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手术植入人脂肪来源干细胞可减轻大鼠实验性肝纤维化。

Surgical implantation of human adipose derived stem cells attenuates experimentally induced hepatic fibrosis in rats.

机构信息

Department of Hepatology, Kanazawa Medical University, Uchinada, Ishikawa, 920-0293, Japan.

Center for Regenerative Medicine, Kanazawa Medical University Hospital, Uchinada, Ishikawa, 920-0293, Japan.

出版信息

Mol Med. 2022 Nov 29;28(1):143. doi: 10.1186/s10020-022-00566-6.

Abstract

BACKGROUND

Mesenchymal stem cells (MSCs) are multipotent stromal cells and could exert hepatoprotective effects against acute liver injury, steatohepatitis, and fibrogenesis. Here, we evaluated the effects of human adipose derived stem cells (hADSCs) to attenuate experimentally induced hepatic fibrosis and early cirrhosis in rats.

METHODS

Hepatic fibrosis was induced by intraperitoneal injections of CCl (0.1 ml/100 g body weight) twice a week for 8 weeks. hADSCs were isolated and cultured on polyethylene discs coated with hydroxyapatite and 2 cm diameter disc was surgically implanted on the right lateral lobe of the liver. Discs implanted without hADSCs served as control. The animals were injected again with CCl once a week for another 8 weeks. All the animals were sacrificed at the end of 16th week.

RESULTS

Serial administrations of CCl resulted in well developed fibrosis and early cirrhosis at 8th week which maintained until the 16th week. Animals treated with hADSC discs depicted over 50% decrease of collagen with significant increase in serum albumin and total protein levels. Immunohistochemical staining for TGF-β1, α-smooth muscle actin, and collagen type I and type III demonstrated marked decrease compared to the animals without hADSC treatment.

CONCLUSIONS

Treatment with hADSCs improved liver functions, markedly reduced hepatic fibrosis and early cirrhosis. Various pleiotropic and paracrine factors secreted from the hADSCs seem to serve as reparative functions in the attenuation of liver cirrhosis. The data demonstrated that treatment with hADSCs can be successfully used as a potent therapeutic method to prevent progression of hepatic fibrosis and related adverse events.

摘要

背景

间充质干细胞(MSCs)是多能基质细胞,可发挥对急性肝损伤、脂肪性肝炎和纤维化的肝保护作用。在此,我们评估了人脂肪来源干细胞(hADSCs)减轻大鼠实验性肝纤维化和早期肝硬化的作用。

方法

通过每周两次腹膜内注射 CCl(0.1ml/100g 体重)诱导肝纤维化 8 周。分离和培养 hADSCs,将其种植在涂有羟磷灰石的聚乙烯盘上,直径 2cm 的圆盘通过手术植入肝右外侧叶。未植入 hADSCs 的圆盘作为对照。所有动物在第 16 周结束时再次每周注射 CCl 一次。

结果

连续给予 CCl 导致第 8 周时纤维化和早期肝硬化明显发展,直到第 16 周仍保持。用 hADSC 圆盘治疗的动物胶原减少超过 50%,血清白蛋白和总蛋白水平显著增加。与未接受 hADSC 治疗的动物相比,TGF-β1、α-平滑肌肌动蛋白、I 型和 III 型胶原的免疫组织化学染色明显减少。

结论

hADSCs 治疗可改善肝功能,显著减少肝纤维化和早期肝硬化。hADSCs 分泌的各种多效和旁分泌因子似乎在减轻肝硬化中发挥修复功能。该数据表明,hADSCs 治疗可成功用作预防肝纤维化和相关不良事件进展的有效治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08ce/9706981/bf1fb14802a4/10020_2022_566_Fig1_HTML.jpg

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