4.6 Article

High Glucose Condition Suppresses Neurosphere Formation by Human Periodontal Ligament-Derived Mesenchymal Stem Cells

Journal

JOURNAL OF CELLULAR BIOCHEMISTRY
Volume 115, Issue 5, Pages 928-939

Publisher

WILEY-BLACKWELL
DOI: 10.1002/jcb.24735

Keywords

PERIODONTAL LIGAMENT-DERIVED MESENCHYMAL STEM CELLS (hPDLSCs); GLUCOSE; NEURONAL DIFFERENTIATION

Funding

  1. Chulalongkorn University [RES560530156-HR]
  2. Government Research Fund
  3. Thailand National Science and Technology Development Agency (NSTDA), Thailand
  4. Thailand Research Fund (Royal Golden Jubilee Scholarship)

Ask authors/readers for more resources

D-Glucose serves many roles in cellular functions, but its role in human periodontal ligament-derived mesenchymal stem cells (hPSLSCs) is yet unknown. Here, the roles of high glucose concentration on neurogenic differentiation by hPDLSCs were investigated. Two-stage neurogenic induction protocol was employed. Cells were maintained in normal neurogenic induction medium, high glucose condition, or high mannose condition. The results showed that high glucose attenuated neurosphere formation efficiency by hPDLSCs in terms of morphology, neurogenic marker expression, without a deleterious effect on cell viability. Contrastingly, neurosphere-derived cells matured in high glucose condition exhibited normal neuronal characteristics compared to the control. During neurosphere formation in high glucose, glucose transporters (GLUTs) mRNA levels were significantly decreased, corresponding with the deprivation of cellular glucose uptake. Further, a glucose uptake inhibitor, cytochalasin B, was used to confirm the deleterious effects of glucose uptake deprivation during neurosphere formation. The results demonstrated that deprivation of glucose uptake attenuated neurosphere formation efficiency by hPDLSCs. Together, the results illustrated that high glucose condition attenuated the efficiency of neurosphere formation but not neuronal maturation, which may occur through the downregulation of GLUTs and the reduction of glucose uptake. J. Cell. Biochem. 115: 928-939, 2014. (c) 2013 Wiley Periodicals, Inc.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available