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In vitro assessment of marrow ‘stem cell’and stromal cell function in aplastic anaemia
Author(s) -
Marsh J. C. W.,
Chang J.,
Testa N. G.,
Hows J. M.,
Dexter T. M.
Publication year - 1991
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1991.tb04426.x
Subject(s) - bone marrow , stromal cell , cd34 , stem cell , progenitor cell , clonogenic assay , haematopoiesis , biology , immunology , microbiology and biotechnology , cell , cancer research , biochemistry
Summary An in vitro model system is described that allows separate assessment of ‘stem cell’and stromal cell function in aplastic anaemia (AA). Seven patients with non‐severe AA, who had responded to immunosuppressive therapy and had haematological evidence of residual marrow function, were studied. Of these, three with otherwise typical AA had an acquired clonal cytogenetic marker. Purified bone marrow haemopoietic progenitors labelled with CD34 monoclonal antibody were positively selected using the fluorescence activated cell sorter (FACS) from both normal subjects and from patients with AA. The generative capacity of the CD34 positive cells was assessed by monitoring the output of granulocyte/macrophage colony forming cells (CFU‐GM) in the non‐adherent layer after inoculation onto irradiated preformed long‐term marrow culture (LTBMC) stromas. Stromal function in AA was assessed by inoculating CD34 positive cells from normal bone marrow onto preformed irradiated stromas from patients with AA. Haemopoietic cell (‘stem cell’) function in AA was assessed by inoculating CD34 positive cells from AA patients onto confluent irradiated normal marrow stromas. Using these crossover/LTBMC experiments, all patients exhibited severe defects in haemopoietic cell function with normal functioning stroma. The proportion of CD34 positive cells present in bone marrow from these patients was reduced compared with controls, they comprised fewer small primitive ‘blast‐like’cells which in normal bone marrow are known to possess marrow repopulating ability, and demonstrated reduced clonogenic potential in short‐term colony assays.