Microenvironmental Regulation of Chondrocyte Plasticity in Endochondral Repair—A New Frontier for Developmental Engineering

The majority of fractures heal through the process of endochondral ossification, in which a cartilage intermediate forms between the fractured bone ends and is gradually replaced with bone. Recent studies have provided genetic evidence demonstrating that a significant portion of callus chondrocytes...

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Main Authors: Sarah A. Wong, Kevin O. Rivera, Theodore Miclau, Eben Alsberg, Ralph S. Marcucio, Chelsea S. Bahney
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-05-01
Series:Frontiers in Bioengineering and Biotechnology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fbioe.2018.00058/full
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spelling doaj-201655a593eb4d48ad1a48c1b72e5c302020-11-24T21:29:17ZengFrontiers Media S.A.Frontiers in Bioengineering and Biotechnology2296-41852018-05-01610.3389/fbioe.2018.00058358233Microenvironmental Regulation of Chondrocyte Plasticity in Endochondral Repair—A New Frontier for Developmental EngineeringSarah A. Wong0Sarah A. Wong1Kevin O. Rivera2Kevin O. Rivera3Theodore Miclau4Eben Alsberg5Ralph S. Marcucio6Ralph S. Marcucio7Chelsea S. Bahney8Department of Orthopaedic Surgery, Orthopaedic Trauma Institute, University of California, San Francisco, San Francisco, CA, United StatesSchool of Dentistry, University of California, San Francisco, San Francisco, CA, United StatesDepartment of Orthopaedic Surgery, Orthopaedic Trauma Institute, University of California, San Francisco, San Francisco, CA, United StatesSchool of Dentistry, University of California, San Francisco, San Francisco, CA, United StatesDepartment of Orthopaedic Surgery, Orthopaedic Trauma Institute, University of California, San Francisco, San Francisco, CA, United StatesDepartment of Orthopaedic Surgery and Biomedical Engineering, Case Western Reserve University, Cleveland, OH, United StatesDepartment of Orthopaedic Surgery, Orthopaedic Trauma Institute, University of California, San Francisco, San Francisco, CA, United StatesSchool of Dentistry, University of California, San Francisco, San Francisco, CA, United StatesDepartment of Orthopaedic Surgery, Orthopaedic Trauma Institute, University of California, San Francisco, San Francisco, CA, United StatesThe majority of fractures heal through the process of endochondral ossification, in which a cartilage intermediate forms between the fractured bone ends and is gradually replaced with bone. Recent studies have provided genetic evidence demonstrating that a significant portion of callus chondrocytes transform into osteoblasts that derive the new bone. This evidence has opened a new field of research aimed at identifying the regulatory mechanisms that govern chondrocyte transformation in the hope of developing improved fracture therapies. In this article, we review known and candidate molecular pathways that may stimulate chondrocyte-to-osteoblast transformation during endochondral fracture repair. We also examine additional extrinsic factors that may play a role in modulating chondrocyte and osteoblast fate during fracture healing such as angiogenesis and mineralization of the extracellular matrix. Taken together the mechanisms reviewed here demonstrate the promising potential of using developmental engineering to design therapeutic approaches that activate endogenous healing pathways to stimulate fracture repair.http://journal.frontiersin.org/article/10.3389/fbioe.2018.00058/fullfractureendochondral ossificationchondrocyte fatedevelopmental engineeringtransdifferentiation
collection DOAJ
language English
format Article
sources DOAJ
author Sarah A. Wong
Sarah A. Wong
Kevin O. Rivera
Kevin O. Rivera
Theodore Miclau
Eben Alsberg
Ralph S. Marcucio
Ralph S. Marcucio
Chelsea S. Bahney
spellingShingle Sarah A. Wong
Sarah A. Wong
Kevin O. Rivera
Kevin O. Rivera
Theodore Miclau
Eben Alsberg
Ralph S. Marcucio
Ralph S. Marcucio
Chelsea S. Bahney
Microenvironmental Regulation of Chondrocyte Plasticity in Endochondral Repair—A New Frontier for Developmental Engineering
Frontiers in Bioengineering and Biotechnology
fracture
endochondral ossification
chondrocyte fate
developmental engineering
transdifferentiation
author_facet Sarah A. Wong
Sarah A. Wong
Kevin O. Rivera
Kevin O. Rivera
Theodore Miclau
Eben Alsberg
Ralph S. Marcucio
Ralph S. Marcucio
Chelsea S. Bahney
author_sort Sarah A. Wong
title Microenvironmental Regulation of Chondrocyte Plasticity in Endochondral Repair—A New Frontier for Developmental Engineering
title_short Microenvironmental Regulation of Chondrocyte Plasticity in Endochondral Repair—A New Frontier for Developmental Engineering
title_full Microenvironmental Regulation of Chondrocyte Plasticity in Endochondral Repair—A New Frontier for Developmental Engineering
title_fullStr Microenvironmental Regulation of Chondrocyte Plasticity in Endochondral Repair—A New Frontier for Developmental Engineering
title_full_unstemmed Microenvironmental Regulation of Chondrocyte Plasticity in Endochondral Repair—A New Frontier for Developmental Engineering
title_sort microenvironmental regulation of chondrocyte plasticity in endochondral repair—a new frontier for developmental engineering
publisher Frontiers Media S.A.
series Frontiers in Bioengineering and Biotechnology
issn 2296-4185
publishDate 2018-05-01
description The majority of fractures heal through the process of endochondral ossification, in which a cartilage intermediate forms between the fractured bone ends and is gradually replaced with bone. Recent studies have provided genetic evidence demonstrating that a significant portion of callus chondrocytes transform into osteoblasts that derive the new bone. This evidence has opened a new field of research aimed at identifying the regulatory mechanisms that govern chondrocyte transformation in the hope of developing improved fracture therapies. In this article, we review known and candidate molecular pathways that may stimulate chondrocyte-to-osteoblast transformation during endochondral fracture repair. We also examine additional extrinsic factors that may play a role in modulating chondrocyte and osteoblast fate during fracture healing such as angiogenesis and mineralization of the extracellular matrix. Taken together the mechanisms reviewed here demonstrate the promising potential of using developmental engineering to design therapeutic approaches that activate endogenous healing pathways to stimulate fracture repair.
topic fracture
endochondral ossification
chondrocyte fate
developmental engineering
transdifferentiation
url http://journal.frontiersin.org/article/10.3389/fbioe.2018.00058/full
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