In vitro morphology viability and cytokine secretion of uterine telocyte‐activated mouse peritoneal macrophages

摘要

Telocytes (TCs), a distinct interstitial cell population, have been identified in the uterus, oviduct and placenta, with multiple proposed potential biological functions. Their unique structure allows them to form intercellular junctions with various immunocytes, both in normal and diseased tissues, suggesting a potential functional relationship with the local immune response. It has been hypothesized that through direct heterocellular junctions or indirect paracrine effects, TCs influence the activity of local immunocytes that are involved in the inflammatory process and in immune‐mediated reproductive abnormalities. However, no reliable cytological evidence for this hypothesis is currently available. In this study, we cultured primary murine uterine TCs and collected TC conditioned media (TCM). Mouse peritoneal macrophages (pMACs) were co‐cultured for 48 hrs with TCM or with DMEM/F12 or lipopolysaccharide (LPS) as negative and positive controls, respectively. Normal uterine TCs with a typical structure and a CD‐34‐positive/vimentin‐positive/c‐kit‐negative immunophenotype were observed during culture. Morphologically, TCM‐treated pMACs displayed an obvious activation/immunoresponse, in contrast to over‐stimulation and cell death after LPS treatment and no sign of activation in the presence of DMEM/F12. Accordingly, a cell counting kit 8 (CCK‐8) assay indicated significant activation of style="fixed-case">pMACs by style="fixed-case">TCM and style="fixed-case">LPS compared to style="fixed-case">DMEM/F12, thus supporting the marked morphological differences among these groups of cells. Furthermore, within a panel of macrophage‐derived cytokines/enzymes, interleukin‐6 ( style="fixed-case">IL‐6) and inducible nitric oxide synthase were significantly elevated in style="fixed-case">TCM‐treated style="fixed-case">pMACs; tumour necrosis factor α, style="fixed-case">IL1‐R1, and style="fixed-case">IL‐10 were slightly, but significantly, up‐regulated; and no changes were observed for transforming growth factor‐β1, style="fixed-case">IL‐1β, style="fixed-case">IL‐23α and style="fixed-case">IL‐18. Our results indicate that style="fixed-case">TCs are not simply innocent bystanders but are rather functional players in the activation of style="fixed-case">pMACs; they trigger and maintain the immune response, likely through indirect paracrine effects. Thus, we provide preliminary in vitro evidence of immunoregulatory and immunosurveillance roles for TCs.