Shaalan Abeer K, Teshima Tathyane H N, Tucker Abigail S, Proctor Gordon B
Centre for Host-Microbiome Interactions, Guy's Hospital, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, UK.
Centre for Craniofacial and Regenerative Biology, Guy's Hospital, Faculty of Dentistry, Oral and Craniofacial Sciences, King's College London, London, UK.
Cell Death Discov. 2021 Jan 18;7(1):16. doi: 10.1038/s41420-020-00393-w.
Little is known about the key molecules that regulate cell division during organogenesis. Here we determine the role of the cell cycle promoter aurora kinase B (AURKB) during development, using embryonic salivary glands (E-SGs) as a model. AURKB is a serine/threonine kinase that regulates key events in mitosis, which makes it an attractive target for tailored anticancer therapy. Many reports have elaborated on the role of AURKB in neoplasia and cancer; however, no previous study has shown its role during organ development. Our previous experiments have highlighted the essential requirement for AURKB during adult exocrine regeneration. To investigate if AURKB is similarly required for progression during embryonic development, we pharmacologically inhibited AURKB in developing submandibular glands (SMGs) at embryonic day (E)13.5 and E16.5, using the highly potent and selective drug Barasertib. Inhibition of AURKB interfered with the expansion of the embryonic buds. Interestingly, this effect on SMG development was also seen when the mature explants (E16.5) were incubated for 24 h with another cell cycle inhibitor Aphidicolin. Barasertib prompted apoptosis, DNA damage and senescence, the markers of which (cleaved caspase 3, γH2AX, SA-βgal and p21, respectively), were predominantly seen in the developing buds. In addition to a reduction in cell cycling and proliferation of the epithelial cells in response to AURKB inhibition, Barasertib treatment led to an excessive generation of reactive oxygen species (ROS) that resulted in downregulation of the acinar differentiation marker Mist1. Importantly, inhibition of ROS was able to rescue this loss of identity, with Mist1 expression maintained despite loss of AURKB. Together, these data identify AURKB as a key molecule in supporting embryonic development and differentiation, while inhibiting senescence-inducing signals during organogenesis.
关于器官发生过程中调节细胞分裂的关键分子,人们了解甚少。在此,我们以胚胎唾液腺(E-SGs)为模型,确定细胞周期促进因子极光激酶B(AURKB)在发育过程中的作用。AURKB是一种丝氨酸/苏氨酸激酶,可调节有丝分裂中的关键事件,这使其成为定制抗癌治疗的一个有吸引力的靶点。许多报告阐述了AURKB在肿瘤形成和癌症中的作用;然而,以前没有研究表明其在器官发育过程中的作用。我们之前的实验强调了AURKB在成体外分泌腺再生过程中的基本需求。为了研究AURKB在胚胎发育过程中是否同样是发育进程所必需的,我们在胚胎第(E)13.5天和E16.5天,使用高效且选择性的药物巴瑞替尼,对发育中的下颌下腺(SMGs)进行AURKB的药理学抑制。抑制AURKB会干扰胚胎芽的扩展。有趣的是,当成熟外植体(E16.5)与另一种细胞周期抑制剂阿非迪霉素孵育24小时时,也观察到了这种对SMG发育的影响。巴瑞替尼引发了细胞凋亡、DNA损伤和衰老,其标志物(分别为裂解的半胱天冬酶3、γH2AX、SA-βgal和p21)主要出现在发育中的芽中。除了因AURKB抑制导致上皮细胞的细胞周期和增殖减少外,巴瑞替尼治疗还导致活性氧(ROS)过度产生,从而导致腺泡分化标志物Mist1的下调。重要的是,抑制ROS能够挽救这种身份丧失,尽管AURKB缺失,但Mist1表达得以维持。总之,这些数据确定AURKB是支持胚胎发育和分化的关键分子,同时在器官发生过程中抑制衰老诱导信号。