Espacio para estudiantes : la bibliotecología y los caminos que nos propone

It made ​​a comment on the value of the library profession and presents the work experience by a group of students from the National University of Mar del Plata on the refurbishment of a neighborhood librar

On the membrane translocation of diphtheria toxin: at low pH the toxin induces ion channels on cells.

Diphtheria toxin (DT) in acidic media forms ion-conducting channels across the plasma membrane and inhibits protein synthesis of both highly and poorly DT-sensitive cell lines. This results in loss of cell potassium and in entry of both sodium and protons with a concomitant rapid lowering of membrane potential. The pH dependency of the permeability changes is similar to that of the inhibition of cell protein synthesis. DT-induced ion channels close when the pH of the external medium is returned to neutrality and cells recover their normal monovalent cation content. Similar permeability changes were induced by two DT mutants defective either in enzymatic activity or in cell binding, but not with a mutant defective in membrane translocation. The implication of these findings for the mechanism of DT membrane translocation is discussed

HDAC inhibitors for muscular dystrophies: progress and prospects

HDAC inhibitors for muscular dystrophies: progress and prospects Duchenne muscular dystrophy (DMD) is the most common and severe form of muscular dystrophy (MD) that affects 1 in 3500–6000 live male births. This lethal X-linked genetic disease is caused by muta- tions in dystrophin gene that leads to a complete absence of the protein, thereby compromising the structural and functional integrity of the dystrophin- associated protein complex (DAPC).[1] The DAPC links the actin cytoskeleton to the extracellular matrix and has an essential role in stabilizing the sarcolemma during repeated cycles of contraction.[2] As such, dystrophin-deficient muscles are vulnerable to mechanical damage and develop progressive muscu- lar weakness, as a consequence of muscle degenera- tion, leading to loss of myofibers, which are ultimately replaced by fibrotic scars and fat deposition.[3] There is still no available cure for DMD, but only palliative treatments that aim to counter muscle loss, thereby extending patient mobility and delaying the onset of respiratory and cardiac problems.[4] The progression of DMD is highly influenced by the ability of dystrophin-deficient muscles to counter mus- cle loss by a regenerative response, which typically defines a clinical latency observed during the early stages of the disease. The gradual exhaustion of such compensatory response coincides with changes in the muscle tissue composition, leading to the progressive formation of fibrotic and adipose tissue in place of contractile fibers. This ‘restriction point’ in the natural history of DMD is due to alterations in the interactions between the cell types that contribute to promote regeneration, eventually culminating with a switch of muscle repair toward fibrotic and fat deposition.[5] In particular, studies in the last decade have revealed the importance of changes in the identity and functional properties of the cellular components of the muscle stem (satellite) cell (MuSC) niche. For instance, the inter- actions between inflammatory cells (e.g. macrophages), interstitial ‘support’ cells (e.g. fibro-adipogenic progeni- tors – FAPs) and MuSCs appear a key determinant to drive the skeletal muscle toward a regeneration or degeneration process.[6,7] This notion has inspired a number of current pharmacological strategies aimed at targeting these cells and the functional networks they establish,[8,9] as an alternative to gene replace- ment and cell-based strategies. Among the pharmacological interventions that aim to slow down the disease progression by targeting key events downstream of the genetic defect, the histone deacetylase inhibitors (HDACi) have recently been translated into a clinical trial, based on the encouraging preclincial data generated in the mouse model of DMD – the mdx mice.[10,11] In principle, the rationale for the use of HDACi in the treatment of DMD was provided by the finding that dystrophin-deficient muscles display an aberrant, con- stitutive activation of HDAC2, as a consequence of reduced nitric oxide (NO)-mediated NO-dependent S-nitrosylation in myofibers.[12] Moreover, recent stu- dies have revealed complex epigenetic networks tar- geted by HDACi in MuSCs and FAPs.