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71.
The Late Miocene Italian brackish Loxoconchidae are herein discussed and illustrated. Three genera and two subgenera have been recognized in the brackish Italian basins: Loxoconcha, Loxocorniculina, Loxoconchissa (Loxoconchissa) and Loxoconchissa (Loxocaspia). Taking into account the diagnostic characters of several Loxoconchidae genera, in this paper Loxocorniculina is raised at a generic rank, Loxocaspia is confirmed as a subgenus within genus Loxoconchissa and several new species are established: Loxoconchissa (Loxoconchissa) kinoi nov. sp., Loxoconchissa (Loxocaspia) cosentinoi nov. sp., Loxoconchissa (Loxocaspia) nuda nov. sp., Loxoconchissa (Loxocaspia) punctata nov. sp., Loxoconchissa (Loxocaspia) reticulata nov. sp., Loxoconchissa (Loxocaspia) tuberosa nov. sp. and Loxoconchissa (Loxocaspia) velonae nov. sp. Loxocorniculina is a typical Paratethyan genus which widespread into the Palaeo-Mediterranean during the late Messinian Lago-Mare event. Loxoconchissa was known to be widespread only in the Paratethyan realm and in this paper it is signalled for the first time in the Late Tortonian-early Messinian of Italy. The palaeobiogeography of these genera is discussed and the observed continuous distribution of Loxocorniculina against the disjunct distribution of Loxoconchissa leads to suggest that this latter genus underwent a passive dispersal via aquatic birds. 相似文献
72.
High salinity alters chloroplast morpho-physiology in a freshwater Kirchneriella species (Selenastraceae) from Ethiopian Lake Awasa 总被引:1,自引:0,他引:1
Ferroni L Baldisserotto C Pantaleoni L Billi P Fasulo MP Pancaldi S 《American journal of botany》2007,94(12):1972-1983
Plants differ in their ability to tolerate salt stress. In aquatic ecosystems, it is important to know the responses of microalgae to increased salinity levels, especially considering that global warming will increase salinity levels in some regions of the Earth, e.g., Ethiopia. A green microalga, Kirchneriella sp. (Selenastraceae, Chlorophyta), isolated from freshwater Lake Awasa in the Rift Valley, Ethiopia, was cultured in media amended with 0, 0.4, 1.9, 5.9, and 19.4 g NaCl·L(-1) adjusted with NaCl to five salinity levels adjusted with NaCl. Growth was monitored for 3 mo, then samples were collected for photosynthetic pigment determinations, microspectrofluorimetric analyses, and micro- and submicroscopic examinations. The best growth was found at 1.9 g NaCl·L(-1). In the chloroplast, excess NaCl affected the coupling of light harvesting complex II and photosystem II (LHCII-PSII), but changes in thylakoid architecture and in the PSII assembly state allowed sufficient integrity of the photosynthetic membrane. The mucilaginous capsule around the cell probably provided partial protection against NaCl excess. On the whole, the microalga is able to acclimate to a range of NaCl concentrations, and this plasticity indicates that Kirchneriella sp. may survive future changes in water quality. 相似文献
73.
74.
Nicolas Tavernier Anna Noatynska Costanza Panbianco Lisa Martino Lucie Van Hove Fran?oise Schwager Thibaut Léger Monica Gotta Lionel Pintard 《The Journal of cell biology》2015,208(6):661-669
The molecular mechanisms governing mitotic entry during animal development are incompletely understood. Here, we show that the mitotic kinase CDK-1 phosphorylates Suppressor of Par-Two 1 (SPAT-1)/Bora to regulate its interaction with PLK-1 and to trigger mitotic entry in early Caenorhabditis elegans embryos. Embryos expressing a SPAT-1 version that is nonphosphorylatable by CDK-1 and that is defective in PLK-1 binding in vitro present delays in mitotic entry, mimicking embryos lacking SPAT-1 or PLK-1 functions. We further show that phospho–SPAT-1 activates PLK-1 by triggering phosphorylation on its activator T loop in vitro by Aurora A. Likewise, we show that phosphorylation of human Bora by Cdk1 promotes phosphorylation of human Plk1 by Aurora A, suggesting that this mechanism is conserved in humans. Our results suggest that CDK-1 activates PLK-1 via SPAT-1 phosphorylation to promote entry into mitosis. We propose the existence of a positive feedback loop that connects Cdk1 and Plk1 activation to ensure a robust control of mitotic entry and cell division timing. 相似文献
75.
