Mesenchymal Stromal Cells Induce Podocyte Protection in the Puromycin Injury Model.
Felipe Mateus OrnellasRodrigo J RamalhoCamilla FanelliMargoth Ramos GarnicaDenise M A C MalheirosSabrina Vargas MartiniMarcelo Marcos MoralesIrene L NoronhaPublished in: Scientific reports (2019)
Podocytes are specialized cells with a limited capacity for cell division that do not regenerate in response to injury and loss. Insults that compromise the integrity of podocytes promote proteinuria and progressive renal disease. The aim of this study was to evaluate the potential renoprotective and regenerative effects of mesenchymal stromal cells (mSC) in a severe form of the podocyte injury model induced by intraperitoneal administration of puromycin, aggravated by unilateral nephrectomy. Bone derived mSC were isolated and characterized according to flow cytometry analyses and to their capacity to differentiate into mesenchymal lineages. Wistar rats were divided into three groups: Control, PAN, and PAN+ mSC, consisting of PAN rats treated with 2 × 105 mSC. PAN rats developed heavy proteinuria, hypertension, glomerulosclerosis and significant effacement of the foot process. After 60 days, PAN rats treated with mSC presented a significant amelioration of all these abnormalities. In addition, mSC treatment recovered WT1 expression, improved nephrin, podocin, synaptopodin, podocalyxin, and VEGF expression, and downregulated proinflammatory Th1 cytokines in the kidney with a shift towards regulatory Th2 cytokines. In conclusion, mSC administration induced protection of podocytes in this experimental PAN model, providing new perspectives for the treatment of renal diseases associated with podocyte damage.
Keyphrases
- high glucose
- diabetic nephropathy
- endothelial cells
- bone marrow
- flow cytometry
- poor prognosis
- stem cells
- cell therapy
- induced apoptosis
- palliative care
- multiple sclerosis
- mesenchymal stem cells
- oxidative stress
- binding protein
- risk assessment
- vascular endothelial growth factor
- single cell
- early onset
- cell cycle arrest
- endoplasmic reticulum stress
- cell proliferation
- soft tissue
- cell death
- body composition
- tissue engineering
- long non coding rna
- stress induced