25 research outputs found
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Effect of reflood prediction uncertainties on LOFT cladding oxidation
The FLOOD4 and RELAP4/MOD6 computer codes, which are used to perform LOFT reflood analysis, have been compared to FLECHT-SET and Semiscale gravity feed tests to provide an evaluation of core reflood prediction techniques and an identification of phenomena important to LOFT reflood behavior. These comparisons provide a basis for estimating uncertainty in cladding temperature history during the LOFT loss-of-coolant experiments (LOCEs). The bounds on the cladding temperature response are then utilized to estimate a range of expected cladding oxidation and embrittlement which is essential for identifying special equipment needed during replacement, storage, and post-test examination of LOFT fuel modules. FLOOD4 couples the system hydraulic response with core heat transfer and steam generation. Four heat transfer correlations simulate the boiling curve and liquid entrainment, fallback and vaporization in the steam generators are modeled. FLOOD4 requires user input multipliers to specify the dispersed flow heat transfer, liquid entrainment and correlations to describe liquid fallback from the upper plenum region. The fraction of liquid vaporized in the steam generators must also be user input
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LOFT fuel rod thermal/mechanical behavior predictions
Best-estimate predictions of LOFT fuel rod behavior during the first LOFT nuclear test series have been made with both RELAP/FLOOD4/FRAP-T and RELAP/SCORE/MOXY computer code combinations. The purpose of the predictions are to test the best-estimate code accuracy by comparison of predictions to subsequent test data and to develop plans for post-test fuel replacements and examinations. The FRAP-T3 computer code was utilized which couples the thermal, mechanical, internal gas, and material property behavior of a nuclear rod during various postulated accident sequences. The cladding deformation models account for elastic-plastic behavior. FRAP-T3 requires coolant conditions to be specified as input boundary conditions. The coolant conditions for the blowdown and refill phases of a loss-of-coolant experiment (LOCE) were calculated with RELAP4/MOD6 and for the reflood portion with FLOOD4
A Universal System for Highly Efficient Cardiac Differentiation of Human Induced Pluripotent Stem Cells That Eliminates Interline Variability
The production of cardiomyocytes from human induced pluripotent stem cells (hiPSC) holds great promise for patient-specific cardiotoxicity drug testing, disease modeling, and cardiac regeneration. However, existing protocols for the differentiation of hiPSC to the cardiac lineage are inefficient and highly variable. We describe a highly efficient system for differentiation of human embryonic stem cells (hESC) and hiPSC to the cardiac lineage. This system eliminated the variability in cardiac differentiation capacity of a variety of human pluripotent stem cells (hPSC), including hiPSC generated from CD34(+) cord blood using non-viral, non-integrating methods.We systematically and rigorously optimized >45 experimental variables to develop a universal cardiac differentiation system that produced contracting human embryoid bodies (hEB) with an improved efficiency of 94.7±2.4% in an accelerated nine days from four hESC and seven hiPSC lines tested, including hiPSC derived from neonatal CD34(+) cord blood and adult fibroblasts using non-integrating episomal plasmids. This cost-effective differentiation method employed forced aggregation hEB formation in a chemically defined medium, along with staged exposure to physiological (5%) oxygen, and optimized concentrations of mesodermal morphogens BMP4 and FGF2, polyvinyl alcohol, serum, and insulin. The contracting hEB derived using these methods were composed of high percentages (64-89%) of cardiac troponin I(+) cells that displayed ultrastructural properties of functional cardiomyocytes and uniform electrophysiological profiles responsive to cardioactive drugs.This efficient and cost-effective universal system for cardiac differentiation of hiPSC allows a potentially unlimited production of functional cardiomyocytes suitable for application to hPSC-based drug development, cardiac disease modeling, and the future generation of clinically-safe nonviral human cardiac cells for regenerative medicine
Present state and future perspectives of using pluripotent stem cells in toxicology research
The use of novel drugs and chemicals requires reliable data on their potential toxic effects on humans. Current test systems are mainly based on animals or in vitro–cultured animal-derived cells and do not or not sufficiently mirror the situation in humans. Therefore, in vitro models based on human pluripotent stem cells (hPSCs) have become an attractive alternative. The article summarizes the characteristics of pluripotent stem cells, including embryonic carcinoma and embryonic germ cells, and discusses the potential of pluripotent stem cells for safety pharmacology and toxicology. Special attention is directed to the potential application of embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) for the assessment of developmental toxicology as well as cardio- and hepatotoxicology. With respect to embryotoxicology, recent achievements of the embryonic stem cell test (EST) are described and current limitations as well as prospects of embryotoxicity studies using pluripotent stem cells are discussed. Furthermore, recent efforts to establish hPSC-based cell models for testing cardio- and hepatotoxicity are presented. In this context, methods for differentiation and selection of cardiac and hepatic cells from hPSCs are summarized, requirements and implications with respect to the use of these cells in safety pharmacology and toxicology are presented, and future challenges and perspectives of using hPSCs are discussed
Individual, social, and environmental factors affecting salivary and fecal cortisol levels in captive pied tamarins (Saguinus bicolor)
This is the peer reviewed version of the following article: Price, E., Coleman, R., Ahsmann, J., Glendewar, G., Hunt, J., Smith, T. & Wormell, D. (2019). Individual, social, and environmental factors affecting salivary and fecal cortisol levels in captive pied tamarins (Saguinus bicolor). American Journal of Primatology, 81(8), which has been published in final form at https://doi.org/10.1002/ajp.23033. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-ArchivingPied tamarins (Saguinus bicolor) are endangered New World primates, and in captivity
appear to be very susceptible to stress. We measured cortisol in 214 saliva samples
from 36 tamarins and in 227 fecal samples from 27 tamarins, and investigated
the effects of age, sex, pregnancy, rearing history, social status, weight, group
composition, and enclosure type using generalized linear mixed models. There was no
effect of age on either fecal or salivary cortisol levels. Female pied tamarins in late
pregnancy had higher fecal cortisol levels than those in early pregnancy, or
nonpregnant females, but there was no effect of pregnancy on salivary cortisol.
