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HOX gene analysis in the osteogenic differentiation of human mesenchymal stem cells
Chae, Song Wha; Jee, Bo Keun; Lee, Joo Yong; Han, Chang Whan; Jeon, Yang-Whan; Lim, Young; Lee, Kweon-Haeng; Rha, Hyoung Kyun; Chae, Gue-Tae.
  • Chae, Song Wha; The Catholic University of Korea. Neuroscience Genome Research Center. Seoul. KR
  • Jee, Bo Keun; The Catholic University of Korea. Neuroscience Genome Research Center. Seoul. KR
  • Lee, Joo Yong; The Catholic University of Korea. Neuroscience Genome Research Center. Seoul. KR
  • Han, Chang Whan; The Catholic University of Korea. College of Medicine. Daejeon St. Mary's Hospital. Department of Orthopedic Surgery. Seoul. KR
  • Jeon, Yang-Whan; The Catholic University of Korea. Our Lady of Mercy Hospital. Department of Psychiatry. Incheon. KR
  • Lim, Young; The Catholic University of Korea. St. Mary's Hospital. Seoul. KR
  • Lee, Kweon-Haeng; The Catholic University of Korea. Neuroscience Genome Research Center. Seoul. KR
  • Rha, Hyoung Kyun; The Catholic University of Korea. Neuroscience Genome Research Center. Seoul. KR
  • Chae, Gue-Tae; The Catholic University of Korea. Institute of Hansen's Disease. Seoul. KR
Genet. mol. biol ; 31(4): 815-823, Sept.-Dec. 2008. tab, graf, ilus
Article Dans Anglais | LILACS | ID: lil-501462
ABSTRACT
Human bone marrow-derived mesenchymal stem cells (hMSCs) have the capacity to differentiate into osteoblasts during osteogenesis. Several studies attempted to identify osteogenesis-related genes in hMSCs. Although HOX genes are known to play a pivotal role in skeletogenesis, their function in the osteogenesis of hMSCs has not yet been investigated in detail. Our aim was to characterize the expression of 37 HOX genes by multiplex RT-PCR to identify the ones most probably involved in osteogenic differentiation. The results showed that the expression patterns of four HOX genes were altered during this process. In particular, the expression levels of HOXC13 and HOXD13 were dramatically changed. Real-time PCR and Western blot analysis were performed in order to further analyze the expression of HOXC13 and HOXD13. The qRT-PCR results showed that transcription of HOXC13 was up-regulated by up to forty times, whereas that of HOXD13 was down-regulated by approximately five times after osteogenic differentiation. The Western blot results for the HOXC13 and HOXD13 proteins also corresponded well with the real-time PCR result. These findings suggest that HOXC13 and HOXD13 might be involved in the osteogenic differentiation of hMSCs.
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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Gènes homéotiques / Cellules souches mésenchymateuses Type d'étude: Étude pronostique Limites du sujet: Humains langue: Anglais Texte intégral: Genet. mol. biol Thème du journal: Génétique Année: 2008 Type: Article Pays d'affiliation: Corée du Sud Institution/Pays d'affiliation: The Catholic University of Korea/KR

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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Gènes homéotiques / Cellules souches mésenchymateuses Type d'étude: Étude pronostique Limites du sujet: Humains langue: Anglais Texte intégral: Genet. mol. biol Thème du journal: Génétique Année: 2008 Type: Article Pays d'affiliation: Corée du Sud Institution/Pays d'affiliation: The Catholic University of Korea/KR