Department of Medical Biochemistry, Oslo University Hospital, 0372, Oslo, Norway.
Department of Microbiology, Oslo University Hospital, 0372, Oslo, Norway.
Nat Commun. 2018 Sep 10;9(1):3665. doi: 10.1038/s41467-018-05578-7.
Epithelial sheet spreading is a fundamental cellular process that must be coordinated with cell division and differentiation to restore tissue integrity. Here we use consecutive serum deprivation and re-stimulation to reconstruct biphasic collective migration and proliferation in cultured sheets of human keratinocytes. In this system, a burst of long-range coordinated locomotion is rapidly generated throughout the cell sheet in the absence of wound edges. Migrating cohorts reach correlation lengths of several millimeters and display dependencies on epidermal growth factor receptor-mediated signaling, self-propelled polarized migration, and a G/G cell cycle environment. The migration phase is temporally and spatially aligned with polarized cell divisions characterized by pre-mitotic nuclear migration to the cell front and asymmetric partitioning of nuclear promyelocytic leukemia bodies and lysosomes to opposite daughter cells. This study investigates underlying mechanisms contributing to the stark contrast between cells in a static quiescent state compared to the long-range coordinated collective migration seen in contact with blood serum.
上皮细胞铺展是一个基本的细胞过程,必须与细胞分裂和分化相协调,以恢复组织完整性。在这里,我们使用连续的血清剥夺和再刺激来重建培养的人角质形成细胞片层中的两相集体迁移和增殖。在这个系统中,在没有伤口边缘的情况下,细胞片层中会迅速产生一阵长程协调的运动。迁移队列达到几毫米的相关长度,并依赖于表皮生长因子受体介导的信号、自我推进的极化迁移和 G1/G0 细胞周期环境。迁移相在时间和空间上与有丝分裂前核迁移到细胞前缘和核早幼粒细胞白血病体和溶酶体的不对称分配到对面的子细胞的极化细胞分裂相匹配。本研究调查了导致静态静止状态下的细胞与接触血清时看到的长程协调集体迁移之间形成鲜明对比的潜在机制。