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The promise(s) of mesenchymal stem cell therapy in averting preclinical diabetes: lessons from in vivo and in vitro model systems

Nagasuryaprasad Kotikalapudi, Samuel Joshua Pragasam Sampath, Sinha Sukesh Narayan, Ramesh Bhonde, Harishankar Nemani, Sathish Kumar Mungamuri, Vijayalakshmi Venkatesan

2021Scientific Reports14 citationsDOIOpen Access PDF

Abstract

Obesity (Ob) poses a significant risk factor for the onset of metabolic syndrome with associated complications, wherein the Mesenchymal Stem Cell (MSC) therapy shows pre-clinical success. Here, we explore the therapeutic applications of human Placental MSCs (P-MSCs) to address Ob-associated Insulin Resistance (IR) and its complications. In the present study, we show that intramuscular injection of P-MSCs homed more towards the visceral site, restored HOMA-IR and glucose homeostasis in the WNIN/GR-Ob (Ob-T2D) rats. P-MSC therapy was effective in re-establishing the dysregulated cytokines. We report that the P-MSCs activates PI3K-Akt signaling and regulates the Glut4-dependant glucose uptake and its utilization in WNIN/GR-Ob (Ob-T2D) rats compared to its control. Our data reinstates P-MSC treatment's potent application to alleviate IR and restores peripheral blood glucose clearance evidenced in stromal vascular fraction (SVF) derived from white adipose tissue (WAT) of the WNIN/GR-Ob rats. Gaining insights, we show the activation of the PI3K-Akt pathway by P-MSCs both in vivo and in vitro (palmitate primed 3T3-L1 cells) to restore the insulin sensitivity dysregulated adipocytes. Our findings suggest a potent application of P-MSCs in pre-clinical/Ob-T2D management.

Topics & Concepts

Mesenchymal stem cellStromal vascular fractionInsulin resistanceAdipose tissueGLUT4PI3K/AKT/mTOR pathwayMedicineCell therapyIn vivoGlucose homeostasisEndocrinologyCancer researchStem cellInternal medicineStromal cellDiabetes mellitusBiologySignal transductionPathologyCell biologyBiotechnologyMesenchymal stem cell researchPancreatic function and diabetesAdipose Tissue and Metabolism
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