TY - JOUR
T1 - The biophysical property of the limbal niche maintains stemness through YAP
AU - Bhattacharya, Swarnabh
AU - Mukherjee, Abhishek
AU - Pisano, Sabrina
AU - Dimri, Shalini
AU - Knaane, Eman
AU - Altshuler, Anna
AU - Nasser, Waseem
AU - Dey, Sunanda
AU - Shi, Lidan
AU - Mizrahi, Ido
AU - Blum, Noam
AU - Jokel, Ophir
AU - Amitai-Lange, Aya
AU - Kaganovsky, Anna
AU - Mimouni, Michael
AU - Socea, Sergiu
AU - Midlij, Mohamad
AU - Tiosano, Beatrice
AU - Hasson, Peleg
AU - Feral, Chloe
AU - Wolfenson, Haguy
AU - Shalom-Feuerstein, Ruby
N1 - © 2023. The Author(s).
PY - 2023/4/24
Y1 - 2023/4/24
N2 - The cell fate decisions of stem cells (SCs) largely depend on signals from their microenvironment (niche). However, very little is known about how biochemical niche cues control cell behavior in vivo. To address this question, we focused on the corneal epithelial SC model in which the SC niche, known as the limbus, is spatially segregated from the differentiation compartment. We report that the unique biomechanical property of the limbus supports the nuclear localization and function of Yes-associated protein (YAP), a putative mediator of the mechanotransduction pathway. Perturbation of tissue stiffness or YAP activity affects SC function as well as tissue integrity under homeostasis and significantly inhibited the regeneration of the SC population following SC depletion. In vitro experiments revealed that substrates with the rigidity of the corneal differentiation compartment inhibit nuclear YAP localization and induce differentiation, a mechanism that is mediated by the TGFβ−SMAD2/3 pathway. Taken together, these results indicate that SC sense biomechanical niche signals and that manipulation of mechano-sensory machinery or its downstream biochemical output may bear fruits in SC expansion for regenerative therapy.
AB - The cell fate decisions of stem cells (SCs) largely depend on signals from their microenvironment (niche). However, very little is known about how biochemical niche cues control cell behavior in vivo. To address this question, we focused on the corneal epithelial SC model in which the SC niche, known as the limbus, is spatially segregated from the differentiation compartment. We report that the unique biomechanical property of the limbus supports the nuclear localization and function of Yes-associated protein (YAP), a putative mediator of the mechanotransduction pathway. Perturbation of tissue stiffness or YAP activity affects SC function as well as tissue integrity under homeostasis and significantly inhibited the regeneration of the SC population following SC depletion. In vitro experiments revealed that substrates with the rigidity of the corneal differentiation compartment inhibit nuclear YAP localization and induce differentiation, a mechanism that is mediated by the TGFβ−SMAD2/3 pathway. Taken together, these results indicate that SC sense biomechanical niche signals and that manipulation of mechano-sensory machinery or its downstream biochemical output may bear fruits in SC expansion for regenerative therapy.
KW - Cell Differentiation
KW - Epithelium, Corneal/metabolism
KW - Limbus Corneae
KW - Mechanotransduction, Cellular
KW - Stem Cell Niche
KW - Stem Cells/metabolism
KW - Humans
KW - YAP-Signaling Proteins/metabolism
UR - http://www.scopus.com/inward/record.url?scp=85153344477&partnerID=8YFLogxK
U2 - 10.1038/s41418-023-01156-7
DO - 10.1038/s41418-023-01156-7
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C2 - 37095157
AN - SCOPUS:85153344477
SN - 1350-9047
VL - 30
SP - 1601
EP - 1614
JO - Cell Death and Differentiation
JF - Cell Death and Differentiation
IS - 6
ER -