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PDF file - 3848K, Figure S1. Pathological doses of cl-CD95L trigger cell migration of TNBC cells. Figure S2. Cl-CD95L induces migration of TNBC cells through a PI3K(p110β)/c-yesdriven signaling pathway. Figure S3. NOX-3-dependent ROS production is instrumental in CD95-mediated cell motility in TNBC cells. Figure S4. Cl-CD95L induces co-localization of CD95 with EGFR. Figure S5. cl-CD95L promotes migration of TNBC cells via EGFR-dependent and EGFindependent signaling pathways.

Sphingonotus is a genus of grasshoppers that contains species groups with several closely related species, among which Sphingonotus caerulans and an unnamed Sphingonotus that are found in continental France. The exact distribution of both species is still under investigation, but it is believed that S. caerulans might be restricted to the northern part of the country, and that Sphingonotus sp. occurs in the southern half and might reach the north east. We explored the genetic identity of Sphingonotus grasshoppers in the upper Rhine Valley of Alsace (northeastern France) using combined fragments of mtDNA ND5 and cytb genes included with other available samples in ML and Bayesian phylogenetic analyses. The results indicate that the five specimens sampled within this region belong to S. caerulans. The actual distribution of Sphingonotus sp. in France remains to be investigated with wider sampling, especially to get a better knowledge on its northern limit.

Even though reptiles are threatened worldwide, few studies address their conservation, especially snakes. The goal of our study was to measure the genetic structure of a widely distributed temperate reptile, the smooth snake Coronella austriaca using eight microsatellite markers in two different areas at the core (Alsace, north-eastern France) and at the edge (Wallonia, southern Belgium) of its range. We sampled 506 individuals in 38 localities (respectively 10 and 28). Analysis of genetic structure conducted with a clustering method detected three clusters in Alsace, one group gathering all populations but two. In Wallonia, differentiation was observed on both sides of the Meuse river and in the Southern Ardenne region (southernmost sampling sites). Spatial autocorrelation analysis showed that individuals share parental relationship up to a distance of 2.8 km in Alsace and up to 10 km in Wallonia. Isolation by distance was detected in Wallonia but the distance explained a very limited part of the differentiation (r = 0.033), whereas no isolation-by-distance pattern was detected in Alsace. Even though genetic differentiation between populations separated by large rivers, highways, or crop fields was detected, dispersal between populations seem currently sufficient to avoid any kind of genetic drift in both regions. These results are strongly contrasting with a previous study in England, suggesting sharp local variation of genetic structuring and diversification between location within the same species, probably related to the position in the distribution area and different densities.

Les recommandations de gestion d’habitat en faveur des Squamates terrestres s’intéressent principalement aux éléments bordiers et délaissent souvent les habitats ouverts comme les prairies. L’observation visuelle et la surveillance régulière d’un réseau de plaques refuges positionnées sur les lisières et le centre d’une prairie permanente non pâturée ont permis de suivre une communauté de Squamates pendant une année au sein du département de la Loire-Atlantique. Nos résultats montrent qu’il existe des différences dans l’exploration de la prairie permanente non pâturée selon les espèces, le mode de thermorégulation, l’âge des individus et le moment de l’année. Les Lacertidae tendent à rester près des lisières, alors que les Serpents et les Orvets fragiles s’aventurent plus loin dans la prairie au cours du temps. Néanmoins, la richesse spécifique diminue lorsque la distance à la lisière augmente. Cette étude nous éclaire sur l’importance de la prise en compte des prairies permanentes non pâturées pour la conservation des Squamates en milieu bocager.

