Clausen O P, Thorud E
J Invest Dermatol. 1980 Jun;74(6):433-6. doi: 10.1111/1523-1747.ep12544614.
Cell kinetic perturbations that resulted in a wave of increased cell division during the 6--8 hr lag period prior to regenerative DNA replication in mouse epidermis were examined. The epidermis was stimulated to proliferate by adhesive tape stripping, and flow cytometric DNA measurements of isolated epidermal basal cells, counting of mitoses, of Colcemid arrested metaphases and of labeled mitoses among basal cells in histologic sections were made. The results showed that mitotic peaks that occur in the pre-replicative period subsequent to tape stripping can be explained by a delay in cell progression through the S phase, followed by subsequent release and partial synchrony in further cell cycle progression. Early peaks of mitoses in epidermis stimulated to proliferate should therefore not, without further evidence, be assumed to originate from cells triggered into division from a resting G2 compartment. The results also indicate an initial delayed cell progression through the G2 phase, whereas the mitotic duration seemed to be initially reduced, indicating that the DNA synthesis phase and the G2 phase are parts of the epidermal cell cycle that may be most vulnerable to various types of influences.
研究了在小鼠表皮再生性DNA复制之前的6-8小时延迟期内导致细胞分裂增加波的细胞动力学扰动。通过胶带剥离刺激表皮增殖,并对分离的表皮基底细胞进行流式细胞术DNA测量,对有丝分裂进行计数,对秋水仙酰胺阻滞的中期进行计数,并对组织学切片中基底细胞中的标记有丝分裂进行计数。结果表明,胶带剥离后复制前期出现的有丝分裂峰可以通过细胞通过S期的进展延迟来解释,随后是进一步细胞周期进展中的释放和部分同步。因此,在没有进一步证据的情况下,不应假定受刺激增殖的表皮中有丝分裂的早期峰源自从静止的G2区室触发进入分裂的细胞。结果还表明细胞通过G2期的初始进展延迟,而有丝分裂持续时间似乎最初缩短,这表明DNA合成期和G2期是表皮细胞周期中可能最易受各种类型影响的部分。