Printer Friendly

Posible papel del gen noggin en el desarrollo mandibular.

Possible Role of Noggin Gene in Mandibular Development

Possivel papel do gene noggin no desenvolvimento mandibular


The lower jaw, teeth, and Meckel's cartilage develop when cells of the cranial neural crest (CNC), which give rise to the dorsal neural tube, migrate into the gill arches (1-3). As the jaw develops, the ectoderm guides patterning into the mesenchyme (3) involving an antagonistic action between a signal of bone morphogenic proteins (BMP-4) and fibroblast growth factor-8 (FGF8) (3,4). BMPs, which belong to the superfamily of transforming growth factor [beta] (TGF-[beta]), operate in a variety of tissues in space and time, requiring adjustment to different levels that ensure their specific responses (5,6). These regulations are given by modulators containing extracellular cysteine-rich domains that are folded in the form of rings of different sizes. Based on the number of ring cysteine domains, they are classified as: (a) 8-ring cysteine proteins, members of DAN (7,8); (b) 9-ring cysteine proteins, twisted gastrulation (tgs) (9,10); and (c) 10-ring cysteine proteins, Chordin (Chd) and Noggin (Nog) (11-14). The latter proteins are encoded by Chd and Nog genes respectively, which are expressed in the pharynx and during early and late formation of the lower jaw (15). Specifically, the Nog gene encodes for the homodimeric Nog protein, which has a molecular weight of 64 KDa, regulates BMPs (14,15), bonds with some BMPs, and prevents its activation by blocking the smad-dependent route (13-16). The Nog gene is a pleiotropic factor that is expressed in both early and late stages of development of various structures derived from ectoderm, such as neural tube, teeth, hair follicle, dermal papilla, and eye (17). Nog is also expressed in tissues derived from the mesoderm and is required for skeletal patterning where it plays a critical role in embryonic chondrogenesis and osteogenesis during the formation of joints. The expression is promoted by Wnt-1 and Shh genes (18). Its role in skeletal physiology has been documented by studies in mice and humans that show that mutations in this gene cause abnormalities in skeletal development (19-21). Computational analyses predicted that the alteration of the Nog heparin-binding site might have caused proximal symphalangism and conductive hearing loss (22). Another study by Matsui and Klingensmith (23) employed the extraction of genes in relevant tissue domains for the formation of upper and lower jaw, in order to determine the role of Nog. They found that the expression of the Nog middle-axial domain is relevant to the development of the first pharyngeal arch in the early stages of development, which in turn promotes the growth of the mandibular right bud, and suggests an indirect mechanism for secondary cleft palate. Based on that evidence, this review aimed at briefly describing the current knowledge regarding the Nog mechanisms that could be involved in mandibular disorders.


The development of the jaw is carried out by multiple processes which include the formation of its skeletal elements, which are derived from cells of the CNC of the first gill arch. In this formation, the condylar development plays an important role, in a form that any alteration level specifically contributes to causing mandibular condyle asymmetries. When the condyle is affected bilaterally, jaw rotation in a posterior-inferior direction is produced causing anterior open bite (24,25). However, if it is affected unilaterally (24), lateral cross bite type occurs. Only the condylar cartilage jaw endures through life and contributes to growth and joint function, becoming a tissue that serves several functions at once (26,27). Studies in human fetuses of 8 weeks of intrauterine life show that the growth of the ramus of both its width and its height is faster than the body of the mandible (28), and this seems to be due to the presence of this cartilage. Previous research which focused on the study of development of the symphysis and condyle (29) found that the cartilage of the mandibular condyle allows the endochondral bone to grow, thus exerting an adaptive role in the growing site, being this growth determined by genetic and epigenetic factors (30); but it can also be influenced by cytokines, hormones, vitamins and mechanical stimuli (31,32). Thus cytokines and the growth factors are molecules that rapidly degrade. Specifically, this latter are involved in the proliferation and differentiation of the cells forming the mandibular condyle. Among them are: The vascular endothelial growth factor (VEGF), insulin growth factor (IGF), FGF, TGF, the related protein parathyroid hormone (PTHrP), Indian hedgehog (Ihh) and BMPs, this of special interest in their specific role in mandibular growth and development (32-35). These growth factors have the role of nuclear transcription factors present in chondrocytes and these latter are found in the Sox and Runx2 family members, which are substantial in the initiation of embryonic growth of the condyle. In Table 1, growth factors and transcription involved in mandibular growth and development and specific action in this region is summarized.

Given the fact that the BMPs act by modulating the growth and development of the 3 mandibular components. The focus will be on understanding how these work. BMPs are synthesized by cells such as osteoblasts, chondrocytes and platelets (52,53) and belong to the family of TGF[sz], except the BMP1. Not only do they act on the bone level but they also have different functions in the formation of organs like the teeth, in embryonic development, repair, apoptosis and chemotaxis of various tissues (54,55). They additionally regulate iron homeostasis and induce intramembranous ossification and chondrogenesis (56). To this day there are 20 types of BMPs that have been grouped according to the similarity of its sequence and its functions. BMPs are dimeric molecules made up of 120 amino acids including cysteine residues highly conserved (57,58), a signal peptide at its N-terminal region composed of 50 to 100 hydrophobic amino acids which guides the protein and its secretory pathway C-terminal prodomain that allows proper folding (59), also contains N- and O-glycosylated sites that give stability and specificity with which the receivers to be coupled (60,61). Signaling pathway of BMPs, is regulated by extra- and intra cellular mediators which may be attached directly to them or any component blocking the transduction signal leading to a decrease in the bone formation (Figure 1). Nog expression blocks the effects of BMPs in osteoblasts, whether they are differentiated or undifferentiated (62). Also it inhibits intramembranous ossification and prevents chondrogenesis. BMPs may act in an autocrine and paracrine form (63).

