RESUMEN
Multiple System Atrophy is a severe neurodegenerative disorder which is characterized by a variable clinical presentation and a broad neuropathological spectrum. The pathogenic mechanisms are almost completely unknown. In the present study, we established a cellular model of MSA by using fibroblasts' primary cultures and performed several experiments to investigate the causative mechanisms of the disease, with a particular focus on mitochondrial functioning. Fibroblasts' analyses (7 MSA-P, 7 MSA-C and 6 healthy controls) displayed several anomalies in patients: an impairment of respiratory chain activity, in particular for succinate Coenzyme Q reductase (pâ¯<â¯0.05), and a reduction of complex II steady-state level (pâ¯<â¯0.01); a reduction of Coenzyme Q10 level (pâ¯<â¯0.001) and an up-regulation of some CoQ10 biosynthesis enzymes, namely COQ5 and COQ7; an impairment of mitophagy, demonstrated by a decreased reduction of mitochondrial markers after mitochondrial inner membrane depolarization (pâ¯<â¯0.05); a reduced basal autophagic activity, shown by a decreased level of LC3 II (pâ¯<â¯0.05); an increased mitochondrial mass in MSA-C, demonstrated by higher TOMM20 levels (pâ¯<â¯0.05) and suggested by a wide analysis of mitochondrial DNA content in blood of large cohorts of patients. The present study contributes to understand the causative mechanisms of Multiple System Atrophy. In particular, the observed impairment of respiratory chain activity, mitophagy and Coenzyme Q10 biosynthesis suggests that mitochondrial dysfunction plays a crucial role in the pathogenesis of the disease. Furthermore, these findings will hopefully contribute to identify novel therapeutic targets for this still incurable disorder.
Asunto(s)
Fibroblastos/patología , Mitocondrias/patología , Atrofia de Múltiples Sistemas/patología , Autofagia , Células Cultivadas , ADN Mitocondrial/análisis , ADN Mitocondrial/metabolismo , Complejo II de Transporte de Electrones/análisis , Complejo II de Transporte de Electrones/metabolismo , Femenino , Fibroblastos/metabolismo , Humanos , Masculino , Potencial de la Membrana Mitocondrial , Mitocondrias/metabolismo , Mitofagia , Atrofia de Múltiples Sistemas/metabolismo , Ubiquinona/análogos & derivados , Ubiquinona/análisis , Ubiquinona/metabolismoRESUMEN
Mitochondrial diseases (MDs) result from alteration of the mitochondrial respiratory chain (MRC) function. Despite the prevalence of MDs in the population, the paucity of animal models available limits the understanding of these disorders. Mutations in SDHA, a gene that codes for the alpha subunit of succinate dehydrogenase (SDH), can cause some forms of MD. SDHA is a crucial contributor to MRC function. In order to expand the range of MD animal models available, we attempted to generate a Sdha knockout rat. Since homozygous Sdha-/- rats could neither be identified in newborn litters, nor as early as embryonic day 14, we evaluated wild-type (WT) and heterozygous Sdha+/- genotypes. No differences in behavioral, biochemical, or molecular evaluations were observed between WT and Sdha+/- rats at 6 weeks or 6 months of age. However, 30% of Sdha+/- rats displayed mild muscle fiber atrophy with rare fibers negative for cytochrome oxidase and SDH on histochemical staining. Collectively, our data provide additional evidence that modeling SDH mutations in rodents may be challenging due to animal viability, and heterozygous rats are insufficiently symptomatic at a phenotypic and molecular level to be of significant use in the study of SDH deficiency.
Asunto(s)
Complejo II de Transporte de Electrones/genética , Complejo II de Transporte de Electrones/metabolismo , Fuerza de la Mano/fisiología , Músculo Esquelético/metabolismo , Músculo Esquelético/patología , Animales , ADN Mitocondrial/genética , ADN Mitocondrial/metabolismo , Complejo II de Transporte de Electrones/análisis , Técnicas de Inactivación de Genes/métodos , Masculino , Músculo Esquelético/química , Ratas , Ratas TransgénicasRESUMEN
BACKGROUND: Periapical inflammatory lesions have been investigated previously, but understanding of pathogenesis of these lesions (granulomas and radicular cysts) at the molecular level is still questionable. Matrix metalloproteinases (MMPs) are enzymes involved in the development of periapical pathology, specifically inflammation and tissue destruction. To elucidate pathogenesis of periapical granulomas and radicular cysts, we undertook a detailed analysis of gene expression of MMP-1, MMP-2 and their tissue inhibitors, TIMP-1 and TIMP-2. METHODS: A total of 149 samples were analyzed using real-time PCR (59 radicular cysts, 50 periapical granulomas and 40 healthy gingiva samples as controls) for expression of MMP-1, MMP-2, TIMP-1 and TIMP-2 genes. The determination of best reference gene for expression analysis of periapical lesions was done using a panel of 12 genes. RESULTS: We have shown that ß-actin and GAPDH are not the most stable reference controls for gene expression analysis of inflammatory periapical tissues and healthy gingiva. The most suitable reference gene was determined to be SDHA (a succinate dehydrogenase complex, subunit A, flavoprotein [Fp]). We found that granulomas (n = 50) and radicular cysts (n = 59) exhibited significantly higher expression of all four examined genes, MMP-1, MMP-2, TIMP-1, and TIMP-2, when compared to healthy gingiva (n = 40; P < 0.05). CONCLUSION: This study has confirmed that the expression of MMP-1, MMP-2, TIMP-1, and TIMP-2 genes is important for the pathogenesis of periapical inflammatory lesions. Since the abovementioned markers were not differentially expressed in periapical granulomas and radicular cysts, the challenge of finding the genetic differences between the two lesions still remains.
