Recherches sur la vie et les oeuvres d'une précieuse / par M. Théry,...

Comprend : [Poèmes de Marie-Anne de La Vigne]

The Hippo Transducer YAP1 Transforms Activated Satellite Cells and Is a Potent Effector of Embryonal Rhabdomyosarcoma Formation.

The role of the Hippo pathway effector YAP1 in soft tissue sarcomas is poorly defined. Here we report that YAP1 activity is elevated in human embryonal rhabdomyosarcoma (ERMS). In mice, sustained YAP1 hyperactivity in activated, but not quiescent, satellite cells induces ERMS with high penetrance and short latency. Via its transcriptional program with TEAD1, YAP1 directly regulates several major hallmarks of ERMS. YAP1-TEAD1 upregulate pro-proliferative and oncogenic genes and maintain the ERMS differentiation block by interfering with MYOD1 and MEF2 pro-differentiation activities. Normalization of YAP1 expression reduces tumor burden in human ERMS xenografts and allows YAP1-driven ERMS to differentiate in situ. Collectively, our results identify YAP1 as a potent ERMS oncogenic driver and a promising target for differentiation therapy.

Revisão dos gêneros Sitalces, Eusitalces e Parasitalces (Orthoptera, Acrididae, Abracrini) e descrição de três novos gêneros

Revisão dos gêneros Sitalces, Eusitalces e Parasitalces (Orthoptera, Acrididae, Abracrini) e descrição de três novos gêneros. Os gêneros sulamericanos de Abracrini Sitalces Stål, 1878, Eusitalces Bruner, 1911, Parasitalces Bruner, 1911, Liebermannacris gen. nov., Robustusacris gen. nov., e Arimacris gen. nov. são revisados, descritos, redescritos e redefinidos. Quatro espécies são novas combinações: Liebermannacris dorsualis (Giglio-Tos, 1898) comb. nov., Liebermannacris punctifrons (Stål,1878) comb. nov., Robustusacris balzapambae (Rehn, 1913) comb. nov., e Arimacris trinitatis (Bruner, 1906) comb. nov., todas removidas de Sitalces Stål, 1878. Nove espécies são novos sinônimos: Sitalces robustus Bruner, 1908 (de S. volxemi Stål, 1878); S. infuscatus Bruner, 1908, S. nudus Bruner, 1908, S. ovatipennis Bruner, 1908, S. madeirensis Rehn, 1916 (de Liebermannacris dorsualis (Giglio-Tos, 1898); S. rubripes Hebard, 1924 (de Robustusacris balzapambae (Rehn, 1913); E. amazonicus Günther, 1940 e S. apolinari Hebard, 1923 (de Eusitalces vittatus Bruner, 1911); E. rubripes Günther, 1940 (de P. vulneratus (Bruner,1919)). Lectótipos e paralectótipos são designados. São fornecidas chaves para identificação, medidas, mapa de distribuição geográfica e ilustrações dos gêneros e espécies.

Traité de l'existence et des attributs de Dieu (Nouvelle édition, accompagnée de notes et précédée d'une introduction et d'une analyse des chapitres, par M. Alph. Aulard,...) / par Fénelon

[Traité de l'existence de Dieu (français). 1878]

Traité de l'existence et des attributs de Dieu ; suivi de Lettres sur divers sujets de métaphysique et de religion / par Fénelon,...

[Traité de l'existence de Dieu (français). 1878]

Notes on the holotype of Anopheles marajoara Galvão & Damasceno (Diptera, Culicidae)

During studies on the dynamics of malaria transmission in Marajó Island, State of Pará, Brazil, Galvão & Damasceno (1942) collected a single specimen of a new species that they named Anopheles (Nyssorhynchus) marajoara Galvão & Damasceno, 1942. Now, examining genitalia slide associated to the holotype, we observed that the ventral claspette of the male genitalia is distinct from those of all other species of the Argyritarsis Section and consequently from members of the complex Anopheles albitarsis Lynch Arribalzaga, 1878. The male genitalia of the slide belong to a specimen of Anopheles aquasalis Curry, 1932, nevertheless, it was originally labeled as Anopheles marajoara. To solve this problem, we are setting aside the male genitalia slide associated with the holotype of Anopheles marajoara and excluding it from the type material. Illustrations of the male genitalia and adult male are included.

Engineered aprotinin for improved stability of fibrin biomaterials.

Fibrin has been long used clinically for hemostasis and sealing, yet extension of use in other applications has been limited due to its relatively rapid resorption in vivo, even with addition of aprotinin or other protease inhibitors. We report an engineered aprotinin variant that can be immobilized within fibrin and thus provide extended longevity. When recombinantly fused to a transglutaminase substrate domain from α(2)-plasmin inhibitor (α(2)PI(1-8)), the resulting variant, aprotinin-α(2)PI(1-8), was covalently crosslinked into fibrin matrices during normal thrombin/factor XIIIa-mediated polymerization. Challenge with physiological plasmin concentrations revealed that aprotinin-α(2)PI(1-8)-containing matrices retained 78% of their mass after 3 wk, whereas matrices containing wild type (WT) aprotinin degraded completely within 1 wk. Plasmin challenge of commercial sealants Omrixil and Tisseel, supplemented with aprotinin-α(2)PI(1-8) or WT aprotinin, showed extended longevity as well. When seeded with human dermal fibroblasts, aprotinin-α(2)PI(1-8)-supplemented matrices supported cell growth for at least 33% longer than those containing WT aprotinin. Subcutaneously implanted matrices containing aprotinin-α(2)PI(1-8) were detectable in mice for more than twice as long as those containing WT aprotinin. We conclude that our engineered recombinant aprotinin variant can confer extended longevity to fibrin matrices more effectively than WT aprotinin in vitro and in vivo.

Acute coronary syndrome after levamisole-adultered cocaine abuse

Cocaine is a well known trigger of acute coronary syndromes. Over the last 10 years levamisole, a veterinary anthelminthic drug has been increasingly used as an adulterant of cocaine. Levamisole was used to treat pediatric nephritic syndrome and rheumatoid arthritis before being withdrawn from the market due to its significant toxicity, i.e. hematological complications and vasculitis. The major complications of levamisole-adultered cocaine reported up to now are hematological and dermatological. The case reported here is of a 25 year old man with a history of cocaine abuse who died at home after complaining of retrosternal pain. Postmortem CT-angiography, autopsy, and chemical and toxicological analyses were performed. An eroded coronary artery plaque was found at the proximal segment of the left anterior descending coronary artery. Two myocardial infarct scars were present in the left ventricle. Microscopic examination of the coronary artery revealed infiltration of eosinophils into the adventitia and intima. Toxicological examination confirmed the presence of cocaine and its metabolites in the peripheral blood, and of levamisole in the urine and pericardial fluid. Eosinophilic inflammatory coronary artery pathologies have been clinically linked to coronary dissection, hypersensitivity coronary syndrome and vasospastic allergic angina. The coronary pathology in the presented case could be a complication of levamisole-adultered cocaine use, in which an allergic or immune-mediated mechanism might play a role. The rise in cocaine addiction worldwide and the increase of levamisole adulterated cocaine highlights the importance of updating our knowledge of the effects of adultered cocaine abuse.