Development of Enthesopathies and Joint Structural Damage in a Murine Model of X-Linked Hypophosphatemia

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Development of Enthesopathies and Joint Structural Damage in a Murine Model of X-Linked Hypophosphatemia. / Faraji-Bellée, Carole-Anne; Cauliez, Axelle; Salmon, Benjamin; Fogel, Olivier; Zhukouskaya, Volha; Benoit, Aurélie; Schinke, Thorsten; Roux, Christian; Linglart, Agnès; Miceli-Richard, Corinne; Chaussain, Catherine; Briot, Karine; Bardet, Claire.

In: FRONT CELL DEV BIOL, Vol. 8, 2020, p. 854.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Faraji-Bellée, C-A, Cauliez, A, Salmon, B, Fogel, O, Zhukouskaya, V, Benoit, A, Schinke, T, Roux, C, Linglart, A, Miceli-Richard, C, Chaussain, C, Briot, K & Bardet, C 2020, 'Development of Enthesopathies and Joint Structural Damage in a Murine Model of X-Linked Hypophosphatemia', FRONT CELL DEV BIOL, vol. 8, pp. 854. https://doi.org/10.3389/fcell.2020.00854

APA

Faraji-Bellée, C-A., Cauliez, A., Salmon, B., Fogel, O., Zhukouskaya, V., Benoit, A., Schinke, T., Roux, C., Linglart, A., Miceli-Richard, C., Chaussain, C., Briot, K., & Bardet, C. (2020). Development of Enthesopathies and Joint Structural Damage in a Murine Model of X-Linked Hypophosphatemia. FRONT CELL DEV BIOL, 8, 854. https://doi.org/10.3389/fcell.2020.00854

Vancouver

Bibtex

@article{2288685469074cf8b2dedfda49b0b09f,
title = "Development of Enthesopathies and Joint Structural Damage in a Murine Model of X-Linked Hypophosphatemia",
abstract = "X-linked hypophosphatemia (XLH) is characterized by rickets and osteomalacia, caused by inactivating mutations in the Phosphate-regulating endopeptidase homolog X-linked (PHEX) gene. With aging, adult patients develop paradoxical heterotopic calcifications of tendons and ligaments at their insertion sites (enthesophytes), and joint alterations. Understanding the progression of this structural damage that severely affects patients' quality of life will help to improve the management of XLH. Here, we characterized the occurrence of enthesophytes and joint alterations through a 12 month in vivo micro-CT follow-up in the Hyp mouse, a murine model of XLH (n = 5 mice per group). Similar to adult patients with XLH, Hyp mice developed calcaneal enthesophytes, hip joint alterations, erosions of the sacroiliac joints and periarticular calcifications. These lesions were already present at month 3 and gradually worsened over time. In sharp contrast, no abnormalities were observed in control mice at early time points. Histological analyses confirmed the presence of bone erosions, calcifications and expansion of mineralizing enthesis fibrocartilage in Hyp mice and their absence in controls and suggested that new bone formation is driven by altered mechanical strain. Interestingly, despite a strong deformation of the curvature, none of the Hyp mice displayed enthesophyte at the spine. Peripheral enthesophytes and joint alterations develop at the early stages of the disease and gradually worsen overtime. Overall, our findings highlight the relevance of this preclinical model to test new therapies aiming to prevent bone and joint complications in XLH.",
author = "Carole-Anne Faraji-Bell{\'e}e and Axelle Cauliez and Benjamin Salmon and Olivier Fogel and Volha Zhukouskaya and Aur{\'e}lie Benoit and Thorsten Schinke and Christian Roux and Agn{\`e}s Linglart and Corinne Miceli-Richard and Catherine Chaussain and Karine Briot and Claire Bardet",
year = "2020",
doi = "10.3389/fcell.2020.00854",
language = "English",
volume = "8",
pages = "854",
journal = "FRONT CELL DEV BIOL",
issn = "2296-634X",
publisher = "Frontiers Media S. A.",

