The role of the plasmalemma in metal tolerance in angiosperms

Evidence for the role of the plasmalemma in metal tolerance of metal resistant ecotypes, cultivars and clones is presented. A range of tolerance mechanisms involving the plasmalemma are discussed including alterations to protein carrier and channel function and synthesis, efflux pumps and maintenance of plasmalemma integrity. Specific examples of such alterations from the literature on Al, As and Cu tolerance, where the plasmalemma has been shown to have a role in tolerance are considered. Tolerance by alterations to plasmalemma function in tolerant ecotypes may also rely on internal metal detoxification mechanisms constitutive in tolerant and non-tolerant plants.     

Dephosphorylation of r Factor by Protein Phosphatase 2A in Synaptosomal Cytosol Fractions, and Inhibition by Aluminum

When the synaptosomal cytosol fraction from rat brain was chromatographed on a DEAE-cellulose column and assayed for protein phosphatases for τ factor and histone H1, two peaks of activities, termed peak 1 (major) and peak 2 (minor), were separated. Each peak was in a single form on Sephacryl S-300 column chromatography. Both peaks 1 and 2 dephosphorylated τ factor phosphorylated by Ca²⁺/calmodulin-dependent protein kinase II and the catalytic subunit of cyclic AMP-dependent protein kinase. The K_m values were in the range of 0.42–0.84 μM for τ factor. There were no differences in kinetic properties of dephosphorylation between the substrates phosphorylated by the two kinases. The phosphatase activities did not depend on Ca²⁺, Mn²⁺, and Mg²⁺. Immunoprecipitation and immunoblotting analysis using polyclonal antibodies to the catalytic subunit of brain protein phosphatase 2A revealed that both protein phosphatases are the holoenzymic forms of protein phosphatase 2A. Aluminum chloride inhibited the activities of both peaks 1 and 2 with IC₅₀ values of 40–60 μM. These results suggest that dephosphorylation of r factor in presynaptic nerve terminals is controlled mainly by protein phosphatase 2A and that the neurotoxic effect of aluminum seems to be related mostly to inhibition of dephosphorylation of τ factor     

Aluminum Inhibits Calpain-Mediated Proteolysis and Induces Human Neurofilament Proteins to Form ProteaseResistant High Molecular Weight Complexes

We studied the effects of aluminum salts on the degradation of human neurofilament subunits (NF-H, NF-M, and NF-L, the high, middle, and low molecular weight subunits, respectively) and other cytoskeletal proteins using calcium-activated neutral proteinase (calpain) purified from human brain. Calpain-mediated proteolysis of NF-L, tubulin, and glial fibrillary acidic protein (GFAP), three substrates that displayed constant digestion rates in vitro, was inhibited by AlCl3 (IC50 = 200 microM) and by aluminum lactate (IC50 = 400 microM). Aluminum salts inhibited proteolysis principally by affecting the substrates directly. After exposure to 400 microM aluminum lactate and removal of unbound aluminum, human cytoskeletal proteins were degraded two- to threefold more slowly by calpain. When cytoskeleton preparations were exposed to aluminum salt concentrations of 100 microM or higher, proportions of NF-M and NF-H formed urea-insoluble complexes of high apparent molecular mass, which were also resistant to proteolysis by calpain. Complexes of tubulin and of GFAP were not observed under the same conditions. Aluminum salts irreversibly inactivated calpain but only at high aluminum concentrations (IC50 = 1.2 and 2.1 mM for aluminum lactate and AlCl3, respectively), although longer exposure to the ion reduced by twofold the levels required for protease inhibition. These interactions of aluminum with neurofilament proteins and the effects on proteolysis suggest possible mechanisms for the impaired axoplasmic transport of neurofilaments and their accumulation in neuronal perikarya after aluminum administration in vivo.     

