Heilige, Heiliges und Heiligkeit in spätantiken Religionskulturen

Was das Heilige ist und wie man darüber sprechen kann, ist eine offene Frage in der religionswissenschaftlichen und theologischen Forschung. Jenseits der klassischen Entwürfe von Durkheim, Otto oder Eliade kann Heiliges heute nur in multiperspektivischer Betrachtung angemessen untersucht werden. Die Beiträge zu diesem Band analysieren Diskurse über Heiliges in spätantiken Religionskulturen: griechisch-römische Religion, Judentum und Christentum. Terminologien, Handlungen und Reflexionen in Bezug auf Heiliges werden in ihrem jeweiligen religiösen Bezugssystem thematisiert, aber darüber hinaus auch miteinander ins Gespräch gebracht. Hierfür dienen Kategorien wie Zeit, Ort, Individuum und Gruppe der Zuordnung der Befunde. Besonderes Augenmerk liegt zudem auf quellensprachlichen und forschungsinternen Begrifflichkeiten von Heiligem sowie auf der geschichtlichen Dynamik von Heiligkeitsvorstellungen. Dieses interdisziplinäre Vorgehen macht Diskontinuitäten und Kontinuitäten des Diskurses über „das Heilige“ in der Vielfalt seiner Erscheinungsformen präziser als bisher identifizierbar.

Römisches Recht als Vergleichsfaktor, insb. in der Lehre von Ignacy Koschembahr-Lyskowski

Ignacy Koschembahr-Lyskowski formulierte gegen Ende des 19. Jh. eine interessante und äusserst aktuelle These über die Rolle des Römischen Rechts in der modernen Privatrechtswissenschaft. Seiner Ansicht nach sollte das klassische Römische Recht heutzutage als Vergleichsfaktor herangezogen werden, um die Fortbildung des Privatrechts mit der jahrhundertelangen Erfahrung römischer Juristen zu bereichern. Somit wird die historische Rechtsvergleichung gegenüber der dogmengeschichtlichen Betrachtung bevorzugt. Das Recht sollte dabei unter Berücksichtigung seiner sozialen Funktion bewertet werden; der historische Vergleich wird bei der Wahl von geeigneten Rechtsmitteln helfen können. Derselbe Gedanke wurde 2008 von Koschembahr-Lyskowskis Nachfolger in Fribourg, P. Pichonnaz, thematisiert (Römisches Recht als tertium comparationis).

Functionalisation of PLLA nanofiber scaffolds using a possible cooperative effect between collagen type I and BMP-2: impact on colonization and bone formation in vivo

The reconstruction of large bone defects after injury or tumor resection often requires the use of bone substitution. Artificial scaffolds based on synthetic biomaterials can overcome disadvantages of autologous bone grafts, like limited availability and donor side morbidity. Among them, scaffolds based on nanofibers offer great advantages. They mimic the extracellular matrix, can be used as a carrier for growth factors and allow the differentiation of human mesenchymal stem cells. Differentiation is triggered by a series of signaling processes, including integrin and bone morphogenetic protein (BMP), which act in a cooperative manner. The aim of this study was to analyze whether these processes can be remodeled in artificial poly-(l)-lactide acid (PLLA) based nanofiber scaffolds in vivo. Electrospun matrices composed of PLLA-collagen type I or BMP-2 incorporated PLLA-collagen type I were implanted in calvarial critical size defects in rats. Cranial CT-scans were taken 4, 8 and 12 weeks after implantation. Specimens obtained after euthanasia were processed for histology and immunostainings on osteocalcin, BMP-2 and Smad5. After implantation the scaffolds were inhomogeneously colonized and cells were only present in wrinkle- or channel-like structures. Ossification was detected only in focal areas of the scaffold. This was independent of whether BMP-2 was incorporated in the scaffold. However, cells that migrated into the scaffold showed an increased ratio of osteocalcin and Smad5 positive cells compared to empty defects. Furthermore, in case of BMP-2 incorporated PLLA-collagen type I scaffolds, 4 weeks after implantation approximately 40 % of the cells stained positive for BMP-2 indicating an autocrine process of the ingrown cells. These findings indicate that a cooperative effect between BMP-2 and collagen type I can be transferred to PLLA nanofibers and furthermore, that this effect is active in vivo. However, this had no effect on bone formation. The reason for this seems to be an unbalanced colonization of the scaffolds with cells, due to insufficient pore size.

Global lymphoid tissue remodeling during a viral infection is orchestrated by a B cell-lymphotoxin-dependent pathway

Adaptive immune responses are characterized by substantial restructuring of secondary lymphoid organs. The molecular and cellular factors responsible for virus-induced lymphoid remodeling are not well known to date. Here we applied optical projection tomography, a mesoscopic imaging technique, for a global analysis of the entire 3-dimensional structure of mouse peripheral lymph nodes (PLNs), focusing on B-cell areas and high endothelial venule (HEV) networks. Structural homeostasis of PLNs was characterized by a strict correlation between total PLN volume, B-cell volume, B-cell follicle number, and HEV length. After infection with lymphocytic choriomeningitis virus, we observed a substantial, lymphotoxin (LT) beta-receptor-dependent reorganization of the PLN microarchitecture, in which an initial B-cell influx was followed by 3-fold increases in PLN volume and HEV network length on day 8 after infection. Adoptive transfer experiments revealed that virus-induced PLN and HEV network remodeling required LTalpha(1)beta(2)-expressing B cells, whereas the inhibition of vascular endothelial growth factor-A signaling pathways had no significant effect on PLN expansion. In summary, lymphocytic choriomeningitis virus-induced PLN growth depends on a vascular endothelial growth factor-A-independent, LT- and B cell-dependent morphogenic pathway, as revealed by an in-depth mesoscopic analysis of the global PLN structure.

Intensity-modulated radiotherapy for a rendu-osler-weber disease patient with recurrent severe epistaxis: a case report

We present a case of a Rendu-Osler-Weber disease patient with recurrent life threatening epistaxis demanding multiple blood transfusions despite of repetitive endoscopic laser and electrocoagulations, endovascular embolisation, septodermoplasty, and long-term intranasal dressings. As alternative treatment modalities repeatedly failed and the patient became almost permanently dependent on nasal dressing, we performed a highly conformal intensity-modulated radiotherapy of the nasal cavity; a total dose of 50 Gy in 2 Gy single fractions was applied. The therapy was very well tolerated, no acute toxicities occurred. Two weeks after the last radiation dose had been applied, the nasal dressing could be removed without problems. Endoscopical control revealed an almost avascular white mucosa without any trace of bleeding spots; previously existing hemangiomas and crusts had disappeared. After a 1-year-follow up, the patient had no significant recurrent epistaxis.