Bagci H, Laurin M, Huber J, Muller W J, Côté J-F
1] Institut de Recherches Cliniques de Montréal (IRCM), Montréal, QC, Canada [2] Department of Anatomy and Cell Biology, McGill University, Montréal, QC, Canada.
Institut de Recherches Cliniques de Montréal (IRCM), Montréal, QC, Canada.
Cell Death Dis. 2014 Aug 14;5(8):e1375. doi: 10.1038/cddis.2014.338.
Throughout life, the tight equilibrium between cell death and the prompt clearance of dead corpses is required to maintain a proper tissue homeostasis and prevent inflammation. Following lactation, mammary gland involution is triggered and results in the death of excessive epithelial cells that are rapidly cleared by phagocytes to ensure that the gland returns to its prepregnant state. Orthologs of Dock1 (dedicator of cytokinesis 1), Elmo and Rac1 (ras-related C3 botulinum toxin substrate 1) in Caenorhabditis elegans are part of a signaling module in phagocytes that is linking apoptotic cell recognition to cytoskeletal reorganization required for engulfment. In mammals, Elmo1 was shown to interact with the phosphatidylserine receptor Bai1 and relay signals to promote phagocytosis of apoptotic cells. Still, the role of the RacGEF Dock1 in the clearance of dying cells in mammals was never directly addressed. We generated two mouse models with conditional inactivation of Dock1 and Rac1 and revealed that the expression of these genes is not essential in the mammary gland during puberty, pregnancy and lactation. We induced mammary gland involution in these mice to investigate the role of Dock1/Rac1 signaling in the engulfment of cell corpses. Unpredictably, activation of Stat3 (signal transducer and activator of transcription 3), a key regulator of mammary gland involution, was impaired in the absence of Rac1 and Dock1 expression. Likewise, failure to activate properly Stat3 was coinciding with a significant delay in the initiation and progression of mammary gland involution in mutant animals. By using an in vitro phagocytosis assay, we observed that Dock1 and Rac1 are essential to mediate engulfment in epithelial phagocytes. In vivo, cell corpses accumulated at late time points of involution in Dock1 and Rac1 mutant mammary glands. Overall, our study demonstrated an unsuspected role for Dock1/Rac1 signaling in the initiation of mammary gland involution, and also suggested a role for this pathway in the clearance of dead cells by epithelial phagocytes.
在整个生命过程中,细胞死亡与及时清除死亡尸体之间的紧密平衡对于维持适当的组织稳态和预防炎症至关重要。哺乳期结束后,乳腺 involution 被触发,导致过量上皮细胞死亡,这些细胞被吞噬细胞迅速清除,以确保腺体恢复到孕前状态。秀丽隐杆线虫中 Dock1(胞质分裂专用蛋白 1)、Elmo 和 Rac1(Ras 相关 C3 肉毒杆菌毒素底物 1)的直系同源物是吞噬细胞中信号模块的一部分,该模块将凋亡细胞识别与吞噬所需的细胞骨架重组联系起来。在哺乳动物中,Elmo1 被证明与磷脂酰丝氨酸受体 Bai1 相互作用,并传递信号以促进凋亡细胞的吞噬作用。然而,RacGEF Dock1 在哺乳动物中对死亡细胞清除的作用从未得到直接研究。我们构建了两个 Dock1 和 Rac1 条件性失活的小鼠模型,并发现这些基因的表达在青春期、怀孕期和哺乳期的乳腺中并非必需。我们在这些小鼠中诱导乳腺 involution,以研究 Dock1/Rac1 信号在细胞尸体吞噬中的作用。出乎意料的是,在缺乏 Rac1 和 Dock1 表达的情况下,乳腺 involution 的关键调节因子 Stat3(信号转导和转录激活因子 3)的激活受到损害。同样,无法正确激活 Stat3 与突变动物乳腺 involution 的起始和进展显著延迟同时发生。通过使用体外吞噬试验,我们观察到 Dock1 和 Rac1 对于介导上皮吞噬细胞中的吞噬作用至关重要。在体内,细胞尸体在 Dock1 和 Rac1 突变乳腺 involution 的后期时间点积累。总体而言,我们的研究证明了 Dock1/Rac1 信号在乳腺 involution 起始中具有意想不到的作用,并且还表明该途径在上皮吞噬细胞清除死亡细胞中发挥作用。