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OCT4A contributes to the stemness and multi-potency of human umbilical cord blood-derived multipotent stem cells (hUCB-MSCs).
Seo, Kwang-Won; Lee, Sae-Rom; Bhandari, Dilli Ram; Roh, Kyoung-Hwan; Park, Sang-Bum; So, Ah-Young; Jung, Ji-Won; Seo, Min-Soo; Kang, Soo-Kyung; Lee, Yong-Soon; Kang, Kyung-Sun.
Affiliation
  • Seo KW; Adult Stem Cell Research Center, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
Biochem Biophys Res Commun ; 384(1): 120-5, 2009 Jun 19.
Article in En | MEDLINE | ID: mdl-19394308
ABSTRACT
The OCT4A gene, a POU homeodomain transcription factor, has been shown to be expressed in embryonic stem cells (ESC) as well as hUCB-MSCs. In this study, the roles played by OCT4A in hUCB-MSCs were determined by stably inhibiting OCT4A with lenti-viral vector-based small hairpin RNA (shRNA). A decreased rate of cell proliferation was observed in OCT4-inhibited hUCB-MSCs. Down-regulation of CCNA2 expression in OCT4-inhibited hUCB-MSCs was confirmed by RT-PCR and real-time RT-PCR analysis in three genetically independent hUCB-MSC clones. Adipogenic differentiation was also suppressed in OCT4-inhibited hUCB-MSCs. The up-regulation of DTX1 and down-regulation of HDAC1, 2, and 4 expressions may be related to this differentiation deformity. The expression of other transcription factors, including SOX2, REX1 and c-MYC, was also affected by OCT4 inhibition in hUCB-MSCs. In conclusion, these finding suggest that OCT4A performs functionally conserved roles in hUCB-MSCs, making its expression biologically important for ex vivo culture of hUCB-MSCs.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Multipotent Stem Cells / Octamer Transcription Factor-3 / Fetal Blood Limits: Humans Language: En Journal: Biochem Biophys Res Commun Year: 2009 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Multipotent Stem Cells / Octamer Transcription Factor-3 / Fetal Blood Limits: Humans Language: En Journal: Biochem Biophys Res Commun Year: 2009 Type: Article