High content image-based cytometry as a tool for nuclear fingerprinting

Cytomics aims at understanding the functional relationships between cellular phenotypes (cytome) and metabolic pathways (proteome) that result from a combination of genetically defined mechanisms (genome) and environmental conditions [1,2]. Although flow-cytometry is able to measure the optical properties of single cells at a rate of >1000 cells per minute it has a limited capability of mapping individual events. To accurately quantify (sub-) cellular characteristics within a natural context there is a fast-growing need for image-based cytometry. Images, obtained with fluorescence microscopy, provide the exact information on signal intensity, location and distribution of specific molecules within intact cell systems (tissue or monolayers) and allow for investigating cellular properties in relation to the cell-ecological context [3]. Previously, we have developed a cytometric approach for scoring DNA lesion endpoints in confocal images of murine fibroblasts [3]. We now present a generalized approach for multivariate phenotypic profiling of individual nuclei using automated fluorescence mosaic microscopy and optimized digital image processing tools. An indefinite number of fields, z-slices and channels can be analyzed; the only prerequisite is the presence of a nuclear counterstain, which is used for the generation of masks. To anticipate for erroneous segmentation of clustered nuclei in dense cell cultures we implemented an iterative conditional segmentation (ics) algorithm that uses both morphological and intensity information from the image (Figure 1). The method makes use of a priori knowledge about the size and shape of nuclei in stringent feedback selection of correctly segmented nuclei. Depending on the degree of clustering, segmentation performance varies between 95% and 100%. Complete analysis of nuclei and subnuclear features for a region of 25 images of 1000x1000 pixels, 3 z-slices and 3 channels only takes ~ 3 minutes or ~ 0.7sec/nucleus. Our method is insensitive to scaling, illumination heterogeneity and variability or non-uniformity of staining. We have successfully applied our system in cell cycle analysis, scoring of transfection efficiency and assessment of (localized) DNA damage in response to genotoxic stress and ionizing radiation

Modulation of gene expression in endothelial cells in response to high LET nickel ion irradiation

Ionizing radiation can elicit harmful effects on the cardiovascular system at high doses. Endothelial cells are critical targets in radiation-induced cardiovascular damage. Astronauts performing a long-term deep space mission are exposed to consistently higher fluences of ionizing radiation that may accumulate to reach high effective doses. In addition, cosmic radiation contains high linear energy transfer (LET) radiation that is known to produce high values of relative biological effectiveness (RBE). The aim of this study was to broaden the understanding of the molecular response to high LET radiation by investigating the changes in gene expression in endothelial cells. For this purpose, a human endothelial cell line (EA.hy926) was irradiated with accelerated nickel ions (Ni) (LET, 183 keV/mu m) at doses of 0.5, 2 and 5 Gy. DNA damage was measured 2 and 24 h following irradiation by gamma-H2AX foci detection by fluorescence microscopy and gene expression changes were measured by microarrays at 8 and 24 h following irradiation. We found that exposure to accelerated nickel particles induced a persistent DNA damage response up to 24 h after treatment. This was accompanied by a downregulation in the expression of a multitude of genes involved in the regulation of the cell cycle and an upregulation in the expression of genes involved in cell cycle checkpoints. In addition, genes involved in DNA damage response, oxidative stress, apoptosis and cell-cell signaling (cytokines) were found to be upregulated. An in silico analysis of the involved genes suggested that the transcription factors, E2F and nuclear factor (NF)-kappa B, may be involved in these cellular responses

The effect of genetic background and dose on non-targeted effects of radiation

Purpose: This work investigates the hypothesis that genetic background plays a significant role in the signalling mechanisms underlying induction and perpetuation of genomic instability following radiation exposure. Materials and methods: Bone marrow from two strains of mice (CBA and C57) were exposed to a range of X-ray doses (0, 0.01, 0.1, 1 and 3 Gy). Different cellular signalling endpoints: Apoptosis, cytokine levels and calcium flux, were evaluated at 2 h, 24 h and 7 d post-irradiation to assess immediate and delayed effects. Results: In CBA (radiosensitive) elevated apoptosis levels were observed at 24 h post X-irradiation, and transforming growth factor-β (TGF-β) levels which increased with time and dose. C57 showed a higher background level of apoptosis, and sustained apoptotic levels 7 days after radiation exposure. Levels of tumor necrosis factor-α (TNF-α were increased in C57 at day 7 for higher X-ray doses. TGF-β levels were higher in CBA, whilst C57 exhibited a greater TNF-α response. Calcium flux was induced in reporter cells on exposure to conditioned media from both strains. Conclusions: These results show genetic and dose specific differences in radiation-induced signalling in the initiation and perpetuation of the instability process, which have potential implications on evaluation of non-targeted effects in radiation risk assessment

