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全反式维甲酸体外处理白血病早幼粒细胞时GPI连接分子的差异调节

Differential regulation of GPI-linked molecules on leukaemic promyelocytes treated in vitro with all-trans retinoic acid.

作者信息

Di Noto R, Schiavone E M, Lo Pardo C, Ferrara F, Manzo C, Vacca C, Del Vecchio L

机构信息

Divisione di Oncologia Sperimentale C, Immunologia, Istituto Nazionale dei Tumori, Fondazione G. Pascale, Naples, Italy.

出版信息

Br J Haematol. 1996 May;93(2):392-3. doi: 10.1046/j.1365-2141.1996.4861027.x.

Abstract

It has been demonstrated that certain cell-surface proteins are anchored to the cell membrane by a unique structure known as the glycosylphosphatidylinositol (GPI) anchor whose absence has been reported on blood cells from patients with paroxysmal nocturnal haemoglobinuria. We have investigated the expression of CD16/Fc(tau)R-III and CD66b GPI linked molecules at the surface of blast cells from five acute promyelocytic leukaemia (APL) patients before and after in vitro stimulation with all-trans retinoic acid (ATRA). We observed that whereas CD66b antigen exhibited a strong ATRA-driven up-regulation in all cases studied, CD16 expression was unaffected by the treatment with the drug.

摘要

已经证明,某些细胞表面蛋白通过一种称为糖基磷脂酰肌醇(GPI)锚的独特结构锚定在细胞膜上,据报道,阵发性夜间血红蛋白尿患者的血细胞缺乏这种结构。我们研究了5例急性早幼粒细胞白血病(APL)患者的原始细胞在全反式维甲酸(ATRA)体外刺激前后,CD16/Fc(τ)R-III和CD66b GPI连接分子在其表面的表达。我们观察到,在所有研究病例中,CD66b抗原均表现出强烈的ATRA驱动的上调,而CD16的表达不受该药物治疗的影响。

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