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截短型乳脂肪球表皮生长因子样因子8通过抑制整合素-转化生长因子β受体相互作用改善肝纤维化。

Truncated Milk Fat Globule-EGF-like Factor 8 Ameliorates Liver Fibrosis via Inhibition of Integrin-TGFβ Receptor Interaction.

作者信息

An Geun Ho, Lee Jaehun, Jin Xiong, Chung Jinwoo, Kim Joon-Chul, Park Jung-Hyuck, Kim Minkyung, Han Choongseong, Kim Jong-Hoon, Woo Dong-Hun

机构信息

Department of New Drug Development, NEXEL Co., Ltd., 8th Floor, 55 Magokdong-ro, Gangseo-gu, Seoul 07802, Korea.

Laboratory of Stem Cells and Tissue Regeneration, Department of Biotechnology, College of Life Sciences and Biotechnology, Science Campus, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, Korea.

出版信息

Biomedicines. 2021 Oct 24;9(11):1529. doi: 10.3390/biomedicines9111529.

Abstract

Milk fat globule-EGF factor 8 (MFG-E8) protein is known as an immunomodulator in various diseases, and we previously demonstrated the anti-fibrotic role of MFG-E8 in liver disease. Here, we present a truncated form of MFG-E8 that provides an advanced therapeutic benefit in treating liver fibrosis. The enhanced therapeutic potential of the modified MFG-E8 was demonstrated in various liver fibrosis animal models, and the efficacy was further confirmed in human hepatic stellate cells and a liver spheroid model. In the subsequent analysis, we found that the modified MFG-E8 more efficiently suppressed transforming growth factor β (TGF-β) signaling than the original form of MFG-E8, and it deactivated the proliferation of hepatic stellate cells in the liver disease environment through interfering with the interactions between integrins (αvβ3 & αvβ5) and TGF-βRI. Furthermore, the protein preferentially delivered in the liver after administration, and the safety profiles of the protein were demonstrated in male and female rat models. Therefore, in conclusion, this modified MFG-E8 provides a promising new therapeutic strategy for treating fibrotic diseases.

摘要

乳脂肪球表皮生长因子8(MFG-E8)蛋白在多种疾病中被视为一种免疫调节剂,我们之前已证明MFG-E8在肝脏疾病中的抗纤维化作用。在此,我们展示了一种截短形式的MFG-E8,其在治疗肝纤维化方面具有更高的治疗效益。改良后的MFG-E8在多种肝纤维化动物模型中展现出增强的治疗潜力,并且在人肝星状细胞和肝球体模型中进一步证实了其疗效。在后续分析中,我们发现改良后的MFG-E8比原始形式的MFG-E8更有效地抑制转化生长因子β(TGF-β)信号传导,并且它通过干扰整合素(αvβ3和αvβ5)与TGF-βRI之间的相互作用,在肝脏疾病环境中使肝星状细胞的增殖失活。此外,该蛋白在给药后优先在肝脏中递送,并且在雄性和雌性大鼠模型中证明了该蛋白的安全性。因此,总之,这种改良后的MFG-E8为治疗纤维化疾病提供了一种有前景的新治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecaf/8615163/a110d01b3298/biomedicines-09-01529-g001.jpg

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