267 research outputs found

    Field Trip for the Gospel

    Get PDF

    Nanocomposite-based dual enzyme system for broad-spectrum scavenging of reactive oxygen species

    Get PDF
    A broad-spectrum reactive oxygen species (ROS)-scavenging hybrid material (CASCADE) was developed by sequential adsorption of heparin (HEP) and poly(L-lysine) (PLL) polyelectrolytes together with superoxide dismutase (SOD) and horseradish peroxidase (HRP) antioxidant enzymes on layered double hydroxide (LDH) nanoclay support. The synthetic conditions were optimized so that CASCADE possessed remarkable structural (no enzyme leakage) and colloidal (excellent resistance against salt-induced aggregation) stability. The obtained composite was active in decomposition of both superoxide radical anions and hydrogen peroxide in biochemical assays revealing that the strong electrostatic interaction with the functionalized support led to high enzyme loadings, nevertheless, it did not interfere with the native enzyme conformation. In vitro tests demonstrated that ROS generated in human cervical adenocarcinoma cells were successfully consumed by the hybrid material. The cellular uptake was not accompanied with any toxicity effects, which makes the developed CASCADE a promising candidate for treatment of oxidative stress-related diseases

    Pnpla3 single nucleotide polymorphism prevalence and association with liver disease in a diverse cohort of persons living with hiv

    Get PDF
    In persons living with HIV (PLWH), there are multiple sources of liver injury. Gene polymorphisms of PNPLA3 (patatin-like phospholipase domain-containing protein 3) have been identified as an important cofactor for increased disease severity in both alcoholic and non-alcoholic steatohepatitis (NASH). We utilized a well-characterized cohort of ethnically and racially diverse patients with HIV to define the prevalence of PNPLA3 SNPs (single nucleotide polymorphism) (rs738409), and to determine the relationship to hepatic steatosis and liver fibrosis. Steatosis was determined using MRI-PDFF (magnetic resonance imaging-determined proton density fat fraction) and fibrosis was estimated using MR Elastography (MRE). From the Miami Area HIV Study (MASH) cohort, 100 HIV positive participants and 40 controls (HCV/HIV = 20; HCV and HIV negative = 20) were evaluated. Nearly 40% of all participants carried the variant G allele associated with increased liver disease severity and 5% were homozygotic GG. The variant SNP occurred most frequently in those self-identified as Hispanic compared to white or Black participants. Hepatic steatosis (\u3e5% fat) was present significantly more often in those without HIV vs. those with (p \u3c 0.001). Putative NAFLD/NASH was found to be present in 6% of tested subjects, who were HIV monoinfected. BMI was lower in those that carried the G allele for PNPLA3. This finding suggests that PNPLA3 may be an independent component to NAFLD (non-alcoholic fatty liver disease)/NASH development and longitudinal follow-up of the cohort is warranted

    Development of a novel renal activity index of lupus nephritis in children & young adults

    Get PDF
    BACKGROUND: Noninvasive estimation of the degree of inflammation seen on kidney biopsy with lupus nephritis (LN) remains difficult. The objective of this study was to develop a Renal Activity Index for Lupus (RAIL) that, based solely on laboratory measures, accurately reflects histological LN activity. METHODS: We assayed traditional LN laboratory tests and 16 urine biomarkers (UBMs) in children (n=47) at the time of kidney biopsy. Histological LN activity was measured by the NIH Activity Index (NIH-AI) and the Tubulointerstitial Activity Index (TIAI). High LN-activity status (vs. moderate/low) was defined as NIH-AI scores \u3e 10 (vs.5 (vs.92% accuracy and LN-activityTIAI status with \u3e80% accuracy. RAIL accuracy was minimally influenced by concomitant LN damage. Accuracies between 71 and 85% were achieved without standardization of the UBMs. The strength of these UBMs to reflect LN-activity status was confirmed by principal component and linear discriminant analyses. CONCLUSION: The RAIL is a robust and highly accurate noninvasive measure of LN-activity. The measurement properties of the RAIL, which reflect the degree of inflammatory changes as seen on kidney biopsy, will require independent validation. This article is protected by copyright. All rights reserved

    Hepatitis E Virus Antibodies in Patients with Chronic Liver Disease

    Get PDF
    In the United States, the seroprevalence rate for hepatitis E virus (HEV) is ≈20%. This study examined HEV seroprevalence in persons with and without chronic liver disease. Our data indicate that HEV seropositivity is high in patients with chronic liver disease and that HEV seroprevalence increases significantly with age

    Autoantibodies to a 140-kd protein in juvenile dermatomyositis are associated with calcinosis

