Hernandez Marylens, Patzig Julia, Mayoral Sonia R, Costa Kevin D, Chan Jonah R, Casaccia Patrizia
Department of Neuroscience, Graduate School of Biological Sciences.
Department of Neuroscience.
J Neurosci. 2016 Jan 20;36(3):806-13. doi: 10.1523/JNEUROSCI.2873-15.2016.
Oligodendrocyte progenitors respond to biophysical or mechanical signals, and it has been reported that mechanostimulation modulates cell proliferation, migration, and differentiation. Here we report the effect of three mechanical stimuli on mouse oligodendrocyte progenitor differentiation and identify the molecular components of the linker of nucleoskeleton and cytoskeleton (LINC) complex (i.e., SYNE1) as transducers of mechanical signals to the nucleus, where they modulate the deposition of repressive histone marks and heterochromatin formation. The expression levels of LINC components increased during progenitor differentiation and silencing the Syne1 gene resulted in aberrant histone marks deposition, chromatin reorganization and impaired myelination. We conclude that spatial constraints, via the actin cytoskeleton and LINC complex, mediate nuclear changes in oligodendrocyte progenitors that favor a default pathway of differentiation. Significance statement: It is recognized that oligodendrocyte progenitors are mechanosensitive cells. However, the molecular mechanisms translating mechanical stimuli into oligodendrocyte differentiation remain elusive. This study identifies components of the mechanotransduction pathway in the oligodendrocyte lineage.
少突胶质前体细胞对生物物理或机械信号有反应,并且据报道机械刺激可调节细胞增殖、迁移和分化。在此,我们报告了三种机械刺激对小鼠少突胶质前体细胞分化的影响,并确定了核骨架与细胞骨架连接复合体(LINC复合体)(即SYNE1)的分子成分作为机械信号向细胞核的转导分子,在细胞核中它们调节抑制性组蛋白标记的沉积和异染色质形成。LINC复合体成分的表达水平在祖细胞分化过程中增加,沉默Syne1基因会导致异常的组蛋白标记沉积、染色质重组和髓鞘形成受损。我们得出结论,通过肌动蛋白细胞骨架和LINC复合体的空间限制介导了少突胶质前体细胞的核变化,这些变化有利于默认的分化途径。意义声明:人们认识到少突胶质前体细胞是机械敏感细胞。然而,将机械刺激转化为少突胶质细胞分化的分子机制仍然难以捉摸。本研究确定了少突胶质细胞谱系中机械转导途径的成分。