Asunto(s)
Periodontitis Crónica/enzimología , Inflamación/genética , Metaloproteinasa 1 de la Matriz/genética , Metaloproteinasa 2 de la Matriz/genética , Periodontitis Periapical/genética , Inhibidor Tisular de Metaloproteinasa-1/genética , Inhibidor Tisular de Metaloproteinasa-2/genética , Actinas/biosíntesis , Actinas/genética , Periodontitis Crónica/genética , Complejo II de Transporte de Electrones/análisis , Complejo II de Transporte de Electrones/genética , Encía/enzimología , Granuloma/enzimología , Granuloma/genética , Humanos , Inflamación/metabolismo , Metaloproteinasa 1 de la Matriz/biosíntesis , Metaloproteinasa 2 de la Matriz/biosíntesis , Granuloma Periapical/enzimología , Granuloma Periapical/genética , Periodontitis Periapical/enzimología , Quiste Radicular/enzimología , Quiste Radicular/genética , Inhibidor Tisular de Metaloproteinasa-1/biosíntesis , Inhibidor Tisular de Metaloproteinasa-2/biosíntesis , Transcripción GenéticaRESUMEN
Despite the established role of SDHB/SDHA immunohistochemistry as a valuable tool to identify patients at risk for familial succinate dehydrogenase-related pheochromocytoma/paraganglioma syndromes, the reproducibility of the assessment methods has not as yet been determined. The aim of this study was to investigate interobserver variability among seven expert endocrine pathologists using a web-based virtual microscopy approach in a large multicenter pheochromocytoma/paraganglioma cohort (n=351): (1) 73 SDH mutated, (2) 105 non-SDH mutated, (3) 128 samples without identified SDH-x mutations, and (4) 45 with incomplete SDH molecular genetic analysis. Substantial agreement among all the reviewers was observed either with a two-tiered classification (SDHB κ=0.7338; SDHA κ=0.6707) or a three-tiered classification approach (SDHB κ=0.6543; SDHA κ=0.7516). Consensus was achieved in 315 cases (89.74%) for SDHB immunohistochemistry and in 348 cases (99.15%) for SDHA immunohistochemistry. Among the concordant cases, 62 of 69 (~90%) SDHB-/C-/D-/AF2-mutated cases displayed SDHB immunonegativity and SDHA immunopositivity, 3 of 4 (75%) with SDHA mutations showed loss of SDHA/SDHB protein expression, whereas 98 of 105 (93%) non-SDH-x-mutated counterparts demonstrated retention of SDHA/SDHB protein expression. Two SDHD-mutated extra-adrenal paragangliomas were scored as SDHB immunopositive, whereas 9 of 128 (7%) tumors without identified SDH-x mutations, 6 of 37 (~16%) VHL-mutated, as well as 1 of 21 (~5%) NF1-mutated tumors were evaluated as SDHB immunonegative. Although 14 out of those 16 SDHB-immunonegative cases were nonmetastatic, an overall significant correlation between SDHB immunonegativity and malignancy was observed (P=0.00019). We conclude that SDHB/SDHA immunohistochemistry is a reliable tool to identify patients with SDH-x mutations with an additional value in the assessment of genetic variants of unknown significance. If SDH molecular genetic analysis fails to detect a mutation in SDHB-immunonegative tumor, SDHC promoter methylation and/or VHL/NF1 testing with the use of targeted next-generation sequencing is advisable.
Asunto(s)
Neoplasias de las Glándulas Suprarrenales/genética , Complejo II de Transporte de Electrones/análisis , Inmunohistoquímica/normas , Paraganglioma/genética , Feocromocitoma/genética , Succinato Deshidrogenasa/análisis , Biomarcadores de Tumor/análisis , Biomarcadores de Tumor/genética , Complejo II de Transporte de Electrones/genética , Humanos , Microscopía/métodos , Mutación , Variaciones Dependientes del Observador , Succinato Deshidrogenasa/genética , Telepatología/métodosRESUMEN
Oncocytomas are tumours predominantly or exclusively composed of oncocytes, cells with granular and eosinophilic cytoplasm filled with mitochondria. Although they can occur in every organ, they are rare in adrenal glands, and in paediatric patients they are even rarer, with only three case reports previously published. We present a preschool child developing Cushing's syndrome due to an adrenocortical oncocytoma, which was confirmed immunohistochemically with antibodies to the mitochondrial electron complex 2. A 5.8-year-old girl presented with clinical features of Cushing's syndrome. ACTH-independent hypercortisolism was confirmed biochemically and a left adrenal mass was detected by imaging and removed by laparotomy. Histopathological analysis revealed a tumour composed of more than 95 % of oncocytes, confirmed immunohistochemically with antibodies to subunits A and B of the mitochondrial enzyme succinate dehydrogenase. Using the Lin-Weiss-Bisceglia score system and the reticulin algorithm, this tumour was categorized as a benign adrenocortical oncocytoma. The patient currently has 64 months of follow-up, without any evidence of relapse of symptoms. To our knowledge, we herein present the youngest patient developing an adrenocortical oncocytoma and the first manifestation of Cushing's syndrome due to this rare neoplasm in paediatric patients. We also emphasize the clinical usefulness of immunohistochemistry to the mitochondrial enzyme succinate dehydrogenase to confirm the oxyphilic nature of adrenocortical oncocytomas.
