Department of Bioengineering University of California Los Angeles Los Angeles CA 90095 USA.
Department of Human Genetics University of California Los Angeles Los Angeles CA 90095 USA.
Adv Sci (Weinh). 2021 Feb 25;8(7):2003516. doi: 10.1002/advs.202003516. eCollection 2021 Apr.
Cell reprogramming is considered a stochastic process, and it is not clear which cells are prone to be reprogrammed and whether a deterministic step exists. Here, asymmetric cell division (ACD) at the early stage of induced neuronal (iN) reprogramming is shown to play a deterministic role in generating elite cells for reprogramming. Within one day, fibroblasts underwent ACD, with one daughter cell being converted into an iN precursor and the other one remaining as a fibroblast. Inhibition of ACD significantly inhibited iN conversion. Moreover, the daughter cells showed asymmetric DNA segregation and histone marks during cytokinesis, and the cells inheriting newly replicated DNA strands during ACD became iN precursors. These results unravel a deterministic step at the early phase of cell reprogramming and demonstrate a novel role of ACD in cell phenotype change. This work also supports a novel hypothesis that daughter cells with newly replicated DNA strands are elite cells for reprogramming, which remains to be tested in various reprogramming processes.
细胞重编程被认为是一个随机过程,目前尚不清楚哪些细胞容易被重编程,以及是否存在确定性步骤。在这里,诱导神经元(iN)重编程早期的不对称细胞分裂(ACD)被证明在产生用于重编程的精英细胞方面起着确定性的作用。在一天内,成纤维细胞经历 ACD,一个子细胞转化为 iN 前体细胞,另一个子细胞保持成纤维细胞状态。ACD 的抑制显著抑制了 iN 的转化。此外,子细胞在有丝分裂过程中表现出不对称的 DNA 分离和组蛋白标记,在 ACD 过程中继承新复制 DNA 链的细胞成为 iN 前体细胞。这些结果揭示了细胞重编程早期阶段的一个确定性步骤,并证明了 ACD 在细胞表型改变中的新作用。这项工作还支持了一个新的假设,即具有新复制 DNA 链的子细胞是用于重编程的精英细胞,这有待在各种重编程过程中进行检验。