Éditeur(s) : HAL CCSD
Résumé : Travaux Pratiques de Biochimie, IUT 2e année. Mise en place d'un réacteur enzymatique. Beta galactosidase. Transformation de l'oNPG en orthonitrophénol et galactose.
https://medihal.archives-ouvertes.fr/medihal-00459243
Terre Sainte, France

Droits : http://creativecommons.org/licenses/by-nc/
medihal-00459243
https://medihal.archives-ouvertes.fr/medihal-00459243
https://medihal.archives-ouvertes.fr/medihal-00459243/image
https://medihal.archives-ouvertes.fr/medihal-00459243/file/tp_biochimie_iut10.jpg

Éditeur(s) : HAL CCSD Nature Publishing Group
Résumé : International audience
Among pregnant women ibuprofen is one of the most frequently used pharmaceutical compounds with up to 28% reporting use. Regardless of this, it remains unknown whether ibuprofen could act as an endocrine disruptor as reported for fellow analgesics paracetamol and aspirin. To investigate this, we exposed human fetal testes (7-17 gestational weeks (GW)) to ibuprofen using ex vivo culture and xenograft systems. Ibuprofen suppressed testosterone and Leydig cell hormone INSL3 during culture of 8-9 GW fetal testes with concomitant reduction in expression of the steroidogenic enzymes CYP11A1, CYP17A1 and HSD17B3, and of INSL3. Testosterone was not suppressed in testes from fetuses younger than 8 GW, older than 10-12 GW, or in second trimester xenografted testes (14-17 GW). Ex vivo, ibuprofen also affected Sertoli cell by suppressing AMH production and mRNA expression of AMH, SOX9, DHH, and COL2A1. While PGE2 production was suppressed by ibuprofen, PGD2 production was not. Germ cell transcripts POU5F1, TFAP2C, LIN28A, ALPP and KIT were also reduced by ibuprofen. We conclude that, at concentrations relevant to human exposure and within a particular narrow â €' early window' of sensitivity within first trimester, ibuprofen causes direct endocrine disturbances in the human fetal testis and alteration of the germ cell biology. © The Author(s) 2017.
ISSN: 2045-2322

hal-01517095
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01517095
DOI : 10.1038/srep44184
PUBMED : 28281692

Éditeur(s) : HAL CCSD Wiley
Résumé : International audience
Mechanical forces influence the growth and shape of virtually all tissues and organs. Recent studies show that increased cell contractibility, growth and differentiation might be normalized by modulating cell tensions. Particularly, the role of these tensions applied by the extracellular matrix during liver fibrosis could influence the hepatocarcinogenesis process. The objective of this study is to determine if 3D stiffness could influence growth and phenotype of normal and transformed hepatocytes and to integrate extracellular matrix (ECM) stiffness to tensional homeostasis. We have developed an appropriate 3D culture model: hepatic cells within three-dimensional collagen matrices with varying rigidity. Our results demonstrate that the rigidity influenced the cell phenotype and induced spheroid clusters development whereas in soft matrices, Huh7 transformed cells were less proliferative, well-spread and flattened. We confirmed that ERK1 played a predominant role over ERK2 in cisplatin-induced death, whereas ERK2 mainly controlled proliferation. As compared to 2D culture, 3D cultures are associated with epithelial markers expression. Interestingly, proliferation of normal hepatocytes was also induced in rigid gels. Furthermore, biotransformation activities are increased in 3D gels, where CYP1A2 enzyme can be highly induced/activated in primary culture of human hepatocytes embedded in the matrix. In conclusion, we demonstrated that increasing 3D rigidity could promote proliferation and spheroid developments of liver cells demonstrating that 3D collagen gels are an attractive tool for studying rigidity-dependent homeostasis of the liver cells embedded in the matrix and should be privileged for both chronic toxicological and pharmacological drug screening.
ISSN: 0730-2312

hal-01196600
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01196600
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01196600/document
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01196600/file/Increasing%203D%20Matrix%20Rigidity_accepted.pdf
DOI : 10.1002/jcb.25356

