METALLOTHIONEIN INDUCTION IN CULTURED RAT HEPATOCYTES BY ARTHRITIC RAT SERUM, ACTIVATED MACROPHAGES, INTERLEUKIN-6, INTERLEUKIN-11 AND LEUKEMIA INHIBITORY FACTOR

Potential mediators of hepatic metallothionein (MT) synthesis in adjuv ant-induced arthritis were investigated in cultured rat hepatocytes. S era from arthritic rats (14 d post-adjuvant treatment) in the presence of Zn (50 mu mol/L) + dexamethasone (Dex; 1 mu mol/L) increased metal lothionein (MT) accumulation by 34% above that obtained with control r at serum with Zn + Dex. Endogenous IL-6 activity in serum from arthrit ic rats was 93 +/- 49 U/mL and was undetectable in control rat serum. The activities of TNF, IL-1 and corticosterone concentrations were the same in control and arthritic rats. The accumulation of MT in hepatoc ytes in the presence of Zn (10 mu mol/L) + Dex (1 mu mol/L) was enhanc ed 29% and 49% by media from lipopolysaccharide (LPS)-stimulated perit oneal macrophage (PMM) and Kupffer cell cultures (KCM), respectively. The response with PMM and KCM was quantitatively the same as that with interleukin-6 (IL-6). Analysis of PMM and KCM showed activities of 1, 000-10,000 U/mL for IL-6, 100-1000 U/mL for TNF and <10,000 U/mL for I L-1, the latter detected only in PMM. LPS alone enhanced the accumulat ion of MT above Zn + Dex ill a dose dependent manner. A significant LP S response was obtained at 5 mg/L with a maximal stimulation above Zn + Dex of 38% at 10 mg/L. This direct stimulation of MT by LPS was not part of the response observed with PMM and KCM where the final LPS con centration in culture was only 0.1 mg/L. Other cytokines capable of sy nergy with Zn + Dex on MT synthesis were investigated. Interleukin-ll (IL-11) increased the Zn + Dex induction in a dose dependent manner wi th maximal stimulation at 100 U/mL of 40%. A small stimulation of 12% above Zn + Dex was obtained with leukaemia inhibitory factor (LIF) at concentrations greater than 100 U/mL. No enhancement of the Zn + Dex r esponse was obtained with interleukin-3 (1000 U/mL), interleukin-4 (10 mu g/L), platelet activating factor (5 nmol/L) or granulocyte-colony stimulating factor (5 mu g/L). Neither IL-11 nor LIF enhanced the resp onse obtained with Zn + Dex + IL-6. The results demonstrate that media tors present in arthritic rat serum and in LPS-stimulated PMM and KCM cause a quantitatively similar response on MT accumulation as IL-6. IL -11 and to a lesser extent LIF, are also potential mediators of MT syn thesis in inflammation.