Aluminum-induced alterations in lipid composition of microsomal membranes from an aluminum-resistant and an aluminum-sensitive cultivar of Triticum aestivum

We have studied the effect of aluminum (Al) on the lipid composition of microsomal membranes isolated from 5-mm root tips of an Al-resistant (T 741) and an Al-sensitive (Katepwa) cultivar of Triticum aestivum L. Exposure of both genotypes to 10 and 50 μ M AeCl₃ for 1 day had no effect on lipid composition; however, decreases in phospholipids and increases in monogalactosyl diacylglycerols, free sterols, free fatty acids and triacylglycerols were observed with prolonged exposure (3 days) to 5O μ M AlCe₃. Several genotype-specific changes were also observed under these conditions. The content of digalactosyl diacylglycerols increased by 66.7% in Katepwa. but decreased slightly in PT 741. Thus, the ratio of rnonogalactosyl diacylglycerols to digalactosyl diacylglycerols increased by 46.2% in PT 741, but decreased by 21.3% in Katepwa. Genotype-specific differences were also observed in steryl lipids. Treatment with Al induced a 70.2% increase in sterylglucosides and a 23.3% increase in acylated sterylglucosides in Katepwa. In contrast, a 18.9% decrease in acylated sterylglucosides and no changes in sterylglucosides were observed in PT 741. Our limited understanding of the effect of membrane composition on membrane structure and function makes it difficult to predict how these changes relate to Al toxicity and resistance. While it is possible that many changes reflect the toxic effects of Al, we believe that changes observed only in the Al-resistant genotype could contribute to continuous growth in the face of Al stress.     

Chronic Exposure to Aluminum Impairs Neuronal Glutamate-Nitric Oxide-Cyclic GMP Pathway

Abstract: Humans are exposed to aluminum from environmental sources and therapeutic treatments. However, aluminum is neurotoxic and is considered a possible etiologic factor in Alzheimer's disease and other neurological disorders. The molecular mechanism of aluminum neurotoxicity is not understood. We tested the effects of aluminum on the glutamate-nitric oxide-cyclic GMP pathway in cultured neurons. Neurons were exposed to 50 µ M aluminum in culture medium for short-term (4 h) or long-term (8–14 days) periods, or rats were prenatally exposed, i.e., 3.7% aluminum sulfate in the drinking water, during gestation. Chronic (but not short-term) exposure of neurons to aluminum decreased glutamate-induced activation of nitric oxide synthase by 38% and the formation of cyclic GMP by 77%. The formation of cyclic GMP induced by the nitric oxide-generating agent S -nitroso- N -acetylpenicillamine was reduced by 33%. In neurons from rats prenatally exposed to aluminum but not exposed to it during culture, glutamate-induced formation of cyclic GMP was inhibited by 81%, and activation of nitric oxide synthase was decreased by 85%. The formation of cyclic GMP induced by S -nitroso- N -acetylpenicillamine was not affected. These results indicate that chronic exposure to aluminum impairs glutamate-induced activation of nitric oxide synthase and nitric oxide-induced activation of guanylate cyclase. Impairment of the glutamate-nitric oxide-cyclic GMP pathway in neurons may contribute to aluminum neurotoxicity.     

铝参与神经原纤维缠结形成的实验研究

目的探讨铝与神经原纤维缠结(NFTs)形成之间的相关性。方法选用16只雌性ICR小鼠,分为正常对照组与染铝组(200mg/kg.bw,染铝8个月)。组织荧光双重染色法观察铝与NFTs在小鼠大脑新皮层神经元内的定位。West-ern blot法半定量检测新皮层内tau蛋白及其磷酸化水平。结果组织荧光染色表明NFTs阳性荧光表达随铝阳性荧光增强而增强,两者分布呈对应关系;Western blot结果显示长期铝暴露导致tau蛋白水平下降(P<0.01,与对照组相比),但磷酸化水平升高(P<0.01,与对照组相比)。结论铝参与大脑新皮层神经元内NFTs形成与累积过程,tau蛋白的过度磷酸化可能是其成因之一。     

铝胁迫对木荷幼苗光合特性的影响及添加盐基阳离子和磷的调节作用

为探讨铝(Al)胁迫对木荷(Schima superba)幼苗光合特征的影响,采用营养液水培的方法,对铝(Al)胁迫下木荷幼苗的光合响应及盐基阳离子(BC)和磷(P)的调节作用进行了研究。结果表明,在低浓度Al(0.25 mmol L–1)处理下,木荷幼苗的光合色素(Chl a、Chl b、Car)含量、光合作用参数(P n、g s、WUE、C i/C a)以及光响应特征参数(P max、AQY、R d、LSP)均呈下降趋势,添加BC或同时添加BC和P均能缓解上述参数的降低。中、高浓度Al(0.75、1.50 mmol L–1)处理,除光合色素含量呈增加趋势外,光合作用参数、光响应特征参数均下降,且下降幅度随Al浓度的升高而增大,添加P比添加BC更能有效缓解Al胁迫对木荷幼苗的影响。这揭示了BC、P在缓解木荷Al胁迫的相对重要性。     

