Nicotinamide phosphoribosyltransferase (NAMPT) is located in both the nucleus and cytoplasm and has multiple biological functions including catalyzing the rate-limiting step in NAD synthesis. Moreover, up-regulated NAMPT expression has been observed in many cancers. However, the determinants and regulation of NAMPT's nuclear transport are not known. Here, we constructed a GFP-NAMPT fusion protein to study NAMPT's subcellular trafficking. We observed that in unsynchronized 3T3-L1 preadipocytes, 25% of cells had higher GFP-NAMPT fluorescence in the cytoplasm, and 62% had higher GFP-NAMPT fluorescence in the nucleus. In HepG2 hepatocytes, 6% of cells had higher GFP-NAMPT fluorescence in the cytoplasm, and 84% had higher GFP-NAMPT fluorescence in the nucleus. In both 3T3-L1 and HepG2 cells, GFP-NAMPT was excluded from the nucleus immediately after mitosis and migrated back into it as the cell cycle progressed. In HepG2 cells, endogenous, untagged NAMPT displayed similar changes with the cell cycle, and in nonmitotic cells, GFP-NAMPT accumulated in the nucleus. Similarly, genotoxic, oxidative, or dicarbonyl stress also caused nuclear NAMPT localization. These interventions also increased poly(ADP-ribosyl) polymerase and sirtuin activity, suggesting an increased cellular demand for NAD. We identified a nuclear localization signal in NAMPT and amino acid substitution in this sequence (424RSKK to ASGA), which did not affect its enzymatic activity, blocked nuclear NAMPT transport, slowed cell growth, and increased histone H3 acetylation. These results suggest that NAMPT is transported into the nucleus where it presumably increases NAD synthesis required for cell proliferation. We conclude that specific inhibition of NAMPT transport into the nucleus might be a potential avenue for managing cancer.
- Klíčová slova
- GFP fusion, NAMPT, cancer, epigenetics, nicotinamide adenine dinucleotide (NAD), nuclear localization, pre–B cell colony enhancing factor (PBEF), sirtuin, visfatin,
- MeSH
- akrylamidy farmakologie MeSH
- aktivní transport - buněčné jádro MeSH
- buněčné jádro metabolismus MeSH
- buňky 3T3-L1 MeSH
- buňky Hep G2 MeSH
- cytoplazma metabolismus MeSH
- histony metabolismus MeSH
- kontrolní body buněčného cyklu MeSH
- lidé MeSH
- mutageneze cílená MeSH
- myši MeSH
- NAD metabolismus MeSH
- nikotinamidfosforibosyltransferasa chemie genetika metabolismus MeSH
- oxidační stres MeSH
- piperidiny farmakologie MeSH
- poly(ADP-ribosa)polymerasy metabolismus MeSH
- proliferace buněk MeSH
- rekombinantní fúzní proteiny chemie genetika metabolismus MeSH
- sirtuiny metabolismus MeSH
- viabilita buněk účinky léků MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- akrylamidy MeSH
- histony MeSH
- N-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(pyridin-3-yl)acrylamide MeSH Prohlížeč
- NAD MeSH
- nikotinamidfosforibosyltransferasa MeSH
- piperidiny MeSH
- poly(ADP-ribosa)polymerasy MeSH
- rekombinantní fúzní proteiny MeSH
- sirtuiny MeSH
Cypress (Cupressus sp.pl) is a genus within the Cupressaceae family. This family covers all of the Earth's continents except for Antarctica, and it includes about 160 species. The most important taxa for allergic diseases belong to five different genera: Cupressus, Hesperocyparis, Juniperus, Cryptomeria, and Chamaecyparis. Cupressaceae species share a common pollen type that can even include the genus Taxus (Taxaceae) when this plant is also present. As Juniperus oxycedrus pollinates in October, Cupressus sempervirens in January and February, Hesperocyparis arizonica (prev. Cupressus arizonica) in February and March, and Juniperus communis in April, the symptomatic period is long-lasting. Due to global warming, the pollination period tends to last longer, and there is a