Matches in SemOpenAlex for { <https://semopenalex.org/work/W4281693500> ?p ?o ?g. }
- W4281693500 endingPage "1237" @default.
- W4281693500 startingPage "1227" @default.
- W4281693500 abstract "RUNX2 is a master osteogenic transcription factor, and mutations in RUNX2 cause the inherited skeletal disorder cleidocranial dysplasia (CCD). Studies have revealed that RUNX2 is not only a downstream target of the bone morphogenetic protein (BMP) pathway but can also regulate the expression of BMPs. However, the underlying mechanism of the regulation of BMPs by RUNX2 remains unknown. In this project, we diagnosed a CCD patient with a 7.86-Mb heterozygous deletion on chromosome 6 containing all exons of RUNX2 by multiplex ligation-dependent probe amplification (MLPA) and whole-genome sequencing (WGS). Bone marrow mesenchymal stem cells (BMSCs) were further extracted from patient alveolar bone fragments (CCD-BMSCs), an excellent natural model to explore the possible mechanism. The osteogenic differentiation ability of CCD-BMSCs was severely affected by RUNX2 heterozygous deletion. Also, BMP4 decreased most in BMP ligands, and CHRDL1, a BMP antagonist, was abnormally elevated in CCD-BMSCs. Furthermore, BMP4 treatment essentially rescued the osteogenic capacity of CCD-BMSCs, and RUNX2 overexpression reversed the abnormal expression of BMP4 and CHRDL1. Notably, we constructed CRISPR/Cas9 Runx2+/m MC3T3-E1 cells, which simulated a variant in CCD-BMSCs, to exclude the interference of other gene deletions and the heterogeneity of the genetic background of primary cells, and verified all findings from the CCD-BMSCs. Moreover, the luciferase reporter experiment showed that RUNX2 could inhibit the transcription of CHRDL1. Through immunofluorescence, the inhibitory effect of CHRDL1 on BMP4/Smad signaling was confirmed in MC3T3-E1 cells. These results revealed that RUNX2 regulated the BMP4 pathway by inhibiting CHRDL1 transcription. We collectively identified a novel RUNX2/CHRDL1/BMP4 axis to regulate osteogenic differentiation and noted that BMP4 might be a valuable therapeutic option for treating bone diseases." @default.
- W4281693500 created "2022-06-13" @default.
- W4281693500 creator A5000149447 @default.
- W4281693500 creator A5023667128 @default.
- W4281693500 creator A5036644714 @default.
- W4281693500 creator A5065111217 @default.
- W4281693500 creator A5070253636 @default.
- W4281693500 creator A5085544823 @default.
- W4281693500 date "2022-05-26" @default.
- W4281693500 modified "2023-10-14" @default.
- W4281693500 title "RUNX2 Regulates Osteoblast Differentiation via the BMP4 Signaling Pathway" @default.
- W4281693500 cites W1502035335 @default.
- W4281693500 cites W1604904418 @default.
- W4281693500 cites W1982627750 @default.
- W4281693500 cites W1987266329 @default.
- W4281693500 cites W1989533590 @default.
- W4281693500 cites W1992016760 @default.
- W4281693500 cites W1993817188 @default.
- W4281693500 cites W1994596418 @default.
- W4281693500 cites W1994964287 @default.
- W4281693500 cites W1998397995 @default.
- W4281693500 cites W1998696289 @default.
- W4281693500 cites W2006048313 @default.
- W4281693500 cites W2006055704 @default.
- W4281693500 cites W2011445064 @default.
- W4281693500 cites W2013714561 @default.
- W4281693500 cites W2033498402 @default.
- W4281693500 cites W2039076982 @default.
- W4281693500 cites W2042125973 @default.
- W4281693500 cites W2081134904 @default.
- W4281693500 cites W2081516778 @default.
- W4281693500 cites W2091052622 @default.
- W4281693500 cites W2092859323 @default.
- W4281693500 cites W2110810005 @default.
- W4281693500 cites W2121551386 @default.
- W4281693500 cites W2152934729 @default.
- W4281693500 cites W2157445945 @default.
- W4281693500 cites W2165213969 @default.
- W4281693500 cites W2172270516 @default.
- W4281693500 cites W2181249761 @default.
- W4281693500 cites W2266017316 @default.
- W4281693500 cites W2283490245 @default.
- W4281693500 cites W2345509148 @default.
- W4281693500 cites W2737751938 @default.
- W4281693500 cites W2899167227 @default.
- W4281693500 cites W2901669407 @default.
- W4281693500 cites W3022006582 @default.
- W4281693500 cites W4210369002 @default.
- W4281693500 cites W2008952152 @default.
- W4281693500 doi "https://doi.org/10.1177/00220345221093518" @default.
- W4281693500 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35619284" @default.
- W4281693500 hasPublicationYear "2022" @default.
- W4281693500 type Work @default.
- W4281693500 citedByCount "4" @default.
- W4281693500 countsByYear W42816935002023 @default.
- W4281693500 crossrefType "journal-article" @default.
- W4281693500 hasAuthorship W4281693500A5000149447 @default.
- W4281693500 hasAuthorship W4281693500A5023667128 @default.
- W4281693500 hasAuthorship W4281693500A5036644714 @default.
- W4281693500 hasAuthorship W4281693500A5065111217 @default.
- W4281693500 hasAuthorship W4281693500A5070253636 @default.
- W4281693500 hasAuthorship W4281693500A5085544823 @default.
- W4281693500 hasConcept C104317684 @default.
- W4281693500 hasConcept C153911025 @default.
- W4281693500 hasConcept C185592680 @default.
- W4281693500 hasConcept C202751555 @default.
- W4281693500 hasConcept C203014093 @default.
- W4281693500 hasConcept C2776363554 @default.
- W4281693500 hasConcept C2778260815 @default.
- W4281693500 hasConcept C2780804394 @default.
- W4281693500 hasConcept C2781080636 @default.
- W4281693500 hasConcept C2781316418 @default.
- W4281693500 hasConcept C31507581 @default.
- W4281693500 hasConcept C54355233 @default.
- W4281693500 hasConcept C62478195 @default.
- W4281693500 hasConcept C86339819 @default.
- W4281693500 hasConcept C86803240 @default.
- W4281693500 hasConcept C95444343 @default.
- W4281693500 hasConceptScore W4281693500C104317684 @default.
- W4281693500 hasConceptScore W4281693500C153911025 @default.
- W4281693500 hasConceptScore W4281693500C185592680 @default.
- W4281693500 hasConceptScore W4281693500C202751555 @default.
- W4281693500 hasConceptScore W4281693500C203014093 @default.
- W4281693500 hasConceptScore W4281693500C2776363554 @default.
- W4281693500 hasConceptScore W4281693500C2778260815 @default.
- W4281693500 hasConceptScore W4281693500C2780804394 @default.
- W4281693500 hasConceptScore W4281693500C2781080636 @default.
- W4281693500 hasConceptScore W4281693500C2781316418 @default.
- W4281693500 hasConceptScore W4281693500C31507581 @default.
- W4281693500 hasConceptScore W4281693500C54355233 @default.
- W4281693500 hasConceptScore W4281693500C62478195 @default.
- W4281693500 hasConceptScore W4281693500C86339819 @default.
- W4281693500 hasConceptScore W4281693500C86803240 @default.
- W4281693500 hasConceptScore W4281693500C95444343 @default.
- W4281693500 hasFunder F4320321001 @default.
- W4281693500 hasIssue "10" @default.
- W4281693500 hasLocation W42816935001 @default.
- W4281693500 hasLocation W42816935002 @default.