The BMPs (Color Purple) begin their signaling by uniting to two different receptor types I and II in the extracellular region causing phosphorylation of proteins. This attachment may activate Smad cytoplasmic proteins, including three classes: the Smad 1, 5 and 8 which bind transcription factors in the nucleus (gene promoter region) important genes for transcription. Another signaling pathway of BMPs is independent Smad, which is initiated by growth factors such as FGF, epidermal growth factor (EGF) and the growth factor (IGF), which in turn activate the MAP kinase (MAPK) pathway that also includes 3 proteins Kinases: Erk, JNK and p38 MAPK. When the BMP (violet) joins the antagonist Nog (Blue), they form the Nog / BMP complex, which results in inhibition and modulation of its signal causing decrease in bone formation.

Noggin gene

The human NOGGIN gene (NOG), with a length of 1.9 kb is located on chromosome 17q22 (NOG; MIM # 602991). Consists of a single exon and encodes a protein of 232 amino acids (NP 005441) with a molecular weight of 25,7 KDa (UniProt NOGG_HUMAN, # Q13253). The protein on the other part is characterized by a carboxy-terminal cysteine-rich, which is used to classify antagonists of BMPs in the different subfamilies: chordin and noggin, DAN and twisted gastrulation (7). The form of this protein is the two axes; one is butterfly-shaped and another called snake-shaped clip, which is rolled around the ligand and occludes BMPs and these binding sites to their type I and II receptors. Nog dimers forming the shaft 1, consisting of two pairs of chains extending [beta] preceded by an N-terminal 20 amino acids that form the axis 2 (CLIP segment) (13) (Figure 2A).

Nog acts as a modulator of BMPs, a regulator of BMP signaling complex: 2, 4, 6, and 7 in particular. Nog has a very important role in embryogenesis, as it influences the differentiation and development of cartilage, skeletal muscle, and neural tissues and craniofacial structures (64). Nog is critical to chondrogenesis and osteogenesis embryonic joint formation (19-21). It is regulated by the FGF-2 and FGF-9 which in recent studies showed that when combined with Nog prolong human embryonic stem cells in vitro (65) they could be used to normalize or balance somehow bone remodeling activity (66).

Noggin/BMP complex

As mentioned earlier, BMPs are important for both embryonic and postnatal skeletal and bone development (67,68). The activity of BMPs is regulated by several soluble antagonists among them Nog are very important because it prevents the binding of BMPs to the surface of its receptors avoiding signal transduction BMPs start on target cells (13,67) (Figure 2B).

Nog antagonistic action occurs in undifferentiated mesenchymal cells that are to be differentiated into osteoblasts (69). However, sometimes antagonists are promiscuous, that is, their role is not limited to BMPs. They can join other members of the superfamily of TGF [beta] (17). For example Nog and sclerotin interact with each other to cancel their respective antagonism (70). This indicates that the function of the antagonists is dependent on its affinity for BMPs with which they interact (62,70). BMP2 interacts or has high affinity for heparin sulfate proteoglycans. Nog and chd also interact with these proteoglycans, however it is not clear whether these associations which are covalent unions, are irreversible at some point (71). What is clear is that the potential for interaction between receptors and ligands may also depend on the concentrations of ligand. For example, at low concentrations it appears that BMPs can join dimeric receptors Type I. Specific receptor affinities have not been determined for all BMPs (60,72-73). It has been found that the BMPs are expressed in a specific time and place in order to regulate the growth of craniofacial elements derived from the neural crest, and that Nog union alters this growth through via binding to type I receptor Alk2 using the Wnt pathway, which results in cleft lip and palate and mandibular hypoplasia (74). Similarly, the loss of these inhibitors of BMPs (Nog-Chd) may affect mandibular growth and positioning of the temporo-mandibular joint, which definitely seems to suggest that, the dose of BMPs is very important (41,75-78). Mutations in the Nog/Bmp complex are manifested in rare skeletal disorders such as the multiple synostosis syndrome 1 (78). Also it has been observed in mouse model that Nog overexpression causes a severe form of osteoporosis, while its haploinsufficiency can act in the protection from arthritis (79). Moreover, Nog transgene expression under the control of skin keratin 14 promoter, cause tumorgenesis, suggesting that this gene may inhibit tumor suppressing properties of the BMPs (80). It has also been reported that Nog, could act as a molecule that maintains pluripotency by short periods from stem cells that are supported on hydrogel matrices, which could be used in case of bone regeneration (81). BMPs can be integrated with other signaling proteins according to cell needs and are regulated from the nucleus epigenetic shape. They also influence growth factors such as FGF, Wnt, Sonic hedgehog (Shh) and Notch in order to develop different tissues. It is unclear what role the BMP antagonist Nog plays in the formation of the craniofacial skeleton, due to its multiple domains of expression during formative stages.

