RESUMEN
Comment on: Yien Y, et al. TMEM14C is required for erythroid mitochondrial heme metabolism. J. Clin. Invest. 2014; 124:4294-4304.
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Células Eritroides/metabolismo , Mitocondrias/metabolismo , Protoporfirinas/fisiología , Animales , Transporte Biológico , Hemo/química , Homeostasis , Humanos , Ratones , Análisis de Secuencia de ARN , Pez CebraRESUMEN
5-Aminolevulinic acid (ALA), the committed intermediate of the heme biosynthesis pathway, shows significant promise for cancer treatment. Here, we identified that in addition to hemA and hemL, hemB, hemD, hemF, hemG and hemH are also the major regulatory targets of the heme biosynthesis pathway. Interestingly, up-regulation of hemD and hemF benefited ALA accumulation whereas overexpression of hemB, hemG and hemH diminished ALA accumulation. Accordingly, by combinatorial overexpression of the hemA, hemL, hemD and hemF with different copy-number plasmids, the titer of ALA was improved to 3.25 g l(-1). Furthermore, in combination with transcriptional and enzymatic analysis, we demonstrated that ALA dehydratase (HemB) encoded by hemB is feedback inhibited by the downstream intermediate protoporphyrinogen IX. This work has great potential to be scaled-up for microbial production of ALA and provides new important insights into the regulatory mechanism of the heme biosynthesis pathway.
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Ácido Aminolevulínico/metabolismo , Escherichia coli/genética , Hemo/biosíntesis , Vías Biosintéticas , Clonación Molecular , Represión Enzimática , Escherichia coli/enzimología , Proteínas de Escherichia coli/genética , Proteínas de Escherichia coli/metabolismo , Ferroquelatasa/genética , Ferroquelatasa/metabolismo , Regulación Bacteriana de la Expresión Génica , Porfobilinógeno Sintasa/genética , Porfobilinógeno Sintasa/metabolismo , Protoporfirinógeno-Oxidasa/genética , Protoporfirinógeno-Oxidasa/metabolismo , Protoporfirinas/fisiología , Regulación hacia ArribaRESUMEN
BACKGROUND: Previous research on fluorescence detection of non-melanoma had mixed results. An accurate non-invasive method for the detection of skin cancer is valuable to dermatologists because of the high incidence of skin cancer among the aging population. One notable difference between the methods of fluorescence detection previously studied was the use of the auto-fluorescence of the skin. Currently, there has not been a direct comparison between both methods of fluorescence detection. OBJECTIVE: To compare the accuracy of PpIX fluorescence and auto-fluorescence normalized PpIX fluorescence detection systems for the localization non-melanoma skin cancers (NMSC). METHODS: We conducted an observer blinded direct comparison of both methods. Thirty patients, 14 females and16 males, mean age 62 (SD = 9 years), skin type I to III and being suspected of having one or more NMSC, visited an independent treatment centre for dermatology. The patients were investigated using a fluorescence detection system capable of both normalized and non-normalized PpIX fluorescence measurements. Liposomal encapsulated 5-aminolevulinic acid was used as a photosensitizer. For each area being investigated, the associated normalized and non-normalized fluorescence measurements were directly compared. The results of the analysis were confirmed by clinical investigation using a dermatoscope. Both methods were evaluated based on the number of true and false positives and the number of true and false negatives. Specificity and sensitivity were calculated. Statistical significance of the findings was determined using Pearson's Chi-squared test. RESULTS: The non-normalized method was found to have a sensitivity of 27 % and a specificity of 39 % and the normalized method has a sensitivity of 97% and a specificity of 100%. This difference is statistically significant (p < 0.05). CONCLUSION: Using auto-fluorescence in PpIX fluorescence detection of NMSC is more accurate that PpIX fluorescence detection alone.
