Modulatory effect of chemokines on porcine endometrial stromal and endothelial cells.

The endometrium undergoes cyclical changes during the estrous cycle and pregnancy. These alterations are controlled by various factors, including cytokines. The present study aimed to screen the effect of several chemokines (CCL2, CCL4, CCL5, CCL8, CXCL2, CXCL8, CXCL9, CXCL10, and CXCL12) on endometrial stromal and endothelial cells. Real-time PCR analysis revealed mRNA expression of all examined chemokines and their receptors in primary stromal cells and undetectable levels of CXCL9, CXCL10, and CXCR3 in endothelial cells. Immunocytochemical staining showed variable distribution of chemokine receptors in stromal and endothelial cells. All examined chemokines enhanced stromal cell proliferation, and CCL2 and CXCL12 also increased the migratory potential of these cells. The evaluation of a possible indirect effect of chemokines on angiogenesis and lymphangiogenesis demonstrated that CXCL12 may potentially negatively affect lymphatic vessel creation. Downregulation of VEGFC mRNA and protein expression was noticed after CXCL12 stimulation. Among all examined chemokines, CCL4 and CCL8 positively affected the proliferation and migration of endothelial cells. The number of capillary-like structures was significantly reduced after CXCL8, CXCL10, and CXCL12 stimulation. In conclusion, among all examined chemokines, CCL2 is thought to act as the modulator of stromal cell functions, whereas CCL4 and CCL8 are suggested to be potent factors directly stimulating blood vessel creation.