Noggin and jaw development

The mandibular development takes place in three components: The first component comprises the prominence of the jaw which grows distally from the embryo. The second component is the formation of teeth (Odontogenesis) and the third component is the development of the supporting structures of the jaw (82,83). The three components require specific modulation of the activity of the BMPs, this has been demonstrated by the ectopic application over the jawbones (22,84-85). It has also been shown that the lack of function of its antagonist Nog results in skeletal defects and neural tube. Nog has a unique role in the early development mandibular (17,86) but acts with Chd for mandibular growth. Apparently both antagonists are also expressed in the three major phases of development of the gill arches and are both expressed around the pharynx and mandibular buttons (22). Winnier et al. in 1995 (87) analyzed the pharyngeal endoderm and ectoderm mandibular BMP-4 mutant mice, finding absence of the development of the early phases of the jaw, with implications in the almost complete loss of the jaw.

Studies in knockout of Nog shows abnormalities in the neural tube and the somites and mandibular defects ranging over a range of phenotypes from the mandibular hypoplasia, passing through an intermediate phenotype micrognathia (poor formation of the jaw) to agnathia (absence of mandibular formation) (88,89). It has also been suggested that gene coding Nog variants can act as a holoprosencephaly aetiological factor for human, in which the presence of the mandibular micrognathism is evident (90). Nog seems to play an important role in the early mandibular development (89) and functions redundantly with Chd for mandibular growth (88,89). Analysis of the NOG gene polymorphisms in Colombian individuals with mandibular micrognathia suggests that this gene is involved in the genesis of this anomaly (91). Studies in mice with mutations in the Nog gene (Nog +/-) have shown micrognathia with incomplete penetrance, a thin jaw and bilateral asymmetries. In general, the most severe defects were found in double mutants than in heterozygotes (40,89).

Similarly, it has been observed that the direct application of Nog regulates the BMPs in chondrogenesis, deducing that the activity of these proteins is increased when the antagonists decrease, and this increase reduces the expression of FGF-8 leading to improper migration of neural crest cells of the first gill arch, causing stunt growth of the bones of the upper and lower jaws. This shows that the coordination of the expression of FGF-8 and BMP-4 in time and adequate space is also critical to the jaw development (92).

Mandibular development therefore appears to be influenced by the modulation occurring in the BMPs by their antagonists, (Nog and Chd). Given that BMP signaling is key to the formation and migration of neural crest cells and jaw formation depends on this migration, alteration of this signal produces, among other craniofacial bone defects, a severe hypertrophic jaw. This is shown in studies conducted in mouse embryos, where expression of BMP-4 and their antagonists was blocked presenting cell death of mesenchymal cells of the mandibular base causing agnathia (9,40).

Considering the above, the hypothesis proposes how mutations in the gene Nog can alter the formation of its protein, which in turn would prevent a proper fitting of the BMPs receivers causing a lack of regulation of their signaling. This leads to overexpression of BMPs generating apoptosis of mesenchymal cells involved in mandibular growth. This lack of growth is based on the dose, going from a range of hypoplasia, micrognathia through agnathia (Figure 3).

The BMPs play an important role in the migration of neural crest cells for the formation of the 3 components of the jaw (thin blue arrows). Mentonian symphysis, teeth and supporting structures such as ascending branches and Meckel's cartilage. Nog modulates of BMPs signal through binding to their receptors in the extracellular space. When the gene which encodes Nog protein suffer impaired function primarily by mutations, the dose of the BMP signaling is increased which leads to lack of migration and death of mesenchymal cells of the neural crest which form the jaw. Therefore this could explain the presence of the different phenotypes according to the dose of signaling and these can range from hypertrophy and / or mandibular hypoplasia, through the micrognathism, up to the total lack of formation of the jaw called agnathia.


In conclusion, in the development of the mandible there are numerous genes involved in each stage of the formation of this structure. By altering these genes, defects occur that affect its growth, leading to abnormalities. Among these defects, the most often is mandibular micrognathia. It is known that the mandibular tissue derived from the neural crest, which in turn interacts with tissue as the endoderm and ectoderm result in the formation of this structure and the BMPs in turn play a key role as a regulator of development of neural crest cells and their derivatives.

It is also known that these BMPs have main antagonists (Nog and Chd) and modulating the signal act in regulating the development of craniofacial structures. The Nog antagonist specifically, plays an essential role and acts as both in the early pleiotropic development in the late development of the jaw and in the presence of BMP 2, 4, 5, 6 and 7 increases its expression in osteoblast cells and chondrocytes.


The mechanisms by which this gene could cause this malformation are not well understood. Therefore is necessary to undergo more molecular studies of the NOG gene and other regulator genes of the BMPs signaling in patients with mandibular micrognathism and mandibular growth alterations, which can give light to the etiology of this anomaly. Epigenetic studies are suggested in order to determine not only the aspects which influence the ethiology of these anomalies from the classic genetics standpoint, but also the environmental factors involved.


For several decades, studies have been conducted on craniofacial development and morphogenesis and have identified alterations in the gene sequences involved in the formation of these tissues. Animal models have also been used in which specific mutations and embryological techniques have been performed, allowing us to determine the importance of different signaling pathways. The Nog gene has recently attracted attention due to its involvement in the development of the mandible and several other craniofacial elements derived from neural crest cells (NCCs). Moreover, a lack of proper Nog function appears to be related to another craniofacial malformation that has one of the highest rates of morbidity in the world, one of them being cleft palate. Several studies using a topical treatment of the noggin recombinant human protein (rh Noggin) in mice with craniosynostosis (premature closure of cranial sutures) have shown that rhNoggin prevents this premature closure and may be a potential medical alternative for treating craniofacial syndromes. Furthermore, rhNoggin may also be used to treat mandibular growth alterations, such as prognathism and micrognathia as well as cleft palate. Viral and non-viral methods have been designed for transgene introduction and are potential strategies for craniofacial regeneration and treatment because more studies are focusing on designing safe gene therapy protocols for a single gene with the long-term goal of using similar protocols to treat complex diseases that involve several genes in their etiology. The use of these ex vivo strategies, such as cell transduction with retroviruses, is promising and may lead to successful treatment. However, it is essential to perform each step carefully, taking into consideration genotoxicity, and to begin integrating gene therapy with craniofacial engineering.


