Author
Listed:
- Young-Hoon Kim
(Graduate School of Biomedical Science and Engineering/College of Medicine, Hanyang University
Brain Korea 21 Plus Project for Medical Sciences, Graduate Program of Nano Science and Technology, Yonsei University College of Medicine)
- Hyun O. Kim
(Yonsei University College of Medicine)
- Eun J. Baek
(Hanyang University College of Medicine)
- Ryo Kurita
(Central Blood Institute, Japanese Red Cross Society)
- Hyuk-Jin Cha
(College of Natural Sciences, Sogang University)
- Yukio Nakamura
(RIKEN BioResource Center)
- Hyongbum Kim
(Graduate School of Biomedical Science and Engineering/College of Medicine, Hanyang University
Brain Korea 21 Plus Project for Medical Sciences, Graduate Program of Nano Science and Technology, Yonsei University College of Medicine)
Abstract
Group O D-negative blood cells are universal donors in transfusion medicine and methods for converting other blood groups into this universal donor group have been researched. However, conversion of D-positive cells into D-negative is yet to be achieved, although conversion of group A or B cells into O cells has been reported. The Rh D blood group is determined by the RHD gene, which encodes a 12-transmembrane domain protein. Here we convert Rh D-positive erythroid progenitor cells into D-negative cells using RHD-targeting transcription activator-like effector nucleases (TALENs). After transfection of TALEN-encoding plasmids, RHD-knockout clones are obtained. Erythroid-lineage cells differentiated from these knockout erythroid progenitor cells do not agglutinate in the presence of anti-D reagents and do not express D antigen, as assessed using flow cytometry. Our programmable nuclease-induced blood group conversion opens new avenues for compatible donor cell generation in transfusion medicine.
Suggested Citation
Young-Hoon Kim & Hyun O. Kim & Eun J. Baek & Ryo Kurita & Hyuk-Jin Cha & Yukio Nakamura & Hyongbum Kim, 2015.
"Rh D blood group conversion using transcription activator-like effector nucleases,"
Nature Communications, Nature, vol. 6(1), pages 1-13, November.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms8451
DOI: 10.1038/ncomms8451
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