Azithromycin alleviates the severity of rheumatoid arthritis via
targeting UPR component GRP78
Abstract
Background and Purpose: Azithromycin (AZM) is a macrolide antibiotic
with well-described anti-inflammatory properties. This study aimed to
substantiate its treatment potential in rheumatoid arthritis (RA).
Experimental Approach: Gene expression profiles were collected by
RNA-sequencing and the effects of AZM were assessed in functional
assays. In vitro and vivo assays for examining the blockade of
glucose-regulated protein 78 (GRP78) actions by AZM: assays for defining
the anti-inflammatory activity of AZM using fibroblast-like synoviocytes
(FLSs) from RA patients as well as collagen-induced arthritis (CIA) in
DBA/1 mice. Identification and characterization of the binding of AZM to
GRP78 using drug affability responsive target stability assay,
proteomics and cellular thermal shift assay. Detect AZM inhibition of
GRP78 and dependence of AZM’s anti-arthritis activity on GRP78. Key
Results: AZM reduced pro-inflammatory factor production, cell migration,
invasion and chemo-attractive potential, enhanced apoptosis, thereby
reducing the deleterious inflammatory response of RA FLSs in vitro. AZM
ameliorated the severity of CIA lesions. Transcriptional analyses
implied that AZM treatment causes impairments in signaling cascades
associated with cholesterol and lipid biosynthetic process. GRP78 was
isolated as a novel target of AZM. AZM-mediated activation of unfolded
protein response (UPR) via inhibiting GRP78 activity is required not
only for inducing the expression of C/EBP-homologous protein (CHOP), but
also for activation of sterol-regulatory element binding protein (SREBP)
and its targeted genes involved in cholesterol and lipid biosynthetic
process. Further, deletion of GRP78 abolished AZM’s anti-arthritis
activity. Conclusion and Implications: These findings confirmed that AZM
is an anti-arthritis therapeutic drug for RA treatment.