[13,14] In particular, studies from Saccone et al. have identified an HDAC-regulated network that controls the func- tional phenotype of FAPs from dystrophic muscles. Treatment with HDACi promotes the expression of two core components of the myogenic transcriptional machinery, MyoD and BAF60c [15] and upregulates three myogenic microRNA involved into muscle differ- entiation (myomiRs; miR-1.2, miR-133 and miR-206) in FAPs. MyomiRs in turn target two alternative BAF60 variants – BAF60 A and B – that when incorporated into the Switch/Sucrose NonFermentable (SWI/SNF) chromatin-remodeling complex would otherwise pro- mote the activation of the fibro-adipogenic program. [14] Thus, HDACi-mediated selection of BAF60 C-based SWI/SNF complex appears to mediate a therapeutic switch of FAP phenotype from pro-fibroadipogenic to pro-myogenic one. Interestingly, FAPs from dystrophic muscles at advanced stage of disease are resistant to the beneficial effects of HDACi, accounting for the stage-specific effect of HDACi previously observed by Mozzetta et al.[9] Genome-wide studies of chromatin accessibility showed that at early stages of the disease, HDACi promote an extensive chromatin remodeling, which was not observed at late stage of the disease. [14] This finding indicates that pharmacological inter- ventions that target FAPs could be used to promote compensatory regeneration, while preventing fibro- adipogenic degeneration of DMD muscles. It also sug- gests that FAPs of dystrophic muscles at late stages of DMD progression might acquire a chromatin conforma- tion that confers resistance to treatments that are © 2015 Taylor & Francis 126 M. SANDONÁ ET AL. otherwise effective at early stages of disease. Understanding the molecular basis of such resistance could reveal novel targets for interventions aimed at restoring the ability of FAPs to support muscle regen- eration rather than fibrosis and fat infiltration in a larger population of patients. Conclusion As preclinical evidence supported the rationale for the use of HDACi in the treatment of DMD, the HDACi Givinostat has been launched as the first epigenetic drug tested in a Phase I/II clinical trial on DMD boys between 8 and 10 years of age that is currently under investigation. Given the potential of HDACi to promote regeneration at the expense of fibro-adipogenic degen- eration, one predicted effect of Givinostat on DMD muscles is to extend the compensatory regeneration and delay the disease progression in patients at early stages of disease progression, Future research should evaluate the efficacy of Givinostat in a larger population of DMD patients and identify molecular criteria and noninvasive biomarkers that define patient responsive- ness and eventually inspire further interventions that sensitize to HDACi unresponsive patients. Expert opinion Three fundamental aspects for the future development of HDACi-based therapies concern a) the identification of biomarkers that help selecting patients for clinical studies and monitoring their responsiveness to the treatments, b) the discovery of complementary approaches that synergize with HDACi to provide an optimal combined therapeutic intervention and c) the potential extension of HDACi-based treatments to other forms of muscular dystrophies. While the analysis of muscle biopsies is currently regarded as the most reliable readout of the histologi- cal effects of HDACi, this procedure is invasive, is lim- ited to one specific muscle and cannot be repeated multiple times during the course of clinical trials. As such, it is currently missing an effective readout of the efficacy of treatment with HDACi or similar pharmaco- logical approaches. Identification of circulating biomar- kers and/or setting noninvasive or semi-invasive procedures for the evaluation of the effects of pharma- cological interventions is clearly a fundamental step to further move forward pro-clinical and clinical research on DMD. Moreover, beyond the beneficial effects on muscle histology, the clinical efficacy of HDACi treatment needs to be correlated with functional tests. Studies with HDACi in mdx mice demonstrated that the morpholo- gical recovery is accompanied by increased muscle strength and exercise performance.[10,11] Thus, match- ing functional tests, such as 6 Minute Walk Test (6MWT) and North Star Ambulatory Assessment, with the histo- logical evaluation of treated muscles, will be mandatory to reveal the efficacy of HDACi and other pharmacolo- gical interventions in DMD patients. Regarding the identification of complementary approaches that synergize with HDACi, the most urgent questions relate to the functional interactions between HDACi and steroids – the standard treatment currently used in the treatment of DMD. In this case, it is inter- esting to note that steroids are typically acting through a nuclear receptor – the glucocorticoid receptor (GR) – whose activity is negatively regulated by an HDAC- containing repressive complex. Moreover, the possibi- lity to combine HDACi-based treatment with emerging strategies toward re-introducing functional dystrophin in DMD muscles (i.e. exon skipping or future CRISPR- based interventions) is supported by a strong rationale consisting of the necessity to protect the newly formed myofibers, induced by HDACi-promoted regeneration, from contraction-mediated regeneration, via dystrophin re-expression. Finally, future research should determine the poten- tial efficacy of HDACi on other forms of muscular dys- trophies that share pathogenic events with DMD, e.g. the shift from compensatory regeneration to fibrosis and fat deposition. Declaration of interest Funding has been received from AFM Telethon and Duchenne Parent Project (DPP-NL). