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Summary: Impact of the UPR pathway on the establishment of the UVB-induced senescent phenotype Skin aging, influenced by a combination of intrinsic and extrinsic factors, leads to damage capable of altering skin functions. Among extrinsic factors, ultraviolet (UV) radiation is responsible for skin photoaging. In particular, these elements lead to an accumulation of senescent cells capable of contributing to the development of age-related pathologies such as skin cancers. Indeed, senescence is accompanied by profound morphological and molecular changes within the cell. This includes a modification of its secretome, which becomes enriched with pro-inflammatory cytokines, growth factors and extracellular matrix remodeling enzymes, altering the characteristics of tissues as they age. Nevertheless, the precise mechanisms leading to the senescent phenotype induced by UVB remain largely unknown. In this context, the main objective of this work was to identify molecular mechanisms underlying the establishment of UVB-induced senescence in normal human dermal fibroblasts (NHDFs), mechanisms that could contribute to skin aging. In vitro, we confirmed that repeated UVB exposures induce premature senescence in NHDFs and that this state is associated with activation of the three branches of the UPR (Unfolded Protein Response) pathway responsible for maintaining homeostasis of the endoplasmic reticulum (ER), the primary secretory compartment. These observations were supported by transcriptomic analysis, revealing regulatory elements linked to major senescence pathways and ER functions in UVB-exposed NHDFs. Subsequently, we showed that the ATF6α branch plays a central role in the occurrence of biomarkers of the UVB-induced senescent phenotype. Indeed, ATF6α invalidation not only protects against UVB-induced morphological changes, but reduces the percentage of SA-βgalactosidase (SA-βgal)-positive cells, prevents persistent DNA damage, and alters the expression of major factors of the senescence-associated secretory phenotype (SASP). As SASP exerts, among other things, a pro-tumoral action, we sought to assess whether the conditioned medium (CM) of UVB-exposed fibroblasts invalidated for ATF6α could impact the migration and invasion potential of melanoma-derived cells. However, we did not observe any ATF6α-dependent pro-migratory or pro-invasive effects.To highlight a potential role for ATF6α in another biological process, we exploited our transcriptomic and secretomic analyses and identified a possible effect of ATF6α on the paracrine control of the skin environment. To explore this, we focused on SASP factors (cytokines and metalloproteases) regulated by ATF6α and whose impact on the tissue environment was known. Next, we treated a reconstructed human epidermis (RHE) model with MC derived from NHDFs exposed to UVB or not, and invalidated or not for ATF6α. Surprisingly, we observed that MC from UVB-exposed NHDFs increased RHE thickness and basal keratinocyte proliferation, via an ATF6α-dependent mechanism. Finally, we identified IL8 as a major paracrine factor involved in this process, since IL-8 blockade by neutralizing antibodies prevents excessive keratinocyte proliferation. In conclusion, we report the role of ATF6α in UVB-induced senescence as well as its impact on the preservation of skin homeostasis under stress conditions notably through the regulation of the expression of SASP components. This suggests that ATF6α and its effectors could be promising targets controlling the effects of skin aging.Abstract: Impact of the UPR pathway on the establishment of the senescent phenotype induced by UVBSkin aging, influenced by a combination of intrinsic and extrinsic factors, can result in damage that has the potential to alter skin functions. Among extrinsic factors, ultraviolet (UV) radiation is responsible for skin photoaging. These factors notably contribute to the accumulation of senescent cells which in turn can contribute to the development of age-related pathologies, including skin cancers. Indeed, senescence is characterized by profound morphological and molecular changes within the cell. This includes a modification of its secretome, which becomes enriched in pro-inflammatory cytokines, growth factors, and matrix-remodeling enzymes, altering tissue characteristics during aging. However, the exact mechanisms driving the senescent phenotype induced by UVB remain largely unknown. In this context, the main objective of this work was to identify the underlying molecular mechanisms responsible for the establishment of UVB-induced senescence in normal human dermal fibroblasts (NHDFs), mechanisms that may play a role in skin aging. In vitro, we confirmed that repeated exposures to UVB induce premature senescence of NHDFs and that this state is associated with the activation of the three branches of the Unfolded Protein Response (UPR), which are responsible for maintaining endoplasmic reticulum (ER) homeostasis, the primary cellular secretion compartment. These observations were supported by transcriptomic analysis, revealing regulatory elements related to major senescence pathways and ER functions in UVB-exposed NHDFs. Subsequently, we demonstrated that the ATF6α branch plays a central role in the development of the UVB-induced senescent phenotype. Indeed, the silencing of ATF6α not only protects against morphological changes induced by UVB, but also reduces the percentage of senescence-associated β-galactosidase (SA-βgal) positive cells, prevents the persistence of DNA damage, and alters the expression of major factors associated with the senescence-associated secretory phenotype (SASP).The SASP, exerting a pro-tumoral action, led us to assess whether the conditioned medium (CM) from UVB-exposed fibroblasts invalidated for ATF6α could impact the migration and invasion potential of melanoma cells. However, we did not observe any ATF6α-dependent pro-migratory or pro-invasive effects. To highlight a potential role of ATF6α in another biological process, we further analyzed our transcriptomic and secretomic analyses and identified a possible effect of ATF6α on the paracrine control of the skin environment. To explore this, we focused on SASP factors (cytokines and metalloproteinases) regulated by ATF6α and whose impact on tissue environment was known. Subsequently, we treated a reconstructed human epidermis (RHE) model with CM from NHDFs exposed or not to UVB and invalidated or not for ATF6α. Surprisingly, we observed that the CM from UVB-exposed NHDFs increased the thickness of the RHE as well as the proliferation of basal keratinocytes, via an ATF6α-dependent mechanism. Finally, we identified IL8 as a major paracrine factor involved in this process, as blocking IL-8 with neutralizing antibodies prevented excessive proliferation of keratinocytes. In conclusion, we report the role of ATF6α in UVB-induced senescence and its impact on the preservation of skin homeostasis under stress conditions, particularly through the regulation of the expression of SASP components. This suggests that ATF6α and its effectors could be promising targets for controlling the effects of skin aging. Jury Prof. Yves POUMAY (Department of Medicine, UNamur), chairmanProf. Florence CHAINIAUX (Department of Biology, UNamur), promoter and secretaryProf. Olivier PLUQUET (Canther, University of Lille), co-promoterProf. Isabelle PETROPULOS (Adaptation Biologique et Vieillissement, Sorbonne Université)Prof. Jérôme LAMARTINE (Laboratoire de Biologie Tissulaire et d'Ingénierie thérapeutique, Université Claude Bernard Lyon 1)Prof. Fabienne FOUFELLE (Maladies métaboliques, diabète et comorbidités, Sorbonne Université)

