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111.
112.
Esteban Grasso Daniel Paparini Vanesa Hauk Gabriela Salamone Claudia Perez Leiros Rosanna Ramhorst 《PloS one》2014,9(5)
Macrophages at the maternal-placental interface coordinate opposite demands under the control of trophoblast cells such as the response against pathogens on one hand, and apoptotic cell clearance and wound healing with the production of suppressor cytokines. Here, we investigated whether trophoblast cells induce maternal monocyte activation towards an alternative activated macrophage profile and whether bacterial or viral stimuli modulate their migratory properties. We used an in vitro model of the maternal-placental interface represented by co-cultures of CD14+ cells isolated from fertile women with first trimester trophoblast cell line (Swan-71 cells) in the presence or absence of pathogen associated molecular pattern (PAMP) stimuli lipopolysaccharide (LPS), peptidoglycan (PGN) or poly [I:C]). Maternal CD14+ cells showed increased CD16 and CD39 expression, both markers associated to an alternative activation profile, with no changes in CD80 expression after trophoblast cell interaction. These changes were accompanied by increased IL-10 and decreased IL-12 production by CD14+ cells. After stimulation with LPS, PGN or poly [I:C], monocytes co-cultured with trophoblast cells had lower production of TNF-α and IL-1β compared with non co-cultured monocytes. Interestingly, monocyte migration towards trophoblast cells was prevented in the presence of LPS or PGN but not after 24h of stimulation with poly [I:C]. LPS or PGN also decreased CCR5, CXCL-8 and CCL5 expression. Finally, trophoblast cells co-cultured with monocytes in the presence of pathological stimuli failed to increase chemokine expression, indicating a bidirectional effect. In conclusion, trophoblast might ‘instruct’ maternal monocytes to express an alternative activation profile and restrain their early recruitment under pathological threats as one of the first strategies to avoid potential tissue damage at the maternal-placental interface. 相似文献
113.
The patterns of pollen deposition in the upper layers of the soil and in biological traps (mosses and lichens) in relation to the widespread and well known vegetational types of the Alps is investigated. The communities studied are beach woods, pine woods (Pinus cembra, P. sylveslris) and alpine pastures. Quantitative correlations between the pollen spectra and the vegetation have been calculated and over, under and equi-represented species delimited. Since representativity differs, in some cases, from that recorded in the literature it is suggested that it would be useful to continue the study in order to improve our understanding of actual pollen deposition and, as a consequence, of the interpretation of fossil pollen data. 相似文献
114.
Background
The chloroplast of eukaryotic microalgae such as Chlamydomonas reinhardtii is a potential platform for metabolic engineering and the production of recombinant proteins. In industrial biotechnology, inducible expression is often used so that the translation or function of the heterologous protein does not interfere with biomass accumulation during the growth stage. However, the existing systems used in bacterial or fungal platforms do not transfer well to the microalgal chloroplast. We sought to develop a simple inducible expression system for the microalgal chloroplast, exploiting an unused stop codon (TGA) in the plastid genome. We have previously shown that this codon can be translated as tryptophan when we introduce into the chloroplast genome a trnWUCA gene encoding a plastidial transfer RNA with a modified anticodon sequence, UCA.Results
A mutated version of our trnWUCA gene was developed that encodes a temperature-sensitive variant of the tRNA. This allows transgenes that have been modified to contain one or more internal TGA codons to be translated differentially according to the culture temperature, with a gradient of recombinant protein accumulation from 35 °C (low/off) to 15 °C (high). We have named this the CITRIC system, an acronym for cold-inducible translational readthrough in chloroplasts. The exact induction behaviour can be tailored by altering the number of TGA codons within the transgene.Conclusions
CITRIC adds to the suite of genetic engineering tools available for the microalgal chloroplast, allowing a greater degree of control over the timing of heterologous protein expression. It could also be used as a heat-repressible system for studying the function of essential native genes in the chloroplast. The genetic components of CITRIC are entirely plastid-based, so no engineering of the nuclear genome is required.115.
116.
Rosa van den Berg Sander Kooijman Raymond Noordam Ashna Ramkisoensing Gustavo Abreu-Vieira Lauren L. Tambyrajah Wieneke Dijk Philip Ruppert Isabel M. Mol Barbara Kramar Rosanna Caputo Laura Sardón Puig Evelien M. de Ruiter Jan Kroon Menno Hoekstra Ronald J. van der Sluis Onno C. Meijer Ko Willems van Dijk Patrick C.N. Rensen 《Cell reports》2018,22(13):3521-3533
117.
Marco Artini Paola Cicatiello Annarita Ricciardelli Rosanna Papa Laura Selan Principia Dardano 《Biofouling》2017,33(7):601-611
Staphylococcus epidermidis is a significant nosocomial pathogen in predisposed hosts because of its capability of forming a biofilm on indwelling medical devices. The initial stage of biofilm formation has a key role in S. epidermidis abiotic surface colonization. Recently, many strategies have been developed to create new anti-biofilm surfaces able to control bacterial adhesion mechanisms. In this work, the self-assembled amphiphilic layers formed by two fungal hydrophobins (Vmh2 and Pac3) have proven to be able to reduce the biofilm formed by different strains of S. epidermidis on polystyrene surfaces. The reduction in the biofilm thickness on the coated surfaces and the preservation of cell vitality have been demonstrated through confocal laser scanning microscope analysis. Moreover, the anti-biofilm efficiency of the self-assembled layers on different medically relevant materials has also been demonstrated using a CDC biofilm reactor. 相似文献
118.
Equine and Canine Anaplasma phagocytophilum Strains Isolated on the Island of Sardinia (Italy) Are Phylogenetically Related to Pathogenic Strains from the United States
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Alberto Alberti Rosanna Zobba Bernardo Chessa Maria Filippa Addis Olivier Sparagano Maria Luisa Pinna Parpaglia Tiziana Cubeddu Gianpaolo Pintori Marco Pittau 《Applied microbiology》2005,71(10):6418-6422
The presence of Anaplasma phagocytophilum, a tick-transmitted zoonotic pathogen, was investigated in Sardinia using a molecular approach. Phylogenetic analysis revealed that Sardinian strains are genetically distinct from the two lineages previously described in Europe and are closely related to strains isolated in different areas of the United States. 相似文献
119.
Reiprich S Stolt CC Schreiner S Parlato R Wegner M 《Molecular biology of the cell》2008,19(4):1575-1586
120.