Pamela Maris Arnaud Blomme Ana Perez Palacios Brunella Costanza Akeila Bellahcène Elettra Bianchi Stephanie Gofflot Pierre Drion Giovanna Elvi Trombino Emmanuel Di Valentin Pino G. Cusumano Sylvie Maweja Guy Jerusalem Philippe Delvenne Eric Lifrange Vincent Castronovo Andrei Turtoi 《PLoS medicine》2015,12(9)
BackgroundBreast cancer is a leading malignancy affecting the female population worldwide. Most morbidity is caused by metastases that remain incurable to date. TGF-β1 has been identified as a key driving force behind metastatic breast cancer, with promising therapeutic implications.ConclusionsOur data show that asporin is a stroma-derived inhibitor of TGF-β1 and a tumor suppressor in breast cancer. High asporin expression is significantly associated with less aggressive tumors, stratifying patients according to the clinical outcome. Future pre-clinical studies should consider options for increasing asporin expression in TNBC as a promising strategy for targeted therapy. 相似文献
76.
Nicolas Tavernier Costanza Panbianco Monica Gotta Lionel Pintard 《Cell cycle (Georgetown, Tex.)》2015,14(15):2394-2398
Mitosis is orchestrated by several protein kinases including Cdks, Plks and Aurora kinases. Despite considerable progress toward understanding the individual function of these protein kinases, how their activity is coordinated in space and time during mitosis is less well understood. In a recent article published in the Journal of Cell Biology, we show that CDK-1 regulates PLK-1 activity during mitosis in C. elegans embryos through multisite phosphorylation of the PLK-1 activator SPAT-1 (Aurora Borealis, Bora in human). SPAT-1 variants mutated on CDK-1 phosphorylation sites results in severe delays in mitotic entry, mimicking embryos lacking spat-1 or plk-1 function. We further show that SPAT-1 phosphorylation by CDK-1 promotes its binding to PLK-1 and stimulates PLK-1 phosphorylation on its activator T-loop by Aurora A kinase in vitro. Likewise, we find that phosphorylation of Bora by Cdk1 promotes phosphorylation of human Plk1 by Aurora A suggesting that this mechanism is conserved in humans. These results indicate that Cdk1 regulates Plk1 by boosting its kinase activity. Here we discuss these recent findings and open questions regarding the regulation of Plk1/PLK-1 by Cdk1/CDK-1 and Bora/SPAT-1. 相似文献
77.
