Cargando…

Col11a1 Regulates Bone Microarchitecture during Embryonic Development

Collagen XI alpha 1 (Col11a1) is an extracellular matrix molecule required for embryonic development with a role in both nucleating the formation of fibrils and regulating the diameter of heterotypic fibrils during collagen fibrillar assembly. Although found in many different tissues throughout the...

Descripción completa

Detalles Bibliográficos
Autores principales: Hafez, Anthony, Squires, Ryan, Pedracini, Amber, Joshi, Alark, Seegmiller, Robert E., Oxford, Julia Thom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4711924/
https://www.ncbi.nlm.nih.gov/pubmed/26779434
http://dx.doi.org/10.3390/jdb3040158
_version_ 1782409984181534720
author Hafez, Anthony
Squires, Ryan
Pedracini, Amber
Joshi, Alark
Seegmiller, Robert E.
Oxford, Julia Thom
author_facet Hafez, Anthony
Squires, Ryan
Pedracini, Amber
Joshi, Alark
Seegmiller, Robert E.
Oxford, Julia Thom
author_sort Hafez, Anthony
collection PubMed
description Collagen XI alpha 1 (Col11a1) is an extracellular matrix molecule required for embryonic development with a role in both nucleating the formation of fibrils and regulating the diameter of heterotypic fibrils during collagen fibrillar assembly. Although found in many different tissues throughout the vertebrate body, Col11a1 plays an essential role in endochondral ossification. To further understand the function of Col11a1 in the process of bone formation, we compared skeletal mineralization in wild-type (WT) mice and Col11a1-deficient mice using X-ray microtomography (micro-CT) and histology. Changes in trabecular bone microstructure were observed and are presented here. Additionally, changes to the periosteal bone collar of developing long bones were observed and resulted in an increase in thickness in the case of Col11a1-deficient mice compared to WT littermates. Vertebral bodies were incompletely formed in the absence of Col11a1. The data demonstrate that Col11a1 depletion results in alteration to newly-formed bone and is consistent with a role for Col11a1 in mineralization. These findings indicate that expression of Col11a1 in the growth plate and perichondrium is essential for trabecular bone and bone collar formation during endochondral ossification. The observed changes to mineralized tissues further define the function of Col11a1.
format Online
Article
Text
id pubmed-4711924
institution National Center for Biotechnology Information
language English
publishDate 2015
record_format MEDLINE/PubMed
spelling pubmed-47119242016-01-13 Col11a1 Regulates Bone Microarchitecture during Embryonic Development Hafez, Anthony Squires, Ryan Pedracini, Amber Joshi, Alark Seegmiller, Robert E. Oxford, Julia Thom J Dev Biol Article Collagen XI alpha 1 (Col11a1) is an extracellular matrix molecule required for embryonic development with a role in both nucleating the formation of fibrils and regulating the diameter of heterotypic fibrils during collagen fibrillar assembly. Although found in many different tissues throughout the vertebrate body, Col11a1 plays an essential role in endochondral ossification. To further understand the function of Col11a1 in the process of bone formation, we compared skeletal mineralization in wild-type (WT) mice and Col11a1-deficient mice using X-ray microtomography (micro-CT) and histology. Changes in trabecular bone microstructure were observed and are presented here. Additionally, changes to the periosteal bone collar of developing long bones were observed and resulted in an increase in thickness in the case of Col11a1-deficient mice compared to WT littermates. Vertebral bodies were incompletely formed in the absence of Col11a1. The data demonstrate that Col11a1 depletion results in alteration to newly-formed bone and is consistent with a role for Col11a1 in mineralization. These findings indicate that expression of Col11a1 in the growth plate and perichondrium is essential for trabecular bone and bone collar formation during endochondral ossification. The observed changes to mineralized tissues further define the function of Col11a1. 2015-12-16 2015 /pmc/articles/PMC4711924/ /pubmed/26779434 http://dx.doi.org/10.3390/jdb3040158 Text en http://creativecommons.org/licenses/by/4.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hafez, Anthony
Squires, Ryan
Pedracini, Amber
Joshi, Alark
Seegmiller, Robert E.
Oxford, Julia Thom
Col11a1 Regulates Bone Microarchitecture during Embryonic Development
title Col11a1 Regulates Bone Microarchitecture during Embryonic Development
title_full Col11a1 Regulates Bone Microarchitecture during Embryonic Development
title_fullStr Col11a1 Regulates Bone Microarchitecture during Embryonic Development
title_full_unstemmed Col11a1 Regulates Bone Microarchitecture during Embryonic Development
title_short Col11a1 Regulates Bone Microarchitecture during Embryonic Development
title_sort col11a1 regulates bone microarchitecture during embryonic development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4711924/
https://www.ncbi.nlm.nih.gov/pubmed/26779434
http://dx.doi.org/10.3390/jdb3040158
work_keys_str_mv AT hafezanthony col11a1regulatesbonemicroarchitectureduringembryonicdevelopment
AT squiresryan col11a1regulatesbonemicroarchitectureduringembryonicdevelopment
AT pedraciniamber col11a1regulatesbonemicroarchitectureduringembryonicdevelopment
AT joshialark col11a1regulatesbonemicroarchitectureduringembryonicdevelopment
AT seegmillerroberte col11a1regulatesbonemicroarchitectureduringembryonicdevelopment
AT oxfordjuliathom col11a1regulatesbonemicroarchitectureduringembryonicdevelopment