Northwestern investigators have identified a novel transcription factor which regulates a signaling mechanism utilized by a fertilized embryo to protect its mother from cellular and environmental stress, according to a recent study to published in the journal Genes and Development.  

The findings have implications for promoting healthy aging by therapeutically targeting age-related protein dysregulation and misfolding, which can lead to the development of many neurodegenerative disorders.  

“Our work is really trying to understand in aging what are the earliest events that we can detect to restore proteostasis, because proteostasis controls the health of every protein. The proteostasis network that controls protein synthesis, folding and clearance is the only cellular pathway that we know of that can prevent or enhance the clearance of amyloid formation,” said Richard Morimoto, PhD, a professor in the Ken and Ruth Davee Department of Neurology and the Bill and Gayle Cook Professor of Biology in the Weinberg Colleges of Arts and Sciences, who was senior author of the study.  

The health of an organism relies on a functional proteome, or the entire set of proteins expressed in every cell of an organism. As an organism naturally ages, proteins exhibit a higher risk of misfolding and aggregating to form amyloid, which play a key role in the development of many neurodegenerative diseases in humans, including Alzheimer’s disease, Parkinson’s disease and cystic fibrosis.  

This “proteostasis collapse” is a phenomenon previously discovered by Morimoto and colleagues by studying C. elegans models of neurodegenerative diseases. C. elegans is a transparent roundworm whose biochemical makeup is similar to that of humans and is used by scientists to better understand human biology, including aging and disease development.  

In a recent study, Morimoto’s group found using C. elegans models of neurodegenerative diseases that a damaged fertilized embryo protects the mother from cellular stress by sending her molecular signals to promote her overall health so that she can produce future generations of healthy eggs.  

The results of a genetic screen performed in C. elegans revealed that when the vitelline layer – the outer shell of the egg – is damaged, the embryo signals to the mother to prevent  proteostasis collapse and to suppress protein aggregation.  

“It was stunning. It was, in a sense, a novel form of transgenerational signaling,” Morimoto said. “That was intriguing because this is about communicating from one tissue, the egg, to the mother.” 

In the current study, using advanced transcriptomics techniques, Morimoto’s team found that this signaling pathway is regulated by a transcription factor called NHR-49, which is known to support gene expression in all metazoans that use eggs, including humans, and regulates lipid metabolism. Lipid metabolism is the breakdown and storage of fatty acids for the cell to use as energy and also supports the conversion of lipids for constructing the cell membrane.  

The findings establish NHR-49 as a key regulator that connects lipid homeostasis and cellular resilience to proteotoxic stress. This signaling pathway could therefore serve as a biomarker and therapeutic target for regulating proteostasis and, ultimately, promoting healthy aging, according to Morimoto.  

“The major emphasis for the future is to now convert this into predictable models that for which we could then target that pathway or that set of genes,” Morimoto said.  

The current study is part of a larger effort led by Morimoto and supported by a recent $32.4 million award from the Hevolution Foundation to improve the understanding of how proteostasis regulates healthy aging and to prevent diseases of protein misfolding.  

“Our ability to identify the machinery and understand what is optimal allows us to then understand how to rejuvenate the cell, the tissue, and the organism against the threats of aging,” Morimoto said.  

Ambre Sala, PhD, a postdoctoral fellow in the Morimoto laboratory, was first author of the study. Co-authors include Rogan Grant, PhD, a Schmidt Science Fellow at Northwestern.  

This work was supported by National Institutes of Health grants RF1AG057296, P01AG054407 and T32AG020506, an ATIP-Avenir grant (Centre National de la Recherche Scientifique Biology), the Daniel F. and Ada L. Rice Foundation, and a postdoctoral fellowship from the American Federation for Aging Research.