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991.
Microgravity tissue engineering 总被引:35,自引:4,他引:31
Lisa E. Freed Gordana Vunjak-Novakovic 《In vitro cellular & developmental biology. Animal》1997,33(5):381-385
Summary Tissue engineering studies were done using isolated cells, three-dimensional polymer scaffolds, and rotating bioreactors operated
under conditions of simulated microgravity. In particular, vessel rotation speed was adjusted such that 10 mm diameter × 2
mm thick cell-polymer constructs were cultivated in a state of continuous free-fall. Feasibility was demonstrated for two
different cell types: cartilage and heart. Conditions of simulated microgravity promoted the formation of cartilaginous constructs
consisting of round cells, collagen and glycosaminoglycan (GAG), and cardiac tissue constructs consisting of elongated cells
that contracted spontaneously and synchronously. Potential advantages of using a simulated microgravity environment for tissue
engineering were demonstrated by comparing the compositions of cartilaginous constructs grown under four different in vitro culture conditions: simulated microgravity in rotating bioreactors, solid body rotation in rotating bioreactors, turbulent
mixing in spinner flasks, and orbital mixing in petri dishes. Constructs grown in simulated microgravity contained the highest
fractions of total regenerated tissue (as a percent of construct dry weight) and of GAG, the component required for cartilage
to withstand compressive force. 相似文献
992.
Gordana Mati Jasmina Kipi Biljana Risti Jadranka Dundjerski Divna Trajkovi 《Cell biology international》1995,19(3):203-213
A mild whole body hyperthermic stress causes a rapid and reversible reduction of rat liver glucocorticoid receptor (GR) binding capacity and affects the stability of the GR-DNA complexes formed after thermal transformation of the receptor. These changes appear to be physiologically relevant, since they are accompanied by a decrease in dexamethasone induction of hepatic tyrosine aminotransferase (TAT). In spite of the decreased rate of the GR degradation in liver cytosol of hyperthermic as compared to control rats, the total amount of the GR and its proteolytic products recognized by BuGR2 monoclonal antibody was found to be lower in the former cytosol, but higher in the respective nuclei. 相似文献
993.
994.
V. Čatská 《Folia microbiologica》1980,25(2):174-176
Differences in the effect of volatile and gaseous metabolites of germinating pea seeds on the germination of spores of Mucor racemosus and macroconidia of Fusarium oxysporum are described. Germination of spores of M. racemosus was inhibited by seed metabolites whereas germination of macroconidia of F. oxysporum was stimulated during the first two days and inhibition occurred only after further two days of germination of the seeds. A pronounced inhibition of germination of spores of both micromycetes took place due to absorption of CO2 from volatile and gaseous metabolites. Absorption of some components of seed metabolites in a KMnO4 solution led to a decrease of the inhibitory effect on germination of spores of M. racemosus and stimulatory effect on germination of macroconidia of F. oxysporum. 相似文献
995.
The adaptation of dermatophytes to antimycotics leads to the development of two independent processes—the induction of degrading
enzyme systems detoxicating the antimycotic to less active or completely inactive derivatives, and temporary resistance, accompanied
by increasing loss of sensitivity of the dermatophytes to the given antimycotics. These processes can both be regarded as
part of the defences of the microbial cell. 相似文献
996.
Diana Bilić-Šobot Valentina Kubale Martin Škrlep Marjeta Čandek-Potokar Maja Prevolnik Povše Gregor Fazarinc 《Archives of animal nutrition》2016,70(5):378-388
This study aimed to evaluate the effect of hydrolysable tannin supplementation on morphology, cell proliferation and apoptosis in the intestine and liver of fattening boars. A total of 24 boars (Landrace × Large white) were assigned to four treatment groups: Control (fed commercial feed mixture) and three experimental groups fed the same diet supplemented with 1%, 2% and 3% of hydrolysable tannin-rich extract. Animals were housed individually with ad libitum access to feed and then slaughtered at 193 d of age and 122 ± 10 kg body weight. Diets supplemented with hydrolysable tannin affected the morphometric traits of the duodenum mucosa as reflected in increased villus height, villus perimeter and mucosal thickness. No effect was observed on other parts of the small intestine. In the large intestine, tannin supplementation reduced mitosis (in the caecum and descending colon) and apoptosis (in the caecum, ascending and descending colon). No detrimental effect of tannin supplementation on liver tissue was observed. The present findings suggest that supplementing boars with hydrolysable tannins at concentrations tested in this experiment has no unfavourable effects on intestinal morphology. On the contrary, it may alter cell debris production in the large intestine and thus reduce intestinal skatole production. 相似文献
997.