    Get PDF
    Objective. The identification of novel autoantibodies in juvenile dermatomyositis (DM) may have etiologic and clinical implications. The aim of this study was to describe autoantibodies to a 140-kd protein in children recruited to the Juvenile DM National Registry and Repository for UK and Ireland.Methods. Clinical data and sera were collected from children with juvenile myositis. Sera that recognized a 140-kd protein by immunoprecipitation were identified. The identity of the p140 autoantigen was investigated by immunoprecipitation/immunodepletion, using commercial monoclonal antibodies to NXP-2, reference anti-p140, and anti-p155/140, the other autoantibody recently described in juvenile DM. DNA sampies from 100 Caucasian children with myositis were genotyped for HLA class II haplotype associations and compared with those from 864 randomly selected UK Caucasian control subjects.Results. Sera from 37 (23%) of 162 patients with juvenile myositis were positive for anti-p140 autoantibodies, which were detected exclusively in patients with juvenile DM and not in patients with juvenile DM-overlap syndrome or control subjects. No anti-p140 antibody-positive patients were positive for other recognized autoantibodies. Immunodepletion suggested that the identity of p140 was consistent with NXP-2 (the previously identified MJ autoantigen). In children with anti-p140 antibodies, the association with calcinosis was significant compared with the rest of the cohort (corrected P < 0.005, odds ratio 7.0, 95% confidence interval 3.0-16.1). The clinical features of patients with anti-p140 autoantibodies were different from those of children with anti-p155/140 autoantibodies. The presence of HLA-DRB1*08 was a possible risk factor for anti-p140 autoantibody positivity.Conclusion. This study has established that anti-p140 autoantibodies represent a major autoantibody subset in juvenile DM. This specificity may identify a further immunogenetic and clinical phenotype within the juvenile myositis spectrum that includes an association with calcinosis

    Pilot study comparing the childhood arthritis and rheumatology research alliance consensus treatment plans for induction therapy of juvenile proliferative lupus nephritis

    Get PDF
    BACKGROUND: To reduce treatment variability and facilitate comparative effectiveness studies, the Childhood Arthritis and Rheumatology Research Alliance (CARRA) published consensus treatment plans (CTPs) including one for juvenile proliferative lupus nephritis (LN). Induction immunosuppression CTPs outline treatment with either monthly intravenous (IV) cyclophosphamide (CYC) or mycophenolate mofetil (MMF) in conjunction with one of three corticosteroid (steroid) CTPs: primarily oral, primarily IV or mixed oral/IV. The acceptability and in-practice use of these CTPs are unknown. Therefore, the primary aims of the pilot study were to demonstrate feasibility of adhering to the LN CTPs and delineate barriers to implementation in clinical care in the US. Further, we aimed to explore the safety and effectiveness of the treatments for induction therapy.METHODS: Forty-one patients were enrolled from 10 CARRA sites. Patients had new-onset biopsy proven ISN/RPS class III or IV proliferative LN, were starting induction therapy with MMF or IV CYC and high-dose steroids and were followed for up to 24 months. Routine clinical data were collected at each visit. Provider reasons for CTP selection were assessed at baseline. Adherence to the CTPs was evaluated by provider survey and medication logs. Complete and partial renal responses were reported at 6 months.RESULTS: The majority of patients were female (83%) with a mean age of 14.7 years, SD 2.8. CYC was used more commonly than MMF for patients with ISN/RPS class IV LN (vs. class III), those who had hematuria, and those with adherence concerns. Overall adherence to the immunosuppression induction CTPs was acceptable with a majority of patients receiving the target MMF (86%) or CYC (63%) dose. However, adherence to the steroid CTPs was poor (37%) with large variability in dosing. Renal response endpoints were exploratory and did not show a significant difference between CYC and MMF.CONCLUSIONS: Overall, the immunosuppression CTPs were followed as intended in the majority of patients however, adherence to the steroid CTPs was poor indicating revision is necessary. In addition, our pilot study revealed several sources of treatment selection bias that will need to be addressed in for future comparative effectiveness research

    LOL2 and LOL5 loci control latex production by laticifer cells in Euphorbia lathyris

