Effects of GSK3β/eEF2K signaling pathway on pulmonary fibrosis in mice / 中国应用生理学杂志

Objective: To investigate the effects of glycogen synthase kinase-3β (GSK3β)/eukaryotic extension factor kinase 2 (eEF2K) signaling pathway on the process of pulmonary fibrosis through in vivo experiments, and find new ideas for clinical treatment of pulmonary fibrosis. Methods: The pulmonary fibrosis model of C57BL/6 male mice was induced by bleomycin with intratracheal injection at the dose of 2 mg/kg. After 14 days of modeling, animals were divided into model group, negative inhibition group and inhibition group (n=5 for each group), and control group was not processed. The inhibition group was treated with TDZD-8 (4 mg/kg) after modeling, the negative inhibition group was given DMSO solution after modeling, and the samples were collected after 28 days. Hematoxylin-eosin staining method was used to detect lung fibrosis in mice and scored according to Ashcroft scale. Expression levels of GSK3β, p-GSK3β, eEF2K, p-eEF2K (Ser70, Ser392, Ser470), precursor protein of matrix metalloproteinase-2 (pro-MMP-2), matrix metalloproteinase-2 (MMP-2), collagen I (Col I), collagen Ⅲ (Col Ⅲ) and α-smooth muscle actin (α-SMA) were detected by Western blot. Results: Compared with control group, the fibrosis score was up-regulated, the expression levels of GSK3β, p-GSK3β, p-eEF2K (Ser70, Ser392, Ser470), pro-MMP-2, MMP-2, Col I, Col Ⅲ and α-SMA were increased, while that of eEF2K was decreased in model group (P＜0.05). Compared with model group, the fibrosis score, expression levels of GSK3β, p-GSK3β, p-eEF2K (Ser70, Ser392, Ser470), pro-MMP-2, MMP-2, Col I, Col Ⅲ and α-SMA were decreased, but the expression level of eEF2K was increased in inhibition group (P＜0.05). Conclusion: GSK3β can activate eEF2K by phosphorylation at the sites of Ser70, Ser392 and Ser470, increase the contents of fibrosis indicators, promote the formation of pulmonary fibrosis, and aggravate lung tissue lesions.

Eukaryotic expression, Co-IP and MS identify BMPR-1B protein-protein interaction network

BACKGROUND: BMPR-1B is part of the transforming growth factor ß super family and plays a pivotal role in ewe litter size. Functional loss of exon-8 mutations in the BMPR-1B gene (namely the FecB gene) can increase both the ewe ovulation rate and litter size. RESULTS: This study constructed a eukaryotic expression system, prepared a monoclonal antibody, and characterized BMPR-1B/FecB protein-protein interactions (PPIs). Using Co-immunoprecipitation coupled to mass spectrometry (Co-IP/MS), 23 proteins were identified that specifically interact with FecB in ovary extracts of ewes. Bioinformatics analysis of selected PPIs demonstrated that FecB associated with several other BMPs, primarily via signal transduction in the ovary. FecB and its associated interaction proteins enriched the reproduction process via BMP2 and BMP4 pathways. Signal transduction was identified via Smads proteins and TGF-beta signaling pathway by analyzing the biological processes and pathways. Moreover, other target proteins (GDF5, GDF9, RhoD, and HSP 10) that interact with FecB and that are related to ovulation and litter size in ewes were identified. CONCLUSIONS: In summary, this research identified a novel pathway and insight to explore the PPi network of BMPR-1B.

Evalúan las probables propiedades terapéuticas de la espirulina / Assessment of the probable therapeutic properties of spirulina

La espirulina es un alga verdeazulada (cianobacteria) que ha sido consumida por los seres humanos durante cientos de años en la región Kanem de Chad y en las regiones lacustres de México. Actualmente se comercializa en todo el mundo como alimento terapéutico. Su potencial como tratamiento de varias enfermedades se encuentra en evaluación. El consumo mundial de espirulina ha clarificado tanto sus potenciales efectos adversos como sus acciones beneficiosas. En este artículo se presenta un breve resumen del uso de la espirulina en el área de la salud.

Mycosporine-like amino acids (MAAs): chemical structure, biosynthesis and significance as UV-absorbing/screening compounds.

Continuous depletion of the stratospheric ozone layer has resulted in an increase in ultraviolet-B (UV-B; 280-315 nm) radiation on the earth's surface which inhibits photochemical and photobiological processes. However, certain photosynthetic organisms have evolved mechanisms to counteract the toxicity of ultraviolet or high photosynthetically active radiation by synthesizing the UV-absorbing/screening compounds, such as mycosporine-like amino acids (MAAs) and scytonemin besides the repair of UV-induced damage of DNA and accumulation of carotenoids and detoxifying enzymes or radical quenchers and antioxidants. Chemical structure of various MAAs, their possible biochemical routes of synthesis and role as photoprotective compounds in various organisms are discussed.

Removal of Cr6+ from aqueous solution by some algae.

Biosorption of Cr6+ from aqueous solution on dried (Halimeda tuna, Sargassum vulgare, Pterocladia capillacea, Hypnea musciformis, Laurencia papillosa) algae were studied with variation in the parameters of pH, initial metal ion concentration and agitation time. From the batch system studies the working sorption pH value was determined as 1.0 for Halimeda tuna and Sargassum vulgare, 2.0 for Pterocladia capillacea and Hypnea musciformis, 3.0 for Laurencia papillosa. The total adsorbed quantities, equilibrium uptakes and total removal percents of Cr6+ were determined by evaluating the breakthrough curves obtained at different inlet Cr6+ concentration for each sorbent. The maximum chromium biosorption occured at 120 min for Halimeda tuna, 180 min for Sargassum vulgare, Hypnea musciformis and Pterocladia capillacea, 60 min for Laurencia papillosa. The suitability of the Freundlich and Langmiur adsorption models were also investigated for each chromium-sorbent system. The results showed that Sargassum vulgare was found suitable for removing chromium from aqueous solution. The maximum sorption capacities of Halimeda tuna, Sargassum vulgare, Pterocladia capillacea, Hypnea musciformis, Laurencia papillosa were determined as 2.3, 33.0, 6.6, 4.7 and 5.3 mgg(-1).