}

RIS

TY - JOUR

T1 - Development of Enthesopathies and Joint Structural Damage in a Murine Model of X-Linked Hypophosphatemia

AU - Faraji-Bellée, Carole-Anne

AU - Cauliez, Axelle

AU - Salmon, Benjamin

AU - Fogel, Olivier

AU - Zhukouskaya, Volha

AU - Benoit, Aurélie

AU - Schinke, Thorsten

AU - Roux, Christian

AU - Linglart, Agnès

AU - Miceli-Richard, Corinne

AU - Chaussain, Catherine

AU - Briot, Karine

AU - Bardet, Claire

PY - 2020

Y1 - 2020

N2 - X-linked hypophosphatemia (XLH) is characterized by rickets and osteomalacia, caused by inactivating mutations in the Phosphate-regulating endopeptidase homolog X-linked (PHEX) gene. With aging, adult patients develop paradoxical heterotopic calcifications of tendons and ligaments at their insertion sites (enthesophytes), and joint alterations. Understanding the progression of this structural damage that severely affects patients' quality of life will help to improve the management of XLH. Here, we characterized the occurrence of enthesophytes and joint alterations through a 12 month in vivo micro-CT follow-up in the Hyp mouse, a murine model of XLH (n = 5 mice per group). Similar to adult patients with XLH, Hyp mice developed calcaneal enthesophytes, hip joint alterations, erosions of the sacroiliac joints and periarticular calcifications. These lesions were already present at month 3 and gradually worsened over time. In sharp contrast, no abnormalities were observed in control mice at early time points. Histological analyses confirmed the presence of bone erosions, calcifications and expansion of mineralizing enthesis fibrocartilage in Hyp mice and their absence in controls and suggested that new bone formation is driven by altered mechanical strain. Interestingly, despite a strong deformation of the curvature, none of the Hyp mice displayed enthesophyte at the spine. Peripheral enthesophytes and joint alterations develop at the early stages of the disease and gradually worsen overtime. Overall, our findings highlight the relevance of this preclinical model to test new therapies aiming to prevent bone and joint complications in XLH.

AB - X-linked hypophosphatemia (XLH) is characterized by rickets and osteomalacia, caused by inactivating mutations in the Phosphate-regulating endopeptidase homolog X-linked (PHEX) gene. With aging, adult patients develop paradoxical heterotopic calcifications of tendons and ligaments at their insertion sites (enthesophytes), and joint alterations. Understanding the progression of this structural damage that severely affects patients' quality of life will help to improve the management of XLH. Here, we characterized the occurrence of enthesophytes and joint alterations through a 12 month in vivo micro-CT follow-up in the Hyp mouse, a murine model of XLH (n = 5 mice per group). Similar to adult patients with XLH, Hyp mice developed calcaneal enthesophytes, hip joint alterations, erosions of the sacroiliac joints and periarticular calcifications. These lesions were already present at month 3 and gradually worsened over time. In sharp contrast, no abnormalities were observed in control mice at early time points. Histological analyses confirmed the presence of bone erosions, calcifications and expansion of mineralizing enthesis fibrocartilage in Hyp mice and their absence in controls and suggested that new bone formation is driven by altered mechanical strain. Interestingly, despite a strong deformation of the curvature, none of the Hyp mice displayed enthesophyte at the spine. Peripheral enthesophytes and joint alterations develop at the early stages of the disease and gradually worsen overtime. Overall, our findings highlight the relevance of this preclinical model to test new therapies aiming to prevent bone and joint complications in XLH.

U2 - 10.3389/fcell.2020.00854

DO - 10.3389/fcell.2020.00854

M3 - SCORING: Journal article

C2 - 33072734

VL - 8

SP - 854

JO - FRONT CELL DEV BIOL

JF - FRONT CELL DEV BIOL

SN - 2296-634X

ER -