Aluminum concentrations in human deciduous enamel and dentin related to dental caries

The aluminum (Al) concentrations in the enamel and dentin of 314 human deciduous teeth were determined in order to examine the relationship between Al and dental caries. The sample teeth were divided into three groups: the sound tooth group, carious tooth group and filled tooth group. The teeth of the carious tooth group were further classified into three groups depending on the stage of caries. The Al content was determined using graphite furnace atomic absorption spectrometry. In both the enamel and dentin, the Al concentrations were unaffected by sex, but did depend on tooth type. In enamel, the Al concentration was significantly higher in the sound tooth group (42.8 +/- 37.3 microg/g) than in the three carious groups (20.7 +/- 17.1-24.9 +/- 22.0 microg/g) and the filled tooth group (27.3 +/- 25.5 microg/g). As for dentin, the Al concentration was also significantly higher in the sound tooth group (36.2 +/- 35.1 microg/g) than in the three carious groups (15.1 +/- 13.3-24.5 +/- 23.4 microg/g) and the filled tooth group (17.2 +/- 20.6 microg/g). Even when analyzing incisors alone, the Al concentrations were significantly higher in the sound tooth group than in the other groups, for both enamel and dentin. Furthermore, the Al levels in carious enamel and dentin did not decrease with the advance of caries. These findings indicated that the deciduous teeth containing higher Al concentrations on average had less caries than the teeth with lower Al concentrations, and suggest that Al acts as a possible cariostatic agent by itself.     

AFLP markers tightly linked to the aluminum-tolerance gene Alt3 in rye (Secale cereale L.)

Rye (Secale cereale L.) is considered to be the most aluminum (Al)-tolerant species among the Triticeae. It has been suggested that aluminum tolerance in rye is controlled by three major genes (Alt genes) located on rye chromosome arms 3RL, 4RL, and 6RS, respectively. Screening of an F₆ rye recombinant inbred line (RIL) population derived from the cross between an Al-tolerant rye (M39A-1–6) and an Al-sensitive rye (M77A-1) showed that a single gene controls aluminum tolerance in the population analyzed. In order to identify molecular markers tightly linked to the gene, we used a combination of amplified fragment length polymorphism (AFLP) and bulked segregant analysis techniques to evaluate the F₆ rye RIL population. We analyzed approximately 22,500 selectively amplified DNA fragments using 204 primer combinations and identified three AFLP markers tightly linked to the Alt gene. Two of these markers flanked the Alt locus at distance of 0.4 and 0.7 cM. Chromosomal localization using cloned AFLP and a restriction fragment length polymorphism (RFLP) marker indicated that the gene was on the long arm of rye chromosome 4R. The RFLP marker (BCD1230) co-segregated with the Alt gene. Since the gene is on chromosome 4R, the gene was designated as Alt3. These markers are being used as a starting point in the construction of a high resolution map of the Alt3 region in rye. Received: 29 March 2000 / Accepted: 9 July 2001     

Cost-effectiveness of five burrow fumigants for managing black-tailed prairie dogs

We evaluated the cost-effectiveness of two solid form burrow fumigants (aluminum phosphide and gas cartridges) and three pressurized gas–liquid burrow fumigants (methyl bromide, chloropicrin, and a methyl bromide–chloropicrin mixture) for managing black-tailed prairie dogs (Cynomys ludovicianus). Fifty-two variable-sized plots, including 25 treatment and 25 control burrows, were established within 13 prairie dog colonies in central Nebraska during spring 1989. Each group of 25 treatment burrows was fumigated with one of the five fumigants according to label directions or manufacturer recommendations. All five fumigants reduced burrow activity 95–98%, as measured by a plugged burrow technique. No significant differences in efficacy (P=0.453) were detected among the five treatments. Total costs for materials and labor for the aluminum phosphide and gas cartridges, excluding application equipment, were twice ($75.00 to $96.88 ha⁻¹) the cost of the pressurized gas–liquid fumigants ($37.67 to $41.76 ha⁻¹). Costs for the application equipment were considerably higher for the pressurized materials. Each treatment required labor for burrow plugging, which accounted for 50–75% of the total cost. None of the products tested met all requirements of a proposed selection criteria for fumigants.