Recibido para publicacion, 24/10/2015

Aceptado para publicacion: 15/12/2015

Disponible en:


The authors acknowledge the support of the office of the Academic Vice President of Pontificia Universidad Javeriana, campus Bogota. The authors declare no conflicts of interest.


(1.) Le Douarin NM, Kalcheim C. The neural crest. 2nd ed. New York, NY: Cambridge University Press; 1999.

(2.) Mina M, Kollar EJ. The induction of odontogenesis in non-dental mesenchyme combined with early murine mandibular arch epithelium. Arch Oral Biol. 1987; 32(2): 123-7.

(3.) Tucker A, Sharpe P. The cutting-edge of mammalian development; how the embryo makes teeth. Nat Rev Genet. 2004 Jul; 5(7): 499-508.

(4.) Neubuser A, Peters H, Balling R, Martin GR. Antagonistic interactions between FGF and BMP signaling pathways: a mechanism for positioning the sites of tooth formation. Cell. 1997 Jul 25; 90 (2): 247-55.

(5.) Walsh DW, Godson C, Brazil DP, Martin F. Extracellular BMP antagonist regulation in development and disease tied up in knots. Trends Cell Biol. 2010 May; 20(5): 244-56. doi: 10.1016/j.tcb.2010.01.008.

(6.) Gazzerro E, Canalis E. Bone morphogenetic proteins and their antagonists. Rev Endocr Metab Disord. 2006 Jun; 7(1-2): 51-65.

(7.) Avsian-Kretchmer O, Hsueh AJ. Comparative genomic analysis of the eight membered ring cystine knot containing bone morphogenetic protein antagonists. Mol Endocrinol. 2004 Jan; 18(1): 1-12.

(8.) Sudo S, Avsian-Kretchmer O, Wang LS, Hsueh AJ. Protein related to DAN and cerberus is a bone morphogenetic protein antagonist that participates in ovarian paracrine regulation. J Biol Chem. 2004 May 28; 279(22): 23134-41.

(9.) Mason ED, Konrad KD, Webb CD, Marsh JL. Dorsal midline fate in Drosophila embryos requires twisted gastrulation, a gene encoding a secreted protein related to human connective tissue growth factor. Genes Dev. 1994 Jul 1; 8(13): 1489-501.

(10.) Ross JJ, Shimmi O, Vilmos P, Petryk A, Kim H, Gaudenz K, Hermanson S, Ekker SC, O'Connor MB, Marsh JL. Twisted gastrulation is a conserved extracellular BMP antagonist. Nature. 2001 Mar 22; 410(6827): 479-83.

(11.) Sasai Y, Lu B, Steinbeisser H, De Robertis EM. Regulation of neural induction by the Chd and Bmp-4 antagonistic patterning signals in Xenopus. Nature. 1995 Jul 27; 376(6538): 333-6.

(12.) Garcia Abreu J, Coffinier C, Larrain J, Oelgeschlager M, De Robertis EM. Chordin like CR domains and the regulation of evolutionarily conserved extracellular signaling systems. Gene. 2002 Apr 3; 287(1-2): 39-47.

(13.) Groppe J, Greenwald J, Wiater E, Rodriguez-Leon J, Economides AN, Kwiatkowski W, Affolter M, Vale WW, Izpisua Belmonte JC, Choe S. Structural basis of BMP signaling inhibition by the cystine knot protein Noggin. Nature. 2002 Dec 12; 420 (6916): 636-42.

(14.) Re'em Kalma Y, Lamb T, Frank D. Competition between noggin and bone morphogenetic protein 4 activities may regulate dorsalization during Xenopus development. Proc Natl Acad Sci USA. 1995 Dec 19; 92(26): 12141-5.

(15.) Smith WC, Harland RM. Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos. Cell. 1992 Sep 4; 70(5): 829-40.

(16.) Zimmerman LB, De Jesus-Escobar JM, Harland RM. The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4. Cell. 1996 Aug 23; 86(4): 599-606.

(17.) McMahon JA, Takada S, Zimmerman LB, Fan CM, Harland RM, McMahon AP. Noggin mediated antagonism of BMP signaling is required for growth and patterning of the neural tube and somite. Genes Dev. 1998 May 15; 12(10): 1438-52.

(18.) Hirsinger E, Duprez D, Jouve C, Malapert P, Cooke J, Pourquie O. Noggin acts downstream of Wnt and Sonic Hedgehog to antagonize BMP4 in avian somite patterning. Development. 1997 Nov; 124(22): 4605-14.

(19.) Pathi S, Rutenberg JB, Johnson RL, Vortkamp A. Interaction of Shh and BMP/Noggin signaling during cartilage differentiation. Dev Biol. 1999 May 15; 209(2): 239-53.

(20.) Gong Y, Krakow D, Marcelino J, Wilkin D, Chitayat D, Babul-Hirji R, Hudgins L, Cremers CW, Cremers FP, Brunner HG, Reinker K, Rimoin DL, Cohn DH, Goodman FR, Reardon W, Patton M, Francomano CA, Warman ML. Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis. Nat Genet. 1999; 21: 302-4.