    Full text link
    [EN] Laticifers are specialized plant cells capable of indefinite elongation that ramify extensively and are responsible for latex biosynthesis and accumulation. However, the mechanisms underlying laticifer cell differentiation, growth and production of latex remain largely unknown. In a search for mutants showing enhanced accumulation of latex we identified two LOT OF LATEX (LOL) loci in Euphorbia lathyris. lol2 and lol5 mutants show enhanced production of latex contained within laticifer cells. The recessive lol2 mutant carries increased biosynthesis of the plant hormone jasmonoyl-isoleucine (JA-Ile) and therefore establishes a genetic link between jasmonic acid (JA) signaling and latex production in laticifers. Instead, heightened production of latex in lol5 plants obeys to enhanced proliferation of laticifer cells. Phylogenetic analysis of laticifer-expressed genes in E. lathyris and in two other latex-bearing species, Euphorbia corallioides and Euphorbia palustris, allowed the identification of canonical JA responsive elements present in the gene promoter regions of laticifer marker genes. Moreover, we identified that the hormone JA functions not as a morphogen for laticifer differentiation but as a trigger for the fill out of laticifers with latex and the associated triterpenoids. The identification of LOL loci represents a further step towards the understanding of mechanisms controlling latex production in laticifer cells.This work was supported by Spanish MINECO (BFU2015 -68199 -R to P.V.) and Generalitat Valenciana (Prometeo 2014/024 to P.V.).Castelblanque, L.; Balaguer Zamora, B.; Marti, C.; Orozco, M.; Vera Vera, P. (2018). LOL2 and LOL5 loci control latex production by laticifer cells in Euphorbia lathyris. New Phytologist. 219(4):1467-1479. https://doi.org/10.1111/nph.15253S146714792194Agrawal, A. A., & Konno, K. (2009). Latex: A Model for Understanding Mechanisms, Ecology, and Evolution of Plant Defense Against Herbivory. Annual Review of Ecology, Evolution, and Systematics, 40(1), 311-331. doi:10.1146/annurev.ecolsys.110308.120307Barres, L., Vilatersana, R., Molero, J., Susanna, A., & Galbany-Casals, M. (2011). Molecular phylogeny of Euphorbia subg. Esula sect. Aphyllis (Euphorbiaceae) inferred from nrDNA and cpDNA markers with biogeographic insights. TAXON, 60(3), 705-720. doi:10.1002/tax.603007Becerra, J. X., & Venable, D. L. (1990). Rapid-Terpene-Bath and «Squirt-Gun» Defense in Bursera schlechtendalii and the Counterploy of Chrysomelid Beetles. Biotropica, 22(3), 320. doi:10.2307/2388545Boffelli, D. (2003). Phylogenetic Shadowing of Primate Sequences to Find Functional Regions of the Human Genome. Science, 299(5611), 1391-1394. doi:10.1126/science.1081331Bonaventure, G., Gfeller, A., RodrĂ­guez, V. M., Armand, F., & Farmer, E. E. (2007). The fou2 Gain-of-Function Allele and the Wild-Type Allele of Two Pore Channel 1 Contribute to Different Extents or by Different Mechanisms to Defense Gene Expression in Arabidopsis. Plant and Cell Physiology, 48(12), 1775-1789. doi:10.1093/pcp/pcm151Chini, A., Fonseca, S., FernĂĄndez, G., Adie, B., Chico, J. M., Lorenzo, O., 
 Solano, R. (2007). The JAZ family of repressors is the missing link in jasmonate signalling. Nature, 448(7154), 666-671. doi:10.1038/nature06006Clough, S. J., & Bent, A. F. (1998). Floral dip: a simplified method forAgrobacterium-mediated transformation ofArabidopsis thaliana. The Plant Journal, 16(6), 735-743. doi:10.1046/j.1365-313x.1998.00343.xBary, A. de, Bower, F. O., & Scott, D. H. (1884). Comparative anatomy of the vegetative organs of the phanerogams and ferns; doi:10.5962/bhl.title.56013De Geyter, N., Gholami, A., Goormachtig, S., & Goossens, A. (2012). Transcriptional machineries in jasmonate-elicited plant secondary metabolism. Trends in Plant Science, 17(6), 349-359. doi:10.1016/j.tplants.2012.03.001Dombrecht, B., Xue, G. P., Sprague, S. J., Kirkegaard, J. A., Ross, J. J., Reid, J. B., 
