Morrison S J, Lagasse E, Weissman I L
Department of Pathology, Stanford University School of Medicine, CA.
Blood. 1994 Jun 15;83(12):3480-90.
We have been unable to reproduce experiments suggesting the existence of three lineage-restricted progenitor populations from mouse bone marrow. Thy1.1loMac-1+B220+ cells were reported to give rise to greatly expanded numbers of myeloid and lymphoid cells, while Thy1.1loMac-1+B220- and Thy1.1loMac-1-B220+ cells were reported to be highly proliferative myeloid and B-lineage-restricted progenitors, respectively. Both Mac-1+ cell types appear to be much less frequent than previously reported, and we observed no activity consistent with their characterization as committed progenitors of expanded numbers of cells. The original identification of these populations may have resulted from a failure to distinguish bonafide signals from autofluorescent background and nonspecific staining. The progenitor activities originally associated with these populations may have been due to hematopoietic stem cell contamination. This study shows that low levels of Mac-1 are expressed on cells with multipotent progenitor activity. Thy1.1loB220+Mac-1- cells can be purified from bone marrow, but in these experiments they do not give rise to detectable levels of progeny on injection into lethally irradiated mice. Thy1.1loB220+Mac-1- cells appear to be pro-B cells without significant proliferation potential in vivo. The finding that the described populations do not have the reported progenitor activities leaves the pathways of stem cell differentiation open to further study.
我们无法重复那些表明小鼠骨髓中存在三种谱系受限祖细胞群体的实验。据报道,Thy1.1loMac-1+B220+细胞可产生大量扩增的髓系和淋巴细胞,而Thy1.1loMac-1+B220-细胞和Thy1.1loMac-1-B220+细胞分别据报道是高度增殖的髓系祖细胞和B谱系受限祖细胞。这两种Mac-1+细胞类型的出现频率似乎比之前报道的要低得多,并且我们没有观察到与它们作为大量细胞的定向祖细胞的特征相符的活性。对这些细胞群体的最初鉴定可能是由于未能将真实信号与自发荧光背景及非特异性染色区分开来。最初与这些细胞群体相关的祖细胞活性可能是由于造血干细胞污染所致。本研究表明,具有多能祖细胞活性的细胞上表达低水平的Mac-1。Thy1.1loB220+Mac-1-细胞可从骨髓中纯化出来,但在这些实验中,将它们注射到受致死性照射的小鼠体内后,不会产生可检测水平的子代细胞。Thy1.1loB220+Mac-1-细胞似乎是前B细胞,在体内没有显著的增殖潜力。所描述的细胞群体不具有所报道的祖细胞活性这一发现,使得干细胞分化途径有待进一步研究。