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- Ferrari, E, et al.
(author)
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Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation
- 2017
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In: Cell death & disease. - : Springer Science and Business Media LLC. - 2041-4889. ; 8:1, s. e2544-
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Journal article (peer-reviewed)abstract
- Cystic fibrosis (CF), the most common lethal monogenic disease in Caucasians, is characterized by recurrent bacterial infections and colonization, mainly by Pseudomonas aeruginosa, resulting in unresolved airway inflammation. CF is caused by mutations in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein, which functions as a chloride channel in epithelial cells, macrophages, and other cell types. Impaired bacterial handling by macrophages is a feature of CF airways, although it is still debated how defective CFTR impairs bacterial killing. Recent evidence indicates that a defective autophagy in CF macrophages leads to alterations of bacterial clearance upon infection. Here we use bone marrow-derived macrophages from transgenic mice to provide the genetic proof that defective CFTR compromises both uptake and clearance of internalized Pseudomonas aeruginosa. We demonstrate that the proteostasis regulator cysteamine, which rescues the function of the most common F508del-CFTR mutant and hence reduces lung inflammation in CF patients, can also repair the defects of CF macrophages, thus restoring both bacterial internalization and clearance through a process that involves upregulation of the pro-autophagic protein Beclin 1 and re-establishment of the autophagic pathway. Altogether these results indicate that cysteamine restores the function of several distinct cell types, including that of macrophages, which might contribute to its beneficial effects on CF.
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- Maiuri, L, et al.
(author)
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Defective proteostasis in celiac disease as a new therapeutic target
- 2019
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In: Cell death & disease. - : Springer Science and Business Media LLC. - 2041-4889. ; 10:2, s. 114-
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Journal article (peer-reviewed)abstract
- Cystic fibrosis (CF) is a disease caused by loss-of-function mutations affecting the CF transmembrane conductance regulator (CFTR), a chloride channel. Recent evidence indicates that CFTR is inhibited by a gluten/gliadin-derived peptide (P31-43), causing an acquired state of CFTR inhibition within the gut that contributes to the pathogenesis of celiac disease (CD). Of note, CFTR inhibition does not only cause intra- and extracellular ion imbalances but also affects proteostasis by activating transglutaminase-2 (TGM2) and by disabling autophagy. These three phenomena (CFTR inhibition, TGM2 activation, and autophagy impairment) engage in multiple self-amplifying circuitries, thus forming an “infernal trio”. The trio hinders enterocytes from returning to homeostasis and instead locks them in an irreversible pro-inflammatory state that ultimately facilitates T lymphocyte-mediated immune responses against another gluten/gliadin-derived peptide (P57–68), which,upon deamidation by activated TGM2, becomes fully antigenic. Hence, the pathogenic protein gliadin exemplifies a food constituent the exceptional immunogenicity of which arises from a combination of antigenicity (conferred by deaminated P57–68) and adjuvanticity (conferred by P31-43). CF can be treated by agents targeting the “infernal trio” including CFTR potentiators, TGM2 inhibitors, and autophagy enhancers. We speculate that such agents may also be used for CD therapy and indeed could constitute close-to-etiological treatments of this enteropathy.
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- Piras, P., et al.
(author)
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Evolution of the sabertooth mandible: A deadly ecomorphological specialization
- 2018
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In: Palaeogeography Palaeoclimatology Palaeoecology. - : Elsevier BV. - 0031-0182. ; 496, s. 166-174
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Journal article (peer-reviewed)abstract
- Saber-toothed cats were armed with formidable weapons. They evolved a number of highly derived morphological features, most notably a pair of extremely long upper canines, which makes them unique within the felid family. Although the sabertooth character evolved several times among carnivorous mammals, sabertooth clades mostly had disjunctive occurrences both in space and time, and no sabertooth is alive today. We studied the rates of phenotypic and taxonomic diversification in the mandible of sabertooths, as compared to the rates calculated for both extinct and extant conical toothed cats. We found that the mandible's shape and physical properties in sabertooth clades evolved at distinctly higher rates than the rest of the felid tree. In addition, sabertooths had similar speciation rate to conical toothed cats, but statistically higher extinction rate. The wealth of morphological specializations required to be a sabertooth, and their tendency to focus on large-sized species as prey, was likely responsible for such high extinction rate, and for the peculiar, disjunctive patterns of sabertooth Glade occurrence in the fossil record.
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