Find out what Aurelien Clement, a master's student in management sciences at the University of Namur, has to say about his Erasmus stay at the University of Laval in Canada.

Dissertation topic: Modelling and Implementation of Blockchain-Based Solutions Supporting Cross-Organized Business Processes Jury compositionPromotersProf. Corentin Burnay, Université de NamurProf. Monique Snoeck, KU LeuvenOther jury membersProf. Sarah Bouraga, Université de NamurDr. Félix Harer, Université de FribourgPro. Estefania Serral Asension, KU LeuvenJury presidentProf. Jean-Jacques Gnabo, Université de Namur

EMBO Courses and Workshops are selected for their excellent scientific quality and timelines, provision of good networking activities for all participants and speaker gender diversity (at least 40% of speakers must be from the underrepresented gender). Organisers are encouraged to implement measures to make the meeting environmentally more sustainable.Upon registration - More info and registration on the EMBO website.

On Thursday May 30, for our last Chill&Sciences of the season, Candy Sonvaux and Alexis Coyette, mathematics researchers, invite you to discover the mathematics where the movements of the planets and the spread of viruses intertwine until they impact our society.Chill&Science: enriching encountersWith nearly 20 years' experience of scientific cafés, the Confluent des Savoirs has set up a new concept of scientific encounters. The Chill&Sciences are a unique opportunity for the public to come and discuss and ask questions of experts on research topics related to current affairs and citizen issues.Come and enjoy the unique, relaxed atmosphere of Quai22. Researchers and experts from the seven faculties of the University of Namur will present their research and discuss with you over a drink (or two, but never without exaggeration).In practiceThe meetings are open to everyone aged 16 and over. Evenings are limited to around 20 people to ensure a relaxed atmosphere and to facilitate discussions. Meetings take place if a minimum of 10 people are registered. Except in exceptional circumstances, meetings take place every 2 months at the University of Namur's cultural space, Quai22, located at n°22 Rue du Séminaire.Tarif Participation in a Chill&Sciences costs 5€. A discounted annual pass is available. Please note: preferential rate for students (discount code: PromoCDS).The booking fee includes a drink* (soft or beer), a snack (chips and cookies) and management fees linked to the organization Unless cancelled by us, bookings are non-refundable. (*additional drinks will be available upon electronic payment.)

Title of the dissertation: Ion implantation in Low-E coatings Low-emissivity (Low-E) coating technology revolutionizes glass applications for windows, offering high optical transparency while reducing heat transfer. They consist of a silver-based thin film deposited on a glass panel by physical vapor deposition. However, these coatings are fragile and must be placed inside a double-glazing cavity where an inert gas resides. Otherwise, they can be easily degraded by bad atmospheric conditions.The thesis approach is to combine low-E technology with a post-treatment of ion implantation. The research question driving this thesis is: how does ion implantation enhance the durability of low-E coatings containing silver?The experiments conducted during the thesis show that implantation indeed increases the coating resistance while having a small impact on its color. However, the treatment degrades the thermal insulation properties. Hence, a series of hypotheses are formulated based on the literature to explain and control this behavior.A deeper investigation shows that implantation impacts the silver nanostructure. First by dewetting the film which allows reorganization into larger crystallites, second by forcing silver mixing at its interface through ballistic ejections. These two phenomena increase the toughness of the silver interface by interlocking effects. However, dewetting has also been linked to thermal insulation properties degradation. Nonetheless, it was shown that using light gas implantation limits the destructive effect (dewetting) while still inducing good durability (due to interface mixing).. Jury Prof. Julien COLAUX (UNamur), presidentProf. Stéphane LUCAS (UNamur), promoter and secretaryDr Amory JACQUES (Service Public de Wallonie)Dr Philippe ROQUINY (AGC Glass Europe)Prof. Rony SNYDERS (University of Mons)

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The morning will be marked by a lecture by Julien Berthaud, a specialist in the social integration of students, who will share his insights on how this integration becomes a genuine vector for success.Then, scientific papers and experience sharing will enrich our knowledge and spark constructive debate. Lunch will be an opportunity to discover innovative student projects, highlighted in an inspiring exhibition.The afternoon promises to be just as stimulating with a round table moderated by Sabine Henry, where experts will discuss service learning, educational entrepreneurship and spirituality. This dynamic dialogue will be followed by a closing activity: the fresco of engagement, a collective brainstorming session that will lay the foundations for an innovative educational game.Join us for this day of exchange and reflection, and help shape the future of education where student engagement and knowledge vivacity will be the cornerstones of a new educational paradigm.

Floriane Goosse, a PhD student at the University of Namur, within the NaDI-CeRCLe research center, has received the prestigious "Best Research Paper Award" for her thesis paper conducted in collaboration with Wafa Hammedi, professor in the Department of Management at UNamur, and Dominik Mahr, from Maastricht University.