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Inositol trisphosphate 3-kinase B (InsP3KB) as a physiological modulator of myelopoiesis

机译:肌醇三磷酸3-激酶B(InsP3KB)作为骨髓生成的生理调节剂

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摘要

Inositol trisphosphate 3-kinase B (InsP3KB) belongs to a family of kinases that convert inositol 1,4,5-trisphosphate (Ins(1,4,5)P3 or IP3) to inositol 1,3,4,5-tetrakisphosphate (Ins(1,3,4,5)P4). Previous studies have shown that disruption of InsP3KB leads to impaired T cell and B cell development as well as hyperactivation of neutrophils. Here, we demonstrate that InsP3KB is also a physiological modulator of myelopoiesis. The InsP3KB gene is expressed in all hematopoietic stem/progenitor cell populations. In InsP3KB null mice, the bone marrow granulocyte monocyte progenitor (GMP) population was expanded, and GMP cells proliferated significantly faster. Consequently, neutrophil production in the bone marrow was enhanced, and the peripheral blood neutrophil count was also substantially elevated in these mice. These effects might be due to enhancement of PtdIns(3,4,5)P3/Akt signaling in the InsP3KB null cells. Phosphorylation of cell cycle-inhibitory protein p21cip1, one of the downstream targets of Akt, was augmented, which can lead to the suppression of the cell cycle-inhibitory effect of p21.
机译:肌醇三磷酸3-激酶B(InsP3KB)属于将肌醇1,4,5-三磷酸(Ins(1,4,5)P3或IP3)转化为肌醇1,3,4,5-四磷酸( Ins(1,3,4,5)P4)。以前的研究表明,破坏InsP3KB会导致T细胞和B细胞发育受损,以及嗜中性粒细胞过度活化。在这里,我们证明InsP3KB也是骨髓生成的生理调节剂。 InsP3KB基因在所有造血干/祖细胞群中表达。在InsP3KB空小鼠中,骨髓粒细胞单核祖细胞(GMP)群体得到了扩大,并且GMP细胞的增殖速度明显加快。因此,这些小鼠中骨髓中的中性粒细胞产生增加,并且外周血中性粒细胞计数也显着增加。这些影响可能是由于InsP3KB空单元格中PtdIns(3,4,5)P3 / Akt信号增强所致。细胞周期抑制蛋白p21cip1(Akt的下游靶标之一)的磷酸化增强,可导致抑制p21的细胞周期抑制作用。

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