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Biomedical subjects

G Russo

Publications and source records attributed to G Russo.

At least 181 records · Page 10Linked to original sources

Non-NMDA receptors mediate glutamate-induced depolarization in frog crista ampullaris.

The effect of glutamate on frog crista ampullaris was investigated in order to assess the potential role of this agent as an afferent transmitter in inner ear organs. Intracellular recordings from single afferent axons in the isolated labyrinth showed that, after blocking synaptic transmission with high concentrations of Mg2+, micro-injections of glutamate elicit a dose-dependent postsynaptic depolarization. The amplitude of depolarization was reduced dose-dependently by the competitive non-NMDA receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione. When Na+ concentration in the bath was progressively reduced, depolarization decreased gradually and disappeared almost completely in Na(+)-free Ringer. On the contrary, complete substitution of Ca2+ ions in the bath was without apparent effects. These results indicate that the postsynaptic depolarization induced by glutamate in frog semicircular canals involves the activation of non-NMDA amino acid receptors.

6-Cyano-7-nitroquinoxaline-2,3-dione↗

Patterns of recovery and change in verbal and nonverbal functions in a case of crossed aphasia: implications for models of functional brain lateralization and localization.

We present a 2-year verbal and nonverbal follow-up of a crossed aphasic patient. The patient had suffered from widespread ischemic damage in the area of right middle cerebral artery, with a parieto-temporal lesion. Three months postonset he showed classical Wernicke's aphasia associated with oral, limb and constructional apraxia and left hemineglect. However, follow-up findings showed a complex, dynamic pattern entirely consistent with cognitive models of language and nonlanguage abilities. Current models of functional brain lateralizations could not satisfactorily account for such longitudinal, fine-grain observations.

Agraphia↗

Incidence of lower respiratory tract infections caused by Mycoplasma, Chlamydia and Legionella: an Italian Multicenter Survey.

A collaborative retrospective study based on serologic diagnosis was conducted to assess the etiological role sustained by privileged pathogens in Italy. The results obtained indicate the Mycoplasma, Chlamydia and Legionella are important etiologic agents of lower respiratory tract infections in Italy since they account for about 31% of the cases taken into consideration in this survey. We found a high incidence of M. pneumoniae (12.3%), C. pneumoniae (10.5%) and L. pneumophila (8.3%). These results are in line with similar figures reported in the recent literature. While the data gathered in our survey do not allow us to clarify the nature of the agents involved in the etiology of the majority (70%) of the respiratory infections occurring in Italy, it seems safe to assume that after Streptococcus pneumoniae and Haemophilus influenzae, the privileged pathogens represent the most common cause of lower respiratory tract infections.

Chlamydia Infections↗

Differential expression of potassium currents by hair cells in thin slices of frog crista ampullaris.

1. Electrical responses in hair cells located in the peripheral regions and in the central region of the frog crista ampullaris were investigated in thin slice preparations by using the whole-cell configuration of the patch-clamp technique. 2. Hair cells from the peripheral regions exhibited mostly a club-like shape and had an average resting potential of -46 mV, whereas cells from the central region had mostly a cylindrical shape and a more negative resting potential (-57 mV). 3. Voltage-clamp recordings revealed that ionic conductances differed in the two epithelial regions. Cells from the peripheral regions exhibited a transient K+ current of A-type (IA) in conjunction with a slow rectifier outward K+ current (IK). Cells from the central region showed little or no IA and generated an IK together with an inward rectifier K+ current (IIR). In both regions, hair cells showed a rapidly activating Ca(2+)-dependent outward K+ current (IK(Ca)) that rapidly inactivated to reach a steady-state level during 150-ms test pulses. 4. IA activated close to -60 mV and was inhibited by 12 mM 4-aminopyridine (4-AP). The time course of this current showed time to peak values of 3-4 ms at 0 mV. Inactivation was fast and almost voltage-independent. The decay time constant was approximately 35 ms at 0 mV. 5. IK was recruited close to -60 mV and activated slowly, reaching peak values in approximately 100 ms at 0 mV. It showed no evidence of inactivation during 150-ms test pulses and it was insensitive to 4-AP. 6. IIR activated at membrane potentials more negative than -90 mV and was blocked by exposure to 6 mM Cs+ or to a K(+)-free medium. This current showed an outward relaxation at potentials more negative than -140 mV, an effect that disappeared after exposure to a Na(+)-free medium. 7. IK(Ca) was recruited close to -40 mV and was inhibited by exposure to a Ca(2+)-free external medium or to 0.5 mM Cd2+. The time to peak of this current was approximately 3 ms at 0 mV and inactivation was very fast and almost independent from the membrane potential. The decay time constant was approximately 4 ms at 0 mV. 8. IK and IA were prominent in hair cells from the peripheral regions, whereas IK accounted for most of the membrane conductance in cells from the central region. The contribution of IK(Ca) was comparable in cells from both epithelial regions.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

[Coronary recanalization in acute myocardial infarction: early coronary angiography].

