作者: E. Fibach , D. Manor , A. Treves , E. A. Rachmilewitz
关键词: Cell biology 、 Immunology 、 Cell culture 、 Stem cell 、 Erythropoiesis 、 Cell division 、 Erythropoietin 、 Biology 、 Erythroid Precursor Cells 、 Population 、 Cell growth
摘要: Most studies of erythropoiesis in vitro have employed cloning methods semisolid medium. We recently described a two-step liquid culture procedure that supports the proliferation and differentiation human erythroid progenitors. In present study, we modified to allow large-scale cultures cells derived from normal donors. The is divided into two phases. first phase, which erythropoietin (Epo) independent, early progenitors multiply differentiate. second, Epo-dependent they mature orthochromatic normoblasts enucleated erythrocytes. Using this procedure, cell yield reached 7.5 x 10(6)/ml total 7 10(8) could be harvested per blood unit. A comparison growth their colony indicated was superior: 1) terms originally cultured mononuclear cell, 2) ml surface area purity resultant population. addition, it permits easier manipulation condition components sampling greater than 1 10(7) at each maturation stage subsequent proerythroblast stage. This might provide an important experimental tool for studying development.