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961.
Opsonization with Antimyelin Antibody Increases the Uptake and Intracellular Metabolism of Myelin in Inflammatory Macrophages 总被引:1,自引:0,他引:1
Jacqueline Trotter Linda J. DeJong Marion Edmonds Smith 《Journal of neurochemistry》1986,47(3):779-789
In most demyelinating diseases, macrophages are believed to be active agents of myelin destruction. In experimental encephalomyelitis, these cells appear to strip off and ingest the myelin lamellae, and myelin debris has been observed within the cell body. We show here in vitro conditions in which rat peritoneal macrophages phagocytose and metabolize CNS myelin lipids. Purified rat myelin, prelabeled in vivo with [14C]acetate, was incubated with preimmune serum or rabbit antiserum to rat CNS myelin and added to macrophage monolayers. Myelin opsonized with antimyelin antibodies was more readily phagocytosed and metabolized by cultured macrophages than untreated myelin or that preincubated with preimmune serum. In the presence of macrophages, levels of myelin polar lipids and cholesterol decreased, whereas radioactive cholesterol ester and triglyceride accumulated. Up to five times as much radioactive cholesterol ester and about twice as much triglyceride accumulated in macrophage cultures containing antibody-treated myelin as in cultures fed preimmune serum-treated myelin or in those incubated with untreated myelin. Both the fatty acid and the cholesterol from cholesterol ester contained radioactive label; therefore, both were derived at least partly from the radioactive myelin lipid. Antiserum to myelin purified from peripheral nerve was almost as effective as that to CNS myelin in stimulating cholesterol metabolism, whereas antiserum to galactocerebroside was about 70% as active. Antiserum to basic protein had less effect, whereas antiserum to the myelin-associated glycoprotein and proteolipid protein was inactive. Of the polar lipids, ethanolamine phosphatide was most degraded in both the antiserum- and preimmune serum-treated myelin, with the diacyl form and plasmalogen form degraded about equally. These experiments indicate that myelin-specific antibodies in inflammatory CNS lesions may participate in and stimulate macrophage-mediated demyelination. 相似文献
962.
Prof. Dr. Christian Girod Jacqueline Trouillas Mireille Raccurt Maurice P. Dubois 《Cell and tissue research》1986,246(2):237-242
Summary With the use of an antibody against bovine S-100 protein, it was possible to reveal a characteristic cell type in the pars distalis and the pars tuberalis of the monkey Macaca irus. In the adenohypophysis of Cercopithecus aethiops, labeled cells were present in the pars distalis, pars tuberalis, and pars intermedia. These cells, so-called folliculo-stellate cells, were found in all pituitaries studied. Surprisingly, an antibody against human S-100 protein did not label the stellate cells of the adenohypophysis. However, in Macaca irus, this antibody gave a strong positive reaction with various other cell types (interstitial cells of the pineal gland, Müller cells of the retina, autonomic ganglionic cells, glial cells of the central nervous system, Schwann cells, Bergmann glia of the cerebellum, fat cells, reticular cells of lymphoid organs). By use of double immunoenzymatic labeling, it was evident that stellate cells are spatially related either to somatotropes, prolactin cells, corticotropes, or to glycoprotein-containing cells. Thus, a specific relationship to a particular endocrine-cell type could not be observed.Dr. M.P. Dubois died in Tours (France) on March 30, 1986, aged 65 相似文献
963.
DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family 总被引:5,自引:4,他引:1
Véronique David Pascale Paul M. Simon J. -Y. Le Gall Renée Fauchet Isabelle Gicquel Isabelle Dugast Loïc Le Mignon Jacqueline Yaouanq D. Cohen M. Bourel 《Human genetics》1986,74(2):113-120
Summary The metabolic error involved in idiopathic hemochromatosis, as well as the underlying genetic defect remain unknown. It has, however, been recently shown that this genetic lesion occurs at a locus linked to the major histocompatibility complex, probably close to the HLA-A locus, and that the disease is recessively transmitted. Therefore, in a family where one subject has idiopathic hemochromatosis his HLA-identical siblings should also be affected. We present here the restriction polymorphism with two MHC class I probes and one DR probe in an exceptional family with three HLA-identical siblings: one (the proband) has a major form of idiopathic hemochromatosis, while the other two are free of any clinical or biochemical signs of the disease. The restriction patterns observed after DNA digestion by enzymes EcoRI, EcoRV, BglII, BamHI, PvuII, TaqI, HincII, and HindIII led to the conclusion that one of the proband's chromosome 6 had undergone two alterations: one, a deletion in the DR region, was revealed by missing fragments all correlated with DR5; the other was an unbalanced cross-over or a genetic conversion in the MHC class I region. This latter alteration was revealed by modifications in the patterns of high molecular weight HindIII bands which hybridize with probe pHLA2 and also by the absence of a HindIII fragment of 7.4 kb hybridized by another class I probe. This latter alteration most likely involved the hemochromatosis gene and could be the first step toward a molecular approach to this gene. 相似文献
964.
Activated macrophages harvested from rat peritoneum were shown to contain phospholipase A1, A2 and lysophospholipase activities which were defined on a series of radiolabelled phospholipid substrates. During in vitro culture of these elicited macrophage populations, phospholipase enzymes were secreted into the culture medium. Radiolabelled myelin, prepared from young rats after intracerebral injection of14C acetate, was used as a substrate to analyze the susceptibility of central nervous system (CNS) myelin to attack by cell-associated and secreted macrophage enzymes. Homogenates of peritoneal macrophages degraded the myelin lipids at acid pH; phosphatidyl choline (PC) and ethanolamine phosphatide (EP) were both degraded with liberation of free fatty acid and small amounts of lysolipids. The ethanolamine lipids were most vulnerable; up to 20% of this fraction was degraded in six hours. Selected batches of macrophage culture supernatant similarly degraded the myelin EP at acid pH. These results suggest that phospholipase enzymes, released from activated macrophages in close proximity to the myelin sheath, may participate in primary demyelination in inflammatory CNS lesions. 相似文献
965.
