Skip to Main content Skip to Navigation
New interface
Journal articles

Single Cell Transcriptomics to Understand HSC Heterogeneity and Its Evolution upon Aging

Abstract : Single-cell transcriptomic technologies enable the uncovering and characterization of cellular heterogeneity and pave the way for studies aiming at understanding the origin and consequences of it. The hematopoietic system is in essence a very well adapted model system to benefit from this technological advance because it is characterized by different cellular states. Each cellular state, and its interconnection, may be defined by a specific location in the global transcriptional landscape sustained by a complex regulatory network. This transcriptomic signature is not fixed and evolved over time to give rise to less efficient hematopoietic stem cells (HSC), leading to a well-documented hematopoietic aging. Here, we review the advance of single-cell transcriptomic approaches for the understanding of HSC heterogeneity to grasp HSC deregulations upon aging. We also discuss the new bioinformatics tools developed for the analysis of the resulting large and complex datasets. Finally, since hematopoiesis is driven by fine-tuned and complex networks that must be interconnected to each other, we highlight how mathematical modeling is beneficial for doing such interconnection between multilayered information and to predict how HSC behave while aging.
Document type :
Journal articles
Complete list of metadata

https://hal-cnrs.archives-ouvertes.fr/hal-03854346
Contributor : Elisabeth Remy Connect in order to contact the contributor
Submitted on : Tuesday, November 15, 2022 - 5:29:49 PM
Last modification on : Wednesday, November 16, 2022 - 3:23:57 AM

Links full text

Identifiers

Collections

Citation

Léonard Hérault, Mathilde Poplineau, Elisabeth Remy, Estelle Duprez. Single Cell Transcriptomics to Understand HSC Heterogeneity and Its Evolution upon Aging. Cells, 2022, 11 (19), pp.3125. ⟨10.3390/cells11193125⟩. ⟨hal-03854346⟩

Share

Metrics

Record views

0