The hormone ABA regulates the oxidative stress state under desiccation in seaweed species; an environmental condition generated during daily tidal changes. Desiccation is one of the most important factors that determine the distribution pattern of intertidal seaweeds. Among most tolerant seaweed is Pyropia orbicularis, which colonizes upper intertidal zones along the Chilean coast. P. orbicularis employs diverse mechanisms of desiccation tolerance (DT) (among others, e.g., antioxidant activation, photoinhibition, and osmo-compatible solute overproduction) such as those used by resurrection plants and bryophytes. In these organisms, the hormone abscisic acid (ABA) plays an important role in regulating responses to water deficit, including gene expression and the activity of antioxidant enzymes. The present study determined the effect of ABA on the activation of antioxidant responses during desiccation in P. orbicularis and in the sensitive species Mazzaella laminarioides and Lessonia spicata. Changes in endogenous free and conjugated ABA, water content during the hydration-desiccation cycle, enzymatic antioxidant activities [ascorbate peroxidase (AP), catalase (CAT) and peroxiredoxine (PRX)], and levels of lipid peroxidation and cell viability were evaluated. The results showed that P. orbicularis had free ABA levels 4-7 times higher than sensitive species, which was overproduced during water deficit. Using two ABA inhibitors (sodium tungstate and ancymidol), ABA was found to regulate the activation of the antioxidant enzymes activities during desiccation. In individuals exposed to exogenous ABA the enzyme activity increased, concomitant with low lipid peroxidation and high cell viability. These results demonstrate the participation of ABA in the regulation of DT in seaweeds, and suggest that regulatory mechanisms with ABA signaling could be of great importance for the adaptation of these organisms to dehydration.
The transcriptional modulation of desiccation tolerance factors in P. orbicularis explains its successful recuperation after water deficit. Differential responses to air exposure clarify seaweed distribution along intertidal rocky zones. Desiccation-tolerant seaweed species, such as Pyropia orbicularis, can tolerate near 96% water loss during air exposure. To understand the phenotypic plasticity of P. orbicularis to desiccation, several tolerance factors were assessed by RT-qPCR, Western-blot analysis, and enzymatic assays during the natural desiccation-rehydration cycle. Comparative enzymatic analyses were used to evidence differential responses between P. orbicularis and desiccation-sensitive species. The results showed that during desiccation, the relative mRNA levels of genes associated with basal metabolism [trehalose phosphate synthase (tps) and pyruvate dehydrogenase (pdh)] were overexpressed in P. orbicularis. Transcript levels related to antioxidant metabolism [peroxiredoxin (prx); thioredoxin (trx); catalase (cat); lipoxygenase (lox); ferredoxin (fnr); glutathione S-transferase (gst)], cellular detoxification [ABC transporter (abc) and ubiquitin (ubq)], and signal transduction [calmodulin (cam)] increased approximately 15- to 20-fold, with the majority returning to basal levels during the final hours of rehydration. In contrast, actin (act) and transcription factor 1 (tf1) transcripts were down-regulated. ABC transporter protein levels increased in P. orbicularis during desiccation, whereas PRX transcripts decreased. The antioxidant enzymes showed higher specific activity in P. orbicularis under desiccation, and sensitive species exhibited enzymatic inactivation and scarce ABC and PRX protein detection following prolonged desiccation. In conclusion, the reported findings contribute towards understanding the ecological distribution of intertidal seaweeds at the molecular and functional levels.
