Reciprocal interaction between mesenchymal stem cells and transit amplifying cells regulates tissue homeostasis

Interaction between adult stem cells and their progeny is critical for tissue homeostasis and regeneration. In multiple organs, mesenchymal stem cells (MSCs) give rise to transit amplifying cells (TACs), which then differentiate into different cell types. However, whether and how MSCs interact with...

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Main Authors: Junjun Jing, Jifan Feng, Jingyuan Li, Hu Zhao, Thach-Vu Ho, Jinzhi He, Yuan Yuan, Tingwei Guo, Jiahui Du, Mark Urata, Paul Sharpe, Yang Chai
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-01-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/59459
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spelling doaj-6ecedfbb88b84e7d8b68adbdbd3b054f2021-05-05T22:42:40ZengeLife Sciences Publications LtdeLife2050-084X2021-01-011010.7554/eLife.59459Reciprocal interaction between mesenchymal stem cells and transit amplifying cells regulates tissue homeostasisJunjun Jing0https://orcid.org/0000-0001-5745-5207Jifan Feng1Jingyuan Li2Hu Zhao3Thach-Vu Ho4https://orcid.org/0000-0001-6293-4739Jinzhi He5Yuan Yuan6Tingwei Guo7Jiahui Du8Mark Urata9Paul Sharpe10https://orcid.org/0000-0003-2116-9561Yang Chai11https://orcid.org/0000-0003-2477-7247Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United States; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Chengdu, ChinaCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United StatesCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United StatesCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United StatesCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United StatesCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United States; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Chengdu, ChinaCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United StatesCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United StatesCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United StatesCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United StatesDepartment of Craniofacial Development and Stem Cell Biology, Dental Institute, Kings College London, London, United KingdomCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, United StatesInteraction between adult stem cells and their progeny is critical for tissue homeostasis and regeneration. In multiple organs, mesenchymal stem cells (MSCs) give rise to transit amplifying cells (TACs), which then differentiate into different cell types. However, whether and how MSCs interact with TACs remains unknown. Using the adult mouse incisor as a model, we present in vivo evidence that TACs and MSCs have distinct genetic programs and engage in reciprocal signaling cross talk to maintain tissue homeostasis. Specifically, an IGF-WNT signaling cascade is involved in the feedforward from MSCs to TACs. TACs are regulated by tissue-autonomous canonical WNT signaling and can feedback to MSCs and regulate MSC maintenance via Wnt5a/Ror2-mediated non-canonical WNT signaling. Collectively, these findings highlight the importance of coordinated bidirectional signaling interaction between MSCs and TACs in instructing mesenchymal tissue homeostasis, and the mechanisms identified here have important implications for MSC–TAC interaction in other organs.https://elifesciences.org/articles/59459mesenchymal stem celltissue homeostasisincisor
collection DOAJ
language English
format Article
sources DOAJ
author Junjun Jing
Jifan Feng
Jingyuan Li
Hu Zhao
Thach-Vu Ho
Jinzhi He
Yuan Yuan
Tingwei Guo
Jiahui Du
Mark Urata
Paul Sharpe
Yang Chai
spellingShingle Junjun Jing
Jifan Feng
Jingyuan Li
Hu Zhao
Thach-Vu Ho
Jinzhi He
Yuan Yuan
Tingwei Guo
Jiahui Du
Mark Urata
Paul Sharpe
Yang Chai
Reciprocal interaction between mesenchymal stem cells and transit amplifying cells regulates tissue homeostasis
eLife
mesenchymal stem cell
tissue homeostasis
incisor
author_facet Junjun Jing
Jifan Feng
Jingyuan Li
Hu Zhao
Thach-Vu Ho
Jinzhi He
Yuan Yuan
Tingwei Guo
Jiahui Du
Mark Urata
Paul Sharpe
Yang Chai
author_sort Junjun Jing
title Reciprocal interaction between mesenchymal stem cells and transit amplifying cells regulates tissue homeostasis
title_short Reciprocal interaction between mesenchymal stem cells and transit amplifying cells regulates tissue homeostasis
title_full Reciprocal interaction between mesenchymal stem cells and transit amplifying cells regulates tissue homeostasis
title_fullStr Reciprocal interaction between mesenchymal stem cells and transit amplifying cells regulates tissue homeostasis
title_full_unstemmed Reciprocal interaction between mesenchymal stem cells and transit amplifying cells regulates tissue homeostasis
title_sort reciprocal interaction between mesenchymal stem cells and transit amplifying cells regulates tissue homeostasis
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2021-01-01
description Interaction between adult stem cells and their progeny is critical for tissue homeostasis and regeneration. In multiple organs, mesenchymal stem cells (MSCs) give rise to transit amplifying cells (TACs), which then differentiate into different cell types. However, whether and how MSCs interact with TACs remains unknown. Using the adult mouse incisor as a model, we present in vivo evidence that TACs and MSCs have distinct genetic programs and engage in reciprocal signaling cross talk to maintain tissue homeostasis. Specifically, an IGF-WNT signaling cascade is involved in the feedforward from MSCs to TACs. TACs are regulated by tissue-autonomous canonical WNT signaling and can feedback to MSCs and regulate MSC maintenance via Wnt5a/Ror2-mediated non-canonical WNT signaling. Collectively, these findings highlight the importance of coordinated bidirectional signaling interaction between MSCs and TACs in instructing mesenchymal tissue homeostasis, and the mechanisms identified here have important implications for MSC–TAC interaction in other organs.
topic mesenchymal stem cell
tissue homeostasis
incisor
url https://elifesciences.org/articles/59459
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