Asunto(s)
Adenoma Oxifílico/diagnóstico , Neoplasias de la Corteza Suprarrenal/diagnóstico , Síndrome de Cushing/diagnóstico , Adenoma Oxifílico/enzimología , Adenoma Oxifílico/patología , Adenoma Oxifílico/cirugía , Neoplasias de la Corteza Suprarrenal/enzimología , Neoplasias de la Corteza Suprarrenal/patología , Neoplasias de la Corteza Suprarrenal/cirugía , Niño , Diagnóstico Diferencial , Complejo II de Transporte de Electrones/análisis , Femenino , Humanos , Inmunohistoquímica , Succinato Deshidrogenasa/análisisRESUMEN
Rett syndrome (RTT) is a severe neurodevelopmental disorder, predominantly caused by mutations in the X-linked Methyl-CpG-binding protein 2 (MECP2) gene. Patients present with numerous functional deficits including intellectual disability and abnormalities of movement. Clinical and biochemical features may overlap with those seen in patients with primary mitochondrial respiratory chain disorders. In the late stages of the disorder, patients suffer from motor deterioration and usually require assisted mobility. Using a mouse model of RTT (Mecp2(tm1Tam)), we studied the mitochondrial function in the hind-limb skeletal muscle of these mice. We identified a reduction in cytochrome c oxidase subunit I (MTCO1) at both the transcript and protein level, in accordance with our previous findings in RTT patient brain studies. Mitochondrial respiratory chain (MRC) enzyme activity of complexes II+III (COII+III) and complex IV (COIV), and glutathione (GSH) levels were significantly reduced in symptomatic mice, but not in the pre-symptomatic mice. Our findings suggest that mitochondrial abnormalities in the skeletal muscle may contribute to the progressive deterioration in mobility in RTT through the accumulation of free radicals, as evidenced by the decrease in reduced glutathione (GSH). We hypothesise that a diminution in GSH leads to an accumulation of free radicals and an increase in oxidative stress. This may impact on respiratory chain function and contribute in part to the progressive neurological and motor deterioration seen in the Mecp2-mutant mouse. Treatment strategies aimed at restoring cellular GSH levels may prove to be a novel target area to consider in future approaches to RTT therapies.
Asunto(s)
Mitocondrias/fisiología , Músculo Esquelético/fisiopatología , Síndrome de Rett/fisiopatología , Animales , Modelos Animales de Enfermedad , Complejo II de Transporte de Electrones/análisis , Complejo III de Transporte de Electrones/análisis , Complejo IV de Transporte de Electrones/análisis , Radicales Libres/toxicidad , Glutatión/análisis , Humanos , Ratones , Mitocondrias/enzimología , Mitocondrias/metabolismo , Estrés OxidativoRESUMEN
The mitochondrion, derived in evolution from an α-proteobacterial progenitor, plays a key metabolic role in eukaryotes. Mitochondria house the electron transport chain (ETC) that couples oxidation of organic substrates and electron transfer to proton pumping and synthesis of ATP. The ETC comprises several multiprotein enzyme complexes, all of which have counterparts in bacteria. However, mitochondrial ETC assemblies from animals, plants and fungi are generally more complex than their bacterial counterparts, with a number of 'supernumerary' subunits appearing early in eukaryotic evolution. Little is known, however, about the ETC of unicellular eukaryotes (protists), which are key to understanding the evolution of mitochondria and the ETC. We present an analysis of the ETC proteome from Acanthamoeba castellanii, an ecologically, medically and evolutionarily important member of Amoebozoa (sister to Opisthokonta). Data obtained from tandem mass spectrometric (MS/MS) analyses of purified mitochondria as well as ETC complexes isolated via blue native polyacrylamide gel electrophoresis are combined with the results of bioinformatic queries of sequence databases. Our bioinformatic analyses have identified most of the ETC subunits found in other eukaryotes, confirming and extending previous observations. The assignment of proteins as ETC subunits by MS/MS provides important insights into the primary structures of ETC proteins and makes possible, through the use of sensitive profile-based similarity searches, the identification of novel constituents of the ETC along with the annotation of highly divergent but phylogenetically conserved ETC subunits.
