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. 2021 May 29;246(17):1928–1937. doi: 10.1177/15353702211010420

Figure 2.

Figure 2.

The ability of HCC cells to induce macrophage recruitment and M2 polarization was abrogated by ligustilide. (a) HCC cells under ligustilide exposure, or not, were co-cultured with PMA-treated THP-1 macrophages using the Transwell co-culture system. Macrophage migration was then analyzed. Macrophages without any treatment were defined as a control group. Scale bars, 100 µM. (b) Flow cytometry was used to detect the percentage of CD14+CD206+ cells in macrophages. (c and d) The mRNA levels of M2 macrophage phenotype markers were determined by qRT-PCR. (e and f) The transcript (e) and release (f) of M2 macrophage marker IL-10 and TGF-β were further explored. *P <0.05 vs. control group. §P <0.05 vs. CC-treated group. (A color version of this figure is available in the online journal.)