In acute myocardial infarction the early patency of the infarct-related artery is positively correlated with improved left ventricular function and survival. Coronary artery reperfusion is commonly achieved by intravenous administration of thrombolytic agents. Methods of mechanical recanalization, mainly percutaneous transluminal coronary angioplasty (PTCA), have been proposed and tested as alternative or adjunctive ways to thrombolysis. Early coronary angiography provides reliable and irreplaceable information concerning mechanical intervention utility and feasibility. Therefore, it is incorporated in the mechanical revascularization strategies at various stages in the setting of acute myocardial infarction. In the primary, direct PTCA strategy early coronary arteriography is done for planning and carrying out mechanical revascularization as an alternative to intravenous thrombolytic therapy. This strategy may be particularly effective in patients presenting with cardiogenic shock, large infarctions, contraindications to thrombolytic therapy, and prior bypass surgery. Coronary angiography in evolving myocardial infarction has also been proposed to set the stage for rescue PTCA when thrombolysis has proved to be ineffective. Nevertheless, there are currently no unequivocal data to judge the value of the rescue PTCA strategy. After unsuccessful thrombolysis, this approach should be considered in patients with a large infarction, with cardiogenic shock, with left ventricular dysfunction and with refractory ischemia. Early, routine coronary angiography after lytic recanalization is not recommended. In fact, the strategy of immediate arteriography plus PTCA after thrombolytic therapy does not improve outcome but leads to several deleterious effects.

Angioplasty, Balloon, Coronary↗

Non invasive recording of CO2 cerebrovascular reactivity in normal subjects and patients with unilateral internal carotid artery stenosis.

CO2 cerebrovascular reactivity has been recorded in 12 healthy volunteers and 10 patients with unilateral > 70% extracranial internal carotid artery (ICA) stenosis, using non invasive techniques. The relative changes of middle cerebral artery blood flow velocity (VMCA) and velocity waveform pulsatility (PIMCA) after that hypocapnia was induced by spontaneous hyperventilation were recorded. 35.5% average VMCA reduction and 63% PIMCA increment of basal values was produced in healthy subjects after hyperventilation. The percentage variation of CO2 Reactivity Index (RI), expressed in terms of VMCA (V-RI) and PIMCA (PI-RI), per mmHg change in pCO2, presents a good right-left side correlation (r = 0.82 and r = 0.83 respectively) in healthy subjects, while a dissociation between V-RI and PI-RI was found in our patients. A significant reduction of PI-RI was also recorded in the group of patients on the side of ICA stenosis. From our data CO2 reactivity index recorded in terms of PI seems to allow a better separation between pathology and normality, without the need to assume a close relationship between velocity and blood flow under the condition considered. Furthermore, PI-RI seems to be a valid index in the evaluation of some attribute pertaining to the distal vascular bed.

Adult↗

[The compression of numerical radiological images].

A digital radiological image is made by a number of pixels, each of them characterized by a definite numerical value obtained by quantization which represents the luminance in that specific image unit. Spatial resolution and dynamic range are the main factors in determining the quality of a digital radiological image. The product of the two above factors defines the global dimensions of the image and is expressed in bits. In conventional radiographic images the global dimension of the image is expressed in MBytes, because of its high spatial and contrast resolution. To reduce the visualization and storage requirements as well as the transmission time of large image data sets, compression algorithms have been recently introduced. These algorithms are based on the fact that often in a digital image parts of the binary data are "redundant", that is they are not necessary for correct image representation. Therefore, compression methods are aimed at reducing both statistical and perceptive redundancy. Statistical redundancy is reduced by means of lossless coding which does not allow to compress images with a ratio higher than 4-5:1 and that--by definition--allows to recover the original image quality. On the other hand "lossy" compression algorithms, which eliminate the perceptive redundancy, are based on the reduction of spatial resolution and dynamic range and on transform-based methods. In particular, the latter have usually been more successful in terms of efficient compression, even when applied to conventional radiographic images. The basic transform procedure can be modified at various levels. JPEG is one of these methods, originally developed for photographic images, which can be usefully applied to radiological images as well. Lossy procedures allow to reach higher compression ratios than lossless methods, but the decrease in information content must be prevented from reducing diagnostic accuracy. In order to assess the diagnostic efficiency of the images compressed with lossy methods, semi-objective analyses are usually performed and ROC curves are produced and evaluated. A model ROC analysis is presented.

