Extracellular calcium promotes bone formation from bone marrow mesenchymal stem cells by amplifying the effects of BMP-2 on SMAD signalling

Understanding the molecular events that regulate osteoblast differentiation is essential for the development of effective approaches to bone regeneration. In this study, we analysed the osteoinductive properties of extracellular calcium in bone marrow-derived mesenchymal stem cell (BM-MSC) different...

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Published in:PloS one Vol. 12; no. 5; p. e0178158
Main Authors: Aquino-Martínez, Rubén, Artigas, Natalia, Gámez, Beatriz, Rosa, José Luis, Ventura, Francesc
Format: Journal Article
Language:English
Published: United States Public Library of Science 25-05-2017
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Abstract Understanding the molecular events that regulate osteoblast differentiation is essential for the development of effective approaches to bone regeneration. In this study, we analysed the osteoinductive properties of extracellular calcium in bone marrow-derived mesenchymal stem cell (BM-MSC) differentiation. We cultured BM-MSCs in 3D gelatin scaffolds with Ca2+ and BMP-2 as osteoinductive agents. Early and late osteogenic gene expression and bone regeneration in a calvarial critical-size defect model demonstrate that extracellular Ca2+ enhances the effects of BMP-2 on Osteocalcin, Runx2 and Osterix expression and promotes bone regeneration in vivo. Moreover, we analysed the molecular mechanisms involved and observed an antagonistic effect between Ca2+ and BMP-2 on SMAD1/5, ERK and S6K signalling after 24 hours. More importantly, a cooperative effect between Ca2+ and BMP-2 on the phosphorylation of SMAD1/5, S6, GSK3 and total levels of β-CATENIN was observed at a later differentiation time (10 days). Furthermore, Ca2+ alone favoured the phosphorylation of SMAD1, which correlates with the induction of Bmp2 and Bmp4 gene expression. These data suggest that Ca2+ and BMP-2 cooperate and promote an autocrine/paracrine osteogenic feed-forward loop. On the whole, these results demonstrate the usefulness of calcium-based bone grafts or the addition of exogenous Ca2+ in bone tissue engineering.
AbstractList Understanding the molecular events that regulate osteoblast differentiation is essential for the development of effective approaches to bone regeneration. In this study, we analysed the osteoinductive properties of extracellular calcium in bone marrow-derived mesenchymal stem cell (BM-MSC) differentiation. We cultured BM-MSCs in 3D gelatin scaffolds with Ca 2+ and BMP-2 as osteoinductive agents. Early and late osteogenic gene expression and bone regeneration in a calvarial critical-size defect model demonstrate that extracellular Ca 2+ enhances the effects of BMP-2 on Osteocalcin , Runx2 and Osterix expression and promotes bone regeneration in vivo . Moreover, we analysed the molecular mechanisms involved and observed an antagonistic effect between Ca 2+ and BMP-2 on SMAD1/5, ERK and S6K signalling after 24 hours. More importantly, a cooperative effect between Ca 2+ and BMP-2 on the phosphorylation of SMAD1/5, S6, GSK3 and total levels of β-CATENIN was observed at a later differentiation time (10 days). Furthermore, Ca 2+ alone favoured the phosphorylation of SMAD1, which correlates with the induction of Bmp2 and Bmp4 gene expression. These data suggest that Ca 2+ and BMP-2 cooperate and promote an autocrine/paracrine osteogenic feed-forward loop. On the whole, these results demonstrate the usefulness of calcium-based bone grafts or the addition of exogenous Ca 2+ in bone tissue engineering.
