RESUMEN
The diagnosis of kidney diseases in tortoises is only possible to a very limited extent on the basis of the general examination due to the development of unspecific disease symptoms. Extensive additional examinations are required to confirm the diagnosis. In addition to blood and urine tests, imaging techniques such as X-ray, computed tomography and MRI are suitable for visualizing the skeletal and organ systems, while additional samples can be taken during an endoscopic examination. There are clear species-specific differences with regard to the reference values of the laboratory parameters, which are in part significantly influenced by environmental influences, the seasons or even gender. It can also be seen that kidney diseases in tortoises kept in captivity are usually very advanced at the time of diagnosis, since these animals, like reptiles in general, show a pronounced lack of symptoms. Annual checks by a veterinarian specialized in reptiles can help to detect diseases at an early stage.
Asunto(s)
Enfermedades Renales , Tortugas , Animales , Enfermedades Renales/diagnóstico por imagen , Enfermedades Renales/veterinaria , Valores de Referencia , Estaciones del AñoRESUMEN
Background: Despite improvements in habitational conditions, kidney disease is relatively common in tortoises. Objectives: Purpose of this study was the establishment of Symmetrical dimethylarginine (SDMA) reference values for clinically healthy Hermann's Tortoises. Animals: Clinically healthy Hermann's Tortoises (n = 131) were included in the period from October 2017 to September 2019. Methods: Creatinine and other biomarkers were tested at IDEXX Laboratories, Germany using residual blood samples from Hermann's tortoises. SDMA was measured with the IDEXX test and verified by liquid chromatography-mass spectrometry at IDEXX Laboratories, USA. Results: SDMA values ranged from 1 to 21 µg/dl (n = 131) for the IDEXX SDMA Test and SDMA values ranged from 1 to 17 µg/dl (n = 82) for LC-MS. For the comparison of the two measuring systems, the following results were obtained R 2 = 0.75 (p < 0.001). Conclusion and Clinical Importance: SDMA can be measured in Hermann's Tortoises and the reference values range in clinically healthy animals is comparable to that of dogs and cats.
RESUMEN
Centrosome morphology and number are frequently deregulated in cancer cells. Here, to identify factors that are functionally relevant for centrosome abnormalities in cancer cells, we established a protein-interaction network around 23 centrosomal and cell-cycle regulatory proteins, selecting the interacting proteins that are deregulated in cancer for further studies. One of these components, LGALS3BP, is a centriole- and basal body-associated protein with a dual role, triggering centrosome hypertrophy when overexpressed and causing accumulation of centriolar substructures when downregulated. The cancer cell line SK-BR-3 that overexpresses LGALS3BP exhibits hypertrophic centrosomes, whereas in seminoma tissues with low expression of LGALS3BP, supernumerary centriole-like structures are present. Centrosome hypertrophy is reversed by depleting LGALS3BP in cells endogenously overexpressing this protein, supporting a direct role in centrosome aberration. We propose that LGALS3BP suppresses assembly of centriolar substructures, and when depleted, causes accumulation of centriolar complexes comprising CPAP, acetylated tubulin and centrin.
Asunto(s)
Antígenos de Neoplasias/metabolismo , Biomarcadores de Tumor/metabolismo , Proteínas Portadoras/metabolismo , Centriolos/metabolismo , Centriolos/patología , Glicoproteínas/metabolismo , Neoplasias/metabolismo , Neoplasias/patología , Animales , Antígenos de Neoplasias/genética , Biomarcadores de Tumor/genética , Proteínas Portadoras/genética , Línea Celular Tumoral , Centriolos/ultraestructura , Cromatografía de Afinidad , Proteínas de la Matriz Extracelular/metabolismo , Regulación Neoplásica de la Expresión Génica , Técnicas de Silenciamiento del Gen , Glicoproteínas/genética , Células HEK293 , Humanos , Hipertrofia , Masculino , Microtúbulos/metabolismo , Microtúbulos/ultraestructura , Neoplasias/genética , Mapas de Interacción de Proteínas , Proteínas Serina-Treonina Quinasas/metabolismo , Transporte de Proteínas , ARN Interferente Pequeño/metabolismo , Ratas , Ratas Sprague-Dawley , Seminoma/genética , Seminoma/patología , Huso Acromático/metabolismo , Huso Acromático/ultraestructuraRESUMEN
Phosphorylation is one of the key mechanisms that regulate centrosome biogenesis, spindle assembly, and cell cycle progression. However, little is known about centrosome-specific phosphorylation sites and their functional relevance. Here, we identified phosphoproteins of intact Drosophila melanogaster centrosomes and found previously unknown phosphorylation sites in known and unexpected centrosomal components. We functionally characterized phosphoproteins and integrated them into regulatory signaling networks with the 3 important mitotic kinases, cdc2, polo, and aur, as well as the kinase CkIIß. Using a combinatorial RNA interference (RNAi) strategy, we demonstrated novel functions for P granule, nuclear envelope (NE), and nuclear proteins in centrosome duplication, maturation, and separation. Peptide microarrays confirmed phosphorylation of identified residues by centrosome-associated kinases. For a subset of phosphoproteins, we identified previously unknown centrosome and/or spindle localization via expression of tagged fusion proteins in Drosophila SL2 cells. Among those was otefin (Ote), an NE protein that we found to localize to centrosomes. Furthermore, we provide evidence that it is phosphorylated in vitro at threonine 63 (T63) through Aurora-A kinase. We propose that phosphorylation of this site plays a dual role in controlling mitotic exit when phosphorylated while dephosphorylation promotes G(2)/M transition in Drosophila SL2 cells.
