Maresin 1 resolves aged‐associated macrophage inflammation to improve bone regeneration. Issue 10 (14th August 2020)

• Record Type: Journal Article
• Authors: Huang, Rong; Vi, Linda; Zong, Xiaohua; Baht, Gurpreet S.
• Is Part Of: FASEB journal. Volume 34:Issue 10(2020)
• Page Start: 13521
• Page End: 13532
• Publication Date: 2020-08-14
• Subjects: bone -- fracture healing -- inflammaging -- macrophage -- osteoblast; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.202001145R
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract: Inflammaging is associated with poor tissue regeneration observed in advanced age. Specifically, protracted inflammation after acute injury has been associated with decreased bone fracture healing and increased rates of nonunion in elderly patients. Here, we investigated the efficacy of using Maresin 1 (MaR1), an omega‐3 fatty acid‐derived pro‐resolving agent, to resolve inflammation after tibial fracture injury and subsequently improving aged bone healing. Aged (24‐month‐old mice) underwent tibial fracture surgery and were either treated with vehicle or MaR1 3 days after injury. Fracture calluses were harvested 7 days, 14 days, 21 days, and 28 days after injury to investigate inflammatory response, cartilage development, bone deposition, and mechanical integrity, respectively. Healing bones from MaR1‐treated mice displayed decreased cartilage formation and increased bone deposition which resulted in increased structural stiffness and increased force to fracture in the later stages of repair. In the early stages, MaR1 treatment decreased the number of pro‐inflammatory macrophages within the fracture callus and decreased the level of inflammatory biomarkers in circulation. In tissue culture models, MaR1 treatment of bone marrow‐derived macrophages from aged mice protected cells form a pro‐inflammatory phenotype and induced an anti‐inflammatory fate. Furthermore, the secretome of MaR1‐treated bone marrow‐derived macrophages was identified as osteoinductive, enhancing osteoblast differentiation of bone marrow stromal cells. Our findings here identify resolution of inflammation, and MaR1 itself, to be a point of intervention to improve aged bone healing.