The role of Matrix Gla Protein in ossification and recovery of the avian growth plate

ECM mineralization is an essential physiologic process in bone, teeth, and hypertrophic cartilage. Matrix Gla Protein (MGP), an inhibitor of mineralization, is expressed by chondrocytes and vascular smooth muscle cells to inhibit calcification of those soft tissues.Tibial Dyschondroplasia (TD), a sk...

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Main Authors: Harel eDan, Stav eSimsa-Maziel, Adi eReich, Dalit eSela-Donenfeld, Efrat eMonsonego-Ornan
Format: Article
Language:English
Published: Frontiers Media S.A. 2012-07-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fendo.2012.00079/full
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author Harel eDan
Stav eSimsa-Maziel
Adi eReich
Dalit eSela-Donenfeld
Efrat eMonsonego-Ornan
author_facet Harel eDan
Stav eSimsa-Maziel
Adi eReich
Dalit eSela-Donenfeld
Efrat eMonsonego-Ornan
author_sort Harel eDan
collection DOAJ
description ECM mineralization is an essential physiologic process in bone, teeth, and hypertrophic cartilage. Matrix Gla Protein (MGP), an inhibitor of mineralization, is expressed by chondrocytes and vascular smooth muscle cells to inhibit calcification of those soft tissues.Tibial Dyschondroplasia (TD), a skeletal abnormality apparent as a plug of non-vascularized, non-mineralized, white opaque cartilage in the tibial growth plate of avian species can serve as a good model for studying process and genes involved in matrix mineralization and calcification. In this work, we studied the involvement of MGP in the development of TD, as well as in the processes of spontaneous and induced recovery from this syndrome. First, we found that during normal bone development, MGP is expressed in specific time and locations, starting from wide spread expression in the yet un-ossified diaphysis during embryonic development, to specific expression in hypertrophic chondrocytes adjacent to the chondro-osseous junction and the secondary ossification center just prior to calcification. In addition, we show that MGP is not expressed in the impaired TD lesion, however when the lesion begins to heal, it strongly express MGP prior to its calcification. Moreover, we show that when calcification is inhibited, a gap is formed between the expression zones of MGP and BMP2 and that this gap is closed during the healing process. To conclude, we suggest that MGP, directly or through interaction with BMP2, plays a role as ossification regulator, rather then simple inhibitor that acts prior to ossification.
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spelling doaj.art-5928b98dee544cf29f3784f404b71ada2022-12-21T19:30:37ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922012-07-01310.3389/fendo.2012.0007927998The role of Matrix Gla Protein in ossification and recovery of the avian growth plateHarel eDan0Stav eSimsa-Maziel1Adi eReich2Dalit eSela-Donenfeld3Efrat eMonsonego-Ornan4The Hebrew UniversityThe Hebrew UniversityThe Hebrew UniversityThe Hebrew UniversityThe Hebrew UniversityECM mineralization is an essential physiologic process in bone, teeth, and hypertrophic cartilage. Matrix Gla Protein (MGP), an inhibitor of mineralization, is expressed by chondrocytes and vascular smooth muscle cells to inhibit calcification of those soft tissues.Tibial Dyschondroplasia (TD), a skeletal abnormality apparent as a plug of non-vascularized, non-mineralized, white opaque cartilage in the tibial growth plate of avian species can serve as a good model for studying process and genes involved in matrix mineralization and calcification. In this work, we studied the involvement of MGP in the development of TD, as well as in the processes of spontaneous and induced recovery from this syndrome. First, we found that during normal bone development, MGP is expressed in specific time and locations, starting from wide spread expression in the yet un-ossified diaphysis during embryonic development, to specific expression in hypertrophic chondrocytes adjacent to the chondro-osseous junction and the secondary ossification center just prior to calcification. In addition, we show that MGP is not expressed in the impaired TD lesion, however when the lesion begins to heal, it strongly express MGP prior to its calcification. Moreover, we show that when calcification is inhibited, a gap is formed between the expression zones of MGP and BMP2 and that this gap is closed during the healing process. To conclude, we suggest that MGP, directly or through interaction with BMP2, plays a role as ossification regulator, rather then simple inhibitor that acts prior to ossification.http://journal.frontiersin.org/Journal/10.3389/fendo.2012.00079/fullChondrocytesThiramBMP-2MGPTibial dyschondroplasia
spellingShingle Harel eDan
Stav eSimsa-Maziel
Adi eReich
Dalit eSela-Donenfeld
Efrat eMonsonego-Ornan
The role of Matrix Gla Protein in ossification and recovery of the avian growth plate
Frontiers in Endocrinology
Chondrocytes
Thiram
BMP-2
MGP
Tibial dyschondroplasia
title The role of Matrix Gla Protein in ossification and recovery of the avian growth plate
title_full The role of Matrix Gla Protein in ossification and recovery of the avian growth plate
title_fullStr The role of Matrix Gla Protein in ossification and recovery of the avian growth plate
title_full_unstemmed The role of Matrix Gla Protein in ossification and recovery of the avian growth plate
title_short The role of Matrix Gla Protein in ossification and recovery of the avian growth plate
title_sort role of matrix gla protein in ossification and recovery of the avian growth plate
topic Chondrocytes
Thiram
BMP-2
MGP
Tibial dyschondroplasia
url http://journal.frontiersin.org/Journal/10.3389/fendo.2012.00079/full
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