Thulium Ion Promotes Apoptosis of Primary Mouse Bone Marrow Stromal Cells

Bone is one of the main target organs for the lanthanides (Ln). Biodistribution studies of Tm-based compounds in vivo showed that bone had significant uptake. But the effect of Tm³⁺ on primary mouse bone marrow stromal cells (BMSCs) has not been reported. So we investigated the effect and underlying mechanisms of Tm³⁺ on BMSCs. Cell viability, cell apoptosis, reactive oxygen species (ROS) level, lactate dehydrogenase (LDH) activity and mitochondrial membrane potential (MMP) were studied. The results indicated that Tm³⁺ increased the viability of BMSCs at concentrations of 1?×?10^?7, 1?×?10^?6, 1?×?10^?5, and 1?×?10^?4 mol/L in a dose-dependent manner, turned to decrease the viability of BMSCs at the highest concentration of 1?×?10^?3 mol/L for 24, 48, and 72 h. Tm³⁺ at 1?×?10^?3 mol/L promoted apoptosis of BMSCs, increased the ROS and LDH levels, and decreased MMP in BMSCs. Taken together, we demonstrated that Tm³⁺ at 1?×?10^?3 mol/L might induce cellular apoptosis through mitochondrial pathway. These results may be helpful for more rational application of Tm-based compounds in the future.     

Lanthanum Induced Primary Neuronal Apoptosis Through Mitochondrial Dysfunction Modulated by Ca2+ and Bcl-2 Family

As a representative element of lanthanide, lanthanum has been widely used in various fields and eventually entered environment and accumulated in human body. Epidemiological and experimental evidences indicated that lanthanum has neurotoxicity; however, the detailed mechanism is still elusive. Here, we chose primary cerebral cortical neurons as model in vitro to investigate the mechanism underlying the toxic effects of lanthanum chloride (LaCl₃). This study revealed the following findings: (1) LaCl₃ treatment (0.01, 0.1, and 1.0 mM for 24 h) reduced the viability of cortical neurons and elevated apoptotic rate significantly in a dose-dependent manner. (2) LaCl₃ triggered mitochondrial apoptotic pathway in cortical neurons, characterized with collapsed mitochondrial membrane potential, release of cytochrome c into cytosol, and increasing expression of activated caspase-3. (3) LaCl₃ elevated intracellular Ca²⁺ concentration, promoted reactive oxygen species generation, and upregulated pro-apoptotic Bax, whereas it downregulated anti-apoptotic Bcl-2 expression and consequently altered Bax/Bcl-2 ratio, which ultimately lead to neuronal mitochondrial apoptosis. Our results demonstrated that toxicity of lanthanum in cortical neurons perhaps partly attributed to enhanced mitochondrial apoptosis due to mitochondrial dysfunction modulated by Ca²⁺ and Bcl-2 family.     

Effects of lanthanum chloride on glutamate level, intracellular calcium concentration and caspases expression in the rat hippocampus

Lanthanum chloride (LaCl₃) can affect neurobehavioral development and impair cognitive abilities. The mechanism underlying LaCl₃-induced neurotoxic effects is still unknown. The purpose of this research was to investigate the neuronal impairment induced by LaCl₃ and discuss the possible mechanism from the aspects of the alteration of glutamate level, intracellular calcium concentration ([Ca²⁺]_i), Bax, Bcl-2 and caspases expression in the hippocampus. Lactational rats were exposed to 0, 0.25, 0.50 and 1.0 % LaCl₃ in drinking water, respectively. Their offspring were exposed to LaCl₃ by parental lactation and then administrated with 0, 0.25, 0.50 and 1.0 % LaCl₃ in drinking water for 1 month. The results showed that 0.25, 0.50 and 1.0 % LaCl₃ exposure induced neuronal impairment in the hippocampus of young rat. Hippocampal glutamate level, [Ca²⁺]_i and ratio of Bax and Bcl-2 expression increased significantly after LaCl₃ exposure. Besides, LaCl₃ exposure increased GRP78, GRP94, GADD153 and p-JNK expression, promoted the activation of caspase-3, caspase-9 and caspase-12, induced PARP cleavage and caused excessive apoptosis. These results indicate that LaCl₃ increases glutamate level, [Ca²⁺]_i and ratio of Bax and Bcl-2 expression, which cause excessive apoptosis by the mitochondrial and endoplasmic reticulum stress-induced pathway, and thus neuronal damages in the hippocampus.     

