Cellular death is vital for health. Without it, we could develop autoimmune diseases or cancers. But a cell’s decision to self-destruct is tightly regulated, so that it only happens to serve the best interests of the body. Now researchers have discovered a novel role for a signaling molecule that was once considered a dispensable player, a discovery that could inform fields of research as diverse as cancer, autoimmunity, and in-utero development. The research was published in Nature Communications, February, 2019.
Years ago, researchers in the field discovered receptors on the surfaces of cells they called “death receptors.” These molecules would send the cell into a cascade of cellular reactions that ended in death. Soon after, three molecules were discovered that contained “death domains,” areas on the molecule that directly interacted with the death receptors and helped relay the message. These molecules proved so essential that without them mice lacking these death-domain molecules died young. At least that was the case in two of the three molecules.
Of the three major death-relaying molecules, RIPK1, FADD, and TRADD, it seemed TRADD was less essential. Without FADD, mice died in utero. Without RIPK1, mice die shortly before or after birth. Without TRADD, mice seemed to do just fine. TRADD had a death domain – it clearly was connected to cell-death pathways – but its main purpose was unclear.
Senior author, Jianke Zhang, PhD, a Professor of Microbiology and Immunology at Jefferson (Philadelphia University + Thomas Jefferson University) has been studying cell-death pathways for decades. Through the work of Dr. Zhang and others, it became clear that the roles of these molecules wasn’t simply to turn on the death signal. Rather, in certain combinations they could protect a cell from death, rather than spur suicide.
Through the work of first author and postdoctoral fellow John Dowling, their most recent paper, the researchers showed that TRADD serves a dual function. In cells lacking the RIPK1 protein, having two copies of the gene TRADD or no copies of it would result in cell death. On the other hand, when only one copy of TRADD gene was present in cells lacking RIPK1, the cells tended to turn off the death signal, and promote cell survival.
“The work sheds new light on the regulation of cell death and survival,” said Dr. Zhang. “In certain contexts, such as in cells that have naturally low RIPK1 expression, TRADD could drive death or promote survival.”
This article has been republished from materials provided by Thomas Jefferson University. Note: material may have been edited for length and content. For further information, please contact the cited source.
Dowling, J. P., Alsabbagh, M., Casale, C. D., Liu, Z., & Zhang, J. (2019). TRADD regulates perinatal development and adulthood survival in mice lacking RIPK1 and RIPK3. Nature Communications, 10(1). doi:10.1038/s41467-019-08584-5