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PMID |
Sentence |
1 |
27723804
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Neutrophils and the primary epithelial cells were found to express the IL-17A receptor subunit IL-17RA, while the expression of IL-17RE was only observed on epithelial cells.
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2 |
27723804
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BCG stimulation specifically reduced neutrophil IL-17RA and epithelial IL-17RE expression.
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3 |
27723804
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Infected epithelial cells and neutrophils were not found to be a source of IL-17 cytokines or the interstitial collagenase MMP-1.
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4 |
27723804
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However, the addition of IFNγ or IL-17A to BCG stimulated primary epithelial cells increased epithelial IL-6 secretion, while the presence of IFNγ reduced neutrophil recruitment.
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5 |
27288334
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The levels of four of them, including vascular endothelial growth factor receptor-3 (VEGFR3), basic fibroblast growth factor (bFGF), interferon gamma (IFNG) and matrix metalloproteinase 1 (MMP1), were quantified using western blot analysis.
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6 |
25924700
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To test the hypothesis that MMP expression in luteal cells is regulated by luteolytic factors, we investigated the effects of prostaglandin F2α (PGF), interferon γ (IFNG) and tumor necrosis factor α (TNF) on the mRNA expression of MMPs and TIMPs in cultured luteal cells.
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7 |
25924700
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To test the hypothesis that MMP expression in luteal cells is regulated by luteolytic factors, we investigated the effects of prostaglandin F2α (PGF), interferon γ (IFNG) and tumor necrosis factor α (TNF) on the mRNA expression of MMPs and TIMPs in cultured luteal cells.
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8 |
25924700
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To test the hypothesis that MMP expression in luteal cells is regulated by luteolytic factors, we investigated the effects of prostaglandin F2α (PGF), interferon γ (IFNG) and tumor necrosis factor α (TNF) on the mRNA expression of MMPs and TIMPs in cultured luteal cells.
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9 |
25924700
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Luteal cells obtained from the CL at the mid-luteal stage (days 8-12 after ovulation) were cultured with PGF (0.01, 0.1, 1 μM), IFNG (0.05, 0.5, 5 nM) and TNF (0.05, 0.5, 0.5 nM) alone or in combination for 24 h.
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10 |
25924700
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Luteal cells obtained from the CL at the mid-luteal stage (days 8-12 after ovulation) were cultured with PGF (0.01, 0.1, 1 μM), IFNG (0.05, 0.5, 5 nM) and TNF (0.05, 0.5, 0.5 nM) alone or in combination for 24 h.
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11 |
25924700
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Luteal cells obtained from the CL at the mid-luteal stage (days 8-12 after ovulation) were cultured with PGF (0.01, 0.1, 1 μM), IFNG (0.05, 0.5, 5 nM) and TNF (0.05, 0.5, 0.5 nM) alone or in combination for 24 h.
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12 |
25924700
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PGF and IFNG significantly increased the expression of MMP-1 mRNA.
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13 |
25924700
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PGF and IFNG significantly increased the expression of MMP-1 mRNA.
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14 |
25924700
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PGF and IFNG significantly increased the expression of MMP-1 mRNA.
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15 |
25924700
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In addition, 1 μM PGF in combination with 5 nM IFNG stimulated MMP-1 and MMP-9 mRNA expression significantly more than either treatment alone.
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16 |
25924700
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In addition, 1 μM PGF in combination with 5 nM IFNG stimulated MMP-1 and MMP-9 mRNA expression significantly more than either treatment alone.
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17 |
25924700
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In addition, 1 μM PGF in combination with 5 nM IFNG stimulated MMP-1 and MMP-9 mRNA expression significantly more than either treatment alone.
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18 |
25924700
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In contrast, IFNG significantly decreased the level of MMP-14 mRNA.
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19 |
25924700
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In contrast, IFNG significantly decreased the level of MMP-14 mRNA.
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20 |
25924700
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In contrast, IFNG significantly decreased the level of MMP-14 mRNA.
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21 |
25924700
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The mRNA expression of TIMP-1, which preferentially inhibits MMP-1, was suppressed by 5 nM INFG.
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22 |
25924700
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The mRNA expression of TIMP-1, which preferentially inhibits MMP-1, was suppressed by 5 nM INFG.
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23 |
25924700
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The mRNA expression of TIMP-1, which preferentially inhibits MMP-1, was suppressed by 5 nM INFG.
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24 |
25924700
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One μM PGF and 5 nM IFNG suppressed TIMP-2 mRNA expression.
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25 |
25924700
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One μM PGF and 5 nM IFNG suppressed TIMP-2 mRNA expression.
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26 |
25924700
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One μM PGF and 5 nM IFNG suppressed TIMP-2 mRNA expression.
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27 |
25924700
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These results suggest a new role of MMPs: luteal MMPs stimulated by PGF and IFNG break down the extracellular matrix surrounding luteal cells, which accelerates detachment from the CL during luteolysis, providing an essential prerequisite for outflow of luteal cells from the CL to lymphatic vessels.
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28 |
25924700
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These results suggest a new role of MMPs: luteal MMPs stimulated by PGF and IFNG break down the extracellular matrix surrounding luteal cells, which accelerates detachment from the CL during luteolysis, providing an essential prerequisite for outflow of luteal cells from the CL to lymphatic vessels.
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29 |
25924700
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These results suggest a new role of MMPs: luteal MMPs stimulated by PGF and IFNG break down the extracellular matrix surrounding luteal cells, which accelerates detachment from the CL during luteolysis, providing an essential prerequisite for outflow of luteal cells from the CL to lymphatic vessels.
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