Algorithms↗

Immune status and immune response to diphtheria-tetanus and polio vaccines in allogeneic bone marrow-transplanted thalassemic patients.

We evaluated the immune status against diphtheria (D), tetanus (T) and polio viruses (PV) and the immune response to re-administration of the respective vaccines in a series of 23 transplanted homozygous beta-thalassemic patients, aged 5-17 years (mean age 12.1 +/- 3.1 years). They had been given compulsory DT toxoids and types 1, 2 and 3 PV vaccine in infancy and had been successfully submitted to allogeneic BMT 2-6 years previously. Prior to revaccination, a high percentage of subjects (from 48% for type 2 PV to 83% for D) had antibody levels below the protective levels and low geometric mean titers (GMTs). After revaccination (three doses of DT toxoids and of inactivated PV vaccine) the percentage of subjects with protective levels of antibodies rose to 86-100% and the GMTs increased markedly. We conclude that: (1) the protection afforded by compulsory DT and PV vaccines administered in infancy is almost entirely lost in beta-thalassemic patients for several years after BMT, (2) revaccination is necessary in these subjects, and (3) at least three doses of DT and PV vaccines must be administered to recover adequate protection.

Adolescent↗

c-fes expression in ontogenetic development and hematopoietic differentiation.

The c-fes protein (NCP92) is a tyrosine-specific protein kinase, capable of both autophosphorylation and phosphorylation of other substrates. We have analysed c-fes RNA expression in human/murine ontogenetic development and in homogeneous populations of embryonic and adult human hematopoietic cells. c-fes expression has been observed in rapidly proliferating embryonic-fetal tissues originating from different germinal layers, but not in adult non-hematopoietic tissues. In particular, a spatially and temporally regulated transcription was observed in the central nervous system and in developing cartilage. Expression in hematopoietic cells was evaluated in progenitors purified from embryonic-fetal liver and adult peripheral blood differentiating gradually and specifically along the erythroid or granulomonocytic lineage. In both embryonic and adult hematopoietic cells c-fes was abundantly expressed in undifferentiated progenitors of both lineages, as well as in differentiated granulomonocytic precursors, but not in erythroblasts. This expression pattern correlates with that of GM-CSF and in part IL-3 receptors (Testa et al., 1993 and our unpublished results). Altogether, these results suggest a possible role for c-fes in signal transduction, in both embryonic non-hematopoietic tissues and embryonic/adult hematopoietic cells, following interaction of growth factors with their tyrosine-kinase negative receptors (i.e., GM-CSF and IL-3 receptors in adult hematopoietic cells and other hypothetical growth factor(s) receptors during embryonic development.

Adult↗

Chromosome walking on the TCL1 locus involved in T-cell neoplasia.

The TCL1 locus on chromosome 14 band q32.1 is frequently involved in the chromosomal translocations and inversions with the T-cell receptor genes observed in several T-cell tumors, including T-prolymphocytic leukemias, acute and chronic leukemias associated with the immunodeficiency syndrome ataxia-telangiectasia, and adult T-cell leukemia. All breakpoints cloned in this area have been mapped to 14q32.1, an area distant approximately 10,000 kb from the immunoglobulin heavy-chain gene locus on chromosome 14q band 32.3. Except for two cases of inversion, no physical linkage of the cloned breakpoints has been reported, nor has a gene been identified in this region. Taking advantage of chromosome-walking techniques and of the P1 phage, we cloned and characterized 450 kb of the germ-line TCL1 locus, starting from the breakpoints of two independent T-cell leukemias. We show that all molecular rearrangements characterized so far map to these clones, indicating not only that this region is the target of chromosomal rearrangements occurring in this area but also that both inversion and translocations occur within a 300-kb region in the T-cell leukemias. In the attempt to identify a candidate oncogene responsible for the malignant transformation, a CpG island centromeric to the inversions and to the translocations has been identified. Two probes near the CpG island have detected sequences conserved among species, as well as two transcripts in the K562 human erythroleukemia cell line. On the basis of these data, a model of activation of the putative TCL1 oncogene is suggested.