Understanding the molecular events that regulate osteoblast differentiation is essential for the development of effective approaches to bone regeneration. In this study, we analysed the osteoinductive properties of extracellular calcium in bone marrow-derived mesenchymal stem cell (BM-MSC) differentiation. We cultured BM-MSCs in 3D gelatin scaffolds with Ca.sup.2+ and BMP-2 as osteoinductive agents. Early and late osteogenic gene expression and bone regeneration in a calvarial critical-size defect model demonstrate that extracellular Ca.sup.2+ enhances the effects of BMP-2 on Osteocalcin, Runx2 and Osterix expression and promotes bone regeneration in vivo. Moreover, we analysed the molecular mechanisms involved and observed an antagonistic effect between Ca.sup.2+ and BMP-2 on SMAD1/5, ERK and S6K signalling after 24 hours. More importantly, a cooperative effect between Ca.sup.2+ and BMP-2 on the phosphorylation of SMAD1/5, S6, GSK3 and total levels of [beta]-CATENIN was observed at a later differentiation time (10 days). Furthermore, Ca.sup.2+ alone favoured the phosphorylation of SMAD1, which correlates with the induction of Bmp2 and Bmp4 gene expression. These data suggest that Ca.sup.2+ and BMP-2 cooperate and promote an autocrine/paracrine osteogenic feed-forward loop. On the whole, these results demonstrate the usefulness of calcium-based bone grafts or the addition of exogenous Ca.sup.2+ in bone tissue engineering.
Understanding the molecular events that regulate osteoblast differentiation is essential for the development of effective approaches to bone regeneration. In this study, we analysed the osteoinductive properties of extracellular calcium in bone marrow-derived mesenchymal stem cell (BM-MSC) differentiation. We cultured BM-MSCs in 3D gelatin scaffolds with Ca2+ and BMP-2 as osteoinductive agents. Early and late osteogenic gene expression and bone regeneration in a calvarial critical-size defect model demonstrate that extracellular Ca2+ enhances the effects of BMP-2 on Osteocalcin, Runx2 and Osterix expression and promotes bone regeneration in vivo. Moreover, we analysed the molecular mechanisms involved and observed an antagonistic effect between Ca2+ and BMP-2 on SMAD1/5, ERK and S6K signalling after 24 hours. More importantly, a cooperative effect between Ca2+ and BMP-2 on the phosphorylation of SMAD1/5, S6, GSK3 and total levels of β-CATENIN was observed at a later differentiation time (10 days). Furthermore, Ca2+ alone favoured the phosphorylation of SMAD1, which correlates with the induction of Bmp2 and Bmp4 gene expression. These data suggest that Ca2+ and BMP-2 cooperate and promote an autocrine/paracrine osteogenic feed-forward loop. On the whole, these results demonstrate the usefulness of calcium-based bone grafts or the addition of exogenous Ca2+ in bone tissue engineering.
Understanding the molecular events that regulate osteoblast differentiation is essential for the development of effective approaches to bone regeneration. In this study, we analysed the osteoinductive properties of extracellular calcium in bone marrow-derived mesenchymal stem cell (BM-MSC) differentiation. We cultured BM-MSCs in 3D gelatin scaffolds with Ca 2+ and BMP-2 as osteoinductive agents. Early and late osteogenic gene expression and bone regeneration in a calvarial critical-size defect model demonstrate that extracellular Ca 2+ enhances the effects of BMP-2 on Osteocalcin , Runx2 and Osterix expression and promotes bone regeneration in vivo . Moreover, we analysed the molecular mechanisms involved and observed an antagonistic effect between Ca 2+ and BMP-2 on SMAD1/5, ERK and S6K signalling after 24 hours. More importantly, a cooperative effect between Ca 2+ and BMP-2 on the phosphorylation of SMAD1/5, S6, GSK3 and total levels of β-CATENIN was observed at a later differentiation time (10 days). Furthermore, Ca 2+ alone favoured the phosphorylation of SMAD1, which correlates with the induction of Bmp2 and Bmp4 gene expression. These data suggest that Ca 2+ and BMP-2 cooperate and promote an autocrine/paracrine osteogenic feed-forward loop. On the whole, these results demonstrate the usefulness of calcium-based bone grafts or the addition of exogenous Ca 2+ in bone tissue engineering.
