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1.
Biochemistry ; 39(18): 5534-42, 2000 May 09.
Article in English | MEDLINE | ID: mdl-10820027

ABSTRACT

The phosholipid bilayer fluidity of isolated mitochondria and phospholipid vesicles after calcium-dependent binding of annexin V was studied using EPR spectroscopy. The membranes were probed at different depths by alternatively using cardiolipin, phosphatidylcholine, or phosphatidylethanolamine spin labeled at position C-5 or C-12 or C-16 of the beta acyl chain. Computer-aided spectral titration facilitated observing and quantitating the EPR spectrum from phospholipid spin labels affected by annexin binding, and spectral mobility was calibrated by comparison with standard spectra scanned at various temperatures. In most cases it was found that binding of the protein to the membranes makes the inner bilayer more rigid up to acyl position C-12 than afterward, in agreement with the previously observed effect in SUVs [Megli, F. M., Selvaggi, M., Liemann, S., Quagliariello, E., and Huber, R. (1998) Biochemistry 37, 10540-10546]. Moreover, in isolated mitochondrial membranes, cardiolipin apparently is more readily affected than the other main phospholipids, while in vesicles made from mitochondrial phospholipids, the different species are affected in essentially the same way. This behavior is consistent with the existence of distinct cardiolipin pools in mitochondria, and with the already advanced hypothesis that these domains are the binding site for annexin V to the isolated organelles [Megli, F. M., Selvaggi, M., De Lisi, A., and Quagliariello, E. (1995) Biochim. Biophys. Acta 1236, 273-278]. Keeping in mind the funcional importance of cardiolipin in the mitochondrial membrane, the question is raised as to whether the observed influence of annexin V binding to this phospholipid and its consequent local fluidity alteration might affect the mitochondrial functionality, at least in vitro.


Subject(s)
Annexin A5/pharmacology , Cardiolipins/chemistry , Lipid Bilayers/chemistry , Membrane Fluidity , Mitochondria, Liver/metabolism , Animals , Binding Sites , Electron Spin Resonance Spectroscopy , Intracellular Membranes/chemistry , Liposomes/chemistry , Membrane Fluidity/drug effects , Phospholipids/chemistry , Protein Binding , Rats , Spin Labels
2.
Nucleic Acids Res ; 27(8): 1890-9, 1999 Apr 15.
Article in English | MEDLINE | ID: mdl-10101198

ABSTRACT

The cDNA for the sea urchin mitochondrial D-loop-binding protein (mtDBP), a 40 kDa protein which binds two homologous regions of mitochondrial DNA (the D-loop region and the boundary between the oppositely transcribed ND5 and ND6 genes), has been cloned. Four different 3'-untranslated regions have been detected that are related to each other in pairs and do not contain the canonical polyadenylation signal. The in vitro synthesised mature protein (348 amino acids), deprived of the putative signal sequence, binds specifically to its DNA target sequence and produces a DNase I footprint identical to that given by the natural protein. mtDBP contains two leucine zippers, one of which is bipartite, and two small N- and C-terminal basic domains. A deletion mutation analysis of the recombinant protein has shown that the N-terminal region and the two leucine zippers are necessary for the binding. Furthermore, evidence was provided that mtDBP binds DNA as a monomer. This rules out a dimerization role for the leucine zippers and rather suggests that intramolecular interactions between leucine zippers take place. A database search has revealed as the most significative homology a match with the human mitochondrial transcription termination factor (mTERF), a protein that also binds DNA as a monomer and contains three leucine zippers forming intramolecular interactions. These similarities, and the observation that mtDBP-binding sites contain the 3'-ends of mtRNAs coded by opposite strands and the 3'-end of the D-loop structure, point to a dual function of the protein in modulating sea urchin mitochondrial DNA transcription and replication.


