RESUMEN
Cleavage of mutant huntingtin (HTT) is an essential process in Huntington's disease (HD), an inherited neurodegenerative disorder. Cleavage generates N-ter fragments that contain the polyQ stretch and whose nuclear toxicity is well established. However, the functional defects induced by cleavage of full-length HTT remain elusive. Moreover, the contribution of non-polyQ C-terminal fragments is unknown. Using time- and site-specific control of full-length HTT proteolysis, we show that specific cleavages are required to disrupt intramolecular interactions within HTT and to cause toxicity in cells and flies. Surprisingly, in addition to the canonical pathogenic N-ter fragments, the C-ter fragments generated, that do not contain the polyQ stretch, induced toxicity via dilation of the endoplasmic reticulum (ER) and increased ER stress. C-ter HTT bound to dynamin 1 and subsequently impaired its activity at ER membranes. Our findings support a role for HTT on dynamin 1 function and ER homoeostasis. Proteolysis-induced alteration of this function may be relevant to disease.
Asunto(s)
Dinamina I/metabolismo , Enfermedad de Huntington/metabolismo , Proteínas Asociadas a Microtúbulos/metabolismo , Proteínas del Tejido Nervioso/metabolismo , Péptidos/metabolismo , Proteolisis , Proteínas de Transporte de Serotonina en la Membrana Plasmática/metabolismo , Animales , Proteínas de Drosophila , Drosophila melanogaster , Dinamina I/genética , Retículo Endoplásmico/genética , Retículo Endoplásmico/metabolismo , Estrés del Retículo Endoplásmico/genética , Humanos , Proteína Huntingtina , Enfermedad de Huntington/genética , Ratones , Proteínas Asociadas a Microtúbulos/genética , Proteínas del Tejido Nervioso/genética , Péptidos/genética , Proteínas de Transporte de Serotonina en la Membrana Plasmática/genéticaRESUMEN
We demonstrate subwavelength sectioning on biological samples with a conventional confocal microscope. This optical sectioning is achieved by the phenomenon of supercritical angle fluorescence, wherein only a fluorophore next to the interface of a refractive index discontinuity can emit propagating components of radiation into the so-called forbidden angles. The simplicity of this technique allows it to be integrated with a high numerical aperture confocal scanning microscope by only a simple modification on the detection channel. Confocal-supercritical angular fluorescence microscopy would be a powerful tool to achieve high-resolution surface imaging, especially for membrane imaging in biological samples.
Asunto(s)
Membrana Celular/metabolismo , Microscopía Confocal/métodos , Animales , Células CHO , Cricetinae , CricetulusRESUMEN
The characterization of vaccine distribution to relevant tissues after in vivo administration is critical to understanding their mechanisms of action. Vaccines based on mRNA lipid nanoparticles (LNPs) are now being widely considered against infectious diseases and cancer. Here, we used in vivo imaging approaches to compare the trafficking of two LNP formulations encapsulating mRNA following intramuscular administration: DLin-MC3-DMA (MC3) and the recently developed DOG-IM4. The mRNA formulated in DOG-IM4 LNPs persisted at the injection site, whereas mRNA formulated in MC3 LNPs rapidly migrated to the draining lymph nodes. Furthermore, MC3 LNPs induced the fastest increase in blood neutrophil counts after injection and greater inflammation, as shown by IL-1RA, IL-15, CCL-1, and IL-6 concentrations in nonhuman primate sera. These observations highlight the influence of the nature of the LNP on mRNA vaccine distribution and early immune responses.
RESUMEN
PURPOSE OF REVIEW: The persistence of HIV-1-infected cells, despite the introduction of the combinatorial antiretroviral therapy, is a major obstacle to HIV-1 eradication. Understanding the nature of HIV reservoir will lead to novel therapeutic approaches for the functional cure or eradication of the virus. In this review, we will update the recent development in imaging applications toward HIV-1/simian immunodeficiency virus (SIV) viral reservoirs research and highlight some of their limitations. RECENT FINDINGS: CD4 T cells are the primary target of HIV-1/SIV and the predominant site for productive and latent reservoirs. This viral reservoir preferentially resides in lymphoid compartments that are difficult to access, which renders sampling and measurements problematical and a hurdle for understanding HIV-1 pathogenicity. Novel noninvasive technologies are needed to circumvent this and urgently help to find a cure for HIV-1. Recent technological advancements have had a significant impact on the development of imaging methodologies allowing the visualization of relevant biomarkers with high resolution and analytical capacity. Such methodologies have provided insights into our understanding of cellular and molecular interactions in health and disease. SUMMARY: Imaging of the HIV-1 reservoir can provide significant insights for the nature (cell types), spatial distribution, and the role of the tissue microenvironment for its in vivo dynamics and potentially lead to novel targets for the virus elimination.