Calcium ions (Ca2+) play important and diverse roles in the regulation of autophagy, cell death and differentiation. Here, we investigated the impact of Ca2+ in regulating acute promyelocytic leukemia (APL) cell fate in response to the anti-cancer agent all-trans retinoic acid (ATRA). We observed that ATRA promotes calcium entry through store-operated calcium (SOC) channels into acute promyelocytic leukemia (APL) cells. This response is associated with changes in the expression profiles of ORAI1 and STIM1, two proteins involved in SOC channels activation, as well as with a significant upregulation of several key proteins associated to calcium signaling. Moreover, ATRA treatment of APL cells led to a significant activation of calcium/calmodulin-dependent protein kinase kinase 2 (CAMKK2) and its downstream effector AMP-activated protein kinase (AMPK), linking Ca2+ signaling to autophagy. Pharmacological inhibition of SOC channels and CAMKK2 enhanced ATRA-induced cell differentiation and death. Altogether, our results unravel an ATRA-elicited signaling pathway that involves SOC channels/CAMKK2 activation, induction of autophagy, inhibition of cellular differentiation and suppression of cell death. We suggest that SOC channels and CAMKK2 may constitute novel drug targets for potentiating the anti-cancer effect of ATRA in APL patients F.M. was supported by a postdoctoral fellowship from the “Aquitaine Regional Council” (to MDM). K.A.-V. is supported by the Mexican National Council of Science and Technology (CONACYT, funding #757821). This work was supported by funds from the Institut National de la Santé et de la Recherche Médicale (INSERM), a grant from SIRIC BRIO (to M.D.M.), Federation de recherche Transbiomed (to M.D-M.) and contributes to the IdEx Université de Paris ANR-18-IDEX-0001. GK is supported by the Ligue contre le Cancer (équipe labellisée); Agence National de la Recherche (ANR)—Projets blancs; AMMICa US23/CNRS UMS3655; Association pour la recherche sur le cancer (ARC); Association “Ruban Rose”; Cancéropôle Ile-de-France; Fondation pour la Recherche Médicale (FRM); a donation by Elior; Equipex Onco-Pheno-Screen; European Joint Programme on Rare Diseases (EJPRD); Gustave Roussy Odyssea, the European Union Horizon 2020 Projects Oncobiome and Crimson; Fondation Carrefour; Institut National du Cancer (INCa); Inserm (HTE); Institut Universitaire de France; LabEx Immuno-Oncology (ANR-18-IDEX-0001); the Leducq Foundation; a Cancer Research ASPIRE Award from the Mark Foundation; the RHU Torino Lumière; Seerave Foundation; SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE); and SIRIC Cancer Research and Personalized Medicine (CARPEM). This study contributes to the IdEx Université de Paris ANR-18-IDEX-0001.

Systemic lupus erythematosus (SLE) is a systemic autoimmune disease characterized by a loss of tolerance toward self-nucleic acids, autoantibody production, interferon expression and signaling, and a defect in the regulatory T (Treg) cell compartment. In this work, we identified that platelets from patients with active SLE preferentially interacted with Treg cells via the P-selectin/P-selectin glycoprotein ligand-1 (PSGL-1) axis. Selectin interaction with PSGL-1 blocked the regulatory and suppressive properties of Treg cells and particularly follicular Treg cells by triggering Syk phosphorylation and an increase in intracytosolic calcium. Mechanistically, P-selectin engagement on Treg cells induced a down-regulation of the transforming growth factor–β axis, altering the phenotype of Treg cells and limiting their immunosuppressive responses. In patients with SLE, we found an up-regulation of P- and E-selectin both on microparticles and in their soluble forms that correlated with disease activity. Last, blocking P-selectin in a mouse model of SLE improved cardinal features of the disease, such as anti-dsDNA antibody concentrations and kidney pathology. Overall, our results identify a P-selectin–dependent pathway that is active in patients with SLE and validate it as a potential therapeutic avenue.