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Ácido Aminolevulínico , Biomarcadores de Tumor/fisiología , Carcinoma/diagnóstico , Queratosis Actínica/diagnóstico , Fármacos Fotosensibilizantes , Protoporfirinas/fisiología , Neoplasias Cutáneas/diagnóstico , Biomarcadores de Tumor/metabolismo , Enfermedad de Bowen/diagnóstico , Enfermedad de Bowen/metabolismo , Enfermedad de Bowen/fisiopatología , Carcinoma/metabolismo , Carcinoma/fisiopatología , Carcinoma Basocelular/diagnóstico , Carcinoma Basocelular/metabolismo , Carcinoma Basocelular/fisiopatología , Reacciones Falso Negativas , Reacciones Falso Positivas , Femenino , Fluorescencia , Humanos , Queratosis Actínica/metabolismo , Queratosis Actínica/fisiopatología , Masculino , Persona de Mediana Edad , Protoporfirinas/metabolismo , Sensibilidad y Especificidad , Método Simple Ciego , Neoplasias Cutáneas/metabolismo , Neoplasias Cutáneas/fisiopatología , Espectrometría de FluorescenciaRESUMEN
Photodynamic therapy (PDT) may cause tumour cell destruction by direct toxicity or by inducing microcirculatory shutdown. Protoporphyrin IX generated from 5-aminolevulinic acid (ALA) has been widely used as an endogenous photosensitiser in PDT. However, the hydrophilic nature of the ALA molecule limits its penetration through the stratum corneum of the skin and cell membranes and thus, ALA alkyl-esters have been developed to improve ALA permeation. The aim of this work was to study Protoporphyrin IX synthesis from ALA and its derivatives ALA methyl ester (Me-ALA) and ALA hexyl ester (He-ALA) in the microvascular endothelial cell line HMEC-1 derived from normal skin, and to evaluate their response to PDT. We found that lower light doses are required to photosensitise HMEC-1 endothelial cells than to photosensitise PAM212 transformed keratinocytes, showing some possible selectivity of ALA-PDT for vascularisation in skin. Employed at concentrations leading to equal Protoporphyrin IX synthesis, ALA, He-ALA and Me-ALA presented the same efficacy of HMEC-1 photosensitisation. However, He-ALA was a promising compound for the use in the enhancement of Protoporphyrin IX in HMEC-1 cells employed at low concentrations at both short and long time exposures whereas Me-ALA should be employed at high concentrations and longer time periods in order to surpass the Protoporphyrin IX levels obtained with ALA. The advantage of Me-ALA over ALA was based on its lower dark toxicity. This is the first work to report vascular cell photosensitisation employing alkyl-esters of ALA, and we demonstrated that these derivatives could exert the same effect as ALA and under certain conditions enhance photosensitisation of vasculature.
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Ácido Aminolevulínico/análogos & derivados , Ácido Aminolevulínico/metabolismo , Células Endoteliales/metabolismo , Fotoquimioterapia , Fármacos Fotosensibilizantes/metabolismo , Protoporfirinas/biosíntesis , Animales , Línea Celular , Células Endoteliales/efectos de la radiación , Humanos , Protoporfirinas/fisiología , Rayos UltravioletaRESUMEN
Human erythropoiesis is a complex multistep developmental process that begins at the level of pluripotent hematopoietic stem cells (HSCs) at bone marrow microenvironment (HSCs niche) and terminates with the production of erythrocytes (RBCs). This review covers the basic and contemporary aspects of erythropoiesis. These include the: (a) cell-lineage restricted pathways of differentiation originated from HSCs and going downward toward the blood cell development; (b) model systems employed to study erythropoiesis in culture (erythroleukemia cell lines and embryonic stem cells) and in vivo (knockout animals: avian, mice, zebrafish, and xenopus); (c) key regulators of erythropoiesis (iron, hypoxia, stress, and growth factors); (d) signaling pathways operating at hematopoietic stem cell niche for homeostatic regulation of self renewal (SCF/c-kit receptor, Wnt, Notch, and Hox) and for erythroid differentiation (HIF and EpoR). Furthermore, this review presents the mechanisms through which transcriptional factors (GATA-1, FOG-1, TAL-1/SCL/MO2/Ldb1/E2A, EKLF, Gfi-1b, and BCL11A) and miRNAs regulate gene pattern expression during erythroid differentiation. New insights regarding the transcriptional regulation of alpha- and beta-globin gene clusters were also presented. Emphasis was also given on (i) the developmental program of erythropoiesis, which consists of commitment to terminal erythroid maturation and hemoglobin production, (two closely coordinated events of erythropoieis) and (ii) the capacity of human embryonic and umbilical cord blood (UCB) stem cells to differentiate and produce RBCs in culture with highly selective media. These most recent developments will eventually permit customized red blood cell production needed for transfusion.
