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71.
Konstantina Marinoglou 《The Yale journal of biology and medicine》2012,85(4):469-480
It has been estimated that a human cell is confronted with 1 million DNA lesions
every day, one fifth of which may originate from the activity of Reactive Oxygen
Species (ROS) alone [1,2]. Terminally differentiated
neurons are highly active cells with, if any, very restricted regeneration
potential [3]. In
addition, genome integrity and maintenance during neuronal development is
crucial for the organism. Therefore, highly accurate and robust mechanisms for
DNA repair are vital for neuronal cells. This requirement is emphasized by the
long list of human diseases with neurodegenerative phenotypes, which are either
caused by or associated with impaired function of proteins involved in the
cellular response to genotoxic stress [4-8]. Ataxia
Telangiectasia Mutated (ATM), one of the major kinases of the DNA Damage
Response (DDR), is a node that links DDR, neuronal development, and
neurodegeneration [2,9-12]. In humans, inactivating mutations of ATM lead to
Ataxia-Telangiectasia (A-T) disease [11,13], which is
characterized by severe cerebellar neurodegeneration, indicating an important
protective function of ATM in the nervous system [14]. Despite the large number of studies on the
molecular cause of A-T, the neuroprotective role of ATM is not well established
and is contradictory to its general proapoptotic function. This review discusses
the putative functions of ATM in neuronal cells and how they might contribute to
neuroprotection. 相似文献
72.
In immersive virtual reality (IVR) it is possible to replace a person’s real body by a life-sized virtual body that is seen from first person perspective to visually substitute their own. Multisensory feedback from the virtual to the real body (such as the correspondence of touch and also movement) can also be present. Under these conditions participants typically experience a subjective body ownership illusion (BOI) over the virtual body, even though they know that it is not their real one. In most studies and applications the posture of the real and virtual bodies are as similar as possible. Here we were interested in whether the BOI is diminished when there are gross discrepancies between the real and virtual body postures. We also explored whether a comfortable or uncomfortable virtual body posture would induce feelings and physiological responses commensurate with the posture. We carried out an experiment with 31 participants in IVR realized with a wide field-of-view head-mounted display. All participants were comfortably seated. Sixteen of them were embodied in a virtual body designed to be in a comfortable posture, and the remainder in an uncomfortable posture. The results suggest that the uncomfortable body posture led to lesser subjective BOI than the comfortable one, but that participants in the uncomfortable posture experienced greater awareness of their autonomic physiological responses. Moreover their heart rate, heart rate variability, and the number of mistakes in a cognitive task were associated with the strength of their BOI in the uncomfortable posture: greater heart rate, lower heart rate variability and more mistakes were associated with higher levels of the BOI. These findings point in a consistent direction—that the BOI over a body that is in an uncomfortable posture can lead to subjective, physiological and cognitive effects consistent with discomfort that do not occur with the BOI over a body in a comfortable posture. 相似文献
73.
74.
Konstantina Fragaki Vincent Procaccio Sylvie Bannwarth Valrie Serre Sean OHearn Prasanth Potluri Gaelle Aug Florence Casagrande Cline Caruba Jean Claude Lambert Vronique Paquis-Flucklinger 《Mitochondrion》2009,9(5):346-352
Mutations within the mitochondrially encoded cytochrome b (MTCYB) gene are heteroplasmic and lead to severe exercise intolerance. We describe an unusual clinical presentation secondary to a novel homoplasmic mutation within MTCYB. The m.15635T > C transition (S297P) was carried by a newborn who presented with a polyvisceral failure. This mutation was responsible for a complex III deficiency. It was homoplasmic in all tissues tested and was undetectable in patient’s mother. Functional analyses, including studies on patient’s cybrid cell lines, demonstrate the pathogenicity of this variant. Our data show that mutations within MTCYB can be responsible for severe phenotype at birth. 相似文献
75.
Carotene production from waste cooking oil by Blakeslea trispora in a bubble column reactor: The role of oxidative stress 下载免费PDF全文
Konstantina Nanou Triantafyllos Roukas Emmanuel Papadakis Parthena Kotzekidou 《Engineering in Life Science》2017,17(7):775-780
The oxidative stress induced by hydroperoxides and reactive oxygen species (ROS) during carotene production from waste cooking oil (WCO) and corn steep liquor (CSL) by the fungus Blakeslea trispora in a bubble column reactor was investigated. The specific activities of the intracellular enzymes superoxide dismutase (SOD) and catalase (CAT) as well as the micromorphology of the fungus were measured in order to study the response of the fungus to oxidative stress. The changes of the morphology of microorganism leaded to pellets formation and documented using a computerized image analysis system. As a consequence of the mild oxidative stress induced by hydroperoxides of WCO and ROS a significant increase in carotene production was obtained. The highest carotene concentration (980.0 mg/l or 51.5 mg/g dry biomass) was achieved in a medium consisted of CSL (80.0 g/L) and WCO (50.0 g/L) at an aeration rate of 5 vvm after 6 days of fermentation. In this case the carotenes produced consisted of β‐carotene (71%), γ‐carotene (26%), and lycopene (3%). The strong oxidative stress in the fungus caused a significant increase of γ‐carotene concentration. Bubble column reactor is a useful fermentation system for carotene production in industrial scale. 相似文献
76.
