Chapman Sandra, McDermott David H, Shen Kui, Jang Moon Kyoo, McBride Alison A
Stem Cell Res Ther. 2014 Apr 28;5(2):60. doi: 10.1186/scrt449.
We previously demonstrated that the lifespan of primary human keratinocytes could be extended indefinitely by culture in the presence of the Rho kinase (ROCK) inhibitor Y-27632. This technique has proven to be very useful in diverse areas of basic and clinical research.
In this follow-up study we determine whether the continual presence of Y-27632 is required for sustained proliferation. We also test whether different ROCK inhibitors can be used for this technique and whether it can also promote indefinite proliferation of animal keratinocytes. We measure keratinocyte gene expression, proliferation, behaviour and lifespan in the presence and absence of Y-27632.
We demonstrate that the extension of lifespan observed by culture of keratinocytes in the presence of fibroblast feeders and a ROCK inhibitor is reversible and that cells senesce gradually when the inhibitor is removed from the medium. Conversely, keratinocytes that are close to the end of their replicative life span can be revived by ROCK inhibition. We demonstrate that different inhibitors of ROCK can also efficiently extend the lifespan of human keratinocytes and that ROCK inhibition extends the lifespan of animal keratinocytes derived from mouse and bovine epithelia. Gene expression analysis of human epidermal keratinocytes cells grown in the presence of Y-27632 demonstrates that ROCK inhibition primarily inhibits keratinocyte differentiation. Live-imaging of keratinocytes cultured with ROCK inhibitors show that the effect of ROCK inhibition on cellular proliferation is immediate and ROCK inhibited cells proliferate rapidly without differentiation or stratification.
ROCK inhibition rapidly and conditionally induces indefinite proliferation of keratinocytes. This method has far-reaching applications for basic research, as well as for regenerative and personalized medicine.
我们之前证明,在Rho激酶(ROCK)抑制剂Y-27632存在的情况下进行培养,原代人角质形成细胞的寿命可以无限延长。该技术已被证明在基础研究和临床研究的各个领域都非常有用。
在这项后续研究中,我们确定持续增殖是否需要持续存在Y-27632。我们还测试了不同的ROCK抑制剂是否可用于该技术,以及它是否也能促进动物角质形成细胞的无限增殖。我们在有和没有Y-27632的情况下测量角质形成细胞的基因表达、增殖、行为和寿命。
我们证明,在成纤维细胞饲养层和ROCK抑制剂存在的情况下培养角质形成细胞所观察到的寿命延长是可逆的,当从培养基中去除抑制剂时,细胞会逐渐衰老。相反,接近其复制寿命末期的角质形成细胞可以通过ROCK抑制得以复苏。我们证明,不同的ROCK抑制剂也能有效地延长人角质形成细胞的寿命,并且ROCK抑制可延长源自小鼠和牛上皮的动物角质形成细胞的寿命。对在Y-27632存在下生长的人表皮角质形成细胞进行基因表达分析表明,ROCK抑制主要抑制角质形成细胞分化。用ROCK抑制剂培养的角质形成细胞的实时成像显示,ROCK抑制对细胞增殖的作用是即时的,ROCK抑制的细胞迅速增殖而不发生分化或分层。
ROCK抑制快速且有条件地诱导角质形成细胞的无限增殖。该方法在基础研究以及再生医学和个性化医学方面具有深远的应用。