339 research outputs found

    Porphyrin biosynthesis in soybean callus tissue system. Isolation, purification and general properties of δ-aminolaevulinate dehydratase

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    Fil:Tigier, H.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Batlle, A.M.d.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Locascio, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina

    Two separate functions of class II (Ia) molecules: T-cell stimulation and B-cell excitation.

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    We have evaluated the role of major histocompatibility complex-encoded class II (Ia) molecules as transmembrane signaling receptors in the T helper cell-dependent activation of B lymphocytes. For these studies, we utilized the murine B-cell lymphoma CH12, which expresses both I-A and I-E class II molecules. In addition, CH12 cells carry IgM of known antigen specificity and require both specific antigen and Ia-restricted T-cell help for the induction of antibody secretion. In this respect, they resemble normal resting B cells. We have studied the ability of antigen-specific or alloreactive T helper cells reactive with either the I-A or the I-E molecules on CH12 to be activated and their ability to stimulate antibody production by CH12. The results show that, although CH12 cells present antigen to T helper cells that interact with either the I-A or the I-E molecules, CH12 cells are stimulated to secrete antibody only by T helper cells reactive with their I-E molecules. Our data demonstrate that class II molecules are transducers of signals for B-cell excitation in addition to serving a restricting function for helper T-cell stimulation. Moreover, the data demonstrate that these two functions, T-cell stimulation and B-cell excitation, are discrete and need not be expressed by the same Ia molecule

    Serum heart-type fatty acid-binding protein and cerebrospinal fluid tau: Marker candidates for dementia with Lewy bodies

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    Background: The measurement of biomarkers in cerebrospinal fluid (CSF) has gained increasing acceptance in establishing the diagnosis of some neurodegenerative diseases. Heart-type fatty acid-binding protein (H-FABP) was recently discovered in CSF and serum of patients with neurodegenerative diseases. Objective: We investigated H-FABP in CSF and serum alone and in combination with CSF tau protein to evaluate these as potential biomarkers for the differentiation between dementia with Lewy bodies (DLB) and Alzheimer's disease (AD). Methods: We established H-FABP and tau protein values in a set of 144 persons with DLB (n = 33), Parkinson disease with dementia (PDD; n = 25), AD (n = 35) and nonclemented neurological controls (NNC; n = 51). Additionally, serum H-FABP levels were analyzed in idiopathic Parkinson disease patients without evidence of cognitive decline (n = 45) using commercially available enzyme-linked immunosorbent assays. We calculated absolute values of HFABP and tau protein in CSF and serum and established relative ratios between the two to obtain the best possible match for the clinical working diagnosis. Results: Serum HFABP levels were elevated in DLB and PDD patients compared with NNC and AD subjects. To better discriminate between DLB and AD, we calculated the ratio of serum H-FABP to CSF tau protein levels. At the arbitrary chosen cutoff ratio >= 8 this quotient reached a sensitivity of 91% and a specificity of 66%. Conclusion: Our results suggest that the measurement of CSF tau protein, together with H-FABP quantification in serum and CSF, and the ratio of serum H-FABP to CSF tau protein represent marker candidates for the differentiation between AD and DLB. Copyright (c) 2007 S. Karger AG, Basel

    Design and evaluation of artificial controllers assisting voluntary balance performance in paraplegia and in stroke

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    The mobility impairment caused by a paralysis like a spinal cord injury or a stroke has, beside many other impacts, an influence on the transfer of signals between the muscles of the lower extremities and the brain. In a paraplegic person, this means that she or he can not stand without holding onto a support or standing in a standing frame while the impact on the ability to balance in a hemiplegic person can be less severe. Although the connection between the muscles and the brain is impaired by the injury, the muscles still retain the ability to contract if innervated. This thesis describes control approaches which combine the remaining voluntary control of the paraplegic and stroke patients with the artificially controlled stimulation of the muscles of the paralysed limbs to aid the subject in balancing. The aim was to develop new control approaches which would assist balance in paraplegic subjects and in stroke. To support standing in paraplegic subjects, the moment generated at the ankle using electrical stimulation of the shank muscles was integrated with the voluntary control of the upper body, resulting in the concept of Integrated Voluntary Control (IVC). In the outer loop the ankle moment produced by the paraplegic subject due to his voluntary upper body movement was estimated using a mathematical model based on the inclination angles of upper and lower body. This estimated ankle moment was then compared with the actual moment applied at the force plates the subject was standing on, and an appropriate stimulation signal was applied to the paralysed shank muscles. Experimental evaluation initially involved four able bodied volunteers in which base line results with stiffness and stiffness-viscosity controllers using a rotating standing platform were obtained. This was extended to the paraplegic subject, where electrical muscle stimulation was used to generate the required ankle moment. The IVC concept was then evaluated with the paraplegic subject and compared to the base line results. Due to the nature of the system and implied perturbation onto the control system controlling the posture of the paraplegic subject the known evaluation values (e.g. rise time, steady state value, overshoot value etc.) are not suitable. Therefore, the variance of a time signal around its mean value was used as an evaluation value which allowed to compare the achieved performance of the paraplegic subject employing the new control approach with the stiffness and stiffness-viscosity controllers directly. To assist balance in stroke patients, a new training approach was introduced based on the concept of integrating the voluntary abilities of the patient with mechanical balance support and sensory electrical stimulation. This concept was evaluated in a training program with one stroke subject which demonstrated the feasibility and potential balance improvement resulting from this approach.EThOS - Electronic Theses Online ServiceGBUnited Kingdo