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock owner- ship or options, expert testimony, grants or patents received or pending, or royalties. References Papers of special note have been highlighted as either of interest (•) or of considerable interest (••) to readers. 1. Dalkilic I, Kunkel LM. Muscular dystrophies: genes to pathogenesis. Curr Opin Genet Dev. 2003;13(3):231–238. 2. Petrof BJ, Shrager JB, Stedman HH, et al. Dystrophin protects the sarcolemma from stresses developed during muscle contraction. Proc Natl Acad Sci USA. 1993;90(8):3710–3714. 3. Straub V, Campbell KP. Muscular dystrophies and the dystrophin-glycoprotein complex. Curr Opin Neurol. 1997;10(2):168–175. 4. Mercuri E, Muntoni F. Muscular dystrophy: new chal- lenges and review of the current clinical trials. Curr Opin Pediatr. 2013;25(6):701–707. DOI:10.1097/ MOP.0b013e328365ace5. 5. Serrano AL, Mann CJ, Vidal B, et al. Cellular and molecular mechanisms regulating fibrosis in skeletal muscle repair and disease. Curr Top Dev Biol. 2011;96:167–201. DOI:10.1016/B978-0-12-385940-2.00007-3. 6. Farup J, Madaro L, Puri PL, et al. Interactions between muscle stem cells, mesenchymal-derived cells and immune cells in muscle homeostasis, regeneration and disease. Cell Death Dis. 2015;6:e1830. DOI:10.1038/ cddis.2015.198. 7. Judson RN, Zhang RH, Rossi FM. Tissue-resident mesenchymal stem/progenitor cells in skeletal muscle: collaborators or saboteurs? Febs J. 2013;280 (17):4100–4108. DOI:10.1111/febs.12370. 8. Lemos DR, Babaeijandaghi F, Low M, et al. Nilotinib reduces muscle fibrosis in chronic muscle injury by promoting TNF-mediated apoptosis of fibro/adipogenic progenitors. Nat Med. 2015;21(7):786–794. DOI:10.1038/nm.3869. 9. Mozzetta C, Consalvi S, Saccone V, et al. Fibroadipogenic progenitors mediate the ability of HDAC inhibitors to promote regeneration in dystrophic muscles of young, but not old Mdx mice. EMBO Mol Med. 2013;5 (4):626–639. DOI:10.1002/emmm.201202096. • Exciting paper studying the fibroadipogenic pro- genitors (FAPs) as cellular determinants of the ben- eficial effects of HDAC inhibitors. FAPs mediate HDACi effects promoting muscles regeneration in a stage-specific manner. 10. Minetti GC, Colussi C, Adami R, et al. Functional and morphological recovery of dystrophic muscles in mice treated with deacetylase inhibitors. Nat Med. 2006;12 (10):1147–1150. • Interesting paper describing the functional and mor- phological effects of HDAC inhibitors treatments. HDAC inhibitors increase myofiber size and counter the functional decline of dystrophic muscles 11. Consalvi S, Mozzetta C, Bettica P, et al. Preclinical studies in the mdx mouse model of Duchenne muscular dystro- phy with the histone deacetylase inhibitor Givinostat. Mol Med. 2013;19:79–87. DOI:10.2119/molmed.2013.00011. •• Excellentpaperdemonstratingtheeffectivenessofa long-term treatment with Givinostat. The findings of this paper provide preclinical basis for a translation on DMD patients. 12. Colussi C, Mozzetta C, Gurtner A, et al. HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment. Proc Natl Acad Sci USA. 2008;105 (49):19183–19187. DOI:10.1073/pnas.0805514105. 13. Cacchiarelli D, Martone J, Girardi E, et al. MicroRNAs involved in molecular circuitries relevant for the Duchenne muscular dystrophy pathogenesis are controlled by the dystrophin/nNOS pathway. Cell Metab. 2010;12(4):341–351. DOI:10.1016/j. cmet.2010.07.008. 14. Saccone V, Consalvi S, Giordani L, et al. HDAC-regulated myomiRs control BAF60 variant exchange and direct the functional phenotype of fibro-adipogenic progenitors in dystrophic muscles. Genes Dev. 2014;28(8):841–857. DOI:10.1101/gad.234468.113. • Fascinating paper determines the molecular mechan- ism that controls the FAPs switch from a fibroadipo- genic to a myogenic phenotype after HDACi treatment. 15. Forcales SV, Albini S, Giordani L, et al. Signal-dependent incorporation of MyoD-BAF60c into Brg1-based SWI/SNF chromatin-remodelling complex. Embo J. 2012;31(2):301–316. DOI:10.1038/emboj. 2011.391. M. Sandoná IRCCS Fondazione Santa Lucia, Rome, Italy DAHFMO, Unit of Histology and Medical Embryology, Sapienza University of Rome, Rome, Italy S. Consalvi IRCCS Fondazione Santa Lucia, Rome, Italy L. Tucciarone IRCCS Fondazione Santa Lucia, Rome, Italy P. L. Puri IRCCS Fondazione Santa Lucia, Rome, Italy Muscle Development and Regeneration Program, Sanford Children’s Health Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA V. Saccone IRCCS Fondazione Santa Lucia, Rome, Ital

