Reinhardt D, Witt O, Miosge N, Herken R, Pekrun A
Department of Paediatrics, Georg-August-University of Goettingen, Germany.
Blood Cells Mol Dis. 2001 Mar-Apr;27(2):399-406. doi: 10.1006/bcmd.2001.0396.
Red cells in hereditary spherocytosis are characterized by a reduced surface area/volume ratio. The mechanisms leading to the loss of membrane material and subsequent elimination of the cells have still not been clarified. It was the aim of the present study to analyze band 3 distribution in the red cell membrane and its putative role in red cell elimination.
METHODS/RESULTS: Immunogold histochemistry was performed to detect band 3 in red cell membranes. Band 3 density and distribution were visualized by electron microscopy. Unsplenectomized spherocytosis patients (n = 12) showed reduced band 3 density and aggregation compared to controls (n = 15) (density: 1.2 +/- 0.1 gold particles/microm circumference of red cell membrane vs 1.5 +/- 0.07 gold particles/microm, x +/- SEM; P < 0.05; aggregation: 0.26 +/- 0.02 aggregates/microm vs 0.3 +/- 0.02 aggregates/microm). By contrast, band 3 density and aggregation were increased in spherocytosis patients who had undergone splenectomy (density: 2.8 +/- 0.1 gold particles/microm vs 2.0 +/- 0.1 gold particles/microm; P < 0.05; aggregation: 1.5 +/- 0.1 aggregates/microm vs 0.5 +/- 0.03 aggregates/microm; P < 0.01). Artificial ageing of red cells from healthy controls (n = 6) led to a significant increase in band 3 aggregation (2.06 +/- 0.2 aggregates/microm vs 0.33 +/- 0.1 aggregates/microm; P(Wilcoxon) < 0.01) but no change in band 3 density. In hereditary spherocytosis (n = 6), both band 3 density and aggregation increased significantly after artificial ageing of the red cells. The elevated band 3 aggregation was associated with a stimulated erythrophagocytosis in vitro.
Band 3 aggregation characterizes the red cells in hereditary spherocytosis. It may be the cause of selective splenic phagocytosis of both spherocytes and senescent erythrocytes.
遗传性球形红细胞增多症中的红细胞特征为表面积/体积比降低。导致膜物质丢失及随后细胞被清除的机制仍未阐明。本研究的目的是分析红细胞膜中带3的分布及其在红细胞清除中的假定作用。
方法/结果:采用免疫金组织化学法检测红细胞膜中的带3。通过电子显微镜观察带3的密度和分布。未行脾切除术的球形红细胞增多症患者(n = 12)与对照组(n = 15)相比,带3密度降低且有聚集现象(密度:1.2±0.1个金颗粒/红细胞膜微米周长,对照组为1.5±0.07个金颗粒/微米,x±SEM;P < 0.05;聚集:0.26±0.02个聚集体/微米,对照组为0.3±0.02个聚集体/微米)。相比之下,行脾切除术的球形红细胞增多症患者带3密度和聚集增加(密度:2.8±0.1个金颗粒/微米,对照组为2.0±0.1个金颗粒/微米;P < 0.05;聚集:1.5±0.1个聚集体/微米,对照组为0.5±0.03个聚集体/微米;P < 0.01)。健康对照组(n = 6)红细胞的人工老化导致带3聚集显著增加(2.06±0.2个聚集体/微米,对照组为0.33±0.1个聚集体/微米;P(Wilcoxon)< 0.01),但带3密度无变化。在遗传性球形红细胞增多症(n = 6)中,红细胞人工老化后带3密度和聚集均显著增加。带3聚集升高与体外红细胞吞噬作用增强相关。
带3聚集是遗传性球形红细胞增多症中红细胞的特征。它可能是球形红细胞和衰老红细胞被选择性脾吞噬的原因。