Enrichment of pluripotent hemopoietic progenitor cells from human bone marrow.
Enrichment of pluripotent hemopoietic progenitor cells from human bone marrow.
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富集人骨髓中的多能造血祖细胞。
DOI:
10.1182/blood.v64.4.774.774
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发表时间:
1984
期刊:
影响因子:
20.3
通讯作者:
M. Beard
中科院分区:
文献类型:
--
作者:
M. Bodger;I. Hann;R. Maclean;M. Beard
Pluripotent hemopoietic progenitor cells (CFU-GEMM, cells forming mixed hemopoietic colonies in methylcellulose) from human bone marrow were enriched 90-fold by positive selection on the fluorescence-activated cell sorter using monoclonal antibody RFB-1. Bone marrow cells were separated by cell size, using log 90 degrees light scatter, and the cell fraction containing CFU-GEMM was further separated by relative fluorescence intensity for the RFB-1 antigen. Further enrichment, up to 150-fold, was achieved by depleting bone marrow of T cells and mature myeloid cells prior to RFB-1 selection. These procedures yield a cell fraction containing 51% blast cells, 2% promyelocytes, and 47% undifferentiated (lymphocyte-like) mononuclear cells, although only 1% of the cells formed a mixed colony. CFU-GEMM are strongly positive for the RFB-1 antigen, whereas morphologically identifiable erythroblasts, myeloblasts, and promyelocytes are weakly RFB-1+. This suggests that the relative concentration of the RFB-1 antigen on bone marrow cells is inversely related to their maturity. The greatly increased recovery of CFU-GEMM after the separation of bone marrow by log 90 degrees light scatter and the removal of T cells and mature myeloid cells suggested that accessory cells that normally regulate the cloning efficiency of CFU-GEMM were removed.
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影响因子:
4.3
作者:
Platsoucas,CD;Beck,JD;Kapoor,N;Good,RA;Gupta,S
通讯作者:
Gupta,S
影响因子:
20.3
作者:
Nicola,NA;Metcalf,D;vonMelchner,H;Burgess,AW
通讯作者:
Burgess,AW
影响因子:
20.3
作者:
Ash,RC;Detrick,DA;Zanjani,ED
通讯作者:
Zanjani,ED
影响因子:
20.3
作者:
Morstyn,G;Nicola,NA;Metcalf,D
通讯作者:
Metcalf,D
影响因子:
2.6
作者:
Wisniewski,D;Platsoucas,C;Strife,A;Lambek,C;Clarkson,B
通讯作者:
Clarkson,B