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超声靶向微泡破坏介导间充质干细胞肾靶向移植促进糖尿病肾病大鼠肾脏修复。

Kidney-targeted transplantation of mesenchymal stem cells by ultrasound-targeted microbubble destruction promotes kidney repair in diabetic nephropathy rats.

机构信息

Department of Ultrasound, Xinqiao Hospital of the Third Military Medical University, 183 Xinqiaozheng Road, Chongqing 400037, China.

出版信息

Biomed Res Int. 2013;2013:526367. doi: 10.1155/2013/526367. Epub 2013 May 27.

DOI:10.1155/2013/526367
PMID:23762850
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3677660/
Abstract

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.

摘要

我们验证了这样一个假设,即超声靶向微泡破坏(UTMD)技术可以增强骨髓间充质干细胞(BM-MSCs)肾靶向移植在糖尿病肾病(DN)大鼠中的肾保护作用。糖尿病通过链脲佐菌素(STZ)注射(60mg/Kg,腹腔内)诱导 Sprague-Dawley 大鼠。在糖尿病发病后 4 周,将 MSC 单独或与 UTMD 联合用于 DN 大鼠。在 MSC 移植后 1、2、4 和 8 周测量随机血糖浓度,在 MSC 移植后 8 周评估血浆胰岛素水平、尿白蛋白排泄率(UAER)值、胰腺和肾脏结构、TGF-β1、突触蛋白和 IL-10 的表达。MSC 移植降低了血糖浓度并减轻了胰岛/β细胞损伤。UTMD 后,肾间质毛细血管的通透性和 VCAM-1 表达增加,这增强了 MSC 向肾脏的归巢和保留。MSC 移植联合 UTMD 通过抑制 TGF-β1 表达和上调突触蛋白和 IL-10 表达来预防肾脏损伤并降低 UAER 值。我们得出结论,MSC 移植可逆转高血糖;UTMD 技术可无创性增加 MSC 向肾脏的归巢并促进 DN 大鼠的肾脏修复。这种非侵入性细胞输送方法可能是可行且有效的,作为糖尿病肾病个性化 MSC 治疗的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/2a132db61732/BMRI2013-526367.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/fce81cef8603/BMRI2013-526367.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/2cdb6ee953ee/BMRI2013-526367.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/870c075f9a48/BMRI2013-526367.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/409c2aee26f6/BMRI2013-526367.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/2a132db61732/BMRI2013-526367.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/fce81cef8603/BMRI2013-526367.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/2cdb6ee953ee/BMRI2013-526367.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/870c075f9a48/BMRI2013-526367.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/409c2aee26f6/BMRI2013-526367.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498c/3677660/2a132db61732/BMRI2013-526367.005.jpg

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