Shibuya Atsushi, Kawashima Hiroaki, Tanaka Masato
a Department of Biotechnology , Tokyo Denki University , Tokyo , Japan.
Hematology. 2018 Oct;23(9):669-675. doi: 10.1080/10245332.2018.1455278. Epub 2018 Apr 6.
In order to investigate the pathophysiology of erythrocyte membrane proteins, 10 patients (6 pre- and 4 post-splenectomy) with hereditary spherocytosis (HS) and other patients with haemolytic anaemia were examined.
The membrane proteins were analysed by biochemical and mass spectrometry.
Reductions in the extracellular membrane of band 3 protein by eosin-5'-maleimide (EMA) binding test were greater in patients with pre-splenectomy HS than in patients with post-splenectomy HS, other types of haemolytic anaemia, and controls. Compared to patients with haemolytic anaemia and healthy controls, the band 3 protein of patients with HS pre- or post-splenectomy was more easily decomposed with N-glycosidase F and by mass spectrometry interactions with degraded low-molecular-weight spectrin and ankyrin. The resulting fragments were observed more frequently in pre-splenectomy than post-splenectomy HS. Haemoglobin-derived peptides were present in patients with haemoglobinopathy (Hb Evans, Hb Sabine) but not in those with haemolytic anaemia and healthy controls.
Haemolysis in patients with HS occurred because the fragile proteins in erythrocytes (band 3, spectrin, and ankyrin) collapsed due to compression during blood circulation in the spleen. Further, haemolysis in patients with haemoglobinopathy occurred owing to membrane damage due to combined spectrin, band 3 with denatured haemoglobin in the vessel during blood circulation.
为了研究红细胞膜蛋白的病理生理学,对10例遗传性球形红细胞增多症(HS)患者(6例脾切除术前和4例脾切除术后)以及其他溶血性贫血患者进行了检查。
通过生化和质谱分析法对膜蛋白进行分析。
嗜酸性-5'-马来酰亚胺(EMA)结合试验显示,脾切除术前HS患者的带3蛋白细胞外膜减少程度大于脾切除术后HS患者、其他类型溶血性贫血患者及对照组。与溶血性贫血患者和健康对照组相比,脾切除术前或术后HS患者的带3蛋白更容易被N-糖苷酶F分解,且通过质谱分析发现其与降解的低分子量血影蛋白和锚蛋白存在相互作用。在脾切除术前HS患者中观察到的这些片段比脾切除术后更频繁。血红蛋白衍生肽存在于血红蛋白病患者(Hb Evans、Hb Sabine)中,但不存在于溶血性贫血患者和健康对照组中。
HS患者发生溶血是因为红细胞中的脆弱蛋白(带3、血影蛋白和锚蛋白)在脾脏血液循环过程中因受压而崩溃。此外,血红蛋白病患者发生溶血是由于血液循环过程中血管内血影蛋白、带3与变性血红蛋白结合导致膜损伤。