$-meson electroproduction cross sections observed in recent experiments.Comment: 53 pages, 23 figures, revtex and epsfig. Minor additions to tex

Deregulation of secondary metabolism in a histone deacetylase mutant of Penicillium chrysogenum

The Pc21 g14570 gene of Penicillium chrysogenum encodes an ortholog of a class 2 histone deacetylase termed HdaA which may play a role in epigenetic regulation of secondary metabolism. Deletion of the hdaA gene induces a significant pleiotropic effect on the expression of a set of polyketide synthase (PKS) and nonribosomal peptide synthetase (NRPS)-encoding genes. The deletion mutant exhibits a decreased conidial pigmentation that is related to a reduced expression of the PKS gene Pc21 g16000 (pks17) responsible for the production of the pigment precursor naphtha-γ-pyrone. Moreover, the hdaA deletion caused decreased levels of the yellow pigment chrysogine that is associated with the downregulation of the NRPS-encoding gene Pc21 g12630 and associated biosynthetic gene cluster. In contrast, transcriptional activation of the sorbicillinoids biosynthetic gene cluster occurred concomitantly with the overproduction of associated compounds . A new compound was detected in the deletion strain that was observed only under conditions of sorbicillinoids production, suggesting crosstalk between biosynthetic gene clusters. Our present results show that an epigenomic approach can be successfully applied for the activation of secondary metabolism in industrial strains of P. chrysogenum