Abstract
Hematopoietic stem cells (HSCs) supply all blood cells throughout life by making use of their self-renewal and multilineage differentiation capabilities. Over the last few years, transplantation of hematopoietic stem and progenitor cell from mobilized blood stem cells, umbilical cord blood and selected CD34+ cells has been used for treatment of patients with hematologic and non-hematologic malignances. The techniques have become available that allow the extensive proliferation, orderly differentiation, functional activation and gene transfer of hematopoietic stem/progenitor cells in ex vivo culture systems. These techniques have now developed to the point at which clinical trials are now underway in a variety of settings for the applications of hematopoietic stem cell transplantation, hematopoietic support after high-dose chemotherapy, immunotherapy of cancers, and gene therapy. The article will discuss the characteristics, detecting assays, surface markers, expansion, orderly differentiation, cell therapy and gene therapy of hematopoietic stem/progenitor cells. Except that, it will also discuss some advanced achievements of stem cell research, such as the multilineage differentiation of marrow-derived mesenchymal stem cells. Some results of different gene expression between stem cells and induced cells by gene chip analysis will be reported.
Similar content being viewed by others
References
Pei XT, Yan CS, Zhu JP. Kinetic changes of CFU-S in a stable or unstable liquid culture system.Acta Physiol Sinica. 1988;40:569.
Wu CT, Pei XT, Cong PJ. Effects of human fetal liver extract on the growth of HL-60 cells.Exp Hematol. 1989;17:304.
Wu CT, Wang YZ, Pei XT. Studies on the suppression of HL-60 cell growth in vitro by low molecular weight suppressor of human fetal liver origin.Leuk Res. 1989;13:825.
Pei XT, Wu CT. Preferential suppression of low molecular weight natural tumor suppressor of human fetal liver origin on the growth of leukemic cells in vitro.Exp Hematol. 1990; 18:927.
Pei XT, Wu CT, Lao MF, et al. Preliminary application of a low molecular weight tumor suppressor in purged autologous bone marrow transplantation.Cancer J. 1992;5:142.
Wu CT, Pei XT, Cao JR, et al. A new pharmacological activity of Dibutyl Phthalate (DBP) on selective elimination of tumor cells from bone marrow.Leuk Res. 1993;17:557.
Pei XT, Wu CT, Coutinho LH, et al. The effect of GM-CSF and IL-3 on the grafting efficiency of umbilical cord blood CD34+ cells.Acta Physiol Sinica 1995;47:485.
de Wynter EA, Coutinho LH, Pei X, et al. Comparison of purity and enrichment of CD34+ cells from bone marrow, umbilical cord and peripheral blood (primed for apheresis) using five separation systems.Stem Cells. 1995;13:524.
Pei XT, Wang LS, Xu L, et al. Isolation and characterization of human CD34+ hematopoietic progenitor cells by highgradient magnetic cell sorting.High Technol Letters 1995;1: 108.
Wu CT, Yang K, Pei XT, et al. Bone marrow purging with Dibutyl Phthalate — experimental basis and a preliminary clinical application.Leuk Res. 1995;19:557.
Wang LS, Wu CT, Pei XT, et al. Dibutyl Phthalate (DBP) purged autologous bone marrow transplantation in the treatment of leukemial.Leuk Res. 1996;20:343.
Wang LS, Wu CT, Pei XT, et al. Purging effect of Dibutyl Phthalate on leukemic cells associated with apoptosis.Leuk Res. 1996;20:989.
Pei Xuetao. Who is hematopoietic stem cell: CD34+ or CD34?Int J Hematol. 1999;70:213.
Du N, Pei XT, Luo CJ, et al. In vitro studies on the expression of FLT3 Ligand regulated by Egr-1 regulated sequence.Immunol J. 2000,16:166.
Author information
Authors and Affiliations
About this article
Cite this article
Pei, X. Stem cell engineering: The new generation of cellular therapeutics. Int J Hematol 76 (Suppl 1), 155–156 (2002). https://doi.org/10.1007/BF03165233
Issue Date:
DOI: https://doi.org/10.1007/BF03165233