The CD34+CD38neg population is significantly increased in haemopoietic cell expansion cultures in serum-free compared to serum-replete conditions:: dissociation of phenotype and function
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Donaldson, C
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Univ Bristol, Div Transplantat Sci, Stem Cell Lab, Med Sch Unit,Southmead Hosp, Bristol BS10 5ND, Avon, EnglandUniv Bristol, Div Transplantat Sci, Stem Cell Lab, Med Sch Unit,Southmead Hosp, Bristol BS10 5ND, Avon, England
Donaldson, C
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Denning-Kendall, P
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Univ Bristol, Div Transplantat Sci, Stem Cell Lab, Med Sch Unit,Southmead Hosp, Bristol BS10 5ND, Avon, EnglandUniv Bristol, Div Transplantat Sci, Stem Cell Lab, Med Sch Unit,Southmead Hosp, Bristol BS10 5ND, Avon, England
Denning-Kendall, P
[1
]
Bradley, B
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Univ Bristol, Div Transplantat Sci, Stem Cell Lab, Med Sch Unit,Southmead Hosp, Bristol BS10 5ND, Avon, EnglandUniv Bristol, Div Transplantat Sci, Stem Cell Lab, Med Sch Unit,Southmead Hosp, Bristol BS10 5ND, Avon, England
Bradley, B
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]
Hows, J
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Univ Bristol, Div Transplantat Sci, Stem Cell Lab, Med Sch Unit,Southmead Hosp, Bristol BS10 5ND, Avon, EnglandUniv Bristol, Div Transplantat Sci, Stem Cell Lab, Med Sch Unit,Southmead Hosp, Bristol BS10 5ND, Avon, England
Hows, J
[1
]
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[1] Univ Bristol, Div Transplantat Sci, Stem Cell Lab, Med Sch Unit,Southmead Hosp, Bristol BS10 5ND, Avon, England
Expansion of haemopoietic stem cells is proposed to combat graft failure in adult recipients following cord blood (CB) transplantation. Cultures are traditionally performed in medium containing FCS, but to transfer expansion to the clinic, 'good manufacturing practice' (GMP) standards are required. This study evaluated expansion cultures in culture bags and serum-free (SF) conditions, to comply with GMP, by analysing subpopulations of CD34(+) cells, colony-forming cells (CFC) and long-term culture initiating cells (LTC-IC), CD34(+) cell analysis has previously been used to measure clonogenic capacity and the CD34(+)CD38(neg) surface phenotype to measure primitive cell numbers. In this study, comparison of expansion in serum-replete medium with that in SF conditions demonstrated a lack of expression of CD38 on CD34(+) cells in the absence of serum. These findings must be considered in clinical studies using in vitro expansion in SF conditions, and the CD34(+)CD38(neg) phenotype should not be used to confirm maintenance, or expansion, of primitive progenitor cells.