Literature DB >> 25387264

Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expression.

Adi Reich1, Alison S Bae, Aileen M Barnes, Wayne A Cabral, Aleksander Hinek, Jennifer Stimec, Suvimol C Hill, David Chitayat, Joan C Marini.   

Abstract

CONTEXT: Patients with type V osteogenesis imperfecta (OI) are heterozygous for a dominant IFITM5 c.-14C>T mutation, which adds five residues to the N terminus of bone-restricted interferon-induced transmembrane-like protein (BRIL), a transmembrane protein expressed in osteoblasts. Type V OI skeletal findings include hyperplastic callus formation, ossification of the forearm interosseous membrane, and dense metaphyseal bands.
OBJECTIVE: The objective of this study was to examine the role of osteoblasts in the active mineralization traits of type V OI and the effect of the IFITM5 mutation on type I collagen.
METHODS: We identified eight patients with the IFITM5 c.-14C>T mutation. Cultured osteoblasts from type V OI patients were used to study osteoblast differentiation and mineralization.
RESULTS: We verified the expression and stability of mutant IFITM5 transcripts. In differentiated type V OI primary osteoblasts in culture, the IFITM5 expression and BRIL level is comparable with control. Both early and late markers of osteoblast differentiation are increased in type V OI osteoblasts. Mineralization, assayed by alizarin red staining, was increased in type V OI osteoblasts compared with control. However, type V OI osteoblasts have significantly decreased COL1A1 transcripts in mid- to late differentiation. Type I collagen protein is concomitantly decreased, with decreased cross-linked collagen in matrix and altered appearance of fibrils deposited in culture.
CONCLUSIONS: This study demonstrates that type V OI mineralization has a gain-of-function mechanism at the osteoblast level, which likely underlies the overactive tissue mineralization seen in patients. Decreased type I collagen expression, secretion, and matrix incorporation establish type V OI as a collagen-related defect.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 25387264      PMCID: PMC4318905          DOI: 10.1210/jc.2014-3082

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  36 in total

1.  Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta.

Authors:  Wayne A Cabral; Weizhong Chang; Aileen M Barnes; MaryAnn Weis; Melissa A Scott; Sergey Leikin; Elena Makareeva; Natalia V Kuznetsova; Kenneth N Rosenbaum; Cynthia J Tifft; Dorothy I Bulas; Chahira Kozma; Peter A Smith; David R Eyre; Joan C Marini
Journal:  Nat Genet       Date:  2007-02-04       Impact factor: 38.330

2.  Bril: a novel bone-specific modulator of mineralization.

Authors:  Pierre Moffatt; Marie-Helene Gaumond; Patrick Salois; Karine Sellin; Marie-Claude Bessette; Eric Godin; Paulo Tambasco de Oliveira; Gerald J Atkins; Antonio Nanci; Gethin Thomas
Journal:  J Bone Miner Res       Date:  2008-09       Impact factor: 6.741

3.  Mutations near amino end of alpha1(I) collagen cause combined osteogenesis imperfecta/Ehlers-Danlos syndrome by interference with N-propeptide processing.

Authors:  Wayne A Cabral; Elena Makareeva; Alain Colige; Anne D Letocha; Jennifer M Ty; Heather N Yeowell; Gerard Pals; Sergey Leikin; Joan C Marini
Journal:  J Biol Chem       Date:  2005-02-22       Impact factor: 5.157

4.  Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta.

Authors:  Aileen M Barnes; Weizhong Chang; Roy Morello; Wayne A Cabral; MaryAnn Weis; David R Eyre; Sergey Leikin; Elena Makareeva; Natalia Kuznetsova; Thomas E Uveges; Aarthi Ashok; Armando W Flor; John J Mulvihill; Patrick L Wilson; Usha T Sundaram; Brendan Lee; Joan C Marini
Journal:  N Engl J Med       Date:  2006-12-28       Impact factor: 91.245

5.  Type V osteogenesis imperfecta: a new form of brittle bone disease.

Authors:  F H Glorieux; F Rauch; H Plotkin; L Ward; R Travers; P Roughley; L Lalic; D F Glorieux; F Fassier; N J Bishop
Journal:  J Bone Miner Res       Date:  2000-09       Impact factor: 6.741

6.  Topological mapping of BRIL reveals a type II orientation and effects of osteogenesis imperfecta mutations on its cellular destination.

Authors:  Alexa Patoine; Marie-Hélène Gaumond; Prashant K Jaiswal; François Fassier; Frank Rauch; Pierre Moffatt
Journal:  J Bone Miner Res       Date:  2014-09       Impact factor: 6.741

Review 7.  Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.

