Transmembrane tumor necrosis factor (TNF)-alpha inhibits adipocyte differentiation by selectively activating TNF receptor 1

Tumor necrosis factor alpha (TNF alpha) is a potent cytokine with multiple biological activities and exists in two forms as follows: a 17-kDa soluble form that is a cleaved product of the 26-kDa transmembrane form (mTNF alpha ), It has been suggested that the transmembrane form of TNF alpha is mainly responsible for localized responses via cell-cell contact. Here, we have e xamined the activities of transmembrane TNF alpha in cultured adipocytes, A non-cleavable transmembrane form of TNF alpha (mTNF alpha 1-9K11E) was exp ressed in several preadipocyte cell lines using retroviral gene transfer, I n wild type preadipocytes carrying both TNF receptors, expression of mTNF D elta 1-9K11E resulted in inhibition of the differentiation program. The ext ent of this varied depending on the nature and strength of the adipogenic s timuli. The TNF receptor responsible for this function was determined by ex pressing mTNF Delta 1-9K11E in preadipocyte cell lines lacking either TNF r eceptor 1 (TNFR1), 2 (TNFR2), or both. In order to confirm the results in t he same cellular background, TNF receptors were also reconstituted in the c ell lines lacking corresponding receptors, These experiments demonstrated t hat TNFR1 was necessary and sufficient for mediating mTNF Delta 1-9K11E-ind uced inhibition of adipogenesis and that this action was similar to that of soluble TNF alpha. In conclusion, our results indicate that mTNF Delta 1-9 K11E is biologically active in cultured adipocytes and can alter the adipog enic program of these cells by selectively activating TNFR1. This may have physiological implications where local TNF alpha actions are thought to be generated at sites such as adipose tissue.