Phagocytic lining cells determine local expression of inflammation in type II collagen–induced arthritis

P Van Lent, AEM Holthuysen… - … : Official Journal of …, 1996 - Wiley Online Library
P Van Lent, AEM Holthuysen, LAM Van Den Bersselaar, N Van Rooijen, LAB Joosten
Arthritis & Rheumatism: Official Journal of the American College …, 1996Wiley Online Library
Objective. To investigate the in vivo role of phagocytic synovial lining cells in the local
expression of inflammation in type II collagen–induced arthritis (CIA) in DBA/1J mice.
Methods. On various days before arthritis induction (day 7, 5, or 2), phagocytic lining cells
were selectively depleted from the synovial layer by injecting multilamellar liposomes
containing clodronate (dichloromethylene diphosphonate) directly into the knee joints. As
controls, either PBS or PBS‐laden liposomes were injected. CIA was induced by immunizing …
Abstract
Objective. To investigate the in vivo role of phagocytic synovial lining cells in the local expression of inflammation in type II collagen–induced arthritis (CIA) in DBA/1J mice.
Methods. On various days before arthritis induction (day 7, 5, or 2), phagocytic lining cells were selectively depleted from the synovial layer by injecting multilamellar liposomes containing clodronate (dichloromethylene diphosphonate) directly into the knee joints. As controls, either PBS or PBS‐laden liposomes were injected. CIA was induced by immunizing mice with heterologous bovine type II collagen in Freund's complete adjuvant. Arthritis onset was synchronized by a single intraperitoneal injection of lipopolysaccharide; arthritis was evaluated in hematoxylin and eosin–stained knee joint sections. Chemotactic activity in synovial washout samples was detected in a Transwell chemotactic assay. Interleukin‐1 (IL‐1) and tumor necrosis factor α (TNFα) protein levels were measured in NOB‐1 and L929 bioassays, respectively. IL‐1 messenger RNA (mRNA) in synovial specimens was measured by reverse transcriptase–polymerase chain reaction. IL‐1 was also detected immunohistologically in knee joint sections.
Results. In clodronate‐laden liposome–treated, lining‐depleted knee joints, there was significantly decreased inflammation compared with controls. Cell influx into the synovium was markedly decreased. Expression of IL‐1 mRNA in the synovium was significantly reduced. IL‐1 was detected only in some cells in the deeper synovial layer, in contrast to controls, in which large numbers of cells in the deeper synovial layer were stained. In synovial washouts from lining‐depleted knee joints, biologically active IL‐1 levels were reduced by 40% at 6 hours after arthritis induction. Most strikingly, chemotactic activity was highly decreased in these synovial washout samples. When IL‐1 or TNFα was injected into the knee joints of immunized mice in which arthritis was not yet expressed, arthritis was not induced in the lining‐depleted joints, whereas marked cell influx was found in control joints.
Conclusion. Our data indicate that phagocytic lining cells play a crucial role in the local expression of inflammation in systemically induced CIA. Phagocytic lining cells probably form an important source of chemotactic factors which are set free upon activation by IL‐1 or TNFα.
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