Nitrate reductase activty: a solution to nitrate problems tested in free and immobilized algal cells in presence of heavy metals

Every organism has different potential to accumulate NO3- from the environment. Nitrate reduction processes are perhaps most significant in maintaining water quality by alteration of nitrate to nitrite. A comparative study between the nitrate reductase NR activity of green and blue green algae in presence of heavy metals is being conducted to present a situation where nitrate reductase process may be affected in presence of heavy metals. Metals interacted negatively with the nitrate reductase activity of a blue green alga, Anacystis nidulans and green algae, Chlorella vulgaris in both free and immobilized state. The activity was more repressed in C. vulgaris in presence of Ni compared to Zn and Cd. However, Cd was more toxic to NR activity in A. nidulans [free state]. Metal dependent variation between free and immobilized cells were found to be significant [P< 0.01] however, the concentration dependent pattern in the activity between free and immobilized state was non significant in both the test organisms. C.vulgaris is more efficient in conversion of nitrate to nitrite compared to A.nidulans in presence of heavy metals

Biological process of arsenic removal using selected microalgae.

In the present investigation, growth of the organisms was reduced due to presence of arsenic (III) and (V) in the culture medium. In comparison to arsenic (V), arsenic (III) had more toxic effect on microalgae. Among the different algal strains, blue green algal species Oscillatoria-Lyngbya mixed culture showed maximum efficiency in removing arsenic (64%) after 21 days of incubation and the same algal species could remove arsenic (III), but 60% after 21 days when incubated in 0.1 mg/l arsenic (III) containing medium. Maximum removal was observed at their exponential growth phase and also so sometime extended to the stationary phase.

Biorecovery of gold.

Recovery of ionic and metallic gold (Au) from a wide variety of solutions by selected species of bacteria, yeasts, fungi, algae, and higher plants is documented. Gold accumulations were up to 7.0 g/kg dry weight (DW) in various species of bacteria, 25.0 g/kg DW in freshwater algae, 84.0 g/kg DW in peat, and 100.0 g/kg DW in dried fungus mixed with keratinous material. Mechanisms of accumulation include oxidation, dissolution, reduction, leaching, and sorption. Uptake patterns are significantly modified by the physicochemical milieu. Crab exoskeletons accumulate up to 4.9 g Au/kg DW; however, gold accumulations in various tissues of living teleosts, decapod crustaceans, and bivalve molluscs are negligible.

Glycosyl-phosphatidylinositols in protozoa structure, biosynthesis and intracellular localisation.

We are investigating the structure and biosynthesis of glycosyl-phosphatidylinositols (GPI) in the protozoa Toxoplasma gondii, Plasmodium falciparum, Plasmodium yoelii and Paramecium primaurelia. This comparison of structural and biosynthesis data should lead us to common and individual features of the GPI-biosynthesis and transport in different organisms.

The effect of salinity on the growth and carotenogenesis in two Chilean strains of Dunaliella salina Teodoresco

We studied the effect of salt concentration on the growth and carotenogenesis in two Chilean strains of Dunaliella salina, CONC-006 and CONC-007, cultivated in two media of different chemical composition J/l and PES, under controlled laboratory conditions. Growth rates, k (div day-1), intrinsic production rates of total carotenoids per unit time rcar (day-1), maximum levels of total carotenoids, K (mg l-1), and maximum production of total carotenoids per unit time, rK/4 (micrograms l-1 day-1) were estimated from growth and carotenogenesis data. The highest maximum productivity of total carotenoids was 978 micrograms l-1 day-1 obtained in CONC-007 at 25 percent NaCl, and the lowest 15 micrograms l-1 day-1, in CONC-006 at 30 percent NaCl, both growing in PES medium. CONC-007 showed the highest growth rates, 0.76 and 0.65 div day-1, at the lowest salt concentration (5 percent) in PES and J/1, respectively. On the contrary, the strain CONC-006 exhibited a different growth pattern in both media. Its maximum growth rate in J/1 was 0.37 div day-1 at 20 percent NaCl, and in PES, 0.53 div day-1 at 5 percent NaCl. According to these results, the best integration of growth and carotenogenesis in CONC-007 was obtained at 15 percent NaCl in J/1 from 10 to 25 percent NaCl in PES and in CONC-006, from 5 to 20 percent NaCl in J/1 and from 5 to 10 percent NaCl in PES

Effects of copper on photosynthetic activity and chlorophyll-a content of chaectoceros radicans Schutte

Chaetoceros radicans was selected to test the effect of copper concentrations of 0.001, 0.005, 0.01, 0.05, 0.1 and 0.5 ppm for 6 days on the photosynthetic activity and chlorophyll-a content under laboratory conditions. The photosynthetic activity decreased with time of exposure and copper concentration. The control photosynthetic activity reached a maximum value at 120 hours and chlorophyll-a at 72 hours. Chaetoceros radicans cultures treated by copper showed a slight decrease in its photosynthetic activity and chlorophyll-a at levels 0.001 and 0.005 ppm, while they rapidly decreased at higher copper concentrations