Resolving the distinct stages in erythroid differentiation based on dynamic changes in membrane protein expression during erythropoiesis

被引:408
作者
Chen, Ke [1 ]
Liu, Jing [1 ]
Heck, Susanne
Chasis, Joel A. [2 ]
An, Xiuli [1 ,3 ]
Mohandas, Narla [1 ]
机构
[1] New York Blood Ctr, Red Cell Physiol Lab, New York, NY 10065 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
[3] Peking Univ, Hlth Sci Ctr, Dept Biophys, Beijing 100191, Peoples R China
关键词
CD44; CD71; erythroblast differentiation; cell adhesion; erythrocyte; RED-CELL MEMBRANE; RETICULOCYTE MATURATION; ASYNCHRONOUS SYNTHESIS; TRANSFERRIN RECEPTOR; UNEQUAL SYNTHESIS; ALPHA-SPECTRIN; BETA-SPECTRIN; BLOOD-CELLS; ERYTHROBLASTS; SKELETON;
D O I
10.1073/pnas.0909296106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Erythropoiesis is the process by which nucleated erythroid progenitors proliferate and differentiate to generate, every second, millions of nonnucleated red cells with their unique discoid shape and membrane material properties. Here we examined the time course of appearance of individual membrane protein components during murine erythropoiesis to throw new light on our understanding of the evolution of the unique features of the red cell membrane. We found that the accumulation of all of the major transmembrane and all skeletal proteins of the mature red blood cell, except actin, accrued progressively during terminal erythroid differentiation. At the same time, and in marked contrast, accumulation of various adhesion molecules decreased. In particular, the adhesion molecule, CD44 exhibited a progressive and dramatic decrease from proerythroblast to reticulocyte; this enabled us to devise a new strategy for distinguishing unambiguously between erythroblasts at successive developmental stages. These findings provide unique insights into the genesis of red cell membrane function during erythroblast differentiation and also offer a means of defining stage-specific defects in erythroid maturation in inherited and acquired red cell disorders and in bone marrow failure syndromes.
引用
收藏
页码:17413 / 17418
页数:6
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