Base Sequence↗

Extrathymic differentiation of T lymphocytes and natural killer cells from human embryonic liver precursors.

Liver cells were isolated on Ficoll/Hypaque gradients from embryos or fetuses at 6-10 weeks of gestation; 2-20% of the cells expressed CD45 or HLA class I surface antigens and 2-6% expressed CD7. Other T- or natural-killer (NK)-cell-lineage-specific markers were undetectable. Liver-cell suspensions cultured in the presence of phytohemagglutinin and recombinant interleukin 2 gave rise to large proportions of CD3+ lymphocytes expressing either alpha/beta or gamma/delta T-cell receptors. This occurred not only in bulk cultures but also when cells were cloned under limiting dilution conditions. Importantly, these figures were obtained also in embryos at 6-8 weeks of gestation, which is before colonization of the thymic rudiment by T-cell precursors. When the same liver-cell suspensions were cultured in the presence of irradiated H9 cells and recombinant interleukin 2 (either in bulk cultures or under cloning conditions), large proportions of cells (or clones) expressed surface CD16 and CD56 antigens and displayed a strong cytolytic activity against both NK-sensitive (K562) and NK-resistant (M14) target cells. In addition, liver-derived T or NK cells expressed functional receptor molecules since they could be activated via either CD3/T-cell receptor or CD16 surface antigens, respectively. Further fractionation of liver cells on the basis of CD45 antigen expression indicated that only CD45+ cells could give rise to T or NK cells in culture. Thus, CD45 can be used as a marker for identification of an early liver-cell population containing T- and NK-cell precursors. That T or NK cells were derived from male embryos and not from the mother was shown by PCR amplification of X and Y chromosomal sequences. Our present data may offer an in vitro model for extrathymic embryonic T-cell maturation that can be used to examine fundamental aspects of human T-cell development and function.

CD3 Complex↗

Human L7a ribosomal protein: sequence, structural organization, and expression of a functional gene.

A cDNA coding for the human L7a ribosomal protein (r-protein) was used to isolate the corresponding gene by screening two human genomic libraries constructed in bacteriophage lambda and in a cosmid vector. One of the cosmid clones isolated, cos1.1, contains the whole L7 alpha gene, composed of eight exons and seven introns spanning 3226 bp. As in other mammalian housekeeping genes, the promoter and the first exon of the L7 alpha reside within a CpG-rich island. Furthermore, similar to the other higher eukaryote r-protein-encoding genes characterized so far, the human L7 alpha gene has a C as the major transcriptional start point localized in a pyrimidine-rich region and lacks a canonical TATA sequence. We show that 130 bp of the human L7 alpha gene 5'-flanking region represent the minimal element required to promote its transcription. This element is strikingly conserved between the mouse and human L7 alpha genes. Finally, a comparison of the human L7 alpha gene coding sequence and the predicted amino acid (aa) sequence with the sequences of mouse L7a, rat L7a, and the homologous yeast L4 shows that the aa sequence has been highly conserved during evolution.

Amino Acid Sequence↗

Chick embryo metanephros: the glycosylation pattern as revealed with lectin conjugates.

Fragments of metanephros were taken from chick embryos and studied from the 7th to the 21st d of incubation. A battery of 7 different horseradish peroxidase-labelled lectins (PNA, ConA, DBA, SBA, LTA, WGA and UEA I) was used to analyse the distribution and changes of carbohydrate moieties in glycoconjugates along the metanephric nephron from the S-shaped body stage onwards. DBA and SBA reacted for a short time at some sites during the considered period of incubation. Provided WGA and ConA reacted with most of the nephric components, the almost ubiquitous presence of N-acetyl-D-glucosamine and alpha-D-mannose was demonstrated. SBA and LTA were found to be good markers of the proximal tubule. On the 12th d of incubation, sialic acid was found in the podocytes, capillary walls, and the connecting and collecting ducts. On the same day, other oligosaccharides were present at the nephric tubular components. The simultaneous presence of sialic acid and other sugar residues may be significant for the identification of the exact stage of incubation at which metanephric activity starts. The possible role of some sugar residues for the regulation of metanephric activity is discussed.

Animals↗