The Effect of Pegylated Antisense Acetylcholinesterase on Hematopoiesis
To determine whether the efficacy of entry and action of antisense oligonucleotides (AS-ODN) on hematopoietic stem cells in vitro could be improved by the addition of polyethylene glycol (PEG), a molecule of PEG was bound to AS- or sense-acetylcholinesterase (AS-ACHE or S-ACHE). The introduction of...
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Veröffentlicht in: | Oligonucleotides 2003-01, Vol.13 (4), p.27-216 |
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Sprache: | eng |
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Zusammenfassung: | To determine whether the efficacy of entry and action of antisense oligonucleotides (AS-ODN) on hematopoietic stem cells
in vitro
could be improved by the addition of polyethylene glycol (PEG), a
molecule of PEG was bound to AS- or sense-acetylcholinesterase (AS-ACHE or S-ACHE). The introduction of 0.1-0.5 μM PEG-AS-ACHE or 0.5 μM AS-ACHE into methylcellulose bone marrow (BM) cultures produced
a doubling in number of colony-forming unit-granulocyte-erythrocyte-macrophage-megakaryocyte (CFU-GEMM) and a 5-fold increase in cell number of the PEG-ODN. Further increase in concentration of the PEG-ODN
reduced colony numbers. PEG-AS-ACHE induced higher colony numbers and greatly increased megakaryocyte (MK) formation when compared with PEG and AS-ACHE added separately to the culture. In addition, differentials
of the CFU-GEMMs indicated there was a direct relationship between MK number and PEG-AS-ACHE concentration. Under these culture conditions, 5 μM PEG alone gave control values of CFU-GEMM. On addition
of FITC-PEG-AS-ACHE to the cell cultures, using confocal microscopy, the nuclei of both early and mature MKs were labeled specifically, whereas all other cellular nuclei were negative to the stain. The
use of PEG-AS-ODN, affording specific delivery of AS-ODN to target cells, increased cell proliferation, and enhanced ODN uptake, may be of potential importance in stem cell expansion for BM transplantation
and gene therapy. |
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ISSN: | 1545-4576 2159-3337 1557-8526 2159-3345 |
DOI: | 10.1089/154545703322460595 |