Asunto(s)
Acanthamoeba castellanii/metabolismo , Proteínas del Complejo de Cadena de Transporte de Electrón/análisis , Proteínas del Complejo de Cadena de Transporte de Electrón/química , Mitocondrias/metabolismo , Acanthamoeba castellanii/genética , Secuencia de Aminoácidos , Biología Computacional , Transporte de Electrón , Proteínas del Complejo de Cadena de Transporte de Electrón/fisiología , Complejo I de Transporte de Electrón/análisis , Complejo I de Transporte de Electrón/química , Complejo I de Transporte de Electrón/fisiología , Complejo II de Transporte de Electrones/análisis , Complejo II de Transporte de Electrones/fisiología , Complejo III de Transporte de Electrones/análisis , Complejo III de Transporte de Electrones/fisiología , Complejo IV de Transporte de Electrones/análisis , Complejo IV de Transporte de Electrones/fisiología , Evolución Molecular , Datos de Secuencia Molecular , ProteomaRESUMEN
Multiple sclerosis is the most common cause of non-traumatic neurological impairment in young adults. An energy deficient state has been implicated in the degeneration of axons, the pathological correlate of disease progression, in multiple sclerosis. Mitochondria are the most efficient producers of energy and play an important role in calcium homeostasis. We analysed the density and function of mitochondria using immunohistochemistry and histochemistry, respectively, in chronic active and inactive lesions in progressive multiple sclerosis. As shown before in acute pattern III and Balo's lesions, the mitochondrial respiratory chain complex IV activity is reduced despite the presence of mitochondria in demyelinated axons with amyloid precursor protein accumulation, which are predominantly located at the active edge of chronic active lesions. Furthermore, the strong non-phosphorylated neurofilament (SMI32) reactivity was associated with a significant reduction in complex IV activity and mitochondria within demyelinated axons. The complex IV defect associated with axonal injury may be mediated by soluble products of innate immunity, as suggested by an inverse correlation between complex IV activity and macrophage/microglial density in chronic lesions. However, in inactive areas of chronic multiple sclerosis lesions the mitochondrial respiratory chain complex IV activity and mitochondrial mass, judged by porin immunoreactivity, are increased within approximately half of large (>2.5 microm diameter) chronically demyelinated axons compared with large myelinated axons in the brain and spinal cord. The axon-specific mitochondrial docking protein (syntaphilin) and phosphorylated neurofilament-H were increased in chronic lesions. The lack of complex IV activity in a proportion of Na(+)/K(+) ATPase alpha-1 positive demyelinated axons supports axonal dysfunction as a contributor to neurological impairment and disease progression. Furthermore, in vitro studies show that inhibition of complex IV augments glutamate-mediated axonal injury (amyloid precursor protein and SMI32 reactivity). Our findings have important implications for both axonal degeneration and dysfunction during the progressive stage of multiple sclerosis.
Asunto(s)
Axones/ultraestructura , Encéfalo/ultraestructura , Complejo IV de Transporte de Electrones/metabolismo , Mitocondrias/ultraestructura , Esclerosis Múltiple/patología , Médula Espinal/ultraestructura , Adulto , Anciano , Anciano de 80 o más Años , Animales , Autopsia , Axones/metabolismo , Western Blotting/métodos , Encéfalo/metabolismo , Células Cultivadas , Enfermedad Crónica , Complejo II de Transporte de Electrones/análisis , Complejo II de Transporte de Electrones/metabolismo , Complejo IV de Transporte de Electrones/análisis , Complejo IV de Transporte de Electrones/antagonistas & inhibidores , Femenino , Ácido Glutámico/farmacología , Humanos , Inmunohistoquímica , Masculino , Ratones , Microscopía Electrónica , Persona de Mediana Edad , Mitocondrias/metabolismo , Esclerosis Múltiple/metabolismo , Azida Sódica/farmacología , Médula Espinal/metabolismoRESUMEN
The mitochondrial metabolic pathway of the parasitic nematode Ascaris suum changes dramatically during its life cycle, to adapt to changes in the environmental oxygen concentration. We previously showed that A. suum mitochondria express stage-specific isoforms of complex II (succinate-ubiquinone reductase: SQR/quinol-fumarate reductase: QFR). The flavoprotein (Fp) and small subunit of cytochrome b (CybS) in adult complex II differ from those of infective third stage larval (L3) complex II. However, there is no difference in the iron-sulfur cluster (Ip) or the large subunit of cytochrome b (CybL) between adult and L3 isoforms of complex II. In the present study, to clarify the changes that occur in the respiratory chain of A. suum larvae during their migration in the host, we examined enzymatic activity, quinone content and complex II subunit composition in mitochondria of lung stage L3 (LL3) A. suum larvae. LL3 mitochondria showed higher QFR activity ( approximately 160 nmol/min/mg) than mitochondria of A. suum at other stages (L3: approximately 80 nmol/min/mg; adult: approximately 70 nmol/min/mg). Ubiquinone content in LL3 mitochondria was more abundant than rhodoquinone ( approximately 1.8 nmol/mg versus approximately 0.9 nmol/mg). Interestingly, the results of two-dimensional bule-native/sodium dodecyl sulfate polyacrylamide gel electrophoresis analyses showed that LL3 mitochondria contained larval Fp (Fp(L)) and adult Fp (Fp(A)) at a ratio of 1:0.56, and that most LL3 CybS subunits were of the adult form (CybS(A)). This clearly indicates that the rearrangement of complex II begins with a change in the isoform of the anchor CybS subunit, followed by a similar change in the Fp subunit.
