Reduced TGF-β Expression and CD206-Positive Resident Macrophages in the Intervertebral Discs of Aged Mice

Age is a key factor in intervertebral disc (IVD) degeneration; however, the changes that occur in IVDs with age are not fully understood. Tissue-resident macrophages are critical for tissue homeostasis and are regulated by transforming growth factor- (TGF-) β . We examined changes in the proportion of resident macrophages in young versus aged mice and the role of TGF- β in regulating resident macrophages in IVDs. IVDs were harvested from 4-month (young) and 18-month-old (aged) C57BL/6J mice. The proportion of macrophages in IVDs was determined using flow cytometry ( n = 5 for each time point) and the expression of Cd11b , Cd206 , and Tgfb genes, which encode CD11b, CD206, and TGF- β protein, respectively, using real-time PCR. To study the role of TGF- β in the polarization of resident macrophages, resident macrophages isolated from IVDs from young and aged mice were treated with recombinant TGF- β with and without a TGF- β inhibitor (SB431542). Additionally, SB431542 was intraperitoneally injected into young and aged mice, and Cd206 expression was examined using real-time PCR ( n = 10 for each time point). The proportion of CD11b+ and CD11b+ CD206+ cells was significantly reduced in aged versus young mice, as was Cd11b , Cd206 , and Tgfb expression. TGF- β /IL10 stimulation significantly increased the expression of Cd206 , an M2 macrophage marker, in disc macrophages from both young and aged mice. Meanwhile, administration of a TGF- β inhibitor significantly reduced Cd206 expression compared to vehicle control in both groups. Conclusion . Resident macrophages decrease with age in IVDs, which may be associated with the concomitant decrease in TGF- β . Our findings provide new insight into the mechanisms of age-related IVD pathology.