Éditeur(s) : HAL CCSD
Résumé : Travaux Pratiques de Biochimie, IUT 2e année. Mise en place d'un réacteur enzymatique. Beta galactosidase. Transformation de l'oNPG en orthonitrophénol et galactose.
https://medihal.archives-ouvertes.fr/medihal-00459249
Terre Sainte, France

Droits : http://creativecommons.org/licenses/by-nc/
medihal-00459249
https://medihal.archives-ouvertes.fr/medihal-00459249
https://medihal.archives-ouvertes.fr/medihal-00459249/image
https://medihal.archives-ouvertes.fr/medihal-00459249/file/tp_biochimie_iut16.jpg

Éditeur(s) : HAL CCSD Public Library of Science
Résumé : International audience
Author Summary Leptospirosis is a common disease in tropical regions around the world. It is caused by a bacteria excreted in environmental waters by mammals, especially rodents, through their urine. Leptospirosis has symptoms similar to other tropical diseases, including dengue fever, and early laboratory diagnosis is crucial to provide both appropriate treatments for patients and rapid control measures when an outbreak occurs. In 2011, we undertook a study to determine the incidence of leptospirosis in two territories (Guadeloupe and Martinique) in the French West Indies by establishing a surveillance network and implementing new diagnostic assays in order to ensure an exhaustive diagnostic analysis. We concluded that leptospirosis was previously significantly under-reported in the French West Indies and we recommended: 1- access to these new diagnostic tests for the entire population for a better detection of leptospirosis patients and, 2- the implementation of an integrated surveillance, alert and prevention system for the disease in this region. Our findings had raised the awareness of this neglected disease in the French West Indies and, as another consequence; new diagnostic tests are now reimbursed by the social security insurance in France
ISSN: 1935-2727

Droits : http://creativecommons.org/licenses/by/
hal-01324701
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01324701
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01324701/document
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01324701/file/journal.pntd.0004668.pdf
DOI : 10.1371/journal.pntd.0004668

Éditeur(s) : HAL CCSD
Résumé : Travaux Pratiques de Biochimie, IUT 2e année. Mise en place d'un réacteur enzymatique. Beta galactosidase. Transformation de l'oNPG en orthonitrophénol et galactose.
https://medihal.archives-ouvertes.fr/medihal-00459246
Terre Sainte, France

Droits : http://creativecommons.org/licenses/by-nc/
medihal-00459246
https://medihal.archives-ouvertes.fr/medihal-00459246
https://medihal.archives-ouvertes.fr/medihal-00459246/image
https://medihal.archives-ouvertes.fr/medihal-00459246/file/tp_biochimie_iut13.jpg

Éditeur(s) : HAL CCSD
Résumé : Travaux Pratiques de Biochimie, IUT 2e année. Mise en place d'un réacteur enzymatique. Beta galactosidase. Transformation de l'oNPG en orthonitrophénol et galactose.
https://medihal.archives-ouvertes.fr/medihal-00459237
Terre Sainte, France

Droits : http://creativecommons.org/licenses/by-nc/
medihal-00459237
https://medihal.archives-ouvertes.fr/medihal-00459237
https://medihal.archives-ouvertes.fr/medihal-00459237/image
https://medihal.archives-ouvertes.fr/medihal-00459237/file/tp_biochimie_iut04.jpg

