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101.
Coordination of cell death and survival is crucial during embryogenesis and adulthood, and alteration of this balance can result in degeneration or cancer. Growth factor receptors such as Met can activate phosphatidyl-inositol-3' kinase (PI3K), a major intracellular mediator of growth and survival. PI3K can then antagonize p53-triggered cell death, but the underlying mechanisms are not fully understood. We used genetic and pharmacological approaches to uncover Met-triggered signaling pathways that regulate hepatocyte survival during embryogenesis. Here, we show that PI3K acts via mTOR (Frap1) to regulate p53 activity both in vitro and in vivo. mTOR inhibits p53 by promoting the translation of Mdm2, a negative regulator of p53. We also demonstrate that the PI3K effector Akt is required for Met-triggered Mdm2 upregulation, in addition to being necessary for the nuclear translocation of Mdm2. Inhibition of either mTOR or Mdm2 is sufficient to block cell survival induced by Hgf-Met in vitro. Moreover, in vivo inhibition of mTOR downregulates Mdm2 protein levels and induces p53-dependent apoptosis. Our studies identify a novel mechanism for Met-triggered cell survival during embryogenesis, involving translational regulation of Mdm2 by mTOR. Moreover, they reinforce mTOR as a potential drug target in cancer. 相似文献
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103.
An Escherichia coli vector to express and purify foreign proteins by fusion to and separation from maltose-binding protein 总被引:50,自引:0,他引:50
C V Maina P D Riggs A G Grandea B E Slatko L S Moran J A Tagliamonte L A McReynolds C D Guan 《Gene》1988,74(2):365-373
A plasmid vector has been constructed that directs the synthesis of high levels (approximately 2% of total cellular protein) of fusions between a target protein and maltose-binding protein (MBP) in Escherichia coli. The MBP domain is used to purify the fusion protein in a one step procedure by affinity chromatography to crosslinked amylose resin. The fusion protein contains the recognition sequence (Ile-Glu-Gly-Arg) for blood coagulation factor Xa protease between the two domains. Cleavage by factor Xa separates the two domains and the target protein domain can then be purified away from the MBP domain by repeating the affinity chromatography step. A prokaryotic (beta-galactosidase) and a eukaryotic (paramyosin) protein have been successfully purified by this method. 相似文献
104.
The epithelial cell lining of the respiratory groove ofAlma emini,an oligochaete glossoscolecid worm that lives in a hydrogen sulfide (H2S)-rich tropical swamp, was investigated by transmission electron microscopy to determine the underlying structural adaptations which enable the worm to subsist in a highly inimical habitat. The epithelium of the respiratory groove is made up of squamous cells with a highly amplified free epithelial surface. The cells are tightly packed with electron dense sulfur metabolizing bodies (SMBs) and contain endosymbiotic bacteria. Presence of sulfur in the electron dense SMBs was confirmed by X-ray microanalysis. Certain eukaryotic cells with prominent filopodia-like cytoplasmic extensions were observed under the epithelial cells and in the muscle tissue. The cells contained numerous heteromorphic endosymbiotic bacteria and scattered SMBs. Both the SMBs and the bacteria are reckoned to be involved in scavenging and detoxifying H2S. The removal of sulfide complexes was observed to occur through excision of blebs formed by epithelial cell membrane elaborations and by exocytosis of crystalline-like particles. These adaptive stratagems generally correspond with those that have been adopted by many marine and hydrothermal vent organisms that occupy sulfide-rich biomes. The congruent adaptive stratagems and ultrastructural morphologies in such a diverse community of organisms have been imposed by a common need to neutralize the insidious effects of H2S in their environments. 相似文献
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107.
Yannan Fan Sylvie Richelme Emilie Avazeri Stéphane Audebert Fran?oise Helmbacher Rosanna Dono Flavio Maina 《PLoS genetics》2015,11(9)
The successive events that cells experience throughout development shape their intrinsic capacity to respond and integrate RTK inputs. Cellular responses to RTKs rely on different mechanisms of regulation that establish proper levels of RTK activation, define duration of RTK action, and exert quantitative/qualitative signalling outcomes. The extent to which cells are competent to deal with fluctuations in RTK signalling is incompletely understood. Here, we employ a genetic system to enhance RTK signalling in a tissue-specific manner. The chosen RTK is the hepatocyte growth factor (HGF) receptor Met, an appropriate model due to its pleiotropic requirement in distinct developmental events. Ubiquitously enhanced Met in Cre/loxP-based Rosa26
stopMet knock-in context (Del-R26
Met) reveals that most tissues are capable of buffering enhanced Met-RTK signalling thus avoiding perturbation of developmental programs. Nevertheless, this ubiquitous increase of Met does compromise selected programs such as myoblast migration. Using cell-type specific Cre drivers, we genetically showed that altered myoblast migration results from ectopic Met expression in limb mesenchyme rather than in migrating myoblasts themselves. qRT-PCR analyses show that ectopic Met in limbs causes molecular changes such as downregulation in the expression levels of Notum and Syndecan4, two known regulators of morphogen gradients. Molecular and functional studies revealed that ectopic Met expression in limb mesenchyme does not alter HGF expression patterns and levels, but impairs HGF bioavailability. Together, our findings show that myoblasts, in which Met is endogenously expressed, are capable of buffering increased RTK levels, and identify mesenchymal cells as a cell type vulnerable to ectopic Met-RTK signalling. These results illustrate that embryonic cells are sensitive to alterations in the spatial distribution of RTK action, yet resilient to fluctuations in signalling levels of an RTK when occurring in its endogenous domain of activity. 相似文献
108.
