Novel contribution to clubfoot pathogenesis: The possible role of extracellular matrix proteins
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F44555601%3A13450%2F19%3A43896038" target="_blank" >RIV/44555601:13450/19:43896038 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/67985823:_____/19:00504465 RIV/00216208:11110/19:10391092 RIV/00216208:11130/19:10391092 RIV/00216208:11510/19:10391092 a 2 dalších
Výsledek na webu
<a href="https://onlinelibrary.wiley.com/doi/10.1002/jor.24211" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1002/jor.24211</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/jor.24211" target="_blank" >10.1002/jor.24211</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Novel contribution to clubfoot pathogenesis: The possible role of extracellular matrix proteins
Popis výsledku v původním jazyce
Idiopathic pes equinovarus (clubfoot) is a congenital deformity of the feet and lower legs. Clubfoot belongs to a group of fibro-proliferative disorders but its origin remains unknown. Our study aimed to achieve the first complex proteomic comparison of clubfoot contracted tissue of the foot (medial side; n=16), with non-contracted tissue (lateral side; n=13). We used label-free mass spectrometry quantification and immunohistochemistry. Seven proteins were observed to be significantly upregulated in the medial side (asporin, collagen type III, V, and VI, versican, tenascin-C, and transforming growth factor beta induced protein) and four in the lateral side (collagen types XII and XIV, fibromodulin, and cartilage intermediate layer protein 2) of the clubfoot. Comparison of control samples from cadavers brought only two different protein concentrations (collagen types I and VI). We also revealed pathological calcification and intracellular positivity of transforming growth factor beta only in the contracted tissue of clubfoot. Most of the 11 differently expressed proteins are strongly related to the extracellular matrix architecture and we assume that they may play specific roles in the pathogenesis of this deformity. These proteins seem to be promising targets for future investigations and treatment of this disease. (c) 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res
Název v anglickém jazyce
Novel contribution to clubfoot pathogenesis: The possible role of extracellular matrix proteins
Popis výsledku anglicky
Idiopathic pes equinovarus (clubfoot) is a congenital deformity of the feet and lower legs. Clubfoot belongs to a group of fibro-proliferative disorders but its origin remains unknown. Our study aimed to achieve the first complex proteomic comparison of clubfoot contracted tissue of the foot (medial side; n=16), with non-contracted tissue (lateral side; n=13). We used label-free mass spectrometry quantification and immunohistochemistry. Seven proteins were observed to be significantly upregulated in the medial side (asporin, collagen type III, V, and VI, versican, tenascin-C, and transforming growth factor beta induced protein) and four in the lateral side (collagen types XII and XIV, fibromodulin, and cartilage intermediate layer protein 2) of the clubfoot. Comparison of control samples from cadavers brought only two different protein concentrations (collagen types I and VI). We also revealed pathological calcification and intracellular positivity of transforming growth factor beta only in the contracted tissue of clubfoot. Most of the 11 differently expressed proteins are strongly related to the extracellular matrix architecture and we assume that they may play specific roles in the pathogenesis of this deformity. These proteins seem to be promising targets for future investigations and treatment of this disease. (c) 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30211 - Orthopaedics
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Orthopaedic Research
ISSN
0736-0266
e-ISSN
—
Svazek periodika
37
Číslo periodika v rámci svazku
3
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
10
Strana od-do
769-778
Kód UT WoS článku
000464419100026
EID výsledku v databázi Scopus
—