The Transplantation Resistance of Type II Diabetes Mellitus Adipose-Derived Stem Cells Is Due to G6PC and IGF1 Genes Related to the FoxO Signaling Pathway.
Michiko HoriguchiYuya TurudomeKentaro UshijimaPublished in: International journal of molecular sciences (2021)
In cases of patients with rapidly progressive diabetes mellitus (DM), autologous stem cell transplantation is considered as one of the regenerative treatments. However, whether the effects of autonomous stem cell transplantation on DM patients are equivalent to transplantation of stem cells derived from healthy persons is unclear. This study revealed that adipose-derived mesenchymal stem cells (ADSC) derived from type II DM patients had lower transplantation efficiency, proliferation potency, and stemness than those derived from healthy persons, leading to a tendency to induce apoptotic cell death. To address this issue, we conducted a cyclopedic mRNA analysis using a next-generation sequencer and identified G6PC3 and IGF1, genes related to the FoxO signaling pathway, as the genes responsible for lower performance. Moreover, it was demonstrated that the lower transplantation efficiency of ADSCs derived from type II DM patients might be improved by knocking down both G6PC3 and IGF1 genes. This study clarified the difference in transplantation efficiency between ADSCs derived from type II DM patients and those derived from healthy persons and the genes responsible for the lower performance of the former. These results can provide a new strategy for stabilizing the quality of stem cells and improving the therapeutic effects of regenerative treatments on autonomous stem cell transplantation in patients with DM.
Keyphrases
- stem cell transplantation
- stem cells
- signaling pathway
- end stage renal disease
- cell death
- ejection fraction
- cell therapy
- high dose
- newly diagnosed
- chronic kidney disease
- pi k akt
- prognostic factors
- epithelial mesenchymal transition
- mesenchymal stem cells
- multiple sclerosis
- transcription factor
- metabolic syndrome
- gene expression
- skeletal muscle
- binding protein
- cell proliferation
- oxidative stress
- quality improvement
- single cell
- endoplasmic reticulum stress
- platelet rich plasma