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排序方式: 共有157条查询结果,搜索用时 15 毫秒
71.
Bita Carrion Carlos P. Huang Cyrus M. Ghajar Suraj Kachgal Ekaterina Kniazeva Noo Li Jeon Andrew J. Putnam 《Biotechnology and bioengineering》2010,107(6):1020-1028
Stem cell niches are composed of numerous microenvironmental features, including soluble and insoluble factors, cues from other cells, and the extracellular matrix (ECM), which collectively serve to maintain stem cell quiescence and promote their ability to support tissue homeostasis. A hallmark of many adult stem cell niches is their proximity to the vasculature in vivo, a feature common to neural stem cells, mesenchymal stem cells (MSCs) from bone marrow and adipose tissue, hematopoietic stem cells, and many tumor stem cells. In this study, we describe a novel 3D microfluidic device (MFD) as a model system in which to study the molecular regulation of perivascular stem cell niches. Endothelial cells (ECs) suspended within 3D fibrin gels patterned in the device adjacent to stromal cells (either fibroblasts or bone marrow‐derived MSCs) executed a morphogenetic process akin to vasculogenesis, forming a primitive vascular plexus and maturing into a robust capillary network with hollow well‐defined lumens. Both MSCs and fibroblasts formed pericytic associations with the ECs but promoted capillary morphogenesis with distinct kinetics. Biochemical assays within the niche revealed that the perivascular association of MSCs required interaction between their α6β1 integrin receptor and EC‐deposited laminin. These studies demonstrate the potential of this physiologically relevant ex vivo model system to study how proximity to blood vessels may influence stem cell multipotency. Biotechnol. Bioeng. 2010;107: 1020–1028. © 2010 Wiley Periodicals, Inc. 相似文献
72.
This paper reports studies on the effects of re-vitrification by the CPS (Closed Pulled Straw) method on the development of 4-cell stage mouse embryos. The procedure involved culturing 2-cell mouse embryos in G-1 medium until the 4-cell stage followed by the division of the normal 4-cell stage embryos into a control group (non-vitrified) and two experimental subgroups (vitrified and re-vitrified). Embryos in the vitrified subgroup were cryopreserved by the CPS vitrification method. In the second experimental subgroup (re-vitrified), embryos that were already vitrified were warmed and cryopreserved again by the same method. There was no significant reduction in the rate of blastocyst formation after vitrification and re-vitrification. However, re-vitrification reduced the total cell number, ICM (inner cell mass) percent and blastocyst diameter (P<0.05). These results showed that vitrification and re-vitrification by the CPS method did not negatively affect the development of vitrified-warmed 4-cell mouse embryos, whereas re-vitrification significantly reduced both the cell number and diameter of blastocysts. 相似文献
73.
Fransiska Malfait Ariana Kariminejad Tim Van Damme Caroline Gauche Delfien Syx Faten Merhi-Soussi Sandrine Gulberti Sofie Symoens Suzanne Vanhauwaert Andy Willaert Bita Bozorgmehr Mohamad Hasan Kariminejad Nazanin Ebrahimiadib Ingrid Hausser Ann Huysseune Sylvie Fournel-Gigleux Anne De Paepe 《American journal of human genetics》2013
74.
Hamid Badali Maydelin Fernández-González Bita Mousavi Maria Teresa Illnait-Zaragozi Juan Carlos González-Rodríguez G. Sybren de Hoog Jacques F. Meis 《Mycopathologia》2013,175(5-6):439-444
We report two cases of chromoblastomycosis due to Fonsecaea pedrosoi and F. monophora in otherwise healthy Cuban males. Direct microscopic examination of biopsies revealed muriform cells, the hallmark of chromoblastomycosis. The suspected agents were recovered in culture, identified on the basis of morphological criteria and confirmed by sequencing of the internal transcribed spacer regions of rDNA. Final treatment consisted of surgical excision. The patients were successfully cured since there was no relapse after a follow-up of more than a year. In vitro antifungal susceptibility testing of both isolates showed that itraconazole and posaconazole had potent activity. High MICs of amphotericin B (2 μg/ml), fluconazole (>64 μg/ml), anidulafungin (8 μg/ml) and caspofungin (8 μg/ml) were found. 相似文献
75.
Bita Naseri Mozhgan Veisi Naier Khaledi 《Archives Of Phytopathology And Plant Protection》2013,46(7-8):349-358
AbstractMacrophomina phaseolina causes charcoal root rot (CRR) in numerous crops worldwide. However, structural progression of CRR epidemics in association with bean agro-ecosystems is little understood. Thus, progression of CRR epidemics in interaction with 13 agro-ecological variables was characterised in 48 commercial bean fields. Frequency of pathogen isolated from root was assessed at vegetative (V3), flowering-podding (R6-7) and pod maturity (R9) growth stages. Two principal factors accounting for 89% of total data variance characterised CRR epidemics. Rhizobial nodulation and cultivation–depth, clay–pH, date–preceding crop, urea–bean class and urea–herbicide interactions accounted for 50% CRR epidemic dynamics. Sixty-five percent of production variance was explained by soil clay, bean class, colonisation, planting date and depth, cultivation method, preceding crop, nodulation, herbicide and urea application. The present findings enabled us to explain a noticeable part of variations in productivity among the bean CRR pathosystems with the help of certain agricultural and environmental events for sustainable agriculture purposes. 相似文献
76.