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Diferenciación Celular/fisiología , Eritropoyesis/fisiología , Regulación de la Expresión Génica/fisiología , Células Madre Hematopoyéticas/citología , Modelos Animales , Modelos Biológicos , Transducción de Señal/fisiología , Animales , Línea Celular , Células Madre Hematopoyéticas/fisiología , Humanos , Factor 1 Inducible por Hipoxia/fisiología , Ratones , Protoporfirinas/fisiologíaRESUMEN
Fhit, the product of tumor suppressor fragile histidine triad (FHIT) gene, exhibits antitumor activity of still largely unknown cellular background. However, it is believed that Fhit-Ap(3)A or Fhit-AMP complex might act as a second class messenger in cellular signal transduction pathway involved in cell proliferation and apoptosis. We demonstrate here for the first time that the photosensitizer, protoporphyrin IX (which is a natural precursor of heme) binds to Fhit protein and its mutants in the active site in vitro. Furthermore, PpIX inhibits the enzymatic activity of Fhit. Simultaneously, PpIX shows lower binding capacity to mutant Fhit-H96N of highly reduced hydrolase activity. In cell-based assay PpIX induced HeLa cell death in Fhit and Fhit-H96N-dependent manner which was measured by means of MTT assay. Moreover, HeLa cells stably expressing Fhit or mutant Fhit-H96N were more susceptible to protoporphyrin IX-mediated photodynamic therapy (2J/cm(2)) than parental cells.
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Ácido Anhídrido Hidrolasas/metabolismo , Proteínas de Neoplasias/metabolismo , Fotoquimioterapia , Protoporfirinas/metabolismo , Ácido Anhídrido Hidrolasas/antagonistas & inhibidores , Ácido Anhídrido Hidrolasas/genética , Ácido Anhídrido Hidrolasas/fisiología , Supervivencia Celular , Células HeLa , Humanos , Mutación , Proteínas de Neoplasias/antagonistas & inhibidores , Proteínas de Neoplasias/genética , Proteínas de Neoplasias/fisiología , Fármacos Fotosensibilizantes , Unión Proteica/genética , Protoporfirinas/fisiología , Sistemas de Mensajero SecundarioRESUMEN
Many small passerine birds worldwide lay white eggs speckled with red, brown and black protoporphyrin pigment spots (maculation). Unlike some patterns of avian eggshell pigmentation which clearly serve a crypsis or signalling function, the ubiquity of maculation among passerines suggests that its origins lie in another function, not specific to any particular ecological or behavioural group. Elsewhere, we have presented evidence that protoporphyrin pigments serve a structural function related to eggshell thickness and calcium availability: eggshell maculation in the great tit Parus major increases with decreasing soil calcium levels, pigments demarcate thinner areas of shell, and both the pigment intensity and distribution are related to shell thickness. Here we show that maculation also affects the rate of water loss from the egg during incubation (approximately Mass Loss per Day or MLD, which is critical to egg viability), but not that of unincubated eggs. We also demonstrate, both by observation and experiment, that the effect of female incubation behaviour on MLD compensates in some way for variation in egg characteristics, and that differences between females in the degree of such compensation are related to differences in clutch maculation. Our results suggest that, while a principal function of maculation in this species may be to strengthen the eggshell, it may also reduce eggshell permeability when large amounts of pigment are used, and that this necessitates a behavioural adjustment from the female during incubation. We discuss these findings and make further testable predictions from our model.
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Comportamiento de Nidificación/fisiología , Óvulo/fisiología , Pigmentación/fisiología , Pájaros Cantores/fisiología , Agua/fisiología , Animales , Femenino , Protoporfirinas/fisiologíaRESUMEN
OBJECTIVE: Photodynamic therapy of Walker tumor after subcutaneous administration of 5-ALA solution using a multiple laser irradiation scheme was monitored by the fluorescence imaging technique to investigate the effectiveness of 5-ALA-PDT. BACKGROUND DATA: Photodynamic therapy (PDT) is a localized cancer treatment based on the selective uptake and retention of photosensitizer at the tumoral level and on the activation of the photosensitizer by a specific wavelength of light, aiming to induce cytotoxic reactions. As a new photosensitizer, the heme precursor 5- aminolevulinic acid has been introduced recently for photodynamic therapy of tumors and precancerous lesions of the skin. It has been shown that the efficacy of topical 5-ALA-PDT is limited for deeper skin tumor by the depth of 5-ALA penetration through the skin. Oral or systemic administration of ALA or the use of different irradiation schemes may improve tumor response to PDT. METHODS: Laser irradiation parameters used in this study were lambda = 635 nm, P = 3 mW, t(exp) = 300 sec, and three sessions. The fluorescence was excitated by monochromatic light of 405 nm. The temporal behavior of PpIX fluorescence was studied by processing and analyzing the fluorescence images acquired just after applying 5-ALA, just before and just after three laser irradiations. RESULTS: The results demonstrate that PpIX is highly selective for tumors areas and a re-accumulation of PpIX appears between laser irradiations. During laser irradiation, the PpIX fluorescence intensity decreases rapidly, reflecting the photodegradation of PpIX. CONCLUSIONS: In conclusion, the use of a multiple laser irradiation scheme, for the activation of reaccumulation of Pp IX (with three steps) is effective for photodynamic therapy of Walker tumor.