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Ciclo Celular , Centrosoma/metabolismo , Proteínas de Drosophila/metabolismo , Drosophila melanogaster/citología , Proteínas de la Membrana/metabolismo , Membrana Nuclear/metabolismo , Proteínas Nucleares/metabolismo , Proteínas Serina-Treonina Quinasas/metabolismo , Animales , Aurora Quinasas , Proteína Quinasa CDC2/genética , Proteína Quinasa CDC2/metabolismo , Quinasa de la Caseína II/genética , Quinasa de la Caseína II/metabolismo , Línea Celular , Proteínas de Drosophila/genética , Drosophila melanogaster/genética , Drosophila melanogaster/metabolismo , Proteínas de la Membrana/análisis , Proteínas Nucleares/análisis , Fosforilación , Proteínas Serina-Treonina Quinasas/genética , Interferencia de ARNRESUMEN
Regulation of centrosome structure, duplication and segregation is integrated into cellular pathways that control cell cycle progression and growth. As part of these pathways, numerous proteins with well-established non-centrosomal localization and function associate with the centrosome to fulfill regulatory functions. In turn, classical centrosomal components take up functional and structural roles as part of other cellular organelles and compartments. Thus, although a comprehensive inventory of centrosome components is missing, emerging evidence indicates that its molecular composition reflects the complexity of its functions. We analysed the Drosophila embryonic centrosomal proteome using immunoisolation in combination with mass spectrometry. The 251 identified components were functionally characterized by RNA interference. Among those, a core group of 11 proteins was critical for centrosome structure maintenance. Depletion of any of these proteins in Drosophila SL2 cells resulted in centrosome disintegration, revealing a molecular dependency of centrosome structure on components of the protein translation machinery, actin- and RNA-binding proteins. In total, we assigned novel centrosome-related functions to 24 proteins and confirmed 13 of these in human cells.
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Proteínas de Ciclo Celular/metabolismo , Centrosoma/química , Proteínas Cromosómicas no Histona/metabolismo , Drosophila/química , Mitosis/fisiología , Animales , Proteínas de Ciclo Celular/genética , Centrosoma/fisiología , Proteínas Cromosómicas no Histona/genética , Drosophila/fisiología , Embrión no Mamífero/metabolismo , Embrión no Mamífero/fisiología , Espectrometría de Masas , Proteómica/métodos , Interferencia de ARNRESUMEN
The spindle assembly checkpoint guards the fidelity of chromosome segregation. It requires the close cooperation of cell cycle regulatory proteins and cytoskeletal elements to sense spindle integrity. The role of the centrosome, the organizing center of the microtubule cytoskeleton, in the spindle checkpoint is unclear. We found that the molecular requirements for a functional spindle checkpoint included components of the large gamma-tubulin ring complex (gamma-TuRC). However, their localization at the centrosome and centrosome integrity were not essential for this function. Thus, the spindle checkpoint can be activated at the level of microtubule nucleation.
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Proteínas de Drosophila/metabolismo , Proteínas Asociadas a Microtúbulos/metabolismo , Mitosis , Huso Acromático/metabolismo , Tubulina (Proteína)/metabolismo , Animales , Proteínas de Ciclo Celular/metabolismo , Línea Celular , Centrosoma/fisiología , Proteínas de Drosophila/genética , Drosophila melanogaster , Proteínas de Homeodominio/genética , Proteínas de Homeodominio/metabolismo , Humanos , Cinetocoros/metabolismo , Proteínas Asociadas a Microtúbulos/genética , Microtúbulos/ultraestructura , Proteínas Quinasas/metabolismo , Proteínas Serina-Treonina Quinasas , Interferencia de ARN , Huso Acromático/ultraestructuraRESUMEN
Classical protocols for the isolation of centrosomes from higher eukaryotic cells are based on enrichment of cell organelles by density gradient centrifugation. Various successful protocols have been described that isolate centrosomes from mammalian tissue culture cells, tissue, clam oocytes, Drosophila, and yeast, to mention only some of the more frequently used sources. The material produced is subsequently used in various assays. These include functional tests such as the microtubule nucleation assay, electron microscopic study of centrosome morphology, and antigen localization; the organelles may also be used for the generation of antibodies. Furthermore, centrosomal preparations have been used for the characterization of their protein composition. The method described here focuses on the isolation of centrosomes from the syncytial stages of the early Drosophila embryo. This is a particularly attractive system because these organelles are not bounded by cellular membranes. Moreover, the abundance of pericentriolar material of these centrosomes produces excellent total protein yields.
