Alveolar regeneration through a Krt8+ transitional stem cell state that persists in human lung fibrosis

肺泡再生是通过一种在人类肺纤维化中持续存在的Krt8+过渡干细胞状态实现的

阅读:5
作者:Maximilian Strunz # ,Lukas M Simon # ,Meshal Ansari ,Jaymin J Kathiriya ,Ilias Angelidis ,Christoph H Mayr ,George Tsidiridis ,Marius Lange ,Laura F Mattner ,Min Yee ,Paulina Ogar ,Arunima Sengupta ,Igor Kukhtevich ,Robert Schneider ,Zhongming Zhao ,Carola Voss ,Tobias Stoeger ,Jens H L Neumann ,Anne Hilgendorff ,Jürgen Behr ,Michael O'Reilly ,Mareike Lehmann ,Gerald Burgstaller ,Melanie Königshoff ,Harold A Chapman ,Fabian J Theis ,Herbert B Schiller

Abstract

The cell type specific sequences of transcriptional programs during lung regeneration have remained elusive. Using time-series single cell RNA-seq of the bleomycin lung injury model, we resolved transcriptional dynamics for 28 cell types. Trajectory modeling together with lineage tracing revealed that airway and alveolar stem cells converge on a unique Krt8 + transitional stem cell state during alveolar regeneration. These cells have squamous morphology, feature p53 and NFkB activation and display transcriptional features of cellular senescence. The Krt8+ state appears in several independent models of lung injury and persists in human lung fibrosis, creating a distinct cell-cell communication network with mesenchyme and macrophages during repair. We generated a model of gene regulatory programs leading to Krt8+ transitional cells and their terminal differentiation to alveolar type-1 cells. We propose that in lung fibrosis, perturbed molecular checkpoints on the way to terminal differentiation can cause aberrant persistence of regenerative intermediate stem cell states.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。