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Granzyme-A deficiency attenuates experimental osteoarthritis in mice, but perforin deficiency does not

OBJECTIVES: This study aims to assess the development of osteoarthritis (OA) in granzyme A- (gzmA) and B- (gzmB) and perforin- (perf) knockout mice. MATERIALS AND METHODS: A total of 75 male and female C57BL/6 (eight to nine-week-old) mice were allocated to: gzmA-deficient (gzmA-/-) (11 females, 8 m...

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Autores principales: Calvo, Jorge, Santiago, Llipsy, Arias, Maykel, Pardo, Julián, Albareda, Jorge, Martínez-Lostao, Luis, García-Alvarez, Felícito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bayçınar Medical Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10367147/
https://www.ncbi.nlm.nih.gov/pubmed/37462629
http://dx.doi.org/10.52312/jdrs.2023.892
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author Calvo, Jorge
Santiago, Llipsy
Arias, Maykel
Pardo, Julián
Albareda, Jorge
Martínez-Lostao, Luis
García-Alvarez, Felícito
author_facet Calvo, Jorge
Santiago, Llipsy
Arias, Maykel
Pardo, Julián
Albareda, Jorge
Martínez-Lostao, Luis
García-Alvarez, Felícito
author_sort Calvo, Jorge
collection PubMed
description OBJECTIVES: This study aims to assess the development of osteoarthritis (OA) in granzyme A- (gzmA) and B- (gzmB) and perforin- (perf) knockout mice. MATERIALS AND METHODS: A total of 75 male and female C57BL/6 (eight to nine-week-old) mice were allocated to: gzmA-deficient (gzmA-/-) (11 females, 8 males), gzmB-deficient (gzmB-/-) (9 females, 8 males), perf-deficient (perf-/-) (10 females, 9 males), and control group (10 females, 10 males). Osteoarthritis was induced in the right knee by instability of the meniscus medial ligament. Sham surgery was practiced in the left knee. Knee samples obtained eight weeks after surgery were stained (Safranin-O) and blindly scored in lateral and medial femur and tibia using the Osteoarthritis Research Society International scale (OARSI) (from Grade 0, cartilage intact to 6, deformation), (five stages from 0, no OA to 4, >50% surface involvement); OARSI score (grade x stage); and a semi-quantitative scale from Grade 0 (normal) to 6 (cartilage erosion >80%). RESULTS: Significantly higher values in all scales in the right knees compared to the left knees in male and female mice were observed (p<0.05). Males of all strains showed in the right knee higher values than females on all scales. Deficiency of perforin did not modify OA severity in any sex. The gzmA-/- females presented less degenerative changes than the other groups. CONCLUSION: Our study results show that sex plays an important role in the development of experimental OA in mice. Deficiency of gzmA can protect from the development of OA in female mice.
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spelling pubmed-103671472023-07-26 Granzyme-A deficiency attenuates experimental osteoarthritis in mice, but perforin deficiency does not Calvo, Jorge Santiago, Llipsy Arias, Maykel Pardo, Julián Albareda, Jorge Martínez-Lostao, Luis García-Alvarez, Felícito Jt Dis Relat Surg Original Article OBJECTIVES: This study aims to assess the development of osteoarthritis (OA) in granzyme A- (gzmA) and B- (gzmB) and perforin- (perf) knockout mice. MATERIALS AND METHODS: A total of 75 male and female C57BL/6 (eight to nine-week-old) mice were allocated to: gzmA-deficient (gzmA-/-) (11 females, 8 males), gzmB-deficient (gzmB-/-) (9 females, 8 males), perf-deficient (perf-/-) (10 females, 9 males), and control group (10 females, 10 males). Osteoarthritis was induced in the right knee by instability of the meniscus medial ligament. Sham surgery was practiced in the left knee. Knee samples obtained eight weeks after surgery were stained (Safranin-O) and blindly scored in lateral and medial femur and tibia using the Osteoarthritis Research Society International scale (OARSI) (from Grade 0, cartilage intact to 6, deformation), (five stages from 0, no OA to 4, >50% surface involvement); OARSI score (grade x stage); and a semi-quantitative scale from Grade 0 (normal) to 6 (cartilage erosion >80%). RESULTS: Significantly higher values in all scales in the right knees compared to the left knees in male and female mice were observed (p<0.05). Males of all strains showed in the right knee higher values than females on all scales. Deficiency of perforin did not modify OA severity in any sex. The gzmA-/- females presented less degenerative changes than the other groups. CONCLUSION: Our study results show that sex plays an important role in the development of experimental OA in mice. Deficiency of gzmA can protect from the development of OA in female mice. Bayçınar Medical Publishing 2023-04-27 /pmc/articles/PMC10367147/ /pubmed/37462629 http://dx.doi.org/10.52312/jdrs.2023.892 Text en Copyright © 2023, Turkish Joint Diseases Foundation https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Article
Calvo, Jorge
Santiago, Llipsy
Arias, Maykel
Pardo, Julián
Albareda, Jorge
Martínez-Lostao, Luis
García-Alvarez, Felícito
Granzyme-A deficiency attenuates experimental osteoarthritis in mice, but perforin deficiency does not
title Granzyme-A deficiency attenuates experimental osteoarthritis in mice, but perforin deficiency does not
title_full Granzyme-A deficiency attenuates experimental osteoarthritis in mice, but perforin deficiency does not
title_fullStr Granzyme-A deficiency attenuates experimental osteoarthritis in mice, but perforin deficiency does not
title_full_unstemmed Granzyme-A deficiency attenuates experimental osteoarthritis in mice, but perforin deficiency does not
title_short Granzyme-A deficiency attenuates experimental osteoarthritis in mice, but perforin deficiency does not
title_sort granzyme-a deficiency attenuates experimental osteoarthritis in mice, but perforin deficiency does not
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10367147/
https://www.ncbi.nlm.nih.gov/pubmed/37462629
http://dx.doi.org/10.52312/jdrs.2023.892
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