Debili N, Robin C, Schiavon V, Letestu R, Pflumio F, Mitjavila-Garcia M T, Coulombel L, Vainchenker W
Institut National de la Santé et de la Recherche Médicale (INSERM) U 362, Institut Gustave Roussy, Cedex, France.
Blood. 2001 Apr 1;97(7):2023-30. doi: 10.1182/blood.v97.7.2023.
The glycoprotein (Gp) IIb/IIIa integrin, also called CD41, is the platelet receptor for fibrinogen and several other extracellular matrix molecules. Recent evidence suggests that its expression is much wider in the hematopoietic system than was previously thought. To investigate the precise expression of the CD41 antigen during megakaryocyte (MK) differentiation, CD34(+) cells from cord blood and mobilized blood cells from adults were grown for 6 days in the presence of stem cell factor and thrombopoietin. Two different pathways of differentiation were observed: one in the adult and one in the neonate cells. In the neonate samples, early MK differentiation proceeded from CD34(+)CD41(-) through a CD34(-)CD41(+)CD42(-) stage of differentiation to more mature cells. In contrast, in the adult samples, CD41 and CD42 were co-expressed on a CD34(+) cell. The rare CD34(+)CD41(+)CD42(-) cell subset in neonates was not committed to MK differentiation but contained cells with all myeloid and lymphoid potentialities along with long-term culture initiating cells (LTC-ICs) and nonobese diabetic/severe combined immune-deficient repopulating cells. In the adult samples, the CD34(+)CD41(+)CD42(-) subset was enriched in MK progenitors, but also contained erythroid progenitors, rare myeloid progenitors, and some LTC-ICs. All together, these results demonstrate that the CD41 antigen is expressed at a low level on primitive hematopoietic cells with a myeloid and lymphoid potential and that its expression is ontogenically regulated, leading to marked differences in the surface antigenic properties of differentiating megakaryocytic cells from neonates and adults. (Blood. 2001;97:2023-2030)
糖蛋白(Gp)IIb/IIIa整合素,也称为CD41,是纤维蛋白原和其他几种细胞外基质分子的血小板受体。最近的证据表明,其在造血系统中的表达比以前认为的要广泛得多。为了研究巨核细胞(MK)分化过程中CD41抗原的精确表达,将来自脐带血的CD34(+)细胞和来自成人的动员血细胞在干细胞因子和血小板生成素存在的情况下培养6天。观察到两种不同的分化途径:一种在成人细胞中,一种在新生儿细胞中。在新生儿样本中,早期MK分化从CD34(+)CD41(-)通过CD34(-)CD41(+)CD42(-)分化阶段发展为更成熟的细胞。相比之下,在成人样本中,CD41和CD42在CD34(+)细胞上共表达。新生儿中罕见的CD34(+)CD41(+)CD42(-)细胞亚群未定向分化为MK,但包含具有所有髓系和淋巴系潜能的细胞以及长期培养起始细胞(LTC-ICs)和非肥胖糖尿病/严重联合免疫缺陷再填充细胞。在成人样本中,CD34(+)CD41(+)CD42(-)亚群富含MK祖细胞,但也包含红系祖细胞、罕见的髓系祖细胞和一些LTC-ICs。总之,这些结果表明,CD41抗原在具有髓系和淋巴系潜能的原始造血细胞上低水平表达,并且其表达受个体发育调控,导致新生儿和成人分化中的巨核细胞表面抗原特性存在明显差异。(《血液》。2001年;97:2023 - 2030)