Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Oct 15;149(20):dev201070.
doi: 10.1242/dev.201070. Epub 2022 Oct 11.

Lessons from early life: understanding development to expand stem cells and treat cancers

Fiona M Bain  1 , James L C Che  1 , Maria Jassinskaja  1 , David G Kent  1
Affiliations
Review

Lessons from early life: understanding development to expand stem cells and treat cancers

Fiona M Bain et al. Development. .

Abstract

Haematopoietic stem cell (HSC) self-renewal is a process that is essential for the development and homeostasis of the blood system. Self-renewal expansion divisions, which create two daughter HSCs from a single parent HSC, can be harnessed to create large numbers of HSCs for a wide range of cell and gene therapies, but the same process is also a driver of the abnormal expansion of HSCs in diseases such as cancer. Although HSCs are first produced during early embryonic development, the key stage and location where they undergo maximal expansion is in the foetal liver, making this tissue a rich source of data for deciphering the molecules driving HSC self-renewal. Another equally interesting stage occurs post-birth, several weeks after HSCs have migrated to the bone marrow, when HSCs undergo a developmental switch and adopt a more dormant state. Characterising these transition points during development is key, both for understanding the evolution of haematological malignancies and for developing methods to promote HSC expansion. In this Spotlight article, we provide an overview of some of the key insights that studying HSC development have brought to the fields of HSC expansion and translational medicine, many of which set the stage for the next big breakthroughs in the field.

Keywords: HSC; Haematopoiesis; Stem cells.

PubMed Disclaimer

Conflict of interest statement

Competing interests The authors declare no competing or financial interests.

Figures

Fig. 1.
Fig. 1.
Regulation of HSC self-renewal during life. During development, particularly in the foetal liver, HSC self-renewal expansion divisions occur in order to produce HSCs to sustain lifelong haematopoiesis. Postnatally, at approximately 3-4 weeks of age in mice, this self-renewal expansion is suppressed (represented by the blue blanket) as HSCs transition to a largely quiescent population. The loss of this suppression of proliferation can result in the aberrant accumulation of immature HSC-like cells (e.g. in leukaemia), but may also be harnessed to expand HSCs transiently outside the body for clinical utility.
See this image and copyright information in PMC

References

    1. Adamo, L., Naveiras, O., Wenzel, P. L., Mckinney-Freeman, S., Mack, P. J., Gracia-Sancho, J., Suchy-Dicey, A., Yoshimoto, M., Lensch, M. W., Yoder, M. C.et al. (2009). Biomechanical forces promote embryonic haematopoiesis. Nature 459, 1131-1135. 10.1038/nature08073 - DOI - PMC - PubMed
    1. Audet, J., Zandstra, P. W., Eaves, C. J. and Piret, J. M. (1998). Advances in hematopoietic stem cell culture. Curr. Opin. Biotechnol. 9, 146-151. 10.1016/S0958-1669(98)80107-9 - DOI - PubMed
    1. Audet, J., miller, C. L., Rose-John, S., Piret, J. M. and Eaves, C. J. (2001). Distinct role of gp130 activation in promoting self-renewal divisions by mitogenically stimulated murine hematopoietic stem cells. Proc. Natl. Acad. Sci. USA 98, 1757-1762. 10.1073/pnas.98.4.1757 - DOI - PMC - PubMed
    1. Audet, J., Miller, C. L., Eaves, C. J. and Piret, J. M. (2002). Common and distinct features of cytokine effects on hematopoietic stem and progenitor cells revealed by dose-response surface analysis. Biotechnol. Bioeng. 80, 393-404. 10.1002/bit.10399 - DOI - PubMed
    1. Azzoni, E., Frontera, V., Anselmi, G., Rode, C., James, C., Deltcheva, E. M., Demian, A. S., Brown, J., Barone, C., Patelli, A.et al. (2021). The onset of circulation triggers a metabolic switch required for endothelial to hematopoietic transition. Cell Rep. 37, 110103. 10.1016/j.celrep.2021.110103 - DOI - PMC - PubMed

Publication types