 Kazan, K. (2007). MYC2 Differentially Modulates Diverse Jasmonate-Dependent Functions in Arabidopsis. The Plant Cell, 19(7), 2225-2245. doi:10.1105/tpc.106.048017Dussourd, D., & Eisner, T. (1987). Vein-cutting behavior: insect counterploy to the latex defense of plants. Science, 237(4817), 898-901. doi:10.1126/science.3616620Ellis, C., Karafyllidis, I., Wasternack, C., & Turner, J. G. (2002). The Arabidopsis Mutant cev1 Links Cell Wall Signaling to Jasmonate and Ethylene Responses. The Plant Cell, 14(7), 1557-1566. doi:10.1105/tpc.002022Frame, B. R., Shou, H., Chikwamba, R. K., Zhang, Z., Xiang, C., Fonger, T. M., 
 Wang, K. (2002). Agrobacterium tumefaciens-Mediated Transformation of Maize Embryos Using a Standard Binary Vector System. Plant Physiology, 129(1), 13-22. doi:10.1104/pp.000653Godoy, M., Franco-Zorrilla, J. M., PĂ©rez-PĂ©rez, J., Oliveros, J. C., Lorenzo, Ó., & Solano, R. (2011). Improved protein-binding microarrays for the identification of DNA-binding specificities of transcription factors. The Plant Journal, 66(4), 700-711. doi:10.1111/j.1365-313x.2011.04519.xHAGEL, J., YEUNG, E., & FACCHINI, P. (2008). Got milk? The secret life of laticifers. Trends in Plant Science, 13(12), 631-639. doi:10.1016/j.tplants.2008.09.005HAO, B. (2000). Laticifer Differentiation in Hevea brasiliensis: Induction by Exogenous Jasmonic Acid and Linolenic Acid. Annals of Botany, 85(1), 37-43. doi:10.1006/anbo.1999.0995Huber, M., Epping, J., Schulze Gronover, C., Fricke, J., Aziz, Z., Brillatz, T., 
 Erb, M. (2016). A Latex Metabolite Benefits Plant Fitness under Root Herbivore Attack. PLOS Biology, 14(1), e1002332. doi:10.1371/journal.pbio.1002332James, J., Tugizimana, F., Steenkamp, P., & Dubery, I. (2013). Metabolomic Analysis of Methyl Jasmonate-Induced Triterpenoid Production in the Medicinal Herb Centella asiatica (L.) Urban. Molecules, 18(4), 4267-4281. doi:10.3390/molecules18044267Jefferson, R. A., Kavanagh, T. A., & Bevan, M. W. (1987). GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. The EMBO Journal, 6(13), 3901-3907. doi:10.1002/j.1460-2075.1987.tb02730.xKonno, K. (2011). Plant latex and other exudates as plant defense systems: Roles of various defense chemicals and proteins contained therein. Phytochemistry, 72(13), 1510-1530. doi:10.1016/j.phytochem.2011.02.016Laosombut, T., Arreewichit, P., Nirapathpongporn, K., Traiperm, P., Kongsawadworakul, P., Viboonjun, U., & Narangajavana, J. (2016). Differential Expression of Methyl Jasmonate-Responsive Genes Correlates with Laticifer Vessel Proliferation in Phloem Tissue of Rubber Tree (Hevea brasiliensis). Journal of Plant Growth Regulation, 35(4), 1049-1063. doi:10.1007/s00344-016-9603-4Lescot, M. (2002). PlantCARE, a database of plant cis-acting regulatory elements and a portal to tools for in silico analysis of promoter sequences. Nucleic Acids Research, 30(1), 325-327. doi:10.1093/nar/30.1.325Lewinsohn, T. M. (1991). The geographical distribution of plant latex. Chemoecology, 2(1), 64-68. doi:10.1007/bf01240668Lorenzo, O., Chico, J. M., SĂĄnchez-Serrano, J. J., & Solano, R. (2004). JASMONATE-INSENSITIVE1 Encodes a MYC Transcription Factor Essential to Discriminate between Different Jasmonate-Regulated Defense Responses in Arabidopsis. The Plant Cell, 16(7), 1938-1950. doi:10.1105/tpc.022319Mahlberg, P. G. (1961). EMBRYOGENY AND HISTOGENESIS IN NERIUM OLEANDER II. ORIGIN AND DEVELOPMENT OF THE NON-ARTICULATED LATICIFER. American Journal of Botany, 48(1), 90-99. doi:10.1002/j.1537-2197.1961.tb11608.xMahlberg, P. G. (1963). Development of Non-Articulated Laticifer in Seedling Axis of Nerium oleander. Botanical Gazette, 124(3), 224-231. doi:10.1086/336195Mahlberg, P. G. (1993). Laticifers: An historical perspective. The Botanical Review, 59(1), 1-23. doi:10.1007/bf02856611Mahlberg, P. G., & Sabharwal, P. S. (1968). ORIGIN AND EARLY DEVELOPMENT OF NONARTICULATED LATICIFERS IN EMBRYOS OF EUPHORBIA MARGINATA. American Journal of Botany, 55(3), 375-381. doi:10.1002/j.1537-2197.1968.tb07389.xMangas, S., Bonfill, M., Osuna, L., Moyano, E., Tortoriello, J., Cusido, R. M., 
