OP0096 DYSREGULATED BONE MARROW STROMAL CELLS IN MODIC TYPE 1 CHANGES. (June 2019)

• Record Type: Journal Article
• Authors: Dudli, Stefan; Haenni, Dominik; Juengel, Astrid; Betz, Michael; Spirig, Jose; Brunner, Florian; Farshad, Mazda; Distler, Oliver
• Is Part Of: Annals of the rheumatic diseases. Volume 78(2019)Supplement 2
• Page Start: 121
• Page End: 121
• Publication Date: 2019-06
• Subjects: Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/annrheumdis-2019-eular.1051
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Background: Modic type 1 changes (MC1) are fibrotic-inflammatory vertebral bone marrow lesions adjacent to degenerating discs. Patient with MC1 often develop low back pain [1]. In MC1, extra-cellular collagen is deposited, myelopoiesis is dysregulated, and bone is rapidly remodeled. These are signs of a chronic inflammation. The cellular mechanisms are unknown, yet bone marrow stromal cells (BMSC) are key regulators of myelopoiesis, can differentiate into collagen-producing cells, and modulate inflammation [2]. Objectives: To link BMSC phenotype and function to molecular changes in MC1. Methods: From patients undergoing lumbar spondylodesis, bone marrow aspirates (n=5 MC1+5 controls, adjacent level healthy bone marrow (Ctrl)) or biopsies (n=2 MC1+2 Ctrl) were taken through pedicle screw trajectory before screw insertion. Biopsies were fixed, dehydrated, and imaged with multiphoton fluorescence microscopy (MPE). Tissue auto-fluorescence and second-harmonics-generation (SHG) of collagen were recorded of full-length biopsies with up to 200 µm penetration depth and qualitatively evaluated. Fluorescence-life-time-imaging-microscopy (FLIM) of the auto-fluorescence signal was performed in key areas of biopsies and single-photon-counting histograms were fitted with a triple-exponential decay function. BMSC were isolated from aspirates by plastic adherence and characterized (passage 2): Sequencing of ribosomal depleted RNA (Illumina Novaseq) with pathway analysis was performed, differentiation capacity was quantified histologically (Wilcoxon test), duplication rate was measured with CellTrace TM (t-test), and stem cell surface marker expression was quantified by flow cytometry (CD14, CD16, CD19, CD34, CD45, CD73, CD90, CD105, CD284 (t-test). Results: Biopsies: Collagen was qualitatively more abundant in MC1 than in Ctrl bone marrow, particularly in areas of adipocyte clusters and around adipocytes (Figure 1, arrows). FLIM was able to distinguish adipocytes (τ=2.1-2.7ns), leukocytes (τ=0.4-0.8ns), erythrocytes (τ=0.2-0.4ns), and collagen (τ<0.15ns) based on their different auto-fluorescent life-times (Figure 1, right). BMSCs: By RNA sequencing 154 genes were differentially expressed between MC1 and Ctrl BMSCs (p≤0.01; log2 ratio≥0.5). Pathway analysis revealed significant alterations in processes important for 'cell adhesion' (p<9.3e-13) and 'extracellular matrix organization' (p<1.8e-7). Aggrecan (fold change=0.25, p<1e-7) and osteopontin (fold change=5.26, p<1e-5) were the first and third top-most differentially regulated genes, indicating a shift away from chondrogenic polarization towards osteogenic polarization. A shift in BMSC polarization was corroborated with differentiation assays: MC1 vs. Ctrl BMSCs had a reduced adipogenic (mean±sd: -33±13%, p=0.03) and chondrogenic (-31±25%, p=0.18) differentiation capacity (Figure 2). In addition, an increased duplication rate of MC1 vs. Ctrl BMSCs (29.3±1.7 vs. 26.2±1.0 hours, p=0.07) was observed, also indicate a change in phenotype. There were no changes in the expression of surface markers. Conclusion: These data suggest that MPE-FLIM is a prime technology to investigate fibrotic pathologies and it allows to morphologically study the importance of BMSCs in MC1. The BMSC/adipocyte axis seem to play a pivotal role in the fibrotic pathomechanism. Adipocytes have not been regarded as pathomechanistically relevant yet and hence open novel targets for therapeutic approaches. Reference: [1] Dudli, et al. Eur Spine J. 2017;26(5):1362-1373. [2] García-García A, et al. Immunol Lett. 2015;168(2):129-135. Disclosure of Interests: Stefan Dudli: None declared, Dominik Haenni: None declared, Astrid Juengel: None declared, Michael Betz: None declared, Jose Spirig: None declared, Florian Brunner: None declared, Mazda Farshad: None declared, Oliver Distler Grant/research support from: Prof. Distler received research funding from Actelion, Bayer, Boehringer Ingelheim and Mitsubishi Tanabe to investigate potential treatments of scleroderma and its complications, Consultant for: Prof. Distler has/had consultancy relationship within the last 3 years with Actelion, AnaMar, Bayer, Boehringer Ingelheim, ChemomAb, espeRare foundation, Genentech/Roche, GSK, Inventiva, Italfarmaco, iQvia, Lilly, medac, MedImmune, Mitsubishi Tanabe Pharma, Pharmacyclics, Novartis, Pfizer, Sanofi, Serodapharm and UCB in the area of potential treatments of scleroderma and its complications. In addition, he had/has consultancy relationship within the last 3 years with A. Menarini, Amgen, Abbvie, GSK, Mepha, MSD, Pfizer and UCB in the field of arthritides and related disorders