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Ácido Aminolevulínico/farmacología , Carcinoma 256 de Walker/tratamiento farmacológico , Fotoquimioterapia/métodos , Fármacos Fotosensibilizantes/farmacología , Protoporfirinas/fisiología , Animales , Carcinoma 256 de Walker/fisiopatología , Carcinoma 256 de Walker/radioterapia , Trasplante de Neoplasias , Protoporfirinas/efectos de la radiación , RatasRESUMEN
This study investigated the role of heme oxygenase (HO)-1 in the cardiac tissue injury of acute ischemia/reperfusion (I/R) in diabetic streptozotocin (STZ)-induced hyperglycemic rats. The effects of 1) hemin, an inducer of HO expression and activity, and 2) zinc protoporphyrin IX (ZnPP-IX), an inhibitor of HO activity, have also been investigated on the tissue injury by I/R and some mediators released in these circumstances. STZ hyperglycemic rats had impaired levels of HO-1 within the cardiac tissue and increased myocardial infarct size (IS) following I/R, as compared with the nondiabetic rats. In these rats, administration of hemin 4 mg/kg 18 h before I/R increases the levels of HO-1 within the tissue. However, the values of HO-1 assayed in these circumstances were significantly lower (P < 0.01) than those assayed in nondiabetic animals subjected to the same procedures; IS was much more extended (P < 0.01) than in the parent nondiabetic group. STZ hyperglycemic rats also predisposed the heart to produce high levels of the cytokines interleukin (IL)-1beta and CXCL8. Subsequent I/R further increased (P < 0.01) the cytokine production, an effect partly prevented by hemin treatment. This recovered the huge number of infiltrated polymorphonuclear (PMN) leukocytes within the cardiac tissue associated with the STZ hyperglycemic state and I/R damage.
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Diabetes Mellitus Experimental/fisiopatología , Proteínas de Choque Térmico/fisiología , Hiperglucemia/fisiopatología , Infarto del Miocardio/patología , Daño por Reperfusión Miocárdica/patología , Miocardio/enzimología , Oxigenasas/fisiología , Animales , Antígeno CD11b/fisiología , Diabetes Mellitus Experimental/sangre , Diabetes Mellitus Experimental/enzimología , Expresión Génica , Proteínas de Choque Térmico/metabolismo , Hemo Oxigenasa (Desciclizante) , Hemina/fisiología , Hiperglucemia/enzimología , Hiperglucemia/patología , Leucocitos Mononucleares , Masculino , Infarto del Miocardio/sangre , Infarto del Miocardio/enzimología , Daño por Reperfusión Miocárdica/sangre , Daño por Reperfusión Miocárdica/enzimología , Miocardio/patología , Oxigenasas/metabolismo , Protoporfirinas/fisiología , Ratas , Ratas Sprague-DawleyRESUMEN
AIMS: The lipid-secreting exocrine Harderian gland contains a large amount of porphyrins (mainly protoporphyrin IX, PPIX) in the glandular cells, the physiological significance of which is rather poorly understood. METHODS: In the present study, the possibility of using Fura-2 to measure intracellular calcium ([Ca2+]c) changes in these cells was assessed. RESULTS: It was found that when Fura-2-loaded cells were excited by light at 340/380 nm, [Ca2+]c increased spontaneously, indicating a photodynamic action powered by light at 340/380 nm. In contrast, with the visible spectrum calcium probe Fluo-3 (lambda(ex) = 475 nm), carbachol at 10 microm induced [Ca2+]c increase; [Ca2+]c did not change without carbachol stimulation. Brief illumination with light at 340/380 nm induced a large [Ca2+]c increase in Fluo-3-loaded cells. Photodynamic stimulation of [Ca2+]c increase was confirmed with an exogenous photosensitizer sulphonated aluminium phthalocyanine (SALPC) and visible light (>580 nm). The wavelength-dependence of the [Ca2+]c increase correlates well with the excitation spectrum of the isolated Harderian glandular cells. CONCLUSION: These data suggest that PPIX present in rat Harderian glandular cells plays the role of a photosensitizer which upon activation by UVA and blue components of daylight and subsequent singlet oxygen generation, triggers [Ca2+]c increase and secretory response. The PPIX photodynamic action may also play a potential role in photic entrainment of the central circadian clock.
