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Details

Autor(en) / Beteiligte
Titel
Micro-vesicles derived from bone marrow stem cells protect the kidney both in vivo and in vitro by microRNA-dependent repairing
Ist Teil von
  • Nephrology (Carlton, Vic.), 2015-09, Vol.20 (9), p.591-600
Ort / Verlag
Australia: Blackwell Publishing Ltd
Erscheinungsjahr
2015
Quelle
Wiley-Blackwell Journals
Beschreibungen/Notizen
  • Aims Micro‐vesicles (MVs) from bone mesenchymal stem cells (MSCs) have been shown to contribute to the recovery of damaged kidney. The aims of the present study are to investigate the biological effects and repair mechanisms of MVs. Methods Micro‐vesicles were obtained from MSC supernatants. In vitro, the proximal tubular epithelial cells (HK‐2) were treated with transforming growth factor (TGF‐β1). The expressions of E‐cadherin and α‐smooth muscle actin (α‐SMA) were evaluated. In vitro, the mice were divided into: control, unilateral ureteral obstruction (UUO), UUO+MSC, and UUO+MV group. MVs and MSCs were injected after surgery. The mice were killed 7/14 days after surgery and handled for further tests. The micro‐RNA expressions were labeled using the miRCURY Hy3/Hy5 Power labeling kit and hybridized on the miRCURY LNA Array. Results In vitro, MV reversed transforming growth factor‐β1 (TGF‐β1)‐induced morphological changes, and firmed the expression of E‐cadherin and reduced the secretion of α‐SMA in HK2 cells. In vivo, the level of blood urea nitrogen (BUN) in the MV and MSC group was lower than the UUO (P < 0.01). The Scr level decreased after 7 days of MV treatment (P < 0.05). Administration of MSC and MV reduced Scr level at day 14 (P < 0.05). The level of serum UA decreased with MV administration (day 7,14, P < 0.01). Herein, a total of 503 expressed miRNAs were detected, of which, 266 were in MSC, including 237 in MVs. Conclusion Micro‐vesicles (MVs) protect kidneys both in vivo and vitro, and MVs are superior to MSCs in some respects. MVs can be a potential therapy in treatment of kidney diseases. Summary at a Glance This paper has had three reviews with mixed recommendations. The topic is novel – use of mesenchymal stem cells to deliver miRNA via endosome vesicles. The English may require some editorial proofing, but otherwise suitable for publication.

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