Collagen X Is Dispensable for Hypertrophic Differentiation and Endochondral Ossification of Human iPSC‐Derived Chondrocytes

ABSTRACT Collagen X is a non‐fibril collagen produced by hypertrophic chondrocytes and was believed to associate with the calcification process of growth plate cartilage. The homozygous loss of Col10a1 gene in mice, however, demonstrated no remarkable effects on growth plate formation or skeletal de...

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Main Authors: Takeshi Kamakura, Yonghui Jin, Megumi Nishio, Sanae Nagata, Masayuki Fukuda, Liping Sun, Shunsuke Kawai, Junya Toguchida
Format: Article
Language:English
Published: Wiley 2023-05-01
Series:JBMR Plus
Subjects:
Online Access:https://doi.org/10.1002/jbm4.10737
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author Takeshi Kamakura
Yonghui Jin
Megumi Nishio
Sanae Nagata
Masayuki Fukuda
Liping Sun
Shunsuke Kawai
Junya Toguchida
author_facet Takeshi Kamakura
Yonghui Jin
Megumi Nishio
Sanae Nagata
Masayuki Fukuda
Liping Sun
Shunsuke Kawai
Junya Toguchida
author_sort Takeshi Kamakura
collection DOAJ
description ABSTRACT Collagen X is a non‐fibril collagen produced by hypertrophic chondrocytes and was believed to associate with the calcification process of growth plate cartilage. The homozygous loss of Col10a1 gene in mice, however, demonstrated no remarkable effects on growth plate formation or skeletal development. To investigate the role of collagen X in human chondrocytes, we established human induced pluripotent stem cells (hiPSCs) with heterozygous (COL10A1+/−) or homozygous (COL10A1−/−) deletions of COL10A1 gene using the dual sgRNA CRISPR/Cas9 system. Several mutant clones were established and differentiated into hypertrophic chondrocytes by a previously reported 3D induction method. No remarkable differences were observed during the differentiation process between parental and mutant cell lines, which differentiated into cells with features of hypertrophic chondrocytes, indicating that collagen X is dispensable for the hypertrophic differentiation of human chondrocytes in vitro. To investigate the effects of collagen X deficiency in vivo, chondrocyte pellets at the proliferating or prehypertrophic stage were transplanted into immunodeficient mice. Proliferating pellet‐derived tissues demonstrated the zonal distribution of chondrocytes with the transition to bone tissues mimicking growth plates, and the proportion of bone tended to be larger in COL10A1−/− tissues. Prehypertrophic pellet‐derived tissues produced trabecular bone structures with features of endochondral ossification, and there was no clear difference between parental‐ and mutant‐derived tissues. A transcriptome analysis of chondrocyte pellets at the hypertrophic phase showed a lower expression of proliferating‐phase genes and a higher expression of calcification‐phase genes in COL10A1−/− pellets compared with parental cell pellets. These in vitro and in vivo data suggested that collagen X is dispensable for the hypertrophic differentiation and endochondral ossification of human iPSC‐derived chondrocytes, though it may facilitate the differentiation process. Thus, COL10A1−/− iPSC lines are useful for investigating the physiological role of collagen X in chondrocyte differentiation. © 2023 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
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spelling doaj.art-44b157d147da47c9aeba1708c52fff2d2023-05-15T09:22:04ZengWileyJBMR Plus2473-40392023-05-0175n/an/a10.1002/jbm4.10737Collagen X Is Dispensable for Hypertrophic Differentiation and Endochondral Ossification of Human iPSC‐Derived ChondrocytesTakeshi Kamakura0Yonghui Jin1Megumi Nishio2Sanae Nagata3Masayuki Fukuda4Liping Sun5Shunsuke Kawai6Junya Toguchida7Department of Regeneration Sciences and Engineering, Institute for Life and Medical Sciences Kyoto University Kyoto JapanDepartment of Regeneration Sciences and Engineering, Institute for Life and Medical Sciences Kyoto University Kyoto JapanDepartment of Fundamental Cell Technology, Center for iPS Cell Research and Application Kyoto University Kyoto JapanDepartment of Fundamental Cell Technology, Center for iPS Cell Research and Application Kyoto University Kyoto JapanDepartment