Altered trabecular bone structure and delayed cartilage degeneration in the knees of collagen VI null mice.

Mutation or loss of collagen VI has been linked to a variety of musculoskeletal abnormalities, particularly muscular dystrophies, tissue ossification and/or fibrosis, and hip osteoarthritis. However, the role of collagen VI in bone and cartilage structure and function in the knee is unknown. In this...

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Main Authors: Susan E Christensen, Jeffrey M Coles, Nicole A Zelenski, Bridgette D Furman, Holly A Leddy, Stefan Zauscher, Paolo Bonaldo, Farshid Guilak
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0033397&type=printable
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author Susan E Christensen
Jeffrey M Coles
Nicole A Zelenski
Bridgette D Furman
Holly A Leddy
Stefan Zauscher
Paolo Bonaldo
Farshid Guilak
author_facet Susan E Christensen
Jeffrey M Coles
Nicole A Zelenski
Bridgette D Furman
Holly A Leddy
Stefan Zauscher
Paolo Bonaldo
Farshid Guilak
author_sort Susan E Christensen
collection DOAJ
description Mutation or loss of collagen VI has been linked to a variety of musculoskeletal abnormalities, particularly muscular dystrophies, tissue ossification and/or fibrosis, and hip osteoarthritis. However, the role of collagen VI in bone and cartilage structure and function in the knee is unknown. In this study, we examined the role of collagen VI in the morphology and physical properties of bone and cartilage in the knee joint of Col6a1(-/-) mice by micro-computed tomography (microCT), histology, atomic force microscopy (AFM), and scanning microphotolysis (SCAMP). Col6a1(-/-) mice showed significant differences in trabecular bone structure, with lower bone volume, connectivity density, trabecular number, and trabecular thickness but higher structure model index and trabecular separation compared to Col6a1(+/+) mice. Subchondral bone thickness and mineral content increased significantly with age in Col6a1(+/+) mice, but not in Col6a1(-/-) mice. Col6a1(-/-) mice had lower cartilage degradation scores, but developed early, severe osteophytes compared to Col6a1(+/+) mice. In both groups, cartilage roughness increased with age, but neither the frictional coefficient nor compressive modulus of the cartilage changed with age or genotype, as measured by AFM. Cartilage diffusivity, measured via SCAMP, varied minimally with age or genotype. The absence of type VI collagen has profound effects on knee joint structure and morphometry, yet minimal influences on the physical properties of the cartilage. Together with previous studies showing accelerated hip osteoarthritis in Col6a1(-/-) mice, these findings suggest different roles for collagen VI at different sites in the body, consistent with clinical data.
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spelling doaj-art-561a9e69dbf7410f8cd64e493e42c3fa2025-08-20T02:05:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0173e3339710.1371/journal.pone.0033397Altered trabecular bone structure and delayed cartilage degeneration in the knees of collagen VI null mice.Susan E ChristensenJeffrey M ColesNicole A ZelenskiBridgette D FurmanHolly A LeddyStefan ZauscherPaolo BonaldoFarshid GuilakMutation or loss of collagen VI has been linked to a variety of musculoskeletal abnormalities, particularly muscular dystrophies, tissue ossification and/or fibrosis, and hip osteoarthritis. However, the role of collagen VI in bone and cartilage structure and function in the knee is unknown. In this study, we examined the role of collagen VI in the morphology and physical properties of bone and cartilage in the knee joint of Col6a1(-/-) mice by micro-computed tomography (microCT), histology, atomic force microscopy (AFM), and scanning microphotolysis (SCAMP). Col6a1(-/-) mice showed significant differences in trabecular bone structure, with lower bone volume, connectivity density, trabecular number, and trabecular thickness but higher structure model index and trabecular separation compared to Col6a1(+/+) mice. Subchondral bone thickness and mineral content increased significantly with age in Col6a1(+/+) mice, but not in Col6a1(-/-) mice. Col6a1(-/-) mice had lower cartilage degradation scores, but developed early, severe osteophytes compared to Col6a1(+/+) mice. In both groups, cartilage roughness increased with age, but neither the frictional coefficient nor compressive modulus of the cartilage changed with age or genotype, as measured by AFM. Cartilage diffusivity, measured via SCAMP, varied minimally with age or genotype. The absence of type VI collagen has profound effects on knee joint structure and morphometry, yet minimal influences on the physical properties of the cartilage. Together with previous studies showing accelerated hip osteoarthritis in Col6a1(-/-) mice, these findings suggest different roles for collagen VI at different sites in the body, consistent with clinical data.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0033397&type=printable
spellingShingle Susan E Christensen
Jeffrey M Coles
Nicole A Zelenski
Bridgette D Furman
Holly A Leddy
Stefan Zauscher
Paolo Bonaldo
Farshid Guilak
Altered trabecular bone structure and delayed cartilage degeneration in the knees of collagen VI null mice.
PLoS ONE
title Altered trabecular bone structure and delayed cartilage degeneration in the knees of collagen VI null mice.
title_full Altered trabecular bone structure and delayed cartilage degeneration in the knees of collagen VI null mice.
title_fullStr Altered trabecular bone structure and delayed cartilage degeneration in the knees of collagen VI null mice.
title_full_unstemmed Altered trabecular bone structure and delayed cartilage degeneration in the knees of collagen VI null mice.
title_short Altered trabecular bone structure and delayed cartilage degeneration in the knees of collagen VI null mice.
title_sort altered trabecular bone structure and delayed cartilage degeneration in the knees of collagen vi null mice
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0033397&type=printable
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