Females had higher salivary cortisol levels than males, but there was no effect of
rearing history. However, for fecal cortisol, there was an interaction between sex and
rearing history. Hand‐reared tamarins overall had higher fecal cortisol levels, but
while male parent‐reared tamarins had higher levels than females who were parent‐
reared, the reverse was true for hand‐reared individuals. There was a trend towards
lower fecal cortisol levels in subordinate individuals, but no effect of status on
salivary cortisol. Fecal but not salivary cortisol levels declined with increasing weight.
We found little effect of group composition on cortisol levels in either saliva or feces,
suggesting that as long as tamarins are housed socially, the nature of the group is of
less importance. However, animals in off‐show enclosures had higher salivary and
fecal cortisol levels than individuals housed on‐show. We suggest that large on‐show
enclosures with permanent access to off‐exhibit areas may compensate for the
effects of visitor disturbance, and a larger number of tamarins of the same species
housed close together may explain the higher cortisol levels found in tamarins living
in off‐show accommodation, but further research is needed
Uncertainty in predicted loft reflooding response: influence on cladding oxidation
Semiscale gravity feed reflood and FLECHT-SET tests have been reviewed to determine phenomena which may be important during LOFT reflood. FLOOD4 and RELAP4/MOD6 predictions for Semiscale and FLECHT-SET tests were compared to experimental data. Based on these comparisons, uncertainties were estimated for the LOFT reflood predictions; these uncertainties were then utilized to bound the extent of cladding oxidation expected for the LOFT L2-3 and L2-4 tests
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Nuclear fuel rod response during LOFT tests L2-2 and L2-3. [PWR]
Comparisons of the measured fuel rod peak cladding temperatures for the first two nuclear loss-of-coolant experiments (LOCE), LOCEs L2-2 and L2-3, are presented. These LOCEs were performed in the Loss-of-Fluid Test (LOFT) facility at the Idaho National Engineering Laboratory. The LOCEs provided a basis for evaluating the effect of initial power on the maximum cladding temperatures during a large break (200%, guillotine) LOCE and identified important core thermal-hydraulic responses that influence the peak cladding temperatures
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LOFT nuclear fuel rod behavior
An overview of the calculational models used to predict fuel rod response for Loss-of-Fluid Test (LOFT) data from the first LOFT nuclear test is presented and discussed and a comparison of predictions with experimental data is made
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Nuclear fuel rod behavior during LOFT experiment L2-2
The Loss-of-Fluid Test (LOFT) Program is providing data to evaluate analytical models used to predict the thermal-hydraulic and fuel rod response of a pressurized water reactor (PWR) under loss-of-coolant accident (LOCA) conditions. The fuel rod response for the first nuclear loss-of-coolant experiment (LOCE), LOCE L2-2, is summarized
Microwell-mediated Control of Embryoid Body Size Regulates Embryonic Stem Cell Fate Via Differential Expression of WNT5a and WNT11
Recently, various approaches for controlling the embryonic stem (ES) cell microenvironment have been developed for regulating cellular fate decisions. It has been reported that the lineage specific differentiation could be affected by the size of ES cell colonies and embryoid bodies (EBs). However, much of the underlying biology has not been well elucidated. In this study, we used microengineered hydrogel microwells to direct ES cell differentiation and determined the role of WNT signaling pathway in directing the differentiation. This was accomplished by forming ES cell aggregates within microwells to form different size EBs. We determined that cardiogenesis was enhanced in larger EBs (450 μm in diameter), and in contrast, endothelial cell differentiation was increased in smaller EBs (150 μm in diameter). Furthermore, we demonstrated that the EB-size mediated differentiation was driven by differential expression of WNTs, particularly noncanonical WNT pathway, according to EB size. The higher expression of WNT5a in smaller EBs enhanced endothelial cell differentiation. In contrast, the increased expression of WNT11 enhanced cardiogenesis. This was further validated by WNT5a-siRNA transfection assay and the addition of recombinant WNT5a. Our data suggest that EB size could be an important parameter in ES cell fate specification via differential gene expression of members of the noncanonical WNT pathway. Given the size-dependent response of EBs to differentiate to endothelial and cardiac lineages, hydrogel microwell arrays could be useful for directing stem cell fates and studying ES cell differentiation in a controlled manner.National Institutes of Health (U.S.) (DE019024, HL092836, and EB007249