Role of RANK-RANKL-OPG Axis in Cranial Suture Homeostasis

Craniosynostosis is a significant disorder affecting 1 in 2500 live births worldwide. Although a large body of work has focused on dural regulation and the contributions of molecular mediators such as fibroblast growth factor, bone morphogenetic protein, and transforming growth factor &bgr;, minimal attention has been directed toward osteoclast function in cranial suture biology. Receptor activator of nuclear factor &kgr;B (RANK) is an essential mediator of osteoclastogenesis and osteoclast activation. In this study, physiologic fusion of posterior frontal sutures in murine development correlated with decreasing protein expression of RANK in comparison to age-matched coronal and sagittal sutures via immunohistochemical survey. However, RANK mRNA did not exhibit a similar pattern suggesting that RANK is regulated at the protein level. Fused cranial sutures in nonsyndromic craniosynostotic children also showed decreased levels of RANK staining in immunohistochemistry in comparison to patent sutures from the same patients. Immunohistochemistry with a RANK ligand antibody did not show differences in fused or patent sutures. Moreover, RANK knockdown in calvarial strip suture cultures displayed increased bone density specifically in the suture line after infection with small interfering RANK viruses. Cranial suture biology, similar to bone biology in general, likely depends on a complex interplay between osteoblasts and osteoclasts. We now report a temporospatial correlation between RANK expression and suture morphology that suggests that osteoclast activity is important in maintenance of cranial suture patency in normal physiology and disease. Furthermore, RANK downregulation promoted suture fusion establishing a causal relationship between the presence of RANK and patency.

[1]  J. Fearon,et al.  Major Morbidity and Mortality Rates in Craniofacial Surgery: An Analysis of 8101 Major Procedures , 2010, Plastic and Reconstructive Surgery.

[2]  S. Goldstein,et al.  Force-Induced Craniosynostosis in the Murine Sagittal Suture , 2009, Plastic and reconstructive surgery.

[3]  T. He,et al.  A comprehensive analysis of the dual roles of BMPs in regulating adipogenic and osteogenic differentiation of mesenchymal progenitor cells. , 2009, Stem cells and development.

[4]  C. Deng,et al.  Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology. , 2009, Developmental biology.

[5]  J. Penninger,et al.  RANK/RANKL: Regulators of Immune Responses and Bone Physiology , 2008, Annals of the New York Academy of Sciences.

[6]  Deepak M. Gupta,et al.  Microarray Analysis of the Role of Regional Dura Mater in Cranial Suture Fate , 2008, Plastic and reconstructive surgery.

[7]  J. Persing,et al.  Familial lambdoid craniosynostosis between father and son. , 2008, The Journal of craniofacial surgery.

[8]  S. Rasmussen,et al.  A population‐based study of craniosynostosis in metropolitan Atlanta, 1989–2003 , 2008, American journal of medical genetics. Part A.

[9]  D. Frim,et al.  Recurrence of Synostosis following Surgical Repair of Craniosynostosis , 2008, Plastic and reconstructive surgery.

[10]  M. Sena-Esteves,et al.  Dihydrotestosterone Stimulates Proliferation and Differentiation of Fetal Calvarial Osteoblasts and Dural Cells and Induces Cranial Suture Fusion , 2007, Plastic and reconstructive surgery.

[11]  V. Kimonis,et al.  Genetics of craniosynostosis. , 2007, Seminars in pediatric neurology.

[12]  A. Burrows,et al.  Noggin Inhibits Postoperative Resynostosis in Craniosynostotic Rabbits , 2007, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[13]  Wei Jiang,et al.  Selection and validation of optimal siRNA target sites for RNAi-mediated gene silencing. , 2007, Gene.

[14]  H. Takayanagi Osteoimmunology: shared mechanisms and crosstalk between the immune and bone systems , 2007, Nature Reviews Immunology.

[15]  B. Burton,et al.  Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations , 2007, American journal of medical genetics. Part A.

[16]  M Brent Seagle,et al.  History of Craniosynostosis Surgery and the Evolution of Minimally Invasive Endoscopic Techniques: The University of Florida Experience , 2007, Annals of plastic surgery.

[17]  M. Longaker,et al.  Isolation and Characterization of Posterofrontal/Sagittal Suture Mesenchymal Cells In Vitro , 2007, Plastic and reconstructive surgery.

[18]  D. David,et al.  Somatic FGFR and TWIST Mutations are not a Common Cause of Isolated Nonsyndromic Single Suture Craniosynostosis , 2007, The Journal of craniofacial surgery.

[19]  É. Arnaud,et al.  Genetic considerations in nonsyndromic midline craniosynostoses: a study of twins and their families. , 2005, Journal of neurosurgery.

[20]  M. Longaker,et al.  Expression and Possible Mechanisms of Regulation of BMP3 in Rat Cranial Sutures , 2005, Plastic and reconstructive surgery.

[21]  Devra B. Becker,et al.  Speech, Cognitive, and Behavioral Outcomes in Nonsyndromic Craniosynostosis , 2005, Plastic and reconstructive surgery.

[22]  J. V. van Aalst,et al.  Craniosynostosis anomalies in twins. , 2005, The Journal of craniofacial surgery.

[23]  P. Marie,et al.  A role for fibroblast growth factor receptor-2 in the altered osteoblast phenotype induced by Twist haploinsufficiency in the Saethre-Chotzen syndrome. , 2005, Human molecular genetics.

[24]  A. Wilkie,et al.  FGFR3 P250R Mutation Increases the Risk of Reoperation in Apparent ‘Nonsyndromic’ Coronal Craniosynostosis , 2005, The Journal of craniofacial surgery.