Résumé : Le genre Crassostrea regroupe de nombreuses espèces dont la répartition mondiale s'étend sur une grande partie des régions côtières des basses et moyennes latitudes. La classification des différentes espèces décrites à partir des critères morphologiques et de répartition géographique est aujourd'hui remise en cause dans de nombreux cas par les nouvelles études utilisent les techniques récentes de biologie moléculaire. C'est en particulier grâce à l'apport des séquences génomiques variables, qu'il a été possible de déterminer différentes espèces présentes sur les côtes africaines et américaines (Lapègue & al.). La présence de l'espèce C. gasar, d'abord décrite en Afrique, a ainsi été montré en Amérique. La répartition de cette espèce sur les deux continents laisse supposer que les barrières géographiques on induit une limitation des flux géniques et donc permis une divergence génétique des populations. Pour confirmer cette hypothèse une étude génétique des populations sur 3 populations de chaque continent a donc été réalisée. Elle s'est basée sur le marqueur nucléaire ITS2, séquence non transcrite et variable du génome nucléaire. Il a donc été possible, grâce aux techniques de RFLP (restriction fragments length polymorphisme) de démontrer une forte différenciation génétique entre les deux continents. Cependant le séquençage montre une divergence nucléotidique faible (3%). Ceci laisse supposer qu'il n'y a pas de flux génique entre les deux continents, et que les populations ont divergé récemment. De plus, le polymorphisme intracontinental observé uniquement en Afrique nous laisse supposer les populations américaines seraient originaires d'Afrique. La mise au point du séquençage et la lecture de deux séquences pour des individus de chaque continent a de plus permis de sélectionner de nouvelles enzymes de restriction utilisable en RFLP pour poursuivre l'étude du polymorphisme entre les populations.

Droits : 2001 Univ. La Rochelle, Ifremer
http://archimer.ifremer.fr/doc/00033/14407/11700.pdf
http://archimer.ifremer.fr/doc/00033/14407/

Éditeur(s) : HAL CCSD
Résumé : Travaux Pratiques de Biochimie, IUT 2e année. Mise en place d'un réacteur enzymatique. Beta galactosidase. Transformation de l'oNPG en orthonitrophénol et galactose.
https://medihal.archives-ouvertes.fr/medihal-00459239
Terre Sainte, France

Droits : http://creativecommons.org/licenses/by-nc/
medihal-00459239
https://medihal.archives-ouvertes.fr/medihal-00459239
https://medihal.archives-ouvertes.fr/medihal-00459239/image
https://medihal.archives-ouvertes.fr/medihal-00459239/file/tp_biochimie_iut06.jpg

Éditeur(s) : HAL CCSD
Résumé : National audience
Il virus dell’epatite C (HCV), a trasmissione parenterale, è stato identificato nel 1989 come il virus responsabile delle epatiti «non A non B». L’infezione colpisce circa 170 milioni di persone nel mondo e 200 000 persone in Francia hanno una replicazione virale attiva. Nei paesi industrializzati, l’epidemia ha accompagnato lo sviluppo della trasfusione sanguigna e della tossicomania endovenosa. I test enzyme-linked immunosorbent assay che individuano gli anticorpi anti-HCV hanno permesso uno screening attendibile dell’infezione a partire dal 1992. La rilevazione dell’acido ribonucleico virale C permette la diagnosi dell’infezione cronica che fa seguito all’epatite acuta in circa l’80% dei casi. La gravità dell’infezione è legata allo sviluppo progressivo di una fibrosi epatica che conduce alla cirrosi dopo una mediana di evoluzione di 30-40 anni. La malattia è, così, responsabile di circa 350 000 decessi per anno nel mondo, legati, in parti uguali, all’insufficienza epatica e al carcinoma epatocellulare. Il trattamento ha compiuto enormi progressi in 20 anni e nuove molecole antivirali sono in corso di sviluppo clinico.
EMC - AKOS - Trattato di Medicina

hal-01154232
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01154232
DOI : 10.1016/S1634-7358(15)70635-2