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Glándula de Harder/fisiología , Fármacos Fotosensibilizantes/farmacología , Protoporfirinas/fisiología , Animales , Calcio/metabolismo , Carbacol/farmacología , Células Cultivadas , Agonistas Colinérgicos/farmacología , Colorantes Fluorescentes , Fura-2/metabolismo , Glándula de Harder/efectos de los fármacos , Indoles/farmacología , Luz , Masculino , Compuestos Organometálicos/farmacología , Protoporfirinas/farmacología , Ratas , Ratas Sprague-Dawley , Rayos UltravioletaRESUMEN
The present study deals with photomodification of the electrical properties of the plasma membrane of an epithelial cell line (opossum kidney (OK) cells). The effect of photofrin II (previously investigated) is compared with that of 5 other membrane-active sensitizers: sulfonated Zn-phthalocyanine, merocyanine 540, rose bengal, methylene blue and protoporphyrin IX (an endogenous sensitizer induced by addition of its biosynthetic precursor 5-aminolaevulinic acid). The study was performed in order to investigate whether photomodification of the ion transport properties of the plasma membrane by membrane-active sensitizers is a general and early event in cellular photosensitization. The changes in the electrical properties were monitored by application of the whole-cell and the inside-out configuration of the patch-clamp technique. Illumination in the presence of the compounds (apart from merocyanine 540) gave rise to similar changes of the electrical properties of the membrane: depolarization of the membrane potential, inactivation of a large-conductance, Ca2+-dependent K+-channel (maxi-KCa), and a strong increase of the leak conductance of the membrane. This similarity indicates the general character of the functional photomodifications by membrane-active sensitizers previously reported for photofrin II.
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Membrana Celular/efectos de los fármacos , Potenciales de la Membrana/efectos de los fármacos , Fármacos Fotosensibilizantes/farmacología , Ácido Aminolevulínico/farmacología , Animales , Línea Celular/efectos de los fármacos , Línea Celular/efectos de la radiación , Membrana Celular/efectos de la radiación , Éter de Dihematoporfirina/farmacología , Conductividad Eléctrica , Indoles/farmacología , Transporte Iónico/efectos de los fármacos , Transporte Iónico/efectos de la radiación , Isoindoles , Riñón , Luz , Azul de Metileno/farmacología , Zarigüeyas , Compuestos Organometálicos/farmacología , Técnicas de Placa-Clamp , Fotoquímica , Protoporfirinas/biosíntesis , Protoporfirinas/fisiología , Pirimidinonas/farmacología , Rosa Bengala/farmacología , Compuestos de ZincRESUMEN
The polymerization of hemoglobin-derived ferric-protoporphyrin IX [Fe(III)PPIX] to inert hemozoin (malaria pigment) is a crucial and unique process for intraerythrocytic plasmodia to prevent heme toxicity and thus a good target for new antimalarials. Quinoline drugs, i.e., chloroquine, and non-iron porphyrins have been shown to block polymerization by forming electronic pi-pi interactions with heme monomers. Here, we report the identification of ferrous-protoporphyrin IX [Fe(II)PPIX] as a novel endogenous anti-malarial. Fe(II)PPIX molecules, released from the proteolysis of hemoglobin, are first oxidized and then polymerized to hemozoin. We obtained Fe(II)PPIX on preparative scale by electrochemical reduction of Fe(III)PPIX, and the reaction was monitored by cyclic voltammetry. Polymerization assays at acidic pH were conducted with the resulting Fe(II)PPIX using a spectrophotometric microassay of heme polymerization adapted to anaerobic conditions and the products characterized by infrared spectroscopy. Fe(II)PPIX (a) did not polymerize and (b) produced a dose-dependent inhibition of Fe(III)PPIX polymerization (IC(50) = 0.4 molar equiv). Moreover, Fe(II)PPIX produced by chemical reduction with thiol-containing compounds gave similar results: a dose-dependent inhibition of heme polymerization was observed using either L-cysteine, N-acetylcysteine, or DL-homocysteine, but not with L-cystine. Cyclic voltammetry confirmed that the inhibition of heme polymerization was due to the Fe(II)PPIX molecules generated by the thiol-mediated reduction of Fe(III)PPIX. These results point to Fe(II)PPIX as a potential endogenous antimalarial and to Fe(III)PPIX reduction as a potential new pharmacological target.