Asunto(s)
Ascariasis/parasitología , Ascaris suum/enzimología , Complejo II de Transporte de Electrones/metabolismo , Mitocondrias Musculares/enzimología , Migración Animal/fisiología , Animales , Anticuerpos Antihelmínticos/análisis , Anticuerpos Antihelmínticos/metabolismo , Ascariasis/enzimología , Ascaris suum/crecimiento & desarrollo , Ascaris suum/fisiología , Western Blotting , Complejo II de Transporte de Electrones/análisis , Complejo II de Transporte de Electrones/química , Electroforesis en Gel de Poliacrilamida , Larva/enzimología , Larva/fisiología , Oxidorreductasas/análisis , Oxidorreductasas/metabolismo , Subunidades de Proteína/análisis , Subunidades de Proteína/metabolismo , Quinonas/análisis , ConejosRESUMEN
We introduce high resolution clear native electrophoresis (CNE) as a powerful technique to resolve enzymatically active mitochondrial complexes from cultured human cell lines and skeletal muscle biopsy samples. Quantitative enzymatic assays can be performed using small amounts of cultured cells with low mitochondria content, for example, around 10 mg of sedimented osteosarcoma cells (wet weight) which is equivalent to around 10 million cells. High resolution CNE offers general advantages for in-gel catalytic activity assays compared to blue native electrophoresis. It seems especially suited for assaying mitochondrial ATP synthase and respiratory chain complexes I and II in cell models of human mitochondrial disorders and for detailed analyses of patient cells and tissues with defects in oxidative phosphorylation.
Asunto(s)
Complejo III de Transporte de Electrones/análisis , Complejo II de Transporte de Electrones/análisis , Complejo IV de Transporte de Electrones/análisis , Complejo I de Transporte de Electrón/análisis , Electroforesis en Gel de Poliacrilamida/métodos , Proteínas Mitocondriales/análisis , Fosforilación Oxidativa , Bioensayo , Biopsia , Catálisis , Línea Celular , Digitonina/química , Electroforesis en Gel Bidimensional , Humanos , Mitocondrias Musculares/enzimología , Reproducibilidad de los Resultados , Manejo de EspecímenesRESUMEN
Mitochondrial parameters in peripheral blood mononuclear cells (PBMC) and their relationship with mitochondrially-driven PBMC apoptosis were investigated in a group of HIV-1-infected long-term nonprogressors (LTNP) and compared with untreated asymptomatic HIV-1 infected typical progressors (TP) and uninfected healthy controls (HC). Twenty-six LTNP, 27 TP and 31 HC were evaluated. Studies were performed in PBMCs. Mitochondrial DNA content (mtDNA) was assessed by quantitative real-time PCR. Activities of mitochondrial respiratory chain complexes (MRC) II, III and IV were determined by spectrophotometry. Caspase-3 activity was assessed by fluorimetry, and caspase-9 activation and Bcl-2 levels were assessed by immunoblotting. mtDNA abundance (p<0.05), MRC complex II (p<0.001), complex III (p<0.01) and complex IV (p=0.01) were lower in the TP group than in the HC group. In the LTNP group these parameters were similar to those of the HC group except for complex II, which was decreased (p<0.01). The PBMC of TP showed the highest overall apoptotic activation, since their caspase-3 activity was greater than that of HC (p<0.05) and LTNP. In the case of LTNP, however, the difference was non-significant. Caspase-9 and the caspase-9/Bcl-2 ratio were both over-expressed in TP compared to HC (p<0.01) and LTNP (p<0.05). Both of these measurements indicate that mitochondrially-driven apoptosis in TP is greater than in LTNP and HC. A relationship between mitochondrial damage and apoptotic activation was found in TP. Mitochondrial damage is associated with increased PBMC apoptosis in patients with active HIV-1 replication (TP). These abnormalities are slight or not present in LTNP.
