RESUMEN

Lipid rafts display a lateral heterogeneity forming membrane microdomains that hold a fundamental role on biological membranes and are indispensable to physiological functions of cells. Oxidative stress in cellular environments may cause lipid oxidation, changing membrane composition and organization, thus implying in effects in cell signaling and even loss of homeostasis. The individual contribution of oxidized lipid species to the formation or disruption of lipid rafts in membranes still remains unknown. Here, we investigate the role of different structures of oxidized phospholipids on rafts microdomains by carefully controlling the membrane composition. Our experimental approach based on fluorescence microscopy of giant unilamellar vesicles (GUV) enables the direct visualization of the impact of hydroperoxidized POPC lipid (referred to as POPCOOH) and shortened chain lipid PazePC (1-palmitoyl-2-azelaoyl-sn-glycero-3-phosphocholine) on phase separation. We found that the molecular structure of oxidized lipid is of paramount importance on lipid mixing and/or demixing. The hydrophobic mismatch promoted by POPCOOH coupled to its cylindrical molecular shape favor microdomains formation. In contrast, the conical shape of PazePC causes disarrangement of lipid 2D organized platforms. Our findings contribute to better unraveling how oxidized phospholipids can trigger formation or disruption of lipid rafts. As a consequence, phospholipid oxidation may indirectly affect association or dissociation of key biomolecules in the rafts thus altering cell signaling and homeostasis.

Asunto(s)

Membrana Dobles de Lípidos/metabolismo , Microdominios de Membrana/efectos de los fármacos , Microdominios de Membrana/metabolismo , Fosfatidilcolinas/metabolismo , Fosfatidilcolinas/farmacología , Membrana Dobles de Lípidos/química , Peroxidación de Lípido/fisiología , Microdominios de Membrana/química , Oxidantes Fotoquímicos/química , Oxidantes Fotoquímicos/farmacología , Oxidación-Reducción , Fosfatidilcolinas/química , Fosforilcolina/análogos & derivados , Fosforilcolina/química , Fosforilcolina/metabolismo , Liposomas Unilamelares/química , Liposomas Unilamelares/metabolismo

RESUMEN

Visible light can induce the generation of singlet oxygen and can cause oxidative stress, especially in melanocytes due to melanin photosensitization. Currently, there is no organic UV-filter that provide visible light protection. Previous studies showed that some antioxidants, such as apigenin (API), chrysin (CRI) and beta-carotene (BTC) besides neutralizing radical chain reactions can also quench singlet oxygen via physical or chemical quenching and exhibit potential for use in photoprotection. Therefore, the aim of this study is to evaluate the efficacy of API, CRI and BTC on the protection against cell death induced by melanin photosensitization and understand the underlying mechanisms that are involved in the protection. Precise protocols of melanogenesis and quantification of singlet oxygen generation were developed. Viability of B16-F10 cells with melanin basal levels and after melanogenesis induction was evaluated after visible light exposure in the presence and absence of API, CRI and BTC. Results showed that API and BTC protected cells from photoinduced cell death API exhibiting superior photoprotective effect. We noticed that the efficiency of cell protection and the rate of singlet oxygen suppression are not well correlated, at least for the studied series of antioxidants, indicating that the anti-radical capacity should be playing a major role in protecting cells against the damage induced by melanin photosensitization. In terms of sun care strategies, both API and BTC offer protection against visible light-induced damages and may be effective topical antioxidants to be added to sunscreens.

Asunto(s)

Antioxidantes/farmacología , Apigenina/farmacología , Flavonoides/farmacología , Melaninas/química , Fármacos Fotosensibilizantes/química , beta Caroteno/farmacología , Animales , Línea Celular Tumoral , Supervivencia Celular/efectos de los fármacos , Supervivencia Celular/efectos de la radiación , Luz , Melaninas/antagonistas & inhibidores , Melanocitos/citología , Melanocitos/efectos de los fármacos , Melanocitos/fisiología , Melanocitos/efectos de la radiación , Ratones , Procesos Fotoquímicos , Fármacos Fotosensibilizantes/antagonistas & inhibidores , Oxígeno Singlete/agonistas , Oxígeno Singlete/química , Oxígeno Singlete/metabolismo

Asunto(s)

Dermatitis Fototóxica/fisiopatología , Lipofuscina/metabolismo , Trastornos por Fotosensibilidad/fisiopatología , Especies Reactivas de Oxígeno/metabolismo , Rayos Ultravioleta/efectos adversos , Células Cultivadas , Humanos , Queratinocitos/efectos de la radiación , Luz , Lipofuscina/efectos de la radiación , Especies Reactivas de Oxígeno/efectos de la radiación , Valores de Referencia , Medición de Riesgo

