Hyaluronidase enhancement of TNF-mediated cell death is reversed by TGF-b1

Chang, Nan-Shan. Hyaluronidase enhancement of TNFmediated cell death is reversed by TGF-b1. Am. J. Physiol. 273 (Cell Physiol. 42): C1987–C1994, 1997.—Both hyaluronidase and transforming growth factor (TGF)-b1 play a significant role in the development of prostate cancer. In this study, the regulation of tumor necrosis factor (TNF)-mediated cell death by hyaluronidase and TGF-b1 was investigated. Preexposure of L929 fibroblasts, prostate LNCaP cells, and epithelial Mv 1 Lu cells to hyaluronidase for a minimum of 12 h resulted in significant enhancement of cell death by TNF. Phosphorylation of p42 and p44 mitogen-activated protein (MAP) kinases was found by stimulation of L929 cells with hyaluronidase for 30 min, indicating that the Raf/MAP kinase-extracellular signal-regulating protein kinase (MEK)/ MAP kinase pathway was activated. However, blocking the activation of upstream MAP kinase kinase (MEK 1 and 2 kinase) by PD-98059 failed to inhibit the hyaluronidaseenhanced TNF killing of cells, suggesting that hyaluronidasemediated degradation of extracellular matrix and membrane components may elicit multiple signaling pathways. As a potent stimulator of extracellular matrix protein synthesis, TGF-b1 blocked the hyaluronidase-enhanced death of L929 and LNCaP cells mediated by TNF. TGF-b1 activated proteintyrosine kinases in L929 cells, in which the tyrosine kinase inhibitors lavendustin A and tyrphostin blocked the activation as well as the TGF-b1 inhibition of hyaluronidase effects. Functional antagonism was also observed between hyaluronidase and TGF-b1 in cell growth regulation. For example, TGF-b1-mediated suppression of epithelial Mv 1 Lu cell growth was abolished by hyaluronidase. Overall, it is demonstrated in this study that hyaluronidase reciprocally antagonized TGF-b1 in the modulation of cell proliferation and TNF-mediated death.