International audience; Although CD95L (also known as FasL) is still predominantly considered as a death ligand that induces apoptosis in infected and transformed cells, substantial evidence indicate that it can also trigger non-apoptotic signaling pathways whose pathophysiological roles remain to be fully elucidated. The transmembrane ligand CD95L belongs to the tumor necrosis factor (TNF) superfamily. After cleavage by metalloprotease, its soluble form (s-CD95L) fails to trigger the apoptotic program but instead induces signaling pathways promoting the aggressiveness of certain inflammatory disorders such as autoimmune diseases and cancers. We propose to evaluate the various pathologies in which the metalloprotease-cleaved CD95L is accumulated and analyze whether this soluble ligand may play a significant role in the pathology progression. Based on the TNFα-targeting therapeutics, we envision that targeting the soluble form of CD95L may represent a very attractive therapeutic option in the pathologies depicted herein.

The complete mitogenome of the lizard Iphisa elegans Gray, 1851 was sequenced using a shotgun approach on an Illumina HiSeq 3000 platform, providing the first mitogenome for Gymnophthalmidae. The genome was 18,622 bp long, with 13 protein-coding genes, two rRNA (12S and 16S), and 22 tRNA, as well as the control region. A maximum likelihood phylogenetic analysis including I. elegans and all other available mitogenomes of Squamata provided a tree in accordance with previous phylogenetic relationships inferred for Squamata.

International audience; CD95 (also known as Fas) is the prototype of death receptors; however, evidence suggests that this receptor mainly implements non-apoptotic signaling pathways such as NF-κB, MAPK, and PI3K that are involved in cell migration, differentiation, survival, and cytokine secretion. At least two different forms of CD95 L exist. The multi-aggregated transmembrane ligand (m-CD95 L) is cleaved by metalloproteases to release a homotrimeric soluble ligand (s-CD95 L). Unlike m-CD95 L, the interaction between s-CD95 L and its receptor CD95 fails to trigger apoptosis, but instead promotes calcium-dependent cell migration, which contributes to the accumulation of inflammatory Th17 cells in damaged organs of lupus patients and favors cancer cell invasiveness. Novel inhibitors targeting the pro-inflammatory roles of CD95/CD95 L may provide attractive therapeutic options for patients with chronic inflammatory disorders or cancer. This review discusses the roles of the CD95/CD95 L pair in cell migration and metastasis.

The complete mitogenome of the lizard Iphisa elegans Gray, 1851 was sequenced using a shotgun approach on an Illumina HiSeq 3000 platform, providing the first mitogenome for Gymnophthalmidae. The genome was 18,622 bp long, with 13 protein-coding genes, two rRNA (12S and 16S), and 22 tRNA, as well as the control region. A maximum likelihood phylogenetic analysis including I. elegans and all other available mitogenomes of Squamata provided a tree in accordance with previous phylogenetic relationships inferred for Squamata.

Information on temperature and composition of planetary mantles can be obtained from electrical conductivity profiles derived from induced magnetic field analysis. This requires a modeling of the conductivity for each mineral phase at conditions relevant to planetary interiors. Interpretation of iron-rich Martian mantle conductivity profile therefore requires a careful modeling of the conductivity of iron-bearing minerals. In this paper, we show that conduction mechanism called small polaron is the dominant conduction mechanism at temperature, water and iron content conditions relevant to Mars mantle. We then review the different measurements performed on mineral phases with various iron content. We show that, for all measurements of mineral conductivity reported so far, the effect of iron content on the activation energy governing the exponential decrease in the Arrhenius law can be modeled as the cubic square root of the iron content. We recast all laboratory results on a common generalized Arrhenius law for iron-bearing minerals, anchored on Earth's mantle values. We then use this modeling to compute a new synthetic profile of Martian mantle electrical conductivity. This new profile matches perfectly, in the depth range [100,1000] km, the electrical conductivity profile recently derived from the study of Mars Global Surveyor magnetic field measurements.

[This corrects the article DOI: 10.1371/journal.pbio.1001090.].