    Prodigal: prokaryotic gene recognition and translation initiation site identification

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    <p>Abstract</p> <p>Background</p> <p>The quality of automated gene prediction in microbial organisms has improved steadily over the past decade, but there is still room for improvement. Increasing the number of correct identifications, both of genes and of the translation initiation sites for each gene, and reducing the overall number of false positives, are all desirable goals.</p> <p>Results</p> <p>With our years of experience in manually curating genomes for the Joint Genome Institute, we developed a new gene prediction algorithm called Prodigal (PROkaryotic DYnamic programming Gene-finding ALgorithm). With Prodigal, we focused specifically on the three goals of improved gene structure prediction, improved translation initiation site recognition, and reduced false positives. We compared the results of Prodigal to existing gene-finding methods to demonstrate that it met each of these objectives.</p> <p>Conclusion</p> <p>We built a fast, lightweight, open source gene prediction program called Prodigal <url>http://compbio.ornl.gov/prodigal/</url>. Prodigal achieved good results compared to existing methods, and we believe it will be a valuable asset to automated microbial annotation pipelines.</p

    COP1 destabilizes DELLA proteins in Arabidopsis

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    DELLA transcriptional regulators are central components in the control of plant growth responses to the environment. This control is considered to be mediated by changes in the metabolism of the hormones gibberellins (GAs), which promote the degradation of DELLAs. However, here we show that warm temperature or shade reduced the stability of a GA-insensitive DELLA allele in Arabidopsis thaliana. Furthermore, the degradation of DELLA induced by the warmth preceded changes in GA levels and depended on the E3 ubiquitin ligase CONSTITUTIVELY PHOTOMORPHOGENIC1 (COP1). COP1 enhanced the degradation of normal and GA-insensitive DELLA alleles when coexpressed in Nicotiana benthamiana. DELLA proteins physically interacted with COP1 in yeast, mammalian, and plant cells. This interaction was enhanced by the COP1 complex partner SUPRESSOR OF phyA-105 1 (SPA1). The level of ubiquitination of DELLA was enhanced by COP1 and COP1 ubiquitinated DELLA proteins in vitro. We propose that DELLAs are destabilized not only by the canonical GA-dependent pathway but also by COP1 and that this control is relevant for growth responses to shade and warm temperature.This work was supported by the Spanish Ministry of Economy, Industry and Competitiveness and Agencia Española de Investigación/Fondo Europeo para el Desarrollo Regional/Unión Europea (grants BIO2016-79133-P to D.A. and BIO2013-46539-R and BIO2016-80551-R to V.R.); the European Union SIGNAT-Research and Innovation Staff Exchange (Grant H2020-MSCA-RISE-2014-644435 to M.A.B., D.A., and J.J.C.); the Argentinian Agencia Nacional de Promoción Científica y Tecnológica (Grant Proyectos de Investigación Científica y Tecnológica-2016-1459 to J.J.C.); Universidad de Buenos Aires (grant 20020170100505BA to J.J.C.); the National Institute of General Medical Sciences of the National Institutes of Health (awards R01GM067837 and R01GM056006 to S.A.K.); the German Research Foundation (DFG) under Germany’s Excellence Strategy/Initiative (Cluster of Excellence on Plant Sciences – Excellence Cluster EXC-2048/1, Project ID 390686111 to M.D.Z.); the International Max Planck Research School of the Max Planck Society; the Universities of Düsseldorf and of Cologne to T.B.; Nordrhein Westfalen Bioeconomy Science Center-FocusLabs CombiCom to N.H. and M.D.Z.; and Ministry of Education, Youth and Sports of the Czech Republic (Project LQ1601 Central European Institute of Technology 2020 to B.B. and M.C.). N.B.-T., E.I., and M.G.-L. were supported by Ministerio de Economía y Competitividad-Formación de Personal Investigador Program fellowships
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