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51.
K. Broberg Janusz Limon E. Pålsson Anders Lindstrand Sören Toksvig-Larsen Nils Mandahl Fredrik Mertens 《Human genetics》1997,101(3):295-298
We have previously reported recurrent clonal chromosomal aberrations in synovia, osteophytes and articular cartilage from
patients with osteoarthritis (OA). In particular, gain of chromosomes 5 and 7 was found to be strongly associated with OA.
In order to exclude the possibility of in vitro artefacts, we studied three to four parallel, independent cultures from ten
samples of synovia and three samples of osteophytes from ten women with primary OA. In all, 40 cultures were cytogenetically
analysed, 39 of which had clonal chromosomal aberrations. The most common aberrations were +7 and +5 which were found in 38
and 12 cultures, respectively. There were striking karyotype similarities among the parallel cultures from each case. Out
of a total of 83 clones, only 11 were unique for one culture, 7 from synovia and 4 from osteophytes. The genetic homogeneity
among different cultures from the same patients excludes the possibility of in vitro artefacts and indicates a widespread
distribution of the cytogenetically aberrant clones in vivo.
Received: 16 July 1997 / Accepted: 25 August 1997 相似文献
52.
Identification of 27-oxo-octacosanoic acid and heptacosane-1,27-dioic acid in Legionella pneumophila
Hermann Moll ers Sonesson Erik Jantzen Reinhard Marre Ulrich Zähringer 《FEMS microbiology letters》1992,97(1-2):1-6
A strain of Escherichia coli having elevated levels of cytochrome bo and lacking the cytochrome bd quinol oxidase was grown in chemostat culture at low copper levels. Such cells had lowered levels of copper and of total cytochrome b. Cytochrome o concentration was unchanged when assayed by conventional CO difference spectroscopy, but apparently diminished by 80% in copper-deficient cells as determined by photodissociation of bound CO at 193 K. This is attributed to depletion of copper in the oxidase of copper-deficient cells, causing rapid recombination of photodissociated CO to haem O. CO recombination was also more sensitive to low intensities of actinic light in copper-depleted oxidase. The results illustrate a further similarity between the active sites of o- and aa3-type terminal oxidases. 相似文献
53.
Herbert Lüers 《Molecular & general genetics : MGG》1955,87(1):93-96
Zusammenfassung Thioxanthon hat sich, in schwacher Konzentration (0,025%) oral appliziert, bei Drosophila als ein sehr schwach, aber nachweisbar wirksames Mutagen erwiesen. Seine Wirksamkeit wurde besonders an der Reaktion der unreifen Stadien der Spermatogenese nachgewiesen. Der Anteil der Chromosomenmutationen ist auffällig hoch. 相似文献
54.
The mechanistic details of mtDNA maintenance in petite-negative yeasts have remained largely unexplored. We report here that the DNA helicase Hmi1p plays a crucial role in mtDNA stability in Candida albicans. Like its counterpart in Saccharomyces cerevisiae, Hmi1p in C. albicans (CaHmi1p) contains a C-terminal mitochondrial targeting signal that is functional in both organisms. Biochemical analysis demonstrates that CaHmi1p is a protein possessing ATP-dependent 3'-5' DNA-unwinding activity. Deletion of both HMI1 alleles does not lead to complete loss of mtDNA in C. albicans; however, substantial fragmentation of the wild-type mitochondrial genome, reduction of mtDNA mass and loss of wild-type nucleoid distribution occur. Specific regions of the mitochondrial genome give rise to mtDNA molecule populations with altered characteristics upon CaHMI1 deletion. Fragmentation of the mitochondrial genome can be reversed by reintroduction of CaHmi1p. This is the first time that a gene required for wild-type mtDNA maintenance in S. cerevisiae has been demonstrated to be nonessential in a petite-negative yeast. 相似文献
55.
Cecilie L. Licht ers B. Marcussen Gregers Wegener† David H. Overstreet‡ Susana Aznar Gitte M. Knudsen 《Journal of neurochemistry》2009,109(5):1363-1374
The 5-hydroxytryptamine (5-HT4 ) receptor may be implicated in depression and is a new potential target for antidepressant treatment. We have investigated the brain 5-HT4 receptor [3 H]SB207145 binding in the Flinders Sensitive Line rat depression model by quantitative receptor autoradiography, and related this to 5-HT transporter ( S )-[ N -methyl-3 H]citalopram binding. We also determined the regulation of 5-HT4 receptor binding by 1, 14, and 21 days of paroxetine administration and subchronic 5-HT depletion, and compared this with changes in 5-HT2A receptor [3 H]MDL100907 binding. In the Flinders Sensitive Line, the 5-HT4 receptor and 5-HT transporter binding were decreased in the dorsal and ventral hippocampus, and the changes in binding were directly correlated within the dorsal hippocampus. Chronic but not acute paroxetine administration caused a 16–47% down-regulation of 5-HT4 receptor binding in all regions evaluated including the basal ganglia and hippocampus, while 5-HT depletion increased the 5-HT4 receptor binding in the dorsal hippocampus, hypothalamus, and lateral globus pallidus. In comparison, the 5-HT2A receptor binding was decreased in the frontal and cingulate cortices after chronic paroxetine administration, and markedly reduced in several regions after 5-HT depletion. Thus, the 5-HT4 receptor binding was decreased in the Flinders Sensitive Line depression model and in response to chronic paroxetine administration. 相似文献
56.
