Selective antagonism by Mg2+ of amino acid-induced depolarization of spinal neurones.

In the isolated frog or rat spinal cord, low concentrations of Mg2+ (0.5-1.00 mM) markedly depress, in a substantially Ca2+-independent manner, ventral root depolarizations produced by dorsal root stimulation and by certain amino acids (e.g. N-methyl-D-aspartate and L-homocysteate) but do not depress depolarizations produced by other excitatory amino acids (e.g. kainate and quisqualate). L-Aspartate-induced depolarizations are more sensitive to Mg2+ then are L-glutamate-induced depolarizations.     

Extracellular Mg2+ regulates intracellular Mg2+ and its subcellular compartmentation in fission yeast, Schizosaccharomyces pombe

Effects of extracellular magnesium ions ([Mg²⁺]_o ) on intracellular free Mg²⁺ ([Mg²⁺]_i ) and its subcellular distribution in single fission yeast cells, Schizosaccharomyces pombe, were studied with digital-imaging microscopy and an Mg²⁺ fluorescent probe (mag-fura-2). Using 0.44 mM [Mg²⁺]_o , [Mg²⁺]_i in yeast cells was 0.91±0.08 mM. Elevation of [Mg²⁺]_o to 1.97 mM induced rapid (within 5 min) increments in [Mg²⁺]_i (2.18±0.11 mM). Lowering [Mg²⁺]_o to 0.06 mM, however, exerted no significant effects on [Mg²⁺]_i (0.93±0.14 mM), at least for periods of up to 30 min. Irrespective of the [Mg²⁺]_o used, the subcellular distribution of [Mg²⁺]_i remained hetero geneous, i.e. where the sub-plasma membrane region >cytoplasm >nucleus. [Mg²⁺] in all three subcellular compartments increased significantly, two- to threefold, concomitant with [Mg²⁺]_i when placed in 1.97 mM [Mg²⁺]_o . We conclude that [Mg²⁺]_i in fission yeast is maintained at a physiologic level when [Mg²⁺]_o is low, but intracellular free Mg²⁺ rapidly rises when [Mg²⁺]_o is elevated. Like most eukaryotic cells, yeast may have a Mg²⁺ transport system(s) which functions to maintain gradients of Mg²⁺ from the outside to inside the cell and among its subcellular compartments. Received 18 April 1996; received after revision 4 July 1996; accepted 26 July 1996     

Diffusion loading conditions determine recovery of protein synthesis in electroporated P3X63 Ag8 cells

Summary Using the suspension cell line P3X63 Ag8 we have studied the impact of the composition of the diffusion medium on cellular protein synthesis under standard electroporation conditions in TBS-Na. This buffer contains the high saline concentration usually present in electroporation-mediated DNA transfection. Electroporation in the presence of TBS-Na resulted in an immediate shut-off of protein synthesis, even though both FITC-dextran (M_r 40 kD) and Semliki Forest virus core protein (M_r 33 kD) were incorporated efficiently into the cytoplasm across the electropores at 0°C. Subsequent resealing of the pores was completed after a 5-min incubation at 37°C. When compared with control cells, overall protein synthesis of electroporated cells recovered slowly to resume a 30% activity after 1 h of incubation at 37°C. We have determined optimal conditions for diffusion loading (which necessitates the presence of ATP, GTP, amino acids, K⁺, Mg²⁺, and Ca²⁺) and resealing (in the presence of K⁺, Mg²⁺, and Ca²⁺), leading to a full and lasting recovery of protein synthesis within 5 min after pore closure.     

The (Na++K+)-ATPase activity in brain of quaking mice

Summary The (Na⁺+K⁺)- and Mg²⁺-dependent ATPase distribution in several brain areas has been investigated in Quaking mutant mice characterized by myelin deficiency. A marked decrease of (Na⁺+K⁺)-ATPase activity has been found in limbic structures, hypothalamus and cerebellum. The Mg²⁺-dependent activity did not change. A possible involvement of the impairment of the (Na⁺+K⁺)-ATPase activity in the seizure susceptibility of this mice is discussed.Chargée de Recherche au CNRS.     

The Ca2+-transport ATPases in smooth muscle

Summary A calmodulin stimulated Ca²⁺-transport ATPase which has many of the characteristics of the erythrocyte type Ca²⁺-transport ATPase has been purified from smooth muscle. In particular, the effect of calmodulin on these transport enzymes is mimiced by partial proteolysis and antibodies against erythrocyte Ca²⁺-transport ATPase also bind to the smooth muscle (Ca²⁺+Mg²⁺)ATPase. A correlation between the distribution of the calmodulin stimulated (Ca²⁺+Mg²⁺)ATPase and (Na⁺+K⁺)ATPase activities in smooth muscle membranes separated by density gradient centrifugation suggests a plasmalemmal distribution of this (Ca²⁺+Mg²⁺)ATPase. A phosphoprotein intermediate in smooth muscle which strongly resembles the corresponding phosphoprotein in sarcoplasmic reticulum of skeletal muscle may indicate the presence in smooth muscle of a similar type of Ca²⁺-transport ATPase.     

