Zuba-Surma E K, Wu W, Ratajczak J, Kucia M, Ratajczak M Z
Stem Cell Institute at James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Mech Ageing Dev. 2009 Jan-Feb;130(1-2):58-66. doi: 10.1016/j.mad.2008.02.003. Epub 2008 Feb 14.
Recently our group identified in murine bone marrow (BM) and human cord blood (CB), a rare population of very small embryonic-like (VSEL) stem cells. We hypothesize that these cells are deposited during embryonic development in BM as a mobile pool of circulating pluripotent stem cells (PSC) that play a pivotal role in postnatal tissue turnover both of non-hematopoietic and hematopoietic tissues. During in vitro co-cultures with murine myoblastic C2C12 cells, VSELs form spheres that contain primitive stem cells. Cells isolated from these spheres may give rise to cells from all three germ layers when plated in tissue specific media. The number of murine VSELs and their ability to form spheres decreases with the age and is reduced in short-living murine strains. Thus, developmental deposition of VSELs in adult tissues may potentially play an underappreciated role in regulating the rejuvenation of senescent organs. We envision that the regenerative potential of these cells could be harnessed to decelerate aging processes.
最近,我们的研究小组在小鼠骨髓(BM)和人类脐带血(CB)中发现了一种罕见的极小胚胎样(VSEL)干细胞群。我们推测,这些细胞在胚胎发育过程中沉积在骨髓中,作为循环多能干细胞(PSC)的一个流动库,在出生后非造血和造血组织的组织更新中起关键作用。在与小鼠成肌C2C12细胞的体外共培养过程中,VSELs形成含有原始干细胞的球体。当接种到组织特异性培养基中时,从这些球体中分离出的细胞可能产生来自所有三个胚层的细胞。小鼠VSELs的数量及其形成球体的能力随年龄增长而减少,在寿命较短的小鼠品系中也会降低。因此,VSELs在成年组织中的发育沉积可能在调节衰老器官的年轻化方面发挥未被充分认识的作用。我们设想,可以利用这些细胞的再生潜力来减缓衰老过程。