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Abstract Number: 2134

Extracellular Adenosine Increases IL-6 Production by Aging Tenocytes and May Contribute to the Age-related Pattern of Polymyalgia Rheumatica

Charmi Shah1, Thomas Garvey 2, Claudia Gohr 1, Elizabeth Mitton-fitzgerald 3 and Ann Rosenthal 3, 1Medical College of Wisconsin, Milwaukee, WI, 2Mayo Clinic, Rochester, MN, 3Medical College of Wisconsin, Milwaukee

Meeting: 2019 ACR/ARP Annual Meeting

Keywords: interleukin 6 and adenosine, polymyalgia rheumatica, tendons

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Session Information

Date: Tuesday, November 12, 2019

Session Title: Miscellanous Rheumatic & Inflammatory Disease Poster III: Autoimmune Conditions and Therapies

Session Type: Poster Session (Tuesday)

Session Time: 9:00AM-11:00AM

Background/Purpose: Polymyalgia rheumatica (PMR) is a common disease preferentially affecting elderly patients.  Characteristically, PMR involves large tendons and muscles around the hips and shoulders. While corticosteroids remain the mainstay of PMR therapy, IL-6 inhibitors have been shown to be effective alternatives to corticosteroids in PMR.  Recent work suggests that IL-6 levels in hip and shoulder regions of PMR patients are higher than circulating levels, thus suggesting local IL-6 production.   The factors stimulating IL-6 release in tendon and muscles of PMR patients are not well defined. An explanation of the strong association of PMR with age also remains unclear.   Adenosine levels are higher with age in some tissues. In myocardial tissue, for example, dysfunction of cellular adenosine transporters leads to accumulation of adenosine in the extracellular space.  While adenosine is often considered to be anti-inflammatory, extracellular adenosine increases IL-6 production in some connective tissue cells.  We sought to determine if elevated levels of adenosine promote IL-6 production in tenocytes, whether this is age-dependent, and whether levels of the adenosine transporter, equilibrative nucleoside transporter 1 (ENT1), vary with age.

Methods: Primary tenocytes were obtained from the patellar tendons of old (3-5 year old) and young (6 month old) pigs using digestion with collagenase.  Cells were plated at 4.5×105 cells/cm2 in DMEM with 10 % fetal calf serum and used within 5 days of culture.  After two days in culture, tenocytes were exposed to fresh DMEM with 0.35 % BSA with no additives (control) or 50 to 200 µM adenosine.  IL-6 levels were measured in the conditioned media with both Western blotting using IL-17 as a positive control and an IL-6 ELISA (R&D Systems) with dose and time response.  ENT1 levels were measured in the cell layer of young and old tenocytes using Western blotting and GAPDH as a loading control.

Results: In old tenocytes, 100 µM of adenosine and 10 ng/mL IL-17 increased media IL-6 levels by Western blot. The IL-6 ELISA showed no measurable amounts of IL-6 in the control of either young or old tenocytes. In old tenocytes, IL-6 levels rose to 666.3 +/- 194.3 pg/ml with 200 µM adenosine at 72 hours (p< 0.002) (Figure 1).    In young tenocytes, there was no measurable IL-6 with any amount or time of adenosine exposure. (Data not shown.)  Similar levels of ENT1 were present in both old and young tenocytes (Figure 2).

Conclusion: As tenocytes age, they may become increasingly responsive to adenosine leading to IL-6 production and an inflammatory response.  While levels of ENT1 protein are similar in old and young tenocytes, additional work will be necessary to determine whether there are differences in adenosine metabolism in old and young tendon.  Further studies of the pro-inflammatory effects of adenosine in older tissues may ultimately result in a better understanding of the pathways underlying the strong association of PMR with advanced age.

Figure 1. Effect of adenosine on tenocyte IL-6 levels. Old tenocytes were incubated with no additives -Control- or 50,100 or 200 uM adenosine. IL-6 levels were measured by ELISA in the media after 24-72 hours. IL-6 levels were not measurable at any time point in the controls. IL-6 levels were significantly increased at 24 hours by 200 uM adenosine -n=6, *= p<0.01- and at 48 and 72 hours by all concentrations of adenosine -n=6, **=p<.001, ***=p=.0002-. IL-6 levels were not measurable in young tenocytes at any time point or with any concentration of adenosine -Data not shown.-

Figure 2. Levels of ENT1 in old and young chondrocytes. Two cultures of old and three cultures of young tenocytes were lysed with RIPA buffer, and similar quantities of protein were run on a 4-12 % Bis-Tris gel. Proteins were transferred to a nitrocellulose membrane and probed with ENT1 antibody. The loading control was GAPDH. There were no differences in the density of the ENT1 bands between old and young tenocytes. Lanes 1 and 2 are old tenocytes, Lanes 3,4 and 5 are young tenocytes.


Disclosure: C. Shah, None; T. Garvey, None; C. Gohr, None; E. Mitton-fitzgerald, None; A. Rosenthal, None.

To cite this abstract in AMA style:

Shah C, Garvey T, Gohr C, Mitton-fitzgerald E, Rosenthal A. Extracellular Adenosine Increases IL-6 Production by Aging Tenocytes and May Contribute to the Age-related Pattern of Polymyalgia Rheumatica [abstract]. Arthritis Rheumatol. 2019; 71 (suppl 10). https://acrabstracts.org/abstract/extracellular-adenosine-increases-il-6-production-by-aging-tenocytes-and-may-contribute-to-the-age-related-pattern-of-polymyalgia-rheumatica/. Accessed January 26, 2021.
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