Audience Academic
Author Artigas, Natalia
Rosa, José Luis
Ventura, Francesc
Gámez, Beatriz
Aquino-Martínez, Rubén
AuthorAffiliation Medical University of South Carolina, UNITED STATES
Departament de Ciències Fisiològiques, Universitat de Barcelona, IDIBELL, L’Hospitalet de Llobregat, Spain
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/28542453$$D View this record in MEDLINE/PubMed
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Copyright COPYRIGHT 2017 Public Library of Science
2017 Aquino-Martínez et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
cc-by (c) Aquino Martínez, Rubén Francisco et al., 2017 info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/3.0/es
2017 Aquino-Martínez et al 2017 Aquino-Martínez et al
Copyright_xml – notice: COPYRIGHT 2017 Public Library of Science
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Competing Interests: The authors have declared that no competing interests exist.
Conceptualization: RAM FV.Data curation: RAM NA BG FV.Formal analysis: RAM NA BG JLR FV.Funding acquisition: FV.Investigation: RAM NA BG FV.Methodology: RAM NA BG FV.Project administration: FV.Resources: FV JLR.Supervision: JLR FV.Validation: RAM NA FV.Visualization: RAM FV.Writing – original draft: RAM FV.
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Snippet Understanding the molecular events that regulate osteoblast differentiation is essential for the development of effective approaches to bone regeneration. In...
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pubmedcentral
csuc
proquest
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pubmed
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
StartPage e0178158
SubjectTerms 1-Phosphatidylinositol 3-kinase
Adherent cells
AKT protein
Alveolar bone
Amplification
Animal models
Animals
Antigenicity
Arches
Assaying
Attachment
Biochemistry
Biocompatibility
Biology and Life Sciences
Biomaterials
Biotechnology
Bone biomaterials
Bone growth
Bone healing
Bone marrow
Bone Marrow Cells - drug effects
Bone Marrow Cells - physiology
Bone Morphogenetic Protein 2 - physiology
Bone morphogenetic proteins
Bone remodeling
Bone turnover
Bones
Bones growth
Calci en l'organisme
Calcification
Calcium
Calcium - pharmacology
Calcium in the body
Cell adhesion
Cell Differentiation - drug effects
Cell Differentiation - physiology
Cells (biology)
Cellular signal transduction
Collagen
Creixement dels ossos
Cèl·lules mare
Defects
Degradation
Degradation products
Differentiation
Engineering
Engineering and Technology
Exposure
Fragmentation
Gene expression
Gene Expression Profiling
Genetic aspects
Glial stem cells
Growth factors
Hay
Homeostasis
Hydroxyapatite
Inactivation
Kinases
Laminar flow
Media
Mesenchymal stem cells
Mesenchymal Stromal Cells - drug effects
Mesenchymal Stromal Cells - physiology
Mice
Mice, Inbred BALB C
Neural stem cells
Ossificació
Ossification
Osteoblasts - drug effects
Osteoblasts - physiology
Osteogenesis
Osteogenesis - drug effects
Osteogenesis - physiology
Osteoprogenitor cells
Pharmacology
Physiological aspects
Physiology
Plates (structural members)
Potassium
Propagation
Proteins
Regulations
Research and Analysis Methods
Shear stress
Signal transduction
Signal Transduction - drug effects
Signal Transduction - physiology
Skeletogenesis
Smad Proteins - physiology
Stem cells
Strontium
Surgical implants
Temperature effects
Tissue engineering
Tissue Scaffolds
Transcription factors
Transducció de senyal cel·lular
Vertebrates
Vertical orientation
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Title Extracellular calcium promotes bone formation from bone marrow mesenchymal stem cells by amplifying the effects of BMP-2 on SMAD signalling
URI https://www.ncbi.nlm.nih.gov/pubmed/28542453
https://www.proquest.com/docview/1902478334
https://search.proquest.com/docview/1903160386
https://recercat.cat/handle/2072/307124
https://pubmed.ncbi.nlm.nih.gov/PMC5444778
https://doaj.org/article/294f9eb7a8254c3aa78f0f80d82f1119
http://dx.doi.org/10.1371/journal.pone.0178158
Volume 12
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