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肾上腺髓质素增强大鼠实验性中风后间充质干细胞的治疗效力。

Adrenomedullin enhances therapeutic potency of mesenchymal stem cells after experimental stroke in rats.

作者信息

Hanabusa Kenichiro, Nagaya Noritoshi, Iwase Takashi, Itoh Takefumi, Murakami Shinsuke, Shimizu Yoshito, Taki Waro, Miyatake Kunio, Kangawa Kenji

机构信息

Department of Regenerative Medicine and Tissue Engineering, National Cardiovascular Center Research Institute, Suita, Osaka, Japan.

出版信息

Stroke. 2005 Apr;36(4):853-8. doi: 10.1161/01.STR.0000157661.69482.76. Epub 2005 Mar 3.

Abstract

BACKGROUND AND PURPOSE

Adrenomedullin (AM) induces angiogenesis and inhibits cell apoptosis through the phosphatidylinositol 3-kinase/Akt pathway. Transplantation of mesenchymal stem cells (MSCs) has been shown to improve neurological deficits after stroke in rats. We investigated whether AM enhances the therapeutic potency of MSC transplantation.

METHODS

Male Lewis rats (n=100) were subjected to 2-hour middle cerebral artery occlusion. Immediately after reperfusion, rats were assigned randomly to receive intravenous transplantation of MSCs plus subcutaneous infusion of AM for 7 days (MSC+AM group), AM infusion alone (AM group), MSC transplantation alone (MSC group), or vehicle infusion (control group). Neurological and immunohistological assessments were performed to examine the effects of these treatments.

RESULTS

Some engrafted MSCs were positive for neuronal and endothelial cell markers, although the number of differentiated MSCs did not differ significantly between the MSC and MSC+AM groups. The neurological score significantly improved in the MSC, AM, and MSC+AM groups compared with the control group. Importantly, improvement in the MSC+AM group was significantly greater than that in the MSC and AM groups. There was marked induction of angiogenesis in the ischemic penumbra in the MSC+AM group, followed by the AM, MSC, and control groups. AM infusion significantly inhibited apoptosis of transplanted MSCs. As a result, the number of engrafted MSCs in the MSC+AM group was significantly higher than that in the MSC group.

CONCLUSIONS

AM enhanced the therapeutic potency of MSCs, including neurological improvement, possibly through inhibition of MSC apoptosis and induction of angiogenesis.

摘要

背景与目的

肾上腺髓质素(AM)通过磷脂酰肌醇3激酶/蛋白激酶B(PI3K/Akt)信号通路诱导血管生成并抑制细胞凋亡。间充质干细胞(MSC)移植已被证明可改善大鼠脑卒中后的神经功能缺损。我们研究了AM是否能增强MSC移植的治疗效果。

方法

100只雄性Lewis大鼠接受2小时大脑中动脉闭塞。再灌注后立即将大鼠随机分为4组,分别接受静脉注射MSC加皮下注射AM共7天(MSC+AM组)、单独注射AM(AM组)、单独进行MSC移植(MSC组)或注射溶剂(对照组)。进行神经学和免疫组织学评估以检验这些治疗的效果。

结果

一些植入的MSC对神经元和内皮细胞标志物呈阳性,尽管MSC组和MSC+AM组之间分化的MSC数量没有显著差异。与对照组相比,MSC组、AM组和MSC+AM组的神经学评分显著改善。重要的是,MSC+AM组的改善明显大于MSC组和AM组。MSC+AM组在缺血半暗带中有明显的血管生成诱导,其次是AM组、MSC组和对照组。注射AM显著抑制了移植MSC的凋亡。结果,MSC+AM组中植入的MSC数量显著高于MSC组。

结论

AM增强了MSC的治疗效果,包括神经功能改善,可能是通过抑制MSC凋亡和诱导血管生成实现的。

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