77.
Kocheva KV Georgiev GI 《Zeitschrift für Naturforschung. C, Journal of biosciences》2008,63(1-2):101-104
The amino acid proline is accumulated in plant tissues in response to a variety of stresses. The existence of two routes for its biosynthesis is well documented. However, little is known about the contribution of each pathway to the accumulation of free proline under stress conditions. In the present study young barley plants were subjected to osmotic stress by treating their roots with 25% polyethylene glycol. Prior to stress imposition roots were incubated for 24 h in nutrient solution containing proline or one of its metabolic precursors: glutamate and ornithine. Free proline quantity in the leaves was measured before and after stress. Relative water content (RWC) was used as a measure of the plant water status. Foliar proline levels showed a significant increase in ornithine- and proline-pretreated plants compared to the control. Nevertheless, no considerable changes in leaf RWC were observed. It was shown that before stress application only ornithine but not glutamate was immediately metabolized to proline. Under stress conditions, however, both precursors were converted into proline. The possible role of this amino acid in the processes of post stress recovery is discussed. 相似文献
78.
Huynh H Wang X Li W Bottini N Williams S Nika K Ishihara H Godzik A Mustelin T 《Journal of immunology (Baltimore, Md. : 1950)》2003,171(12):6661-6671
Sec14p homology domains are found in a large number of proteins from plants, yeast, invertebrates, and higher eukaryotes. We report that the N-terminal Sec14p homology domain of the human protein tyrosine phosphatase PTP-MEG2 binds phosphatidylinositol-3,4,5-trisphosphate (PtdIns(3,4,5)P(3)) in vitro and colocalizes with this lipid on secretory vesicle membranes in intact cells. Point mutations that prevented PtdIns(3,4,5)P(3) binding abrogated the capacity of PTP-MEG2 to induce homotypic secretory vesicle fusion in cells. Inhibition of cellular PtdIns(3,4,5)P(3) synthesis also rapidly reversed the effect of PTP-MEG2 on secretory vesicles. Finally, we show that several different phosphoinositide kinases colocalize with PTP-MEG2, thus allowing for local synthesis of PtdIns(3,4,5)P(3) in secretory vesicle membranes. We suggest that PTP-MEG2 through its Sec14p homology domain couples inositide phosphorylation to tyrosine dephosphorylation and the regulation of intracellular traffic of the secretory pathway in T cells. 相似文献
79.
Ioannou Maria Zacharouli Konstantina Doukas Sotirios G. Diamantidis Michael D. Tsangari Vaya Karakousis Konstantinos Koukoulis George K. Vageli Dimitra P. 《Journal of molecular histology》2022,53(4):753-762
Journal of Molecular Histology - Hemophagocytic lymphohistiocytosis (HLH) constitutes a life-threatening inflammatory syndrome. Postmortem histological findings of bone marrow (BM) from COVID-19... 相似文献
80.
Nika K Tautz L Arimura Y Vang T Williams S Mustelin T 《The Journal of biological chemistry》2007,282(49):36000-36009
Src family kinases are suppressed by a "tail bite" mechanism, in which the binding of a phosphorylated tyrosine in the C terminus of the protein to the Src homology (SH) 2 domain in the N-terminal half of the protein forces the catalytic domain into an inactive conformation stabilized by an additional SH3 interaction. In addition to this intramolecular suppressive function, the SH2 domain also mediates intermolecular interactions, which are crucial for T cell antigen receptor (TCR) signaling. To better understand the relative importance of these two opposite functions of the SH2 domain of the Src family kinase Lck in TCR signaling, we created three mutants of Lck in which the intramolecular binding of the C terminus to the SH2 domain was strengthened. The mutants differed from wild-type Lck only in one to three amino acid residues following the negative regulatory tyrosine 505, which was normally phosphorylated by Csk and dephosphorylated by CD45 in the mutants. In the Lck-negative JCaM1 cell line, the Lck mutants had a much reduced ability to transduce signals from the TCR in a manner that directly correlated with SH2-Tyr(P)(505) affinity. The mutant with the strongest tail bite was completely unable to support any ZAP-70 phosphorylation, mitogen-activated protein kinase activation, or downstream gene activation in response to TCR ligation, whereas other mutants had intermediate abilities. Lipid raft targeting was not affected. We conclude that Lck is regulated by a weak tail bite to allow for its activation and service in TCR signaling, perhaps through a competitive SH2 engagement mechanism. 相似文献