The use of patient-derived breast tissue explants to study macrophage polarization and the effects of environmental chemical exposure
Ex vivo mammary explant systems are an excellent model to study interactions between epithelium and stromal cell types because they contain physiologically relevant heterotypic interactions in the background of genetically diverse patients. The intact human mammary tissue, termed patient derived explant (PDE), can be used to investigate cellular responses to a wide variety of external stimuli in situ. For this study, we examined the impact of cytokines or environmental chemicals on macrophage phenotypes. We demonstrate that we can polarize macrophages within human breast tissue PDEs toward M1 or M2 through the addition of IFN-+LPS or IL-4+IL-13 respectively. Elevated expression levels of M(IFN-+LPS) markers (HLADRA and CXCL10) or M(IL-4+IL-13) markers (CD209 and CCL18) were observed in cytokine treated tissues. We also examined the impact of the endocrine disrupting chemical, benzophenone-3 (BP3) on PDEs and measured significant, yet varying effects on macrophage polarization. Furthermore, a subset of the PDEs respond to IL-4 +IL-13 through down regulation of E-cadherin and upregulation of Vimentin which is reminiscent of EMT changes. Finally, we were able to show immortalized non-malignant breast epithelial cells can exhibit EMT characteristics when exposed to growth factors secreted by M(IL-4+IL-13) macrophages. Taken together, the PDE model system is an outstanding preclinical model to study early tissue resident immune responses and effects on epithelial and stromal responses to stimuli found both endogenously in the breast as well as exogenously due to exposures.
Keywords: EMT; Macrophage Polarization; Patient-Derived Explant; oxybenzone.
Gregory KJ, Morin SM, Kubosiak A, Ser-Dolansky J, Schalet B, Jerry DJ, Schneider SS. The use of patient-derived breast tissue explants to study macrophage polarization and the effects of environmental chemical exposure. Immunol Cell Biol. 2020 Jul 26. doi: 10.1111/imcb.12381.