Literature DB >> 12955857

Physiology and pathophysiology of the growth plate.

R Tracy Ballock1, Regis J O'Keefe.   

Abstract

Longitudinal growth of the skeleton is a result of endochondral ossification that occurs at the growth plate. Through a sequential process of cell proliferation, extracellular matrix synthesis, cellular hypertrophy, matrix mineralization, vascular invasion, and eventually apoptosis, the cartilage model is continually replaced by bone as length increases. The regulation of longitudinal growth at the growth plate occurs generally through the intimate interaction of circulating systemic hormones and locally produced peptide growth factors, the net result of which is to trigger changes in gene expression by growth plate chondrocytes. This review highlights recent advances in genetics and cell biology that are illuminating the important regulatory mechanisms governing the structure and biology of the growth plate, and provides selected examples of how studies of human mutations have yielded a wealth of new knowledge regarding the normal biology and pathophysiology of growth plate cartilage.

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Year:  2003        PMID: 12955857     DOI: 10.1002/bdrc.10014

Source DB:  PubMed          Journal:  Birth Defects Res C Embryo Today        ISSN: 1542-975X


  43 in total

1.  MicroRNA-34a modulates cytoskeletal dynamics through regulating RhoA/Rac1 cross-talk in chondroblasts.

Authors:  Dongkyun Kim; Jinsoo Song; Sunhyo Kim; Hyang Mi Park; Churl-Hong Chun; Jongkyung Sonn; Eun-Jung Jin
Journal:  J Biol Chem       Date:  2012-02-20       Impact factor: 5.157

2.  Choline kinase beta is required for normal endochondral bone formation.

Authors:  Zhuo Li; Gengshu Wu; Roger B Sher; Zohreh Khavandgar; Martin Hermansson; Gregory A Cox; Michael R Doschak; Monzur Murshed; Frank Beier; Dennis E Vance
Journal:  Biochim Biophys Acta       Date:  2014-03-14

3.  Microarray analyses of gene expression during chondrocyte differentiation identifies novel regulators of hypertrophy.

Authors:  Claudine G James; C Thomas G Appleton; Veronica Ulici; T Michael Underhill; Frank Beier
Journal:  Mol Biol Cell       Date:  2005-08-31       Impact factor: 4.138

4.  Loss of β-catenin induces multifocal periosteal chondroma-like masses in mice.

Authors:  Leslie Cantley; Cheri Saunders; Marta Guttenberg; Maria Elena Candela; Yoichi Ohta; Rika Yasuhara; Naoki Kondo; Federica Sgariglia; Shuji Asai; Xianrong Zhang; Ling Qin; Jacqueline T Hecht; Di Chen; Masato Yamamoto; Satoru Toyosawa; John P Dormans; Jeffrey D Esko; Yu Yamaguchi; Masahiro Iwamoto; Maurizio Pacifici; Motomi Enomoto-Iwamoto
Journal:  Am J Pathol       Date:  2012-12-25       Impact factor: 4.307

Review 5.  Disorders of the growth plate.

Authors:  Chanika Phornphutkul; Philip A Gruppuso
Journal:  Curr Opin Endocrinol Diabetes Obes       Date:  2009-12       Impact factor: 3.243

Review 6.  Nonproliferative and Proliferative Lesions of the Rat and Mouse Skeletal Tissues (Bones, Joints, and Teeth).

Authors:  Stacey Fossey; John Vahle; Philip Long; Scott Schelling; Heinrich Ernst; Rogely Waite Boyce; Jacquelin Jolette; Brad Bolon; Alison Bendele; Matthias Rinke; Laura Healy; Wanda High; Daniel Robert Roth; Michael Boyle; Joel Leininger
Journal:  J Toxicol Pathol       Date:  2016-07-29       Impact factor: 1.628

7.  Microarray analysis of perichondral and reserve growth plate zones identifies differential gene expressions and signal pathways.

Authors:  Mingliang Zhang; Meredith R Pritchard; Frank A Middleton; Jason A Horton; Timothy A Damron
Journal:  Bone       Date:  2008-05-09       Impact factor: 4.398

8.  Septoclast deficiency accompanies postnatal growth plate chondrodysplasia in the toothless (tl) osteopetrotic, colony-stimulating factor-1 (CSF-1)-deficient rat and is partially responsive to CSF-1 injections.

Authors:  Alison Gartland; April Mason-Savas; Meiheng Yang; Carole A MacKay; Mark J Birnbaum; Paul R Odgren
Journal:  Am J Pathol       Date:  2009-11-05       Impact factor: 4.307

9.  Wnt/beta-catenin and retinoic acid receptor signaling pathways interact to regulate chondrocyte function and matrix turnover.

Authors:  Rika Yasuhara; Takahito Yuasa; Julie A Williams; Stephen W Byers; Salim Shah; Maurizio Pacifici; Masahiro Iwamoto; Motomi Enomoto-Iwamoto
Journal:  J Biol Chem       Date:  2009-10-26       Impact factor: 5.157

10.  Loss of ATRX in chondrocytes has minimal effects on skeletal development.

Authors:  Lauren A Solomon; Jennifer R Li; Nathalie G Bérubé; Frank Beier
Journal:  PLoS One       Date:  2009-09-23       Impact factor: 3.240

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