3,701 research outputs found

    The retinoblastoma protein:multitasking to suppress tumorigenesis

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    Tumor suppressor activity of the retinoblastoma protein pRB is preserved despite loss of interaction with E2F transcription factors (E2F) or proteins harboring a leucine-x-cysteine-x-glutamic acid motif (LxCxE, where x is any amino acid). This indicates that pRB uses several parallel pathways to suppress tumorigenesis, which may also include E2F- and LxCxE-independent interactions

    Is the Effect of Forest Structure on Bird Diversity Modified by Forest Productivity?

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    Currently, the most common strategy when managing forests for biodiversity at the landscape scale is to maintain structural complexity within stands and provide a variety of seral stages across landscapes. Advances in ecological theory reveal that biodiversity at continental scales is strongly influenced by available energy (i.e., climate factors relating to heat and light and primary productivity). This paper explores how available energy and forest structural complexity may interact to drive biodiversity at a regional scale. We hypothesized that bird species richness exhibits a hump-shaped relationship with energy at the regional scale of the northwestern United States. As a result, we hypothesized that the relationship between energy and richness within a landscape is positive in energy-limited landscapes and flat or decreasing in energy-rich landscapes. Additionally, we hypothesized that structural complexity explains less of the variation in species richness in energy-limited environments and more in energy-rich environments and that the slope of the relationship between structural complexity and richness is greatest in energy-rich environments. We sampled bird communities and vegetation across seral stages and biophysical settings at each of five landscapes arrayed across a productivity gradient from the Pacific Coast to the Rocky Mountains within the five northwestern states of the contiguous United States. We analyzed the response of richness to structural complexity and energy covariates at each landscape. We found that (1) richness had a hump-shaped relationship with available energy across the northwestern United States, (2) the landscape-scale relationships between energy and richness were positive or hump shaped in energy-limited locations and were flat or negative in energy-rich locations, (3) forest structural complexity explained more of the variation in bird species richness in energy-rich landscapes, and (4) the slope of the relationship between forest structural complexity and richness was steepest in energy-limited locations. In energy-rich locations, forest managers will likely increase landscape-scale bird diversity by providing a range of forest structural complexity across all seral stages. In low-energy environments, bird diversity will likely be maximized by managing local high-energy hotspots judiciously and adjusting harvest intensities in other locations to compensate for slower regeneration rates

    THE POTENTIAL EFFECT OF MINI-TRAMPOLINE STIFFNESS ON TAKE-OFF BEHAVIOUR OF GYMNASTS – A METHODOLOGICAL STUDY

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    The purpose of this study was to compare two mini-trampolines with different spring constant in regard to their effect on take-off mechanics. It was expected that the softer (36 springs) trampoline would lead to a longer contact time and a higher take-off impulse. To assess reaction forces during jumps a flexible force insole was used simultaneously with the measurement of run-in velocity by timing gates. Results showed no significant differences in contact mechanics or contact time indicating that the difference between these two trampolines is only marginal. Therefore, this study provides mainly a novel measurement approach to assess the effect of equipment changes in trampolining. Future studies are warranted to assess the athlete-equipment interaction in greater detail

    Retinoic acid has different effects on UCP1 expression in mouse and human adipocytes

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    BACKGROUND: Increased adipose thermogenesis is being considered as a strategy aimed at preventing or reversing obesity. Thus, regulation of the uncoupling protein 1 (UCP1) gene in human adipocytes is of significant interest. Retinoic acid (RA), the carboxylic acid form of vitamin A, displays agonist activity toward several nuclear hormone receptors, including RA receptors (RARs) and peroxisome proliferator-activated receptor δ (PPARδ). Moreover, RA is a potent positive regulator of UCP1 expression in mouse adipocytes. RESULTS: The effects of all-trans RA (ATRA) on UCP1 gene expression in models of mouse and human adipocyte differentiation were investigated. ATRA induced UCP1 expression in all mouse white and brown adipocytes, but inhibited or had no effect on UCP1 expression in human adipocyte cell lines and primary human white adipocytes. Experiments with various RAR agonists and a RAR antagonist in mouse cells demonstrated that the stimulatory effect of ATRA on UCP1 gene expression was indeed mediated by RARs. Consistently, a PPARδ agonist was without effect. Moreover, the ATRA-mediated induction of UCP1 expression in mouse adipocytes was independent of PPARγ coactivator-1α. CONCLUSIONS: UCP1 expression is differently affected by ATRA in mouse and human adipocytes. ATRA induces UCP1 expression in mouse adipocytes through activation of RARs, whereas expression of UCP1 in human adipocytes is not increased by exposure to ATRA

    An siRNA-based method for efficient silencing of gene expression in mature brown adipocytes

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    Brown adipose tissue is a promising therapeutic target for opposing obesity, glucose intolerance and insulin resistance. The ability to modulate gene expression in mature brown adipocytes is important to understand brown adipocyte function and delineate novel regulatory mechanisms of non-shivering thermogenesis. The aim of this study was to optimize a lipofection-based small interfering RNA (siRNA) transfection protocol for efficient silencing of gene expression in mature brown adipocytes. We determined that a critical parameter was to deliver the siRNA to mature adipocytes by reverse transfection, i.e. transfection of non-adherent cells. Using this protocol, we effectively knocked down both high- and low-abundance transcripts in a model of mature brown adipocytes (WT-1) as well as in primary mature mouse brown adipocytes. A functional consequence of the knockdown was confirmed by an attenuated increase in uncoupled respiration (thermogenesis) in response to β-adrenergic stimulation of mature WT-1 brown adipocytes transfected with uncoupling protein 1 siRNA. Efficient gene silencing was also obtained in various mouse and human white adipocyte models (3T3-L1, primary mouse white adipocytes, hMADS) with the ability to undergo “browning.” In summary, we report an easy and versatile reverse siRNA transfection protocol to achieve specific silencing of gene expression in various models of mature brown and browning-competent white adipocytes, including primary cells
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