Reprogramming cellular identity during intestinal regeneration
Research output: Contribution to journal › Review › peer-review
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Reprogramming cellular identity during intestinal regeneration. / Larsen, Hjalte L; Jensen, Kim B.
In: Current Opinion in Genetics & Development, Vol. 70, 2021, p. 40-47.Research output: Contribution to journal › Review › peer-review
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TY - JOUR
T1 - Reprogramming cellular identity during intestinal regeneration
AU - Larsen, Hjalte L
AU - Jensen, Kim B
N1 - Copyright © 2021 The Author(s). Published by Elsevier Ltd.. All rights reserved.
PY - 2021
Y1 - 2021
N2 - The intestine is a vital organ mediating absorption of nutrients and water. Following tissue damage, the intestine mounts a remarkable regenerative response by reprogramming cellular identity to facilitate reinstatement of homeostasis. Here we review recent advances within intestinal regenerative biology and the emerging concept of fetal-like reprogramming, in which the adult intestinal epithelium transiently enters a repair-associated state reminiscent of ontologically pre-existing stages. We focus on molecular mechanisms governing reprogramming of cellular identity via epithelial-mesenchymal crosstalk, and how novel approaches in organoid technologies enable identification and characterisation of cell-autonomous repair responses within epithelial cells. Transitioning from the single-cell level to tissue scale, we discuss clonal selection following regeneration and associated pathological repurcussions such as cancer and chronic inflammatory diseases.
AB - The intestine is a vital organ mediating absorption of nutrients and water. Following tissue damage, the intestine mounts a remarkable regenerative response by reprogramming cellular identity to facilitate reinstatement of homeostasis. Here we review recent advances within intestinal regenerative biology and the emerging concept of fetal-like reprogramming, in which the adult intestinal epithelium transiently enters a repair-associated state reminiscent of ontologically pre-existing stages. We focus on molecular mechanisms governing reprogramming of cellular identity via epithelial-mesenchymal crosstalk, and how novel approaches in organoid technologies enable identification and characterisation of cell-autonomous repair responses within epithelial cells. Transitioning from the single-cell level to tissue scale, we discuss clonal selection following regeneration and associated pathological repurcussions such as cancer and chronic inflammatory diseases.
U2 - 10.1016/j.gde.2021.05.005
DO - 10.1016/j.gde.2021.05.005
M3 - Review
C2 - 34062491
VL - 70
SP - 40
EP - 47
JO - Current Opinion in Genetics & Development
JF - Current Opinion in Genetics & Development
SN - 0959-437X
ER -
ID: 271536295