Reciprocal induction of tumor necrosis factor‐α and interleukin‐β activity mediates fibronectin synthesis in coronary artery smooth muscle cells

Journal of Cellular Physiology - Tập 163 Số 1 - Trang 19-29 - 1995
Silvana Molossi1,2, Nadine Clausell1,2, Marlene Rabinovitch1,2
1Departments of Pediatrics, Pathology and Medicine, University of Toronto, Toronto, Ontario, Canada
2Division of Cardiovascular Research, Research Institute, The Hospital For Sick Children, Toronto, Ontario, Canada, M5G 1X8

Tóm tắt

AbstractWe previously demonstrated an immune‐inflammatory response associated with increased expression of interleukin (IL)‐β and fibronectin in graft coronary arteriopathy in piglets following heterotopic heart transplant. Further studies showed that increased endogenously produced IL‐β was upregulating fibronectin production by donor coronary artery (CA) smooth muscle cells (SMC). Since co‐induction of IL‐β and tumor necrosis factor (TNF)‐α has been shown in other systems, we investigated the possible interaction between these cytokines in regulating fibronectin production in CA SMC. First, we documented increased TNF‐α expression in vivo in donor compared to host CA. Next, synthesis of fibronectin was measured in host and donor CA SMC following [35S]‐methionine radiolabeling and gelatin‐sepharose extraction. As previously shown with IL‐β, increased donor CA SMC fibronectin synthesis was reduced to host levels in the presence of TNF‐α antibodies, and exogenous TNF‐α upregulated fibronectin synthesis in host CA SMC to levels in donor cells. In normal CA SMC, TNF‐α‐stimulated fibronectin production was downregulated to or below control levels in the presence of IL‐β antibodies. Likewise, IL‐β‐stimulated fibronectin synthesis was downregulated to control levels when TNF‐α neutralizing antibodies were added. Combining TNF‐α and IL‐β enhanced fibronectin production over that observed with either cytokine alone, but was not additive. Thus, our studies suggest that vascular SMC fibronectin synthesis is regulated by reciprocal induction of IL‐β and TNF‐α activity and provide the first demonstration of a ‘cytokine loop’ modulating matrix production. © 1995 Wiley‐Liss, Inc.

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