H+-dependent inorganic phosphate transporter in breast cancer cells: Possible functions in the tumor microenvironment

Tumor microenvironment has a high concentration of inorganic phosphate (Pi), which is actually a marker for tumor progression. Regarding Pi another class of transporter has been recently studied, an H⁺-dependent Pi transporter, that is stimulated at acidic pH in Caco2BBE human intestinal cells. In this study, we characterized the H⁺-dependent Pi transport in breast cancer cell (MDA-MB-231) and around the cancer tissue. MDA-MB-231 cell line presented higher levels of H⁺-dependent Pi transport as compared to other breast cell lines, such as MCF-10A, MCF-7 and T47-D. The Pi transport was linear as a function of time and exhibited a Michaelis-Menten kinetic of K_m = 1.387 ± 0.1674 mM Pi and V_max = 198.6 ± 10.23 Pi × h^?1 × mg protein^?1 hence reflecting a low affinity Pi transport. H⁺-dependent Pi uptake was higher at acidic pH. FCCP, Bafilomycin A1 and SCH28080, which deregulate the intracellular levels of protons, inhibited the H⁺-dependent Pi transport. No effect on pHi was observed in the absence of inorganic phosphate. PAA, an H⁺-dependent Pi transport inhibitor, reduced the Pi transport activity, cell proliferation, adhesion, and migration. Arsenate, a structural analog of Pi, inhibited the Pi transport. At high Pi conditions, the H⁺-dependent Pi transport was five-fold higher than the Na⁺-dependent Pi transport, thus reflecting a low affinity Pi transport. The occurrence of an H⁺-dependent Pi transporter in tumor cells may endow them with an alternative path for Pi uptake in situations in which Na⁺-dependent Pi transport is saturated within the tumor microenvironment, thus regulating the energetically expensive tumor processes.     

Phosphate uptake, efflux and deficiency in the water fern, Azolla

High phosphorus status (High-P) Azolla mexicana plants (P content 15.5 μmoles g fr wt^?1, doubling time ca. 2.2 d) and Low-P plants with early signs of P-deficiency (P content 6.2 μmoles g fr wt^?1, doubling time ca. 3.2 d) were used to study Pi uptake, efflux and deficiency. When High-P plants were transferred to medium lacking Pi, uptake capacity increased 1.5-fold within 12 h and before any detectable change in growth rate (24–48 h). When High-P and Low-P plants were compared, uptake rates from 0.3–10000 mmoles m^?3 Pi were 2.6–1.7 times higher in Low-P than High-P plants (18–1150 vs 7–665 μmoles g fr wt^?1 h^?1). The relationship of uptake rate to concentration was interpreted as arising from a combined operation of a high- and a low-affinity uptake system. Higher uptake in Low-P plants involved a 3.4-fold increase in V_max (high affinity), no change in K_m (high affinity), and a 1.5 to two-fold increase in both V_max (low affinity) and Km (low affinity). Rates of P efflux into 1–1000 mmoles m^?3 Pi were 1.7 to two times higher from High-P than Low-P plants (12–22 vs 7–11 μmoles g fr wt^?1 h^?1). Below 1 mmole m^?3 Pi, uptake and efflux rates were similar: the equilibrium concentration, at which net uptake was zero, was 0.22 mmoles m^?3 for High-P plants and 0.05 mmoles m^?3 for Low-P plants. Similar results were obtained with A. filiculoides. P transport characteristics of Azolla, a fern, are closely comparable with those of higher plants. Its high P requirement in the field arises from its ecological rather than physiological behaviour. We interpret the field behaviour by exploring the relationship between Azolla growth rate in the field, plant P concentration in the field, Pi transport rates required to support such growth, and Pi concentrations in pond waters. The transport characteristics which must operate in the field match those of Low-P plants in the laboratory, not High-P plants. Thus, Pi uptake in High-P plants should be interpreted as repressed from the normal state, instead of that in Low-P plants being induced.     