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Fraccionamiento Celular/métodos , Centrifugación por Gradiente de Densidad/métodos , Centrosoma/ultraestructura , Embrión no Mamífero/citología , Animales , Centrosoma/inmunología , Drosophila melanogaster , Técnica del Anticuerpo FluorescenteRESUMEN
BACKGROUND: Pathogenic Yersinia species (Y. enterocolitica, Y. pestis, Y. pseudotuberculosis) share a type three secretion system (TTSS) which allows translocation of effector proteins (called Yops) into host cells. It is believed that proteins are delivered through a hollow needle with an inner diameter of 2-3 nm. Thus transport seems to require substrates which are essentially unfolded. Recent work from different groups suggests that the Yersinia TTSS cannot accommodate substrates which are folded prior to secretion. It was suggested that folding is prevented either by co-translational secretion or by the assistance of specific Yop chaperones (called Sycs). RESULTS: In this study we have fused YopE secretion signals of various length to the mouse dihydrofolate reductase (DHFR) in order to analyse the DHFR folding state prior to secretion. We could demonstrate that secretion-deficient as well as secretion-competent YopE-DHFR fusions complexed to SycE can be efficiently purified from Yersinia cytosol by affinity chromatography using methotrexate-agarose. This implies the folding of the DHFR fusion moiety despite SycE binding and contradicts the previously presented model of folding inhibition by chaperone binding. Secretion-deficient YopE-DHFR fusions caused severe jamming of the TTSS. This observation contradicts the co-translational secretion model. CONCLUSIONS: We present evidence that the Yersinia TTSS is familiar with the processing of transport substrates which are folded prior to secretion. We therefore predict that an unfoldase is involved in type III secretion.
Asunto(s)
Proteínas de la Membrana Bacteriana Externa/metabolismo , Yersinia enterocolitica/metabolismo , Proteínas de la Membrana Bacteriana Externa/genética , Proteínas Bacterianas/metabolismo , Transporte Biológico Activo , Pliegue de Proteína , Señales de Clasificación de Proteína/genética , Señales de Clasificación de Proteína/fisiología , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Tetrahidrofolato Deshidrogenasa/genética , Tetrahidrofolato Deshidrogenasa/metabolismo , Transactivadores/metabolismo , Yersinia enterocolitica/crecimiento & desarrolloRESUMEN
The flagellum is believed to be the common ancestor of all type III secretion systems (TTSSs). In Yersinia enterocolitica, expression of the flagellar TTSS and the Ysc (Yop secretion) TTSS are inversely regulated. We therefore hypothesized that the Ysc TTSS may adopt flagellar motor components in order to use the pathogenicity-related translocon in a drill-like manner. As a prerequisite for this hypothesis, we first tested a requirement for the proton motive force by both systems using the protonophore carbonyl cyanide m-chlorophenylhydrazone (CCCP). Motility as well as type III-dependent secretion of Yop proteins was inhibited by CCCP. We deleted motAB, which resulted in an immotile phenotype. This mutant, however, secreted amounts of Yops to the supernatant comparable to those of the wild type. Translocation of Yops into host cells was also not affected by the motAB deletion. Virulence of the mutant was comparable to that of the wild type in the mouse oral infection model. Thus, the hypothesis that the Ysc TTSS might adopt flagellar motor components was not confirmed. The finding that, in addition to consumption of ATP, Ysc TTSS requires the proton motive force is discussed.
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Proteínas Bacterianas/metabolismo , Fuerza Protón-Motriz/fisiología , Yersinia enterocolitica/metabolismo , Animales , Carbonil Cianuro m-Clorofenil Hidrazona/farmacología , Flagelos/metabolismo , Ratones , Virulencia/genética , Virulencia/fisiología , Yersinia enterocolitica/efectos de los fármacos , Yersinia enterocolitica/patogenicidadRESUMEN
All pathogenic Yersinia species (Y. enterocolitica, Y. pestis, and Y. pseudotuberculosis) share a type three secretion system (TTSS) that allows translocation of effector proteins into host cells. Yersinia enterocolitica SycH is a chaperone assisting the transport of the effector YopH and two regulatory components of the TTSS, YscM1 and YscM2. We have recombinantly expressed SycH in Escherichia coli. Purification of tag-free SycH to near homogeneity was achieved by combining ammonium sulfate precipitation, anion exchange chromatography, and gel filtration. Functionality of purified SycH was proven by demonstrating binding to YopH. SycH crystals were grown that diffracted to 2.94A resolution. Preliminary crystallographic data and biochemical findings suggest that SycH forms homotetramers. SycH may therefore represent a novel class of TTSS chaperones. In addition, we found that YopH was enzymatically active in the presence of SycH. This implies that the function of the secretion chaperone SycH is not to keep YopH in a globally unfolded state prior to secretion.