Globally, fisheries are challenged by the combined impacts of overfishing, degradation of ecosystems and impacts of climate change, while fisheries livelihoods are further pressured by conservation policy imperatives. Fishers' adaptive responses to these pressures, such as exiting from a fishery to pursue alternative livelihoods, determine their own vulnerability, as well as the potential for reducing fishing effort and sustaining fisheries. The willingness and ability to make particular adaptations in response to change, such as exiting from a declining fishery, is influenced by economic, cultural and institutional factors operating at scales from individual fishers to national economies. Previous studies of exit from fisheries at single or few sites, offer limited insight into the relative importance of individual and larger-scale social and economic factors. We asked 599 fishers how they would respond to hypothetical scenarios of catch declines in 28 sites in five western Indian Ocean countries. We investigated how socioeconomic variables at the individual-, household- and site-scale affected whether they would exit fisheries. Site-level factors had the greatest influence on readiness to exit, but these relationships were contrary to common predictions. Specifically, higher levels of infrastructure development and economic vitality - expected to promote exit from fisheries - were associated with less readiness to exit. This may be due to site level histories of exit from fisheries, greater specialisation of fishing households, or higher rewards from fishing in more economically developed sites due to technology, market access, catch value and government subsidies. At the individual and household scale, fishers from households with more livelihood activities, and fishers with lower catch value were more willing to exit. These results demonstrate empirically how adaptive responses to change are influenced by factors at multiple scales, and highlight the importance of understanding natural resource-based livelihoods in the context of the wider economy and society. 相似文献
109.
A H Tashjian M E Lomedico D Maina 《Biochemical and biophysical research communications》1978,81(3):798-806
Thyrotropin-releasing hormone (TRH) or 50 mM K+ stimulated the acute release of prolactin from the GH4C1 strain of rat pituitary cells in culture. The enhanced release of prolactin was inhibited in a dose-related manner by the Ca+2 antagonist Co+2 (2.0 to 0.5 mM) as well as by the Ca+2 chelator EGTA (1.0 mM). Co+2 also reduced spontaneous basal prolactin release. There was partial reversal of the inhibitory effect of Co+2 (2.0 mM) by Ca+2 (2.0 mM) and complete reversal of the inhibitory effect of EGTA (1.0 mM) by Ca+2 (2.0 mM). The enhanced release of prolactin stimulated by 50 mM K+ was maximal by 10–20 minutes in medium containing 0.67 to 0.74 mM Ca+2. Na+ (50 mM) did not mimic the effect of high K+. We conclude that Ca+2 is an essential cation in mediating the actions of high external K+ and TRH on the release of prolactin by GH4C1 cells. 相似文献
110.
Tönges L Ostendorf T Lamballe F Genestine M Dono R Koch JC Bähr M Maina F Lingor P 《Journal of neurochemistry》2011,117(5):892-903
Hepatocyte growth factor (HGF) is known to promote the survival and foster neuritic outgrowth of different subpopulations of CNS neurons during development. Together with its corresponding receptor c-mesenchymal-epithelial transition factor (Met), it is expressed in the developing and the adult murine, rat and human CNS. We have studied the role of HGF in paradigms of retinal ganglion cell (RGC) regeneration and cell death in vitro and in vivo. After application of recombinant HGF in vitro, survival of serum-deprived RGC-5 cells and of growth factor-deprived primary RGC was significantly increased. This was shown to be correlated to the phosphorylation of c-Met and subsequent activation of serine/threonine protein kinase Akt and MAPK downstream signalling pathways involved in neuronal survival. Furthermore, neurite outgrowth of primary RGC was stimulated by HGF. In vivo, c-Met expression in RGC was up-regulated after optic nerve axotomy lesion. Here, treatment with HGF significantly improved survival of axotomized RGC and enhanced axonal regeneration after optic nerve crush. Our data demonstrates that exogenously applied HGF has a neuroprotective and regeneration-promoting function for lesioned CNS neurons. We provide strong evidence that HGF may represent a trophic factor for adult CNS neurons, which may play a role as therapeutic target in the treatment of neurotraumatic and neurodegenerative CNS disorders. 相似文献