The death receptor CD95 (also known as Fas) induces apoptosis through protein/protein association and the formation of the death-inducing signaling complex. On the other hand, in certain biological conditions, this receptor recruits different proteins and triggers the formation of another complex designated motility-inducing signaling complex, which promotes cell migration and inflammation. This pathway relies on a short sequence of CD95, called calcium-inducing domain (CID), which interacts with the phospholipase PLCγ1. To better understand how CID/PLCγ1 interaction occurs, we synthesized different α-AA peptides mimicking CID. Some of these peptidomimetics are as potent as the natural peptide to disrupt the CID/PLCγ1 interaction and cell migration, and showed improved pharmacokinetic properties. We also generated biotinyl- and palmitoyl-labelled peptidomimetics, useful chemico-biological tools to further explore the pro-inflammatory signal of CD95, which plays an important role in the pathogenesis of lupus and other autoimmune diseases.

International audience; Anomaloglossus is a species-rich genus of frogs endemic to the Guiana Shield that still harbors several unnamed species. Within the A. stepheni species group (which includes four valid nominal species), A. baeobatrachus has an uncertain taxonomic status, notably because the holotype was an unvouchered specimen depicted in a popular journal. Another member of this group, A. leopardus, was only superficially described, lacking information on the sex of specimens in the type series and on advertisement call. Therefore, these two taxa need clarifications in order to allow the description of the extant undescribed species. In this paper, we redescribe A. baeobatrachus based on newly collected material from the species type locality and provide information about its reproductive ecology. We also provide an amended definition of A. leopardus using newly collected material from its type locality. These two species form a clade along with a third species from the Eastern Guiana Shield, which is also described herein. The reproductive biology of A. baeobatrachus and A. stepheni is very similar. Both species have endotrophic and nidicolous tadpoles, despite being distantly related, suggesting independent evolution of this breeding mode. The new species and A. leopardus, on the other hand, have exotrophic tadpoles.

We investigate the deformation localization at brittle–ductile transition in axisymmetric compression tests of rock analogue material GRAM1 made of bonded rigid particles. This transition in rocks (as well as in GRAM1) is recognized by the formation of a network of conjugate deformation localization bands in the postmortem rock samples and by a shallow stress reduction followed by a stress plateau in stress–strain curves. GRAM1 is much weaker than hard rocks. Therefore, brittle–ductile transition occurs in GRAM1 at a low confining pressure, 0.3 MPa, which is much smaller than that for real rocks. This allows using a transparent pressure cell and applying the digital image correlation technique to visualize the deformation evolution. Taking advantage of this technique and of the detailed characterization of GRAM1’s constitutive properties in the previous studies, we show that the initiation of deformation localization bands occurs in the dilatant (positive dilatancy factor $$\beta$$ ) and strain-softening (negative hardening modulus $$h$$ ) deformation regime. During the band evolution, the deformation within it becomes compactive ( $$\beta$$ 0), which causes the band to widen and new bands to form successively resulting in a progressively densified band network. The formation of a conjugate band network at brittle–ductile transition is thus due to the transition from dilatancy to compaction and from softening to hardening during the inelastic straining.

International audience; CD95L is a transmembrane ligand (m-CD95L) that is cleaved by metalloproteases to release a soluble ligand (s-CD95L). Unlike m-CD95L, interaction between s-CD95L and CD95 fails to recruit caspase-8 and FADD to trigger apoptosis and instead induces a Ca2+ response via docking of PLC gamma 1 to the calcium-inducing domain (CID) within CD95. This signaling pathway induces accumulation of inflammatory Th17 cells in damaged organs of lupus patients, thereby aggravating disease pathology. A large-scale screen revealed that the HIV protease inhibitor ritonavir is a potent disruptor of the CD95-PLC gamma 1 interaction. A structure-activity relationship approach highlighted that ritonavir is a peptidomimetic that shares structural characteristics with CID with respect to docking to PLC gamma 1. Thus, we synthesized CID peptidomimetics abrogating both the CD95-driven Ca2+ response and transmigration of Th17 cells. Injection of ritonavir and the CID peptidomimetic into lupus mice alleviated clinical symptoms, opening a new avenue for the generation of drugs for lupus patients.