Inhibition ofE. coli ATPase activity by a troponin component,TN-I,and by mitochondrial ATPase inhibitor

Summary The enzymic activity of Mg²⁺-or Ca²⁺-stimulated ATPase fromEscherichia coli was inhibited by one of the troponin components, TN-I, and by mitochondrial ATPase inhibitor (F₁-inhibitor). The inhibitory ability of component TN-I against Mg²⁺-stimulated ATPase activity was lost after digestion of component TN-I with trypsin. The Mg²⁺-stimulated ATPase activity inhibited by component TN-I was completely restored by the addition of another troponin component, TN-C.     

Ketoconazole,an inhibitor of calcium transport in skeletal muscle sarcoplasmic reticulum

Summary Ketoconazole, an antimycotic agent, inhibits calcium binding and accumulation, and induces calcium release in sarcoplasmic reticulum. The Mg²⁺-ATPase and the (Ca²⁺+Mg²⁺)-ATPase activities are stimulated at low but inhibited at high concentrations of ketoconazole.The author wishes to thank Dr K. S. Cheah for discussion and Mr C. C. Ketteridge for preparing the sarcoplasmic reticulum and carrying out the ATPase assays.     

Effects of Mn2+ and Mg2+ on the pigeon liver pyruvate kinase

Riassunto Mn²⁺ and Mg²⁺ attivano la piruvato cinasi di fegato di piccione in maniera distinta. In presenza di basse concentrationi di fosfoenolpiruvato Mn⁺ é piú efficace di Mg²⁺ ed é attivatore dell'enzima saturato da Mg²⁺. Piruvato cinasi (EC 2.7.1.40).

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This work was supported by a grant from the Consiglio Nazionale delle Ricerche, Roma, Italia.Silvia Baldi is a fellow of the Italian C.N.R.     

Metal binding to myosin and to myosin DTNB-light chain

Summary The effects of various divalent cations, Ca²⁺, Mg²⁺ and Mn²⁺ on the intrinsic fluorescence of heavy meromyosin (HMM) and myosin 5,5-dithio-bis-(2-nitrobenzoate) DTNB-light chain of rabbit striated muscle, are compared. At pH 6.4, the fluorescence change induced by the metal ions is present only in the isolated light chain and disappears in HMM, thus indicating an interaction between the heavy and light chains with respect to the binding of the metal ions. Whereas Mg²⁺ binds more strongly than Ca²⁺ to myosin, this order is reversed in the case of the DTNB-light chain.     

Interaction of polyamines or their precursors with the calcium-controlled secretion of peroxidase by sugarbeet cells

Summary Three polyamines tested (cadaverine, spermidine and spermine) and their 2 precursors (the amino acids arginine and ornithine) inhibit the Ca²⁺-mediated secretion of peroxidases by sugarbeet cells in suspension culture at concentrations ranging from 10^–15 to 10^–5M. In the absence of exogenous Ca²⁺, spermine added at higher concentrations mimics the activatory effect of Ca²⁺, the other polyamines being without effect.Supported by the Belgian FRFC (grant No. 2.9009.75 to T.G.) and the Swiss National Foundation for Scientific Research (grant No. 3.140-0.81 to C.P. and H.G.).     

TRPM7 is regulated by halides through its kinase domain

Transient receptor potential melastatin 7 (TRPM7) is a divalent-selective cation channel fused to an atypical α-kinase. TRPM7 is a key regulator of cell growth and proliferation, processes accompanied by mandatory cell volume changes. Osmolarity-induced cell volume alterations regulate TRPM7 through molecular crowding of solutes that affect channel activity, including magnesium (Mg²⁺), Mg-nucleotides and a further unidentified factor. Here, we assess whether chloride and related halides can act as negative feedback regulators of TRPM7. We find that chloride and bromide inhibit heterologously expressed TRPM7 in synergy with intracellular Mg²⁺ ([Mg²⁺]_i) and this is facilitated through the ATP-binding site of the channel’s kinase domain. The synergistic block of TRPM7 by chloride and Mg²⁺ is not reversed during divalent-free or acidic conditions, indicating a change in protein conformation that leads to channel inactivation. Iodide has the strongest inhibitory effect on TRPM7 at physiological [Mg²⁺]_i. Iodide also inhibits endogenous TRPM7-like currents as assessed in MCF-7 breast cancer cells, where upregulation of SLC5A5 sodium-iodide symporter enhances iodide uptake and inhibits cell proliferation. These results indicate that chloride could be an important factor in modulating TRPM7 during osmotic stress and implicate TRPM7 as a possible molecular mechanism contributing to the anti-proliferative characteristics of intracellular iodide accumulation in cancer cells.     