Subject(s)
DNA, Mitochondrial/metabolism , DNA-Binding Proteins/genetics , Leucine Zippers , Mitochondria , Amino Acid Sequence , Animals , Base Sequence , Binding Sites , Cloning, Molecular , DNA, Complementary , DNA-Binding Proteins/metabolism , Humans , Molecular Sequence Data , Sea Urchins/genetics , Sequence Analysis, DNA
3.
FEBS Lett ; 444(2-3): 291-5, 1999 Feb 12.
Article in English | MEDLINE | ID: mdl-10050777

ABSTRACT

The effect of 3'-azido-3'-deoxythymidine on nucleoside diphosphate kinase of isolated rat liver mitochondria has been studied. This is done by monitoring the increase in the rate of oxygen uptake by nucleoside diphosphate (TDP, UDP, CDP or GDP) addition to mitochondria in state 4. It is shown that 3'-azido-3'-deoxythymidine inhibits the mitochondrial nucleoside diphosphate kinase in a competitive manner, with a Ki value of about 10 microM as measured for each tested nucleoside diphosphate. It is also shown that high concentrations of GDP prevent 3'-azido-3'-deoxythymidine inhibition of the nucleoside diphosphate kinase.


Subject(s)
Enzyme Inhibitors/pharmacology , Mitochondria, Liver/enzymology , Nucleoside-Diphosphate Kinase/antagonists & inhibitors , Zidovudine/pharmacology , Animals , Atractyloside/analogs & derivatives , Atractyloside/pharmacology , Binding, Competitive , Cytidine Diphosphate/pharmacokinetics , Guanosine Diphosphate/pharmacokinetics , Kinetics , Mitochondria, Liver/drug effects , Oligomycins/pharmacology , Oxygen Consumption/drug effects , Rats , Thymine Nucleotides/pharmacokinetics , Uridine Diphosphate/pharmacokinetics
4.
Gen Pharmacol ; 31(4): 531-8, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9792211

ABSTRACT

1. The subject of this review is the interaction between AZT (zidovudine) and mitochondria as described in papers dealing with AZT therapy both in AIDS patients and in model systems--that is, in cultured cells and in isolated mitochondria. 2. The structure and function of mitochondria are briefly described with discussion of the theoretical frame for a detailed bioenergetic investigation. 3. Experimental work is reported showing that mitochondria are cell AZT targets: changes in the structure and function induced by long-term AZT therapy as investigated both in AIDS patients and in model systems. 4. The AZT inhibition of energy-supplying reactions is considered in detail in studies dealing with long-term treatment and studies in which AZT was added to isolated mitochondria. In particular, adenylate kinase, ADP/ATP translocase and DNA polymerase gamma are reported as molecular targets of AZT. 5. Some perspectives of AZT therapy from the study of the effect of AZT on mitochondrion biochemistry are briefly reported.


Subject(s)
Acquired Immunodeficiency Syndrome/drug therapy , Mitochondria/drug effects , Zidovudine/pharmacology , Animals , Cells, Cultured , DNA Polymerase gamma , DNA, Mitochondrial/drug effects , DNA-Directed DNA Polymerase/drug effects , Dideoxynucleotides , Humans , In Vitro Techniques , Mitochondria/physiology , Mitochondria/ultrastructure , Thymine Nucleotides/pharmacology , Zidovudine/analogs & derivatives
5.
FEBS Lett ; 435(1): 6-10, 1998 Sep 11.
Article in English | MEDLINE | ID: mdl-9755848

ABSTRACT

We show here that TPP --> TMP conversion can take place in rat liver mitochondria. This occurs via the novel, putative TPP pyrophosphatase localised in the mitochondrial matrix, as shown both by digitonin titration and by an HPLC enzyme assay carried out on the mitochondrial matrix fraction. Certain features of the reaction, including the substrate and pH dependence, are reported. Additional evidence is given that externally added TMP can cross the mitochondrial membrane in a manner consistent with the occurrence of a carrier-mediated process. This can occur both via the TPP translocator and via a novel translocator, inhibited by CAT but different from the ADP/ATP carrier.


Subject(s)
Intracellular Membranes/metabolism , Mitochondria, Liver/metabolism , Thiamine Monophosphate/metabolism , Thiamine Pyrophosphate/metabolism , Animals , Atractyloside/analogs & derivatives , Atractyloside/metabolism , Binding, Competitive , Biological Transport , Catalysis , Hydrolysis , Intracellular Membranes/enzymology , Male , Mitochondria, Liver/enzymology , Rats , Rats, Wistar , Spectrometry, Fluorescence , Thiamine Pyrophosphate/antagonists & inhibitors
6.
Biochemistry ; 37(29): 10540-6, 1998 Jul 21.
Article in English | MEDLINE | ID: mdl-9671526