International audience; The Lesser Antilles are a densely populated region where local populations and industrial facilities are concentrated at the coastlines, and are therefore exposed to many rapid-onset hazards such as hurricanes and tsunamis. However, the historical catalog of these events is too short to allow risk assessment and return period estimations, and it needs to be completed with long-term records of washover deposits in coastal sedimentary environments such as lagoons. In this study, two sediment cores were taken in March 2018 in a small coastal lagoon on Scrub Island (northeastern Caribbean). Sedimentological, geochemical, microfaunal and chronological analyses enabled us to identify 25 sandy layers resulting from high-energy-marine floods. Two of these layers were interpreted as tsunami deposits based on sedimentological (rip-up clast of the underlying cohesive substrate and internal mud laminae), and geochemical evidence. The most recent deposit is associated with the transatlantic tsunami triggered by the 1755 CE Lisbon earthquake. The older one is the thickest sandy layer recorded in the lagoon, with an age range of 1364-1469 cal. CE, as determined using 14 C dating. This event was recorded in sedimentary archives of both the northern and the southern part of the Caribbean, with its large spatial extent, supporting a distant tsunamigenic origin. The 23 remaining sandy layers were interpreted as storm deposits, based on sedimentological and chronological data, with the three most recent layers being correlated with historical hurricanes. This new 1600 year-long record displays similarities with that of the Bahamas, with the periods of intense hurricane activity being in antiphase with those of the northeastern US coast. This regional comparison may provide evidence for a latitudinal forcing of hurricane tracks through time in relation to climate fluctuations.

Objective Plasmacytoid dendritic cells (PDCs) play a central role in pathogenesis of systemic lupus erythematosus (SLE) through their unique ability to produce large amounts of type I interferon (IFN) upon Toll-like receptor 7 (TLR-7) and TLR-9 triggering. PDCs express specific surface regulatory receptors involved in negative regulation of IFNα secretion. These receptors use the γ-chain of high-affinity Fc receptor (FcR) for IgE, FcɛRI. We undertook this study to test our hypothesis that IgE engagement of FcɛRI on PDCs may impact IFNα production in SLE patients. Methods Serum levels of total IgE were measured in healthy volunteers, SLE patients, and patients with IgE-dependent allergic disorders. FcɛRI expression on PDCs from SLE patients was evaluated by flow cytometry. Purified PDCs were incubated with monoclonal IgE for 24 hours, then stimulated for 18 hours with TLR agonists or immune complexes (ICs). IFNα production by PDCs was detected by quantitative real-time polymerase chain reaction (PCR) and enzyme-linked immunosorbent assay. Expression of TLR-7, TLR-9, and IFN regulatory factor 7 (IRF-7) in PDCs was quantified by quantitative real-time PCR. Results We observed significantly higher IgE levels in SLE patients with quiescent disease than in those with active disease. In SLE patients, IgE levels correlated inversely with disease activity. IgE levels were not associated with the presence of antinuclear IgE. Purified PDCs treated for 24 hours with monoclonal IgE up-regulated FcɛRI expression in an IgE dose–dependent manner. IgE-treated PDCs significantly decreased IFNα secretion and down-regulated CCR7 expression upon stimulation with TLR-7 and TLR-9 ligands and ICs from lupus patients. IgE treatment down-regulated expression of TLR-9 and IRF-7. Conclusion Our results support the notion that IgE plays a protective role in SLE pathogenesis through the modulation of inflammatory response by PDCs.

