Publication | Open Access
Kidney-Targeted Transplantation of Mesenchymal Stem Cells by Ultrasound-Targeted Microbubble Destruction Promotes Kidney Repair in Diabetic Nephropathy Rats
65
Citations
33
References
2013
Year
Tissue EngineeringCell TherapyEngineeringAdult Stem CellImmunologyRenal InflammationDiabetic Nephropathy RatsBiomedical EngineeringPancreas TransplantationRenoprotective EffectInsulin SignalingUtmd TechniqueRegenerative MedicineMscs TransplantationMatrix BiologyInsulin DeliveryChronic Kidney DiseaseStem CellsCell TransplantationMesenchymal Stem CellsIslet Cell ManufacturingCell BiologyMesenchymal Stem CellIslet TransplantationUrologyDiabetesKidney-targeted TransplantationDiabetic Kidney DiseaseStem-cell TherapyMedicineNephrologyKidney Research
We test the hypothesis that ultrasound-targeted microbubble destruction (UTMD) technique increases the renoprotective effect of kidney-targeted transplantation of bone-marrow-derived mesenchymal stem cells (BM-MSCs) in diabetic nephropathy (DN) rats. Diabetes was induced by streptozotocin injection (60 mg/Kg, intraperitoneally) in Sprague-Dawley rats. MSCs were administered alone or in combination with UTMD to DN rats at 4 weeks after diabetes onset. Random blood glucose concentrations were measured at 1, 2, 4, and 8 weeks, and plasma insulin levels, urinary albumin excretion rate (UAER) values, the structures of pancreas and kidney, the expressions of TGF- β 1, synaptopodin, and IL-10 were assessed at 8 weeks after MSCs transplantation. MSCs transplantation decreased blood glucose concentrations and attenuated pancreatic islets/ β cells damage. The permeability of renal interstitial capillaries and VCAM-1 expression increased after UTMD, which enhanced homing and retention of MSCs to kidneys. MSCs transplantation together with UTMD prevented renal damage and decreased UAER values by inhibiting TGF- β 1 expression and upregulating synaptopodin and IL-10 expression. We conclude that MSCs transplantation reverts hyperglycemia; UTMD technique noninvasively increases the homing of MSCs to kidneys and promotes renal repair in DN rats. This noninvasive cell delivery method may be feasible and efficient as a novel approach for personal MSCs therapy to diabetic nephropathy.
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