The Effects of Mn2+ on the Proliferation, Osteogenic Differentiation and Adipogenic Differentiation of Primary Mouse Bone Marrow Stromal Cells

The effects of Mn²⁺ on the proliferation, osteogenic and adipogenic differentiation of BMSCs were evaluated by employing MTT, ΔΨm, cell cycle, ALP activity, collagen production, ARS and oil red O stain assays. The results indicated that Mn²⁺ decreased the viability at most concentrations for 24 h, but the viability was increased with prolonging incubation time. Mn²⁺ at the concentrations of 1?×?10^-7 and 1?×?10^-6?mol/L decreased ΔΨm in the BMSCs for 48 h. Mn²⁺ induced G2/M phase cell cycle arrest at tested concentrations. On day 7 and 10, the effect of Mn²⁺ on the osteogenic differentiation depended on concentration, but it inhibited osteogenic differentiation at all tested concentrations for 14 d. The effect of Mn²⁺ on the synthesis of collagen of BMSCs depended on concentration for 7 d, but Mn²⁺ inhibited the synthesis of collagen at all tested concentrations for 10 d. On day 14, Mn²⁺ inhibited the formation of mineralized matrix nodules of BMSCs at all tested concentrations, the inhibitory effect turned to be weaker with prolonging incubation time. Mn²⁺ promoted the adipogenic differentiation of BMSCs at all tested concentrations for 10 d, but had no effect with prolonging incubation time. These findings suggested the effects of Mn²⁺ on the proliferation, osteogenic differentiation and adipogenic differentiation of BMSCs are very complicated, concentration and incubation time are key factors for switching the biological effects of Mn²⁺ from damage to protection.     

Comparison of the effects of lanthanum,cerium and praseodymium on rumen fermentation,nutrient digestion and plasma biochemical parameters in beef cattle

The objectives of the trial were to compare the effects of supplementing rare earth elements (REE) lanthanum (La), cerium (Ce) and praseodymium (Pr) on rumen fermentation, nutrient digestion, methane (CH₄) production, nitrogen (N) balance and plasma biochemical parameters in beef cattle. Four Simmental male cattle, aged 12 months, with initial average liveweight of 333 ± 9 kg and fitted with rumen cannulas, were fed with a basal ration composed of concentrate mixture and maize silage. Animals received a basal ration without adding REE (Control) or three treatments, i.e. supplementing LaCl₃, CeCl₃ or PrCl₃ at 204 mg/kg DM to the basal ration, respectively, which were allocated in a 4 × 4 Latin square design. Each experimental period lasted 15 d, consisting of 12 d for pre-treatment and three subsequent days for sampling. Results showed that all tested levels of REE tended to increase neutral detergent fibre digestibility (p = 0.064) and tended to decrease rumen CH₄ production (p = 0.056). Supplementing LaCl₃ and CeCl₃ decreased total N excretion and urinary N excretion, increased N retention (p < 0.05), tended to increase total urinary purine derivatives (PD) (p = 0.053) and microbial N flow (p = 0.095), whereas supplementing PrCl₃ did not affect N retention, urinary PD and microbial N flow. No differences were found in the effects of nutrient digestibility, CH₄ production and plasma biochemical parameters among LaCl₃, CeCl₃ and PrCl₃. Further trials using graded levels of LaCl₃, CeCl₃ and PrCl₃ in a wide range are needed to obtain more pronounced results for comparing effects of La, Ce and Pr on rumen fermentation and nutrient digestion in beef cattle.     

Effect of lanthanide chloride on photosynthesis and dry matter accumulation in tobacco seedlings

To investigate the physiological effects of rare earth ions, we have studied the effect of LaCl₃ on the photosynthetic light reactions in tobacco (Nicotiana tobacum). When treated with 5–20 mg/L LaCl₃ in Hoagland solution by water culture, the dry matter accumulation of different parts in tobacco, the content of chlorophyll increased gradually, but decreased when the concentration of LaCl₃ was ≥ 50 mg/L. The optimum concentration for growth appeared to be about 20 mg/L of LaCl₃ in nutrient solution. La³⁺ promoted the activities of the Hill reaction, Mg²⁺-ATPase, and stimulated the rate of photophosphorylation in chloroplast at low concentrations, but inhibited them at high concentrations. It is concluded that La³⁺ stimulated the growth of tobacco seedlings and accelerated the photosynthetic light reactions at suitable concentration in vivo.     

