Ma Kexue, Zhang Yumei, Song Gege, Wu Meng, Chen Guangwen
College of Life Sciences, Henan Normal University, Xinxiang, China.
Front Physiol. 2018 Sep 4;9:1223. doi: 10.3389/fphys.2018.01223. eCollection 2018.
Planarians undergo continuous body size remodeling under starvation or during regeneration. This process likely involves autophagy and autophagic cell death, but this hypothesis is supported by few studies. To test this hypothesis, we cloned and characterized autophagy-related gene 7 () from the planarian (). The full-length cDNA of measures 2272 bp and includes a 2082-bp open reading frame encoding 693 amino acids with a molecular weight of 79.06 kDa. The deduced amino acid sequence of contains a conserved ATP-binding site and a catalytic active site of an E1-like enzyme belonging to the ATG7 superfamily. transcripts are mainly expressed in intestinal tissues of the intact animals. After amputation, was highly expressed at the newly regenerated intestinal branch on days 3-7 of regeneration and in the old tissue of the distal intestinal branch on day 10 of regeneration. However, knockdown of by RNAi did not affect planarian regeneration and did not block autophagosome formation, which indicates that autophagy is more complex than previously expected. Interestingly, TEM clearly confirmed that autophagy and autophagic cell death occurred in the old tissues of the newly regenerated planarians and clearly revealed that the dying cell released vesicles containing cellular cytoplasmic contents into the extracellular space. Therefore, the autophagy and autophagic cell death that occurred in the old tissue not only met the demand for body remodeling but also met the demand for energy supply during planarian regeneration. Collectively, our work contributes to the understanding of autophagy and autophagic cell death in planarian regeneration and body remodeling.
涡虫在饥饿或再生过程中会持续进行体型重塑。这一过程可能涉及自噬和自噬性细胞死亡,但这一假说仅得到了少数研究的支持。为了验证这一假说,我们从真涡虫中克隆并鉴定了自噬相关基因7()。的全长cDNA为2272 bp,包含一个2082 bp的开放阅读框,编码693个氨基酸,分子量为79.06 kDa。推导的氨基酸序列包含一个保守的ATP结合位点和一个属于ATG7超家族的E1样酶的催化活性位点。转录本主要在完整动物的肠道组织中表达。截肢后,在再生第3 - 7天新再生的肠分支以及再生第10天远端肠分支的旧组织中高表达。然而,通过RNA干扰敲低并没有影响涡虫的再生,也没有阻止自噬体的形成,这表明自噬比之前预期的更为复杂。有趣的是,透射电子显微镜清楚地证实了自噬和自噬性细胞死亡发生在新再生涡虫的旧组织中,并且清楚地显示垂死细胞将含有细胞质内容物的囊泡释放到细胞外空间。因此,旧组织中发生的自噬和自噬性细胞死亡不仅满足了体型重塑的需求,也满足了涡虫再生过程中的能量供应需求。总的来说,我们的工作有助于理解涡虫再生和体型重塑过程中的自噬和自噬性细胞死亡。