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121.
122.
Dominique Le Grand Michel Solsona Renate Rosengarten francois Poumarat 《FEMS microbiology letters》1996,144(2-3):267-275
Abstract The variability of predominant Mycoplasma bovis surface antigens in the presence of specific immune pressure was analyzed in an in vitro assay to determine if M. bovis could escape immune destruction. We have shown that serum antibodies from immunized or experimentally infected calves and monoclonal antibodies which specifically react with previously characterized or as yet undefined major M. bovis membrane surface proteins cause repression of expression or shortening of the target protein, or induce switching to expression of an antigenically distinct variant protein. We have further demonstrated that removal of the inducing antibody results in reversion to the original phenotype. These results suggest that the level of expression and the length of M. bovis surface antigens in the host is modulated by cognate antibodies. According to the surface antigenic variation systems, random selection of preexisting variants resistant to antibody-mediated inhibition or direct regulation of gene expression may be means by which this organism evades host immune defences. 相似文献
123.
B. M. Culik K. Pütz R. P. Wilson C. A. Bost Y. Le Maho J. -L. Verselin 《Polar Biology》1996,16(5):371-378
Core temperature was determined in two king penguins living in the wild at Ile de la Possession, Crozel Archipelago, using
implantable four-channel temperature loggers. Core temperatures derived from bird no. 1 (sensor placed under the sternum,
in the vicinity of the liver and upper stomach) were closely correlated with diving activity (as determined by an external
light recorder), and ranged from 38.3°C, (on land) to a minimum of 37.2°C during a dive. Core temperatures measured in bird
no. 2 showed that temperatures near the heart were generally 1°C lower than those under the sternum or in the lower abdomen.
Core temperatures declined continuously during dives (by 0.8, 1.2 and 2.7°C in the lower abdomen, under the sternum and near
the heart, respectively) and showed precipitous drops to 35°C, probably associated with ingestion of food. Temperatures measured
near the heart fluctuated over a period of 288 s, corresponding to the duration (from the literature) of the surface/dive
cycle. The relevance of these findings with respect to diving physiology, blood perfusion of tissues, tissue metabolism and
aerobic dive limits is discussed. 相似文献
124.
John O. Hui John Le Viswanatham Katta Robert Rosenfeld Michael F. Rohde Mitsuru Haniu 《Journal of Protein Chemistry》1996,15(4):351-358
Human neurotrophin-3 (NT-3) is a member of the nerve growth factor (NGF) family of neurotrophic factors, and the recombinant protein is being developed as a therapeutic for neurodegenerative diseases. The final product purity and lot-to-lot variation are monitored routinely by peptide mapping. However, only the N-terminal region of NT-3 was susceptible to proteolysis under native conditions. Complete digestion required that the protein be chemically modified by reduction and S-alkylation prior to proteolysis. Complete proteolytic degradation of the protein was achieved simply by an intial denaturation of NT-3 in 6 M guanidinium chloride (pH 6) for 2 hr at 37°C, followed by a tenfold dilution with the digestion buffer (0.1 M Tris-HCl, 1 mM CaCl2 at pH 7.0) and immediate addition of chymotrypsin at 1% by weight. Direct comparison of the peptide map with an identical aliquot that had been reduced and alkylated also allowed the establishment of the cystine linkages present in NT-3: Cys14 to Cys79, Cys57 to Cys108, and Cys67 to Cys110. This disulfide structure is homologous to the NGF family of neurotrophic factors. 相似文献
125.
126.
127.
M. C. Léglise P. Darodes de Tailly J. L. Vignot M. A. Le Bot A.-M. Le Roux C. Riché 《Cell biology and toxicology》1996,12(1):39-53
A cellular model of hematopoiesis which would be more convenient than bone marrow (BM) progenitors and directly relevant to human pathology is needed in order to investigate xenobiotic toxicity. Human umbilical cord blood (HCB), previously shown to be able to repopulate BM, provides a powerful in vitro model of normal human hematopoiesis. In order to validate the use of normal HCB progenitors as targets for dose-related myelosuppression, we used clonogenic assays and expansion in a liquid culture of progenitor-enriched cell suspensions from HCB. A series of 8 reference molecules, doxorubicin, cytosine-arabinoside, 5-fluorouracil, 3-azido-3-deoxythymidine, acetylsalicyclic acid, sodium valproate and two cephalosporin antibiotics, were tested. In vitro 50% inhibition concentrations (IC50) were compared to those observed or reported with BM progenitors, and to the values of plasma concentrations from treated patients. HCB progenitors as in vitro targets for cytotoxic molecules were easy to access and handle, and their use was sensitive, specific and reproducible. They gave results similar to BM progenitors and allowed a qualitative approach to cellular metabolism and toxicity using morphological, flow cytometric and chromatographic methods.Abbreviations ARA-CC
cytosine arabinoside
- AS
acetylsalicylic acid
- AZTT
3-azido-3-deoxythymidine
- BFUU
burst-forming units
- BM
bone marrow
- CFU
colony-forming units
- DOXX
doxorubicin
- FU
5-fluorouracil
- glyAA
glyAcophorin A
- HCB
human umbilical cord blood
- IU
international units
- PCMEM
human placenta-conditioned medium
- VA
sodium valproate 相似文献
128.
