Defining relative cell cycle lengths in mixed cell populations

Defining relative cell cycle lengths in mixed cell populations

Defining relative cell cycle lengths in mixed cell populations


Brian DeVeale

University of Windsor


FUNDER: Katelyn Bedard Bone Marrow Association (KBBMA)

DURATION: 2023-2024

Related Programs:
Nucleus Cores:

Mammalian development from a single-cell zygote requires extensive cell division, differentiation, and morphogenesis. Coordination between cell division and differentiation is cirital for both embryogenesis and adult homeostasis, and severence of this coordination causes many types of cancer. Despite division kinetics being a fundamental aspect of cell biology, the relative cell cycle lengths of distinct cell types during development and homeostasis remain largely unknown. By using population kinetics (POPKIN) and focusing on cell cycle regulation during development and homeostasis, and tumorigensis, this will increase the understanding of hematopoietic stem cells (HSCs) and their development for regenerative medicine and population dynamics within tumours. 

The exploration of POPKIN offers a direct means to compare the proliferation dynamics of the entire HSC compartment while offering a readout of the expression changes assocaited with altered proliferation dynamics. 
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