Howard Hughes Medical Institute, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Mol Cell Biol. 2010 Mar;30(6):1329-40. doi: 10.1128/MCB.00795-09. Epub 2010 Jan 11.
The c-Jun NH(2)-terminal kinase (JNK) is implicated in proliferation. Mice with a deficiency of either the Jnk1 or the Jnk2 genes are viable, but a compound deficiency of both Jnk1 and Jnk2 causes early embryonic lethality. Studies using conditional gene ablation and chemical genetic approaches demonstrate that the combined loss of JNK1 and JNK2 protein kinase function results in rapid senescence. To test whether this role of JNK was required for stem cell proliferation, we isolated embryonic stem (ES) cells from wild-type and JNK-deficient mice. We found that Jnk1(-/-) Jnk2(-/-) ES cells underwent self-renewal, but these cells proliferated more rapidly than wild-type ES cells and exhibited major defects in lineage-specific differentiation. Together, these data demonstrate that JNK is not required for proliferation or self-renewal of ES cells, but JNK plays a key role in the differentiation of ES cells.
c-Jun NH(2)-末端激酶(JNK)参与增殖。缺乏 Jnk1 或 Jnk2 基因的小鼠是有活力的,但同时缺乏 Jnk1 和 Jnk2 会导致早期胚胎致死。使用条件性基因缺失和化学遗传学方法的研究表明,JNK1 和 JNK2 蛋白激酶功能的联合缺失会导致快速衰老。为了测试 JNK 的这种作用是否需要干细胞增殖,我们从野生型和 JNK 缺陷型小鼠中分离出胚胎干细胞(ES 细胞)。我们发现 Jnk1(-/-) Jnk2(-/-) ES 细胞经历了自我更新,但这些细胞比野生型 ES 细胞增殖得更快,并表现出线粒体特异性分化的主要缺陷。总之,这些数据表明 JNK 对于 ES 细胞的增殖或自我更新不是必需的,但 JNK 在 ES 细胞的分化中起着关键作用。