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Antimaláricos/farmacología , Compuestos Ferrosos/farmacología , Hemo/fisiología , Hemina/antagonistas & inhibidores , Pigmentos Biológicos/antagonistas & inhibidores , Plasmodium falciparum/crecimiento & desarrollo , Protoporfirinas/fisiología , Animales , Antimaláricos/química , Electroquímica , Eritrocitos/fisiología , Compuestos Ferrosos/sangre , Hemina/metabolismo , Humanos , Oxidación-Reducción , Pigmentos Biológicos/sangre , Plasmodium falciparum/efectos de los fármacos , Polímeros/metabolismo , Protoporfirinas/sangre , Protoporfirinas/toxicidad , Compuestos de Sulfhidrilo/farmacologíaRESUMEN
Glutathione-S-transferase (GST) activity has been detected in rodent (Plasmodium berghei, P. yoelii), simian (P. knowlesi) and human (P. falciparum) malarial parasites, and in different intraerythrocytic stages of P. knowlesi (schizont > ring > trophozoite). In chloroquine-resistant strains of rodent and human malarial parasites GST activity significantly increases compared to sensitive strains. Further, the increase in enzyme activity is directly related to drug pressure of resistant P. berghei. Complete inhibition of chloroquine-sensitive and resistant P. berghei glutathione-S-transferase activities was observed at 2.5 and 5. micrometer concentration of hemin, respectively. An inverse relationship was found between the heme level and enzyme activity of chloroquine-resistant and sensitive P. berghei. Chloroquine, artemisinin, and primaquine noticeably inhibited GST activity in P. knowlesi.
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Glutatión Transferasa/fisiología , Plasmodium berghei/enzimología , Plasmodium falciparum/enzimología , Plasmodium knowlesi/enzimología , Plasmodium yoelii/enzimología , Animales , Antimaláricos/metabolismo , Antimaláricos/farmacología , Cloroquina/metabolismo , Cloroquina/farmacología , Cricetinae , Resistencia a Medicamentos , Hemo/análisis , Hemo/fisiología , Humanos , Macaca mulatta/parasitología , Mesocricetus/parasitología , Ratones/parasitología , Plasmodium berghei/química , Plasmodium berghei/efectos de los fármacos , Plasmodium berghei/crecimiento & desarrollo , Plasmodium falciparum/química , Plasmodium falciparum/efectos de los fármacos , Plasmodium falciparum/crecimiento & desarrollo , Plasmodium knowlesi/química , Plasmodium knowlesi/efectos de los fármacos , Plasmodium knowlesi/crecimiento & desarrollo , Plasmodium yoelii/química , Plasmodium yoelii/efectos de los fármacos , Plasmodium yoelii/crecimiento & desarrollo , Protoporfirinas/análisis , Protoporfirinas/fisiologíaRESUMEN
Heme-binding protein 23 kDa (HBP23) belongs to the antioxidant family of peroxiredoxins and binds heme with high affinity. In vivo treatment of rats with heme induced expression of HBP23 mRNA levels in liver coordinately with that of the heme degrading enzyme heme oxygenase-1 (HO-1). In primary rat hepatocyte cultures Sn-, Co-, and Zn-metalloprotoporphyrin as well as the heme precursor protoporphyrin IX increased the HBP23 mRNA expression to a level similar to that elicited by heme. Heme-dependent induction of HBP23 mRNA was prevented by pretreatment with actinomycin D, indicating a transcriptional mechanism of gene induction. The results suggest that the coordinate gene regulation pattern of HBP23 and HO-1 plays a physiological role against oxidative stress.
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Proteínas Portadoras/genética , Hemoproteínas/genética , Hígado/fisiología , Metaloporfirinas/fisiología , Protoporfirinas/fisiología , Animales , Células Cultivadas , Cicloheximida/farmacología , Dactinomicina/farmacología , Expresión Génica/efectos de los fármacos , Hemo/farmacología , Hemo Oxigenasa (Desciclizante)/genética , Proteínas de Unión al Hemo , Masculino , Inhibidores de la Síntesis de la Proteína/farmacología , ARN Mensajero/genética , Ratas , Ratas Wistar , Transcripción Genética/efectos de los fármacosRESUMEN
Porphyromonas gingivalis has been shown to require hemin or hemoglobin for in vitro growth. We have previously shown that protoporphyrin IX and inorganic iron can replace the hemin requirement, suggesting that the hemin requirement of this microorganism is actually a porphyrin requirement. We examined the effect of protoporphyrin IX limitation to P. gingivalis strain A7A1-28 in the presence of sufficient iron on growth characteristics, proteolytic enzyme production, virulence in a mouse abscess model, and expression of membrane proteins. Bacterial cells were grown in medium varying between 0 to 5 microM reduced growth by at least 50%. Protoporphyrin IX availability did not affect proteolytic enzyme production or virulence in a mouse abscess model. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of membrane preparations demonstrated that protoporphyrin IX limitation induced the expression of new proteins at 42, 34, 30, 29, and 18 kDa and suppressed the production of proteins at 47, 27, 17, and 15 kDa. These studies suggest that in vivo protoporphyrin availability may modulate membrane protein expression and in turn affect host immune responses against P. gingivalis.
