Literature DB >> 21473688

Gene expression profiles and metabolic changes in embryonic neural progenitor cells under low oxygen.

Ling-Ling Zhu1, Tong Zhao, Xin huang, Zhao-hui Liu, Li-ying Wu, Kui-wu Wu, Ming Fan.   

Abstract

Hypoxia promotes the proliferation of neural progenitor cells (NPCs), and low oxygen is a useful tool for expansion of NPCs in vitro. To further understand the regulation of the mechanisms involved, we first identified the gene expression profile of NPCs and characterized their metabolic changes in vitro under 3% oxygen. NPCs derived from E13.5 rat mesencephalon were cultured under either normoxia or hypoxia for 24 h and 72 h. Total RNA was subjected to cDNA microarray analysis of 5705 genes. The results showed that approximately 1.24% of gene expression changed under low oxygen at the two time points. Among the 142 differentially expressed genes, the greatest number was involved in glycolysis and metabolism. The metabolic changes of NPCs under low oxygen conditions were also assayed. The glucose content in the conditioned medium incubated in low oxygen decreased significantly; however, the levels of pyruvate and lactic acid increased compared to conditioned medium cultured in normoxia. The NPCs under low oxygen consumed more glucose and produced energy by glycolysis. The information gained from gene expression and metabolic analyses of NPCs under low oxygen conditions will provide new approaches for the evaluation of NPCs as potential in vivo cellular therapeutics.

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Year:  2011        PMID: 21473688     DOI: 10.1089/cell.2010.0043

Source DB:  PubMed          Journal:  Cell Reprogram        ISSN: 2152-4971            Impact factor:   1.987


  7 in total

Review 1.  Oxygen levels and the regulation of cell adhesion in the nervous system: a control point for morphogenesis in development, disease and evolution?

Authors:  Kathryn L Crossin
Journal:  Cell Adh Migr       Date:  2012 Jan-Feb       Impact factor: 3.405

Review 2.  The Role of Metabolic Plasticity in Blood and Brain Stem Cell Pathophysiology.

Authors:  Catherine J Libby; Jonathan McConathy; Victor Darley-Usmar; Anita B Hjelmeland
Journal:  Cancer Res       Date:  2019-10-01       Impact factor: 12.701

3.  Arctic ground squirrel neuronal progenitor cells resist oxygen and glucose deprivation-induced death.

Authors:  Kelly L Drew; Matthew Wells; Rebecca McGee; Austin P Ross; Judith Kelleher-Andersson
Journal:  World J Biol Chem       Date:  2016-02-26

4.  Inhibition of monocarboxylate transporter-4 depletes stem-like glioblastoma cells and inhibits HIF transcriptional response in a lactate-independent manner.

Authors:  K S Lim; K J Lim; A C Price; B A Orr; C G Eberhart; E E Bar
Journal:  Oncogene       Date:  2013-09-30       Impact factor: 9.867

5.  Hypoxia-induced alternative splicing in endothelial cells.

Authors:  Julia E Weigand; Jes-Niels Boeckel; Pascal Gellert; Stefanie Dimmeler
Journal:  PLoS One       Date:  2012-08-02       Impact factor: 3.240

6.  Disruption of the monocarboxylate transporter-4-basigin interaction inhibits the hypoxic response, proliferation, and tumor progression.

Authors:  Dillon M Voss; Raffaella Spina; David L Carter; Kah Suan Lim; Constance J Jeffery; Eli E Bar
Journal:  Sci Rep       Date:  2017-06-27       Impact factor: 4.379

7.  Neural progenitor cells-secreted exosomal miR-210 induced by hypoxia influences cell viability.

Authors:  Ming Zhao; Yan Gao; Fei Wang; Xiang Cheng; Tong Zhao; Yongqi Zhao; Ming Fan; Lingling Zhu
Journal:  Neuroreport       Date:  2020-08-05       Impact factor: 1.703

  7 in total

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