Microglia/macrophage-derived human CCL18 promotes glioma progression via CCR8-ACP5 axis analyzed in humanized slice model

在人源化切片模型中分析小胶质细胞/巨噬细胞衍生的人类 CCL18 通过 CCR8-ACP5 轴促进神经胶质瘤进展

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作者:Yimin Huang, Edyta Motta, Cynthia Nanvuma, Leonard D Kuhrt, Yang Yuan, Pengfei Xia, Malgorzata Lubas, Shuai Zhu, Marina Schnauss, Niyeti Qazi, Feng Hu, Huaqiu Zhang, Ting Lei, Michael Synowitz, Charlotte Flüh, Helmut Kettenmann

Abstract

Factors released from glioma-associated microglia/macrophages (GAMs) play a crucial role in glioblastoma multiforme (GBM) progression. Here, we study the importance of CCL18, a cytokine expressed in human but not in rodent GAMs, as a modulator of glioma growth. Since CCL18 signaling could not be studied in classical mouse glioma models, we developed an approach by transplanting induced pluripotent stem cell-derived human microglia and human glioma cells into mouse brain slices depleted of their intrinsic microglia. We observe that CCL18 promotes glioma cell growth and invasion. Chemokine (C-C motif) receptor 8 (CCR8) is identified as a functional receptor for CCL18 on glioma cells, and ACP5 (acid phosphatase 5) is revealed as an important part of the downstream signaling cascade for mediating glioma growth. We conclude, based on the results from an in vitro, ex vivo humanized glioma model and an in vivo GBM model that microglia/macrophage-derived CCL18 promotes glioma growth.

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