trend for Cupressaceae bioclimate niches to migrate north. In Mediterranean areas, C. sempervirens (Italian cypress or Mediterranean cypress) is by far the most common pollinating species. It accounts for half of the total pollination level. The group 1 major allergens belong to the pectate-lyase family, and members share 70 to 97% sequence homology within the different Cupressaceae. Group 2 allergens correspond to the polygalacturonase protein family, while group 3, a minor allergen, belongs to the family of "thaumatin-like proteins," a pathogenesis-related protein 5. Group 4 allergens are Ca++-binding protein (4 EF-hands). Aside from these four groups, about 15 other allergens have been reported. Prominent among these is a basic low-molecular mass cross-reactive allergen that was identified recently, and which is suspected to be involved in pollen food syndromes which are common with peach and citrus. The prevalence of cypress allergy in the general population ranges from 0.6 to 3%, depending on the degree of exposure to the pollen. Depending on the geographic area and the studied population, 9 to 65% of outpatients consulting an allergist may have sensitization to cypress pollen. Repeated cross-sectional studies performed at different time intervals have demonstrated a threefold increase in the percentage of cypress allergy around the Mediterranean area. Risk factors include a genetic predisposition and/or a strong exposure to pollen, and the natural history of cypress allergy allows identification of a subgroup of patients as allergic rather than atopic. Concerning the clinical expression, rhinitis is the most prevalent symptom, while conjunctivitis is the most disabling. Pharmacological treatment of cypress allergies is not different from that of other seasonal allergies. Immunotherapy has been used, initially by subcutaneous injections, but currently mostly through the sublingual route. Although clinical trials have included only a limited number of patients, it has proven effective and safe. Avoidance can be implemented at the individual level, as well as at the community level, through the use of alternative plants, low-pollinating cypresses, or by trimming hedges before pollination.
- Klíčová slova
- Aerobiology, Allergens, Botanic, clinic, Cypress pollen, Epidemiology,
- MeSH
- alergeny imunologie MeSH
- biologické markery MeSH
- celosvětové zdraví MeSH
- chromatografie kapalinová MeSH
- cypřiš (rod) škodlivé účinky klasifikace MeSH
- lidé MeSH
- opylení MeSH
- pyl imunologie ultrastruktura MeSH
- sezónní alergická rýma diagnóza epidemiologie imunologie terapie MeSH
- spektrometrie hmotnostní - ionizace laserem za účasti matrice MeSH
- stromy škodlivé účinky MeSH
- zkřížené reakce MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- alergeny MeSH
- biologické markery MeSH
Traditional supplements of selenium generally have a low degree of absorption and increased toxicity. Therefore, it is imperative to develop innovative systems as transporters of selenium compounds, which would raise the bioavailability of this element and allow its controlled release in the organism. Nanoscale selenium has attracted a great interest as a food additive especially in individuals with selenium deficiency, but also as a therapeutic agent without significant side effects in medicine. This review is focused on the incorporation of nanotechnological applications, in particular exploring the possibilities of a more effective way of administration, especially in selenium-deficient organisms. In addition, this review summarizes the survey of knowledge on selenium nanoparticles, their biological effects in the organism, advantages, absorption mechanisms, and nanotechnological applications for peroral administration.
