作者: Ariela Benigni , Susanna Tomasoni , Lorena Longaretti , Cinzia Rota , Marina Morigi
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摘要: Bone marrow–mesenchymal stem cells (BM-MSC) ameliorate renal dysfunction and repair tubular damage of acute kidney injury by locally releasing growth factors, including the insulin-like factor-1 (IGF-1). The restricted homing BM-MSC at site led us to investigate a possible gene-based communication mechanism between cells. Human (hBM-MSC) released microparticles exosomes (Exo) enriched in mRNAs. A selected pattern transcripts was detected Exo versus parental expressed IGF-1 receptor (IGF-1R), but not mRNA, while hBM-MSC contained both R- lacking IGF-1R exposed hBM-MSC-derived acquired human transcript that translated corresponding protein. Transfer mRNA from cisplatin-damaged proximal (proximal epithelial cell [PTEC]) increased PTEC proliferation. Coincubation damaged with soluble further enhanced These fi...