Chatterjee Sreoshi, Bhardwaj Nitin, Saxena Rajiv K
School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
Faculty of Life Sciences and Biotechnology, South Asian University, New Delhi, India.
PLoS One. 2016 Nov 21;11(11):e0166878. doi: 10.1371/journal.pone.0166878. eCollection 2016.
Repeated weekly injections of rat erythrocytes produced autoimmune hemolytic anemia (AIHA) in C57BL/6 mice after 5-6 weeks. Using the double in vivo biotinylation (DIB) technique, recently developed in our laboratory, turnover of erythrocyte cohorts of different age groups during AIHA was monitored. Results indicate a significant decline in the proportion of reticulocytes, young and intermediate age groups of erythrocytes, but a significant increase in the proportion of old erythrocytes in blood circulation. Binding of the autoantibody was relatively higher to the young erythrocytes and higher levels of intracellular reactive oxygen species (ROS) were also seen in these cells. Erythropoietic activity in the bone marrows and the spleen of AIHA induced mice was examined by monitoring the relative proportion of erythroid cells at various stages of differentiation in these organs. Cells at different stages of differentiation were enumerated flow cytometrically by double staining with anti-Ter119 and anti-transferrin receptor (CD71) monoclonal antibodies. Erythroid cells in bone marrow declined significantly in AIHA induced mice, erythroblast C being most affected (50% decline). Erythroblast C also recorded high intracellular ROS level along with increased levels of membrane-bound autoantibody. No such decline was observed in spleen. A model of AIHA has been proposed indicating that binding of autoantibodies may not be a sufficient condition for destruction of erythroid cells in bone marrow and in blood circulation. Last stage of erythropoietic differentiation in bone marrow and early stages of erythrocytes in blood circulation are specifically susceptible to removal in AIHA.
每周重复注射大鼠红细胞,5至6周后在C57BL/6小鼠中诱发了自身免疫性溶血性贫血(AIHA)。利用我们实验室最近开发的双体内生物素化(DIB)技术,监测了AIHA期间不同年龄组红细胞群体的更新情况。结果表明,网织红细胞、年轻和中年红细胞群体的比例显著下降,但血液循环中衰老红细胞的比例显著增加。自身抗体与年轻红细胞的结合相对较高,并且在这些细胞中也观察到较高水平的细胞内活性氧(ROS)。通过监测AIHA诱导小鼠骨髓和脾脏中不同分化阶段红系细胞的相对比例,检测了其造血活性。通过用抗Ter119和抗转铁蛋白受体(CD71)单克隆抗体进行双重染色,流式细胞术对不同分化阶段的细胞进行计数。AIHA诱导小鼠的骨髓红系细胞显著减少,其中幼红细胞C受影响最大(减少50%)。幼红细胞C还记录到细胞内ROS水平升高以及膜结合自身抗体水平增加。脾脏中未观察到此类减少。已提出AIHA模型,表明自身抗体的结合可能不是骨髓和血液循环中红系细胞破坏的充分条件。骨髓中红细胞生成分化的最后阶段以及血液循环中红细胞的早期阶段在AIHA中特别容易被清除。