摘要
采用 TUNEL 法对 2 6例骨髓增生异常综合征 (MDS)、11例巨幼细胞贫血 (Meg A)、8例阵发性血红蛋白尿 (PNH)、6例 Evans综合征患者和 10例正常健康志愿者的骨髓单个核细胞 (BMMNC)凋亡进行探讨。结果发现 ,5 0 % MDS呈现凋亡过度 ,Meg A、PNH和 Evans综合征患者与对照组无显著差异。 MDS患者凋亡累及粒、红、巨三系各阶段造血细胞 ,随病情演变 ,凋亡程度渐下降。提示凋亡过度为 MDS无效造血机制之一 ,病情演变可能与异常克隆逃逸凋亡有关 ,抗凋亡疗法可试用于早期 MDS。
Apoptosis of bone marrow mononuclear cells(BMMNC)was demonstrated using terminal deoxytransferase(TdT)-mediated dUTP nick end labeling(TUNEL)method in 26 myelodysplastic syndromes(MDS)patients,11 megaloblastic anemia(MegA),8 paroxysmal nocturnal hemoglobinuria(PNH)and 6 Evans syndromes patients.Apoptosis was significantly increased in MDS,no difference of apoptosis was found between MegA,PNH,Evans syndromes and normal controls.Apoptosis was seen in myeloid blasts,maturing myeloid cells,nucleated erythroid cells and megakaryocyte cells in MDS patients.As MDS progressing,apoptosis gradually decreased.These results suggest that excess apoptosis is one of factors leading to ineffective hematopoiesis in MDS.MDS clinical progression may be associated with escaping from apoptosis of myelodysplastic progenitors.Therapy of anti-apoptosis could be used in early MDS patients.
出处
《山东医药》
CAS
北大核心
2001年第5期7-8,共2页
Shandong Medical Journal