A new method to create synthetic neurons allows researchers to investigate how the human brain makes metabolic building blocks essential for the survival of all living organisms. A second study describes a core enzyme involved in the synthesis of these building blocks, called purines, and how the enzyme might change during infection by herpes simplex virus.
A team led by researchers from Penn State optimized a new method to create the neuron-like cells.
“These newly developed neuron-like cells allowed us to investigate purine formation in a specialized cell type for the first time. We were interested in neurons because they require a lot of energy and therefore need to produce purines efficiently. We were also curious how the synthesis process might be affected by infection with herpes simplex virus, an energetically demanding virus that takes up residence in neurons,”
said Moriah Szpara, assistant professor of biochemistry and molecular biology at Penn State and senior author of both papers.
FGAMS
When demand for purines is high in a cell, a complex composed of many enzymes called the purinosome forms to enable faster production of these important chemicals. The researchers investigated an enzyme called phosphoribosyl formylglycinamidine synthase (FGAMS), a core component of the purinosome.
To better understand the role of FGAMS in purine production, they looked at where and how much of the enzyme is expressed in rodent brain slices, rodent neurons, human non-neuronal cells, and the human neuron-like cells cultivated with the new technique.
“Studying human neurons has been challenging because we haven’t had a good laboratory model to study them. We can use neurons from rodents or chick embryos, but they don’t give us the same information as human cells. Most studies require large numbers of cells, so we developed a method to take a commonly available cell line and shape it into cells that look and act like neurons. This new method will allow us to start asking the backlog of questions we have about neurons, like how purines are synthesized in the brain,”
said Colleen Mangold, a postdoctoral researcher at Penn State and an author of both studies.
In the neuron-like cells and in rodent neurons and brain slices, FGAMS was expressed in a number of locations throughout the neuron, including near mitochondria and microtubules. Because FGAMS is also found near these structures in non-neuronal cells, the researchers suspect that purinosome formation may be conserved across different cell types.
Herpes Simplex Virus 1
The researchers also investigated the effect of infection with herpes simplex virus 1 (HSV1) on the purine biosynthesis protein FGAMS both in neurons and in non-neuronal cells. HSV1 initially infects an individual at the skin surface and proceeds to set up a lifelong infection in neurons that cannot be cleared by the immune system.
Because purines may play a role in the replication of HSV1, the high metabolic load of the virus might deplete purine resources and affect purine synthesis.
“Infection with HSV1 induced clustering of FGAMS in the non-neuronal cells, which model the skin phase of infection, while FGAMS appeared to be constantly clustered and activated in neuronal cells. We suspect that the purinosome is assembled only on an as-needed basis in non-neuronal cells, but that high energetic demands in neurons may necessitate the purinosome being present all of the time,”
said Stephen Benkovic, Evan Pugh Professor of Chemistry and Holder of the Eberly Family Chair in Chemistry at Penn State and an author of the purine formation paper.
“Viruses like HSV1 survive by establishing a lifelong infection in neurons,” said Szpara, “and there is growing evidence suggesting links between chronic viral infections and late-life neurocognitive diseases. We are continuing to investigate the potential connections between the burdens of viral infection and the high metabolic demands of neurons to see if there are avenues to prevent damage and improve long-term neuronal health.
Because the results from the neuron-like cells mirror those in the rodent brain slices and neurons, this study highlights the utility of these cells as a new model system for studying neurons and how viruses affect them.
References:
Mangold, C. A., Yao, P. J., Du, M., Freeman, W. M., Benkovic, S. J. and Szpara, M. L. Expression of the purine biosynthetic enzyme phosphoribosyl formylglycinamidine synthase (FGAMS) in neurons. J. Neurochem. doi:10.1111/jnc.14304
Mackenzie M. Shipley, Colleen A. Mangold, Chad V. Kuny and Moriah L. Szpara. Differentiated Human SH-SY5Y Cells Provide a Reductionist Model of Herpes Simplex Virus 1 Neurotropism. J. Virol. December 2017 vol. 91 no. 23 e00958-17
Last Updated on April 25, 2023