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Similar Influences (similar + influence)
Selected AbstractsGap junctional communication in human osteoclasts in vitro and in vivoJOURNAL OF CELLULAR AND MOLECULAR MEDICINE, Issue 6a 2008A. F. Schilling Abstract Bone-forming cells are known to be coupled by gap junctions, formed primarily by connexin43 (Cx43). The role of Cx43 in osteoclasts has so far only been studied in rodents, where Cx43 is important for fusion of mononuclear precursors to osteoclasts. Given the potential importance for human diseases with pathologically altered osteoclasts, we asked whether a similar influence of Cx43 can also be observed in osteoclasts of human origin. For this purpose, Cx43 mRNA expression was studied in a time course experiment of human osteoclast differentiation by RT-PCR. Localization of Cx43 in these cells was determined by immunohistochemistry and confocal microscopy. For the assessment of the effect of gap junction inhibition on cell fusion, gap junctions were blocked with heptanol during differentiation of the cells and the cells were then evaluated for multinuclearity. Paraffin sections of healthy bone and bone from patients with Paget's disease and giant cell tumour of the bone were used to study Cx43 expression in vivo. We found mRNA and protein expression of Cx43 in fully differentiated osteoclasts as well as in precursor cells. This expression decreased in the course of differentiation. Consistently, we found a lower expression of Cx43 in osteoclasts than in bone marrow precursor cells in the histology of healthy human bone. Blockade of gap junctional communication by heptanol led to a dose-dependent decrease in multinuclearity, suggesting that gap junctional communication precedes cell fusion of human osteoclasts. Indeed, we found a particularly strong expression of Cx43 in the giant osteoclasts of patients with Paget's disease and giant cell tumour of the bone. These results show that gap junctional communication is important for fusion of human mononuclear precursor cells to osteoclasts and that gap junctional Cx43 might play a role in the regulation of size and multinuclearity of human osteoclasts in vivo. [source] The significance of small herbivores in structuring annual grasslandJOURNAL OF VEGETATION SCIENCE, Issue 2 2007Halton A. Peters Abstract Question: Herbivores can play a fundamental role in regulating the composition and structure of terrestrial plant communities. Relatively inconspicuous but nevertheless ubiquitous gastropods and small mammals are usually considered to influence grassland communities through distinct modes. 1. Do terrestrial gastropods and small mammals, either alone or in combination, influence plant community composition of an intact annual grassland? 2. Do these herbivores influence the plant size structure of the dominant grass Avena? Location: Jasper Ridge Biological Preserve (37°24' N, 122° 13' W, elevation 150 m) in northern California. Methods: Animal exclosures were used to examine the single and combined influences of these herbivores on annual grassland production, community composition, and plant size structure during the growing season of an intact annual grassland. Results: The removal and exclusion of the herbivores increased the prevalence of grasses relative to legumes and non-legume forbs; increased total production of above-ground plant biomass; and increased mean plant size and exacerbated size hierarchies in populations of Avena. The effect of both gastropods and small mammals, alone and in combination, was characterized by temporal oscillations in the relative dominance of grasses in plots with vs. without herbivores. Conclusions: Both groups of herbivores are important controllers of California annual grassland that exert similar influences on production and composition. While other factors appear to determine the absolute number of individuals in this plant community, selective consumption of grasses by gastropods and small mammals partially offsets the competitive advantages associated with their early germination. [source] Tests for presynaptic modulation of corticospinal terminals from peripheral afferents and pyramidal tract in the macaqueTHE JOURNAL OF PHYSIOLOGY, Issue 1 2006A. Jackson The efficacy of sensory input to the spinal cord can be modulated presynaptically during voluntary movement by mechanisms that depolarize afferent terminals and reduce transmitter release. It remains unclear whether similar influences are exerted on the terminals of descending fibres in the corticospinal pathway of Old World primates and man. We investigated two signatures of presynaptic inhibition of the macaque corticospinal pathway following stimulation of the peripheral nerves of the arm (median, radial and ulnar) and the pyramidal tract: (1) increased excitability of corticospinal axon terminals as revealed by changes in antidromically evoked cortical potentials, and (2) changes in the size of the corticospinal monosynaptic field potential in the spinal cord. Conditioning stimulation of the pyramidal tract increased both the terminal excitability and monosynaptic fields with similar time courses. Excitability was maximal between 7.5 and 10 ms following stimulation and returned to baseline within 40 ms. Conditioning stimulation of peripheral nerves produced no statistically significant effect in either measure. We conclude that peripheral afferents do not exert a presynaptic influence on the corticospinal pathway, and that descending volleys may produce autogenic terminal depolarization that is correlated with enhanced transmitter release. Presynaptic inhibition of afferent terminals by descending pathways and the absence of a reciprocal influence of peripheral input on corticospinal efficacy would help to preserve the fidelity of motor commands during centrally initiated movement. [source] Glutathione peroxidase and viral replication: Implications for viral evolution and chemopreventionBIOFACTORS, Issue 1-4 2001Alan M. Diamond It is likely that several of the biological effects of selenium are due to its effects on selenoprotein activity. While the effects of the anti-oxidant selenoprotein glutathione peroxidase (GPx) on inhibiting HIV activation have been well documented, it is clear that increased expression of this enzyme can stimulate the replication and subsequent appearance of cytopathic effects associated with an acutely spreading HIV infection. The effects of GPx on both phases of the viral life cycle are likely mediated via its influence on signaling molecules that use reactive oxygen species, and similar influences on signaling pathways may account for some of the anti-cancer effects of selenium. Similarly, selenium can alter mutagenesis rates in both viral genomes and the DNA of mammalian cells exposed to carcinogens. Comparisons between the effects of selenium and selenoproteins on viral infections and carcinogenesis may yield new insights into the mechanisms of action of this element. [source] | ||||||||||