Asunto(s)
Porphyromonas gingivalis/metabolismo , Protoporfirinas/fisiología , Absceso/microbiología , Animales , Proteínas de la Membrana Bacteriana Externa/biosíntesis , Benzoilarginina-2-Naftilamida/metabolismo , Medios de Cultivo , Endopeptidasas/biosíntesis , Femenino , Humanos , Modelos Lineales , Ratones , Ratones Endogámicos BALB C , Porphyromonas gingivalis/crecimiento & desarrollo , Porphyromonas gingivalis/patogenicidad , Protoporfirinas/metabolismo , VirulenciaRESUMEN
Exogenous provision of 5-aminolevulinic acid (ALA) to many tissues results in the accumulation of sufficient quantities of the endogenous photosensitizer protoporphyrin IX (PpIX) via the heme biosynthetic pathway, to produce a photodynamic effect when exposed to activating light. Therefore, ALA may be considered the only current photodynamic therapy (PDT) agent in clinical development that is a biochemical precursor of a photosensitizer. Topical ALA application, followed by exposure to activating light (ALA PDT), has been reported effective for the treatment of a variety of dermatologic diseases including cutaneous superficial and nodular basal cell carcinoma, Bowen's disease, actinic (solar) keratoses, and T cell lymphoma. Local internal application of ALA has also been used for selective endometrial ablation in animal model systems and, in human clinical studies, it has shown selective formation of PpIX within the endometrium. PpIX induced by ALA application has also been used as a fluorescence detection marker for photodiagnosis (PD) of cancer and dysplastic conditions of the urinary bladder and other organs. Systemic, oral administration of ALA has been used for ALA PDT of superficial head and neck cancer, various gastrointestinal cancers, and the condition known as Barrett's esophagus. This paper reviews the current clinical and development status of ALA PDT and PD.
Asunto(s)
Ácido Aminolevulínico/uso terapéutico , Neoplasias/tratamiento farmacológico , Fotoquimioterapia/métodos , Protoporfirinas/biosíntesis , Ácido Aminolevulínico/metabolismo , Animales , Endometrio/metabolismo , Femenino , Neoplasias Gastrointestinales/tratamiento farmacológico , Humanos , Terapia por Láser , Neoplasias/diagnóstico , Protoporfirinas/fisiología , Neoplasias Cutáneas/diagnóstico , Neoplasias Cutáneas/tratamiento farmacológico , Enfermedades de la Vejiga Urinaria/diagnósticoRESUMEN
Endogenous protoporphyrin IX (PpIX) synthesis after delta-aminolaevulinic acid (ALA) administration occurs in cancer cells in vivo; PpIX, which has a short half-life, may thus constitute a good alternative to haematoporphyrin derivative (HPD) (or Photofrin). This study assesses the ability of the human hepatocarcinoma cell line HepG2 to synthesize PpIX in vitro from exogenous ALA, and compares ALA-induced toxicity and phototoxicity with the photodynamic therapy (PDT) effects of HPD on this cell line. ALA induced a dose-dependent dark toxicity, with 79% and 66% cell survival for 50 and 100 micrograms ml-1 ALA respectively after 3 h incubation; the same treatment, followed by laser irradiation (lambda = 632 nm, 25 J cm-2), induced a dose-dependent phototoxicity, with 54% and 19% cell survival 24 h after PDT. Whatever the incubation time with ALA, a 3 h delay before light exposure was found to be optimal to reach a maximum phototoxicity. HPD induced a slight dose-dependent toxicity in HepG2 cells and a dose- and time-dependent phototoxicity ten times greater than that of ALA-PpIX PDT. After 3 h incubation of 2.5 and 5 micrograms ml-1 HPD, followed by laser irradiation (lambda = 632 nm, 25 J cm-2), cell survival was 59% and 24% respectively at 24 h. Photoproducts induced by light irradiation of porphyrins absorb light in the red spectral region at longer wavelengths than the original porphyrins. The possible enhancement of PDT effects after HepG2 cell incubation with ALA or HPD was investigated by irradiating cells successively with red light (lambda = 632 nm) and light (lambda = 650 nm)(ABSTRACT TRUNCATED AT 250 WORDS)
Asunto(s)
Ácido Aminolevulínico/farmacología , Carcinoma Hepatocelular/terapia , Hematoporfirinas/farmacología , Fármacos Fotosensibilizantes/farmacología , Protoporfirinas/biosíntesis , Carcinoma Hepatocelular/metabolismo , Citometría de Flujo , Humanos , Rayos Láser , Modelos Biológicos , Fototerapia , Protoporfirinas/fisiología , Sales de Tetrazolio/metabolismo , Tiazoles/metabolismo , Factores de Tiempo , Células Tumorales CultivadasRESUMEN
The peripheral benzodiazepine receptor (PBzR) is associated with the outer mitochondrial membrane. Protoporphyrin IX (PPIX), an endogenous substance with high affinity for the PBzR, induced the inner membrane permeability transition (MPT) in respiring liver mitochondria de-energized by carbonyl cyanide p-trifluoromethoxyphenylhydrazone. Cyclosporin A (CyA), an inhibitor of the permeability transition, prevented this effect. In cultured hepatocytes, the MPT was measured as an increased [3H]sucrose-accessible space sensitive to CyA. Nanomolar concentrations of PPIX potentiated the induction of the MPT and the extent of cell killing in hepatocyte cultures de-energized by rotenone. CyA prevented the enhanced cell killing by PPIX. PPIX did not increase the rate or extent of ATP depletion, the loss of the mitochondrial membrane potential, or the accumulation of long chain acyl-CoA thioesters. The association of the PBzR with the voltage-dependent anion channel of the outer mitochondrial membrane and with the adenine nucleotide carrier of the inner membrane suggests that this complex mediates the transport of PPIX across the mitochondrial membranes. In turn, this same complex participates in the MPT. Thus, the same structural complex (PBzR, voltage-dependent anion channel, and adenine nucleotide carrier) can interact with the endogenous substrate PPIX to result in different functional consequences depending on the state of mitochondrial energization.
