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P4HA1下调通过促进M1小胶质细胞极化抑制胶质瘤侵袭性。

P4HA1 Down-Regulation Inhibits Glioma Invasiveness by Promoting M1 Microglia Polarization.

作者信息

Wang Qiyan, Zhang Junwen, Fang Sheng, Wang Jialin, Han Xiangming, Liu Fusheng, Jin Guishan

机构信息

Brain Tumor Research Center, Beijing Neurosurgical Institute, Beijing Laboratory of Biomedical Materials, Beijing Tiantan Hospital Affiliated to Capital Medical University, Beijing, 10070, People's Republic of China.

出版信息

Onco Targets Ther. 2021 Mar 8;14:1771-1782. doi: 10.2147/OTT.S299977. eCollection 2021.

Abstract

BACKGROUND

Polarization of microglia cells in the glioma microenvironment is closely related to the malignant progression and invasion of gliomas. Prolyl 4-hydroxylase subunit α1 (P4HA1) is the rate-limiting subunit of prolyl 4-hydroxylase (P4H). In previous studies, we showed that P4HA1 could promote the proliferation, migration, and invasion of glioma cells, but the specific mechanisms through which this occurs have not been fully elucidated.

MATERIALS AND METHODS

Interactions between glioma and microglia cells were analyzed using bioinformatics. Then, co-culture models were used to obtain conditioned media. To characterize microglial cell polarization, we used PCR and immunofluorescence. Proliferation and invasion assays were used to explore the biological behavior of glioma cells affected by microglia. Finally, marker expression was detected using immunohistochemistry in glioblastoma multiform (GBM) specimens.

RESULTS

Knockdown of P4HA1 resulted in reduced chemotaxis of microglia toward GBM cells and increased polarization of microglia toward the M1 phenotype. The changed microglial polarization state, in turn, inhibited the proliferation and invasion of GBM cells. Moreover, in GBM tissue specimens, the P4HA1 expression level is negatively correlated with that of the CD86 microglia M1-specific marker.

CONCLUSION

Our results show that P4HA1 promotes immunosuppressive microenvironment formation by cross-talk between GBM and microglia cells and indirectly increases the aggressiveness of GBM.

摘要

背景

胶质瘤微环境中微胶质细胞的极化与胶质瘤的恶性进展和侵袭密切相关。脯氨酰4-羟化酶亚基α1(P4HA1)是脯氨酰4-羟化酶(P4H)的限速亚基。在先前的研究中,我们表明P4HA1可以促进胶质瘤细胞的增殖、迁移和侵袭,但具体机制尚未完全阐明。

材料与方法

使用生物信息学分析胶质瘤细胞与微胶质细胞之间的相互作用。然后,使用共培养模型获得条件培养基。为了表征微胶质细胞的极化,我们使用了聚合酶链反应(PCR)和免疫荧光法。使用增殖和侵袭试验来探究微胶质细胞对胶质瘤细胞生物学行为的影响。最后,在多形性胶质母细胞瘤(GBM)标本中使用免疫组织化学检测标志物表达。

结果

敲低P4HA1导致微胶质细胞对GBM细胞的趋化性降低,且微胶质细胞向M1表型的极化增加。微胶质细胞极化状态的改变反过来又抑制了GBM细胞的增殖和侵袭。此外,在GBM组织标本中,P4HA1表达水平与微胶质细胞M1特异性标志物CD86的表达水平呈负相关。

结论

我们的结果表明,P4HA1通过GBM细胞与微胶质细胞之间的相互作用促进免疫抑制微环境的形成,并间接增加GBM的侵袭性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8103/7954035/d17a68cee425/OTT-14-1771-g0001.jpg

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