Éditeur(s) : Actes de colloques Ifremer, Tahiti, French Polynesia, 20 Feb - 4 Mar 1989, n°9, chap. 17, pp.171-181
Résumé : Symptoms recalling a nutritional pathology and more precisely a process of lipid peroxydation were observed during the last years in seabass Dicentrarchus labrax and other fishes cultured in tropical marine condition, Ocyurus chrysurus and Lutjanus analis . They included dark coloration, skin ulceration, lethargy, anorexy, emaciation. Histological examinations showed hepatic fatty degenerative lesions, pancreatitis, muscular degeneration and retinal atrophy. Additional vitamins E and C in the food suppressed that pathological symptoms. The previously evoked clinical or histological signs were not achieved in spite of an increase of the level of hepatic, muscular or blood malondialdehyde and of the conjugated dienes of the perivisceral fat. In the same time, hepatic and muscular tocopherol decreased. These experiments also showed the feasibility and the interest of different analyses in the characterization of such a pathology: hemolysis test and activity of enzymes such as erythrocytic catalase or superoxyde dismutase and plasma glutathione peroxydase. Another nutritional disease is worth describing again, the Granulomatous Hypertyrosinaemia. It was essentially investigated in turbot Scophtalmus maximus but other fish species such as sea bream Chrysophris aurata are often affected.

Droits : info:eu-repo/semantics/openAccess
http://archimer.ifremer.fr/doc/1989/acte-1501.pdf
http://archimer.ifremer.fr/doc/00000/1501/

Éditeur(s) : HAL CCSD
Résumé :  
The spatial genetic differentiation among European beech stands in western Germany was analysed by a new method. The genetic structure at 8 enzyme gene loci of 100 sampled populations was used as data base. The data represent authors' own results and published data from 8 different studies. For 10 geographic distance classes [h] from 0 to 500 km, the average genetic distance between the populations for each single gene locus, a gene-pool distance and the semivariances of genetic diversity gam were computed. Significant deviation from random spatial genetic structure was tested by permutation analysis. In many cases (Lap-B, Mdh-B, Mdh-C and 6Pgdh-C) the mean genetic distance between stands with spatial distance up to 200 km was significantly smaller and the genetic distance between stands with geographic distances of 200 and 400 km was significantly greater than expected for random spatial genetic structure. Similar tendencies were found for the gene-pool distance and the semivariances of diversity. Kriging, as a method for spatial interpolation, was used to draw synthetic maps of the spatial patterns of allelic frequencies and genetic diversity. The influence of postglacial recolonisation and regeneration with foreign seed material on the spatial genetic patterns are discussed
Forest genetics

hal-01032093
https://hal.archives-ouvertes.fr/hal-01032093

Éditeur(s) : HAL CCSD Wiley
Résumé : International audience
The Caribbean bivalves Codakia orbicularis (Linnée, 1758) and C. orbiculata (Montagu, 1808) live in seagrass beds of Thalassia testudinum and harbor intracellular sulfuroxidizing gamma-proteobacteria. These bacterial symbionts fix CO2 via the Calvin Benson cycle and provide organic compounds to the bivalve. During experimentally induced starvation, no reduced sulfur compounds and no organic particle food are available; the symbionts could be considered as the sole nutrient source of the host bivalve. A previous study has shown that the intracellular bacterial population decreased considerably during starvation and that bacterial endosymbionts were not released by the bivalves. In this study, the activity of two lysosomal marker enzymes (acid phosphatase and arylsulfatase) was detected using cytochemical experiments coupled with energy-dispersive X-ray transmission electron microscopy during sulfide and organic particle starvation. The degradation of bacterial endosymbionts began after 2 weeks of starvation in C. orbiculata and after 3 weeks in C. orbicularis. Degradation processes seem to be continuous over several months and could be responsible for the disappearance of the bacterial endosymbionts within the gills during starvation. These data suggest that the host use symbionts as a nutrient source to survive a hunger crisis. The carbon transfer from the symbionts to the host could be flexible and could consist in transfer of organic matter, “milking,” under normal feeding conditions and digestion of the symbionts under starved conditions.
ISSN: 1059-910X

Droits : info:eu-repo/semantics/OpenAccess
hal-01206367
https://hal.univ-antilles.fr/hal-01206367
https://hal.univ-antilles.fr/hal-01206367/document
https://hal.univ-antilles.fr/hal-01206367/file/revised%20version%20to%20be%20submitted%20to%20the%20editor3oct.pdf
DOI : 10.1002/jemt.22458