ABSTRACT

The fluidity of the hydrophobic interior of phospholipid vesicles after calcium-dependent binding of human annexin V (AVH) was studied using EPR spectroscopy. Vesicles (SUVs) composed of PC or PE and an acidic phospholipid (alternatively PS, PA, or CL) were probed at different bilayer depths by either phosphatidylcholine, or the accompanying acidic phospholipid, bearing a spin label probe at position C-5, C-12, or C-16 of the sn-2 acyl chain. Alternatively, the vesicle surface was probed with a polar head spin labeled PE (PESL). The EPR spectra of annexin-bound bilayer domain(s) were obtained by computer spectral subtraction. The order parameter values (S) from the resulting difference spectra revealed that the bilayer hydrophobic interior has a greatly altered fluidity gradient, with an increased rigidity up to the C-12 position. Thereafter, the rigidification progressively vanished. The effect is not linked to the phospholipid class, since all the acidic phospholipid spectra, as well as phosphatidylcholine, shared the same sensitivity to the bound protein. The observed membrane rigidification appears to parallel the "crystallizing" tendency of vesicle-bound annexin V, but may not be involved in the calcium channeling activity of this protein.


Subject(s)
Annexin A5/metabolism , Calcium/metabolism , Lipid Bilayers/metabolism , Liposomes/metabolism , Membrane Fluidity , Annexin A5/physiology , Cardiolipins/metabolism , Cyclic N-Oxides/metabolism , Electron Spin Resonance Spectroscopy , Humans , Phosphatidylglycerols/metabolism , Phosphatidylserines/metabolism , Protein Binding , Spin Labels
7.
FEBS Lett ; 424(3): 155-8, 1998 Mar 13.
Article in English | MEDLINE | ID: mdl-9539141

ABSTRACT

Rat heart mitochondrial membranes exposed to the free radicals generating system tert-butylhydroperoxide/Cu2+ undergo lipid peroxidation as evidenced by the accumulation of thyobarbituric acid reactive substances. Mitochondrial lipid peroxidation resulted in a marked loss of both cytochrome c oxidase activity and cardiolipin content. The alterations in the properties of cytochrome c oxidase were confined to a decrease in the maximal activity (Vmax) with no change in the affinity (Km) with respect to the substrate cytochrome c. Various lipid soluble antioxidants could prevent the lipid peroxidation reaction and the associated loss of cytochrome c oxidase activity. External added cardiolipin but no other phospholipids, nor peroxidized cardiolipin was able to prevent the loss of cytochrome oxidase activity induced by lipid peroxidation. These results establish a close correlation between oxidative damage to cardiolipin and alterations in the cytochrome oxidase activity and may prove useful in probing molecular mechanism of free radicals induced peroxidative damage of mitochondria which has been proposed to contribute to aging and to chronic degenerative diseases.


Subject(s)
Cardiolipins/metabolism , Electron Transport Complex IV/metabolism , Lipid Peroxidation , Mitochondria, Heart/metabolism , Animals , Cardiolipins/pharmacology , Electron Transport Complex IV/drug effects , Male , Malondialdehyde/metabolism , Mitochondria, Heart/drug effects , Oxygen/metabolism , Peroxides/pharmacology , Rats , Rats, Inbred Strains , Thiobarbituric Acid Reactive Substances/metabolism , tert-Butylhydroperoxide
8.
Eur J Biochem ; 249(3): 777-85, 1997 Nov 01.
Article in English | MEDLINE | ID: mdl-9395326

ABSTRACT

In order to gain some insight into mitochondrial flavin biochemistry, rat liver mitochondria essentially free of lysosomal and microsomal contamination were prepared and their capability to metabolise externally added and endogenous FAD and FMN tested both spectroscopically and via HPLC. The existence of two novel mitochondrial enzymes, namely FAD pyrophosphatase (EC 3.6.1.18) and FMN phosphohydrolase (EC 3.1.3.2), which catalyse FAD-->FMN and FMN-->riboflavin conversion, respectively, is shown. They differ from each other and from extramitochondrial enzymes, as judged by their pH profile and inhibitor sensitivity, and can be separated in a partial FAD pyrophosphatase purification. Digitonin titration and subfractionation experiments show that FAD pyrophosphatase is located in the outer mitochondrial membrane and FMN phosphohydrolase in the intermembrane space. Since these enzymes can metabolise endogenous FAD and FMN, which are made available by using both Triton X-100 and the effector oxaloacetate, a proposal is made that FAD pyrophosphatase and FMN phosphohydrolase play a major role in mitochondrial flavoprotein turnover.