966.
A study of the anterior sensory receptors of male and female Asplanchna brightwelli by scanning electron microscopy reveals some important differences in the region surrounding the mouth. In the male, the ventrolateral sensory bristles, the pseudotrochus, the inner and the outer buccal tufts and the mastax receptors are absent. The oral receptors are reduced. Transmission electron microscopy of these receptors shows that they consist of ciliated sensory cells surrounded by epithelial supporting cells. The distal ends of the cilia of the mastax receptors are modified; the cilia of the other receptors differ only in their length and rootlet structure from the locomotor cilia of the cingulum. A consideration of the feeding behaviour of Asplanchna leads us to suppose that these sensory cilia function in mechanoreception and in chemoreception. 相似文献
967.
Geneviève Kayser Paul Lambotte Paul Falmagne Carine Capiau Jacqueline Zanen Jean-Marie Ruysschaert 《Biochemical and biophysical research communications》1981,99(2):358-363
Conductance measurements on planar lipid bilayers demonstrate that CB1, a CNBr peptide of diphtheria toxin fragment B located in its middle region, possesses the unique property to destabilize the lipid bilayer organization. It is suggested that a segment of 25 amino acids in the N-terminal sequence of CB1 could be responsible for this effect. Its very low polarity, its predicted amphipathic helical structure and a helix length corresponding to the thickness of the hydrocarbon region of the lipid bilayer should specifically favor its insertion in the membrane. The existence of such a transverse lipid-associating domain could confer upon the molecule the properties leading to the anchoring of diphtheria toxin in the cytoplasmic membrane. 相似文献
968.
Jacqueline Barra Plana Barrand Marie-Hélène Blondelet Philippe Brachet 《Molecular & general genetics : MGG》1980,177(4):607-613
Summary Upon starvation, amoebae of the mutant strain HPX235 are unable to aggregate. Previous work has shown that this aggregateless character was associated with a nearly complete block in the production of the phosphodiesterase by these cells. Aggregation of the HPX235 amoebae can be induced with exogenous phosphodiesterase. In the present work, we show that both the aggregateless character and the block in phosphodiesterase production appear to result from the same recessive mutation, allocated to I.g.IV. Two other mutant strains displaying a comparable phenotype (HPX262 and HP594) were shown by complementation to belong to the same locus pdsA. Unlike wild type cells, the mutants of the locus pdsA cannot be induced to produce phosphodiesterase following treatment of the cells with exogenous cAMP, whether exogenous phosphodiesterase is present or not in the starvation buffer. It is concluded that pdsA is either the structural gene for the phosphodiesterase or a controlling element whose integrity is required for phosphodiesterase production. Mutations in pdsA share secondary effects among which the abnormally low production of the phosphodiesterase inhibitor. However, this effect can be overcome upon addition of exogenous phosphodiesterase, and most likely results from the lack of cAMP hydrolysis.The late development is also affected in pdsA mutants. Aggregates formed in the presence of exogenous phosphodiesterase cannot culminate normally. This suggests that the level of cAMP hydrolysis also plays a role during the late stages of development of Dictyostelium discoideum.Abbreviations used cAMP
adenosine 3,5-cyclic monophosphoric acid
- l.g.
linkage group
- PDE
3,5-cAMP phosphodiesterase 相似文献
969.
Olivier Huisman Richard D'Ari Jacqueline George 《Molecular & general genetics : MGG》1980,177(4):629-636
Summary Brief exposure of an Escherichia coli tif lon strain to 40° results in subsequent prolonged inhibition of cell division (part of the SOS response), which is completely and specifically suppressed by sfiA and sfiB mutations. This sfi dependent division inhibition requires protein synthesis during the 40° incubation period, implying the existence of a tif-inducible protein which results in cell division arrest. sfi dependent division inhibition is also induced early during thymine starvation in tif
+ cells; at later times a sfi independent mechanism of division arrest is invoked as well.In lon mutants, known to lack a protease, the sfi dependent division inhibition is amplified, perhaps due to stabilization of the inducible protein involved in division arrest. In these strains the P1 lysogenization defect and the filamentation observed after a nutritional shift-up are sfi dependent, suggesting that P1 infection and nutritional shift-up may also induce the protein involved in division arrest. Bacteria are known to increase in size following a shift-up. Thus the latter observation suggests that the SOS response may be not only a last resort in time of distress but also a means permitting better adaptation of the cells to their environment.After five years of heroic struggle against cancer, Jacqueline George passed away 14 August 1979. Despite weakened health and debilitating therapy she continued to stimulate and participate in the work of the microbial genetics group which she had created 相似文献
970.
Summary Six Algerian patients with 0 thalassemia are presented, in addition to the two patients already reported (Godet et al., 1977). Family studies indicate that all the patients had homozygous thalassemia characterized by absence of globin chain synthesis in peripheral blood. The clinical severity varies from one family to the other and within the same family, from typical Cooley's anemia to thalassemia intermedia and appears to be related to the child death rate observed in each family. The / biosynthetic ratio was 0.36–0.40 in seven patients and 0.2 in the most seriously affected patient. The mRNA content in peripheral reticulocytes was less than 1.5% of mRNA in seven patients and 13.3% in one patient. These results indicate that Algerians homozygous for thalassemia are heterozygous at the clinical, biochemical and molecular levels. 相似文献