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首页> 外文期刊>Leukemia and lymphoma >Inhibition of class II phosphoinositide 3-kinase gamma expression by p185(Bcr-Abl) contributes to impaired chemotaxis and aberrant homing of leukemic cells.
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Inhibition of class II phosphoinositide 3-kinase gamma expression by p185(Bcr-Abl) contributes to impaired chemotaxis and aberrant homing of leukemic cells.

机译:p185(Bcr-Abl)抑制II类磷酸肌醇3-激酶γ的表达有助于白血病细胞的趋化性和异常归巢。

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摘要

The expression of p185(Bcr-Abl) in Ba/F3 cells inhibits the chemotactic response of these cells to SDF1alpha. A mutant p185(Bcr-Abl) with deletion of amino acids from 176 to 426 (p185(Delta176-426)) is deficient in suppressing SDF1alpha-stimulated chemotaxis. Comparison of the gene expression profiles among parental Ba/F3 cells and cells transformed by p185(Bcr-Abl) and p185(Delta176-426) reveals that class II phosphoinositide 3-kinase gamma (PI3KC2gamma) expression is markedly down-regulated by p185(Bcr-Abl) but not p185(Delta176-426). Furthermore, knockdown of PI3KC2gamma expression in p185(Delta176-426) cells is sufficient to suppress SDF1alpha-stimulated chemotaxis and to promote infiltration of these cells into the liver. Together, these studies suggest that inhibition of PI3KC2gamma expression may represent a mechanism by which Bcr-Abl suppresses SDF1alpha-induced chemotaxis and induces abnormal homing of leukemic cells.
机译:Ba / F3细胞中p185(Bcr-Abl)的表达抑制了这些细胞对SDF1alpha的趋化反应。具有从176到426个氨基酸缺失的突变体p185(Bcr-Abl)(p185(Delta176-426))不足以抑制SDF1alpha刺激的趋化性。比较亲代Ba / F3细胞和经p185(Bcr-Abl)和p185(Delta176-426)转化的细胞之间的基因表达谱,发现II类磷酸肌醇3-激酶γ(PI3KC2γ)的表达明显受p185的下调( Bcr-Abl),但不包含p185(Delta176-426)。此外,敲低p185(Delta176-426)细胞中PI3KC2γ的表达足以抑制SDF1alpha刺激的趋化性并促进这些细胞向肝脏的浸润。总之,这些研究表明,抑制PI3KC2γ的表达可能代表Bcr-Abl抑制SDF1alpha诱导的趋化性并诱导白血病细胞归巢的机制。

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