Abstract
AbstractInfertility is thought to be caused by genetic mutations and dysfunction in the cellular niche where spermatogenesis takes place. An understanding of the specialized cellular processes which drive spermatogenesis is needed to develop treatments; however, the development of in vitro systems to study these cells has been hindered by our reliance on rarely available human testicular tissues for research. Human induced pluripotent stem cells (hiPSCs) can be used to derive human testicular-like cells, and thus provide an avenue for the development of in vitro testicular model systems. Therefore, this study set out to engineer a human testicular tissue model using hiPSCs for the first time. We demonstrate the ability of hiPSC-derived testicular cells to self-organize and mature into testicular-like tissues using organoid culture. Moreover, we show that hiPSC-derived testicular organoids promote testicular somatic cell maturation and spermatogenesis up to the post-meiotic spermatid stage. These hiPSC-derived testicular organoids have the potential to replace rarely available primary testicular tissues to further infertility research in an in vitro setting.
Publisher
Cold Spring Harbor Laboratory
Reference87 articles.
1. Chen H , Mruk D , Xiao X , Cheng CY . Human Spermatogenesis and Its Regulation. In: Winters SJ , Huhtaniemi IT , editors. Male Hypogonadism: Basic, Clinical and Therapeutic Principles. Cham: Springer International Publishing; 2017. p. 49–72.
2. The adult human testis transcriptional cell atlas
3. The Dynamic Transcriptional Cell Atlas of Testis Development during Human Puberty
4. Wu X , Lu M , Yun D , Gao S , Chen S , Hu L , et al. Single cell ATAC-Seq reveals cell type-specific transcriptional regulation and unique chromatin accessibility in human spermatogenesis. Hum Mol Genet. 2021.
5. The Mammalian Spermatogenesis Single-Cell Transcriptome, from Spermatogonial Stem Cells to Spermatids
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献