4.5 Review

Paligenosis: Cellular Remodeling During Tissue Repair

Journal

ANNUAL REVIEW OF PHYSIOLOGY
Volume 84, Issue -, Pages 461-483

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev-physiol-061121-035954

Keywords

dedifferentiation; regeneration; injury; metaplasia

Categories

Funding

  1. US Department of Defense, through the PRCRP [W81XWH-20-1-0630]
  2. US National Institutes of Health (NIH) [T32 DK007130-42]
  3. NIH [R21 AI156236]
  4. Digestive Disease Research Core Centers Pilot and Feasibility Grant [P30DK052574]
  5. Doris Duke Charitable Foundation Fund to Retain Clinical Scientists
  6. American Gastroenterological Association grant [AGA2021-5101]
  7. NIH National Cancer Institute grant [T32 CA009547]
  8. NIH National Cancer Institute [R01CA239645, R01CA246208]
  9. National Institute of Diabetes and Digestive and Kidney Diseases [R21 DK111369, R01DK094989, R01DK105129, R01DK110406]
  10. BETRNet [U54 CA163060]

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Multi-cellular organisms utilize cell plasticity rather than unidirectional differentiation to replenish cells, with mechanisms such as mature cells re-entering the cell cycle to regenerate damaged tissue. While plasticity benefits organisms, it also comes with potential oncogenic risks.
Complex multicellular organisms have evolved specific mechanisms to replenish cells in homeostasis and during repair. Here, we discuss how emerging technologies (e.g., single-cell RNA sequencing) challenge the concept that tissue renewal is fueled by unidirectional differentiation from a resident stem cell. We now understand that cell plasticity, i.e., cells adaptively changing differentiation state or identity, is a central tissue renewal mechanism. For example, mature cells can access an evolutionarily conserved program (paligenosis) to reenter the cell cycle and regenerate damaged tissue. Most tissues lack dedicated stem cells and rely on plasticity to regenerate lost cells. Plasticity benefits multicellular organisms, yet it also carries risks. For one, when long-lived cells undergo paligenotic, cyclical proliferation and redifferentiation, they can accumulate and propagate acquired mutations that activate oncogenes and increase the potential for developing cancer. Lastly, we propose a new framework for classifying patterns of cell proliferation in homeostasis and regeneration, with stem cells representing just one of the diverse methods that adult tissues employ.

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