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1 Institute of Medical Science, University of Toronto, and the Ontario Cancer Institute,
Toronto, Canada.
Marrow from 28 nonleukemic individuals
was separated by adherence to glass or
plastic into nonadherent (NA) and adherent
populations. The NA populations were
found to be more dependent for colony
formation in culture on added colonystimulating activity (CSA) than unseparated marrow suspensions, and therefore
proved useful for CSA assays. Quantitative
reconstitution procedures were used to
assay CSA-producing cells. Either increasing numbers of irradiated unseparated
marrow, or adherent cells derived from
varying numbers of marrow cells, were
used to restore colony-forming efficiency
to NA populations. Assay procedures for
CSA-producing cells were applied to four
patients with acute leukemia prior to
treatment. In all four instances, a defect in
CSA-producing cells was demonstrated.
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