A. Le Ralec 《BioControl》1995,40(1):87-93
Using transmission electron microscopy, egg content is studied in 10 parasitoid species, which either feed on host hemolymph or do not. As expected, hydropic eggs were found to contain little yolk which is only lipoid. In host-feeding species, the yolk contains a great number of typical protein bodies whereas in species that do not host-feed and which produce large eggs, the yolk contain very different bodies. 相似文献
129.
C. Kevers B. Bisbis F. Le Dily J. P. Billard C. Huault Th. Gaspar 《In vitro cellular & developmental biology. Plant》1995,31(2):122-126
The transfer of light-cultured green normal (N) and white habituated (HNO) sugarbeet callus to darkness reduced the growth
of N callus and improved growth and delayed necrosis in the HNO callus. The decrease of dry matter of N callus under darkness
was accompanied by a reduced content of carotenoids and by decreased CO2 fixation, which was compensated by an increased dependency on externally supplied sucrose. The levels of some organic nitrogen
compounds such as glutamate, proline, and free polyamines were not affected by transfer to darkness of N or HNO callus. Darkness
decreased ethylene emissions in both callus types. In the HNO callus, the sucrose growth dependency and the CO2 fixation were unaffected by darkness. Chlorophylls were absent both in light and darkness, whereas some carotenoids were
accumulated in the HNO callus only in dark conditions. In another connection, a significant increase of peroxidase activity,
which did not occur in the N callus, was induced by darkness in the HNO callus. A decreased content of thio-barbituric acid
(TBA)-reactive substances was measured in the HNO callus transferred to darkness, whereas an increase was noticed in the N
callus placed in the same conditions. These metabolic changes and the reduction of cellular damage in darkness revealed light-induced
stress reactions leading to necrosis and to reduced growth of HNO callus. It appeared that darkness allowed the HNO callus
to avoid the photooxidation stress. Therefore, the favorable effect of darkness on HNO growth might be explained by the suppression
of photooxidative damage due to the absence of carotenoids. The higher peroxidase activity in the HNO callus maintained in
darkness raised the problem of heme synthesis in this heterotrophic callus. 相似文献
130.
An RNA pseudoknot is an essential structural element of the internal ribosome entry site located within the hepatitis C virus 5' noncoding region. 总被引:8,自引:2,他引:6
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Translation of the human hepatitis C virus (HCV) RNA genome occurs by a mechanism known as "internal ribosome entry." This unusual strategy of translation is employed by naturally uncapped picornaviral genomic RNAs and several cellular mRNAs. A common feature of these RNAs is a relatively long 5' noncoding region (NCR) that folds into a complex secondary structure harboring an internal ribosome entry site (IRES). Evidence derived from the use of dicistronic expression systems, combined with an extensive mutational analysis, demonstrated the presence of an IRES within the HCV 5'NCR. The results of our continued mutational analysis to map the critical structural elements of the HCV IRES has led to the identification of a pseudoknot structure upstream of the initiator AUG. The evidence presented in this study is based upon the mutational analysis of the putative pseudoknot structure. This is further substantiated by biochemical and enzymatic probing of the wild-type and mutant 5'NCR. Further, the thermodynamic calculations, based upon a modified RNAKNOT program, are consistent with the presence of a pseudoknot structure located upstream of the initiator AUG. Maintenance of this structural element is critical for internal initiation of translation. The pseudoknot structure in the 5'NCR represents a highly conserved feature of all HCV subtypes and members of the pestivirus family, including hog cholera virus and bovine viral diarrhea virus. 相似文献