INT211906
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Significant increases of circulating cells expressing the EPC phenotype were observed at days 2 (36.12% compared to pre-treatment control p = 0.04) and 7 (95.35% compared to pretreatment control, p = .001) as shown in Figure 5.
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Stem-Kine augments circulation of cells with EPC phenotype | |||||||||||||||
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Stem-Kine increases circulating cells with EPC activity | |||||||||||||||
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According to our previous transcript profiling, three highly expressed transcripts for each EPC type were chosen; HLA-DRA, lysozyme, and CD14 for eEPCs, and caveolin1, VE-cadherin, and vWF for OECs. | |||||||||||||||
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CB-derived as opposed to PB-derived eEPCs and OECs were also included in transcriptomic analysis as it has been suggested that foetal blood may represent a richer EPC source than adult peripheral blood [23,24]. | |||||||||||||||
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An alternative approach to isolate EPCs from peripheral or umbilical cord blood utilizes in vitro culture and this consistently produces two distinct EPC subtypes which have been named as early EPCs (eEPCs) and Outgrowth endothelial cells (OECs) [11]. | |||||||||||||||
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Furthermore, eEPC gene expression patterns partially matched monocytes, and OECs were closely linked to DMECs. | |||||||||||||||
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In conclusion, the current study suggests feasibility of significant mobilization of cells expressing hematopoietic stem cell and EPC markers and properties. | |||||||||||||||
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Heat maps generated using GenePattern software for the top 30 distinctly expressed transcripts in each EPC subtype show expression patterns at the gene level consistent with hierarchical cluster analysis (Figure 4B, C). | |||||||||||||||
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Therefore, to elucidate and differentiate the expressed phenotypes of endothelial progenitors, eEPC and OEC transcriptomes were directly compared with monocytes and endothelial cells. | |||||||||||||||
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Using a single component (PC1) it was possible to separate samples into two groups; one containing the three eEPC biological replicates with a high PC1 value, and other group with the three OEC biological replicates showing a low PC1 value (Figure 1D). | |||||||||||||||
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Heat maps generated using GenePattern software for the top 30 distinctly expressed transcripts in each EPC subtype show expression patterns at the gene level consistent with hierarchical cluster analysis (Figure 4B, C). | |||||||||||||||
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Currently, the combinations of CD133+CD34+KDR+, CD34+KDR+, or CD14+CD34low [9], [10], [11], are widely used to define or select cells that express properties attributed to EPC. | |||||||||||||||
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Nevertheless, there are ongoing debates about the definition of true EPC, as well as the availability of a reliable method to assess their quantity and quality, functional status, and therapeutic application. | |||||||||||||||
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Patients with ACS were further stratified for troponin T positivity to account for potential effects of myocardial necrosis on EPC levels. | |||||||||||||||
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An approximate F statistic approached significance (P = 0.07), indicating weak evidence in favour of a different relationship between age and both HSC and EPC for the SUD and N-SUD groups with the SUD group having lower numbers of both HSC's and EPC's compared with NA group members of equivalent age. | |||||||||||||||
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Therefore, to elucidate and differentiate the expressed phenotypes of endothelial progenitors, eEPC and OEC transcriptomes were directly compared with monocytes and endothelial cells. | |||||||||||||||
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