CD95L is a transmembrane ligand (m-CD95L) that is cleaved by metalloproteases to release a soluble ligand (s-CD95L). Unlike m-CD95L, interaction between s-CD95L and CD95 fails to recruit caspase-8 and FADD to trigger apoptosis and instead induces a Ca

A large portion of the amphibian species occurring in Amazonia remains undescribed. A recent study on species delineation in Anomaloglossus , a genus endemic to the Guiana Shield, demonstrated the existence of two undescribed species previously identified as A. degranvillei , which we describe herein. In addition to divergence at the molecular level, these two new taxa are also distinguished by subtle morphological characters and substantial differences in the advertisement calls (note length, dominant frequency, note structure). One species occurs in the hilly lowlands of north-eastern French Guiana and is mainly distinguished from its closest relatives by a small body size (15.9–18.8 mm in males) and by vocalisations characterized by the emission of short notes of 0.09 s on average. The other species is only known from the Itoupe Massif in southern French Guiana and is mainly distinguished from its closest relatives by a moderate body size (19.4–20.4 mm in males) and by vocalisations characterized by the emission of long notes of 0.23 s on average. We also provide amended definitions for two previously described species in the A. degranvillei species group: A. degranvillei , which is endemic to a few massifs in central French Guiana, and A. surinamensis , which is distributed throughout Suriname and French Guiana. The new species described here and A. degranvillei have very narrow ranges within French Guiana and seem to have rapidly declined during the last decade. Therefore, we suggest A. degranvillei and A. dewynteri to be considered as “Critically Endangered” and A. blanci as “Vulnerable” according to the IUCN standards.

A master coordinator of cell growth, mTORC1 is activated by different metabolic inputs, particularly the metabolism of glutamine (glutaminolysis), to control a vast range of cellular processes, including autophagy. As a well-recognized tumour promoter, inhibitors of mTORC1 such as rapamycin have been approved as anti-cancer agents, but their overall outcome in patients is rather poor. Here we show that mTORC1 also presents tumour suppressor features in conditions of nutrient restrictions. Thus, the activation of mTORC1 by glutaminolysis during nutritional imbalance inhibits autophagy and induces apoptosis in cancer cells. Importantly, rapamycin treatment reactivates autophagy and prevents the mTORC1-mediated apoptosis. We also observe that the ability of mTORC1 to activate apoptosis is mediated by the adaptor protein p62. Thus, the mTORC1-mediated upregulation of p62 during nutrient imbalance induces the binding of p62 to caspase 8 and the subsequent activation of the caspase pathway. Our data highlight the role of autophagy as a survival mechanism upon rapamycin treatment., Inhibitors of the mTORC1 pathway are considered anti-cancer drugs. Here, the authors show that on nutrient restriction, glutaminolysis-induced activation of mTORC1 induces apoptosis via inhibiting autophagy, highlighting that under such conditions inhibition of mTORC1 results in survival of cancer cells.

This paper presents, for the first time, the evolution of local strain fields around intragranular cracking in polycrystalline ice, at the onset of tertiary creep. Owing to the high homologous temperature conditions and relatively low compressive stress applied, stress concentration at crack tips is relaxed by plastic mechanisms associated with dynamic recrystallization. Strain field evolution followed by Digital Image Correlation indirectly shows the redistribution of stresses during crack opening, but also driven by crack tip plasticity mechanisms and recrystallization. Such redistribution induces modifications in the local strain deformation bands, and crack closure during deformation. A strong interaction between cracking and dynamic recrystallization is therefore evidenced at the ductile to brittle transition in ice deformed at high homologous temperature.

Multiplexed bioluminescence resonance energy transfer (BRET) assays were developed to monitor the activation of several functional transient receptor potential (TRP) channels in live cells and in real time. We probed both TRPV1 intramolecular rearrangements and its interaction with Calmodulin (CaM) under activation by chemical agonists and temperature. Our BRET study also confirmed that: (1) capsaicin and heat promoted distinct transitions, independently coupled to channel gating, and that (2) TRPV1 and Ca2+-bound CaM but not Ca2+-free CaM were preassociated in resting live cells, while capsaicin activation induced both the formation of more TRPV1/CaM complexes and conformational changes. The BRET assay, based on the interaction with Calmodulin, was successfully extended to TRPV3 and TRPV4 channels. We therefore developed a full-spectral three-color BRET assay for analyzing the specific activation of each of the three TRPV channels in a single sample. Such key improvement in BRET measurement paves the way for the simultaneous monitoring of independent biological pathways in live cells.