Nanoparticle-induced neuronal toxicity across placental barriers is mediated by autophagy and dependent on astrocytes

The potential for maternal nanoparticle (NP) exposures to cause developmental toxicity in the fetus without the direct passage of NPs has previously been shown, but the mechanism remained elusive. We now demonstrate that exposure of cobalt and chromium NPs to BeWo cell barriers, an in vitro model of the human placenta, triggers impairment of the autophagic flux and release of interleukin-6. This contributes to the altered differentiation of human neural progenitor cells and DNA damage in the derived neurons and astrocytes. Crucially, neuronal DNA damage is mediated by astrocytes. Inhibiting the autophagic degradation in the BeWo barrier by overexpression of the dominant-negative human ATG4BC74A significantly reduces the levels of DNA damage in astrocytes. In vivo, indirect NP toxicity in mice results in neurodevelopmental abnormalities with reactive astrogliosis and increased DNA damage in the fetal hippocampus. Our results demonstrate the potential importance of autophagy to elicit NP toxicity and the risk of indirect developmental neurotoxicity after maternal NP exposure

Radiation-induced protein redistribution and modification involved in DNA damage response and intercellular communication

Human cells are exposed to a wide range of stressors that influence their responses on different levels. There are strong indications that cells endure these stressors as an entity. Increasing evidence suggests that individual cells are not closed systems isolated from their environment but continuously exchange information with each other. Two non-targeted effects were studied: (1) Bystander effects occur when non-treated cells – that are in contact with exposed cells either through the medium or gap junctions – reveal effects similar to those seen in exposed cells. (2) In adaptive response, cells – either directly or indirectly exposed – are influenced by a prior treatment. Both phenomena were studied using high throughput cytometry and multiplex array screening. Central in this investigation was H2AX, a protein belonging to the histon complex that plays an important role in DNA damage response. In response to double stranded breaks (DSB) H2AX is phosphorylated (γH2AX) and is considered as signal enhancer for the DSB repair pathway. The DNA damage response of human fibroblast was analyzed and H2AX analysis revealed the presence of a bystander effect and an adaptive response. In addition, we analyzed the cytokines that were present in the culture medium after exposure to ionizing radiation. We could also link the upregulation of γH2AX in bystander cells to the presence of these secreted cytokines in the culture medium. In line with the above-mentioned results we analyzed the DNA damage response in fibroblasts exposed to cosmic radiation during the Foton M3 space mission. This fully automated mission lasted for 12 days and completed 190 orbits around the earth. During the space experiment, we tested and validated a compact, biological dosimeter, which can be used in future space flights. Finally, we focused on a specific signaling molecule, cyclophilin B (CypB). CypB is secreted into the culture medium, but has the necessary signal peptides for an efficient retrograde transport to the nucleus. In order to identify the various peptide sequences necessary for these relocalizations, different GFP constructs were made. We identified a nucleolar localization sequence that allowed transport of CypB and could link CypB to a role in rDNA transcription

Interplanetary space travel and long-term habitation on mars

Robotic planetary exploration has enabled scientists to gather valuable data and understanding about the composition and origin of extraterrestrial structures. However, despite its tremendous possibilities, human exploration is a natural next step. Manned missions to Mars are becoming more feasible and as such the irresistible attraction for mankind to explore this neighbouring planet is growing. Especially since 2004, with the president of the United States outlining specific objectives for future exploration, including missions to the Moon, Mars and beyond these aspirations have become tangible. A prerequisite for a manned mission to Mars, requires an extensive, durable life supporting system which should recycle waste. Preferable also produce additional eatable substances and/or additives in a safe and efficient manner with a high reliability to perform in harsh space conditions