Angiopoietin-Like 4 Is Involved in the Poor Angiogenic Potential of High Glucose-Insulted Bone Marrow Stem Cells.
10.4070/kcj.2014.44.3.177
- Author:
Yong Sook KIM
1
;
Hea Jin KANG
;
Moon Hwa HONG
;
Wan Seok KANG
;
Nakwon CHOE
;
Hyun KOOK
;
Myung Ho JEONG
;
Youngkeun AHN
Author Information
1. Research Laboratory of Cardiovascular Regeneration, Chonnam National University Hospital, Gwangju, Korea. cecilyk@hanmail.net
- Publication Type:In Vitro ; Original Article
- Keywords:
Stem cells;
Diabetes mellitus;
ANGPTL4 protein, rat;
MicroRNAs
- MeSH:
Adipokines;
Animals;
Blotting, Western;
Bone Marrow*;
Diabetes Mellitus;
DNA;
Enzyme-Linked Immunosorbent Assay;
Gene Expression;
Glucose;
Humans;
Mesenchymal Stromal Cells;
MicroRNAs;
Oxytocin;
Plasmids;
Polymerase Chain Reaction;
Rats;
Stem Cells*;
Up-Regulation
- From:Korean Circulation Journal
2014;44(3):177-183
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND AND OBJECTIVES: Diabetes is reported to reduce the function or number of progenitor cells. We compared the gene expression patterns of bone marrow-derived mesenchymal stem cells from diabetic (DM-BMCs) and healthy (non-DM-BMCs) rats and suggested Angiopoietin-like 4 (Angptl4) could be a responsible factor for impaired angiogenesis of DM-BMCs. SUBJECTS AND METHODS: BMCs were isolated from DM or non-DM rat, and in vitro angiogenesis activity was compared by tube formation assay on Matrigel and complementary deoxyribonucleic acid expression was analyzed by microarray with or without oxytocin treatment. Human BMCs (hBMCs) were treated with high glucose, and were performed polymerase chain reaction, Western blot, and enzyme-linked immunosorbent assay. Angptl4 plasmid DNA and micro ribonucleic acid-132 (miR-132) were transfected to immortalized hBMCs. RESULTS: In vitro angiogenesis assay showed the impaired tube formation in DM-BMCs, and slightly recovery by oxytocin treatment. Angptl4, an adipokine, was upregulated in DM-BMCs compared to non-DM-BMCs. Oxytocin treatment reduced Angptl4 in DM-BMCs. In hBMCs, overexpression of Angptl4 attenuated the tube formation. In addition to Angptl4, miR-132 was increased by high glucose treatment. Collectively, high glucose resulted in impaired tube formation through miR-132 induction and Angptl4 upregulation in BMCs. CONCLUSION: Our results show that the angiogenic activity of BMCs is impaired by high glucose stress, which would be mediated by Angptl4 and miR-132.