Subject(s)
Acid Phosphatase/metabolism , Flavin Mononucleotide/metabolism , Flavin-Adenine Dinucleotide/metabolism , Mitochondria, Liver/enzymology , Nucleotidases/metabolism , Pyrophosphatases/metabolism , Acid Phosphatase/isolation & purification , Adenosine Monophosphate/pharmacology , Animals , Cell Fractionation , Chromatography, High Pressure Liquid , Flavoproteins/isolation & purification , Flavoproteins/metabolism , Fluorescence , Hydrolysis , Kinetics , Male , Mitochondria, Liver/metabolism , Oxaloacetates/pharmacology , Pyrophosphatases/isolation & purification , Rats , Rats, Wistar
9.
Eur J Biochem ; 247(1): 52-8, 1997 Jul 01.
Article in English | MEDLINE | ID: mdl-9249008

ABSTRACT

A binding protein for single-stranded DNA was purified from Paracentrotus lividus egg mitochondria to near homogeneity by chromatography on DEAE-Sephacel and single-stranded-DNA-cellulose. The protein consists of a single polypeptide of about 15 kDa. Glycerol gradient sedimentation analysis suggested that P. lividus mitochondrial single-stranded-DNA-binding protein exists as a homo-oligomer, possibly a tetramer, in solution. The protein shows a stronger preference for poly(dT) with respect to single-stranded M13, poly(dI) and poly(dC). Binding to poly(dA) takes place with much lower affinity. The binding-site size, determined by gel mobility-shift experiments with oligonucleotides of different length, is approximately 45 nucleotides. The binding to single-stranded DNA occurs with low or no cooperativity and is not influenced by ionic strength. The protein has a very high affinity for the DNA: its apparent macroscopic association constant is 2x10(9) M(-1), a value which is the highest among the mitochondrial single-stranded-DNA-binding proteins characterized to date. The lack of cooperativity and the high association constant represent distinctive features of this protein and might be related to the peculiar mechanism of sea urchin mitochondrial DNA replication.


Subject(s)
DNA, Single-Stranded/metabolism , DNA-Binding Proteins/isolation & purification , Mitochondria/chemistry , Sea Urchins/chemistry , Animals , DNA-Binding Proteins/chemistry , DNA-Binding Proteins/metabolism , Ovum/chemistry
10.
Biochem Pharmacol ; 53(7): 913-20, 1997 Apr 04.
Article in English | MEDLINE | ID: mdl-9174103

ABSTRACT

To gain some insight into the mechanism by which 3'-azido-3'-deoxythymidine (AZT) impairs mitochondrial metabolism, [14C]AZT uptake by rat liver mitochondria (RLM) in vitro was investigated. AZT accumulated in mitochondria in a time-dependent manner and entered the mitochondrial matrix. The rate of AZT uptake into mitochondria showed a hyperbolic dependence on the drug concentration and was inhibited by mersalyl, a thiol reagent that cannot enter mitochondria, thus showing that a membrane protein is involved in AZT transport. Investigation into the capability of AZT to affect certain mitochondrial carriers demonstrated that AZT was able to impair the ADP/ATP translocator, but had no effect on Pi, dicarboxylate, tricarboxylate, or oxodicarboxylate carriers. AZT inhibited ADP/ATP antiport in either mitochondria or mitoplasts in a competitive manner with different sensitivity (Ki values were 18.3 +/- 2.9 and 70.2 +/- 5.8 microM, respectively). Consistent with this were isotopic measurements showing that AZT accumulates in the intermembrane space. AZT does not use ADP/ATP carrier to enter mitochondria, as shown by the failure of both carboxyatractyloside (CAT) to inhibit AZT transport into mitochondria and AZT to induce ATP efflux from ATP-loaded mitochondria. ADP/ATP translocator impairment by AZT as one of the biochemical processes responsible for the ATP deficiency syndrome is discussed.