Pourgholaminejad A Jamali A Samadi-Foroushani M Amari A Mirzaei R Ansaripour B Khansari N Aghasadeghi MR Baban B Hadjati J 《Cellular immunology》2011,271(2):360-364
CpG motifs have been advanced as agents that stimulate the maturation of DCs for immunotherapy. The present study tested the hypothesis that multiple doses of CpG-matured DC vaccine would be efficacious for complete eradication of experimentally-induced tumor. Accordingly, WEHI164 cells were implanted subcutaneously in the flank of BALB/c mice. During DC culture, tumor lysate was added to immature DCs followed by addition of CpG or non-CpG control 4–6 h later. A total of three doses of CpG or non-CpG control-matured DCs were injected around tumors. The results showed that multiple doses of CpG-matured DCs led to considerable decrease in cytotoxicity of lymphocytes and significantly increased tumor growth rate compared to a single dose. Further, mice which received three doses of the vaccine also displayed significant FoxP3 in tumor tissue. In conclusion, multiple doses of CpG-matured DCs exhibited decreased anti-tumor immunity in association with increased expression of FoxP3. 相似文献
77.
The ability of MSCs (mesenchymal stem cells) to differentiate between other cell types makes these cells an attractive therapeutic tool for cell transplantation. This project was designed to improve transdifferentiation of human MSCs into liver cells using IGF-I (insulin-like growth factor 1) which, despite its important role in liver development, has not been used for in vitro hepatic differentiation. In the present study, the MSCs derived from healthy human bone marrow samples were cultured and characterized by immunophenotyping and differentiation potential into osteoblast and adipocytes. Transdifferentiation into hepatocyte-like cells was performed in the presence/absence of IGF-I in combination with predefined hepatic differentiation cocktail. To evaluate transdifferentiation, morphological features, immuno-cytochemical staining of specific biological markers and hepatic functions were assessed. Morphological assessment and evaluation of glycogen content, albumin and AFP (α-feto protein) expression as well as albumin and urea secretion revealed statistically significant difference between experimental groups compared with the control. Morphology and function (albumin secretion) of IGF-I-treated cells were significantly better than IGF-I-free experimental group. To the best of our knowledge, our study is the first to demonstrate that the combination of IGF-I with the predefined hepatic differentiation cocktail will significantly improve the morphological features of the differentiated cells and albumin secretion. 相似文献
78.
Background
Endothelial permeability is involved in injury, inflammation, diabetes and cancer. It is partly regulated by the thrombin-, histamine-, and VEGF-mediated myosin-light-chain (MLC) activation pathways. While these pathways have been investigated, questions such as temporal effects and the dynamics of multi-mediator regulation remain to be fully studied. Mathematical modeling of these pathways facilitates such studies. Based on the published ordinary differential equation models of the pathway components, we developed an integrated model of thrombin-, histamine-, and VEGF-mediated MLC activation pathways.Results
Our model was validated against experimental data for calcium release and thrombin-, histamine-, and VEGF-mediated MLC activation. The simulated effects of PAR-1, Rho GTPase, ROCK, VEGF and VEGFR2 over-expression on MLC activation, and the collective modulation by thrombin and histamine are consistent with experimental findings. Our model was used to predict enhanced MLC activation by CPI-17 over-expression and by synergistic action of thrombin and VEGF at low mediator levels. These may have impact in endothelial permeability and metastasis in cancer patients with blood coagulation.Conclusion
Our model was validated against a number of experimental findings and the observed synergistic effects of low concentrations of thrombin and histamine in mediating the activation of MLC. It can be used to predict the effects of altered pathway components, collective actions of multiple mediators and the potential impact to various diseases. Similar to the published models of other pathways, our model can potentially be used to identify important disease genes through sensitivity analysis of signalling components. 相似文献79.
80.
Glycosphingolipid expression in pig aorta: identification of possible target antigens for human natural antibodies 总被引:4,自引:1,他引:3
Total non-acid glycosphingolipids were isolated from the aortas of more
than 80 pigs. The glycolipids were separated by HPLC, analysed by thin-
layer chromatography, and tested for reactivity with monoclonal anti- blood
group antibodies. The fractions were structurally characterized by NMR
spectroscopy and mass spectrometry. Reactivity with both anti- blood group
A and H antibodies was seen. The major glycosphingolipid constituents were
globotri- and globotetraosylceramides and blood group H
pentaglycosylceramides based on type 1 and type 2 core saccharide chains.
Globopentaosylceramides, blood group H hexaglycosylceramides based on type
4 chain, and blood group A hexaglycosylceramides based on type 1 core chain
were also present. Two structures, that may be important targets for human
antibodies initiating hyperacute rejection following pig to human
xenotransplantation, were present as minor constituents compared to the
blood group components. These were Galalpha1,3neolactotetraosylceramide and
a Galalpha1, 3Lexstructure. A Leb/Y hexaglycosylceramide was also present.
相似文献