Bögler O, Wren D, Barnett S C, Land H, Noble M
Ludwig Institute for Cancer Research, London, United Kingdom.
Proc Natl Acad Sci U S A. 1990 Aug;87(16):6368-72. doi: 10.1073/pnas.87.16.6368.
Bipotential oligodendrocyte-type-2 astrocyte (O-2A) progenitor cells, which give rise to oligodendrocytes and type-2 astrocytes in cultures of rat optic nerve, are one of the few cell types in which most aspects of proliferation and differentiation can be manipulated in a defined in vitro environment. Previous studies have shown that O-2A progenitors exposed to platelet-derived growth factor (PDGF) divide as migratory bipolar cells a limited number of times, with a cell cycle time of 18 hr, before clonally related progenitors differentiate into nondividing oligodendrocytes with a timing similar to that seen in vivo. In contrast, O-2A progenitors grown in the absence of mitogen do not divide but instead differentiate prematurely into oligodendrocytes, and progenitors exposed to appropriate inducing factors differentiate into type-2 astrocytes. We now have found that O-2A progenitors can be induced to undergo continuous self-renewal in the absence of oligodendrocytic differentiation by exposure to a combination of PDGF and basic fibroblast growth factor (bFGF). With the exception of the inhibition of differentiation, the O-2A progenitors exposed to PDGF and bFGF behaved similarly to those exposed to PDGF alone. In contrast, progenitors exposed to basic bFGF alone were multipolar, had a cell-cycle length of 45 hr, showed little migratory behavior, underwent premature oligodendrocytic differentiation, and did not cease division upon expression of oligodendrocyte marker antigens. Thus, inhibition of differentiation required the presence of both mitogens. Our results demonstrate that PDGF and bFGF act on O-2A progenitors as both inducers of division and as regulators of differentiation that modulate multiple aspects of O-2A progenitor development and, additionally, reveal a previously unrecognized means of regulating self-renewal processes, wherein cooperation between growth factors promotes continuous division in the absence of differentiation.
双潜能少突胶质细胞 - 2型星形胶质细胞(O - 2A)祖细胞在大鼠视神经培养物中可分化为少突胶质细胞和2型星形胶质细胞,是少数几种在特定体外环境中其增殖和分化的大多数方面都能被操控的细胞类型之一。先前的研究表明,暴露于血小板衍生生长因子(PDGF)的O - 2A祖细胞作为迁移性双极细胞分裂有限次数,细胞周期为18小时,然后克隆相关祖细胞分化为不分裂的少突胶质细胞,其时间进程与体内所见相似。相比之下,在没有有丝分裂原的情况下生长的O - 2A祖细胞不分裂,而是过早分化为少突胶质细胞,而暴露于适当诱导因子的祖细胞则分化为2型星形胶质细胞。我们现在发现,通过暴露于PDGF和碱性成纤维细胞生长因子(bFGF)的组合,O - 2A祖细胞可以在不发生少突胶质细胞分化的情况下被诱导进行持续自我更新。除了分化受到抑制外,暴露于PDGF和bFGF的O - 2A祖细胞的行为与仅暴露于PDGF的祖细胞相似。相比之下,仅暴露于碱性bFGF的祖细胞是多极的,细胞周期长度为45小时,迁移行为很少,过早发生少突胶质细胞分化,并且在表达少突胶质细胞标记抗原后不会停止分裂。因此,分化的抑制需要两种有丝分裂原的存在。我们的结果表明,PDGF和bFGF作为分裂诱导剂和分化调节剂作用于O - 2A祖细胞,调节O - 2A祖细胞发育的多个方面,此外,还揭示了一种以前未被认识的调节自我更新过程的方式,即生长因子之间的协同作用促进在无分化情况下的持续分裂。