50-FOLD Enrichment of CD34+ cells directly from cord blood in a single density separation

To date, extensive enrichment of progenitor cells from cord blood has required at least two steps, with cell losses incurred at each step. We have developed a simple technique, called RosetteSep™, to enrich progenitor cells directly from whole cord blood in a single step, significantly reducing the...

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Bibliographic Details
Published in:Experimental hematology Vol. 28; no. 7; p. 48
Main Authors: Peters, C.E, Clarke, E, Glimm, H, Lansdorp, P.M, C.J.Eaves, Thomas, T.E
Format: Journal Article
Language:English
Published: Elsevier Inc 01.07.2000
ISSN:0301-472X
Online Access:Get full text
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Summary:To date, extensive enrichment of progenitor cells from cord blood has required at least two steps, with cell losses incurred at each step. We have developed a simple technique, called RosetteSep™, to enrich progenitor cells directly from whole cord blood in a single step, significantly reducing the cell losses seen with other multi-step systems. This approach combines the specificity of antibody (Ab) mediated cell separation with the ease of density gradient centrifugation. A cocktail of bispecific Ab reagents selectively couples cell surface antigens on unwanted cells to erythrocytes present in the sample, producing cell/RBC rosettes. The rosetted cells are pelleted in a standard Ficoll (1.077 g/mL) separation; the desired, unlabeled cells are recovered at the Ficoll:plasma interface. Progenitors were enriched from whole cord blood using two different Ab cocktails: a 4 Ab cocktail (anti- CD2, CD14, CD19, and CD66b) and an 8 Ab cocktail (anti- CD2, CD3, CD14, CD16, CD19, CD24, CD56, and CD66b). Enrichment and % recovery of colony forming cells (CFC) with the 4 Ab cocktail was 9 ± 2 fold and 43 ± 4%, and with the 8 Ab cocktail was 40 ± 9 fold and 43 ± 15%. In summary, the RosetteSep™ method offers high purity and high recovery of progenitors directly from whole cord blood.
ISSN:0301-472X
DOI:10.1016/S0301-472X(00)00239-3