Modeling dynamics and function of bone marrow cells in mouse liver regeneration

Pedone, Elisa, 1985-; Olteanu, Vlad Aris; Marucci, Lucia; Muñoz-Martin, Maria Isabel; Youssef, Sameh A.; de Bruin, Alain; Cosma, Maria Pia, 1970-

doi:http://dx.doi.org/10.1016/j.celrep.2016.12.008

Modeling dynamics and function of bone marrow cells in mouse liver regeneration

License

Citation

Pedone E, Olteanu V, Marucci L, Muñoz-Martin MI, Youssef SA, de Bruin A et al. Modeling Dynamics and Function of Bone Marrow Cells in Mouse Liver Regeneration. Cell Reports. 2017 Jan;18(1):107-21. DOI: 10.1016/j.celrep.2016.12.008

Abstract

In rodents and humans, the liver can efficiently restore its mass after hepatectomy. This is largely attributed to the proliferation and cell cycle re-entry of hepatocytes. On the other hand, bone marrow cells (BMCs) migrate into the liver after resection. Here, we find that a block of BMC recruitment into the liver severely impairs its regeneration after the surgery. Mobilized hematopoietic stem and progenitor cells (HSPCs) in the resected liver can fuse with hepatocytes, and the hybrids proliferate earlier than the hepatocytes. Genetic ablation of the hybrids severely impairs hepatocyte proliferation and liver mass regeneration. Mathematical modeling reveals a key role of bone marrow (BM)-derived hybrids to drive proliferation in the regeneration process, and predicts regeneration efficiency in experimentally non-testable conditions. In conclusion, BM-derived hybrids are essential to trigger efficient liver regeneration after hepatectomy.