Asunto(s)
Infecciones por VIH/patología , Sobrevivientes de VIH a Largo Plazo , Leucocitos Mononucleares/patología , Mitocondrias/patología , Adulto , Apoptosis , Caspasa 3/análisis , Caspasa 9/análisis , Células Cultivadas , ADN Mitocondrial/análisis , Complejo II de Transporte de Electrones/análisis , Complejo II de Transporte de Electrones/metabolismo , Complejo III de Transporte de Electrones/análisis , Complejo III de Transporte de Electrones/metabolismo , Complejo IV de Transporte de Electrones/análisis , Complejo IV de Transporte de Electrones/metabolismo , Femenino , Fluorometría , VIH-1/crecimiento & desarrollo , Humanos , Immunoblotting , Leucocitos Mononucleares/química , Leucocitos Mononucleares/citología , Masculino , Persona de Mediana Edad , Mitocondrias/genética , Reacción en Cadena de la Polimerasa/métodos , Proteínas Proto-Oncogénicas c-bcl-2/análisis , EspectrofotometríaRESUMEN
Clear native electrophoresis and blue native electrophoresis are microscale techniques for the isolation of membrane protein complexes. The Coomassie Blue G-250 dye, used in blue native electrophoresis, interferes with in-gel fluorescence detection and in-gel catalytic activity assays. This problem can be overcome by omitting the dye in clear native electrophoresis. However, clear native electrophoresis suffers from enhanced protein aggregation and broadening of protein bands during electrophoresis and therefore has been used rarely. To preserve the advantages of both electrophoresis techniques we substituted Coomassie dye in the cathode buffer of blue native electrophoresis by non-colored mixtures of anionic and neutral detergents. Like Coomassie dye, these mixed micelles imposed a charge shift on the membrane proteins to enhance their anodic migration and improved membrane protein solubility during electrophoresis. This improved clear native electrophoresis offers a high resolution of membrane protein complexes comparable to that of blue native electrophoresis. We demonstrate the superiority of high resolution clear native electrophoresis for in-gel catalytic activity assays of mitochondrial complexes I-V. We present the first in-gel histochemical staining protocol for respiratory complex III. Moreover we demonstrate the special advantages of high resolution clear native electrophoresis for in-gel detection of fluorescent labeled proteins labeled by reactive fluorescent dyes and tagged by fluorescent proteins. The advantages of high resolution clear native electrophoresis make this technique superior for functional proteomics analyses.
Asunto(s)
Complejo III de Transporte de Electrones/análisis , Complejo II de Transporte de Electrones/análisis , Complejo IV de Transporte de Electrones/análisis , Complejo I de Transporte de Electrón/análisis , Proteínas Mitocondriales/análisis , Tampones (Química) , Colorantes , Detergentes , Electroforesis en Gel de Poliacrilamida/métodos , Micelas , Colorantes de RosanilinaRESUMEN
BACKGROUND: A reliable and sensitive complex I assay is an essential tool for the diagnosis of mitochondrial disorders, but current spectrophotometric assays suffer from low sensitivity, low specificity, or both. This deficiency is mainly due to the poor solubility of coenzyme-Q analogs and reaction mixture turbidity caused by the relatively high concentrations of tissue extract that are often required to measure complex I. METHODS: We developed a new spectrophotometric assay to measure complex I in mitochondrial fractions and applied it to muscle and cultured fibroblasts. The method is based on measuring 2,6-dichloroindophenol reduction by electrons accepted from decylubiquinol, reduced after oxidation of NADH by complex I. The assay thus is designed to avoid nonspecific NADH oxidation because electrons produced in these reactions are not accepted by decylubiquinone, resulting in high rotenone sensitivity. RESULTS: The assay was linear with time and amount of mitochondria. The K(m) values for NADH and 2,6-dichloroindophenol in muscle mitochondria were 0.04 and 0.017 mmol/L, respectively. The highest complex I activities were measured with 0.07 mmol/L decylubiquinone and 3.5 g/L bovine serum albumin. The latter was an essential component of the reaction mixture, increasing the solubility of decylubiquinone and rotenone. In patients with previously diagnosed complex I deficiencies, the new assay detected the complex I deficiencies in both muscle and fibroblasts. CONCLUSIONS: This spectrophotometric assay is reproducible, sensitive, and specific for complex I activity because of its high rotenone sensitivity, and it can be applied successfully to the diagnosis of complex I deficiencies.
Asunto(s)
Complejo I de Transporte de Electrón/análisis , Fibroblastos/química , Mitocondrias/química , Músculo Esquelético/química , Piel/química , Células Cultivadas , Complejo I de Transporte de Electrón/deficiencia , Complejo I de Transporte de Electrón/genética , Complejo II de Transporte de Electrones/análisis , Humanos , Enfermedades Mitocondriales/diagnóstico , Músculo Esquelético/citología , Reproducibilidad de los Resultados , Sensibilidad y Especificidad , Piel/citología , EspectrofotometríaRESUMEN
Utilizando las técnicas moleculares de SSCP y RAPD se pudo evidenciar rápida y claramente la variabilidad genética en Colombia de larvas del céstodo Taenia solium analizando fragmentos de genes de ADN mitocondrial y fragmentos aleatorios de ADN nuclear. El ADN estudiado se obtuvo de ocho aislados de cisticercos de cerdo provenientes de tres departamentos de Colombia: Antioquia, Nariño y Sucre. Los fragmentos obtenidos por PCR de los genes NADH deshidrogenasa 1 (ND1) y citocromo oxidasa c subunidad I (COI) al ser denaturados y analizados en geles no denaturantes de acrilamida, mostraron al menos tres patrones diferentes por cada gen analizado, verificando que estos genes conservados mitocondriales son polimórficos en T. solium colombiana. Por otra parte, los cebadores decaméricos de RAPD produjeron patrones polimórficos, corroboraron la diversidad genética entre los diferentes aislamientos analizados.