Asunto(s)
Infecciones por VIH , VIH-1 , Síndrome de Inmunodeficiencia Adquirida del Simio , Virus de la Inmunodeficiencia de los Simios , Animales , Linfocitos T CD4-Positivos , Infecciones por VIH/tratamiento farmacológico , VIH-1/genética , Humanos , Macaca mulatta , Carga Viral , Latencia del Virus , Replicación ViralRESUMEN
We have employed atomic force microscope-based infrared spectroscopy (AFM-IR) to spatially map energy storage polymers inside individual bacteria Rhodobacter capsulatus. AFM-IR allows chemical mapping of sub-cellular features with a spatial resolution of <100 nm. We have used key absorption bands of the energy storage polymer polyhydroxybutyrate (PHB) known from FTIR to spatially map the molecular distribution of PHB inside bacteria. We have also compared FTIR measurements on bulk PHB with AFM-IR measurements of PHB inside bacteria. We observe a shift in the location of the carbonyl absorption peak between bulk PHB and PHB inside bacteria. We have also used finite element analysis to model AFM-IR measurements of PHB granules, allowing for estimation of the real size of the granules. We have also performed transmission electron microscopy (TEM) of R. capsulatus to determine the size distribution of the PHB granules. Sizes measured by AFM-IR correspond well to TEM measurements.
Asunto(s)
Hidroxibutiratos/química , Microscopía de Fuerza Atómica/métodos , Nanopartículas/química , Espectroscopía Infrarroja por Transformada de Fourier/métodos , Microscopía Electrónica de Transmisión , Tamaño de la Partícula , Polímeros/química , Rhodobacter capsulatus/químicaRESUMEN
Recent whooping cough (pertussis) outbreaks in many countries highlight the crucial need for a better understanding of the pathogenesis of Bordetella pertussis infection of the respiratory tract. The baboon is a recently described preclinical model for the study of B. pertussis infection and may be ideal for the evaluation of new pertussis vaccines. However, many pathophysiological aspects, including bacterial localization and interactions, have yet to be described in this model. Here, we used a baboon model of infection with a fluorescent GFP-expressing B. pertussis strain, derived from European clinical isolate B1917. Juvenile baboons were used to evaluate susceptibility to infection and transmission. Non-invasive in vivo imaging procedures, using probe-based confocal endomicroscopy coupled with bronchoscopy, were developed to track fluorescent bacterial localization and cellular interactions with host cells in the lower respiratory tract of infected animals. All B1917-GFP-challenged animals developed classical pertussis symptoms, including paroxysmal cough, nasopharyngeal colonization, and leukocytosis. In vivo co-localization with antigen presenting cells and progressive bacterial colonization of the lower airways were also assessed by imaging during the first weeks of infection. Our results demonstrate that in vivo imaging can be used to assess bacterial colonization and to point out interactions in a baboon model of pertussis.
Asunto(s)
Bordetella pertussis/crecimiento & desarrollo , Pulmón/microbiología , Tos Ferina/diagnóstico por imagen , Tos Ferina/transmisión , Animales , Bordetella pertussis/genética , Modelos Animales de Enfermedad , Proteínas Fluorescentes Verdes/genética , Papio , Vacuna contra la Tos Ferina/administración & dosificación , Tos Ferina/microbiología , Tos Ferina/prevención & controlRESUMEN
In this paper, we will employ two microscopy techniques, transmission electron microscopy and infrared nanospectromicroscopy, to study the production of polyhydroxybutyrate in Rhodobacter capsulatus and to evaluate the influence of glucose and acetone on the production yield. The results overlap which leads us to a consistent conclusion, highlighting that each technique brings specific and complementary information. By using electron microscopy and infrared nanospectromicroscopy we have proved that both glucose and acetone had a positive effect on the biopolymer production, although the first study done by Fourier transform infrared spectroscopy only identified the effect of acetone. In conclusion, we have now established a method to be able to perform fast diagnostic for PHB production.