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Biomedical subjects

J Haag

Publications and source records attributed to J Haag.

At least 19 recordsLinked to original sources

IL-1beta, but not BMP-7 leads to a dramatic change in the gene expression pattern of human adult articular chondrocytes--portraying the gene expression pattern in two donors.

Anabolic and catabolic cytokines and growth factors such as BMP-7 and IL-1beta play a central role in controlling the balance between degradation and repair of normal and (osteo)arthritic articular cartilage matrix. In this report, we investigated the response of articular chondrocytes to these factors IL-1beta and BMP-7 in terms of changes in gene expression levels. Large scale analysis was performed on primary human adult articular chondrocytes isolated from two human, independent donors cultured in alginate beads (non-stimulated and stimulated with IL-1beta and BMP-7 for 48 h) using Affymetrix gene chips (oligo-arrays). Biostatistical and bioinformatic evaluation of gene expression pattern was performed using the Resolver software (Rosetta). Part of the results were confirmed using real-time PCR. IL-1beta modulated significantly 909 out of 3459 genes detectable, whereas BMP-7 influenced only 36 out of 3440. BMP-7 induced mainly anabolic activation of chondrocytes including classical target genes such as collagen type II and aggrecan, while IL-1beta, both, significantly modulated the gene expression levels of numerous genes; namely, IL-1beta down-regulated the expression of anabolic genes and induced catabolic genes and mediators. Our data indicate that BMP-7 has only a limited effect on differentiated cells, whereas IL-1beta causes a dramatic change in gene expression pattern, i.e. induced or repressed much more genes. This presumably reflects the fact that BMP-7 signaling is effected via one pathway only (i.e. Smad-pathway) whereas IL-1beta is able to signal via a broad variety of intracellular signaling cascades involving the JNK, p38, NFkB and Erk pathways and even influencing BMP signaling.

Aged↗

IL-1beta and BMPs--interactive players of cartilage matrix degradation and regeneration.

Intact human adult articular cartilage is central for the functioning of the articulating joints. This largely depends on the integrity of its extracellular matrix, given the high loading forces during movements in particular in the weight-bearing joints. Unlike the first impression of a more or less static tissue, articular cartilage shows - albeit in the adult organism a slow--tissue turnover. Thus, one of the most important questions in osteoarthritis research is to understand the balance of catabolic and anabolic factors in articular cartilage as this is the key to understand the biology of cartilage maintenance and degeneration. Anabolic and catabolic pathways are very much intermingled in articular cartilage. The balance between anabolism and catabolism is titrated on numerous levels, starting from the mediator-synthesizing cells which express either catabolic or anabolic factors. Also, on the level of the effector cells (i.e. chondrocytes) anabolic and catabolic gene expression compete for a balance of matrix homeostasis, namely the synthesis of matrix components and the expression and activation of matrix-degrading proteases. Also, there are multiple layers of intracellular cross-talks in between the anabolic and catabolic signalling pathways. Maybe the most important lesson from this overview is the notion that the anabolic-catabolic balance as such counts and not so much sufficient net anabolism or limited catabolism alone. Thus, it might be neither the aim of osteoarthritis therapy to foster anabolism nor to knock down catabolism, but the balance of anabolic-catabolic activities as a total might need proper titration and balancing.

Bone Morphogenetic Proteins↗

Bone morphogenetic protein-7 expression and activity in the human adult normal kidney is predominantly localized to the distal nephron.

