Dataset Information

IGF-1R Promotes Symmetric Self-Renewal and Migration of Alkaline Phosphatase⁺ Germ Stem Cells through HIF-2α-OCT4/CXCR4 Loop under Hypoxia.

ABSTRACT: Hypoxia cooperates with endocrine signaling to maintain the symmetric self-renewal proliferation and migration of embryonic germline stem cells (GSCs). However, the lack of an appropriate in vitro cell model has dramatically hindered the understanding of the mechanism underlying this cooperation. Here, using a serum-free system, we demonstrated that hypoxia significantly induced the GSC mesenchymal transition, increased the expression levels of the pluripotent transcription factor OCT4 and migration-associated proteins (SDF-1, CXCR4, IGF-1, and IGF-1R), and activated the cellular expression and translocalization of the CXCR4-downstream proteins ARP3/pFAK. The underlying mechanism involved significant IGF-1/IGF-1R activation of OCT4/CXCR4 expression through HIF-2α regulation. Picropodophyllin-induced inhibition of IGF-1R phosphorylation significantly suppressed hypoxia-induced SDF-1/CXCR4 expression and cell migration. Furthermore, transactivation between IGF-1R and CXCR4 was involved. In summary, we demonstrated that niche hypoxia synergistically cooperates with its associated IGF-1R signaling to regulate the symmetric division (self-renewal proliferation) and cell migration of alkaline phosphatase-positive GSCs through HIF-2α-OCT4/CXCR4 during embryogenesis.

SUBMITTER: Kuo YC

PROVIDER: S-EPMC5830933 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature

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Publications

IGF-1R Promotes Symmetric Self-Renewal and Migration of Alkaline Phosphatase<sup>+</sup> Germ Stem Cells through HIF-2α-OCT4/CXCR4 Loop under Hypoxia.

Kuo Yung-Che YC Au Heng-Kien HK Hsu Jue-Liang JL Wang Hsiao-Feng HF Lee Chiung-Ju CJ Peng Syue-Wei SW Lai Ssu-Chuan SC Wu Yu-Chih YC Ho Hong-Nerng HN Huang Yen-Hua YH

Stem cell reports 20180104 2

Hypoxia cooperates with endocrine signaling to maintain the symmetric self-renewal proliferation and migration of embryonic germline stem cells (GSCs). However, the lack of an appropriate in vitro cell model has dramatically hindered the understanding of the mechanism underlying this cooperation. Here, using a serum-free system, we demonstrated that hypoxia significantly induced the GSC mesenchymal transition, increased the expression levels of the pluripotent transcription factor OCT4 and migra ...[more]

PMID: 29307582

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Project description:Primary bone tumor, also known as osteosarcoma (OS), is the most common primary malignancy of bone in children and young adults. Current treatment protocols yield a 5-year survival rate of near 70% although approximately 80% of patients have metastatic disease at the time of diagnosis. However, long-term survival rates have remained virtually unchanged for nearly four decades, largely due to our limited understanding of the disease process. One major signaling pathway that has been implicated in human OS tumorigenesis is the insulin-like growth factor (IGF)/insulin-like growth factor-1 receptor (IGF1R) signaling axis. IGF1R is a heterotetrameric α2β2 receptor, in which the α subunits comprise the ligand binding site, whereas the β subunits are transmembrane proteins containing intracellular tyrosine kinase domains. Although numerous strategies have been devised to target IGF/IGF1R axis, most of them have failed in clinical trials due to the lack of specificity and/or limited efficacy. Here, we investigated whether a more effective and specific blockade of IGF1R activity in human OS cells can be accomplished by employing dominant-negative IGF1R (dnIGF1R) mutants. We engineered the recombinant adenoviruses expressing two IGF1R mutants derived from the α (aa 1-524) and β (aa 741-936) subunits, and found that either dnIGF1Rα and/or dnIGF1Rβ effectively inhibited cell migration, colony formation, and cell cycle progression of human OS cells, which could be reversed by exogenous IGF1. Furthermore, dnIGF1Rα and/or dnIGF1Rβ inhibited OS xenograft tumor growth in vivo, with the greatest inhibition of tumor growth shown by dnIGF1Rα. Mechanistically, the dnIGF1R mutants down-regulated the expression of PI3K/AKT and RAS/RAF/MAPK, BCL2, Cyclin D1 and most EMT regulators, while up-regulating pro-apoptotic genes in human OS cells. Collectively, these findings strongly suggest that the dnIGF1R mutants, especially dnIGF1Rα, may be further developed as novel anticancer agents that target IGF signaling axis with high specificity and efficacy.

Dataset Information

IGF-1R Promotes Symmetric Self-Renewal and Migration of Alkaline Phosphatase⁺ Germ Stem Cells through HIF-2α-OCT4/CXCR4 Loop under Hypoxia.

Publications

IGF-1R Promotes Symmetric Self-Renewal and Migration of Alkaline Phosphatase<sup>+</sup> Germ Stem Cells through HIF-2α-OCT4/CXCR4 Loop under Hypoxia.

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Dataset Information

IGF-1R Promotes Symmetric Self-Renewal and Migration of Alkaline Phosphatase+ Germ Stem Cells through HIF-2α-OCT4/CXCR4 Loop under Hypoxia.

Publications

IGF-1R Promotes Symmetric Self-Renewal and Migration of Alkaline Phosphatase<sup>+</sup> Germ Stem Cells through HIF-2α-OCT4/CXCR4 Loop under Hypoxia.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets

IGF-1R Promotes Symmetric Self-Renewal and Migration of Alkaline Phosphatase⁺ Germ Stem Cells through HIF-2α-OCT4/CXCR4 Loop under Hypoxia.