- Klíčová slova
- anticancer effect, antimicrobial activity, biomedicine, drug delivery, nanoparticles, oxidative stress, protective effect,
- MeSH
- aplikace orální MeSH
- lékové transportní systémy metody MeSH
- lidé MeSH
- nanočástice aplikace a dávkování chemie MeSH
- nanomedicína metody MeSH
- nanotechnologie MeSH
- potravinářské přísady aplikace a dávkování chemie MeSH
- selen aplikace a dávkování farmakokinetika MeSH
- střevní sliznice účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- potravinářské přísady MeSH
- selen MeSH
- MeSH
- alergeny chemie imunologie MeSH
- antigeny rostlinné chemie imunologie MeSH
- gibereliny chemie imunologie MeSH
- hmotnostní spektrometrie MeSH
- imunoglobulin E imunologie MeSH
- lidé MeSH
- potravinová alergie diagnóza imunologie MeSH
- pyl chemie imunologie MeSH
- rostlinné proteiny chemie imunologie MeSH
- sekvence aminokyselin MeSH
- zkřížené reakce imunologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- dopisy MeSH
- práce podpořená grantem MeSH
- Názvy látek
- alergeny MeSH
- antigeny rostlinné MeSH
- gibereliny MeSH
- imunoglobulin E MeSH
- rostlinné proteiny MeSH
Selenium is an essential trace element important for many physiological processes, especially for the functions of immune and reproductive systems, metabolism of thyroid hormones, as well as antioxidant defense. Selenium deficiency is usually manifested by an increased incidence of retention of placenta, metritis, mastitis, aborts, lowering fertility and increased susceptibility to infections. In calves, lambs and kids, the selenium deficiency demonstrates by WMD (white muscle disease), in foals and donkey foals, it is associated with incidence of WMD and yellow fat disease, and in pigs it causes VESD (vitamin E/selenium deficiency) syndrome. The prevention of these health disorders can be achieved by an adequate selenium supplementation to the diet. The review summarizes the survey of knowledge on selenium, its biological significance in the organism, the impact of its deficiency in mammalian livestock (comparison of ruminants vs. non-ruminants, herbivore vs. omnivore) and possibilities of its peroral administration. The databases employed were as follows: Web of Science, PubMed, MEDLINE and Google Scholar.
- Klíčová slova
- antioxidant, donkeys, horses, metallomics, oxidative stress, ruminants, selenium,
- MeSH
- lidé MeSH
- potravní doplňky MeSH
- savci metabolismus MeSH
- selen nedostatek metabolismus fyziologie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- selen MeSH
The response of nutrient status and biochemical processes in (i) Wistar and (ii) spontaneously hypertensive (SHR) rats upon dietary intake of selenium- (Se-) enriched defatted rapeseed (DRS) and/or vitamin E fortification was examined to assess the health benefit of DRS in animal nutrition. Twenty-four individuals of each type of rat were used: The control group was fed with an untreated diet (Diet A). In Diets B and C, soybean meal was replaced with defatted DRS, which comprised 14% of the total diet. The selenized DRS application resulted in ~3-fold increase of Se content in the diet. Diet C was also fortified with the addition of vitamin E, increasing the natural content by 30%. The Se content of the blood and kidneys tended to increase in the DRS groups, where the changes were significant (P < 0.05) only in the case of SHR rats. The iodine (I) content and the proportion of iodide in rat livers indicated a lower transformation rate of iodide into organoiodine compounds compared to the control. Slight and ambiguous alterations in the antioxidative response of the rat were observed in the DRS groups, but the addition of vitamin E to the diet helped to moderate these effects.
- MeSH
- Brassica rapa * MeSH
- fortifikované potraviny * MeSH
- krysa rodu Rattus MeSH
- ledviny metabolismus MeSH
- potkani inbrední SHR MeSH
- potkani inbrední WKY MeSH
- potravní doplňky * MeSH
- selen * krev farmakologie MeSH
- vitamin E farmakologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- selen * MeSH
- vitamin E MeSH
The aim of this study was to contribute to clarifying the role of 6S RNA in the development and control of antibiotic biosynthesis in Streptomyces coelicolor. Due to the low energetic cost of gene silencing via 6S RNA, it is an easy and rapid means of down-regulating the expression of specific genes in response to signals from changes in the environment. The expression of 6S RNA in S. coelicolor is not constitutive, and its accumulation is adapted to changes in nutritional conditions. The 6S RNA of S. coelicolor is capable of interacting with RNA polymerase β β' subunits and is a template for the transcription of short pRNAs. Deletion of the ssrS gene from S. coelicolor affects the growth rate and causes changes in the expression of several pathway-specific genes involved in actinorhodin biosynthesis. The complementation of the ΔssrS strain with ssrS gene restored the wild-type levels of growth and actinorhodin production. We conclude that 6S RNA contributes to the optimization of cellular adaptation and is an important factor involved in the regulation of growth and expression of key genes for the biosynthesis of actinorhodin.
