中段
细胞生物学
生物
脱落
有丝分裂
劈理沟
中心体
电池极性
细胞分裂
胞质分裂
细胞命运测定
调节器
极性(国际关系)
CDC42型
塞普汀
细胞
微管
细胞周期
遗传学
转录因子
基因
作者
L Dionne,Xiaojing Wang,Rytis Prekeris
标识
DOI:10.1016/j.ceb.2015.04.010
摘要
At late mitosis, the mother cell divides by the formation of a cleavage furrow, leaving two daughter cells connected by a thin intercellular bridge. During ingression of the cleavage furrow, the central spindle microtubules are compacted to form the structure known as the midbody (MB). The MB is situated within the intercellular bridge, with the abscission site sometimes occurring on one side of the MB. As a result of this one-sided (asymmetric) abscission, only one daughter cell can inherit the post-mitotic MB. Interestingly, recent studies have identified post-mitotic MBs as novel signaling platforms regulating stem cell fate and proliferation. Additionally, MBs were proposed to serve a role of polarity cues during the neurite outgrowth and apical lumen formation. Thus, abscission and MB inheritance is clearly a highly regulated cellular event that can affect development and various other cellular functions. In this review we discuss the latest findings regarding post-mitotic MB functions, as well as the machinery regulating MB inheritance and accumulation.
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