Bone morphogenetic protein-7 (BMP)-7 plays an important role during fetal kidney development. In the adult, BMP-7 is most strongly expressed in the kidney compared to other organs, but the exact expression pattern as well as the function of BMP-7 is unclear. The major aim of the present study was to define which parts of the human kidney do physiologically express BMP-7 and which cells appear to be targets of BMP activity by showing phosphorylated BMP-receptor-associated Smads 1, 5, or 8 and inhibitor of differentiation factor 1 (ID1) expression. BMP-7 expression was localized by immunohistology to the epithelia of the distal tubule as well as the collecting ducts (CDs). Phospho-Smads 1/5/8 and ID1 expression largely colocalized with BMP-7 and was also localized in the epithelia of the distal tubule and the CDs. This was confirmed by polymerase chain reaction-based mRNA expression analysis. In vitro, proximal tubular cells (PTCs) expressed BMP receptors and BMP-receptor-associated Smads and were reactive to BMP-7. Our data indicate that BMP-7 expression in the adult human kidney appears to be more restricted than in the fetal situation and predominantly found in the distal nephron. Also, evidence of in vivo BMP signalling (i.e. phospho-Smads and ID1 expression) was found there. These findings suggest that BMP-7 plays a physiological role mostly in this part of the kidney. Still, as reported previously, PTCs are responsive to BMP-7, but presumably not in an autocrine or paracrine mode in normal adult kidneys.

Bone Morphogenetic Protein 7↗

Comparison of the chondrosarcoma cell line SW1353 with primary human adult articular chondrocytes with regard to their gene expression profile and reactivity to IL-1beta.

OBJECTIVE: In this study, the human chondrosarcoma cell line SW1353 was investigated by gene expression analysis in order to validate it as an in vitro model for primary human (adult articular) chondrocytes (PHCs). METHODS: PHCs and SW1353 cells were cultured as high density monolayer cultures with and without 1ng/ml interleukin-1beta (IL-1beta). RNA was isolated and assayed using a custom-made oligonucleotide microarray representing 312 chondrocyte-relevant genes. The expression levels of selected genes were confirmed by real-time polymerase chain reaction and the gene expression profiles of the two cell types, both with and without IL-1beta treatment, were compared. RESULTS: Overall, gene expression profiling showed only very limited similarities between SW1353 cells and PHCs at the transcriptional level. Similarities were predominantly seen with respect to catabolic effects after IL-1beta treatment. In both cell systems matrix metalloproteinase-1 (MMP-1), MMP-3 and MMP-13 were strongly induced by IL-1beta, without significant induction of MMP-2. IL-6 was also found to be up-regulated by IL-1beta in both cellular models. On the other hand, intercellular mediators such as leukemia inhibitory factor (LIF) and bone morphogenetic protein-2 (BMP-2) were not induced by IL-1beta in SW1353 cells, but significantly up-regulated in PHCs. Bioinformatical analysis identified nuclear factor kappa-B (NFkappaB) as a common transcriptional regulator of IL-1beta induced genes in both SW1353 cells and PHCs, whereas other transcription factors were only found to be relevant for individual cell systems. CONCLUSION: Our data characterize SW1353 cells as a cell line with only a very limited potential to mimic PHCs, though SW1353 cells can be of value to study the induction of protease expression within cells, a phenomenon also seen in chondrocytes.

Aged↗

Fly motion vision is based on Reichardt detectors regardless of the signal-to-noise ratio.

The computational structure of an optimal motion detector was proposed to depend on the signal-to-noise ratio (SNR) of the stimulus: At low SNR, the optimal motion detector should be a correlation or "Reichardt" type, whereas at high SNR, the detector would employ a gradient scheme [Potters, M. & Bialek, W. (1994) J. Physiol. (Paris) 4, 1755-1775]. Although a large body of experiments supports the Reichardt detector as the processing scheme leading to direction selectivity in fly motion vision, in most of these studies the SNR was rather low. We therefore reinvestigated the question over a much larger SNR range. Using 2-photon microscopy, we found that local dendritic [Ca(2+)] modulations, which are characteristic of Reichardt detectors, occur in response to drifting gratings over a wide range of luminance levels and contrasts. We also explored, as another fingerprint of Reichardt detectors, the dependence of the velocity optimum on the pattern wavelength. Again, we found Reichardt-typical behavior throughout the whole luminance and contrast range tested. Our results, therefore, provide strong evidence that only a single elementary processing scheme is used in fly motion vision.

Algorithms↗

Orientation tuning of motion-sensitive neurons shaped by vertical-horizontal network interactions.