of Regeneration Sciences and Engineering, Institute for Life and Medical Sciences Kyoto University Kyoto JapanDepartment of Regeneration Sciences and Engineering, Institute for Life and Medical Sciences Kyoto University Kyoto JapanDepartment of Fundamental Cell Technology, Center for iPS Cell Research and Application Kyoto University Kyoto JapanDepartment of Regeneration Sciences and Engineering, Institute for Life and Medical Sciences Kyoto University Kyoto JapanABSTRACT Collagen X is a non‐fibril collagen produced by hypertrophic chondrocytes and was believed to associate with the calcification process of growth plate cartilage. The homozygous loss of Col10a1 gene in mice, however, demonstrated no remarkable effects on growth plate formation or skeletal development. To investigate the role of collagen X in human chondrocytes, we established human induced pluripotent stem cells (hiPSCs) with heterozygous (COL10A1+/−) or homozygous (COL10A1−/−) deletions of COL10A1 gene using the dual sgRNA CRISPR/Cas9 system. Several mutant clones were established and differentiated into hypertrophic chondrocytes by a previously reported 3D induction method. No remarkable differences were observed during the differentiation process between parental and mutant cell lines, which differentiated into cells with features of hypertrophic chondrocytes, indicating that collagen X is dispensable for the hypertrophic differentiation of human chondrocytes in vitro. To investigate the effects of collagen X deficiency in vivo, chondrocyte pellets at the proliferating or prehypertrophic stage were transplanted into immunodeficient mice. Proliferating pellet‐derived tissues demonstrated the zonal distribution of chondrocytes with the transition to bone tissues mimicking growth plates, and the proportion of bone tended to be larger in COL10A1−/− tissues. Prehypertrophic pellet‐derived tissues produced trabecular bone structures with features of endochondral ossification, and there was no clear difference between parental‐ and mutant‐derived tissues. A transcriptome analysis of chondrocyte pellets at the hypertrophic phase showed a lower expression of proliferating‐phase genes and a higher expression of calcification‐phase genes in COL10A1−/− pellets compared with parental cell pellets. These in vitro and in vivo data suggested that collagen X is dispensable for the hypertrophic differentiation and endochondral ossification of human iPSC‐derived chondrocytes, though it may facilitate the differentiation process. Thus, COL10A1−/− iPSC lines are useful for investigating the physiological role of collagen X in chondrocyte differentiation. © 2023 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.https://doi.org/10.1002/jbm4.10737GROWTH PLATECHONDROCYTE AND CARTILAGE BIOLOGYDISEASES AND DISORDERS OF/RELATED TO BONECOLLAGENBONE MATRIX
spellingShingle Takeshi Kamakura
Yonghui Jin
Megumi Nishio
Sanae Nagata
Masayuki Fukuda
Liping Sun
Shunsuke Kawai
Junya Toguchida
Collagen X Is Dispensable for Hypertrophic Differentiation and Endochondral Ossification of Human iPSC‐Derived Chondrocytes
JBMR Plus
GROWTH PLATE
CHONDROCYTE AND CARTILAGE BIOLOGY
DISEASES AND DISORDERS OF/RELATED TO BONE
COLLAGEN
BONE MATRIX
title Collagen X Is Dispensable for Hypertrophic Differentiation and Endochondral Ossification of Human iPSC‐Derived Chondrocytes
title_full Collagen X Is Dispensable for Hypertrophic Differentiation and Endochondral Ossification of Human iPSC‐Derived Chondrocytes
title_fullStr Collagen X Is Dispensable for Hypertrophic Differentiation and Endochondral Ossification of Human iPSC‐Derived Chondrocytes
title_full_unstemmed Collagen X Is Dispensable for Hypertrophic Differentiation and Endochondral Ossification of Human iPSC‐Derived Chondrocytes
title_short Collagen X Is Dispensable for Hypertrophic Differentiation and Endochondral Ossification of Human iPSC‐Derived Chondrocytes
title_sort collagen x is dispensable for hypertrophic differentiation and endochondral ossification of human ipsc derived chondrocytes
topic GROWTH PLATE
CHONDROCYTE AND CARTILAGE BIOLOGY
DISEASES AND DISORDERS OF/RELATED TO BONE
COLLAGEN
BONE MATRIX
url https://doi.org/10.1002/jbm4.10737
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