Growth response of komatsuna (Brassica rapa var. peruviridis) to root and foliar applications of phosphite

Soil and hydroponic culture experiments were conducted to investigate the effects of phosphite (Phi) as phosphorus (P) fertilizer via root and foliar applications on the growth and P supply of komatsuna. In both experiments, root P treatments were combinations of Phi and phosphate (Pi) at different Pi:Phi ratios, for a total of high P level (92 mg P pot^?1; the soil experiment) or low P level (0.05 mM P; the hydroponic experiment). Foliar P treatments were deionized water (control), a Pi solution and a Phi solution at low concentration of 0.05% P₂O₅. In both experiments, shoot dry weight of plants significantly decreased as Pi:Phi ratio decreased. In the soil experiment, plants grew abnormally at a Pi:Phi ratio of 25:75 and died when P was applied to soil entirely as Phi form (0:100 treatment). In the hydroponic experiment, no visible damage was found in shoot but root growth was strongly inhibited with severe damage symptoms at low Pi:Phi ratios. Total P concentration in plant decreased significantly with decreasing Pi:Phi ratio, especially in the hydroponic experiment. Foliar application of Phi although greatly increased total P of plants compared to that of Pi in both experiments, it did not improve but further decreased plant growth at low Pi:Phi ratios in the soil experiment and at all Pi:Phi ratios in the hydroponic experiment. The results of this study clearly indicated that Phi could not be used as P fertilizer by komatsuna plants via both application methods and could not substitute P at any rate at either low or high level. No beneficial effect of Phi was detected even when it was applied at low rate or applied in combination with Pi at different ratios. The effects of Phi were strongly dependent on the P nutrition status of plants; and plants that were not sufficiently fertilized with Pi may become vulnerable to Phi even at low levels.     

Effect of salinity on phosphate accumulation and injury in soybean

Certain soybean [Glycine max (L.) Merr.] cultivars that are grown in saline nutrient cultures are killed when the inorganic phosphate (Pi) concentration in the substrate exceeds 0.10 mM. To determine the role of Na and Cl on this adverse salinity×Pi interaction, four cultivars, Clark, Clark 63, Lee, and Lee 74 were grown in the greenhouse in nutrient solutions salinized with 1) Cl and NO₃ salts to produce treatments with variable amounts of Cl or 2) with NaCl or KCl and CaCl₂ to obtain treatments with and without Na. At an osmotic potential of ?0.34 MPa, all salts enhanced Pi uptake and accumulation in the tissue of plants grown in ≧0.12 mM substrate Pi. Leaf Cl concentration was linearly related (r²≥0.9) to the mole fraction (mf) of Cl in the substrate, therefore excess substrate NO₃ did not greatly influence leaf Cl accumulation. Foliar injury was only observed on plants grown in saline solutions at high Pi (≥0.12 mM) and was not alleviated when KCl replaced NaCl in the substrate. This indicates that Na did not play a direct role in the salinity×Pi interaction. However, as the mf of Cl increased, severity of injury increased. The severity of injury, and its symptoms, were dependent upon leaf P and Cl concentration. Plants died when Cl and P in their leaves exceeded 800 and 600 mmol kg^?1 dry wt, respectively (e.g., Clark 63 grown at mf of Cl=1). The necrotic leaves were beige in color. Leaves that contained P in excess of 600 mmol kg^?1 dry wt and Cl between 150–200 mmol kg^?1 dry wt, were severely injured and reddish-brown in color (e.g., Clark 63 at mf of Cl=1/4 and Lee 74 Pi grown at mf of Cl=1). When leaf Cl was below 150 mmol kg^?1 dry wt, development of reddish-brown coloration in the leaves was sporadic. The adverse salinity×Pi interaction observed on these soybean variaties, therefore, was caused by a synergistic interaction between P and Cl in the leaves.     