We measured the orientation tuning of two neurons of the fly lobula plate (H1 and H2 cells) sensitive to horizontal image motion. Our results show that H1 and H2 cells are sensitive to vertical motion, too. Their response depended on the position of the vertically moving stimuli within their receptive field. Stimulation within the frontal receptive field produced an asymmetric response: upward motion left the H1/H2 spike frequency nearly unaltered while downward motion increased the spike frequency to about 40% of their maximum responses to horizontal motion. In the lateral parts of their receptive fields, no such asymmetry in the responses to vertical image motion was found. Since downward motion is known to be the preferred direction of neurons of the vertical system in the lobula plate, we analyzed possible interactions between vertical system cells and H1 and H2 cells. Depolarizing current injection into the most frontal vertical system cell (VS1) led to an increased spike frequency, hyperpolarizing current injection to a decreased spike frequency in both H1 and H2 cells. Apart from VS1, no other vertical system cell (VS2-8) had any detectable influence on either H1 or H2 cells. The connectivity of VS1 and H1/H2 is also shown to influence the response properties of both centrifugal horizontal cells in the contralateral lobula plate, which are known to be postsynaptic to the H1 and H2 cells. The vCH cell receives additional input from the contralateral VS2-3 cells via the spiking interneuron V1.

Animals↗

Adaptation of response transients in fly motion vision. I: Experiments.

Two types of transient responses have been investigated in fly motion-sensitive neurons in the past: the impulse and the step response. In response to a brief motion pulse, cells show a sudden rise in activity followed by an exponential decay ('impulse response'). In response to the onset of a constant velocity stimulus, cells exhibit transient oscillations before settling to a steady-state value ('step response'). Since the impulse response has been shown to shorten when tested after presentation of an adapting motion stimulus, we investigated whether adaptation also occurs during the step response. We tested this hypothesis by recording extracellularly the response of the H1-cell in the lobula plate of the blowfly Calliphora vicina to gratings of varying pattern contrasts and drift velocity. We found that the transient oscillations of the step response strongly depend on the pattern contrast: at low contrasts, oscillations lasted for several seconds, whereas at high contrasts, they settled within fractions of a second. This suggests that motion adaptation occurs during the initial period of the stimulus presentation and is dependent on the contrast of the motion stimulus. Using identical stimulus parameters (contrast and temporal frequency) for the adapting stimulus and testing the impulse response afterwards, we found that the impulse response and the transient period in the step response shortened in a similar way. We then analyzed the dynamic of the transients oscillations produced by ongoing motion of a square wave pattern in the anti-preferred direction (null direction) of H1. As observed for preferred direction motion, we found that the duration and amplitude of those transients shortened as the contrast and the velocity of the pattern increased, and that the oscillations disappeared when a blank screen instead of a pattern was presented before the onset of motion. Under both stimulus conditions, i.e. grating and blank screen before motion onset, the steady-state response level showed the same dependence on the contrast and temporal frequency of the pattern. When we analyzed the responses of the cell to pattern of various sizes and contrasts moving in the preferred direction of the cell, we found that increments in the size affected the overall amplitude of both the transient oscillations and the steady-state response level, whereas the duration of the oscillations only depended on the local pattern contrast. We also tested the impulse response before and after the presentation of an adapting stimulus presented in either the same or a different location of the visual field. The response shortened only when both the adapting and the test stimuli were presented at the same location. These last experiments demonstrate a strictly local mechanism of adaptation affecting the response transients of both the impulse and the step response.

Adaptation, Ocular↗

Neural networks in the cockpit of the fly.

