Mucin 1, a signal transduction membrane-bound mucin, is present in human disctissue and is downregulated in vitro by exposure to IL-1β or TNF-α

Background: Back pain and disc degeneration have a growing socioeconomic healthcare impact. Mucin 1 (MUC1) is a transmembrane glycoprotein whose extracellular and intracellular domains participate in cellular signaling. Little is currently known about the presence or role of MUC1 in human disc degeneration. Methods: In this IRB-approved research study, 29 human disc specimens were analyzed for MUC1 immunohistochemical localization and gene expression, and annulus fibrosus (annulus) cells were also isolated and cultured in 3D. Microarray analysis assessed expression levels of MUC1 in healthy and degenerated disc tissue and in cells exposed to proinflammatory cytokines (IL-1 beta or TNF-alpha). Results: MUC1 was shown to be present in annulus cells at the protein level using immunochemistry, and its expression was significantly upregulated in annulus tissue from more degenerated grade V discs compared to healthier grade I-II discs (rho = 0.02). A significant positive correlation was present between the percentage of MUC1-positive cells and disc grade (rho = 0.009). MUC1 expression in annulus cells cultured in 3D was also analyzed following exposure to IL-1 beta or TNF-a; exposure produced significant MUC1 downregulation (p chi = 0.0006). Conclusions: Here we present the first data for the constitutive presence of MUC1 in the human disc, and its altered expression during disc degeneration. MUC1 may have an important role in disc aging and degeneration by acting as a regulator in the hypoxic environment, helping disc cells to survive under hypoxic conditions by stabilization and by activation of HIF-1a as previously recognized in pancreatic cancer cells.