Asunto(s)
Hígado/efectos de los fármacos , Mitocondrias Hepáticas/fisiología , Protoporfirinas/fisiología , Receptores de GABA-A/metabolismo , Rotenona/farmacología , Adenosina Trifosfato/metabolismo , Animales , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Diazepam/farmacología , Sinergismo Farmacológico , Membranas Intracelulares/efectos de los fármacos , Membranas Intracelulares/fisiología , Isoquinolinas/farmacología , Ligandos , Hígado/citología , Masculino , Potenciales de la Membrana/fisiología , Permeabilidad/efectos de los fármacos , Ratas , Ratas Sprague-DawleyRESUMEN
1. Zinc-protoporphyrin-IX (ZnPP-IX) is an inhibitor of the enzyme heme-oxygenase-2 (HO-2) and consequently has been used to examine the role of carbon monoxide production in neural tissues. We have measured voltage-gated Ca current in AtT-20 pituitary cells using the whole-cell patch-clamp technique and have assessed the effects of extracellularly applied ZnPP-IX and related compounds. 2. Ca currents evoked by depolarizing steps from a holding potential of -90 mV were of the high-threshold, slowly inactivating type. Fifty-six percent of this current was blocked by 10 microM nifedipine and 16% by 3 microM omega-conotoxin with the remainder resistant to both drugs in combination, suggesting that the total Ca current was a mixture of L, N, and possibly P-type conductances. 3. Bath application of ZnPP-IX resulted in an irreversible, dose-dependent attenuation of Ca current. Five micromolar ZnPP-IX produced a 62% reduction of peak current amplitude with no shift in the current-voltage relation, 0.5 microM produced a 19% reduction, and 0.05 microM produced a variable response, either a small transient attenuation or potentiation. 4. The attenuation of Ca current by 5 microM ZnPP-IX could be nearly completely blocked by co-application of superoxide dismutase in the bath (90 U/ml) but not by addition of an inhibitor of cGMP-dependent protein kinase to the internal saline (KT5823, 1 microM). 5. Other inhibitors of heme-oxygenase with similar potency such as tin-protoporphyrin-IX (Sn-PP-IX) and Zn-deuteroporphyrin-bis-glycol (ZnBG) did not attenuate Ca current when applied at 5microM.(ABSTRACT TRUNCATED AT 400 WORDS)
Asunto(s)
Canales de Calcio/fisiología , Calcio/fisiología , Protoporfirinas/fisiología , Transmisión Sináptica/fisiología , Monóxido de Carbono/metabolismo , Línea Celular , Radicales Libres , Guanilato Ciclasa/fisiología , Hemo Oxigenasa (Desciclizante)/fisiología , Potenciales de la Membrana/fisiologíaRESUMEN
Carbon monoxide, which is formed endogenously from heme catabolism catalyzed by heme oxygenase and shares some of the chemical and biological properties of nitric oxide, may play a similar role as a widespread signal transduction mechanism for the regulation of cell function and communication. Zinc protoporphyrin, an inhibitor of heme oxygenase, prevents induction of long-term potentiation. Zinc protoporphyrin is an endogenous substance and we suggest that it has a physiological role, by modulating heme oxygenase activity and, therefore, formation of carbon monoxide from heme. This in turn would modulate long-term potentiation, memory, and cognitive function.