Morphological and Molecular Diversity of the Neglected Genus Rhizomastix Alexeieff, 1911 (Amoebozoa: Archamoebae) with Description of Five New Species
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Eliška Zadrobílková Pavla Smejkalová Giselle Walker Ivan Čepička 《The Journal of eukaryotic microbiology》2016,63(2):181-197
The genus Rhizomastix is a poorly known group of amoeboid heterotrophic flagellates living as intestinal commensals of insects, amphibians or reptiles, and as inhabitants of organic freshwater sediments. Eleven Rhizomastix species have been described so far, but DNA sequences from only a single species have been published. Recently, phylogenetic analyses confirmed a previous hypothesis that the genus belongs to the Archamoebae; however, its exact position therein remains unclear. In this study we cultured nine strains of Rhizomastix, both endobiotic and free‐living. According to their light‐microscopic morphology and SSU rRNA and actin gene analyses, the strains represent five species, of which four are newly described here: R. bicoronata sp. nov., R. elongata sp. nov., R. vacuolata sp. nov. and R. varia sp. nov. In addition, R. tipulae sp. nov., living in the intestine of crane flies, is separated from the type species, R. gracilis. We also examined the ultrastructure of R. elongata sp. nov., which revealed that it is more complicated than the previously described R. libera. Our data show that either the endobiotic lifestyle of some Rhizomastix species has arisen independently from other endobiotic archamoebae, or the free‐living members of this genus represent a secondary switch from the endobiotic lifestyle. 相似文献
998.
Angeliki?Balasopoulou Biljana?Stankovi? Angeliki?Panagiotara Gordana?Nik?evic Brock?A.?Peters Anne?John Effrosyni?Mendrinou Apostolos?Stratopoulos Aigli?Ioanna?Legaki Vasiliki?Stathakopoulou Aristoniki?Tsolia Nikolaos?Govaris Sofia?Govari Zoi?Zagoriti Konstantinos?Poulas Maria?Kanariou Nikki?Constantinidou Maro?Krini Kleopatra?Spanou Nedeljko?Radlovic Bassam?R.?Ali Joseph?Borg Radoje?Drmanac George?Chrousos Sonja?Pavlovic Eleftheria?Roma Branka?Zukic George?P.?Patrinos Theodora?KatsilaEmail author 《Human genomics》2016,10(1):34
Background
Celiac disease is a complex chronic immune-mediated disorder of the small intestine. Today, the pathobiology of the disease is unclear, perplexing differential diagnosis, patient stratification, and decision-making in the clinic.Methods
Herein, we adopted a next-generation sequencing approach in a celiac disease trio of Greek descent to identify all genomic variants with the potential of celiac disease predisposition.Results
Analysis revealed six genomic variants of prime interest: SLC9A4 c.1919G>A, KIAA1109 c.2933T>C and c.4268_4269delCCinsTA, HoxB6 c.668C>A, HoxD12 c.418G>A, and NCK2 c.745_746delAAinsG, from which NCK2 c.745_746delAAinsG is novel. Data validation in pediatric celiac disease patients of Greek (n?=?109) and Serbian (n?=?73) descent and their healthy counterparts (n?=?111 and n?=?32, respectively) indicated that HoxD12 c.418G>A is more prevalent in celiac disease patients in the Serbian population (P?<?0.01), while NCK2 c.745_746delAAinsG is less prevalent in celiac disease patients rather than healthy individuals of Greek descent (P?=?0.03). SLC9A4 c.1919G>A and KIAA1109 c.2933T>C and c.4268_4269delCCinsTA were more abundant in patients; nevertheless, they failed to show statistical significance.Conclusions
The next-generation sequencing-based family genomics approach described herein may serve as a paradigm towards the identification of novel functional variants with the aim of understanding complex disease pathobiology.999.
Blanka Stiburkova Dana Gabrikova Pavel Čepek Pavel Šimek Pavol Kristian Elizabeth Cordoba-Lanus 《Nucleosides, nucleotides & nucleic acids》2016,35(10-12):529-535
ABSTRACTThe Roma represents a transnational ethnic group, with a current European population of 8–10 million. The evolutionary process that had the greatest impact on the gene pool of the Roma population is called the founder effect. Renal hypouricemia (RHUC) is a rare heterogenous inherited disorder characterized by impaired renal urate reabsorption. The affected individuals are predisposed to recurrent episodes of exercise-induced nonmyoglobinuric acute kidney injury and nephrolithiasis. To date, more than 150 patients with a loss-of-function mutation for the SLC22A12 (URAT1) gene have been found, most of whom are Asians. However, RHUC 1 patients have been described in a variety of ethnic groups (e.g., Arab Israelis, Iraqi Jews, Caucasians, and Roma) and in geographically noncontiguous countries. This study confirms our previous findings regarding the high frequency of SLC22A12 variants observed. Frequencies of the c.1245_1253del and c.1400C>T variants were found to be 1.92% and 5.56%, respectively, in a subgroup of the Roma population from five regions in three countries: Slovakia, Czech Republic, and Spain. Our findings suggested that the common dysfunction allelic variants of URAT1 exist in the general Roma population and thus renal hypouricemia should be kept in differential diagnostic algorithm on Roma patients with defect in renal tubular urate transport. This leads to confirm that the genetic drift in the Roma have increased the prevalence of hereditary disorders caused by very rare variants in major population. 相似文献
1000.