Increased SCF/c-kit by hypoxia promotes autophagy of human placental chorionic plate-derived mesenchymal stem cells via regulating the phosphorylation of mTOR

Youjin Lee, Jieun Jung, Kyung Jin Cho, Seung Kwan Lee, Jong Wan Park, Il Hoan Oh, Gi Jin Kim

Research output: Contribution to journalArticle

39 Citations (Scopus)

Abstract

Hypoxia triggers physiological and pathological cellular processes, including proliferation, differentiation, and death, in several cell types. Mesenchymal stem cells (MSCs) derived from various tissues have self-renewal activity and can differentiate towards multiple lineages. Recently, it has been reported that hypoxic conditions tip the balance between survival and death by hypoxia-induced autophagy, although the underlying mechanism is not clear. The objectives of this study are to compare the effect of hypoxia on the self-renewal of bone marrow-derived mesenchymal stem cells (BM-MSCs) and placental chorionic plate-derived mesenchymal stem cells (CP-MSCs) and to investigate the regulatory mechanisms of self-renewal in each MSC type during hypoxia. The expression of self-renewal markers (e.g., Oct4, Nanog, Sox2) was assessed in both cell lines. PI3K and stem cell factor (SCF) expression gradually increased in CP-MSCs but were markedly downregulated in BM-MSCs by hypoxia. The phosphorylation of ERK and mTOR was augmented by hypoxia in CP-MSCs compared to control. Also, the expression of LC3 II, a component of the autophagosome and the hoof-shaped autophagosome was detected more rapidly in CP-MSCs than in BM-MSCs under hypoxia. Hypoxia induced the expression of SCF in CP-MSCs and increased SCF/c-kit pathway promotes the self-renewal activities of CP-MSCs via an autocrine/paracrine mechanism that balances cell survival and cell death events by autophagy. These activities occur to a greater extent in CP-MSCs than in BM-MSCs through regulating the phosphorylation of mTOR. These findings will provide useful guidelines for better understanding the function of SCF/c-kit in the self-renewal and autophagy-regulated mechanisms that promote of MSC survival.

Original languageEnglish
Pages (from-to)79-88
Number of pages10
JournalJournal of cellular biochemistry
Volume114
Issue number1
DOIs
Publication statusPublished - 2013 Jan 1

Fingerprint

Phosphorylation
Stem Cell Factor
Autophagy
Stem cells
Mesenchymal Stromal Cells
Cell Hypoxia
Bone
Bone Marrow
Hypoxia
Cell Survival
Cells
Hoof and Claw
Cell death
Pathologic Processes
Phosphatidylinositol 3-Kinases

Keywords

  • AUTOPHAGY
  • BONE MARROW-DERIVED MESENCHYMAL STEM CELLS (BM-MSCs)
  • HYPOXIA
  • PLACENTAL CHORIONIC PLATE-DERIVED MESENCHYMAL STEM CELLS (CP-MSCs)
  • SELF-RENEWAL
  • STEM CELL FACTOR (SCF)

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Increased SCF/c-kit by hypoxia promotes autophagy of human placental chorionic plate-derived mesenchymal stem cells via regulating the phosphorylation of mTOR. / Lee, Youjin; Jung, Jieun; Cho, Kyung Jin; Lee, Seung Kwan; Park, Jong Wan; Oh, Il Hoan; Kim, Gi Jin.

In: Journal of cellular biochemistry, Vol. 114, No. 1, 01.01.2013, p. 79-88.

Research output: Contribution to journalArticle

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AU - Park, Jong Wan

AU - Oh, Il Hoan

AU - Kim, Gi Jin

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