Transforming growth factor-beta promotes 'death by neglect' in post-activated human T cells

Transforming growth factor-beta (TGF-beta) is central to the wound repair p rocesses that follow local trauma and inflammation. In order to mimic the e arly events of wound-healing, we studied the effects of TGF-beta on mitogen -stimulated peripheral blood cells. TGF-beta added at the initiation of mit ogenesis did not significantly alter T-cell activation, proliferation. CD45 isoform switching, or activation-induced cell death. By contrast, TGF-beta added 72 hr post activation (or later) enhanced the cumulative increase in apoptotic T cells. TGF-beta had no effect on mitogen-induced up-regulation of Fas (CD95) or Fas ligand and did not enhance killing of the Fas-sensiti ve Jurkat cell line by activated T cells. Furthermore, TGF-beta had no dire ct effect on levels of mRNA for members of the bcl family (bcl-X, bfl-1, bi k, bak, bax, bcl-2 and mol-1). These findings suggest that TGF-beta does no t directly induce apoptosis via the Fas system or by direct effects on bcl proteins. However, interleukin-2, which can 'rescue' lymphocytes from spont aneous apoptosis due to cytokine deprivation. abolished the pro-apoptotic e ffects of TGF-beta on post-activated T cells. thus demonstrating that TGF-b eta increases the cytokine-dependence of T cells for survival. We propose a novel role for TGF-beta in the suppression of inflammation by promoting th e elimination of post-activated T cells once the initiating stimulus has be en resolved.