Temperature and duration of heating of sunflower oil affect ruminal biohydrogenation of linoleic acid in vitro

Sunflower oil heated at 110 or 150°C for 1, 3, or 6 h was incubated with ruminal content in order to investigate the effects of temperature and duration of heating of oil on the ruminal biohydrogenation of linoleic acid in vitro. When increased, these 2 parameters acted together to decrease the disappearance of linoleic acid in the media by inhibiting the isomerization of linoleic acid, which led to a decrease in conjugated linoleic acids and trans-C18:1 production. Nevertheless, trans-10 isomer production increased with heating temperature, suggesting an activation of Δ9-isomerization, whereas trans-11 isomer production decreased, traducing an inhibition of Δ12-isomerization. The amount of peroxides generated during heating was correlated with the proportions of biohydrogenation intermediates so that they might explain, at least in part, the observed effects. The effects of heating temperature and duration on ruminal bacteria community was assessed using capillary electrophoresis single-strand conformation polymorphism. Ruminal bacterial population significantly differed according to heating temperature, but was not affected by heating duration. Heating of fat affected ruminal biohydrogenation, at least in part because of oxidative products generated during heating, by altering enzymatic reactions and bacterial population

Ruminal bacterial community change in response to diet-induced variation of ruminal trans-10 fatty acids

Trans fatty acids (FA) are produced during the biohydrogenation of linoleic acid in the rumen. Because of their health‐promoting properties, trans‐11 isomers, which are usually the most abundant biohydrogenation intermediates, are most desirable (1). However, in high yielding dairy cows, when high concentrate diets containing fat are fed to cows, a shift from trans‐11 to trans‐10 FA can occur, therefore, trans‐10 isomers can become the predominant biohydrogenation intermediates, inducing milk fat depression in dairy cows(2) and having possible detrimental effects on human health(3). The aim of this work was to study the bacterial community dynamics in response to diet‐induced trans‐10 FA shift

From high throughput 454 GS FLX data analysis process of 16S RNA gene sequences using barcoding to bacterial community exploration

From high throughput 454 GS FLX data analysis process of 16S RNA gene sequences using barcoding to bacterial community exploratio

Eigenschappen en toekomstperspectieven van mesenchymale stamcellen bij honden

The therapeutic use of canine mesenchymal stem cells (cMSC) is rapidly expanding. MSC are stromal cells, which show multipotent stem cell properties in vitro. They possess trophic, immunoregulatory, antimicrobial and hematopoiesis-supportive properties. Moreover, injected MSC are able to migrate to sites of hypoxia and inflammation. Recently, more evidence has become available showing that MSC may originate from pericytes. Different microenvironments as well as non-standardized methods for their isolation and expansion lead to heterogeneous cell populations. Further research is essential in order to use these promising therapies without restrictions in dogs

The ruminal level of trans-10 fatty acids of dairy cows is linked to the composition of bacterial community

The ruminal level of trans-10 fatty acids of dairy cows is linked to the composition of bacterial communit

Off-target and tumor-specific accumulation of monocytes, macrophages and myeloid-derived suppressor cells after systemic injection

Solid tumors frequently coexist with a degree of local chronic inflammation. Recruited myeloid cells can therefore be considered as interesting vehicles for tumor-targeted delivery of therapeutic agents. Using in vivo imaging, the short-term accumulation of systemically injected monocytes, macrophages and myeloid-derived suppressor cells (MDSCs) was compared in mice bearing fat pad mammary carcinomas. Monocytes and macrophages demonstrated almost identical in vivo and ex vivo distribution patterns with maximal tumor-associated accumulation seen 48 hours after injection that remained stable over the 4-day follow-up period. However, a substantial accumulation of both cell types was also seen in the liver, spleen and lungs albeit decreasing over time in all three locations. The MDSCs exhibited a similar distribution pattern as the monocytes and macrophages, but demonstrated a better relative on-target fraction over time. Overall, our findings highlight off-target cell accumulation as a major obstacle in the use of myeloid cells as vehicles for therapeutic tumor-targeted agents and indicate that their short-term on-target accumulation is mainly of nonspecific nature