Subject(s)
Mitochondria, Liver/metabolism , Mitochondrial ADP, ATP Translocases/antagonists & inhibitors , Zidovudine/metabolism , Animals , Carbon Radioisotopes , Chromatography, High Pressure Liquid , Dose-Response Relationship, Drug , Intracellular Membranes/metabolism , Male , Rats , Rats, Wistar , Zidovudine/pharmacology
11.
FEBS Lett ; 406(1-2): 136-8, 1997 Apr 07.
Article in English | MEDLINE | ID: mdl-9109403

ABSTRACT

Cardiolipin is a major mitochondrial membrane lipid and plays a pivotal role in mitochondrial function. We have recently suggested a possible involvement of this phospholipid in the age-linked decline of cytochrome c oxidase activity in rat heart mitochondria [G. Paradies et al. (1993) Arch. Gerontol. Geriatr. 16, 263-272]. The aim of this work was to test our earlier proposal. We have investigated whether addition of exogenous cardiolipin to mitochondria is able to reverse, in situ, the age-linked decrease in the cytochrome oxidase activity. The method of fusion of liposomes with mitochondria developed by Hackenbrock [Hackenbrock and Chazotte (1986) Methods Enzymol. 125, 35-45] was employed in order to enrich the mitochondria cardiolipin content. We demonstrate that the lower cytochrome c oxidase activity in heart mitochondria from aged rats can be fully restored to the level of young control rats by exogenously added cardiolipin. No restoration was obtained with other phospholipids or with peroxidized cardiolipin. Our data support a key role for cardiolipin in the age-linked decline of rat heart mitochondrial cytochrome c oxidase activity.


Subject(s)
Aging/metabolism , Cardiolipins/metabolism , Electron Transport Complex IV/metabolism , Mitochondria, Heart/enzymology , Animals , Male , Phospholipids/metabolism , Rats , Rats, Inbred F344
12.
Biochim Biophys Acta ; 1362(2-3): 193-200, 1997 Dec 31.
Article in English | MEDLINE | ID: mdl-9540850

ABSTRACT

Changes in mitochondrial fatty acid metabolism may underlie the decline in cardiac function in the hypothyroid animals. The effect of hypothyroidism on fatty acid oxidation, carnitine-acylcarnitine translocase activity and lipid composition in rat heart mitochondria has been examined. Rates of mitochondrial fatty acid oxidation as well as carnitine-carnitine and carnitine-palmitoylcarnitine exchange reactions were all depressed in heart mitochondria isolated from hypothyroid rats. Kinetic analysis of the carnitine-carnitine exchange reaction showed that the hypothyroid state affects the Vmax of this process, while having no effect on the K(m) value. Heart mitochondrial inner membrane lipid composition was significantly altered in hypothyroid rats. Cardiolipin, particularly, was found to decrease (by around 36%). Alterations in fatty acid pattern of mitochondrial inner membrane preparations from hypothyroid rats were also found. The effects of the hypothyroid state on fatty acids oxidation, carnitine translocase activity and phospholipid composition were completely reversed by following treatment of hypothyroid rats with thyroid hormone. A lower cardiolipin content in the mitochondrial inner membrane offers a plausible mechanism to explain the decline in the translocase activity in hypothyroidism.


Subject(s)
Carnitine Acyltransferases/metabolism , Hypothyroidism/metabolism , Mitochondria, Heart/metabolism , Phospholipids/metabolism , Animals , Cardiolipins/metabolism , Cell-Free System , Fatty Acids/metabolism , Kinetics , Oxidation-Reduction , Oxygen Consumption , Phosphatidylcholines/metabolism , Phosphatidylethanolamines/metabolism , Rats , Rats, Wistar , Triiodothyronine/pharmacology
13.
FEBS Lett ; 397(2-3): 260-2, 1996 Nov 18.
Article in English | MEDLINE | ID: mdl-8955359

ABSTRACT

The effect of hyperthyroidism on fatty acid oxidation and on carnitine-acylcarnitine translocase activity in rat heart mitochondria has been studied. The rates of palmitoylcarnitine supported respiration as well as the carnitine-palmitoylcarnitine exchange reaction were both stimulated (approx. 36%) in heart mitochondria from hyperthyroid rats. Kinetic analysis of the carnitine-carnitine exchange reaction showed that thyroid hormone affects the Vmax of this process, while having no effect on the Km values. The level of cardiolipin was significantly higher (approx. 40%) in heart mitoplasts from hyperthyroid rats than from the control rats. It can be concluded that thyroid hormones produce a stimulation of heart mitochondrial carnitine translocase activity and that the basis of this effect is likely an increase in the cardiolipin content.


