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Phosphate/Pyrophosphate and MV-related Proteins in Mineralisation: Discoveries from Mouse Models

During the process of matrix vesicle (MV)-mediated initiation of mineralisation, chondrocytes and osteoblasts mineralise the extracellular matrix by promoting the seeding of basic calcium phosphate crystals of hydroxyapatite (HA) along the collagen fibrils. This orchestrated process is carefully reg...

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Detalles Bibliográficos
Autores principales: Zhou, Xiaoying, Cui, Yazhou, Zhou, Xiaoyan, Han, Jinxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3372882/
https://www.ncbi.nlm.nih.gov/pubmed/22719218
http://dx.doi.org/10.7150/ijbs.4538
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author Zhou, Xiaoying
Cui, Yazhou
Zhou, Xiaoyan
Han, Jinxiang
author_facet Zhou, Xiaoying
Cui, Yazhou
Zhou, Xiaoyan
Han, Jinxiang
author_sort Zhou, Xiaoying
collection PubMed
description During the process of matrix vesicle (MV)-mediated initiation of mineralisation, chondrocytes and osteoblasts mineralise the extracellular matrix by promoting the seeding of basic calcium phosphate crystals of hydroxyapatite (HA) along the collagen fibrils. This orchestrated process is carefully regulated by the balanced action of propagators and inhibitors of calcification. The primary antagonistic regulators of extracellular matrix mineralisation are phosphate (Pi) and inorganic pyrophosphate (PPi). Studies in mouse models and in humans have established critical roles for Pi/PPi homeostasis in biomineralisation. In this review, we present the regulators of Pi/PPi, as derived from animal models, and discuss their clinical relevance to physiological and pathological mineralisation.
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spelling pubmed-33728822012-06-20 Phosphate/Pyrophosphate and MV-related Proteins in Mineralisation: Discoveries from Mouse Models Zhou, Xiaoying Cui, Yazhou Zhou, Xiaoyan Han, Jinxiang Int J Biol Sci Review During the process of matrix vesicle (MV)-mediated initiation of mineralisation, chondrocytes and osteoblasts mineralise the extracellular matrix by promoting the seeding of basic calcium phosphate crystals of hydroxyapatite (HA) along the collagen fibrils. This orchestrated process is carefully regulated by the balanced action of propagators and inhibitors of calcification. The primary antagonistic regulators of extracellular matrix mineralisation are phosphate (Pi) and inorganic pyrophosphate (PPi). Studies in mouse models and in humans have established critical roles for Pi/PPi homeostasis in biomineralisation. In this review, we present the regulators of Pi/PPi, as derived from animal models, and discuss their clinical relevance to physiological and pathological mineralisation. Ivyspring International Publisher 2012-06-01 /pmc/articles/PMC3372882/ /pubmed/22719218 http://dx.doi.org/10.7150/ijbs.4538 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Review
Zhou, Xiaoying
Cui, Yazhou
Zhou, Xiaoyan
Han, Jinxiang
Phosphate/Pyrophosphate and MV-related Proteins in Mineralisation: Discoveries from Mouse Models
title Phosphate/Pyrophosphate and MV-related Proteins in Mineralisation: Discoveries from Mouse Models
title_full Phosphate/Pyrophosphate and MV-related Proteins in Mineralisation: Discoveries from Mouse Models
title_fullStr Phosphate/Pyrophosphate and MV-related Proteins in Mineralisation: Discoveries from Mouse Models
title_full_unstemmed Phosphate/Pyrophosphate and MV-related Proteins in Mineralisation: Discoveries from Mouse Models
title_short Phosphate/Pyrophosphate and MV-related Proteins in Mineralisation: Discoveries from Mouse Models
title_sort phosphate/pyrophosphate and mv-related proteins in mineralisation: discoveries from mouse models
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3372882/
https://www.ncbi.nlm.nih.gov/pubmed/22719218
http://dx.doi.org/10.7150/ijbs.4538
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