A Novel Osteogenic Cell Line That Differentiates Into GFP-Tagged Osteocytes and Forms Mineral With a Bone-Like Lacunocanalicular Structure.


Journal

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
ISSN: 1523-4681
Titre abrégé: J Bone Miner Res
Pays: United States
ID NLM: 8610640

Informations de publication

Date de publication:
06 2019
Historique:
received: 17 07 2018
revised: 15 02 2019
accepted: 22 02 2019
pubmed: 19 3 2019
medline: 7 8 2020
entrez: 19 3 2019
Statut: ppublish

Résumé

Osteocytes, the most abundant cells in bone, were once thought to be inactive, but are now known to have multifunctional roles in bone, including in mechanotransduction, regulation of osteoblast and osteoclast function and phosphate homeostasis. Because osteocytes are embedded in a mineralized matrix and are challenging to study, there is a need for new tools and cell models to understand their biology. We have generated two clonal osteogenic cell lines, OmGFP66 and OmGFP10, by immortalization of primary bone cells from mice expressing a membrane-targeted GFP driven by the Dmp1-promoter. One of these clones, OmGFP66, has unique properties compared with previous osteogenic and osteocyte cell models and forms 3-dimensional mineralized bone-like structures, containing highly dendritic GFP-positive osteocytes, embedded in clearly defined lacunae. Confocal and electron microscopy showed that structurally and morphologically, these bone-like structures resemble bone in vivo, even mimicking the lacunocanalicular ultrastructure and 3D spacing of in vivo osteocytes. In osteogenic conditions, OmGFP66 cells express alkaline phosphatase (ALP), produce a mineralized type I collagen matrix, and constitutively express the early osteocyte marker, E11/gp38. With differentiation they express osteocyte markers, Dmp1, Phex, Mepe, Fgf23, and the mature osteocyte marker, Sost. They also express RankL, Opg, and Hif1α, and show expected osteocyte responses to PTH, including downregulation of Sost, Dmp1, and Opg and upregulation of RankL and E11/gp38. Live cell imaging revealed the dynamic process by which OmGFP66 bone-like structures form, the motile properties of embedding osteocytes and the integration of osteocyte differentiation with mineralization. The OmGFP10 clone showed an osteocyte gene expression profile similar to OmGFP66, but formed less organized bone nodule-like mineral, similar to other osteogenic cell models. Not only do these cell lines provide useful new tools for mechanistic and dynamic studies of osteocyte differentiation, function, and biomineralization, but OmGFP66 cells have the unique property of modeling osteocytes in their natural bone microenvironment. © 2019 American Society for Bone and Mineral Research.

Identifiants

pubmed: 30882939
doi: 10.1002/jbmr.3720
pmc: PMC7350928
mid: NIHMS1587736
doi:

Substances chimiques

Biomarkers 0
Dmp1 protein, mouse 0
Extracellular Matrix Proteins 0
Fgf23 protein, mouse 0
Minerals 0
Parathyroid Hormone 0
Green Fluorescent Proteins 147336-22-9
Fibroblast Growth Factor-23 7Q7P4S7RRE

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

979-995

Subventions

Organisme : NIH HHS
ID : S10 OD021665
Pays : United States
Organisme : NCRR NIH HHS
ID : S10 RR027668
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG039355
Pays : United States
Organisme : NIH/Shared Instrumentation Program
ID : S10-RR027668
Pays : International
Organisme : NIH/NIAMS
ID : R21-AR071563
Pays : International
Organisme : NIAMS NIH HHS
ID : R21 AR071563
Pays : United States
Organisme : NIH/NIA
ID : P01-AG039355
Pays : International
Organisme : NIH/Shared Instrumentation Program
ID : S10-OD021665
Pays : International
Organisme : NIH/NIAMS
ID : R21- AR054449
Pays : International
Organisme : NIAMS NIH HHS
ID : R21 AR054449
Pays : United States

Informations de copyright

© 2019 American Society for Bone and Mineral Research.

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Auteurs

Kun Wang (K)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.

Lisa Le (L)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.

Brad M Chun (BM)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.

LeAnn M Tiede-Lewis (LM)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.

Lora A Shiflett (LA)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.

Matthew Prideaux (M)

Department of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.

Richard S Campos (RS)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.

Patricia A Veno (PA)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.

Yixia Xie (Y)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.

Vladimir Dusevich (V)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.

Lynda F Bonewald (LF)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.
Department of Anatomy and Cell Biology, School of Medicine, Indiana University, Indianapolis, IN, USA.
Department of Orthopaedic Surgery, Indiana University, Indianapolis, IN, USA.

Sarah L Dallas (SL)

Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri, Kansas City, Kansas City, MO, USA.

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