(21.) Tylzanowski P, Mebis L, Luyten FP. The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects. Dev Dyn. 2006 Jun; 235(6): 1599-607.

(22.) Sawako M, Kazunori N, Hideki M, Satoko U, Yuko M, Hiroki K, Tatsuo M. A mutation in the heparin-binding site of noggin as a novel mechanism of proximal symphalangism and conductive hearing loss. Biochem Biophys Res Commun. 2014 May 9; 447(3): 496-502. doi: 10.1016/j. bbrc.2014.04.015.

(23.) Matsui M, Klingensmith J. Multiple tissue-specific requirements for the BMP antagonist Noggin in development of the mammalian craniofacial skeleton. Dev Biol. 2014 Aug 15; 392(2): 168-81. doi: 10.1016/j.ydbio. 2014.06.006.

(24.) Arnett GW, Milam SB, Gottesman L. Progressive mandibular retrusion-idiopathic condylar resorption. Part I. Am J Orthod Dentofacial Orthop. 1996 Jul; 110(1): 8-15.

(25.) Bryndahl F, Eriksson L, Legrell PE, Isberg A. Bilateral TMJ disk displacement induces mandibular retrognathia. J Dent Res. 2006 Dec; 85(12): 1118-23.

(26.) Symons NBB. Studies on the growth and form of the mandible. Dent Rec (London). 1951 Mar; 71(3): 41-53.

(27.) Copray JC, Jansen HW, Duterloo HS. Growth and growth pressure of mandibular condylar and some primary cartilages of the rat in vitro. Am J Orthod Dentofacial Orthop. 1986 Jul; 90(1): 19-28.

(28.) Bareggi R, Sandrucci MA, Baldini G, Grill V, Zweyer M, Narducci P. Mandibular growth rates in human fetal development. Arch Oral Biol. 1995 Feb; 40(2): 119-25.

(29.) Ben-Ami Y, Lewinson D, Silbermann M. Structural characterization of the mandibular condyle in human fetuses: light and electron microscopy studies. Acta Anat (Basel). 1992; 145(1): 79-87.

(30.) Enlow DH. Handbook of facial growth. 3rd ed. Philadelphia, PA: W. B. Saunders; 1990.

(31.) Ramirez-Yanez GO, Young WG, Daley TJ, Waters MJ. Influence of growth hormone on the mandibular condyle of rats. Arch Oral Biol. 2004 Jul; 49(7): 585-90.

(32.) Carlevaro MF, Cermelli S, Cancedda R, Descalzi Cancedda F. Vascular endotelial growth Factor (VEFG) en cartilage neovascularization and chondrocyte differentiation: Autoparacrine role during endochondral bone formation. J Cell Sci. 2000 Jan; 113 (Pt 1): 59-69.

(33.) Xiong H, Rabie AB, Haag U. Neovascularization and mandibular condylar bone remodeling in adult rats under mechanical strain. Front Biosci. 2005 Jan 1; 10: 74-82.

(34.) Papadopoulou AK, Papachristou DJ, Charzoupoulos SA, Pirttiniemi P, Papavassiliou AG, Baudra EK. Load application induces changes in the expression levels of Sox9, FGFR-3 and VEFG in condylar chondrocytes. FEBS Lett. 2007 May 15; 581(10): 2041-6.

(35.) Mohan S, Baylink DJ. Bone growth factors. Clin Orthop Relat Res. 1991 Feb; (263): 30-48.

(36.) Minuto F, Palermo C, Arbigo M, Barreca AM. The IGF system and Bone. J Endocrinol Invest. 2005; 28(8 Suppl): 8-10.

(37.) Alini M, Marriott A, Chen T, Abe S, Poole AR. A novel angiogenic molecule produced at the time condrocyte hypertrophy during endochondral formation. Dev Biol. 1996 May 25; 176(1): 124-32.

(38.) Ornitz DM, Marie PJ. FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease. Genes Dev. 2002 Jun 15; 16(12): 1446-65.

(39.) Frank DU, Fotheringham LK, Brewer JA, Muglia LJ, Tristani-Firouzi M, Capecchi MR, Moon AM. An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome. Development. 2002 Oct; 129(19): 4591-603.

(40.) Trumpp A, Depew MJ, Rubenstein JL, Bishop JM, Martin GR. Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch. Genes Dev. 1999 Dec 1; 13(23): 3136-48.

(41.) Ballock RT, Heydemann A, Wakefield LM, Flanders KC, Roberts AB, Sporn MB. TGF-beta-1 prevents hypertrophy of epiphyseal condrocytes: Regulation of gene expression for cartilage matrix proteins and metalloproteases. Dev Biol. 1993 Aug; 158(2): 414-29.

(42.) Li XB, Zhou Z, Luo SJ. Expressions of IGF-1 and TGF-[beta]1 in the condylar cartilages of rapidly growing rats. Chin J Dent Res. 1998 Sep; 1(2): 52-6.

(43.) Delatte M, Von den Hoff JW, Malta JC, Kuijpers-Jagtman AM. Growth regulation of the rat mandibular condyle and femoral head by transforming growth factor- (beta) 1, fibroblast growth factor-2 and insulin-like growth factor -1. Eur J Orthod. 2005 Feb; 27(1): 17-26.

(44.) Vortkamp A, Lee K, Lanske B, Segre GV, Kronenberg HM, Tabin CJ. Regulation of rate of cartilage differentiation by Indian Hedgehog and PTH-related protein. Science. 1996 Aug 2; 273(5275): 613-22.