Involvement of thiols in the induction of inward current induced by silver in frog skeletal muscle membrane

Exposure of voltage-clamped frog skeletal muscle fibres to silver caused a maintained inward current which could be carried by Ca²⁺, Mg²⁺ or Na⁺. Inorganic Ca²⁺ channel blockers and dithiothreitol (SH reducing agent) diminished this current, but a Na⁺ channel blocker did not. Thus, silver activates the Ca²⁺ channel by acting on SH groups in a Ca²⁺ channel protein.     

Effects of various inhibitors and 2,4-dinitrophenol on adenosine triphosphatase from Malpighian tubules ofLocusta migratoria L

Summary Both Mg²⁺-ATPase and HCO ₃ ^– -stimulated ATPase activity were inhibited by sodium azide and to a lesser extent ethacrynic acid and amiloride. 1 mM DNP stimulated Mg²⁺-ATPase activity by 22% and HCO ₃ ^– -stimulated ATPase activity by 7%.     

Zur Metallspezifität der Hexokinase

Summary The activity of hexokinase has been determined in the presence of different metal ions. Besides Mg²⁺, the ions Co²⁺, Ni²⁺, Mn²⁺, Zn²⁺, and Cd²⁺ show remarkable activation. The differences are explained by superposition of an activating and an inhibiting function. The specifity problem is discussed.     

Sulfhydryl oxidation induces calcium release from fragmented sarcoplasmic reticulum even in the presence of glutathione

Alcian blue and plumbagin induced transient Ca²⁺ release from fragmented sarcoplasmic reticulum. Dithiothreitol (DTT) and glutathione (GSH) partially blocked Ca²⁺ release induced by these oxidizing compounds. Pretreatment of alcian blue and plumbagin with DTT or GSH for more than 1 min was required to abolish the ability of the oxidizing compounds to release Ca²⁺. Mg²⁺ and ruthenium red completely blocked alcian blue-and plumbagin-induced Ca²⁺ release. These results suggest that oxidation of sulfhydryls on Ca²⁺ release channels induces Ca²⁺ release even in the presence of GSH in situ.     

Insulin-like effect of dichloroacetic acid on hexose transport in Swiss 3T3 cells

Summary Hexose transport in Swiss 3T3 cells was increased by treatment with dichloroacetic acid as well as by treatment with insulin. Neither extra-nor intracellular Ca²⁺ was found to be involved in their stimulatory action. On the other hand, the removal of intracellular Mg²⁺ resulted in a loss of the stimulation. These results suggest that dichloroacetic acid stimulates the hexose transport in Mg²⁺-dependent manner, similar to that of insulin.This work was supported in part by Grants-in-Aid for Scientific Research from the Ministry of Education, Science and Culture, and the Ministry of Health and Welfare of Japan.     

Dissociation-constants of metal-ion-complexes with alkaline phosphatase from pig kidney

Summary Using metal-ion buffers it was possible to remove Zn²⁺, Mg²⁺ and Mn²⁺ ions of pig kidney alkaline phosphatase reversibly. The dissociation constants obtained are K_EMg:4·10^–7 M, K_EMn:4·10^–8 M and K_EZn:8·10^–13 M (22°C, pH:9.6, :0.07).Acknowledgement: The authors thank Dr.H. U. Wolf for helpful suggestions and valuable discussion and MissH. Köth for technical assistance.     

Activation and specificity of alkaline phosphatase of a mineralizing collagen-rich system

Summary Alkaline phosphatase from tibia tendon ofMeleagris gallopavo L. was highly purified. The enzyme activation by different ions was measured. Mg²⁺ showed a high activation with a broader spectrum of phosphomonoester hydrolization. The in vivo Mg²⁺ concentration was an optimum for in vitro activation.Dedicated to Prof. Dr. G. Pfefferkorn on the occasion of his 65^th birthday.We thank Deutsche Forschungsgemeinschaft for support.     

Effects of Ca2+ and Mg2+ on motility of sea urchin spermatozoa

Summary Swimming speed of sea urchin spermatozoa, measured by a light scattering technique, did not change with 0-20 mM Ca²⁺ in the medium. The speed was maximum at the normal concentration of Mg²⁺ (49 mM) in sea water.Supported by grants-in-aid from the Ministry of Education, Science and Culture, Japan, and a grant from the Ford Foundation.