Flies have been buzzing around on earth for over 300 million years. During this time they have radiated into more than 125,000 different species (Yeates and Wiegmann 1999), so that, by now, roughly every tenth described species is a fly. They thus represent one of the most successful animal groups on our planet. This evolutionary success might, at least in part, be a result of their acrobatic maneuverability, which enables them, for example, to chase mates at turning velocities of more than 3000 degrees s(-1) with delay times of less than 30 ms (Land and Collett 1974; Wagner 1986). It is this fantastic behavior, which has initiated much research during the last decades, both on its sensory control and the biophysical and aerodynamic principles of the flight output (Dickinson et al. 1999, 2000). Here, we review the current state of knowledge about the neural processing of visual motion, which represents one sensory component intimately involved in flight control. Other reviews on this topic have been published with a similar (Hausen 1981, 1984; Hausen and Egelhaaf 1989; Borst 1996) or different emphasis (Frye and Dickinson 2001; Borst and Dickinson 2002). Because of space limitations, we do not review the extensive work that has been done on fly motion-sensitive neurons to advance our understanding of neural coding (Bialek et al. 1991; Rieke et al. 1997; de Ruyter et al. 1997, 2000; Haag and Borst 1997, 1998; Borst and Haag 2001). Unless stated otherwise, all data presented in the following were obtained on the blowfly Calliphora vicina which we will often casually refer to as 'the fly'.

Animals↗

Differentiating between low and high susceptibility to schizophrenia in twins: the significance of dermatoglyphic indices in relation to other determinants of brain development.

Both the skin and the brain develop from the same ectoderm and it is thought, therefore, that dermatoglyphics are informative for early disturbances in brain development in schizophrenia. This study was aimed at investigating the differences in both digital and palmar dermatoglyphic indices between twins discordant for schizophrenia and control twins. Furthermore, the significance of dermatoglyphic indices in relation to other determinants of brain development with regard to the susceptibility to schizophrenia was investigated. Data on dermatoglyphic indices of the hand and the palm were obtained from 21 same-sex discordant and 37 same-sex control twins. For 19 discordant and 25 control twins, there was also data available on brain volumes. Non-genetic intra-uterine circumstances early in pregnancy (10-13 weeks of gestation) are associated with a susceptibility to schizophrenia, since both the twins with schizophrenia and the unaffected co-twins showed more fluctuating asymmetry of the finger ridges (P<0.01), and marginally higher absolute finger ridge counts (P=0.06) than control twin pairs. Fluctuating asymmetry of the finger ridges was as important as whole brain and left hippocampal volumes in differentiating twins with a high susceptibility to schizophrenia from those with a low susceptibility.

Adult↗

Recurrent network interactions underlying flow-field selectivity of visual interneurons.

Motion-sensitive large-field neurons found at higher processing stages in many species often exhibit a remarkable selectivity for particular flow fields. However, the underlying neural mechanisms are not yet understood. We studied this problem in the so-called lobula plate tangential cells (LPTCs) of the fly. Investigating the connectivity between LPTCs by means of dual recordings, we find two types of connections: (1) heterolateral connections between LPTCs of both hemispheres and (2) ipsilateral connections between LPTCs within one lobula plate. The circuit is suitable to amplify incoming, dendritic signals in the case of rotatory flow fields and to reduce them in the case of other flow-field structures. In addition to feedforward connectivity, thus, the flow-field selectivity of LPTCs may be significantly attributable to recurrent excitation involving the network of large-field neurons in both brain hemispheres.

Action Potentials↗

The surface structure of trypanosomes in relation to their molecular phylogeny.

Molecular phylogenetic analysis using genes coding for ribosomal RNA and proteins suggests that trypanosomes are monophyletic. Salivarian trypanosomes showing antigenic variation of the variant surface glycoprotein (VSG) diverged from non-Salivarian trypanosomes some 200-300 million years ago. Representatives of the non-Salivarian group, the mammalian parasite, Trypanosoma cruzi, and the fresh-water fish trypanosome, T. carassii, are characterised by surfaces dominated by carbohydrate-rich mucin-like glycoproteins, which are not subject to antigenetic variation. It is suggested that this latter surface structure is typical for non-Salivarian trypanosomes as well as members of the other Kinetoplastid suborder, the Bodonina. This would imply that at some point in time in the evolution of the Salivaria the highly abundant and comparatively poorly immunogenetic mucin-like molecules must have been replaced for equally abundant but highly immunogenic VSG-like molecules. While the selective advantage for such a unique transition is difficult to imagine, the subsequent diversification of VSG genes/molecules may have been comparatively straightforward because even the most limited form of antigenic variation would have extended the duration of infection in the vertebrate and thus would have increased the chance for transfer to the vector.

