Integrin alpha11 is an Osteolectin receptor and is required for the maintenance of adult skeletal bone mass

We previously discovered a new osteogenic growth factor that is required to maintain adult skeletal bone mass, Osteolectin/Clec11a. Osteolectin acts on Leptin Receptor+ (LepR+) skeletal stem cells and other osteogenic progenitors in bone marrow to promote their differentiation into osteoblasts. Here...

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Main Authors: Bo Shen, Kristy Vardy, Payton Hughes, Alpaslan Tasdogan, Zhiyu Zhao, Rui Yue, Genevieve M Crane, Sean J Morrison
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2019-01-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/42274
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spelling doaj-11ece7aac9664addae25d57ca4079e312021-05-05T17:18:32ZengeLife Sciences Publications LtdeLife2050-084X2019-01-01810.7554/eLife.42274Integrin alpha11 is an Osteolectin receptor and is required for the maintenance of adult skeletal bone massBo Shen0https://orcid.org/0000-0002-5237-6144Kristy Vardy1Payton Hughes2Alpaslan Tasdogan3Zhiyu Zhao4https://orcid.org/0000-0001-6308-6997Rui Yue5Genevieve M Crane6https://orcid.org/0000-0001-9274-0214Sean J Morrison7https://orcid.org/0000-0003-1587-8329Children’s Research Institute, University of Texas Southwestern Medical Center, Dallas, United StatesChildren’s Research Institute, University of Texas Southwestern Medical Center, Dallas, United StatesChildren’s Research Institute, University of Texas Southwestern Medical Center, Dallas, United StatesChildren’s Research Institute, University of Texas Southwestern Medical Center, Dallas, United StatesChildren’s Research Institute, University of Texas Southwestern Medical Center, Dallas, United StatesInstitute of Regenerative Medicine, Shanghai East Hospital, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Sciences and Technology, Tongji University, Shanghai, ChinaChildren’s Research Institute, University of Texas Southwestern Medical Center, Dallas, United StatesChildren’s Research Institute, University of Texas Southwestern Medical Center, Dallas, United States; Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, United States; Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, United StatesWe previously discovered a new osteogenic growth factor that is required to maintain adult skeletal bone mass, Osteolectin/Clec11a. Osteolectin acts on Leptin Receptor+ (LepR+) skeletal stem cells and other osteogenic progenitors in bone marrow to promote their differentiation into osteoblasts. Here we identify a receptor for Osteolectin, integrin α11, which is expressed by LepR+ cells and osteoblasts. α11β1 integrin binds Osteolectin with nanomolar affinity and is required for the osteogenic response to Osteolectin. Deletion of Itga11 (which encodes α11) from mouse and human bone marrow stromal cells impaired osteogenic differentiation and blocked their response to Osteolectin. Like Osteolectin deficient mice, Lepr-cre; Itga11fl/fl mice appeared grossly normal but exhibited reduced osteogenesis and accelerated bone loss during adulthood. Osteolectin binding to α11β1 promoted Wnt pathway activation, which was necessary for the osteogenic response to Osteolectin. This reveals a new mechanism for maintenance of adult bone mass: Wnt pathway activation by Osteolectin/α11β1 signaling.https://elifesciences.org/articles/42274osteogenesisOsteolectinskeletal stem cellintegrinboneWnt signaling
collection DOAJ
language English
format Article
sources DOAJ
author Bo Shen
Kristy Vardy
Payton Hughes
Alpaslan Tasdogan
Zhiyu Zhao
Rui Yue
Genevieve M Crane
Sean J Morrison
spellingShingle Bo Shen
Kristy Vardy
Payton Hughes
Alpaslan Tasdogan
Zhiyu Zhao
Rui Yue
Genevieve M Crane
Sean J Morrison
Integrin alpha11 is an Osteolectin receptor and is required for the maintenance of adult skeletal bone mass
eLife
osteogenesis
Osteolectin
skeletal stem cell
integrin
bone
Wnt signaling
author_facet Bo Shen
Kristy Vardy
Payton Hughes
Alpaslan Tasdogan
Zhiyu Zhao
Rui Yue
Genevieve M Crane
Sean J Morrison
author_sort Bo Shen
title Integrin alpha11 is an Osteolectin receptor and is required for the maintenance of adult skeletal bone mass
title_short Integrin alpha11 is an Osteolectin receptor and is required for the maintenance of adult skeletal bone mass
title_full Integrin alpha11 is an Osteolectin receptor and is required for the maintenance of adult skeletal bone mass
title_fullStr Integrin alpha11 is an Osteolectin receptor and is required for the maintenance of adult skeletal bone mass
title_full_unstemmed Integrin alpha11 is an Osteolectin receptor and is required for the maintenance of adult skeletal bone mass
title_sort integrin alpha11 is an osteolectin receptor and is required for the maintenance of adult skeletal bone mass
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2019-01-01
description We previously discovered a new osteogenic growth factor that is required to maintain adult skeletal bone mass, Osteolectin/Clec11a. Osteolectin acts on Leptin Receptor+ (LepR+) skeletal stem cells and other osteogenic progenitors in bone marrow to promote their differentiation into osteoblasts. Here we identify a receptor for Osteolectin, integrin α11, which is expressed by LepR+ cells and osteoblasts. α11β1 integrin binds Osteolectin with nanomolar affinity and is required for the osteogenic response to Osteolectin. Deletion of Itga11 (which encodes α11) from mouse and human bone marrow stromal cells impaired osteogenic differentiation and blocked their response to Osteolectin. Like Osteolectin deficient mice, Lepr-cre; Itga11fl/fl mice appeared grossly normal but exhibited reduced osteogenesis and accelerated bone loss during adulthood. Osteolectin binding to α11β1 promoted Wnt pathway activation, which was necessary for the osteogenic response to Osteolectin. This reveals a new mechanism for maintenance of adult bone mass: Wnt pathway activation by Osteolectin/α11β1 signaling.
topic osteogenesis
Osteolectin
skeletal stem cell
integrin
bone
Wnt signaling
url https://elifesciences.org/articles/42274
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