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p185(Bcr-Abl) 抑制 II 类磷酸肌醇 3-激酶 γ 的表达导致白血病细胞趋化作用受损和归巢异常。

Inhibition of class II phosphoinositide 3-kinase gamma expression by p185(Bcr-Abl) contributes to impaired chemotaxis and aberrant homing of leukemic cells.

机构信息

Department of Internal Medicine, Texas Tech University Health Sciences Center, Amarillo, Texas, USA.

出版信息

Leuk Lymphoma. 2010 Jun;51(6):1098-107. doi: 10.3109/10428191003754624.

Abstract

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.

摘要

p185(Bcr-Abl) 的表达抑制了 Ba/F3 细胞对 SDF1alpha 的趋化反应。缺失了 176 到 426 个氨基酸的突变 p185(Bcr-Abl)(p185(Delta176-426))缺乏对 SDF1alpha 刺激的趋化作用的抑制作用。比较亲本 Ba/F3 细胞和被 p185(Bcr-Abl) 和 p185(Delta176-426) 转化的细胞的基因表达谱,发现 II 类磷酸肌醇 3-激酶γ(PI3KC2γ)的表达被 p185(Bcr-Abl)显著下调,但 p185(Delta176-426)则没有。此外,在 p185(Delta176-426)细胞中敲低 PI3KC2γ的表达足以抑制 SDF1alpha 刺激的趋化作用,并促进这些细胞向肝脏浸润。总之,这些研究表明,抑制 PI3KC2γ的表达可能是 Bcr-Abl 抑制 SDF1alpha 诱导的趋化作用并诱导白血病细胞异常归巢的一种机制。

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