Allan E. Johnson Fredrik Jeppsson† Johan Sandell‡ David Wensbo‡ Jan A. M. Neelissen§ ers Juréus Peter Ström‡ Henrietta Norman† Lars Farde¶ Samuel P. S. Svensson† 《Journal of neurochemistry》2009,108(5):1177-1186
The presence of β‐amyloid plaques in brain is a hallmark of Alzheimer’s disease (AD) and serves as a biomarker for confirmation of diagnosis postmortem. Positron emission tomography (PET) radioligands such as Pittsburgh compound B ([11C]‐2‐(3‐fluoro‐4‐methylamino‐phenyl)‐benzothiazol‐6‐ol) (PIB) binds selectively to β‐amyloid and are promising new tools supporting the clinical diagnoses of AD. In addition, such methodology may be useful for evaluation of new drugs aiming at reduction of amyloid plaque load. The objective of this study is to develop a new amyloid selective PET radioligand with higher signal‐to‐background ratio when compared with existing amyloid PET ligands. The lead compound, AZD2184, (2‐[6‐(methylamino)pyridin‐3‐yl]‐1,3‐benzothiazol‐6‐ol) was found to have high affinity for amyloid fibrils in vitro (Kd: 8.4 ± 1.0 nM). Two minutes after i.v. administration in rats, about 1% of the dose was in brain. In vitro autoradiography on cortical brain sections from amyloid‐beta precursor protein/presenilin 1 (APP/PS1) mice and AD patients showed that while [3H]AZD2184 and [3H]PIB are mutually displaceable, [3H]AZD2184 displays a higher signal‐to‐background ratio primarily by virtue of lower background binding levels. The ratio of binding ability in prefrontal cortex (high plaque load) to subcortical white matter (background) was 4.5 for [3H]AZD2184 and 0.8 for [3H]PIB at 1 nM. In adjacent cortical sections from APP/PS1 mouse as well as from AD cortical tissue, [3H]AZD2184 and antibodies to human β‐amyloid labeled identical structures. In vivo administration of [3H]AZD2184 to APP/PS1 mice further showed that [3H]AZD2184 labels amyloid deposits with low non‐specific background binding. Taken together, the pre‐clinical profile of AZD2184 in relation to the reference ligand PIB, suggests that 11C‐labeled AZD2184 is a potential radioligand for PET‐visualization of β‐amyloid deposits in the living human brain. 相似文献
57.
58.
59.
Broberg CS Giraud GD Schultz JM Thornburg KL Hohimer AR Davis LE 《American journal of physiology. Regulatory, integrative and comparative physiology》2003,285(3):R649-R655
In response to chronic fetal anemia, coronary blood flow, maximal coronary conductance, and coronary reserve increase. We sought to determine whether chronic fetal anemia alters left ventricular (LV) function in adulthood. We studied adult sheep that had been made anemic for 20 days in utero by phlebotomy. They were transfused just before birth. At 7 mo of age, LV function was measured by pressure-volume loops at rest and during hypoxic stress. The in utero anemia group (n = 8) did not differ from controls (n = 5) with respect to hematocrit, heart and body weight, or baseline hemodynamic parameters. However, the effect of hypoxia (relative to baseline) on multiple indexes of systolic function was different between the two groups. End-systolic elastance increased in the in utero anemia group (baseline to hypoxia) by 4.15 +/- 3.47 mmHg/ml (mean +/- SD) but changed little in controls (0.24 +/- 0.45), which shows that the response to hypoxia was significantly different (P < 0.01) between groups. Similarly, the maximum derivative of LV pressure with respect to time increased in the in utero anemia group (486 +/- 340 mmHg/s,) but on average fell in the controls (-503 +/- 211 mmHg/s) with the response again being significantly different (P < 0.03). We conclude that in sheep, perinatal anemia can alter cardiac responses to hypoxic stress in the adult long after restoration of normocythemia. 相似文献
60.
Broberg P 《Genome biology》2002,3(9):preprint00-23