ABSTRACT. In rocky shores, desiccation is triggered by daily tide changes, and experimental evidence suggests that local distribution of algal species across the intertidal rocky zone is related to their capacity to tolerate desiccation. In this context, the permanence of Pyropia columbina in the high intertidal rocky zone is explained by its exceptional physiological tolerance to desiccation. This study explored the metabolic pathways involved in tolerance to desiccation in the Chilean P. columbina, by characterizing its transcriptome under contrasting conditions of hydration. We obtained 1,410 ESTs from two subtracted cDNA libraries in naturally hydrated and desiccated fronds. Results indicate that transcriptome from both libraries contain transcripts from diverse metabolic pathways related to tolerance. Among the transcripts differentially expressed, 15% appears involved in protein synthesis, processing and degradation, 14.4% are related to photosynthesis and chloroplast, 13.1% to respiration and mitochondrial function (NADH dehydrogenase and cytochrome c oxidase proteins), 10.6% to cell wall metabolism, and 7.5% are involved in antioxidant activity, chaperone and defense factors (catalase, thioredoxin, heat shock proteins, cytochrome P450). Both libraries highlight the presence of genes/proteins never described before in algae. This information provides the first molecular work regarding desiccation tolerance in P. columbina, and helps, to some extent, explaining the classical patterns of ecological distribution described for algae across the intertidal zone. Keywords: Pyropia, desiccation stress, ESTs, seaweeds, transcriptomics, proteins. Expresión diferencial de genes en Pyropia columbina (Bangiales, Rhodophyta)bajo hidratación y desecación natural RESUMEN. En zonas rocosas costeras, la desecación es gatillada por cambios diarios en los niveles de marea, y la evidencia experimental indica que la distribución de las algas en la zona intermareal está relacionada con su capacidad para tolerar la desecación. En este contexto, la presencia de Pyropia columbina en la zona alta del intermareal se explica por su excepcional tolerancia fisiológica a la desecación. Este estudio explora las vías metabólicas involucradas en la tolerancia a la desecación en P. columbina, a través de la caracterización de su transcriptoma bajo condiciones de hidratación contrastantes. Se obtuvo 1,410 ESTs provenientes de dos librerías de substracción de cDNA de frondas naturalmente hidratadas y desecadas. Los transcriptomas de ambas librerías contienen transcritos de diversas rutas metabólicas relacionadas a la tolerancia. Entre los transcritos expresados 15% están involucrados en la síntesis de proteínas, su procesamiento y degradación, 14,4% asociados a fotosíntesis y cloroplasto, 13,1% a respiración y función mitocondrial, 10,6% al metabolismo de la pared celular y 7,5% a la actividad antioxidante, proteínas chaperonas y factores de defensa (catalasa, tiorredoxina, proteínas de shock térmico, citocromo P450). En ambas librerías se de...
Novel Magnesium Oxide (MgO) nanoparticles (NPs) modified with the polymer poliethylene glycol (PEG) were synthesized as carrier for the anticancer drug 2-Methoxyestradiol (2ME) to improve its clinical application. The functionalized NPs were characterized by Infrared spectroscopy with Fourier transform to elucidate the vibration modes of this conjugate, indicating the formation of the MgO-PEG-2ME nanocomposite. The studies of absorption and liberation determined that MgO-PEG-2ME NPs incorporated 98.51 % of 2ME while liberation of 2ME was constant during 7 days at pH 2, 5 and 7.35. Finally, the MgO-PEG-2ME NPs decreased the viability of the prostate cancer cell line LNCap suggesting that this nanocomposite is suitable as a drug delivery system for anticancer prostate therapy. 12March 15, 2019 1/9 2-Metoxyestradiol (2ME) has antitumor activity in several types of cancer of the 13 reproductive tract as prostate, cervix, ovary or endometrium. 2ME exerts its anticancer 14 activity via anti-proliferative, apoptotic or antiangiogenic effects on tumor cells [7]. 15 Despite to be considerate as a promising anticancer drug it has an unfavorable kinetic 16 with a low solubility in water; Thus, it is necessary to find new ways to facilitate its 17 administration to the human body. In this context, the nanoparticles (NPs) as drug 18 carriers can play a fundamental role to improvement biological parameters. Actually, it 19 has been proposed that polymeric NPs [8] or TiO 2 NPs coated with polyethylene glycol 20 (PEG) could be useful tools to load 2ME [9]. In the searching for new NPs suitable for 21 medical use, MgO NPs are also an excellent candidate because they are bio-friendly [10]. 22 It has been shown that MgO NPs are not toxic for a variety of human cell lines at 23 concentrations under 300 µg/ml [10]. MgO NPs has been also used as a carrier for the 24 antincancer drug doxorubicin indicating its utility for a controlled system of drugs 25 delivery [11, 12]. In this work, we first performed the physicochemical characterization 26 of MgO NPs coated with PEG and loaded with 2ME (MgO-PEG-2ME). The efficiency 27 of absortion and liberation of 2ME was then analyzed. Finally, the effect of 28 MgO-PEG-2ME NPs on the prostate cell line LnCap was assessed. 29 Materials and Methods 30 Synthesis MgO nanoparticles 31 The MgO NPs were obtained by the sol-gel method route assisted with cetyltrimethyl 32 ammonium bromide C 19 H 4 2BrN (CTAB) as a surfactant to reduce the agglomeration of 33 the NPs [13]. 1:1 molar solution of magnesium acetate, Mg(CH 3 COO) 2 4H 2 O (99,5 %, 34 MERK, USA) and tartaric acid C 4 H 6 O 6 to (99,5 %, MERK, USA) was prepared in 35 ethanol and added dropwise over 10 ml of a 0.001 M of CTAB in water at 60 • C. The 36solution was stirred vigorously for 20 hours to achieve gel formation. Once the gel is 37 formed, it was dried and before calcined at 600 • C for 6 hours to give MgO [14]. 38MgO nanoparticles functionalized with PEG and 2ME loading. 39MgO NPs were covered with poliethylene glycol 600 (PEG600; Sigma...
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.