Establishment of an immortalized human erythroid cell line sustaining differentiation potential without inducible gene expression system

被引:0
|
作者
Svetlana Soboleva
Ryo Kurita
Naoko Kajitani
Hugo Åkerstrand
Kenichi Miharada
机构
[1] Lund University,Division of Molecular Medicine and Gene Therapy, Lund Stem Cell Center
[2] Japanese Red Cross Society,Department of Research and Development, Central Blood Institute
[3] Lund University,Division of Medical Microbiology
[4] Lund University,Division of Molecular Hematology, Lund Stem Cell Center
[5] Kumamoto University,International Research Center for Medical Sciences
来源
Human Cell | 2022年 / 35卷
关键词
Red blood cells; Immortalized erythroid cell lines; HPV-E6/E7; Enucleation; Hemoglobin;
D O I
暂无
中图分类号
学科分类号
摘要
Ex vivo manufactured red blood cells (RBC) generated from immortalized erythroid cell lines which can continuously grow are expected to become a significant alternative in future transfusion therapies. The ectopic expression of human papilloma virus (HPV) E6/E7 gene has successfully been employed to establish these cell lines. To induce differentiation and maturation of the immortalized cell lines, terminating the HPV-E6/E7 expression through a gene induction system has been believed to be essential. Here, we report that erythroid cell lines established from human bone marrow using simple expression of HPV-E6/E7 are capable of normal erythroid differentiation, without turning gene expression off. Through simply changing cell culture conditions, a newly established cell line, Erythroid Line from Lund University (ELLU), is able to differentiate toward mature cells, including enucleated reticulocytes. ELLU is heterogeneous and, unexpectedly, clones expressing adult hemoglobin rapidly differentiate and produce fragile cells. Upon differentiation, other ELLU clones shift from fetal to adult hemoglobin expression, giving rise to more mature cells. Our findings propose that it is not necessary to employ gene induction systems to establish immortalized erythroid cell lines sustaining differentiation potential and describe novel cellular characteristics for desired functionally competent clones.
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页码:408 / 417
页数:9
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