Journal of Tissue Engineering and Reconstructive Surgery ›› 2024, Vol. 20 ›› Issue (1): 58-.

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Effects of CX3CR1 on skeletal muscle microfibers,ERK/MAPK signaling pathway and inflammatory response in rats with traumatic osteomyelitis

  

  • Published:2024-03-07

Abstract:

Objective To explore the effects of CX3CR1 on inflammatory response, skeletal muscle microfibers and ERK/MAPK signaling pathway in rats with traumatic osteomyelitis. Methods Thirty SPF SD male rats were selected and divided into healthy group, model group and CX3CR1 inhibition group according to random number table method, with an average of
10 in each group. Traumatic osteomyelitis model was established in model group and CX3CR1 inhibition group. The healthy
group and model group were routinely injected with normal saline intraperitoneally every day, and the CX3CR1 intervention
group was treated by injecting CX3CR1 neutralizing antibody into the residual cavity. Serum levels of inflammatory cytokines
interleukin (IL-6, IL-10, IL-1β, TGF-β) were detected by ELISA, skeletal muscle microfibers were detected by X-ray
Norden score, and pathological changes were observed by HE staining. Extracellular regulated protein kinase 1/2(ERK1/2),
mitogen activated protein kinase (MAPK) protein and mRNA in femur were detected by Western blotting and PCR. Results
Compared with the healthy group, the contents of TGF- β, IL-1β, IL-10, IL-6 and other inflammatory factors were
increased in the model group (P<0.05). Compared with model group, the content of inflammatory factors in CX3CR1 inhibitory group was decreased (P<0.05). Compared with the healthy group, the X-ray Norden score of the model group was increased over time (P<0.05). Compared with model group, X-ray Norden score of CX3CR1 inhibition group was decreased(P<0.05). HE staining showed that the bone cortex in the healthy group was intact. In the model group, there was a large
number of inflammatory cell infiltration, focal abscess, and area necrosis. In the CX3CR1 inhibitory group, the large cortical
bone was significantly improved and the inflammatory response was reduced. Compared with healthy group, ERK1/2 and
MAPK protein and mRNA in model group were increased (P<0.05). Compared with model group, the protein and mRNA ofERK1/2 and MAPK in CX3CR1 inhibition group were decreased (P<0.05). Conclusion Inhibition of CX3CR1 can improvethe disease response in traumatic osteomyelitis rats, which may be related to decreased inflammatory response, ERK/MAPK
and improved skeletal muscle microfibers

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