Subject(s)
Carnitine Acyltransferases/metabolism , Hyperthyroidism/enzymology , Mitochondria, Heart/enzymology , Animals , Cardiolipins/metabolism , Carnitine/metabolism , Fatty Acids/metabolism , Male , Oxidation-Reduction , Oxygen Consumption , Palmitoylcarnitine/metabolism , Rats , Rats, Wistar
14.
Eur J Biochem ; 241(1): 171-7, 1996 Oct 01.
Article in English | MEDLINE | ID: mdl-8898903

ABSTRACT

Proline/glutamate antiport in rat kidney mitochondria has been studied in terms of two different features: energy dependence and glutamate-carrier contribution to accomplish proline movement across the mitochondrial membrane. Energy dependence of the proline/glutamate antiporter in rat kidney mitochondria has been investigated by means of both spectroscopic measurements and isotopic techniques, using either normal or [14C]glutamate-loaded mitochondria. The sensitivity of the proline/glutamate antiport to the ionophores valinomycin and nigericin, under conditions in which delta psi and delta pH are selectively affected, shows that the exchange is energy dependent. Measurements of both membrane potential and proton movement across the mitochondrial membrane suggest that proline/glutamate antiport is driven by the electrochemical proton gradient via the delta psi dependent proline/glutamate translocator and delta pH-dependent glutamate/OH- carrier. Such a carrier provides for re-uptake of glutamate that has already passed out of the mitochondria in exchange with incoming proline, made possible by the existence of a separate pool of glutamate in the intermembrane space, directly shown by means of HPLC measurements.


Subject(s)
Antiporters/metabolism , Glutamic Acid/metabolism , Mitochondria/metabolism , Proline/metabolism , ATP-Binding Cassette Transporters/metabolism , Amino Acid Transport System X-AG , Animals , Ionophores/pharmacology , Kidney/metabolism , Kinetics , Membrane Potentials/drug effects , Models, Biological , Nigericin/pharmacology , Phenazines/metabolism , Protons , Rats , Valinomycin/pharmacology
15.
Biochem Biophys Res Commun ; 226(2): 566-71, 1996 Sep 13.
Article in English | MEDLINE | ID: mdl-8806674

ABSTRACT

Different proteolytic enzymes were tested for their ability to degrade the myelin basic protein of the central nervous system, purified in two different forms, the lipid-free form and the lipid-bound form. As shown by SDS gel electrophoresis only clostripain, a thiol protease, was able to distinguish between the two MBPs since it degraded MBP only in the lipid-free form. The failure to degrade lipid-bound MBP by clostripain could not be ascribed to the presence of lipids, since the other proteolytic enzymes tested degraded both MBPs independently from lipids giving fragments with different size. These results may be related to different conformations of MBPs possibly relevant for the study of myelin structure and antigenic properties of the protein.


Subject(s)
Cysteine Endopeptidases/metabolism , Lipid Metabolism , Myelin Basic Protein/metabolism , Animals , Cattle , Electrophoresis, Polyacrylamide Gel , Hydrolysis , Metalloendopeptidases/metabolism , Protein Binding , Serine Endopeptidases/metabolism
17.
Biochem Mol Biol Int ; 38(2): 297-306, 1996 Feb.
Article in English | MEDLINE | ID: mdl-8850525

ABSTRACT

In order to gain some insight into the mechanism by which nicotinamide nucleotides localize in mitochondria, NMN was added to rat liver mitochondria, with NAD synthesis tested both enzymatically and by means of HPLC. Evidence is given that the mitochondrial matrix contains a specific NMN adenylyltransferase (E.C. 2.7.7.1.), inhibited by PPi, AMP and ADP-ribose. Some features of this enzyme, including the substrate, pH and temperature dependence were also investigated.