Bocchi L Savi M Graiani G Rossi S Agnetti A Stillitano F Lagrasta C Baruffi S Berni R Frati C Vassalle M Squarcia U Cerbai E Macchi E Stilli D Quaini F Musso E 《PloS one》2011,6(3):e17750
Heart repair by stem cell treatment may involve life-threatening arrhythmias. Cardiac progenitor cells (CPCs) appear best suited for reconstituting lost myocardium without posing arrhythmic risks, being commissioned towards cardiac phenotype. In this study we tested the hypothesis that mobilization of CPCs through locally delivered Hepatocyte Growth Factor and Insulin-Like Growth Factor-1 to heal chronic myocardial infarction (MI), lowers the proneness to arrhythmias. We used 133 adult male Wistar rats either with one-month old MI and treated with growth factors (GFs, n = 60) or vehicle (V, n = 55), or sham operated (n = 18). In selected groups of animals, prior to and two weeks after GF/V delivery, we evaluated stress-induced ventricular arrhythmias by telemetry-ECG, cardiac mechanics by echocardiography, and ventricular excitability, conduction velocity and refractoriness by epicardial multiple-lead recording. Invasive hemodynamic measurements were performed before sacrifice and eventually the hearts were subjected to anatomical, morphometric, immunohistochemical, and molecular biology analyses. When compared with untreated MI, GFs decreased stress-induced arrhythmias and concurrently prolonged the effective refractory period (ERP) without affecting neither the duration of ventricular repolarization, as suggested by measurements of QTc interval and mRNA levels for K-channel α-subunits Kv4.2 and Kv4.3, nor the dispersion of refractoriness. Further, markers of cardiomyocyte reactive hypertrophy, including mRNA levels for K-channel α-subunit Kv1.4 and β-subunit KChIP2, interstitial fibrosis and negative structural remodeling were significantly reduced in peri-infarcted/remote ventricular myocardium. Finally, analyses of BrdU incorporation and distribution of connexin43 and N-cadherin indicated that cytokines generated new vessels and electromechanically-connected myocytes and abolished the correlation of infarct size with deterioration of mechanical function. In conclusion, local injection of GFs ameliorates electromechanical competence in chronic MI. Reduced arrhythmogenesis is attributable to prolongation of ERP resulting from improved intercellular coupling via increased expression of connexin43, and attenuation of unfavorable remodeling. 相似文献
78.
Viscomi C Bottani E Civiletto G Cerutti R Moggio M Fagiolari G Schon EA Lamperti C Zeviani M 《Cell metabolism》2011,14(1):80-90
Increased mitochondrial biogenesis by activation of PPAR- or AMPK/PGC-1α-dependent homeostatic pathways has been proposed as a treatment for mitochondrial disease. We tested this hypothesis on three recombinant mouse models characterized by defective cytochrome c-oxidase (COX) activity:?a knockout (KO) mouse for Surf1, a knockout/knockin mouse for Sco2, and a muscle-restricted KO mouse for Cox15. First, we demonstrated that double-recombinant animals overexpressing PGC-1α in skeletal muscle on a Surf1 KO background showed robust induction of mitochondrial biogenesis and increase of mitochondrial respiratory chain activities, including COX. No such effect was obtained by treating both Surf1(-/-) and Cox15(-/-) mice with the pan-PPAR agonist bezafibrate, which instead showed adverse effects in either model. Contrariwise, treatment with the AMPK agonist AICAR led to partial correction of COX deficiency in all three models, and, importantly, significant motor improvement up to normal in the Sco2(KO/KI) mouse. These results open new perspectives for therapy of mitochondrial disease. 相似文献
79.
P. Franchetti L. Cappellacci G. Abu Sheikha M. Grifantini A. G. Loi A. De Montis 《Nucleosides, nucleotides & nucleic acids》2013,32(3-5):607-610
Abstract The syntheses and antiviral activity of analogues of the anti-HIV agents PMEA, PMEDAP, (R)-PMPA, (R)-PMPDAP are described. In these analogues the adenine moiety is replaced by 4,6-diamino-5-nitro-pyrimidine (the aglycon of clitocine) or 2,4,6-triamino-5-nitro-pyrimidine. The synthesis of similar acyclic phosphonates related to PMEG and (R)-2′-methyl-PMEG is also reported. Some compounds proved to be active as anti-HIV agents. 相似文献
80.
Cecilia Bozzetti Federico Quaini Anna Squadrilli Marcello Tiseo Caterina Frati Costanza Lagrasta Cinzia Azzoni Lorena Bottarelli Maricla Galetti Angela Alama Silvana Belletti Rita Gatti Antonio Passaro Angela Gradilone Andrea Cavazzoni Roberta Alfieri Pier Giorgio Petronini Mara Bonelli Angela Falco Cecilia Carubbi Giuseppe Pedrazzi Rita Nizzoli Nadia Naldi Carmine Pinto Andrea Ardizzoni 《PloS one》2015,10(11)