 PalazĂłn, J. (2006). The effect of methyl jasmonate on triterpene and sterol metabolisms of Centella asiatica, Ruscus aculeatus and Galphimia glauca cultured plants. Phytochemistry, 67(18), 2041-2049. doi:10.1016/j.phytochem.2006.06.025Memelink, J., Verpoorte, R., & Kijne, J. W. (2001). ORCAnization of jasmonate-responsive gene expression in alkaloid metabolism. Trends in Plant Science, 6(5), 212-219. doi:10.1016/s1360-1385(01)01924-0Mertens, J., Pollier, J., Vanden Bossche, R., Lopez-Vidriero, I., Franco-Zorrilla, J. M., & Goossens, A. (2015). The bHLH Transcription Factors TSAR1 and TSAR2 Regulate Triterpene Saponin Biosynthesis in Medicago truncatula. Plant Physiology, 170(1), 194-210. doi:10.1104/pp.15.01645Mertens, J., Van Moerkercke, A., Vanden Bossche, R., Pollier, J., & Goossens, A. (2016). Clade IVa Basic Helix–Loop–Helix Transcription Factors Form Part of a Conserved Jasmonate Signaling Circuit for the Regulation of Bioactive Plant Terpenoid Biosynthesis. Plant and Cell Physiology, 57(12), 2564-2575. doi:10.1093/pcp/pcw168Metcalfe, C. R. (1967). Distribution of latex in the plant kingdom. Economic Botany, 21(2), 115-127. doi:10.1007/bf02897859Nessler, C. L., & Mahlberg, P. G. (1981). CYTOCHEMICAL LOCALIZATION OF CELLULASE ACTIVITY IN ARTICULATED, ANASTOMOSING LATICIFERS OF PAPAVER SOMNIFERUM L. (PAPAVERACEAE). American Journal of Botany, 68(5), 730-732. doi:10.1002/j.1537-2197.1981.tb12405.xPauwels, L., InzĂ©, D., & Goossens, A. (2009). Jasmonate-inducible gene: what does it mean? Trends in Plant Science, 14(2), 87-91. doi:10.1016/j.tplants.2008.11.005Pickard, W. F. (2008). Laticifers and secretory ducts: two other tube systems in plants. New Phytologist, 177(4), 877-888. doi:10.1111/j.1469-8137.2007.02323.xPirrello, J., Leclercq, J., Dessailly, F., Rio, M., Piyatrakul, P., Kuswanhadi, K., 
 Montoro, P. (2014). Transcriptional and post-transcriptional regulation of the jasmonate signalling pathway in response to abiotic and harvesting stress in Hevea brasiliensis. BMC Plant Biology, 14(1). doi:10.1186/s12870-014-0341-0RamĂ­rez, V., Van der Ent, S., GarcĂ­a-Andrade, J., Coego, A., Pieterse, C. M., & Vera, P. (2010). OCP3 is an important modulator of NPR1-mediated jasmonic acid-dependent induced defenses in Arabidopsis. BMC Plant Biology, 10(1), 199. doi:10.1186/1471-2229-10-199Rouster, J., Leah, R., Mundy, J., & Cameron-Mills, V. (1997). Identification of a methyl jasmonate-responsive region in the promoter of a lipoxygenase 1 gene expressed in barley grain. The Plant Journal, 11(3), 513-523. doi:10.1046/j.1365-313x.1997.11030513.xSĂĄnchez-Bel, P., SanmartĂ­n, N., Pastor, V., Mateu, D., Cerezo, M., Vidal-Albalat, A., 
 Flors, V. (2017). Mycorrhizal tomato plants fine tunes the growth-defence balance upon N depleted root environments. Plant, Cell & Environment, 41(2), 406-420. doi:10.1111/pce.13105Staswick, P. E., Su, W., & Howell, S. H. (1992). Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant. Proceedings of the National Academy of Sciences, 89(15), 6837-6840. doi:10.1073/pnas.89.15.6837Suzuki, H., Reddy, M. S. S., Naoumkina, M., Aziz, N., May, G. D., Huhman, D. V., 
 Dixon, R. A. (2004). Methyl jasmonate and yeast elicitor induce differential transcriptional and metabolic re-programming in cell suspension cultures of the model legume Medicago truncatula. Planta, 220(5), 696-707. doi:10.1007/s00425-004-1387-2Tamari, G., Borochov, A., Atzorn, R., & Weiss, D. (1995). Methyl jasmonate induces pigmentation and flavonoid gene expression in petunia corollas: A possible role in wound response. Physiologia Plantarum, 94(1), 45-50. doi:10.1111/j.1399-3054.1995.tb00782.
    • 

    corecore