Authors:  Joan C Marini; Antonella Forlino; Wayne A Cabral; Aileen M Barnes; James D San Antonio; Sarah Milgrom; James C Hyland; Jarmo Körkkö; Darwin J Prockop; Anne De Paepe; Paul Coucke; Sofie Symoens; Francis H Glorieux; Peter J Roughley; Alan M Lund; Kaija Kuurila-Svahn; Heini Hartikka; Daniel H Cohn; Deborah Krakow; Monica Mottes; Ulrike Schwarze; Diana Chen; Kathleen Yang; Christine Kuslich; James Troendle; Raymond Dalgleish; Peter H Byers
Journal:  Hum Mutat       Date:  2007-03       Impact factor: 4.878

8.  Natural history of hyperplastic callus formation in osteogenesis imperfecta type V.

Authors:  Moira S Cheung; Francis H Glorieux; Frank Rauch
Journal:  J Bone Miner Res       Date:  2007-08       Impact factor: 6.741

9.  Deposition and selective degradation of structurally-abnormal type I collagen in a collagen matrix produced by osteogenesis imperfecta fibroblasts in vitro.

Authors:  J F Bateman; S B Golub
Journal:  Matrix Biol       Date:  1994-04       Impact factor: 11.583

10.  Human bone cells in vitro.

Authors:  P G Robey; J D Termine
Journal:  Calcif Tissue Int       Date:  1985-09       Impact factor: 4.333

View more
  16 in total

Review 1.  Bone biology: insights from osteogenesis imperfecta and related rare fragility syndromes.

Authors:  Roberta Besio; Chi-Wing Chow; Francesca Tonelli; Joan C Marini; Antonella Forlino
Journal:  FEBS J       Date:  2019-07-05       Impact factor: 5.542

2.  Integrated analysis of miRNA and mRNA transcriptomic reveals antler growth regulatory network.

Authors:  Boyin Jia; Linlin Zhang; Yifan Zhang; Chenxia Ge; Fuhe Yang; Rui Du; Hengxing Ba
Journal:  Mol Genet Genomics       Date:  2021-03-26       Impact factor: 3.291

Review 3.  IFITM5 mutations and osteogenesis imperfecta.

Authors:  Nobutaka Hanagata
Journal:  J Bone Miner Metab       Date:  2015-06-02       Impact factor: 2.626

4.  Type V osteogenesis imperfecta undergoing surgical correction for scoliosis.

Authors:  Morgan Jones; Lee Breakwell; Ashley Cole; Paul Arundel; Nick Bishop
Journal:  Eur Spine J       Date:  2018-02-19       Impact factor: 3.134

5.  Hypermineralization and High Osteocyte Lacunar Density in Osteogenesis Imperfecta Type V Bone Indicate Exuberant Primary Bone Formation.

Authors:  Stéphane Blouin; Nadja Fratzl-Zelman; Francis H Glorieux; Paul Roschger; Klaus Klaushofer; Joan C Marini; Frank Rauch
Journal:  J Bone Miner Res       Date:  2017-06-26       Impact factor: 6.741

6.  Specific Characteristic of Hyperplastic Callus in a Larger Cohort of Osteogenesis Imperfecta Type V.

Authors:  Wen-Bin Zheng; Jing Hu; Jia Zhang; Zheng Yang; Ou Wang; Yan Jiang; Wei-Bo Xia; Xiao-Ping Xing; Wei Yu; Mei Li
Journal:  Calcif Tissue Int       Date:  2022-01-06       Impact factor: 4.333

Review 7.  Osteogenesis imperfecta and therapeutics.

Authors:  Roy Morello
Journal:  Matrix Biol       Date:  2018-03-11       Impact factor: 11.583

8.  Clinical and Molecular Characterization of Osteogenesis Imperfecta Type V.

Authors:  Evelise Brizola; Eduardo P Mattos; Jessica Ferrari; Patricia O A Freire; Raquel Germer; Juan C Llerena; Têmis M Félix
Journal:  Mol Syndromol       Date:  2015-09-03

Review 9.  Osteogenesis Imperfecta: Mechanisms and Signaling Pathways Connecting Classical and Rare OI Types.

Authors:  Milena Jovanovic; Gali Guterman-Ram; Joan C Marini
Journal:  Endocr Rev       Date:  2022-01-12       Impact factor: 19.871

10.  Effects of the overexpression of IFITM5 and IFITM5 c.-14C>T mutation on human osteosarcoma cells.

Authors:  Bao-Yan Liu; Yan-Qin Lu; Feng Han; Yong Wang; Xin-Kai Mo; Jin-Xiang Han
Journal:  Oncol Lett       Date:  2016-11-23       Impact factor: 2.967

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.