Subject(s)
Adenosine Triphosphate/metabolism , Mitochondria, Liver/metabolism , NAD/biosynthesis , Nicotinamide Mononucleotide/metabolism , Nicotinamide-Nucleotide Adenylyltransferase/metabolism , Adenosine Diphosphate Ribose/pharmacology , Adenosine Monophosphate/pharmacology , Animals , Diphosphates , Hydrogen-Ion Concentration , Male , Mitochondria, Liver/enzymology , NADP/biosynthesis , Rats , Substrate Specificity
18.
Oncol Rep ; 3(4): 753-7, 1996 Jul.
Article in English | MEDLINE | ID: mdl-21594449

ABSTRACT

Thyroid cell growth and function both in vivo and in vitro, are mainly regulated by TSH. Recent studies have shown that growth factors including insulin-like growth factors (IGF-1) have an important role in the control of thyrocyte proliferation and differentiation. The aim of this study was to evaluate the expression of the IGF-1 gene by Northern analysis and the IGF-1 tissue protein by radioimmunoassay in multinodular euthyroid goiters. The study population consisted of 20 patients with multinodular goiter (14 females and 6 males) living in a non endemic geographic area. All patients were euthyroid at the time of surgery and submitted to total or subtotal thyroidectomy. Samples of normal thyroid tissue were obtained from three patients who were operated due to laryngeal carcinomas. The IGF-1 protein content was increased in non toxic multinodular goiter, 22 ng/g vs. 14 in controls (p<0.03), as was IGF-1 gene expression (p<0.05). The increase in the steady state mRNA content correlated with the increase in the protein content (r=0.665; p<0.005). These results suggest that IGF-1 may play a role in proliferation events involved in benign hyperplastic thyroid diseases.

19.
Mech Ageing Dev ; 84(2): 103-12, 1995 Oct 13.
Article in English | MEDLINE | ID: mdl-8788238

ABSTRACT

Age-related changes in mitochondrial fatty acids metabolism may underlie the progressive decline in cardiac function. The effect of aging and acute treatment with acetyl-L-carnitine on fatty acids oxidation and on carnitine-acylcarnitine translocase activity in rat heart mitochondria was studied. Rates of palmitoylcarnitine supported respiration as well as carnitine-carnitine and carnitine-palmitoylcarnitine exchange reactions were all depressed (approx. 35%) in heart mitochondria from aged rats. These effects were almost completely reversed following treatment of aged rats with acetyl-L-carnitine. Heart mitochondrial cardiolipin content was significantly reduced (approx. 38%) in aged rats. Treatment of aged rats with acetyl-L-carnitine restored the level of cardiolipin to that of young rats. It is suggested that acetyl-L-carnitine is able to reverse age-related decrement in mitochondrial carnitine-acylcarnitine exchange activity by restoring the normal cardiolipin content.


Subject(s)
Acetylcarnitine/pharmacology , Aging/metabolism , Cardiolipins/metabolism , Carnitine Acyltransferases/metabolism , Fatty Acids/metabolism , Mitochondria, Heart/enzymology , Animals , Male , Oxidation-Reduction , Rats , Rats, Inbred F344
20.
Biochem Biophys Res Commun ; 215(3): 800-7, 1995 Oct 24.
Article in English | MEDLINE | ID: mdl-7488044

ABSTRACT

Sensitivity to digestion with pronase has been used to show that the precursor form of mitochondrial aspartate aminotransferase, the form lacking the N-terminal presequence, that with a deletion of the first 9 residues and mutants of the mature enzyme in which residue Cys-166 is mutated to alanine or serine, all retain unfolded conformations after synthesis in a reticulocyte lysate. In the presence of lysed mitochondria the various forms of mitochondrial aspartate aminotransferase retained their susceptibilities to pronase in a way that mirrored the efficiencies with which they are imported into intact mitochondria. The results are interpreted as showing that the presequence of mitochondrial aspartate aminotransferase is not uniquely required for interaction with cytosolic factors required to maintain the newly synthesised protein in a form competent for interacting with, and being imported into, mitochondria.


Subject(s)
Aspartate Aminotransferases/chemistry , Cysteine , Mitochondria, Liver/enzymology , Point Mutation , Pronase/metabolism , Protein Conformation , Alanine , Animals , Aspartate Aminotransferases/biosynthesis , Aspartate Aminotransferases/metabolism , Cell-Free System , Kinetics , Mutagenesis, Site-Directed , Plasmids , Rats , Recombinant Fusion Proteins/biosynthesis , Recombinant Fusion Proteins/chemistry , Recombinant Fusion Proteins/metabolism , Serine , Tetrahydrofolate Dehydrogenase/chemistry , Tetrahydrofolate Dehydrogenase/metabolism
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