Molybdenum trioxide enhances viability,osteogenic differentiation and extracellular matrix formation of human bone marrow-derived mesenchymal stromal cells

BackgroundMetals and their ions allow specific modifications of the biological properties of bioactive materials that are intended for application in bone tissue engineering. While there is some evidence about the impact of particles derived from orthopedic Cobalt-Chromium-Molybdenum (Co-Cr-Mo) alloys on cells, there is only limited data regarding the influence of the essential trace element Mo and its ions on the viability, osteogenic differentiation as well as on the formation and maturation of the primitive extracellular matrix (ECM) of primary human bone marrow-derived stromal cells (BMSCs) available so far.MethodsIn this study, the influence of a wide range of molybdenum (VI) trioxide (MoO₃), concentrations on BMSC viability was evaluated via measurement of fluorescein diacetate metabolization. Thereafter, the impact of three non-cytotoxic concentrations of MoO₃ on the cellular osteogenic differentiation as well as on ECM formation and maturation of BMSCs was assessed.ResultsMoO₃ had no negative influence on BMSC viability in most tested concentrations, as viability was in fact even enhanced. Only the highest concentration (10 mM) of MoO₃ showed cytotoxic effects. Cellular osteogenic differentiation, measured via the marker enzyme alkaline phosphatase was enhanced by the presence of MoO₃ in a concentration-dependent manner. Furthermore, MoO₃ showed a positive influence on the expression of relevant marker genes for osteogenic differentiation (osteopontin, osteocalcin and type I collagen alpha 1) and on the formation and maturation of the primitive ECM, as measured by collagen deposition and ECM calcification.ConclusionMoO₃ is considered as an attractive candidate for supplementation in biomaterials and qualifies for further research.     

Effects of extracellular calcium on viability and osteogenic differentiation of bone marrow stromal cells in vitro

Bone marrow stromal cells (BMSCs) have been extensively used for tissue engineering. However, the effect of Ca²⁺ on the viability and osteogenic differentiation of BMSCs has yet to be evaluated. To determine the dose-dependent effect of Ca²⁺ on viability and osteogenesis of BMSCs in vitro, BMSCs were cultured in calcium-free DMEM medium supplemented with various concentrations of Ca²⁺ (0, 1, 2, 3, 4, and 5 mM) from calcium citrate. Cell viability was analyzed by MTT assay and osteogenic differentiation was evaluated by alkaline phosphatase (ALP) assay, Von Kossa staining, and real-time PCR. Ca²⁺ stimulated BMSCs viability in a dose-dependent manner. At slightly higher concentrations (4 and 5 mM) in the culture, Ca²⁺ significantly inhibited the activity of ALP on days 7 and 14 (P < 0.01 or P < 0.05), significantly suppressed collagen synthesis (P < 0.01 or P < 0.05), and significantly elevated calcium deposition (P < 0.01) and mRNA levels of osteocalcin (P < 0.01 or P < 0.05) and osteopontin (P < 0.01 or P < 0.05). Therefore, elevated concentrations of extracellular calcium may promote cell viability and late-stage osteogenic differentiation, but may suppress early-stage osteogenic differentiation in BMSCs.     

Biomass production of Tolypothrix tenuis as a basic component of a cyanobacterial biofertilizer

The influence of artificial illumination on upstream and downstream operations for biomass production of Tolypothrix tenuis as a basic component of a powdered cyanobacterial biofertilizer was studied. Cultures were operated semi-continuously for 18 months at harvesting frequencies of 4, 7, 10, and 14 days in two vertical plate photobioreactors of 1.5 and 5 cm of light path and illuminated at two different light intensities: high (290 μmol photons m^?2 s^?1) and normal (60 μmol photons m^?2 s^?1). Biomass was separated by self-flocculation and finally processed as a dried powder. The cellular concentration and volumetric productivity were superior in photobioreactors of short light path at high light intensity, while the overall areal productivity was higher in the photobioreactor of 5 cm at normal light intensity with weekly harvest frequency. The viability preservation of the dried and milled biomass was greatly enhanced by the use of halogen lamps and subsequent ionic flocculation with 10 mM MgSO₄ plus 10 mM CaCl₂. An optimum value of the retained viability index (RVI₁₀) was maintained for 24 months, while a sharp viability declination and cellular death were produced after 12 months with fluorescent tubes, which represents a relevant aspect in the commercialization step of this type of biofertilizer.     