Asunto(s)
Animales , Marcadores Genéticos , Variación Genética , Reacción en Cadena de la Polimerasa/métodos , Taenia solium/crecimiento & desarrollo , Taenia solium/genética , ADN Mitocondrial/análisis , Colombia , Complejo II de Transporte de Electrones/análisis , Datos de Secuencia Molecular , NADH Deshidrogenasa/análisis , Polimorfismo Genético , Polimorfismo Conformacional Retorcido-Simple , Técnica del ADN Polimorfo Amplificado Aleatorio , Porcinos , Taenia solium/aislamiento & purificaciónRESUMEN
Antinecrotic activity of 2-ethyl-6-methyl-3 oxipyridin succinate (mexidol) and pentoxifylline (trental) was investigated on 32 mail rats with average body-weight of 170-220 g. Under the influence of mexidol and trental, which were injected 15 min before the insection of skin graft and then once per day during 3 days, necrotized area of skin graft is reduced by 22 and 15%, the amount of lost keranocytes--by 33 and 30%. In skin graft homogenates under the influence of mexidol rises the reduced under ischemia succinate dehydrogenase activity, while under trental influence it does not change. Under the influence of mexidol and trental on third day content of ATP rises by 29,5 and 19,5 %, ADP increases and decreases by 27%, creatinphosphate--by 33 and 21% correspondingly. Trentale improves elasticity of erythrocytes. It is suggested, that positive effect of mexidol on skin graft is conditioned by its ability to activate succinate-dependent detour in oxygen phosphorilation chain of mitochondries and to raise content of ubiquinone, whereas the effect of trental relates with intensification of microcirculation, delivery of oxygen on periphery. That allows recommending combined use of preparations in ischemia of skin.
Asunto(s)
Supervivencia de Injerto/efectos de los fármacos , Pentoxifilina/farmacología , Picolinas/farmacología , Trasplante de Piel/patología , Piel/irrigación sanguínea , Colgajos Quirúrgicos/patología , Adenosina Difosfato/análisis , Adenosina Trifosfato/análisis , Animales , Complejo II de Transporte de Electrones/análisis , Isquemia/patología , Queratinocitos/efectos de los fármacos , Masculino , Necrosis/patología , Fosfocreatina/análisis , Ratas , Piel/citologíaRESUMEN
Reamberin in a dose of 25 mg/kg (succinate concentration) was injected intravenously for 3 days starting from the 1st hour after skin ischemia modeling. This treatment decreased activities of lactate dehydrogenase, aspartate transaminase, and creatine phosphokinase in skin homogenates by 1.6 times, 19%, and 51.3%, respectively. The index of cytolysis decreased by 18%. Reamberin had an energotropic effect, which manifested in an increase in the total ATP content and concentration of creatine phosphate (by 16 and 10%, respectively). After administration of Reamberin, activity of the succinate-ubiquinone reductase system increased by 17%. Under these conditions succinate dehydrogenase activity exceeded the normal by 21%. Reamberin had no effect on the mitochondrial NADH-ubiquinone reductase system in dermal cells during skin ischemia. Superoxide dismutase activity in the area of necrosis increased to the control level on day 3 of treatment with Reamberin. Activities of catalase and glutathione peroxidase increased by 13 and 19%, respectively. Our results indicate that the course of intravenous treatment with Reamberin for 3 days contributes to an increase in reserve capacities of the antioxidant protection system and produces a protective effect during skin ischemia.
Asunto(s)
Antioxidantes/administración & dosificación , Isquemia/prevención & control , Mitocondrias/efectos de los fármacos , Piel/irrigación sanguínea , Piel/efectos de los fármacos , Succinatos/administración & dosificación , Adenosina Trifosfato/análisis , Adenosina Trifosfato/metabolismo , Animales , Aspartato Aminotransferasas/análisis , Aspartato Aminotransferasas/metabolismo , Creatina Quinasa/análisis , Creatina Quinasa/metabolismo , Complejo II de Transporte de Electrones/análisis , Complejo II de Transporte de Electrones/metabolismo , Isquemia/enzimología , L-Lactato Deshidrogenasa/análisis , L-Lactato Deshidrogenasa/metabolismo , Masculino , Fosfocreatina/análisis , Fosfocreatina/metabolismo , Ratas , Ratas Endogámicas , Piel/enzimología , Superóxido Dismutasa/análisis , Superóxido Dismutasa/metabolismoRESUMEN
Respiratory oxidative phosphorylation represents a central functionality in plant metabolism, but the subunit composition of the respiratory complexes in plants is still being defined. Most notably, complex II (succinate dehydrogenase) and complex IV (cytochrome c oxidase) are the least defined in plant mitochondria. Using Arabidopsis mitochondrial samples and 2D Blue-native/SDS-PAGE, we have separated complex II and IV from each other and displayed their individual subunits for analysis by tandem mass spectrometry and Edman sequencing. Complex II can be discretely separated from other complexes on Blue-native gels and consists of eight protein bands. It contains the four classical SDH subunits as well as four subunits unknown in mitochondria from other eukaryotes. Five of these proteins have previously been identified, while three are newly identified in this study. Complex IV consists of 9-10 protein bands, however, it is more diffuse in Blue-native gels and co-migrates in part with the translocase of the outer membrane (TOM) complex. Differential analysis of TOM and complex IV reveals that complex IV probably contains eight subunits with similarity to known complex IV subunits from other eukaryotes and a further six putative subunits which all represent proteins of unknown function in Arabidopsis . Comparison of the Arabidopsis data with Blue-native/SDS-PAGE separation of potato and bean mitochondria confirmed the protein band complexity of these two respiratory complexes in plants. Two-dimensional Blue-native/Blue-native PAGE, using digitonin followed by dodecylmaltoside in successive dimensions, separated a diffusely staining complex containing both TOM and complex IV. This suggests that the very similar mass of these complexes will likely prevent high purity separations based on size. The documented roles of several of the putative complex IV subunits in hypoxia response and ozone stress, and similarity between new complex II subunits and recently identified plant specific subunits of complex I, suggest novel biological insights can be gained from respiratory complex composition analysis.
