BackgroundMicroenvironment cues involved in melanoma progression are largely unknown. Melanoma is highly influenced in its aggressive phenotype by the changes it determinates in its microenvironment, such as pH decrease, in turn influencing cancer cell invasiveness, progression and tissue remodelling through an abundant secretion of exosomes, dictating cancer strategy to the whole host. A role of exosomes in driving melanoma progression under microenvironmental acidity was never described.MethodsWe studied four differently staged human melanoma lines, reflecting melanoma progression, under microenvironmental acidic pHs pressure ranging between pH 6.0–6.7. To estimate exosome secretion as a function of tumor stage and environmental pH, we applied a technique to generate native fluorescent exosomes characterized by vesicles integrity, size, density, markers expression, and quantifiable by direct FACS analysis.Functional roles of exosomes were tested in migration and invasion tests. Then we performed a comparative proteomic analysis of acid versus control exosomes to elucidate a specific signature involved in melanoma progression.ResultsWe found that metastatic melanoma secretes a higher exosome amount than primary melanoma, and that acidic pH increases exosome secretion when melanoma is in an intermediate stage, i.e. metastatic non-invasive.We were thus able to show that acidic pH influences the intercellular cross-talk mediated by exosomes. In fact when exposed to exosomes produced in an acidic medium, pH naïve melanoma cells acquire migratory and invasive capacities likely due to transfer of metastatic exosomal proteins, favoring cell motility and angiogenesis.A Prognoscan-based meta-analysis study of proteins enriched in acidic exosomes, identified 11 genes (HRAS, GANAB, CFL2, HSP90B1, HSP90AB1, GSN, HSPA1L, NRAS, HSPA5, TIMP3, HYOU1), significantly correlating with poor prognosis, whose high expression was in part confirmed in bioptic samples of lymph node metastases.ConclusionsA crucial step of melanoma progression does occur at melanoma intermediate –stage, when extracellular acidic pH induces an abundant release and intra-tumoral uptake of exosomes. Such exosomes are endowed with pro-invasive molecules of clinical relevance, which may provide a signature of melanoma advancement.Electronic supplementary materialThe online version of this article (10.1186/s13046-018-0915-z) contains supplementary material, which is available to authorized users.

BackgroundToxoplasmosis is caused by the apicomplexan parasite Toxoplasma gondii and can be acquired either congenitally or via the oral route. In the latter case, transmission is mediated by two distinct invasive stages, i.e., bradyzoites residing in tissue cysts or sporozoites contained in environmentally resistant oocysts shed by felids in their feces. The oocyst plays a central epidemiological role, yet this stage has been scarcely investigated at the molecular level and the knowledge of its expressed proteome is very limited.ResultsUsing one-dimensional gel electrophoresis coupled to liquid chromatography-linked tandem mass spectrometry, we analysed total or fractionated protein extracts of partially sporulated T. gondii oocysts, producing a dataset of 1304 non reduntant proteins (~18% of the total predicted proteome), ~59% of which were classified according to the MIPS functional catalogue database. Notably, the comparison of the oocyst dataset with the extensively covered proteome of T. gondii tachyzoite, the invasive stage responsible for the clinical signs of toxoplasmosis, identified 154 putative oocyst/sporozoite-specific proteins, some of which were validated by Western blot. The analysis of this protein subset showed that, compared to tachyzoites, oocysts have a greater capability of de novo amino acid biosynthesis and are well equipped to fuel the Krebs cycle with the acetyl-CoA generated through fatty acid β-oxidation and the degradation of branched amino acids.ConclusionsThe study reported herein significantly expanded our knowledge of the proteome expressed by the oocyst/sporozoite of T. gondii, shedding light on a stage-specifc subset of proteins whose functional profile is consistent with the adaptation of T. gondii oocysts to the nutrient-poor and stressing extracellular environment.