Effects of saline root environment (NaCl) on nitrate and potassium uptake kinetics for rose plants: a Michaelis–Menten modelling approach

Greenhouse-grown cut flower roses are often irrigated with moderately saline irrigation water. The salt/ballast ions are either present initially in poor quality raw water or reclaimed municipal water, or accumulated in greenhouse irrigation water that is captured and reused. Such ions can inhibit root absorption of essential nutrients. The objective of this work was to quantify the influence of NaCl concentration on the uptake of nitrate and potassium by roses and develop a predictive model of uptake inhibition based on NaCl, NO₃ ^?, and K⁺ concentration. One year-old rose plants (Rosa spp. ‘Kardinal’ on ‘Natal Briar’ rootstock) were moved into growth chambers where nitrogen and potassium depletion were monitored during 6 days. Eight different initial NaCl treatments varying from zero to 65 mol m^?3 were used and within these there were two initial NO₃ ^? and K⁺ concentrations: high concentration (HC, 7.0 mol m^?3 and 2.6 mol m^?3 NO₃ ^? and K⁺ respectively) or low concentration (LC, 3.5 mol m^?3 and 1.3 mol m^?3 NO₃ ^? and K⁺ respectively). Plant NO₃ ^? uptake was negatively affected by NaCl concentration. NO₃ ^? maximum influx (I_max) declined from 5.1 µmol to 2.5 µmol per gram of plant dry weight per hour as NaCl concentration increased from zero to 65 mol m^?3. A modified Michaelis–Menten (M–M) equation taking into account inhibition by NaCl provided the best fit for NO₃ ^? uptake in response to varying NaCl concentration. K⁺ uptake was unaffected by NaCl concentration. A M–M equation that did not include inhibition was suitable for describing K⁺ uptake at varying NaCl concentration. The resulting empirical models could assist with decision making, such as: adjustment of NO₃ ^? fertilization based on NaCl concentration, necessity of water desalinization, or determination of the desired leaching fraction.     

Multi-scale measurements and modeling of denitrification in streams with varying flow and nitrate concentration in the upper Mississippi River basin, USA

Denitrification is an important net sink for NO₃ ^? in streams, but direct measurements are limited and in situ controlling factors are not well known. We measured denitrification at multiple scales over a range of flow conditions and NO₃ ^? concentrations in streams draining agricultural land in the upper Mississippi River basin. Comparisons of reach-scale measurements (in-stream mass transport and tracer tests) with local-scale in situ measurements (pore-water profiles, benthic chambers) and laboratory data (sediment core microcosms) gave evidence for heterogeneity in factors affecting benthic denitrification both temporally (e.g., seasonal variation in NO₃ ^? concentrations and loads, flood-related disruption and re-growth of benthic communities and organic deposits) and spatially (e.g., local stream morphology and sediment characteristics). When expressed as vertical denitrification flux per unit area of streambed (U _denit, in μmol N m^?2 h^?1), results of different methods for a given set of conditions commonly were in agreement within a factor of 2–3. At approximately constant temperature (~20 ± 4°C) and with minimal benthic disturbance, our aggregated data indicated an overall positive relation between U _denit (~0–4,000 μmol N m^?2 h^?1) and stream NO₃ ^? concentration (~20–1,100 μmol L^?1) representing seasonal variation from spring high flow (high NO₃ ^?) to late summer low flow (low NO₃ ^?). The temporal dependence of U _denit on NO₃ ^? was less than first-order and could be described about equally well with power-law or saturation equations (e.g., for the unweighted dataset, U _denit ≈26 * [NO₃ ^?]^0.44 or U _denit ≈640 * [NO₃ ^?]/[180 + NO₃ ^?]; for a partially weighted dataset, U _denit ≈14 * [NO₃ ^?]^0.54 or U _denit ≈700 * [NO₃ ^?]/[320 + NO₃ ^?]). Similar parameters were derived from a recent spatial comparison of stream denitrification extending to lower NO₃ ^? concentrations (LINX2), and from the combined dataset from both studies over 3 orders of magnitude in NO₃ ^? concentration. Hypothetical models based on our results illustrate: (1) U _denit was inversely related to denitrification rate constant (k1_denit, in day^?1) and vertical transfer velocity (v _f,denit, in m day^?1) at seasonal and possibly event time scales; (2) although k1_denit was relatively large at low flow (low NO₃ ^?), its impact on annual loads was relatively small because higher concentrations and loads at high flow were not fully compensated by increases in U _denit; and (3) although NO₃ ^? assimilation and denitrification were linked through production of organic reactants, rates of NO₃ ^? loss by these processes may have been partially decoupled by changes in flow and sediment transport. Whereas k1_denit and v _f,denit are linked implicitly with stream depth, NO₃ ^? concentration, and(or) NO₃ ^? load, estimates of U _denit may be related more directly to field factors (including NO₃ ^? concentration) affecting denitrification rates in benthic sediments. Regional regressions and simulations of benthic denitrification in stream networks might be improved by including a non-linear relation between U _denit and stream NO₃ ^? concentration and accounting for temporal variation.     