Lack of resolution on species boundaries and distribution can hamper inferences in many fields of biology, notably biogeography and conservation biology. This is particularly true in megadiverse and under surveyed regions such as Amazonia, where species richness remains vastly underestimated. Integrative approaches using a combination of phenotypic and molecular evidence have proved extremely successful in reducing knowledge gaps in species boundaries, especially in animal groups displaying high levels of cryptic diversity like amphibians. Here we combine molecular data (mitochondrial 16S rRNA and nuclear TYR, POMC, and RAG1) from 522 specimens of Anomaloglossus, a frog genus endemic to the Guiana Shield, including 16 of the 26 nominal species, with morphometrics, bioacoustics, tadpole development mode, and habitat use to evaluate species delineation in two lowlands species groups. Molecular data reveal the existence of 18 major mtDNA lineages among which only six correspond to described species. Combined with other lines of evidence, we confirm the existence of at least 12 Anomaloglossus species in the Guiana Shield lowlands. Anomaloglossus appears to be the only amphibian genus to have largely diversified within the eastern part of the Guiana Shield. Our results also reveal strikingly different phenotypic evolution among lineages. Within the A. degranvillei group, one subclade displays acoustic and morphological conservatism, while the second subclade displays less molecular divergence but clear phenotypic divergence. In the A. stepheni species group, a complex evolutionary diversification in tadpole development is observed, notably with two closely related lineages each displaying exotrophic and endotrophic tadpoles. (C) 2017 Elsevier Inc. All rights reserved.

// Florent Dufour 1, 2 , Thibault Rattier 1, 2 , Andrei Alexandru Constantinescu 1, 2 , Luciana Zischler 1, 2, 3 , Aymeric Morle 1, 2 , Hazem Ben Mabrouk 4 , Etienne Humblin 1, 2 , Guillaume Jacquemin 1, 2 , Eva Szegezdi 5 , Fabien Delacote 6 , Naziha Marrakchi 4 , Gilles Guichard 7 , Catherine Pellat-Deceunynck 8 , Pierre Vacher 9 , Patrick Legembre 10 , Carmen Garrido 1, 2, 11 , Olivier Micheau 1, 2, 11 1 INSERM, UMR866, « Equipe labellisee Ligue contre le Cancer » and Laboratoire d’Excellence LipSTIC, Dijon, France 2 Univ. Bourgogne Franche-Comte, Dijon, France 3 Pos-graduacao emCiencias da Saude, Escola de Medicina, Pontificia Univ. Catolica do Parana, Curitiba, Parana, Brazil 4 Laboratoire des Venins et Biomolecules Therapeutiques LR11IPT08, Institut Pasteur de Tunis, Tunis, Tunisia 5 Department of Biochemistry and National Centre for Biomedical Engineering Science, National University of Ireland, Galway, Ireland 6 Cellectis, Paris, France 7 Univ. de Bordeaux, CNRS, IPB, UMR 5248, CBMN, Institut Europeen de Chimie et de Biologie, Pessac, France 8 INSERM, UMR892, CNRS 6299, Universite de Nantes, Nantes, France 9 INSERM U1218, Univ. de Bordeaux, Institut Bergonie, Bordeaux, France 10 CLCC Eugene Marquis, INSERM ER440 Oncogenesis, Stress & Signaling, Rennes, France 11 Centre Georges-Francois Leclerc, Dijon, France Correspondence to: Micheau Olivier, email: olivier.micheau@inserm.fr Keywords: receptor, TRAIL, signaling, apoptosis, cancer Received: September 02, 2016 Accepted: November 30, 2016 Published: December 27, 2016 ABSTRACT TRAIL induces selective tumor cell death through TRAIL-R1 and TRAIL-R2. Despite the fact that these receptors share high structural homologies, induction of apoptosis upon ER stress, cell autonomous motility and invasion have solely been described to occur through TRAIL-R2. Using the TALEN gene-editing approach, we show that TRAIL-R1 can also induce apoptosis during unresolved unfolded protein response (UPR). Likewise, TRAIL-R1 was found to co-immunoprecipitate with FADD and caspase-8 during ER stress. Its deficiency conferred resistance to apoptosis induced by thaspigargin, tunicamycin or brefeldin A. Our data also demonstrate that tumor cell motility and invasion-induced by TRAIL-R2 is not cell autonomous but induced in a TRAIL-dependant manner. TRAIL-R1, on the other hand, is unable to trigger cell migration owing to its inability to induce an increase in calcium flux. Importantly, all the isogenic cell lines generated in this study revealed that apoptosis induced TRAIL is preferentially induced by TRAIL-R1. Taken together, our results provide novel insights into the physiological functions of TRAIL-R1 and TRAIL-R2 and suggest that targeting TRAIL-R1 for anticancer therapy is likely to be more appropriate owing to its lack of pro-motile signaling capability.

