Literature DB >> 23566293

MAPK/ERK Signaling Pathway Analysis in Primary Osteoblasts From Patients With Nonsyndromic Sagittal Craniosynostosis.

Sun-Don Kim, Garima Yagnik, Michael L Cunningham, Jinoh Kim, Simeon A Boyadjiev.   

Abstract

OBJECTIVE: The MAPK/ERK signaling pathway has been implicated in several craniosynostosis syndromes and represents a plausible target for therapeutic management of craniosynostosis. The causes of sagittal nonsyndromic craniosynostosis (sNSC) have not been well understood and the role that MAPK/ERK signaling cascade plays in this condition warrants an investigation. We hypothesized that MAPK-signaling is misregulated in calvarial osteoblasts derived from patients with sNSC.
METHODS: In order to analyze if the MAPK/ERK pathway is perturbed in sNSC, we established primary calvarial osteoblast cell lines from patients undergoing surgery for correction of this congenital anomaly. Appropriate negative and positive control cell lines were used for comparison, and we examined the levels of phosphorylated ERK by immunoblotting.
RESULTS: Primary osteoblasts from patients with sNSC showed no difference in ERK1/2 phosphorylation with or without FGF2 stimulation as compared with control osteoblasts.
CONCLUSION: Under the described test conditions, we did not observe convincing evidence that MAPK/ERK signaling contributes to the development of sNSC.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23566293      PMCID: PMC3708983          DOI: 10.1597/12-136

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  40 in total

Review 1.  Clinical dividends from the molecular genetic diagnosis of craniosynostosis.

Authors:  Andrew O M Wilkie; Elena G Bochukova; Ruth M S Hansen; Indira B Taylor; Sahan V Rannan-Eliya; Jo C Byren; Steven A Wall; Lina Ramos; Margarida Venâncio; Jane A Hurst; Anthony W O'rourke; Louise J Williams; Anneke Seller; Tracy Lester
Journal:  Am J Med Genet A       Date:  2007-08-15       Impact factor: 2.802

2.  Craniosynostosis-associated gene nell-1 is regulated by runx2.

Authors:  Thien Truong; Xinli Zhang; Dharmini Pathmanathan; Chia Soo; Kang Ting
Journal:  J Bone Miner Res       Date:  2007-01       Impact factor: 6.741

3.  A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis?

Authors:  D Johnson; S A Wall; S Mann; A O Wilkie
Journal:  Eur J Hum Genet       Date:  2000-08       Impact factor: 4.246

4.  Runx2 is a common target of transforming growth factor beta1 and bone morphogenetic protein 2, and cooperation between Runx2 and Smad5 induces osteoblast-specific gene expression in the pluripotent mesenchymal precursor cell line C2C12.

Authors:  K S Lee; H J Kim; Q L Li; X Z Chi; C Ueta; T Komori; J M Wozney; E G Kim; J Y Choi; H M Ryoo; S C Bae
Journal:  Mol Cell Biol       Date:  2000-12       Impact factor: 4.272

5.  Attenuation of signaling pathways stimulated by pathologically activated FGF-receptor 2 mutants prevents craniosynostosis.

Authors:  V P Eswarakumar; F Ozcan; E D Lew; J H Bae; F Tomé; C J Booth; D J Adams; I Lax; J Schlessinger
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-28       Impact factor: 11.205

6.  Down-regulation of ubiquitin ligase Cbl induced by twist haploinsufficiency in Saethre-Chotzen syndrome results in increased PI3K/Akt signaling and osteoblast proliferation.

Authors:  Hind Guenou; Karim Kaabeche; Cécilie Dufour; Hichem Miraoui; Pierre J Marie
Journal:  Am J Pathol       Date:  2006-10       Impact factor: 4.307

Review 7.  Genetics of craniosynostosis.

Authors:  Virginia Kimonis; June-Anne Gold; Trevor L Hoffman; Jayesh Panchal; Simeon A Boyadjiev
Journal:  Semin Pediatr Neurol       Date:  2007-09       Impact factor: 1.636

Review 8.  Genetic analysis of non-syndromic craniosynostosis.

Authors:  S A Boyadjiev
Journal:  Orthod Craniofac Res       Date:  2007-08       Impact factor: 1.826

9.  RNA interference and inhibition of MEK-ERK signaling prevent abnormal skeletal phenotypes in a mouse model of craniosynostosis.

Authors:  Vivek Shukla; Xavier Coumoul; Rui-Hong Wang; Hyun-Seok Kim; Chu-Xia Deng
Journal:  Nat Genet       Date:  2007-08-12       Impact factor: 38.330

10.  Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations.

Authors:  Marianne L Seto; Anne V Hing; Jocelyn Chang; Ming Hu; Kathleen A Kapp-Simon; Pravin K Patel; Barbara K Burton; Alex A Kane; Matthew D Smyth; Richard Hopper; Richard G Ellenbogen; Kevin Stevenson; Matthew L Speltz; Michael L Cunningham
Journal:  Am J Med Genet A       Date:  2007-04-01       Impact factor: 2.802

View more
  3 in total

1.  BBS9 gene in nonsyndromic craniosynostosis: Role of the primary cilium in the aberrant ossification of the suture osteogenic niche.

Authors:  Marta Barba; Lorena Di Pietro; Luca Massimi; Maria Concetta Geloso; Paolo Frassanito; Massimo Caldarelli; Fabrizio Michetti; Stefano Della Longa; Paul A Romitti; Concezio Di Rocco; Alessandro Arcovito; Ornella Parolini; Gianpiero Tamburrini; Camilla Bernardini; Simeon A Boyadjiev; Wanda Lattanzi
Journal:  Bone       Date:  2018-04-17       Impact factor: 4.398

Review 2.  Genetic advances in craniosynostosis.

Authors:  Wanda Lattanzi; Marta Barba; Lorena Di Pietro; Simeon A Boyadjiev
Journal:  Am J Med Genet A       Date:  2017-02-04       Impact factor: 2.802

3.  GLI1 and AXIN2 Are Distinctive Markers of Human Calvarial Mesenchymal Stromal Cells in Nonsyndromic Craniosynostosis.

Authors:  Lorena Di Pietro; Marta Barba; Chiara Prampolini; Sabrina Ceccariglia; Paolo Frassanito; Alessia Vita; Enrico Guadagni; Davide Bonvissuto; Luca Massimi; Gianpiero Tamburrini; Ornella Parolini; Wanda Lattanzi
Journal:  Int J Mol Sci       Date:  2020-06-19       Impact factor: 5.923

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.