Abstract

The basal cell compartment in many epithelial tissues is generally believed to serve as an important pool of stem cells. However, basal cells are heterogenous and the stem cell subpopulation within basal cells is not well elucidated. Here we uncover that the core epithelial-to-mesenchymal transition (EMT) inducer Zeb1 is expressed in a prostate basal cell subpopulation. The Zeb1+ prostate epithelial cells are multipotent prostate basal stem cells (PBSCs) that can self-renew and generate functional prostatic glandular structures at the single-cell level. Genetic ablation studies reveal an indispensable role for Zeb1 in prostate basal cell development. Utilizing unbiased single-cell transcriptomic analysis of over 9000 mouse prostate basal cells, we confirm the existence of the Zeb1+ basal cell subset. Moreover, Zeb1+ epithelial cells can be detected in mouse and human prostate tumors. Identification of the PBSC and its transcriptome profile is crucial to advance our understanding of prostate development and tumorigenesis.

Heterogeneous populations of basal cells in the prostate epithelium contain stem cells. Here the authors show that Zeb1 marks a pool of prostate epithelial stem cells that self-renew, generate prostate glandular structures with all 3 epithelial cell types and are required for prostate basal cell development.

Details

Title
Identification of a Zeb1 expressing basal stem cell subpopulation in the prostate
Author
Wang, Xue 1 ; Xu, Haibo 2 ; Cheng Chaping 1 ; Ji Zhongzhong 1   VIAFID ORCID Logo  ; Zhao, Huifang 3 ; Sheng Yaru 3 ; Li, Xiaoxia 3 ; Wang, Jinming 3 ; Yu, Shu 3 ; He Yuman 3 ; Fan Liancheng 4 ; Dong Baijun 4   VIAFID ORCID Logo  ; Xue, Wei 4 ; Wai Chua Chee 5   VIAFID ORCID Logo  ; Wu, Dongdong 6   VIAFID ORCID Logo  ; Wei-Qiang, Gao 1 ; He, Zhu Helen 5   VIAFID ORCID Logo 

 Shanghai Jiao Tong University, State Key Laboratory of Oncogenes and Related Genes, Renji-Med-X Stem Cell Research Center, Department of Urology, Ren Ji Hospital, School of Medicine and School of Biomedical Engineering, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293); Shanghai Jiao Tong University, Med-X Research Institute, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293) 
 Kunming Institute of Sciences, State Key Laboratory of Genetic Resources and Evolution, Kunming, China (GRID:grid.16821.3c); University of Chinese Academy of Sciences, Beijing, China (GRID:grid.410726.6) (ISNI:0000 0004 1797 8419) 
 Shanghai Jiao Tong University, State Key Laboratory of Oncogenes and Related Genes, Renji-Med-X Stem Cell Research Center, Department of Urology, Ren Ji Hospital, School of Medicine and School of Biomedical Engineering, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293) 
 Shanghai Jiao Tong University, Department of Urology, Ren Ji Hospital, School of Medicine, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293) 
 Shanghai Jiao Tong University, State Key Laboratory of Oncogenes and Related Genes, Renji-Med-X Stem Cell Research Center, Department of Urology, Ren Ji Hospital, School of Medicine and School of Biomedical Engineering, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293); Shanghai Jiao Tong University, Department of Urology, Ren Ji Hospital, School of Medicine, Shanghai, China (GRID:grid.16821.3c) (ISNI:0000 0004 0368 8293) 
 Kunming Institute of Sciences, State Key Laboratory of Genetic Resources and Evolution, Kunming, China (GRID:grid.16821.3c) 
Publication year
2020
Publication date
2020
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2351473214
Copyright
This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.