(45.) Vortkamp A, Pathi S, Peretti GM, Caruso EM, Zaleske DJ, Tabin CJ. Recapitulation of signals regulating embryonic bone formation during postnatal growth and in fracture repair. Mech Dev. 1998 Feb; 71(1-2): 65-76.

(46.) Shibukawa Y, Young B, Wu C, Yamada S, Long F, Pacifi M, Koyama E. Temporomandibular joint formation and condyle growth require Indian hedgehog signaling. Dev Dyn. 2007 Feb; 236(2): 426-34.

(47.) Ueno T, Kagawa T, Kanou M, Fujii T, Fukunaga J, Mizukawa N, Sugahara T, Yamamoto T. Immunohistochemical observations of cellular differentiation and proliferation in endochondral bone formation from grafted periosteum: Expression and localization of BMP-2 and-4 in the grafted periosteum. J Craniomaxillofac Surg. 2003 Dec; 31(6): 356-61.

(48.) Ng LJ, Weatley S, Muscat GEO, Conway-Campbell J, Bowles J, Wrigth E, Bell DM, Tam PP, Cheah KS, Koopman P. SOX9 binds DNA, activates transcription and coexpresses with type II collagen during chondrogenesis in the mouse. Dev Biol. 1997 Mar 1; 183(1): 108-21.

(49.) Rabie AB, She TT, Haag U. Functional appliance therapy accelerates and enhances condylar growth. Am J Orthod Dentofacial Orthop. 2002 Oct; 122(4): 401-9.

(50.) Stottmann RW, Anderson RM, Klingensmith J. The BMP antagonists Chordin and Noggin have essential but redundant roles in mouse mandibular outgrowth. Dev Biol. 2001 Dec 15; 240(2): 457-73.

(51.) Rabie AB, Tang GH, Hagg U. Cbfa1 couples chondrocytes, maturation and endochondral ossification in rat mandibular condylar cartilage. Arch Oral Biol. 2004 Feb; 49(2): 109-18.

(52.) Pecina M, Vukicevic S. Biological aspects of bone, cartilage and tendon regeneration. Int Orthop. Dec 2007 31(6): 719-20.

(53.) Sipe JB, Zhang J, Waits C, Skikne B, Garimella R, Anderson HC. Localization of bone morphogenetic proteins (BMPs)-2, -4, and -6 within megakaryocytes and platelets. Bone. 2004 Dec; 35(6): 1316-22.

(54.) Ducy P, Karsenty G. The family of bone morphogenetic proteins Kidney Int. 2000 Jun; 57(6): 2207-14.

(55.) Lissenberg-Thunnissen SN, de Gorter DJ, Sier CF, Schipper IB. Use and efficacy of bone morphogenetic proteins in fracture healing. Int Orthop. 2011 Sep; 35(9): 1271-80. doi: 10.1007/s00264-011-1301-z.

(56.) Leboy P, Grasso-Knight G, D'Angelo M, Volk SW, Lian JV, Drissi H, Stein GS, Adams SL. Smad-Runx interactions during chondrocyte maturation. See comment in PubMed Commons belowJ Bone Joint Surg Am. 2001; 83-A Suppl 1(Pt 1): S15-22.

(57.) Butler SJ, Dodd J. A role for BMP heterodimers in roof plate-mediated repulsion of commissural axons. Neuron. 2003 May 8; 38(3): 389-401.

(58.) Griffith DL, Keck, PC. Sampath TK, Rueger DC, Carlson WD. Three-dimensional structure of recombinant human osteogenic protein 1: structural paradigm for the transforming growth factor beta superfamily. Proc Natl Acad Sci USA. 1996 Jan 23; 93(2): 878-83.

(59.) Miyazono K, Hellman U, Wernstedt C, Heldin CH. Latent high molecular weight complex of transforming growth factor beta 1. Purification from human platelets and structural characterization. J Biol Chem. 1988 May 5; 263(13): 6407-15.

(60.) Heinecke K, Seher A, Schmitz W, Mueller TD, Sebald W, Nickel J. Receptor oligomerization and beyond: a case study in bone morphogenetic proteins. BMC Biol. 2009 Sep 7; 7: 59. doi: 10.1186/1741-7007-7-59.

(61.) Lowery JW. Amich JM, Andonian A, Rosen V. N-linked glycosylation of the bone morphogenetic protein receptor type 2 (BMPR2) enhances ligand binding. Cell Mol Life Sci. 2014 Aug; 71(16): 3165-72. doi: 10.1007/s00018-013-1541-8.

(62.) Gazzerro E, Gangji V, Canalis E. Bone morphogenetic proteins induce the expression of noggin, which limits their activity in cultured rat osteoblasts. J Clin Invest. 1998 Dec 15; 102(12): 2106-14.

(63.) Carreira AC, Lojudice FH, Halcsik E, Navarro RD, Sogayar MC, Granjeiro JM. Bone morphogenetic proteins: facts, challenges, and future perspectives. J Dent Res. 2014 Apr; 93(4): 335-45. doi: 10.1177/0022034513518561.

(64.) Wang G, Zhang H, Zhao Y, Li J, Cai J, Wang P , Meng S, Feng J, Miao C, Ding M, Li D, Deng H. Noggin and bFGF cooperate to maintain the pluripotency of human embryonic stem cells in the absence of feeder layers. Biochem Biophys Res Commun. 2005 May 13; 330(3): 934-42.