Etude par pyroséquençage haut débit (454) de l’implantation des bactéries au niveau du rumen du veau laitier, de sa naissance au sevrage

Objectif : Décrire la séquence temporelle d'implantation de la population bactérienne au niveau du rumen chez le veau, de la naissance jusqu'au sevrage, via des outils de microbiologie moléculaire

Cryptococcal transmigration across a model brain blood-barrier: Evidence of the Trojan horse mechanism and differences between Cryptococcus neoformans var. grubii strain H99 and Cryptococcus gattii strain R265

© 2015 Institut Pasteur. Cryptococcus neoformans (. Cn) and Cryptococcus gattii (Cg) cause neurological disease and cross the BBB as free cells or in mononuclear phagocytes via the Trojan horse mechanism, although evidence for the latter is indirect. There is emerging evidence that Cn and the North American outbreak Cg strain (R265) more commonly cause neurological and lung disease, respectively. We have employed a widely validated in vitro model of the BBB, which utilizes the hCMEC/D3 cell line derived from human brain endothelial cells (HBEC) and the human macrophage-like cell line, THP-1, to investigate whether transport of dual fluorescence-labelled Cn and Cg across the BBB occurs within macrophages. We showed that phagocytosis of Cn by non-interferon (IFN)-γ stimulated THP-1 cells was higher than that of Cg. Although Cn and Cg-loaded THP-1 bound similarly to TNF-activated HBECs under shear stress, more Cn-loaded macrophages were transported across an intact HBEC monolayer, consistent with the predilection of Cn for CNS infection. Furthermore, Cn exhibited a higher rate of expulsion from transmigrated THP-1 compared with Cg. Our results therefore provide further evidence for transmigration of both Cn and Cg via the Trojan horse mechanism and a potential explanation for the predilection of Cn to cause CNS infection

Mesure in vitro de l'activité de la communauté bactérienne ruminale

Les techniques modernes de biologie moléculaire permettent une description de la micropopulation ruminale. L’étude de l’activité de cette population sur les principaux constituants de la ration est souvent réalisée in vitro. L’objectif de cette étude était de vérifier si la population bactérienne est active mais n’évolue pas pendant une courte incubation in vitro, ce qui permettrait de mettre en relation le profil et l’activité des bactéries. La communauté bactérienne mise à incuber in vitro n’a pas évolué, ni en quantité, ni en structure ou en diversité, ce qui suggère que les conditions de culture n’entraînent pas une sélection de certaines espèces au cours des 6 premières heures. Cette communauté est restée active, puisque capable de dégrader les différents substrats : matières azotées, glucides et lipides. Une mesure in vitro de l’activité microbienne est donc possible, et pourrait s’avérer intéressante à associer aux techniques de biologie moléculaire afin de mieux caractériser la communauté bactérienne d’un prélèvement

Mononuclear but not polymorphonuclear phagocyte depletion increases circulation times and improves mammary tumor-homing efficiency of donor bone marrow-derived monocytes

Tumor associated macrophages are an essential part of the tumor microenvironment. Consequently, bone marrow-derived monocytes (BMDMs) are continuously recruited to tumors and are therefore seen as ideal delivery vehicles with tumor-targeting properties. By using immune cell depleting agents and macroscopic in vivo fluorescence imaging, we demonstrated that removal of endogenous monocytes and macrophages (but not neutrophils) leads to an increased tumor accumulation of exogenously administered BMDMs. By means of intravital microscopy (IVM), we confirmed our macroscopic findings on a cellular level and visualized in real time the migration of the donor BMDMs in the tumors of living animals. Moreover, IVM also revealed that clodronate-mediated depletion drastically increases the circulation time of the exogenously administered BMDMs. In summary, these new insights illustrate that impairment of the mononuclear phagocyte system increases the circulation time and tumor accumulation of donor BMDMs