Dynamic Autophagy Map in Mouse Female Germ Cells Throughout the Fetal to Postnatal Life
Dynamic Autophagy Map in Mouse Female Germ Cells Throughout the Fetal to Postnatal Life
复制标题
DOI:
10.1007/s43032-022-00940-z
复制
发表时间:
2022-05
影响因子:
2.9
通讯作者:
Gurong Jiang;Li Zhang;Jiexiang Zhao;Lin Li;Zhenqin Huang;Zhijian Wang
中科院分区:
文献类型:
--
作者:
Gurong Jiang;Li Zhang;Jiexiang Zhao;Lin Li;Zhenqin Huang;Zhijian Wang
Autophagy plays vital roles in mouse female germ cells, but the potential mechanism is largely unknown. In this study, by interrogating single-cell RNA-seq dataset, we investigated the dynamic expression of autophagy-related genes in seven types of germ cells (mitosis, pre-leptotene, leptotene, zygotene, pachytene, diplotene, and dictyate) and discovered stage-specific autophagy-related genes. Using immunofluorescence (IF) and transmission electron microscopy (TEM), autophagy activity and autophagosome numbers were revealed from mitosis to follicular assembly (E12.5 (embryonic day 12.5) to P5 (postnatal day 5)). Furthermore, single-sample gene set enrichment analysis (ssGSEA) was performed to validate the autophagy kinetics from E12.5 to P5. Our study proved that the mitosis, diplotene, and dictyate female germ cells had relatively higher autophagy activity among the seven subtypes. In summary, our work provided an autophagy map, suggesting that autophagy was complicated in mouse female germ cell development from the fetal to postnatal life, which paved a new insight for deciphering the autophagy regulatory networks for cell-fate transition and female infertility issues like primary ovarian insufficiency (POI).