(65.) Schwaninger R, Rentsch CA, Wetterwald A, van der Pluijm G, Lowik CW, Ackermann K, Pyerin W, Hamdy FC, Thalmann GN, Cecchini MG. Lack of noggin expression by cancer cells is a determinant of the osteoblast response in bone metastases. Am J Pathol. 2007 Jan; 170(1): 160-75.

(66.) Anderson RM, Lawrence AR, Stottmann RW, Bachiller DJ, Klingensmith J. Chordin and noggin promote organizing centers of forebrain development in the mouse. Development. 2002 Nov; 129(21): 4975-87

(67.) Reddi AH. Role of morphogenetic proteins in skeletal tissue engineering and regeneration. Nat Biotechnol. 1998 Mar; 16(3): 247-52.

(68.) Sampath TK, Maliakal JC, Hauschka PV, Jones WK, Sasak H, Tucker RF, White KH, Coughlin JE, Tucker MM, Pang RH. Recombinant human osteogenic protein-1 (hOP-1) induces new bone formation in vivo with a specific activity comparable with natural bovine osteogenic protein and stimulates osteoblast proliferation and differentiation in vitro. J Biol Chem. 1992 Oct 5; 267(28): 20352-62.

(69.) Wozney JM, Rosen V. Bone morphogenetic protein and bone morphogenetic protein gene family in bone formation and repair. Clin Orthop Relat Res. 1998 Jan; (346): 26-37

(70.) Winkler DG, Yu C, Geoghegan JC, Ojala EW, Skonier JE, Shpektor D, Sutherland MK, Latham JA. Noggin and sclerostin bone morphogenetic protein antagonists form a mutually inhibitory complex. J Biol Chem. 2004 Aug 27; 279(35): 36293-8.

(71.) Abe E, Yamamoto M, Taguchi Y, Lecka-Czernik B, O'Brien CA, Economides AN, Stahl N, Jilka RL, Manolagas SC. Essential requirement of BMPs-2/4 for both osteoblast and osteoclast formation in murine bone marrow cultures from adult mice: antagonism by noggin. J Bone Miner Res. 2000 Apr; 15(4): 663-73.

(72.) Koenig BB, Cook JS, Wolsing DH, Ting J, Tiesman JP, Correa PE. Characterization and cloning of a receptor for BMP-2 and BMP-4 from NIH 3T3 cells. Mol Cell Biol. 1994 Sep; 14(9): 5961-74.

(73.) Greenwald J, Groppe J, Gray P, Wiater E, Kwiatkowski W, Vale W. The BMP7/ActRII extracellular domain complex provides new insights into the cooperative nature of receptor assembly. Mol Cell. 2003 Mar; 11(3): 605-17.

(74.) Dudas M, Sridurongrit S, Nagy A, Okazaki K, Kaartinen V. Craniofacial defects in mice lacking BMP type I receptor Alk2 in neural crest cells. Mech Dev. 2004 Feb; 121(2): 173-82.

(75.) Ekanayake S, Hall BK. The in vivo and in vitro effects of bone morphogenetic protein-2 on the development of the chick mandible. Int J Dev Biol. 1997 Feb; 41(1): 67-81.

(76.) Mina M, Wang YH, Ivanisevic AM, Upholt WB, Rodgers B. Region- and stage-specific effects of FGFs and BMPs in chick mandibular morphogenesis. Dev Dyn. 2002 Mar; 223(3): 333-52.

(77.) Wilson J, Tucker AS. Fgf and Bmp signals repress the expression of Bapx1 in the mandibular mesenchyme and control the position of the developing jaw joint. Dev Biol. 2004 Feb 1; 266(1): 138-50.

(78.) Brown DJ, Kim T, Petty E, Downs C, Martin D, Strouse PJ, Moroi SE, Milunsky JM, Lesperance MM. Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin. Am J Hum Genet. 2002 Sep; 71(3): 618-24. doi: 10.1086/342067.

(79.) Lories JU, Daans M, Derese I, Matthys P, Kasran A, Tylzanowski P, Ceuppens JL, Luyten FP. Noggin haploinsufficiency differentially affects tissue responses in destructive and remodeling arthritis. Arthritis Rheum. 2006 Jun; 54(6): 1736-46.

(80.) Sharov A, Mardaryev A, Sharova T, Grachtchouk M, Atoyan R, Byers R, Seykora JT, Overbeek P, Dlugosz A, Botchkarev VA. Bone morphogenetic protein antagonist noggin promotes skin tumorigenesis via stimulation of the Wnt and Shh signaling pathways. Am J Pathol. 2009 Sep; 175(3): 1303-14. doi: 10.2353/ajpath.2009.090163.

(81.) Chaturvedi G, Simone P, Ain R, Soares MJ, Wolf MW. Noggin maintains pluripotency of human embryonic stem cells grown on Matrigel. Cell Prolif. 2009 Aug; 42(4): 425-33. doi: 10.1111/j.1365-2184.2009.00616.x.

(82.) Jernvall J, Thesleff I. Reiterative signaling and patterning during mammalian tooth morphogenesis. Mech Dev. 2000 Mar 15; 92(1): 19-29.

(83.) Thesleff I, Sharpe P. Signaling networks regulating. Mech Dev. 1997 Oct; 67(2): 111-23.

(84.) Barlow AJ, Francis-West PH. Ectopic application of recombinant BMP-2 and BMP-4 can change patterning of developing chick facial primordial. Development. 1997 Jan; 124(2): 391-8.

