LPS-Induced Inflammation Prior to Injury Exacerbates the Development of Post-Traumatic Osteoarthritis in Mice

Abstract

Osteoarthritis (OA) is a debilitating and painful disease characterized by the progressive loss of articular cartilage. Post-traumatic osteoarthritis (PTOA) is an injury-induced type of OA that persists in an asymptomatic phase for years before it becomes diagnosed in~50% of injured individuals. Although PTOA is not classified as an inflammatory disease, it has been suggested that inflammation could be a major driver of PTOA development. Here we examined whether a state of systemic inflammation induced by lipopolysaccharide (LPS) administration 5-days before injury would modulate PTOA outcomes. RNA-seq analysis at 1-day post-injury followed by micro-computed tomography (μCT) and histology characterization at 6 weeks post-injury revealed that LPS administration causes more severe PTOA phenotypes. These phenotypes included significantly higher loss of cartilage and subchondral bone volume. Gene expression analysis showed that LPS alone induced a large cohort of inflammatory genes previously shown to be elevated in synovial M1 macrophages of rheumatoid arthritis (RA) patients, suggesting that systemic LPS produces synovitis. This synovitis was sufficient to promote PTOA in MRL/MpJ mice, a strain previously shown to be resistant to PTOA. The synovium of LPS-treated injured joints displayed an increase in cellularity, and immunohistological examination confirmed that this increase was in part attributable to an elevation in type 1 macrophages. LPS induced the expression of Tlr7 and Tlr8 in both injured and uninjured joints, genes known to be elevated in RA. We conclude that inflammation before injury is an important risk factor for the development of PTOA and that correlating patient serum endotoxin levels or their state of systemic inflammation with PTOA progression may help develop new, effective treatments to lower the rate of PTOA in injured individuals.

Antibiotic Treatment Prior to Injury Improves Post-Traumatic Osteoarthritis Outcomes in Mice

“…Lipopolysaccharides (LPSs) administered five days prior to the joint injury did not elicit any significant changes in the bone phenotype when compared to the AB-treated uninjured bones. However, as previously reported [ 10 ], LPS administration alone was sufficient to modulate the cartilage phenotype on both the contralateral and injured joints towards a more severe phenotype ( Figure 3 E,F). LPS injured joints showed an enhanced thinning of the femoral cartilage that was distinguishable from the cartilage of the VEH and AB injured groups ( Figure 3 b,d,f).…”

“…In the joint, however, a change in the M1/M2 ratio may be critical in PTOA progression and development. Histological examination of the injured joints indicated a hyperplastic synovium that appeared to have significant cellular infiltration on LPS- and AB-treated injured joints ( Figure 3 dd,ff; asterisk), and this morphology was similar to that of LPS-treated injured joints previously described [ 10 ]. To determine whether AB treatment prior to ACL rupture altered the composition of M1 and M2 cells in the injured joint, we used M1/M2 specific antibody markers to distinguish these subtypes by immunohistochemistry ( Figure 4 ).…”

“…Published literature suggests that the gut microbiome has an indirect effect on bone through changes to the immune system and inflammatory cytokines [ 8 , 9 ]. Commensals aid in immune-regulation by releasing microbial associated molecular patterns (MAMPs) such as lipopolysaccharides (LPSs) that bind and activate toll-like receptors ( Tlr ); LPSs have been shown to bind to Tlr4 [ 9 , 10 , 11 , 12 , 13 , 14 ]. This activation causes an inflammatory cascade that releases inflammatory cytokines and interferons which act as transcription factors to induce naïve immune cells to mature [ 15 , 16 , 17 ].…”

“…Furthermore, we have previously shown that elevated levels of LPSs negatively impact bone by promoting bone loss and accelerate post-traumatic osteoarthritis (PTOA) development. We also showed that LPS administration prior to injury elevates Tlr5/7/8 transcription in the joint [ 10 , 21 ]. TNF-α promotes osteoclastogenesis by increasing RANK-L expression in bone marrow cells and therefore elevating the number of osteoclast precursor cells [ 20 , 22 , 23 , 24 ].…”

Impact of endotoxins in gelatine hydrogels on chondrogenic differentiation and inflammatory cytokine secretionin vitro

“…Like other pathogen-associated molecular patterns (PAMPs), endotoxins may affect cell metabolism 14,15 and are able to trigger the immune system to initiate a pro-inflammatory cascade 16 , which may affect several cellular functions. For example, endotoxins are suggested to play a role in the pathogenesis of OA 17,18 , and in vitro cultured chondrocytes were shown to produce less collagen type II and more matrix metalloproteinase (MMP)-3 in response to lipopolysaccharides (LPS) in a dose-dependent fashion 19 .…”