Asunto(s)
Complejo II de Transporte de Electrones/análisis , Complejo IV de Transporte de Electrones/análisis , Proteínas de Plantas/análisis , Secuencia de Aminoácidos , Arabidopsis/genética , Arabidopsis/metabolismo , Complejo II de Transporte de Electrones/química , Complejo II de Transporte de Electrones/genética , Complejo IV de Transporte de Electrones/química , Complejo IV de Transporte de Electrones/genética , Electroforesis en Gel Bidimensional/métodos , Fabaceae/genética , Fabaceae/metabolismo , Espectrometría de Masas/métodos , Datos de Secuencia Molecular , Proteínas de Plantas/química , Proteínas de Plantas/genética , Análisis de Secuencia de Proteína , Homología de Secuencia de Aminoácido , Solanum tuberosum/genética , Solanum tuberosum/metabolismoRESUMEN
This study addresses an application of pyridine nucleotide enzymatic analyses to evaluate the activity of the mitochondrial electron transport chain (reduced nicotinamide adenine dinucleotide (NADH) oxidase) and Complexes I and II in samples of human muscle as small as approximately 10 mg wet weight. Key aspects in this adaptation are the use of high-performance liquid chromatography with fluorescence detection of NADH and use of alamethicin, a channel-forming antibiotic that enables an unrestricted access of substrates into the mitochondrial matrix. The procedure includes disintegration of tissue by Polytron homogenizer, extraction of myosin from myofibrillar fragments by KCl/pyrophosphate to facilitate release of mitochondria, and preparation of fractions of subsarcolemmal and intermyofibrillar mitochondria. Oxidation of NADH or succinate is assayed in the presence of 40 microg/ml alamethicin and the reaction is terminated by H(2)SO(4), which also destroys the remaining NADH. Nicotinamide adenine dinucleotide (NAD) or fumarate concentrations are measured using alcohol dehydrogenase or fumarase plus malic dehydrogenase reactions, respectively. Generation of NADH, assessed in auxiliary reactions in the presence of hydrazine, is strictly proportional to NAD or fumarate content across a concentration range of 1-20 microM. NADH is quantitatively analyzed with a detection limit of 3-5 pmol by HPLC using a reverse-phase Hypersil ODS column connected to a fluorescence detector.
Asunto(s)
Cromatografía Líquida de Alta Presión/métodos , Complejo II de Transporte de Electrones/análisis , Complejo I de Transporte de Electrón/análisis , Mitocondrias Musculares/enzimología , Músculo Esquelético/enzimología , NAD/química , Alameticina/química , Transporte de Electrón , Humanos , Oxidación-Reducción , Sensibilidad y Especificidad , Ácido Succínico/química , Ácidos Sulfúricos/químicaRESUMEN
Pulmonary hypertension syndrome (PHS) is a metabolic disease associated with the rapid growth rate of modern broilers. Broilers susceptible to PHS experience sustained elevation of pulmonary arterial pressure leading to right ventricular hypertrophy and ultimately heart failure. Previous studies have shown that mitochondrial function is defective in broilers with PHS; they use oxygen less efficiently than broilers without PHS. In this study mitochondrial electron transport chain (ETC) protein levels were compared in cardiac tissues from PHS resistant and susceptible line broilers using quantitative immunoblots. Seven of 9 anti-mammalian mitochondrial ETC protein antibodies tested exhibited cross-species reactivity. Six ETC proteins were differentially expressed in the right ventricles of broilers raised under simulated high altitude conditions (2,900 m above sea level). Four ETC proteins were present at higher levels in resistant line birds without PHS than in resistant line birds with PHS or in susceptible line birds with or without PHS. One ETC protein was present at higher levels in broilers without PHS than in broilers with PHS in both lines, and one ETC protein was present at lower levels in susceptible line birds without PHS than in susceptible line birds with PHS or in resistant line birds with or without PHS. Interestingly, differential expression of mitochondrial ETC proteins was not observed in the right ventricles of broilers raised at local altitude (390 m above sea level) nor was it observed in the left ventricles of broilers exposed to simulated high altitude. These results suggest that higher levels of mitochondrial ETC proteins in right ventricle cardiac muscle may be correlated with resistance to PHS in broilers.