Muscle-specific microRNAs as biomarkers of Duchenne Muscular Dystrophy progression and response to therapies

Recent studies have revealed the contribution of fibro-adipogenic progenitors (FAPs) to the pathogenesis and progression of Duchenne Muscular Dystrophy (DMD). While FAPs direct compensatory regeneration at early stages of disease, as the disease progresses they contribute to the progressive replacement of contractile myofibers with fibrotic scars and fatty infiltration. Using the mouse model of DMD – the mdx mice - we have recently reported that FAPs mediate the ability of HDAC inhibitors (HDACi) to promote muscle regeneration and prevent fibro-adipogenic degeneration at early stages of disease. This effect is mediated by the induction of myomiRs that, in turn, target the SWI/SNF components BAF60A and B, thereby favoring the formation of BAF60C-based SWI/SNF complex, which directs the switch from the fibro-adipogenic to the myogenic lineage. Here we show direct evidence of induction of miR-206 and BAF60C, and reduction of BAF60A, in FAPs isolated from mdx muscles exposed to the HDACi Trichostatin A (TSA). We also discuss how increased expression of myomiRs in dystrophic muscles can be integrated with circulating myomiRs to provide accurate biomarkers of disease progression and response to treatment

Fluorescence lifetime heterogeneity in aggregates of LHCII revealed by time-resolved microscopy.

Two-photon excitation, time-resolved fluorescence microscopy was used to investigate the fluorescence quenching mechanisms in aggregates of light-harvesting chlorophyll a/b pigment protein complexes of photosystem II from green plants (LHCII). Time-gated microscopy images show the presence of large heterogeneity in fluorescence lifetimes not only for different LHCII aggregates, but also within a single aggregate. Thus, the fluorescence decay traces obtained from macroscopic measurements reflect an average over a large distribution of local fluorescence kinetics. This opens the possibility to resolve spatially different structural/functional units in chloroplasts and other heterogeneous photosynthetic systems in vivo, and gives the opportunity to investigate individually the excited states dynamics of each unit. We show that the lifetime distribution is sensitive to the concentration of quenchers contained in the system. Triplets, which are generated at high pulse repetition rates of excitation (>1 MHz), preferentially quench domains with initially shorter fluorescence lifetimes. This proves our previous prediction from singlet-singlet annihilation investigations (Barzda, V., V. Gulbinas, R. Kananavicius, V. Cervinskas, H. van Amerongen, R. van Grondelle, and L. Valkunas. 2001. Biophys. J. 80:2409-2421) that shorter fluorescence lifetimes originate from larger domains in LHCII aggregates. We found that singlet-singlet annihilation has a strong effect in time-resolved fluorescence microscopy of connective systems and has to be taken into consideration. Despite that, clear differences in fluorescence decays can be detected that can also qualitatively be understood