白头翁皂苷通过靶向 STAT6 介导的 M2 型巨噬细胞极化抑制黑色素瘤实验性肺转移。

Pulsatilla Saponins Inhibit Experimental Lung Metastasis of Melanoma via Targeting STAT6-Mediated M2 Macrophages Polarization.

机构信息

Center for Translational Medicine, Jiangxi Key Laboratory of Traditional Chinese Medicine in Prevention and Treatment of Vascular Remodeling Associated Disease, Jiangxi University of Chinese Medicine, Nanchang 330006, China.

The Second Affiliated Hospital, Jiangxi University of Chinese Medicine, Nanchang 330006, China.

出版信息

Molecules. 2023 Apr 24;28(9):3682. doi: 10.3390/molecules28093682.

Abstract

(PS) extracts from Pulsatilla chinensis (Bge.) Regel, are a commonly used traditional Chinese medicine. In the previous study, we found displayed anti-tumor activity without side effects such as bone marrow suppression. However, the mechanism of the anti-tumor effect was not illustrated well. Since M2-like tumor-associated macrophages (TAMs) that required activation of the signal transducer and activator of transcription 6 (STAT6) for polarization are the important immune cells in the tumor microenvironment and play a key role in tumor progress and metastasis, this study aimed to confirm whether could inhibit the development and metastasis of tumors by inhibiting the polarization of M2 macrophages. We investigated the relevance of M2 macrophage polarization and the anti-tumor effects of in vitro and in vivo. In vitro, could decrease the mRNA level of M2 marker genes Arg1, Fizz1, Ym1, and CD206, and the down-regulation effect of phosphorylated STAT6 induced by IL-4; moreover, the conditioned medium (CM) from bone marrow-derived macrophages (BMDM) treated with could inhibit the proliferation and migration of B16-F0 cells. In vivo, could reduce the number of lung metastasis loci, down-regulate the expression of M2 marker genes, and suppress the expression of phosphorylated STAT6 in tumor tissues. Furthermore, we used AS1517499 (AS), a STAT6 inhibitor, to verify the role of PS on M2 macrophage polarization both in vitro and in vivo. We found that failed to further inhibit STAT6 activation; the mRNA level of Arg1, Fizz1, Ym1, and CD206; and the proliferation and migration of B16-F0 cells after AS1517499 intervention in vitro. Similar results were obtained in vivo. These results illustrated that could effectively suppress tumor progress by inhibiting the polarization of M2 macrophages via the STAT6 signaling pathway; this revealed a novel mechanism for its anti-tumor activity.

摘要

(PS)提取物来源于白头翁(Bge.)Regel,是一种常用的传统中药。在之前的研究中,我们发现它具有抗肿瘤活性,且无骨髓抑制等副作用。然而,其抗肿瘤作用的机制并未得到很好的阐明。由于 M2 样肿瘤相关巨噬细胞(TAMs)需要激活信号转导和转录激活因子 6(STAT6)极化,它们是肿瘤微环境中的重要免疫细胞,在肿瘤进展和转移中发挥关键作用,因此本研究旨在证实是否可以通过抑制 M2 巨噬细胞的极化来抑制肿瘤的发展和转移。我们在体外和体内研究了 M2 巨噬细胞极化与白头翁的抗肿瘤作用之间的相关性。在体外,白头翁可以降低 M2 标志物基因 Arg1、Fizz1、Ym1 和 CD206 的 mRNA 水平,以及 IL-4 诱导的磷酸化 STAT6 的下调作用;此外,用白头翁处理的骨髓来源巨噬细胞(BMDM)的条件培养基(CM)可以抑制 B16-F0 细胞的增殖和迁移。在体内,白头翁可以减少肺转移灶的数量,下调肿瘤组织中 M2 标志物基因的表达,并抑制磷酸化 STAT6 的表达。此外,我们使用 STAT6 抑制剂 AS1517499(AS)在体外和体内验证了白头翁对 M2 巨噬细胞极化的作用。我们发现,AS 干预后,白头翁不能进一步抑制 STAT6 激活、Arg1、Fizz1、Ym1 和 CD206 的 mRNA 水平以及 B16-F0 细胞的增殖和迁移。在体内也得到了类似的结果。这些结果表明,白头翁可以通过 STAT6 信号通路有效抑制 M2 巨噬细胞的极化,从而抑制肿瘤的进展,揭示了其抗肿瘤活性的新机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be7/10179893/b13df5db1f34/molecules-28-03682-g001.jpg

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