Intracellular calcium signals regulate cell function and cell survival by controlling many processes. CD95 engagement results in distinct intracellular calcium signals that control the cell fate, apoptosis, or survival, depending on the ligand (membrane or soluble). Intracellular calcium determination is an exquisite readout to explore the molecular mechanisms elicited by CD95 engagement. The most widely applied methods for studying calcium signaling pathways use fluorescent indicators and imaging methods with fluorescence microscopy. This technical approach, however, requires many precautions that we discuss in this chapter.

This paper presents, for the first time, the evolution of the local heterogeneous strain field around intra-granular cracking in polycrystalline ice, at the onset of tertiary creep. Owing to the high homologous temperature conditions and relatively low compressive stress applied, stress concentration at the crack tips is relaxed by plastic mechanisms associated with dynamic recrystallization. Strain field evolution followed by digital image correlation (DIC) directly shows the redistribution of strain during crack opening, but also the redistribution driven by crack tip plasticity mechanisms and recrystallization. Associated local changes in microstructure induce modifications of the local stress field evidenced by crack closure during deformation. At the ductile-to-brittle transition in ice, micro-cracking and dynamic recrystallization mechanisms can co-exist and interact, the later being efficient to relax stress concentration at the crack tips.

GA101/obinutuzumab is a novel type II anti-CD20 monoclonal antibody (mAb), which is more effective than rituximab (RTX) in preclinical and clinical studies when used in combination with chemotherapy. Ca2+ signaling was shown to play a role in RTX-induced cell death. This report concerns the effect of GA101 on Ca2+ signaling and its involvement in the direct cell death induced by GA101. We reveal that GA101 triggered an intracellular Ca2+ increase by mobilizing intracellular Ca2+ stores and activating Orai1-dependent Ca2+ influx in non-Hodgkin lymphoma cell lines and primary B-Cell Chronic Lymphocytic Leukemia (B-CLL) cells. According to the cell type, Ca2+ was mobilized from two distinct intracellular compartments. In Raji, BL2, and B-CLL cells, GA101 induced a Ca2+ release from lysosomes, leading to the subsequent lysosomal membrane permeabilization and cell death. Inhibition of this calcium signaling reduced GA101-induced cell death in these cells. In SU-DHL-4 cells, GA101 mobilized Ca2+ from the endoplasmic reticulum (ER). Inhibition of ER replenishment, by blocking Orai1-dependent Ca2+ influx, led to an ER stress and unfolded protein response (UPR) which sensitized these cells to GA101-induced cell death. These results revealed the central role of Ca2+ signaling in GA101&rsquo, s action mechanism, which may contribute to designing new rational drug combinations improving its clinical efficacy.