Literature DB >> 16584876

Analysis of fracture healing by large-scale transcriptional profile identified temporal relationships between metalloproteinase and ADAMTS mRNA expression.

Kevin Wang1, Prashanth Vishwanath, Gabriel S Eichler, Maisa O Al-Sebaei, Cory M Edgar, Thomas A Einhorn, Temple F Smith, Louis C Gerstenfeld.   

Abstract

The aim of this study was to validate the use of transcriptional profiling as a means of characterizing the complex interactions of the thousands of genes that are expressed during fracture healing. Standard mid-diaphyseal tibia fractures were generated in C57/B6 murine tibiae and the transcriptional expression of approximately 13,000 genes was assessed. Three time points after fracture were assessed: day 3, representative of the inflammatory phase; day 10, representative of the peak of cartilage formation; and day 21, representative of the period of primary bone formation and coupled remodeling. A self-organizing mapping approach of the data revealed the temporal relationships between the expression of mRNAs for extracellular matrix proteins and the proteases that degrade the proteoglycan and collagenous matrices. A broad group of extracellular matrix protein mRNAs representative of basement membranes, blood vessels and cartilage all showed elevated expression over the first 21 days of fracture healing. The sorting of the data identified an orderly temporal expression of the metalloproteinases and ADAMTS during the progression of fracture healing with (MMP2/MMP14/TIMP2) and ADAMTS4 and 15 preceding the expression of (MMP9/MMP13). Based on their patterns of expression, relative to the known activities of the encoded proteolytic enzymes, our results suggest that the dissolution of cartilage protoeglycans proceeds before the underlying collagenous components of the matrix are removed. The exclusion of several mRNAs that are normally expressed by osteoclasts in the profiles of mRNAs from days 3 and 10 suggests that osteoclastic activity was largely absent during the early periods of cartilage tissue formation and that proteoglycan and specific collagenase activities, precedes or is prerequisite to later osteoclast infiltration into the remodeling tissues.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16584876     DOI: 10.1016/j.matbio.2006.02.001

Source DB:  PubMed          Journal:  Matrix Biol        ISSN: 0945-053X            Impact factor:   11.583


  24 in total

1.  Genetic variation in the patterns of skeletal progenitor cell differentiation and progression during endochondral bone formation affects the rate of fracture healing.

Authors:  Karl J Jepsen; Christopher Price; Lee J Silkman; Fred H Nicholls; Phillip Nasser; Bin Hu; Nicole Hadi; Michael Alapatt; Stephanie N Stapleton; Sanjeev Kakar; Thomas A Einhorn; Louis C Gerstenfeld
Journal:  J Bone Miner Res       Date:  2008-08       Impact factor: 6.741

Review 2.  Biological perspectives of delayed fracture healing.

Authors:  K D Hankenson; G Zimmerman; R Marcucio
Journal:  Injury       Date:  2014-06       Impact factor: 2.586

3.  Identification of a thrombin cleavage site and a short form of ADAMTS-18.

Authors:  Jianhui Wang; Wei Zhang; Zanhua Yi; Shiyang Wang; Zongdong Li
Journal:  Biochem Biophys Res Commun       Date:  2012-02-23       Impact factor: 3.575

Review 4.  Border patrol: insights into the unique role of perlecan/heparan sulfate proteoglycan 2 at cell and tissue borders.

Authors:  Mary C Farach-Carson; Curtis R Warren; Daniel A Harrington; Daniel D Carson
Journal:  Matrix Biol       Date:  2013-08-31       Impact factor: 11.583

5.  Urine matrix metalloproteinases (MMPs) as biomarkers for the progression of fracture healing.

Authors:  Nathan A Wigner; Nitin Kulkarni; Mark Yakavonis; Megan Young; Brian Tinsley; Brett Meeks; Thomas A Einhorn; Louis C Gerstenfeld
Journal:  Injury       Date:  2012-03       Impact factor: 2.586

6.  Changes in matrix protein gene expression associated with mineralization in the differentiating chick limb-bud micromass culture system.

Authors:  Cristina C Teixeira; Jenny Xiang; Rani Roy; Valery Kudrashov; Itzhak Binderman; Philipp Mayer-Kuckuk; Adele L Boskey
Journal:  J Cell Biochem       Date:  2011-02       Impact factor: 4.429

Review 7.  Overview of skeletal repair (fracture healing and its assessment).

Authors:  Elise F Morgan; Anthony De Giacomo; Louis C Gerstenfeld
Journal:  Methods Mol Biol       Date:  2014

8.  Analysis of αSMA-labeled progenitor cell commitment identifies notch signaling as an important pathway in fracture healing.

Authors:  Brya G Matthews; Danka Grcevic; Liping Wang; Yusuke Hagiwara; Hrvoje Roguljic; Pujan Joshi; Dong-Guk Shin; Douglas J Adams; Ivo Kalajzic
Journal:  J Bone Miner Res       Date:  2014       Impact factor: 6.741

9.  BMP2 is essential for post natal osteogenesis but not for recruitment of osteogenic stem cells.

Authors:  M V Bais; N Wigner; M Young; R Toholka; D T Graves; E F Morgan; L C Gerstenfeld; T A Einhorn
Journal:  Bone       Date:  2009-05-03       Impact factor: 4.398

10.  Transcriptional analysis of fracture healing and the induction of embryonic stem cell-related genes.

Authors:  Manish Bais; Jody McLean; Paola Sebastiani; Megan Young; Nathan Wigner; Temple Smith; Darrell N Kotton; Thomas A Einhorn; Louis C Gerstenfeld
Journal:  PLoS One       Date:  2009-05-05       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.