Literature DB >> 9707341

Bone formation via cartilage models: the "borderline" chondrocyte.

P Bianco1, F D Cancedda, M Riminucci, R Cancedda.   

Abstract

Increasing evidence substantiates the view that death is not necessarily the only fate of hypertrophic chondrocytes and that, when exposed to the right microenvironment, these cells can further differentiate to osteoblast-like cells and contribute to initial bone formation. In vitro, when replated as adherent cells in the presence of ascorbic acid, hypertrophic chondrocytes resume cell proliferation, switch from the synthesis of the cartilage-characteristic type II and X collagens to the synthesis of type I collagen, and organize a mineralizing bone matrix. In vivo, expression of bone specific markers by growth plate chondrocytes occurs initially in early hypertrophic cells located at the mid-diaphysis and directly facing the osteogenic perichondrium. In bones formed via cartilage models, the first mineralized bone matrix (the earliest bony collar preceding vascular invasion and the onset of endochondral bone formation) is deposited at the outer aspect of the mid-diaphysis between rows of early hypertrophic chondrocytes and osteoblasts, which are arranged in a peculiar "vis à vis" fashion. The "vis à vis" organization of perichondrial osteogenic cells and peripheral early hypertrophic chondrocytes suggests that the latter cells are exposed -- compared to their cognate, the central hypertrophic chondrocytes -- to a specific microenvironment composed of unique matrix-originating signals and cellular cross-talks. A major role in the differentiation control of, and interaction between, hypertrophic chondrocytes and osteogenic perichondrial cells is certainly played by the Indian Hedgehog/PTHrP signalling system. We propose that all early hypertrophic chondrocytes have the inherent potential to differentiate to osteoblast-like cells and to contribute to initial bone formation, but that only chondrocytes positioned at the "borderland" between cartilage and (non-cartilage) osteogenic tissues undergo further differentiation to bone producing cells. We call these hypertrophic chondrocytes "borderline chondrocytes" to emphasize both their specific location and their dual differentiation potential. Hypertrophic chondrocytes located in different cartilage areas are exposed to an inappropriate matrix and endocrine/paracrine environment, cannot differentiate to osteoblast-like cells and therefore undergo apoptosis.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9707341     DOI: 10.1016/s0945-053x(98)90057-9

Source DB:  PubMed          Journal:  Matrix Biol        ISSN: 0945-053X            Impact factor:   11.583


  35 in total

1.  An improved collagen scaffold for skeletal regeneration.

Authors:  Serafim M Oliveira; Rushali A Ringshia; Racquel Z Legeros; Elizabeth Clark; Michael J Yost; Louis Terracio; Cristina C Teixeira
Journal:  J Biomed Mater Res A       Date:  2010-08       Impact factor: 4.396

Review 2.  A Second Career for Chondrocytes-Transformation into Osteoblasts.

Authors:  Lena Ingeborg Wolff; Christine Hartmann
Journal:  Curr Osteoporos Rep       Date:  2019-06       Impact factor: 5.096

Review 3.  Lessons on skeletal cell plasticity from studying jawbone regeneration in zebrafish.

Authors:  Sandeep Paul; J Gage Crump
Journal:  Bonekey Rep       Date:  2016-11-16

Review 4.  Evolutionary origin of endochondral ossification: the transdifferentiation hypothesis.

Authors:  Fret Cervantes-Diaz; Pedro Contreras; Sylvain Marcellini
Journal:  Dev Genes Evol       Date:  2016-12-01       Impact factor: 0.900

5.  Growth Plate Borderline Chondrocytes Behave as Transient Mesenchymal Precursor Cells.

Authors:  Koji Mizuhashi; Mizuki Nagata; Yuki Matsushita; Wanida Ono; Noriaki Ono
Journal:  J Bone Miner Res       Date:  2019-05-06       Impact factor: 6.741

Review 6.  Signaling pathways regulating cartilage growth plate formation and activity.

Authors:  William E Samsa; Xin Zhou; Guang Zhou
Journal:  Semin Cell Dev Biol       Date:  2016-07-11       Impact factor: 7.727

7.  Dual non-viral gene delivery from microparticles within 3D high-density stem cell constructs for enhanced bone tissue engineering.

Authors:  Alexandra McMillan; Minh Khanh Nguyen; Tomas Gonzalez-Fernandez; Peilin Ge; Xiaohua Yu; William L Murphy; Daniel J Kelly; Eben Alsberg
Journal:  Biomaterials       Date:  2018-01-03       Impact factor: 12.479

Review 8.  Skeletal stem cells: insights into maintaining and regenerating the skeleton.

Authors:  Maxwell A Serowoky; Claire E Arata; J Gage Crump; Francesca V Mariani
Journal:  Development       Date:  2020-03-11       Impact factor: 6.868

9.  Perfusion Enhances Hypertrophic Chondrocyte Matrix Deposition, But Not the Bone Formation.

Authors:  Jonathan C Bernhard; Elizabeth Hulphers; Bernhard Rieder; James Ferguson; Dominik Rünzler; Thomas Nau; Heinz Redl; Gordana Vunjak-Novakovic
Journal:  Tissue Eng Part A       Date:  2018-03-02       Impact factor: 3.845

10.  Bromodomain and Extra-terminal (BET) Protein Inhibitors Suppress Chondrocyte Differentiation and Restrain Bone Growth.

Authors:  Ningning Niu; Rui Shao; Guang Yan; Weiguo Zou
Journal:  J Biol Chem       Date:  2016-11-07       Impact factor: 5.157

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.