| Literature DB >> 33296684 |
Fumio Arai1, Patrick S Stumpf2, Yoshiko M Ikushima3, Kentaro Hosokawa4, Aline Roch5, Matthias P Lutolf5, Toshio Suda6, Ben D MacArthur7.
Abstract
Changes in stem cell activity may underpin aging. However, these changes are not completely understood. Here, we combined single-cell profiling with machine learning and in vivo functional studies to explore how hematopoietic stem cell (HSC) divisions patterns evolve with age. We first trained an artificial neural network (ANN) to accurately identify cell types in the hematopoietic hierarchy and predict their age from single-cell gene-expression patterns. We then used this ANN to compare identities of daughter cells immediately after HSC divisions and found that the self-renewal ability of individual HSCs declines with age. Furthermore, while HSC cell divisions are deterministic and intrinsically regulated in young and old age, they are variable and niche sensitive in mid-life. These results indicate that the balance between intrinsic and extrinsic regulation of stem cell activity alters substantially with age and help explain why stem cell numbers increase through life, yet regenerative potency declines.Entities:
Keywords: aging; artificial neural network; hematopoietic stem cell; machine learning; self-renewal
Year: 2020 PMID: 33296684 DOI: 10.1016/j.cels.2020.11.004
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304