Ion gradients in xylem exudate and guttation fluid related to tissue ion levels along primary leaves of barley

The concentration of ions in plant cells and tissues is an essential factor in determining physiological function. In the present study, we established that concentration gradients of mobile ions exist in both xylem exudates and tissues within a barley (Hordeum vulgare) primary leaf. For K⁺ and NO₃^?, ion concentrations generally decreased from the leaf base to the tip in both xylem exudates and tissues. Ion gradients were also found for Pi and Cl^? in the xylem. The hydathode strongly absorbed Pi and re‐translocated it to the rest of the plant, whereas Cl^? was extruded. The ion concentration gradients developed early during leaf growth, increased as the tissue aged and remained under both high and low transpiration conditions. Measurement of the expression profiles of Pi, K⁺ and NO₃^? transporters along the longitudinal axis of the leaf revealed that some transporters are more expressed at the hydathode, but for most transporters, there was no significant variation along the leaf. The mechanisms by which longitudinal ion gradients develop in leaves and their physiological functions are discussed.     

High extracellular Ca2+ enhances the adipocyte accumulation of bone marrow stromal cells through a decrease in cAMP

Bone marrow stromal cells (BMSCs) are common progenitors of both adipocytes and osteoblasts. We recently suggested that increased [Ca²⁺]_o caused by bone resorption might accelerate adipocyte accumulation in response to treatment with both insulin and dexamethasone. In this study, we investigated the mechanism by which high [Ca²⁺]_o enhances adipocyte accumulation.We used primary mouse BMSCs and evaluated the levels of adipocyte accumulation by measuring Oil Red O staining. CaSR agonists (both Ca²⁺ and Sr²⁺) enhanced the accumulation of adipocytes among BMSCs in response to treatment with both insulin and dexamethasone. We showed that high [Ca²⁺]_o decreases the concentration of cAMP using ELISA. Real-time RT-PCR revealed that increasing the intracellular concentration of cAMP (both chemical inducer (1 μM forskolin and 200 nM IBMX) and a cAMP analog (10 μM pCPT-cAMP)) suppressed the expression of PPARγ and C/EBPα. In addition, forskolin, IBMX, and pCPT-cAMP inhibited the enhancement in adipocyte accumulation under high [Ca²⁺]_o in BMSCs. However, this inhibited effect was not observed in BMSCs that were cultured in a basal concentration of [Ca²⁺]_o. We next observed that the accumulation of adipocytes in the of bone marrow of middle-aged mice (25–40 weeks old) is higher than that of young mice (6 weeks old) based on micro CT. ELISA results revealed that the concentration of cAMP in the bone marrow mononuclear cells of middle-aged mice is lower than that of young mice. These data suggest that increased [Ca²⁺]_o caused by bone resorption might accelerate adipocyte accumulation through CaSR following a decrease in cAMP.     