(85.) Wang Y-H, Rutherford B, Uphot W, Mina M. Effects of BMP-7 on mouse tooth mesenchyme and chick mandibular mesenchyme. Dev Dyn. 1999 Dec;216(4-5): 320-35.

(86.) Semba I, Nonaka K, Takahashi I, Takahashi K, Dashner R, Shum L, Nuckolls GH, Slavkin HC. Positionally-dependent chondrogenesis induced by BMP4 is co-regulated by Sox9 and Msx2. Dev Dyn. 2000 Apr; 217(4): 401-14.

(87.) Winnier G, Blessing M, Labosky PA, Hogan BL. Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse. Genes Dev. 1995 Sep 1; 9(17): 2105-16.

(88.) Wijgerde M, Karp S, McMahon J, McMahon AP. Noggin antagonism of BMP4 signaling controls development of the axial skeleton in the mouse. Dev Biol. 2005 Oct 1; 286(1): 149-57

(89.) Bachiller D, Klingensmith J, Kemp C, Belo JA, Anderson RM, May SR, McMahon JA, McMahon AP, Harland RM, Rossant J, De Robertis EM. The organizer factors Chordin and Noggin are required for mouse forebrain development. Nature. 2000 Feb 10; 403(6770): 658-61.

(90.) Lana-Elola E, Tylzanowski P, Takatalo M, Alakurtti K, Veistinen L, Mitsiadis TA, Graf D, Rice R, Luyten FP, Rice DP. Noggin null allele mice exhibit a microform of holoprosencephaly. Hum Mol Genet. 2011 Oct 15; 20(20): 4005-15. doi: 10.1093/hmg/ddr329.

(91.) Gutierrez S, Gomez M, Rey A, Prieto JC. Polymorphisms of the noggin gene and mandibular micrognathia: a first approximation. Acta Odontol Latinoam. 2010; 23(1): 13-9.

(92.) Schmotzer CL, Shehata BM. Two cases of agnathia (otocephaly): with review of the role of fibroblast growth factor (FGF8) and bone morphogenetic protein (BMP4) in patterning of the first branchial arch. Pediatr Dev Pathol. 2008, Jul-Aug; 11 (4): 321-4.


Sandra Gutierrez Prieto

Diana Torres Lopez

Mariluz Gomez Rodriguez

Adriana Garcia Robayo

Sandra Gutierrez Prieto Odontologa, magistra y PhD en Ciencias Biologicas, docente investigadora del Centro de Investigaciones Odontologicas, Pontificia Universidad Javeriana, Bogota, Colombia.

Diana Torres Lopez Bacteriologa, PhD en Ciencias Biologicas, docente investigadora, Pontificia Universidad Javeriana, Bogota, Colombia.

Mariluz Gomez Rodriguez Bacteriologa, magistra en Biologia, Pontificia Universidad Javeriana, Bogota, Colombia. PhD en Biologia Molecular, Instituto Gulbenkian de Ciencias, Portugal. Profesora, Pontificia Universidad Javeriana, Cali, Colombia.

Adriana Garcia Robayo Bacteriologa, Magistra y PhD en Ciencias Biologicas, docente investigadora del Centro de Investigaciones Odontologicas, Pontificia Universidad Javeriana, Bogota, Colombia.



Name                           Action at mandible

VEFG         Express at chondrocytes for the induction of bone
             formation in development and adaptation to mechanical
             charges (33,34).

IGF          Involves in the growth and development of tooth,
             mandible, maxillary and tongue (36,37).

FGF          Express in chondrocytes.

             FGF-2 is highly expressed in the absence of mechanical
             charge, reduces MEC production that directs to
             bone formation.

             FGFR-3 induces chondrocytes proliferation. Mutations of
             FGFR-3 cause skeletal dysplasia such achondroplasia

             FGF-8 expression is critical for jaw development (39),
             as well as for facial mesenchymal neural crest derived
             and growth regulation of facial primordium (40).

TGF          TGF[beta]-1 is strongly expressed at mature layers and
             hypertrophic condyle of mandible (39,40) l Also
             increases proliferation and synthesis of
             glycosaminoglycans, and decreases chondrocytes
             hypertrophy and bone mineralization (41).

PTHrP and    Regulates proliferation and growth of chondrocyte.
Ihh          Prevents chondrocyte hypertrophy (PTHrP). Blocks
             ossification (Ihh) and is involved at the early
             formation of TMJ (42-46)

BMPs         Modulates growth and development of the 3 mandible
             components (47) l Wnt inhibits part of chondro-genesis
             activity by BMP-2.

Sox 9        Regulates chondrocytes for collagen type II production
             at the cartilage (48,49).

RunX-2       Express in osteoblasts and mesenchymal condensation
(cbfal)      prechondrogenic. Regulates hypertrophy chon-drocytes,
             calcification of bone matrix and differentiation of
             osteoblasts and osteoclasts (50,51).
COPYRIGHT 2015 Pontificia Universidad Javeriana
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2015 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Author:Gutierrez Prieto, Sandra; Torres Lopez, Diana; Gomez Rodriguez, Mariluz; Garcia Robayo, Adriana
Publication:Universitas Odontologica
Date:Jul 1, 2015
Previous Article:Eficiencia del proceso de esterilizacion de las limas primarias EaveOne[R].
Next Article:Biodentine: un nuevo material en terapia pulpar.

Terms of use | Privacy policy | Copyright © 2018 Farlex, Inc. | Feedback | For webmasters