Phosphoinositide signalling system in red blood cells of patients with hereditary spherocytosis.

Biomedica biochimica acta Pub Date : 1991-01-01
A Strunecká, L Krpejsová, E Kmonícková, H Hrůsová, H Jakoubková, T Marík, V Brabec
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Abstract

Hereditary spherocytosis (HS) is characterised with many deviations of red blood cells properties. We investigated a group of 14 patients with mild HS, 7 of whom were splenectomised. We found changes in the content and/or turnover of polyphosphoinositides and phosphatidic acid accompanied by the higher generation of inositol 1,4,5-trisphosphate. We suggest that the activation of the phosphoinositide signalling system may be crucial for the manifestation of HS.

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遗传性球形红细胞增多症患者红细胞中的磷酸肌肽信号系统。
遗传性球形红细胞增多症(HS)的特点是红细胞性质的许多偏差。我们研究了14例轻度HS患者,其中7例进行了脾切除术。我们发现,随着肌醇1,4,5-三磷酸的增加,多磷酸肌醇和磷脂酸的含量和/或周转也发生了变化。我们认为,磷脂肌苷信号系统的激活可能是HS表现的关键。
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