- MeSH
- antibakteriální látky biosyntéza MeSH
- bakteriální RNA genetika metabolismus MeSH
- delece genu MeSH
- DNA řízené RNA-polymerasy metabolismus MeSH
- nekódující RNA genetika metabolismus MeSH
- regulace genové exprese u bakterií * MeSH
- Streptomyces coelicolor genetika růst a vývoj metabolismus MeSH
- testy genetické komplementace MeSH
- vazba proteinů MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 6S RNA MeSH Prohlížeč
- antibakteriální látky MeSH
- bakteriální RNA MeSH
- DNA řízené RNA-polymerasy MeSH
- nekódující RNA MeSH
- RNA polymerase beta subunit MeSH Prohlížeč
Autophagy is essential for successful white adipocyte differentiation but the data regarding the timing and relevance of autophagy action during different phases of adipogenesis are limited. We subjected 3T3-L1 preadipocytes to a standard differentiation protocol and inhibited the autophagy within time-limited periods (days 0-2; 2-4; 4-6; 6-8) by asparagine or 3-methyladenine. In the normal course of events, both autophagy flux and the mRNA expression of autophagy related genes (Atg5, Atg12, Atg16, beclin 1) is most intensive at the beginning of differentiation (days 0-4) and then declines. The initiation of differentiation is associated with a 50% reduction of the mitochondrial copy number on day 2 followed by rapid mitochondrial biogenesis. Preadipocytes and differentiated adipocytes differ in the mRNA expression of genes involved in electron transport (Nufsd1, Sdhb, Uqcrc1); ATP synthesis (ATP5b); fatty acid metabolism (CPT1b, Acadl); mitochondrial transporters (Hspa9, Slc25A1) and the TCA cycle (Pcx, Mdh2) as well as citrate synthase activity. Autophagy inhibition during the first two days of differentiation blocked both phenotype changes (lipid accumulation) and the gene expression pattern, while having no or only a marginal effect over any other time period. Similarly, autophagy inhibition between days 0-2 inhibited mitotic clonal expansion as well as mitochondrial network remodeling. In conclusion, we found that autophagy is essential and most active during an initial stage of adipocyte differentiation but it is dispensable during its later stages. We propose that the degradation of preadipocyte cytoplasmic structures, predominantly mitochondria, is an important function of autophagy during this phase and its absence prevents remodeling of the mitochondrial gene expression pattern and mitochondrial network organization.
- Klíčová slova
- 3T3-L1 cells, Adipocytes, Autophagy, Differentiation, Mitochondria, Preadipocytes,
- MeSH
- adipogeneze účinky léků genetika MeSH
- asparagin farmakologie MeSH
- autofagie účinky léků genetika MeSH
- buněčná diferenciace účinky léků genetika MeSH
- buňky 3T3-L1 MeSH
- mitochondrie účinky léků metabolismus MeSH
- myši MeSH
- tukové buňky cytologie účinky léků MeSH
- vývojová regulace genové exprese účinky léků genetika MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- asparagin MeSH
Silent information regulators are NAD(+)-dependent enzymes that display differential specificity toward acetylated substrates. This report provides first evidence for deacetylation activity of CobB1 in Streptomyces coelicolor. The protein is highly conserved in streptomycetes. The CobB1 protein catalytically removes the acetyl group from acetylated bovine serum albumin. In the absence of NAD+ or when NAD+ was substituted with nicotinamide, deacetylation was stopped. We isolated gene encoding AcetylCoA synthetaseA. The recombinant enzyme produces Acetyl-CoA from acetate. The highest acsA-mRNA level was detected in cells from the exponential phase of growth, and then decreased in transition and stationary phases of growth. Acetylated acsA loses the ability to transfer acetate to CoA. Deacetylation of the enzyme required CobB1, ATP-Mg2, and NAD+. Using specific antibodies against acetylated lys, CobB1, and acsA, we found relationship between level of CobB1 and acetylation of acsA, indicating that CobB1 is involved in regulating the acetylation level of acsA and consequently its activity. It was found that 1-acetyl-tetrahydroxy and 1-acetyl pentahydroxy antraquinone inhibit the deacetylation activity of CobB1.
