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1.
Plant Cell Rep ; 42(11): 1841-1843, 2023 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-37632539

RESUMO

KEY MESSAGE: OsHsp18.0 plays a key role in cross-protection of rice seedlings from damages to photochemical systems and cellular membranes, caused by Cd and Cu stresses.


Assuntos
Metais Pesados , Oryza , Oryza/genética , Metais Pesados/toxicidade , Plântula/genética , Cádmio/toxicidade
2.
Environ Res ; 214(Pt 2): 113802, 2022 11.
Artigo em Inglês | MEDLINE | ID: mdl-35810813

RESUMO

Heavy metal release from harsh ultramafic settings influences microbial diversity and function in soil ecology. This study aimed to determine how serpentine mineralosphere bacterial assemblies and their functions differed in two different plate-tectonic plains and mining exposure sites under heavy metal release conditions. The results showed that the Proteobacteria, Actinobacteria, Cyanobacteria, Planctomycetes, and Chloroflexi were the most abundant bacterial groups among all the sites. The log10-based LDA scores highlighted that some specific groups of bacterial assemblies were enriched in plate-tectonic plains and mining activity areas of the serpentine mineralosphere. Functional prediction revealed that the abundance of heavy metal (Cr and Ni) resistance and biogeochemical cycles involving functional KEGG orthology varied in samples from plate-tectonic plains and mining activity sites. The bipartite plot showed that the enrichment of the biogeochemical cycle and heavy metal resistance functional genes correlated with the abundance of serpentine mineralosphere bacterial groups at a 0.005% confidence level. The co-occurrence network plot revealed that the interconnection pattern of the indigenous bacterial assemblies changed in different plate-tectonic plains and mining exposure areas. Finally, this study concluded that due to heavy metal release, the variation in bacterial assemblies, their functioning, and intercommunity co-occurrence patterns were clarified the synergetic effect of mineral-microbial geochemical weathering process in serpentine mining areas.


Assuntos
Metais Pesados , Microbiota , Poluentes do Solo , Bactérias/genética , Metais Pesados/análise , Minerais , Solo , Microbiologia do Solo , Poluentes do Solo/análise
3.
J Biomed Opt ; 19(7): 77004, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25036215

RESUMO

Measuring tissue oxygenation in vivo is of interest in fundamental biological as well as medical applications. One minimally invasive approach to assess the oxygen partial pressure in tissue (pO2) is to measure the oxygen-dependent luminescence lifetime of molecular probes. The relation between tissue pO2 and the probes' luminescence lifetime is governed by the Stern-Volmer equation. Unfortunately, virtually all oxygen-sensitive probes based on this principle induce some degree of phototoxicity. For that reason, we studied the oxygen sensitivity and phototoxicity of dichlorotris(1, 10-phenanthroline)-ruthenium(II) hydrate [Ru(Phen)] using a dedicated optical fiber­based, time-resolved spectrometer in the chicken embryo chorioallantoic membrane. We demonstrated that, after intravenous injection, Ru(Phen)'s luminescence lifetime presents an easily detectable pO2 dependence at a low drug dose (1 mg∕kg) and low fluence (120 mJ∕cm2 at 470 nm). The phototoxic threshold was found to be at 10 J∕cm2 with the same wavelength and drug dose, i.e., about two orders of magnitude larger than the fluence necessary to perform a pO2 measurement. Finally, an illustrative application of this pO2 measurement approach in a hypoxic tumor environment is presented.


Assuntos
Corantes Fluorescentes/química , Imagem Óptica/métodos , Oxigênio/análise , Fenantrolinas/química , Rutênio/química , Animais , Linhagem Celular Tumoral , Embrião de Galinha , Membrana Corioalantoide/irrigação sanguínea , Membrana Corioalantoide/química , Membrana Corioalantoide/efeitos dos fármacos , Membrana Corioalantoide/metabolismo , Corantes Fluorescentes/farmacocinética , Corantes Fluorescentes/toxicidade , Humanos , Neoplasias Experimentais , Fibras Ópticas , Imagem Óptica/instrumentação , Compostos Organometálicos/química , Compostos Organometálicos/farmacocinética , Compostos Organometálicos/toxicidade , Pressão Parcial , Fenantrolinas/farmacocinética , Fenantrolinas/toxicidade , Rutênio/farmacocinética , Rutênio/toxicidade , Distribuição Tecidual
4.
Biochem Pharmacol ; 89(2): 171-84, 2014 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-24565908

RESUMO

Cervical cancer, the second most common malignancy among women, is mainly caused by human papilloma virus (HPV) infection. In HPV-positive cervical cancer cells, the activity of p53 and the induction of p21 are inhibited by the HPV oncoproteins E6 and E7. Therefore, blocking the activity of E6 and E7 would serve as an important therapeutic target in these cancer cells. In this study, anisomelic acid (AA), a natural compound belonging to the same diterpenoid family of bioactive compounds as taxol, was found to deplete the E6 and E7 proteins in HPV-positive cervical cancer cells. Consequently, p53 and the p53-responsive gene, p21, were dramatically induced, leading to G2/M-phase cell cycle arrest. AA-mediated cell cycle arrest and p21 expression were canceled when p53 was down-regulated by p53-shRNA. AA also induced p53-independent intrinsic apoptosis by depletion of the cellular inhibitor of apoptosis protein 2 (cIAP2) whose proteosomal degradation is inhibited by E6. The in ovo chick embryo chorioallantoic membrane (CAM) assay showed that anisomelic acid inhibited the tumor growth of the cervical cancer SiHa cells. AA is revealed to hold a novel action modality based on specific targeting of the HPV oncoproteins, which restores p53-mediated growth arrest and induces apoptosis by terminating E6-mediated cIAP2 stabilization.


Assuntos
Diterpenos/farmacologia , Diterpenos/uso terapêutico , Papillomavirus Humano 6/metabolismo , Proteínas E7 de Papillomavirus/antagonistas & inibidores , Neoplasias do Colo do Útero/virologia , Animais , Embrião de Galinha , Relação Dose-Resposta a Droga , Feminino , Células HeLa , Papillomavirus Humano 6/efeitos dos fármacos , Humanos , Células MCF-7 , Proteínas E7 de Papillomavirus/metabolismo , Neoplasias do Colo do Útero/tratamento farmacológico
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