Animals↗

Spatial distribution and characteristics of voltage-gated calcium signals within visual interneurons.

Most of our knowledge about insect calcium currents is derived from studies on cultured or dissociated somata. So far, only little data on calcium currents are available for neurons including their dendritic and presynaptic structures. Here we combined the switched-electrode voltage-clamp technique with optical recording using calcium-sensitive dyes in identified fly visual interneurons in vivo to characterize the voltage dependence and dynamics of calcium currents quantitatively and in a spatially resolved way. For all three cell types considered, i.e., centrifugal horizontal (CH), horizontal system (HS), and vertical system (VS) cells, the activation curve is rather flat and covers a voltage range from -60 to -20 mV in dendritic as well as presynaptic areas of the cells. The calcium increase is fastest for CH cells with a time constant of approximately 70 ms. In HS and VS cells, the time constant amounts to 400-700 ms. The calcium dynamics as determined in different regions of the cells are similar except for a small segment between the axon and the dendrite in HS and VS cells, where the calcium increase is significantly faster. In summary, the results show the existence of a low-voltage-activated calcium current with little or no inactivation in dendritic as well as presynaptic regions of fly lobula plate tangential cells.

Animals↗

Freshwater fish trypanosomes: definition of two types, host control by antibodies and lack of antigenic variation.

Haemoflagellates of the genus Trypanosoma are prevalent in freshwater fishes and are transmitted by leeches as vectors. As demonstrated by sequence comparisons of nuclear small subunit rRNA genes, trypanosomes isolated from several fish species at different localities can be divided into at least 2 closely related types, designated Type A and Type B. A clone derived from a Type A isolate from carp (Cyprinus carpio) was used to study the anti-parasite immune response in specified pathogen-free outbred carp. Infection leads to an initial rise in parasitaemia in the blood followed by a sharp decline in all fish (acute phase). Thereafter, in some carp, parasites become undetectable both in the blood and in internal organs while, in others, low numbers can be found in the blood for up to 1 year (chronic phase). Fish that have controlled an acute infection with the clone are not only protected against an homologous challenge infection, but also against the infection with parasite lines derived from carp in the chronic phase of infection. Passive immunization experiments with IgM purified from serum of recovered carp indicate that the infection is controlled by antibodies. The anti-parasite antibody level in recovered carp remains high for many months although the parasitaemia is controlled at very low levels and the half life of IgM, t1/2 = 22.5 days, is comparatively short. The effective control of trypanosomes in laboratory infections is in contrast to the high prevalence in natural and farmed freshwater fish populations.

Animals↗

Active membrane properties and signal encoding in graded potential neurons.

We investigated the influence of active membrane properties on the precision by which the stimulus velocity is encoded in the membrane potential of a motion-sensitive interneuron in the blowfly. The so-called HS-cells respond to visual motion stimuli with a graded shift in membrane potential. Superimposed on this graded response are small spike-like events. This "mixed" visual response mode can be modified by current injection in two different ways. (1) By ongoing injection of hyperpolarizing current, the spike-like events are turned into full-blown action potentials, and (2) by injection of depolarizing current, the spike-like events become completely suppressed. The visual response then consists of a graded shift of membrane potential only. As a measure of the fidelity, we calculated the coherence between the motion stimulus and the response of the cell elicited with different electrical manipulations of the cell. We found that the coherence was highest for the cell at rest. Any electrical manipulation resulted in a reduced coherence. This was attributable partly to a lower signal-to-noise ratio and partly to an increased nonlinearity in the response. By applying a threshold operation we transformed the analog membrane response into an all-or-none spike train. A comparison between these two ways of signal representation revealed that more information about the stimulus velocity is inherent in the analog membrane potential than in the spike train.

Action Potentials↗

The molecular phylogeny of trypanosomes: evidence for an early divergence of the Salivaria.