[25]  V. Centonze,et al.  Altered Twist1 and Hand2 dimerization is associated with Saethre-Chotzen syndrome and limb abnormalities , 2005, Nature Genetics.

[26]  K. Aleck Craniosynostosis syndromes in the genomic era. , 2004, Seminars in pediatric neurology.

[27]  J. Szatkowski,et al.  Characterization of the distinct orthotopic bone-forming activity of 14 BMPs using recombinant adenovirus-mediated gene delivery , 2004, Gene Therapy.

[28]  E. Carver,et al.  Craniosynostosis in Twist heterozygous mice: A model for Saethre‐Chotzen syndrome , 2002, The Anatomical record.

[29]  T. Beaty,et al.  Genetic and Environmental Risk Factors for Sagittal Craniosynostosis , 2002, The Journal of craniofacial surgery.

[30]  S. Bartlett,et al.  Craniosynostosis and altered patterns of fetal TGF-beta expression induced by intrauterine constraint. , 2002, Plastic and reconstructive surgery.

[31]  M. Bourgeois,et al.  Craniosynostosis and fetal exposure to sodium valproate. , 2001, Journal of neurosurgery.

[32]  R. Kirschner,et al.  Toward an Understanding of Nonsyndromic Craniosynostosis: Altered Patterns of TGF-&bgr; Receptor and FGF Receptor Expression Induced by Intrauterine Head Constraint , 2001, Annals of plastic surgery.

[33]  S. Herring,et al.  Osteoprotegerin, a Crucial Regulator of Bone Metabolism, Also Regulates B Cell Development and Function1 , 2001, The Journal of Immunology.

[34]  J. Hurst,et al.  Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification , 2000, Nature Genetics.

[35]  J. Bonaventure,et al.  Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcome. , 2000, Journal of neurosurgery.

[36]  D L Lacey,et al.  RANK is the intrinsic hematopoietic cell surface receptor that controls osteoclastogenesis and regulation of bone mass and calcium metabolism. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[37]  J. Goldblatt,et al.  Craniosynostosis in Western Australia, 1980-1994: a population-based study. , 1999, American journal of medical genetics.

[38]  S. Morony,et al.  OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis , 1999, Nature.

[39]  R. Maxson,et al.  Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: a possible mechanism for MSX2-mediated craniosynostosis in humans. , 1999, Developmental biology.

[40]  J. McCarthy,et al.  Immunclocalization of Basic Fibroblast Growth Factor and Fibroblast Growth Factor Receptor‐1 and Receptor‐2 in Rat Cranial Sutures , 1998, Plastic and reconstructive surgery.

[41]  J. McCarthy,et al.  Studies in Cranial Suture Biology: Regional Dura Mater Determines Overlying Suture Biology , 1998, Plastic and reconstructive surgery.

[42]  R. Steinman,et al.  TRANCE (Tumor Necrosis Factor [TNF]-related Activation-induced Cytokine), a New TNF Family Member Predominantly Expressed in T cells, Is a Dendritic Cell–specific Survival Factor , 1997, The Journal of experimental medicine.

[43]  R. Dubose,et al.  A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function , 1997, Nature.

[44]  Brian R. Wong,et al.  TRANCE Is a Novel Ligand of the Tumor Necrosis Factor Receptor Family That Activates c-Jun N-terminal Kinase in T Cells* , 1997, The Journal of Biological Chemistry.

[45]  J. McCarthy,et al.  Studies in Cranial Suture Biology: Regional Dura Mater Determines in Vitro Cranial Suture Fusion , 1997, Plastic and reconstructive surgery.

[46]  Roger Hudgins,et al.  A Longitudinal, Statistical Study of Reoperation Rates in Craniosynostosis , 1997, Plastic and reconstructive surgery.

[47]  C. Raffel,et al.  Surgical treatment of craniosynostosis: outcome analysis of 250 consecutive patients. , 1997, Pediatrics.

[48]  G Shimamoto,et al.  Osteoprotegerin: A Novel Secreted Protein Involved in the Regulation of Bone Density , 1997, Cell.

[49]  Michael T. Longaker,et al.  Studies in Cranial Suture Biology: IV. Temporal Sequence of Posterior Frontal Cranial Suture Fusion in the Mouse , 1996, Plastic and reconstructive surgery.

[50]  J. McCarthy,et al.  Studies in Cranial Suture Biology: Part II. Role of the Dura in Cranial Suture Fusion , 1996, Plastic and reconstructive surgery.

[51]  J G McCarthy,et al.  Studies in cranial suture biology: in vitro cranial suture fusion. , 1996, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

[52]  C. Bonaïti‐pellié,et al.  Genetic study of nonsyndromic coronal craniosynostosis. , 1995, American journal of medical genetics.

[53]  J. Penninger,et al.  Novel functions of RANK(L) signaling in the immune system. , 2010, Advances in experimental medicine and biology.

[54]  M. Cohen Perspectives on craniosynostosis: sutural biology, some well-known syndromes, and some unusual syndromes. , 2009, The Journal of craniofacial surgery.

[55]  J. Hukki,et al.  Single suture craniosynostosis: diagnosis and imaging. , 2008, Frontiers of oral biology.

[56]  M. Passos-Bueno,et al.  Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations. , 2008, Frontiers of oral biology.

[57]  J. Szatkowski,et al.  Osteogenic activity of the fourteen types of human bone morphogenetic proteins (BMPs). , 2003, The Journal of bone and joint surgery. American volume.

[58]  K. Kinzler,et al.  A simplified system for generating recombinant adenoviruses. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[59]  L. Melton,et al.  A population-based study of craniosynostosis. , 1990, Journal of clinical epidemiology.