Depletion of macrophages deteriorates bisphosphonate-related osteonecrosis of the jaw-like lesions in mice

• Published in: Bone (New York, N.Y.) N.Y.), 2023-12, Vol.177, p.116899, Article 116899
• Main Authors: Kozutsumi, Ryohei, Kuroshima, Shinichiro, Al-Omari, Farah A., Hayano, Hiroki, Nakajima, Kazunori, Kakehashi, Hiroe, Sawase, Takashi
• Format: Article
• Language: English
• Subjects: Animals; Bisphosphonate-Associated Osteonecrosis of the Jaw - drug therapy; Bisphosphonates; Bone Density Conservation Agents - adverse effects; BRONJ; Diphosphonates - therapeutic use; Macrophages; Maxilla; Mice; Osteoclasts; Wound healing; X-Ray Microtomography; Zoledronic Acid - therapeutic use
• ISSN: 8756-3282; 1873-2763; 1873-2763
• DOI: 10.1016/j.bone.2023.116899

Bisphosphonate-related osteonecrosis of the jaw (BRONJ) is a potentially intractable disease with no definitive pathophysiology and no treatment and prevention strategies. This study aimed to investigate whether time-selective depletion of macrophages worsens BRONJ-like lesions in mice. A murine model of high-prevalence BRONJ-like lesions in combination with zoledronate/chemotherapeutic drug administration and tooth extraction was created according to the methods of our previous studies. Daily intra-oral submucosal administration of clodronate-loaded liposomes, which temporarily depletes systemic macrophages, was performed immediately after tooth extraction. Spleens, femora, tibiae, and maxillae were dissected 2 weeks after extraction to evaluate BRONJ-like lesions and systemic conditions by micro-computed tomography analysis, histomorphometric and immunofluorescent analyses, and serum chemistry with ELISA. Depletion of macrophages significantly decreased the numbers of local and systemic macrophages and osteoclasts on the bone surface, which markedly worsened osseous healing, with increased necrotic bone and empty lacunae in the existing alveolar bone and newly formed bone in the extraction sockets, and soft tissue healing, with decreased collagen production and increased infiltration of polymorphonuclear cells. Interestingly, the depletion of macrophages significantly shifted macrophage polarization to M1 macrophages through an increase in F4/80+CD38+ M1 macrophages and a decrease in F4/80+CD163+ M2 macrophages, with decreases in the total number of F4/80+ macrophages. These data demonstrated that severe inhibition of osteoclasts in bone tissue and polarization shifting of macrophages in soft tissue are essential factors associated with BRONJ. •Clodronate-loaded liposomes (CLLs) deteriorated BRONJ-like lesions in mice.•CLLs significantly decreased numbers of osteoclasts and macrophages in systemic and local tissues.•F4/80+CD38+ M1 macrophages accumulated in BRONJ-like lesions with CCLs.•F4/80+CD163+ M2 macrophages decreased in BRONJ-like lesions with CCLs.•The M1/M2 ratio shifted to M1 macrophages in the connective tissue of BRONJ-like lesions.