4.8 Article

Quantitative lineage analysis identifies a hepato-pancreato-biliary progenitor niche

Journal

NATURE
Volume 597, Issue 7874, Pages 87-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-021-03844-1

Keywords

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Funding

  1. MDC in the Helmholtz Association
  2. Helmholtz Association
  3. European Union [800981]
  4. BIH (Tr. PhD) fellowship
  5. EMBO Short-Term Fellowship [7853]

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Studies on single cells have shown significant heterogeneity in stem cell and progenitor compartments, highlighting continuous differentiation and plasticity during organogenesis. The hepato-pancreato-biliary system relies on a small endoderm progenitor compartment, leading to various adult tissues. The existence of cellular plasticity in this system is reflected in genetic syndromes and congenital malformations affecting the liver, pancreas, and gall bladder.
Studies based on single cells have revealed vast cellular heterogeneity in stem cell and progenitor compartments, suggesting continuous differentiation trajectories with intermixing of cells at various states of lineage commitment and notable degrees of plasticity during organogenesis(1-5). The hepato-pancreato-biliary organ system relies on a small endoderm progenitor compartment that gives rise to a variety of different adult tissues, including the liver, pancreas, gall bladder and extra-hepatic bile ducts(6,7). Experimental manipulation of various developmental signals in the mouse embryo has underscored important cellular plasticity in this embryonic territory(6). This is reflected in the existence of human genetic syndromes as well as congenital malformations featuring multi-organ phenotypes in liver, pancreas and gall bladder(6). Nevertheless, the precise lineage hierarchy and succession of events leading to the segregation of an endoderm progenitor compartment into hepatic, biliary and pancreatic structures have not yet been established. Here we combine computational modelling approaches with genetic lineage tracing to accurately reconstruct the hepato-pancreato-biliary lineage tree. We show that a multipotent progenitor subpopulation persists in the pancreato-biliary organ rudiment, contributing cells not only to the pancreas and gall bladder but also to the liver. Moreover, using single-cell RNA sequencing and functional experiments we define a specialized niche that supports this subpopulation in a multipotent state for an extended time during development. Together these findings indicate sustained plasticity underlying hepato-pancreato-biliary development that might also explain the rapid expansion of the liver while attenuating pancreato-biliary growth.

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