TY - JOUR
T1 - Cellular Reprogramming of Human Peripheral Blood Cells
AU - Zhang, Xiao Bing
N1 - Funding Information:
The author thanks Amanda Neises, Justin Brier-Jones, Rui-Jun Su and Jason Kiroyan for helpful discussion and critical reading of the manuscript. This work was supported by the Grants for Research and School Partnerships (GRASP) Award from the Loma Linda University and U.S. Army Medical Research Acquisition Activity (USAMRAA) Concept Award (Grant No. W81XWH-11-1-0607 ).
PY - 2013/10
Y1 - 2013/10
N2 - Breakthroughs in cell fate conversion have made it possible to generate large quantities of patient-specific cells for regenerative medicine. Due to multiple advantages of peripheral blood cells over fibroblasts from skin biopsy, the use of blood mononuclear cells (MNCs) instead of skin fibroblasts will expedite reprogramming research and broaden the application of reprogramming technology. This review discusses current progress and challenges of generating induced pluripotent stem cells (iPSCs) from peripheral blood MNCs and of in vitro and in vivo conversion of blood cells into cells of therapeutic value, such as mesenchymal stem cells, neural cells and hepatocytes. An optimized design of lentiviral vectors is necessary to achieve high reprogramming efficiency of peripheral blood cells. More recently, non-integrating vectors such as Sendai virus and episomal vectors have been successfully employed in generating integration-free iPSCs and somatic stem cells.
AB - Breakthroughs in cell fate conversion have made it possible to generate large quantities of patient-specific cells for regenerative medicine. Due to multiple advantages of peripheral blood cells over fibroblasts from skin biopsy, the use of blood mononuclear cells (MNCs) instead of skin fibroblasts will expedite reprogramming research and broaden the application of reprogramming technology. This review discusses current progress and challenges of generating induced pluripotent stem cells (iPSCs) from peripheral blood MNCs and of in vitro and in vivo conversion of blood cells into cells of therapeutic value, such as mesenchymal stem cells, neural cells and hepatocytes. An optimized design of lentiviral vectors is necessary to achieve high reprogramming efficiency of peripheral blood cells. More recently, non-integrating vectors such as Sendai virus and episomal vectors have been successfully employed in generating integration-free iPSCs and somatic stem cells.
KW - Cell fate conversion
KW - Hematopoietic cells
KW - Induced pluripotent stem cells
KW - Peripheral blood
KW - Reprogramming
UR - http://www.scopus.com/inward/record.url?scp=84886406593&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84886406593&partnerID=8YFLogxK
U2 - 10.1016/j.gpb.2013.09.001
DO - 10.1016/j.gpb.2013.09.001
M3 - Review article
C2 - 24060839
SN - 1672-0229
VL - 11
SP - 264
EP - 274
JO - Genomics, Proteomics and Bioinformatics
JF - Genomics, Proteomics and Bioinformatics
IS - 5
ER -