Optimized culture medium for the production of flavonoids from <Emphasis Type="Italic">Orostachys cartilaginea</Emphasis> V.N. Boriss. callus cultures

The optimal culture medium for the production of flavonoid compounds from Orostachys cartilaginea V. N. Boriss. calluses was studied. In callus cultures of O. cartilaginea, the flavonoid monomer content, in decreasing order was kaempferol-3-O-rutinoside (Kp-3-rut), quercetin 3-O-glucoside (Qc-3-glc), epicatechin gallate (Ecg), kaempferide (Ke), and quercetin (Qc). The results of the uniform design experiment indicated that the production of Qc, Ke, Qc-3-glc, Kp-3-rut, and total flavonoids were satisfactory in callus grown on full salt strength (1×) of Murashige and Skoog (MS) medium supplemented with 3.5 mg L^?1 6-benzylaminopurine (BA) and 0.1 mg L^?1 1-naphthalene acetic acid (NAA). By contrast, only Ecg was found in callus grown on 0.75× MS medium supplemented with 1.5 mg L^?1 BA and 0.3 mg L^?1 NAA. A phosphate concentration of 1.25 mM in the MS medium favored the production of Qc and Ke, whereas 0.75 mM phosphate was optimal for the production of Ecg, Qc-3-glc, Kp-3-rup, and total flavonoids. The NH₄ ⁺/NO₃ ^? ratios of 30/30 mM in the MS medium promoted Ke, Ecg, Qc-3-glc, Kp-3-rup, and total flavonoid production. However, a NH₄ ⁺/NO₃ ^? ratio of 20/40 mM enhanced Qc production. The effect of sucrose concentrations on the accumulation of different flavonoid monomers was comparatively more regular. The flavonoid content increased as the sucrose concentration increased from 20 to 40 g L^?1, peaked at 40 g L^?1, and decreased at concentrations greater than 40 g L^?1. Therefore, 40 g L^?1 sucrose was optimal for the production of the five flavonoid monomers and total flavonoids. The present findings demonstrate the possibility of producing flavonoid compounds from O. cartilaginea callus.     

Platinum concentration in PM2.5 in the Mexico City Metropolitan Area: relationship to meteorological conditions

Abstract

Platinum (Pt) concentrations in PM_2.5 were evaluated by means of inductively coupled plasma mass spectrometry (ICP-MS) to evaluate the spatial and temporal behavior and to assess trends. Samples were taken from five representative sites in the Mexico City Metropolitan Area (MCMA): Tlalnepantla-northwest (NW), San Agustin-northeast (NE), La Merced -center (C), Coyoacan-southwest (SW), and Universidad Autonoma Metropolitana Iztapalapa-southeast (SE). Under three weather conditions: dry warm (DW-April), rainy (R-August), and dry cold (DC-November) in 2013. We found that the PM_2.5 median mass concentration was 24?μg m^?3?±?15?μg m^?3 while Pt concentration was 55?pg m^?3?±?15?pg m^?3 (median, interquartile range). Seasonal trend was identified: the concentrations decreased significantly in the following order DC?>?R>DW. No spatial distribution was observed. Interestingly, among other meteorically parameters, wind intensity resulted to be the major factor for the dispersion of Pt in PM2.5 in MCMA. Furthermore, we found that Pt concentrations increased significantly by 19.6% between 2011 and 2013. Regardless of the increase in Pt, carbon monoxide (CO) levels decreased opposite to a rise in vehicular fleet. These results urge for environment public policies that address the upward tendency of Pt levels especially in urban areas.     

The effect of ammonium ions on membrane potential and anion flux in roots of barley and tomato

The effects of ammonium (0–5 mol m^?3) on root hair membrane potential and on the influx of nitrate and phosphate were investigated in roots of intact barley and tomato plants. In both species, addition of ammonium to the medium bathing the roots caused an almost immediate depolarization of the membrane potential; the depolarization was greater at higher concentrations of ammonium. Influx of ¹³NC₃^? and ³²Pi was inhibited over the same time scale and concentration range. In tomato roots, there was little further depolarization of the membrane potential or inhibition of anion influx at ammonium concentrations above 0.4 mol m^?3. In barley roots, the inhibition of nitrate influx and the depolarization of the membrane potential did not saturate below 5 mol m^?3 ammonium.