The malaria parasite invades the terminally differentiated erythrocytes, where it grows and multiplies surrounded by a parasitophorous vacuole. Plasmodium blood stages translocate newly synthesized proteins outside the parasitophorous vacuole and direct them to various erythrocyte compartments, including the cytoskeleton and the plasma membrane. Here, we show that the remodeling of the host cell directed by the parasite also includes the recruitment of dematin, an actin-binding protein of the erythrocyte membrane skeleton and its repositioning to the parasite. Internalized dematin was found associated with Plasmodium 14-3-3, which belongs to a family of conserved multitask molecules. We also show that, in vitro, the dematin-14-3-3 interaction is strictly dependent on phosphorylation of dematin at Ser 124 and Ser 333 , belonging to two 14-3-3 putative binding motifs. This study is the first report showing that a component of the erythrocyte spectrin-based membrane skeleton is recruited by the malaria parasite following erythrocyte infection.The Plasmodium parasite, the etiologic agent of malaria, invades the host red blood cell (RBC), 2 where it grows and multiplies within a parasitophorous vacuole (PV). The PV membrane (PVM) represents an interface between the parasite and the host erythrocyte. A subset of parasite proteins is exported beyond the PVM by a recently discovered secretory system directed by a pentameric amino acid sequence motif (PEXE(L/H)T) (1, 2). Additional pathways might flank this unusual export machinery because a number of parasite proteins that do not contain the PEXE(L/H)T motif are also exported to erythrocyte sites (3). The parasite generates novel membrane compartments to sustain protein trafficking. For example, in Plasmodium falciparum-infected RBCs (iRBCs), the so-called Maurer's clefts, organelles anchored to the RBC cytoskeleton, are responsible for the assembly and targeting of parasite adhesive proteins to the erythrocyte surface. Exported proteins are routed to different erythrocyte compartments, including the host membrane skeleton, leading to extensive remodeling of the host cell.The erythrocyte skeleton is anchored to the phospholipid bilayer through two major protein bridges; one connects the integral membrane protein band 3 to spectrin via ankyrin, whereas the other involves the junctional complex, which connects the C-terminal end of spectrin to short actin protofilaments (4, 5). Protein 4.1, dematin, and adducin are components of the junctional complex. Protein 4.1, p55, and the transmembrane glycophorin C form a well characterized ternary complex, which tethers the junctional complex to the plasma membrane (6). The membrane receptors glucose transporter-1 GLUT1 (7) and Band 3 (8) directly bind to dematin and/or adducin, providing alternative links to the erythrocyte plasma membrane.Several P. falciparum exported proteins bring about coordinated remodeling of the spectrin-based erythrocyte membrane skeleton (3, 9). One of the best characterized examples is the knob-associa...

The aim of the study was to evaluate the airborne contamination by polycyclic aromatic hydrocarbons (PAHs) and some heavy metals (arsenic [As], cadmium [Cd], chromium [Cr], copper [Cu], nickel [Ni], lead [Pb], and zinc [Zn]) of different pollution scenarios around a solid-waste landfill in central Italy using the lichen Pseudovernia furfuracea as a monitoring tool. For this purpose, eight stations around a landfill characterized by different air pollution sources (industrial, agricultural, residential areas, and roads with different traffic intensities), together with three stations far from the landfill (control areas), were monitored using a set of 22 lichen samples (11 samples analysed for PAHs and metals after 4 months, and 11 samples analysed for metals after 8 months). After 4 months of exposure, the lichen content of all of the analysed elements was greater than that in the pre-exposed lichens. In addition, the Cu and Pb concentration after 8 months was greater than the level after 4 months. The order of metal concentration was Zn > Pb > Cu (or Cu > Pb) > Cr > Ni > As > Cd in all cases. The range of ∑11PAHs concentration was 634-1,371 ng/g dw (three to seven times greater than the amount in the pre-exposed lichens). The ∑11PAHs were dominated (>70 %) by compounds with three aromatic rings. The comparison of the levels of air pollutants among the monitored stations shows nonrelevant spatial patterns between the landfill stations and the control areas; the levels of PAHs and metals found in the lichen samples around the landfill seemed to be more related to the general diffusion of these pollutants in that area.

The exposure of the human body to microgravity, conditions that occurs during space flights, causes significant changes in the cardiovascular system. Many cell types have been involved in these changes, and the endothelium seems to play a major role. In endothelial cells (EC), it has been shown that modeled low gravity impairs nitric oxide synthesis, cell adhesion, extracellular matrix composition, cytoskeleton organization, cytokines, and growth factors secretion. Nevertheless, detailed analysis of EC physiological changes induced by microgravity exposure is still lacking. Secretome analysis is one of the most promising approaches for the identification of biomarkers directly related to the physiopathological cellular state. In this study, we analyzed in details the modifications of EC secretome by using umbilical vein endothelial (HUVE) cells exposed to modeled low gravity conditions. By adopting a two-dimensional (2-D) proteomic approach, in conjunction with a technique for the compression of the dynamic range of proteins, we observed that modeled low gravity exposure of HUVE cells affected the secretion of proteins involved in the regulation of cytoskeleton assembly. Moreover, by using Luminex® suspension array systems, we found that the low gravity condition decreased in ECs the secretion of some key pro-inflammatory cytokines, including IL-1α and IL-8, and of the pro-angiogenic factor bFGF. On the contrary, microgravity increase the secretion of two chemokines (Rantes and Eotaxin), involved in leukocytes recruitment.