Regulation of tumour necrosis factor-alpha release from human adipose tissue in vitro

Abstract

Tumour necrosis factor-alpha (TNF-α), secreted by cells of the macrophage-monocyte lineage, has a well established role in inflammation and host-defence. The more recent discovery that adipocytes also secrete TNF-α has led to a substantial body of research implicating this molecule in the insulin resistance of obesity. However, little is known about the normal regulation of TNF-α release from human adipose tissue. In particular, it is not known whether adipocyte production of TNF-α is responsive to similar or different molecular regulators than those relevant to macrophages. TNF-α release from cultured human adipose tissue and isolated adipocytes was examined using an ELISA. Insulin, cortisol or the thiazolidinedione, BRL 49653, did not have a significant effect on TNF-α release from adipose tissue or isolated adipocytes. In contrast, lipopolysaccaride (LPS), a major stimulus of TNF-α protein production in monocytes and macrophages, resulted in a fivefold stimulation of TNF-α release from human adipose tissue. Significant stimulation of TNF-α release was also seen from isolated adipocytes, indicating that the increase in TNF-α release from adipose tissue in the presence of LPS is unlikely to be entirely attributable to contaminating monocytes or macrophages. Consistent with this observation was the finding that mRNA for CD14, a known cellular receptor for LPS, is expressed in human adipocytes. The increase in TNF-α protein release in response to LPS was blocked by an inhibitor of the matrix metalloproteinase responsible for the cleavage of the membrane-bound proform of TNF-α, indicating that this release represented regulated secretion and was not due to cell lysis. In conclusion, the regulation of TNF-α protein release from human adipose tissue and isolated adipocytes appears to be similar to its regulation in cell types more traditionally implicated in host defence. The production by the adipocyte of a range of molecules involved in host defence - TNF-α, factors D, B and C3, interleukin-6, and macrophage colony-stimulating factor - suggest that this cell type may make a significant contribution to innate immunity.