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原始贴壁人类造血祖细胞的表型与子代

Phenotype and progeny of primitive adherent human hematopoietic progenitors.

作者信息

Gordon M Y, Lewis J L, Grand F H, Marley S B, Goldman J M

机构信息

LRF Centre for Adult Leukaemia, Royal Postgraduate Medical School, London, UK.

出版信息

Leukemia. 1996 Aug;10(8):1347-53.

PMID:8709641
Abstract

Hematopoietic progenitor cells can be classified as plastic- and stroma-adherent (P+S+), stroma-adherent (P-S+) and non-adherent (P-S-). Both P+S+ and P-S+ populations are detected in delta (delta) culture systems where they produce non-adherent (P-S-) granulocyte-macrophage colony-forming cells (CFU-GM) and erythroid burst-forming units (BFU-E). Here we demonstrate that the plastic-adherent progenitor cells (P delta cells) comprise 5-10 percent of the CD34+, population in adult human marrow. Moreover, they do not express CD3 or CD22 and 88 percent of them are CD38-, 88 percent are CD33- and 74 percent are HLA-DR-. Production of CFU-GM by purified plastic-adherent CD34+, adherent cells was 60 percent of the number produced by recombined CD34+, and CD34- fractions. We have shown also that the plastic-adherent P+S+ cells are the precursors of the stroma-adherent P-S+ cells (S delta cells), day 21 cobblestone-area forming cells (CAFC) and cells capable of sustained hematopoiesis in a modified long-term bone marrow culture system. These observations support the primitive nature of P delta cells and establish a phenotypic sequence of plastic and stroma adherence through stroma adherence to non-adherence in hematopoietic cell development. To further investigate the relationship between P delta cells, S delta cells and long-term culture-initiating cells (LTCIC), we cultured whole mononuclear cell tractions and plastic-adherent cell-depleted mononuclear cell fractions in long-term culture and in the S delta assay. The results indicated the P delta cells were inhibited in the presence of stromal cells.

摘要

造血祖细胞可分为可塑性和基质黏附性(P+S+)、基质黏附性(P-S+)和非黏附性(P-S-)。在δ培养系统中可检测到P+S+和P-S+群体,它们在该系统中产生非黏附性(P-S-)粒细胞-巨噬细胞集落形成细胞(CFU-GM)和红系爆式集落形成单位(BFU-E)。在此我们证明,可塑性黏附祖细胞(Pδ细胞)占成人骨髓中CD34+群体的5%-10%。此外,它们不表达CD3或CD22,其中88%为CD38-,88%为CD33-,74%为HLA-DR-。纯化的可塑性黏附CD34+黏附细胞产生CFU-GM的数量是重组CD34+和CD34-组分产生数量的60%。我们还表明,可塑性黏附的P+S+细胞是基质黏附性P-S+细胞(Sδ细胞)、第21天鹅卵石区域形成细胞(CAFC)以及在改良的长期骨髓培养系统中能够持续造血的细胞的前体。这些观察结果支持了Pδ细胞的原始特性,并确立了造血细胞发育过程中从可塑性黏附到基质黏附再到非黏附的表型序列。为了进一步研究Pδ细胞、Sδ细胞与长期培养起始细胞(LTCIC)之间的关系,我们在长期培养和Sδ测定中培养了全单核细胞组分和去除可塑性黏附细胞的单核细胞组分。结果表明,在存在基质细胞的情况下,Pδ细胞受到抑制。

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