Chronic infections with trypanosomes dwelling extracellularly in the blood and tissues of their hosts are observed in all vertebrate classes. We present here a molecular phylogenetic reconstruction of trypanosome evolution based on nucleotide sequences of small subunit rRNA genes. The evolutionary tree suggests an ancient split into one branch containing all Salivarian trypanosomes and a branch containing all non-Salivarian lineages. The latter branch splits into a clade containing bird, reptilian and Stercorarian trypanosomes infecting mammals and a clade with a branch of fish trypanosomes and a branch of reptilian/amphibian lineages. The branching order of the non-Salivarian trypanosomes supports host-parasite cospeciation scenarios, but also suggests host switches, e.g. between bird and reptilian trypanosomes. The tree is discussed in relation to the modes of adaptation that allow trypanosomes to infect immunocompetent vertebrates. Most importantly, the early divergence of the Salivarian lineages suggests that the presence of a dense proteinaceous surface coat that is subject to antigenic variation is a unique invention of this group of parasites.

Animals↗

Cultivation of bloodstream forms of Trypanosoma carassii, a common parasite of freshwater fish.

Trypanosoma carassii (syn. T. danilewskyi) is a widespread parasite of carp and other cyprinid as well as some noncyprinid freshwater fish. It lives extracellularly in the blood and tissues of its hosts, causing chronic infections. In this paper the isolation of T. carassii from fish blood and the propagation and cloning of bloodstream forms in vitro are described. By several criteria, cultured and fish-derived trypomastigotes are indistinguishable. The culture system should be useful for the biochemical characterization of this trypanosome and its interaction with the fish immune system.

Animals↗

Dendritic computation of direction selectivity and gain control in visual interneurons.

The extraction of motion information from time varying retinal images is a fundamental task of visual systems. Accordingly, neurons that selectively respond to visual motion are found in almost all species investigated so far. Despite its general importance, the cellular mechanisms underlying direction selectivity are not yet understood in most systems. Blocking inhibitory input to fly visual interneurons by picrotoxinin (PTX), we demonstrate that their direction selectivity arises largely from interactions between postsynaptic signals elicited by excitatory and inhibitory input elements, which are themselves only weakly tuned to opposite directions of motion. Their joint activation by preferred as well as null direction motion leads to a mixed reversal potential at which the postsynaptic response settles for large field stimuli. Assuming the activation ratio of these opponent inputs to be a function of pattern velocity can explain how the postsynaptic membrane potential saturates with increasing pattern size at different levels for different pattern velocities ("gain control"). Accordingly, we find that after blocking the inhibitory input by PTX, gain control is abolished.

Animals↗

Encoding of visual motion information and reliability in spiking and graded potential neurons.

We investigated the information about stimulus velocity inherent in the membrane signals of two types of directionally selective, motion-sensitive interneurons in the fly visual system. One of the cells, the H1-cell, is a spiking neuron, whereas the other, the HS-cell, encodes sensory information mainly by a graded shift of its membrane potential. Using a pseudo-random velocity waveform by which a visual grating is moving along the horizontal axis of the eye, both cell types follow the stimulus velocity at higher precision than in response to a step-like velocity function. To measure how much information about the stimulus velocity is preserved in the cellular responses, we calculated the coherence between the stimulus and the neural signals as a function of stimulus frequency. At frequencies up to approximately 10 Hz motion information is well contained in the electrical signals of HS- and H1-cells: For HS-cells the coherence value amounts to approximately 70%, and for H1-cells this value is approximately 60%. Comparing these values with the coherence expected from a linear encoding reveals that the fidelity of the original stimulus is deteriorated in the neural signal partly by neural noise and partly by the nonlinearity inherent in the process of visual motion detection. The degree to which this nonlinearity contributes to the decrease in coherence depends on the maximum velocity used in the experiments; the smaller the stimulus amplitude, the higher the coherence and, thus, the smaller the nonlinearity in encoding of stimulus motion. All these results are in agreement with model simulations in which visual motion is processed by an array of local motion detectors, the spatially integrated output of which is considered the equivalent of the neural signals of HS- and H1-cells.

Animals↗