Éditeur(s) : HAL CCSD Springer Verlag
Résumé : International audience
The temperate symbiotic sea anemone Anemonia viridis, a member of the Cnidaria phylum, is a relevant experimental model to investigate the molecular and cellular events involved in the preservation or in the rupture of the symbiosis between the animal cells and their symbiotic microalgae, commonly named zooxanthellae. In order to increase research tools for this model, we developed a primary culture from A. viridis animal cells. By adapting enzymatic dissociation protocols, we isolated animal host cells from a whole tentacle in regeneration state. Each plating resulted in a heterogeneous primary culture consisted of free zooxanthellae and many regular, small rounded and adherent cells (of 3-5 mu m diameter). Molecular analyses conducted on primary cultures, maintained for 2 weeks, confirmed a specific signature of A. viridis cells. Further serial dilutions and micromanipulation allowed us to obtain homogenous primary cultures of the small rounded cells, corresponding to A. viridis ``epithelial-like cells''. The maintenance and the propagation over a 4 weeks period of primary cells provide, for in vitro cnidarian studies, a preliminary step for further investigations on cnidarian cellular pathways notably in regard to symbiosis interactions.
ISSN: 0920-9069

hal-01546173
https://hal.archives-ouvertes.fr/hal-01546173
DOI : 10.1007/s10616-013-9566-2

Éditeur(s) : HAL CCSD
Résumé : Travaux Pratiques de Biochimie, IUT 2e année. Mise en place d'un réacteur enzymatique. Beta galactosidase. Transformation de l'oNPG en orthonitrophénol et galactose.
https://medihal.archives-ouvertes.fr/medihal-00459251
Terre Sainte, France

Droits : http://creativecommons.org/licenses/by-nc/
medihal-00459251
https://medihal.archives-ouvertes.fr/medihal-00459251
https://medihal.archives-ouvertes.fr/medihal-00459251/image
https://medihal.archives-ouvertes.fr/medihal-00459251/file/tp_biochimie_iut17.jpg

Éditeur(s) : HAL CCSD
Résumé : Predicting, modelling and analysing the metabolism of xenobiotics, foreign substances to an organism, using computer methods, has been a major challenge for the scientific community for many years. This thesis aims to implement multiscale computing methods for predicting and analyzing the metabolism of xenobiotics. A first focus of this study was on the construction and de novo automatic annotation of metabolic graphs combining high sensitivity and precision. These graphs thus provide the prediction of the metabolism of xenobiotics in humans, as well as the genotoxicity of the molecules and atoms that make up xenobiotics. Then, the work focused on the implementation of a dynamic mathematical model modelling enzymatic competition effects through the development of a methodology allowing the exploitation of limited biological data while limiting inherent biases.
Prédire, modéliser et analyser le métabolisme de xénobiotiques, substances étrangères à un organisme, à l’aide de méthodes informatiques est un challenge majeur mobilisant la communauté scientifique depuis de nombreuses années. Cette thèse vise à implémenter des méthodes informatiques multi-échelles pour prédire et analyser le métabolisme des xénobiotiques. Un premier axe de cette étude portait sur la construction et l’annotation automatique de novo de graphes métaboliques combinant fortes sensibilités et précisions. Ces graphes fournissent ainsi la prédiction du métabolisme de xénobiotiques chez l’homme, ainsi que la génotoxicité des molécules et atomes qui le composent. Puis, le travail s’est orienté sur l’implémentation d’un modèle mathématique dynamique modélisant des effets de compétition enzymatique à travers le développement d’une méthodologie permettant l’exploitation de données biologiques restreintes tout en limitant les biais inhérents.
https://hal-univ-rennes1.archives-ouvertes.fr/tel-01659375

tel-01659375
https://hal-univ-rennes1.archives-ouvertes.fr/tel-01659375
https://hal-univ-rennes1.archives-ouvertes.fr/tel-01659375/document
https://hal-univ-rennes1.archives-ouvertes.fr/tel-01659375/file/these.pdf