RESUMEN

Mobilization of specific mechanisms of regulated cell death is a promising alternative to treat challenging illness such as neurodegenerative disease and cancer. The use of light to activate these mechanisms may provide a route for target-specific therapies. Two asymmetric porphyrins with opposite charges, the negatively charged TPPS2a and the positively charged CisDiMPyP were compared in terms of their properties in membrane mimics and in cells. CisDiMPyP interacts to a larger extent with model membranes and with cells than TPPS2a, due to a favorable electrostatic interaction. CisDiMPyP is also more effective than TPPS2a in damaging membranes. Surprisingly, TPPS2a is more efficient in causing photoinduced cell death. The lethal concentration on cell viability of 50% (LC50) found for TPPS2a was ~3.5 (raw data) and ~5 (considering photosensitizer incorporation) times smaller than for CisDiMPyP. CisDiMPyP damaged mainly mitochondria and triggered short-term phototoxicity by necro-apoptotic cell death. Photoexcitation of TPPS2a promotes mainly lysosomal damage leading to autophagy-associated cell death. Our data shows that an exact damage in lysosome is more effective to diminish proliferation of HeLa cells than a similar damage in mitochondria. Precisely targeting organelles and specifically triggering regulated cell death mechanisms shall help in the development of new organelle-target therapies.

Asunto(s)

Apoptosis/efectos de los fármacos , Bencenosulfonatos/farmacología , Lisosomas/efectos de los fármacos , Fármacos Fotosensibilizantes/farmacología , Porfirinas/farmacología , Compuestos de Piridinio/farmacología , Apoptosis/efectos de la radiación , Bencenosulfonatos/química , Membrana Celular/efectos de los fármacos , Membrana Celular/efectos de la radiación , Supervivencia Celular/efectos de los fármacos , Supervivencia Celular/efectos de la radiación , Células HeLa , Humanos , Cinética , Luz , Lisosomas/metabolismo , Lisosomas/efectos de la radiación , Membranas Artificiales , Mitocondrias/efectos de los fármacos , Mitocondrias/metabolismo , Mitocondrias/efectos de la radiación , Fotoquimioterapia , Fármacos Fotosensibilizantes/química , Porfirinas/química , Compuestos de Piridinio/química , Electricidad Estática , Relación Estructura-Actividad

RESUMEN

Neste trabalho são apresentados estudos do efeito de interfaces nas propriedades fotofísicas e fotoquímicas do azul de metileno (AM) e de derivados fenotiazínicos com o intuito de avaliar o potencial destes compostos como fotossensibilizadores (FS) em terapia fotodinâmica. As propriedades físico-químicas do AM foram estudadas em soluções de SDS e observou-se que a presença do AM em solução altera o equilíbrio entre as micelas de SDS, -diminuindo o valor da concentração micelar crítica de 7mmolL-1 para 70µmoIL-1. A presença das micelas em solução também interfere nas propriedades do AM. Em baixas concentrações de SDS há formação de dímeros de AM, constatados pelo aumento da absorbância em 580nm e diminuição da emissão de fluorescência. A caracterização das espécies transientes mostrou a existência de moléculas de azul de metileno no estado triplete (3AM) e de oxigênio singlete em soluções com altas concentrações de SDS e a formação de espécies radicalares do AM em baixas concentrações do tensoativo. Esta observação sugere que o mecanismo fotoquímico do AM é dependente da sua concentração local próxima de interfaces carregadas. As interações do AM e de alguns de seus derivados fenotiazínicos (tionina, azure A e azure B) com vesículas e com células...

Asunto(s)

Hipoxia/tratamiento farmacológico , Azul de Metileno/farmacocinética , Azul de Metileno/síntesis química , Fotoquimioterapia/efectos adversos , Fotoquimioterapia , Neoplasias/tratamiento farmacológico , Oxígeno Singlete/efectos de la radiación , Materiales Biomiméticos , Técnicas de Cultivo de Célula , Espectrofotometría , Análisis Espectral

RESUMEN

Methylene blue (MB) is a molecule that has been playing important roles in microbiology and pharmacology for some time. It has been widely used to stain living organisms, to treat methemoglobinemia, and lately it has been considered as a drug for photodynamic therapy (PDT). In this review, we start from the fundamental photophysical, photochemical and photobiological characteristics of this molecule and evolved to show in vitro and in vivo applications related to PDT. The clinical cases shown include treatments of basal cell carcinoma, Kaposi's Sarcoma, melanoma, virus and fungal infections. We concluded that used together with a recently developed continuous light source (RL50(®)), MB has the potential to treat a variety of cancerous and non-cancerous diseases, with low toxicity and no side effects.