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Borstgrasrasen, ein prägender Bestandteil der Kulturlandschaft im Schwarzwald, sind in starkem Wandel begriffen, der in erster Linie von Änderungen der Landnutzung abhängt. Um die funktionellen Zusammenhänge in den Borstgrasrasen abbilden zu können, werden die dort vorkommenden Arten zu funktionellen Pflanzentypen gruppiert. Für diese Klassifikation der Arten werden Merkmale herangezogen, die funktionell mit der Reaktion der Arten auf unterschiedlich intensive Beweidung oder Pflege in Zusammenhang stehen. Zum einen wird an ausgewählten Merkmalen, die vor Ort gemessen wurden, überprüft, wie sie bei ausgewählten Arten innerhalb und zwischen Beständen und schließlich auch zwischen den Arten variieren, um deren Eignung für eine Klassifikation zu prüfen. Zum anderen werden Eigenschaften für eine Reihe von Arten aus der Merkmals-Datenbank LEDA abgefragt und zur Ableitung von funktionellen Pflanzentypen (PFTs) mittels numerischer Klassifikation verwendet. Es zeigt sich, dass einige Eigenschaften wie die spezifische Blattfläche (SLA) eine gute Eignung für die Differenzierung von Arten und Beständen haben, da sie nur bei einigen Arten und zudem wenig plastisch auf unterschiedlich intensive Beweidung reagieren. Andere Merkmale, wie das C/N-Verhältnis der Blätter, variieren sehr stark innerhalb einiger Arten und eignen sich somit weniger für eine Klassifikation. Diese ergibt 17 PFTs, die zunächst nach der Lebensform unterschieden werden und dann insbesondere nach den Kriterien Anordnung der Blätter, spezifische Blattfläche und Blattfläche weiter untergliedert werden Einige PFTs zeigen klar unterschiedliche Deckungswerte in verschiedenen Typen von Borstgrasrasen. Andere tragen nicht zur Differenzierung der Rasen bei, da sie in den unterschiedlichen Borstgrasrasen durchgehend Matrixarten enthalten oder überall nur spärlich auftreten. Eine grafische Auswertung nach dem ordinalen LHS-Ansatz (je eine Achse für SLA, Wuchshöhe und Samenmasse) zeigt eine einigermaßen klare Differenzierung der meisten der o. g. Typen von Borstgrasrasen. So sind beide Ansätze, PFT und LHS, geeignet, um eine Zuordnung des Nutzungstyps der Borstgrasrasen vorzunehmen.
Tissue injury and inflammation may result in chronic pain, a severe debilitating disease that is associated with great impairment of quality of life. An increasing body of evidence indicates that members of the Rab family of small GTPases contribute to pain processing; however, their specific functions remain poorly understood. Here, we found using immunofluorescence staining and in situ hybridization that the small GTPase Rab27a is highly expressed in sensory neurons and in the superficial dorsal horn of the spinal cord of mice. Rab27a mutant mice, which carry a single-nucleotide missense mutation of Rab27a leading to the expression of a nonfunctional protein, show reduced mechanical hyperalgesia and spontaneous pain behavior in inflammatory pain models, while their responses to acute noxious mechanical and thermal stimuli is not affected. Our study uncovers a previously unrecognized function of Rab27a in the processing of persistent inflammatory pain in mice.
Organelles are surrounded by membranes with a distinct lipid and protein composition. While it is well established that lipids affect protein functioning and vice versa, it has been only recently suggested that elevated membrane protein concentrations may affect the shape and organization of membranes. We therefore analyzed the effects of high chloroplast envelope protein concentrations on membrane structures using an in vivo approach with protoplasts. Transient expression of outer envelope proteins or protein domains such as CHUP1-TM–GFP, outer envelope protein of 7 kDa–GFP, or outer envelope protein of 24 kDa–GFP at high levels led to the formation of punctate, circular, and tubular membrane protrusions. Expression of inner membrane proteins such as translocase of inner chloroplast membrane 20, isoform II (Tic20-II)–GFP led to membrane protrusions including invaginations. Using increasing amounts of DNA for transfection, we could show that the frequency, size, and intensity of these protrusions increased with protein concentration. The membrane deformations were absent after cycloheximide treatment. Co-expression of CHUP1-TM–Cherry and Tic20-II–GFP led to membrane protrusions of various shapes and sizes including some stromule-like structures, for which several functions have been proposed. Interestingly, some structures seemed to contain both proteins, while others seem to contain one protein exclusively, indicating that outer and inner envelope dynamics might be regulated independently. While it was more difficult to investigate the effects of high expression levels of membrane proteins on mitochondrial membrane shapes using confocal imaging, it was striking that the expression of the outer membrane protein Tom20 led to more elongate mitochondria. We discuss that the effect of protein concentrations on membrane structure is possibly caused by an imbalance in the lipid to protein ratio and may be involved in a signaling pathway regulating membrane biogenesis. Finally, the observed phenomenon provides a valuable experimental approach to investigate the relationship between lipid synthesis and membrane protein expression in future studies.
Introduction: The German PID-NET registry was founded in 2009, serving as the first national registry of patients with primary immunodeficiencies (PID) in Germany. It is part of the European Society for Immunodeficiencies (ESID) registry. The primary purpose of the registry is to gather data on the epidemiology, diagnostic delay, diagnosis, and treatment of PIDs.
Methods: Clinical and laboratory data was collected from 2,453 patients from 36 German PID centres in an online registry. Data was analysed with the software Stata® and Excel.
Results: The minimum prevalence of PID in Germany is 2.72 per 100,000 inhabitants. Among patients aged 1–25, there was a clear predominance of males. The median age of living patients ranged between 7 and 40 years, depending on the respective PID. Predominantly antibody disorders were the most prevalent group with 57% of all 2,453 PID patients (including 728 CVID patients). A gene defect was identified in 36% of patients. Familial cases were observed in 21% of patients. The age of onset for presenting symptoms ranged from birth to late adulthood (range 0–88 years). Presenting symptoms comprised infections (74%) and immune dysregulation (22%). Ninety-three patients were diagnosed without prior clinical symptoms. Regarding the general and clinical diagnostic delay, no PID had undergone a slight decrease within the last decade. However, both, SCID and hyper IgE- syndrome showed a substantial improvement in shortening the time between onset of symptoms and genetic diagnosis. Regarding treatment, 49% of all patients received immunoglobulin G (IgG) substitution (70%—subcutaneous; 29%—intravenous; 1%—unknown). Three-hundred patients underwent at least one hematopoietic stem cell transplantation (HSCT). Five patients had gene therapy.
Conclusion: The German PID-NET registry is a precious tool for physicians, researchers, the pharmaceutical industry, politicians, and ultimately the patients, for whom the outcomes will eventually lead to a more timely diagnosis and better treatment.