Hypoxic priming of mESCs accelerates vascular-lineage differentiation through HIF1-mediated inverse regulation of Oct4 and VEGF

Sae Won Lee, Han Kyul Jeong, Ji Young Lee, Jimin Yang, Eun Ju Lee, Su Yeon Kim, Seock Won Youn, Jaewon Lee, Woo Jean Kim, Kyu Won Kim, Jeong Mook Lim, Jong Wan Park, Young Bae Park, Hyo Soo Kim

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

Hypoxic microenvironment plays an important role in determining stem cell fates. However, it is controversial to which direction between self-renewal and differentiation the hypoxia drives the stem cells. Here, we investigated whether a short exposure to hypoxia (termed 'hypoxic-priming') efficiently directed and promoted mouse embryonic stem cells (mESCs) to differentiate into vascular-lineage. During spontaneous differentiation of embryoid bodies (EBs), hypoxic region was observed inside EB spheroids even under normoxic conditions. Indeed, hypoxia-primed EBs more efficiently differentiated into cells of vascular-lineage, than normoxic EBs did. We found that hypoxia suppressed Oct4 expression via direct binding of HIF-1 to reverse hypoxia-responsive elements (rHREs) in the Oct4 promoter. Furthermore, vascular endothelial growth factor (VEGF) was highly upregulated in hypoxia-primed EBs, which differentiated towards endothelial cells in the absence of exogenous VEGF. Interestingly, this differentiation was abolished by the HIF-1 or VEGF blocking. In vivo transplantation of hypoxia-primed EBs into mice ischemic limb elicited enhanced vessel differentiation. Collectively, our findings identify that hypoxia enhanced ESC differentiation by HIF-1-mediated inverse regulation of Oct4 and VEGF, which is a novel pathway to promote vascular-lineage differentiation.

Original languageEnglish (US)
Pages (from-to)924-938
Number of pages15
JournalEMBO Molecular Medicine
Volume4
Issue number9
DOIs
StatePublished - Sep 1 2012

Fingerprint

Embryoid Bodies
Vascular Endothelial Growth Factor A
Blood Vessels
Stem Cells
Body Regions
Mouse Embryonic Stem Cells
Hypoxia
Cell Lineage
Extremities
Endothelial Cells
Transplantation

Keywords

  • Embryoid bodies
  • Endothelial cells
  • Mesoderm differentiation
  • Mouse embryonic stem cells
  • Niche

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Hypoxic priming of mESCs accelerates vascular-lineage differentiation through HIF1-mediated inverse regulation of Oct4 and VEGF. / Lee, Sae Won; Jeong, Han Kyul; Lee, Ji Young; Yang, Jimin; Lee, Eun Ju; Kim, Su Yeon; Youn, Seock Won; Lee, Jaewon; Kim, Woo Jean; Kim, Kyu Won; Lim, Jeong Mook; Park, Jong Wan; Park, Young Bae; Kim, Hyo Soo.

In: EMBO Molecular Medicine, Vol. 4, No. 9, 01.09.2012, p. 924-938.

Research output: Contribution to journalArticle

Lee, SW, Jeong, HK, Lee, JY, Yang, J, Lee, EJ, Kim, SY, Youn, SW, Lee, J, Kim, WJ, Kim, KW, Lim, JM, Park, JW, Park, YB & Kim, HS 2012, 'Hypoxic priming of mESCs accelerates vascular-lineage differentiation through HIF1-mediated inverse regulation of Oct4 and VEGF', EMBO Molecular Medicine, vol. 4, no. 9, pp. 924-938. https://doi.org/10.1002/emmm.201101107
Lee, Sae Won ; Jeong, Han Kyul ; Lee, Ji Young ; Yang, Jimin ; Lee, Eun Ju ; Kim, Su Yeon ; Youn, Seock Won ; Lee, Jaewon ; Kim, Woo Jean ; Kim, Kyu Won ; Lim, Jeong Mook ; Park, Jong Wan ; Park, Young Bae ; Kim, Hyo Soo. / Hypoxic priming of mESCs accelerates vascular-lineage differentiation through HIF1-mediated inverse regulation of Oct4 and VEGF. In: EMBO Molecular Medicine. 2012 ; Vol. 4, No. 9. pp. 924-938.
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