INT185261
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Nevertheless, OLIG2 is expressed in human OPC [45] and is necessary for specification and differentiation of human OPC [44]. | |||||||||||||||
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We determined that MP are able to mature and develop fundamental functions of normal motoneurons in vitro (expressing OLIG2, ISL1, and HOXC5), including directional growth of long axons, confirming the results from the previous study [11]. | |||||||||||||||
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A ventralizing effect of RA was also observed by upregulation of OLIG2 expression, probably at the expense of IRX3, in agreement with previous findings suggesting that OLIG2 suppresses IRX3 [59] and interacts with progenitor homeodomain proteins, thus activating motor neuron differentiation pathway and HB9 gene. | |||||||||||||||
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OLIGO-2 expression is relatively specific for oligodendrogliomas [8], and the combination of OLIGO-2 and GFAP expression provides further support for the diagnosis. | |||||||||||||||
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OLIGO-2 expression is relatively specific for oligodendrogliomas [8], and the combination of OLIGO-2 and GFAP expression provides further support for the diagnosis. | |||||||||||||||
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Double immunohistochemistry shows co-expression of Pax6/RC2, Olig2/RC2, Olig2/Pax6 (Figure 5C), and Pax6/Emx2 (Figure S1) in virtually every cell. | |||||||||||||||
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Double immunohistochemistry shows co-expression of Pax6/RC2, Olig2/RC2, Olig2/Pax6 (Figure 5C), and Pax6/Emx2 (Figure S1) in virtually every cell. | |||||||||||||||
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Analyzing the transcription phenotype of obtained OPC at day 42, we observed strong expression of OLIG2 [4244], which gives rise to motoneurons during the neurogenic phase. | |||||||||||||||
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To determine whether the neural progenitors have strictly rostral character we next examined the expression of caudal markers (Figures 4F and 4G) such as class I (IRX3, PAX6, PAX7) and class II (OLIG2, NKX2.2, NKX6.1), homeodomein proteins important for motoneuron differentiation [33], [34] and found them highly expressed at D7 and D42. | |||||||||||||||
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The nucleus was positive for OLIGO-2 and the cytoplasm was positive for GFAP on immunohistochemical staining (Figure6, 7). | |||||||||||||||
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All NS cells examined express the same panel of radial glia markers (Figures 5A and S2), plus the neural precursor markers Sox2, Sox3, and Emx2, and the bHLH (basic helixloop helix) transcription factors Olig2 and Mash1 (Figure 5B). | |||||||||||||||
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The presence of Olig2 and Mash1 is not characteristic of dorsal forebrain, and may reflect the ex vivo environment and a response to FGF-2. | |||||||||||||||
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Approximately 31% of hCNS-SCns remained nestin positive suggesting that they remain undifferentiated, however of the cells that differentiated the majority differentiated along the oligodendrocyte lineage expressing the immature Olig2 marker or the mature APC-CC1 marker (41%) and nearly as many differentiated into ß-tubulin III-positive neurons (38%). | |||||||||||||||
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