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Mandible exosomal ssc-mir-133b regulates tooth development in miniature swine via endogenous apoptosis

机译:下颌骨外泌体ssc-mir-133b通过内源性凋亡调节小猪的牙齿发育

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摘要

Signal transduction between different organs is crucial in the normal development of the human body. As an important medium for signal communication, exosomes can transfer important information, such as microRNAs (miRNAs), from donors to receptors. MiRNAs are known to fine-tune a variety of biological processes, including maxillofacial development; however, the underlying mechanism remains largely unknown. In the present study, transient apoptosis was found to be due to the expression of a miniature swine maxillofacial-specific miRNA, ssc-mir-133b. Upregulation of ssc-mir-133b resulted in robust apoptosis in primary dental mesenchymal cells in the maxillofacial region. Cell leukemia myeloid 1 (Mcl-1) was verified as the functional target, which triggered further downstream activation of endogenous mitochondria-related apoptotic processes during tooth development. More importantly, mandible exosomes were responsible for the initial apoptosis signal. An animal study demonstrated that ectopic expression of ssc-mir-133b resulted in failed tooth formation after 12 weeks of subcutaneous transplantation in nude mice. The tooth germ developed abnormally without the indispensable exosomal signals from the mandible.
机译:不同器官之间的信号转导对于人体的正常发育至关重要。作为信号通讯的重要媒介,外泌体可以将重要的信息(例如microRNA(miRNA))从供体传递到受体。已知MiRNA可微调多种生物学过程,包括颌面发育。但是,其基本机制仍然未知。在本研究中,发现瞬时凋亡是由于微型猪颌面特异性miRNA ssc-mir-133b的表达所致。 ssc-mir-133b的上调在上颌面区域的原代牙齿间充质细胞中导致强大的凋亡。细胞白血病髓样1(Mcl-1)被证实是功能性靶标,它在牙齿发育过程中触发了内源性线粒体相关凋亡过程的进一步下游活化。更重要的是,下颌骨外泌体负责最初的细胞凋亡信号。一项动物研究表明,在裸鼠皮下移植12周后,异位表达ssc-mir-133b导致牙齿形成失败。没有下颌骨必不可少的外泌体信号,牙胚异常发育。

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