International Journal Of Bilogical Sciences
.: Home > International Journal Of Bilogical Sciences > 2014 > Volume 10 Number 8 > Mengrui Wu1,2, Yi-Ping Li1, 2, Guochun Zhu2, Yun Lu2, Yiping Wang1,2, Joel Jules2, Matthew McConnell2, Rosa Serra3, Jian-Zhong Shao1, Wei Chen2
Chondrocyte-specific Knockout of Cbfβ Reveals the Indispensable Function of Cbfβ in Chondrocyte Maturation, Growth Plate Development and Trabecular Bone Formation in Mice
Mengrui Wu1,2, Yi-Ping Li1, 2, Guochun Zhu2, Yun Lu2, Yiping Wang1,2, Joel Jules2, Matthew McConnell2, Rosa Serra3, Jian-Zhong Shao1, Wei Chen2
1. Institute of Genetics, Life Science College, Zhejiang University, Hangzhou, Zhejiang, 310058, People’s Republic of China. 2. Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. 3. Department of Cell, Development, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Corresponding author: Wei Chen, MD: Department of Pathology, University of Alabama at Birmingham, SHEL 815, 1825 University Blvd, Birmingham, AL 35294, USA, Tel: 205.975.2605, Fax: 205.975.4919, E-mail: email@example.com or Yi-Ping Li, PhD: Department of Pathology, University of Alabama at Birmingham, SHEL 810, 1825 University Blvd, Birmingham, AL 35294, USA, Tel: 205.975.2606, Fax: 205 975.4919, E-mail: firstname.lastname@example.org
Despite years of research into bone formation, the mechanisms by which transcription factors specify growth plate development and trabecular bone formation remain unclear and the role of hypertrophic chondrocytes in trabeculae morphogenesis is controversial. To study the role of Core binding factor beta (Cbfβ) in postnatal cartilage development and endochondral bone formation, we generated chondrocyte-specific Cbfβ–deficient mice (Cbfβf/fCol2α1-Cre mice) using floxed alleles of Cbfβ (Cbfβf/f) and Cre driven by the Collagen 2α1 promoter (Col2α1-Cre). Cbfβf/fCol2α1-Cre mice evaded developmental and newborn lethality to survive to adulthood and displayed severe skeletal malformation. Cbfβf/fCol2α1-Cre mice had dwarfism, hypoplastic skeletons, defective bone mineralization, shortened limbs, shortened sternum bodies, and un-calcified occipital bones and hyoid bones. In the long bone cartilage, the resting zone was elongated, and chondrocyte proliferation and hypertrophy were impaired in Cbfβf/fCol2α1-Cre mice, which led to deformation of the growth plates. Primary spongiosa formation was delayed, diaphysis was shortened and trabecular bone formation was almost absent in the mutant mice. In addition, lamellar bone formation in the secondary spongiosa was also impaired. However, osteoclast formation in the trabecular bone was not affected. Cbfβ deficiency led to down-regulation of chondrocyte-regulating genes [i.e, patched (Ptc1), Cyclin D1 and Indian hedgehog (Ihh)] in the cartilage. Interestingly, the expression of Runx2 and Runx3 was not changed in the cartilage of the mutants. Collectively, the results revealed that Cbfβ is crucial for postnatal skeletal development and endochondral bone formation through its function in growth plate development and chondrocyte proliferation and differentiation. This study also revealed that chondrocyte maturation, mediated by Cbfβ, was critical to trabecular bone morphogenesis. Significantly, these findings provide insight into the role of Cbfβ in postnatal skeletogenesis, which may assist in the development of new therapies for osteoporosis.
Cbfβ, Runx, Indian hedgehog (Ihh), skeletal development, chondrocyte proliferation and hypertrophy, endochondral bone formation.
Date Deposited : 12 Feb 2016 10:53
Official URL: http://www.ijbs.com/v10i8
Last Modified : 12 Feb 2016 10:53
Volume 10, Number 8, - 2014 , ISSN 1449-2288
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