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991.
992.
993.
Van Landeghem G; Haese P; Lamberts L; Barata J; DeBroe M 《Nephrology, dialysis, transplantation》1997,12(8):1692-1698
Background: The association between aluminium and
dialysis encephalopathy and deterioration of the neurological state during
desferrioxamine treatment of dialysis patients is well established. At
present little is known about the speciation and the mechanisms underlying
the element's neurotoxicity. Methods. Aluminium speciation was performed in
cerebrospinal fluid samples of acutely aluminium-intoxicated dialysis
patients using a recently developed high-performance liquid
chromatographic/electro-thermal atomic absorption spectrometric hybrid
method. Results: Baseline cerebrospinal fluid
aluminium levels of samples taken shortly after the intoxication were low
but elevated (5.0±2.0 &mgr;g/l, n=3) as compared to subjects
with normal renal function (<1 &mgr;g/l). In contrast to the
situation noted in serum and to the iron speciation in cerebrospinal fluid,
aluminium was not bound to transferrin but appeared as two distinct
compounds, the main fraction eluting at the elution volume of aluminium
citrate/silicate. The second compound was not identified. Forty-four hours
after desferrioxamine administration the cerebrospinal fluid aluminium
levels had increased up to a concentration of 10.3±2.5
&mgr;g/l (n=3). This was accompanied by a change in the speciation
profile with aluminium appearing at the elution volume of aluminoxamine.
Conclusion: Our findings may contribute to a better
understanding of the neurotoxic effects of aluminium and its
desferrioxamine chelate in dialysis patients. 相似文献
994.
F. M. RAAPHORST R. LANGLOIS VAN DEN BERGH J. L. M. WAAIJER J. M. VOSSEN & M. J. D. VAN TOL 《Scandinavian journal of immunology》1997,46(3):292-297
Fetal B lymphocytes in mice and humans use a limited number of the available VH gene segments. Mouse fetal B cells primarily utilize 3' VH elements, suggesting that the localization of these elements determines their rearrangement frequency. The previously reported non-random usage of human VH genes has been more difficult to explain. In this study the authors analysed the expression of the most proximal 3' human VH element (VH 6) using a monoclonal antibody (JE-6). VH 6 expression was assessed in various B cell differentiation stages from fetal liver, bone marrow and spleen at 12–20 weeks of gestation. The authors demonstrate that the level of VH 6 expression does not exceed a stochastic usage frequency. This suggests that the localization of VH 6 does not significantly promote its expression during human fetal life, and that other factors must affect the usage of VH genes during human fetal development. 相似文献
995.
996.
Three hundred and twenty samples of subgingival plaque were obtained from 80 caucasian girls, ranging from 10 to 13 years of age. The samples were analyzed to verify the influence of age upon colonization of the gingival sulcus by microorganisms potentially pathogenic to the periodontal tissues. The gingival and plaque status were evaluated through the gingival index (GI) and plaque index (PlI) and the microflora was assessed by the enzymatic method benzoyl-arginine-naphthylamide (BANA). The results of the BANA test were positive for 62.50% of the tested individuals and 40% of the examined sites. The influence of age was statistically significant on BANA reactivity, and the number of positive sites was greater at 11 (57.5%) than at 12 years (28.8%). 相似文献
997.
C M Kyaw C R De Araujo M R Lima E G S Gondim M M Brígido L G Giugliano 《Infection, genetics and evolution》2003,3(2):111-117
Diffusely adhering Escherichia coli (E. coli) strains (DAEC) represent a potential cause of diarrhoea in infants, and the detection of type three secretion system (TTSS) genes in DAEC would substantiate their pathogenic nature. In this work, four isolates of DAEC, recovered from stools of diarrhoeic children, were analysed by PCR, in order to detect the presence of TTSS genes. Primers targeted to the escC, escJ, escN and escV, some of the most conserved TTSS genes in enteropathogenic and enterohaemorrhagic Escherichia coli (EPEC and EHEC), were used in order to verify the occurrence of homologous genes in our DAEC isolates. By this approach, we were able to characterise DNA fragments corresponding to putative escJ and escN genes in all DAEC isolates. Furthermore, DNA fragments homologous to the escC and escV genes were also amplified from all isolates. Besides the similarity found among the DAEC esc homologues with EPEC and EHEC esc genes, the nucleotide sequence analysis of the flanking regions of the amplified DNA fragments suggests that the putative DAEC esc genes are organised in the same manner as observed in EPEC and in EHEC strains. The results described here provide strong evidence for the presence of a TTSS in the DAEC strains analysed, implicating a pathogenic nature of these isolates. 相似文献
998.
Koichi Masuda Robert L Sah Michael J Hejna Eugene J-M A Thonar 《Journal of orthopaedic research》2003,21(1):139-148
Most attempts to tissue-engineer cartilage have involved seeding of cultured cells into a biological or synthetic scaffold. We have developed a novel two-step culture approach that makes possible the in vitro formation of cartilaginous-like tissue by mature adult bovine chondrocytes without the aid of a synthetic matrix. The first step consists of culturing chondrocytes under conditions that maintain their rounded shape and their molecular phenotype as assessed by type II collagen and aggrecan production. This step was accomplished by culturing the isolated chondrocytes in alginate beads until the cells have reestablished a proteoglycan-rich cell-associated matrix (CM). The second step consists of culturing the cells with their CM, after recovery from the beads, on a tissue culture insert with a porous membrane. In this study, young adult bovine articular chondrocytes were cultured in alginate beads in the presence of 10% or 20% fetal bovine serum (FBS). After 7 days of culture, the alginate beads were dissolved by incubating the beads for 20 min in sodium citrate buffer, a calcium chelator. Following a brief centrifugation, the cells with their CM were recovered, resuspended in medium containing 10% or 20% FBS and seeded onto a tissue culture insert. After 1 week of culture on the insert, the individual cells with their CM progressively became incorporated into a mass of cartilaginous tissue. Culture with 20% FBS resulted in the best formation of tissues. These tissues, easily recovered from the insert, were then subjected to biochemical and histological analyses. The biochemical results showed that the chondrocytes remain phenotypically stable in the tissues. The de novo tissue has a relatively high ratio of PG/collagen. Histological examination of the tissue revealed it contained a cartilage-like matrix strongly stained with toluidine blue. This scaffold-free system appears ideal to study, in vitro, the development of transplantable cartilaginous tissue. 相似文献
999.
1000.