- MeSH
- acetát-CoA-ligasa biosyntéza chemie genetika MeSH
- acetylace MeSH
- anthrachinony chemie MeSH
- bakteriální proteiny biosyntéza chemie izolace a purifikace MeSH
- genetická transkripce MeSH
- inhibitory enzymů chemie MeSH
- katalytická doména MeSH
- konzervovaná sekvence MeSH
- molekulární sekvence - údaje MeSH
- posttranslační úpravy proteinů * MeSH
- regulace genové exprese u bakterií MeSH
- rekombinantní proteiny antagonisté a inhibitory biosyntéza chemie MeSH
- sekvence aminokyselin MeSH
- sekvenční seřazení MeSH
- sirtuiny antagonisté a inhibitory biosyntéza chemie MeSH
- Streptomyces coelicolor enzymologie růst a vývoj metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 1-acetyl-2,4,5,7-tetrahydroxyanthraquinone MeSH Prohlížeč
- 1-acetyl-2,4,5,7,8-pentahydroxyanthraquinone MeSH Prohlížeč
- acetát-CoA-ligasa MeSH
- anthrachinony MeSH
- bakteriální proteiny MeSH
- inhibitory enzymů MeSH
- rekombinantní proteiny MeSH
- sirtuiny MeSH
OBJECTIVES: We studied a) mitogen lectin (PHA) evoked changes of Na+/K+-ATPase activity in functionally different lymphocytes or brain cortex cells and b) quantitative relationship between PHA- evoked early enzyme activation and late lymphocyte proliferation were analyzed. MATERIALS AND METHODS: We performed biochemical analyses of Pi released from ATP by Na+/K+-ATPase activity. Lymphocyte proliferation was assayed by 3H-thymidine incorporation. RESULTS: We demonstrated PHA stimulated Na+/K+-ATPase activity of mouse spleen lymphocytes or freshly isolated brain cortex cells. Besides this, we estimated high stimulation of Na+/K+-ATPase activity and subsequent late 3H-thymidine incorporation into pig lymphocytes as both PHA dose and K+ ion concentration dependent. CONCLUSIONS: Thus, early PHA dose-dependent stimulation of Na+/K+-ATPase activity is a more general response in different animal species and functionally different cells. We measured both cell type- and PHA-dose dependent enzyme activity stimulation. We can suggest that intensity of early PHA induced Na+/K+-ATPase activation could be in relationship to subsequent elevated level of T lymphocyte proliferation. The Na+/K+-ATPase can be a part of mitogen lectin evoked signal transduction mechanisms.
- MeSH
- aktivace lymfocytů účinky léků MeSH
- buněčné kultury MeSH
- draslík farmakologie MeSH
- fytohemaglutininy farmakologie MeSH
- mitogeny farmakologie MeSH
- mozková kůra účinky léků metabolismus MeSH
- myši inbrední CBA MeSH
- myši MeSH
- prasata MeSH
- slezina účinky léků metabolismus MeSH
- sodíko-draslíková ATPasa metabolismus MeSH
- T-lymfocyty metabolismus MeSH
- thymus účinky léků metabolismus MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- draslík MeSH
- fytohemaglutininy MeSH
- mitogeny MeSH
- phytohemagglutinin L protein, Phaseolus vulgaris MeSH Prohlížeč
- sodíko-draslíková ATPasa MeSH