Why Do Some Neurons Degenerate and Die in Alzheimer’s Disease, but Not Others?

Summary: Study reveals the molecular clues as to why some neurons are susceptible to death in Alzheimer’s disease while others aren’t.

Source: Gladstone Institute

In the brain of a person with Alzheimer’s disease, neurons degenerate and die, slowly eliminating memories and cognitive skills. However, not all neurons are impacted equally. Some types of neurons in certain brain regions are more susceptible, and even among those subtypes–mysteriously–some perish and some do not.

Researchers at Gladstone Institutes have uncovered molecular clues that help explain what makes some neurons more susceptible than others in Alzheimer’s disease.

In a study published in the journal Nature Neuroscience, the scientists present evidence that neurons with high levels of the protein apolipoprotein E (apoE) are more sensitive to degeneration, and that this susceptibility is linked to apoE’s regulation of immune-response molecules within neurons.

“This is the first time such a link has been established, which is quite exciting and could open new paths to developing treatments for Alzheimer’s disease,” says Gladstone Senior Investigator Yadong Huang, MD, PhD, senior author of the study.

Finding Clues by Comparing Individual Neurons

ApoE has long been a focus of Alzheimer’s disease research because people carrying a gene that produces a particular form of apoE (called apoE4) have a higher risk of developing the disease.

For this study, Huang and his team harnessed recent advancements in single-cell analysis to study the potential role of apoE in the variable susceptibility of neurons in Alzheimer’s disease.

Specifically, they applied a technique known as single-nucleus RNA sequencing, which reveals the extent to which the different genes in any given cell are expressed and converted into RNA, the intermediate between genes and proteins. This approach allowed them to compare individual cells within a cell type, as well as across different cell types.

The researchers used this technique to study brain tissue from both healthy mice and mouse models of Alzheimer’s disease. They also analyzed publicly available data for human brain tissue–some from healthy brains and some with varying degrees of Alzheimer’s disease or mild cognitive impairment.

In both mice and humans, the analysis showed that neurons varied greatly in their extent of apoE expression, even within the same subtype. In addition, the amount of apoE expression was strongly linked to the expression of immune-response genes, which also varied significantly among neurons.

Digging deeper, the researchers examined the connection between apoE and the immune response genes. They found that, in both mouse and human neurons, high levels of apoE turned on genes in the major histocompatibility complex class-I (MHC-I). MHC-I is part of a pathway involved in eliminating excess synapses (connections between neurons) during brain development, and may also alert the immune system to damaged neurons and synapses in the adult brain.

“This was an intriguing clue that by controlling the expression of MHC-I in neurons, apoE might help determine which neuron should be recognized and cleared by the immune system,” says Kelly Zalocusky, PhD, first author of the study and a scientist in Huang’s lab at Gladstone.

A Process Gone Awry Leads to the Progressive Destruction of Neurons

The team found that, in brain tissue, the proportion of neurons expressing high levels of apoE and MHC-I genes fluctuates in a way that closely matches neurodegeneration and the progression of Alzheimer’s disease.

They observed this relationship both in mouse models of Alzheimer’s disease and in human brain tissue at different stages of neurodegeneration. Their work also revealed a causal link between the expression of MHC-I induced by apoE and the increase in tangled aggregates of a protein called tau, which is a hallmark of Alzheimer’s disease and is a good predictor of neurodegeneration.

So, taken together, what do all these findings mean?

“We think that, normally, apoE turns on the expression of MHC-I in a small number of damaged neurons to produce ‘eat me’ signals that mark the neurons for destruction by the immune cells,” says Huang, who is also director of the Center for Translational Advancement at Gladstone, as well as professor of neurology and pathology at UC San Francisco.

“You don’t want to keep damaged neurons around because they could malfunction and cause problems.”

This shows a brain and a hand
The researchers used this technique to study brain tissue from both healthy mice and mouse models of Alzheimer’s disease. Image is in the public domain

But in Alzheimer’s disease, the scientists think this normal process for clearing out damaged neurons may become overactivated in a larger number of cells, leading to the progressive loss of neurons.

In other words, aging brains may face stressors that boost the amount of apoE in some neurons past healthy levels. The study shows that neurons carrying the form of apoE associated with increased risk of Alzheimer’s disease, apoE4, are particularly susceptible to these stressors. This excess apoE turns on the expression of MHC-I, marking these neurons for destruction.

Meanwhile, neurons with lower levels of apoE remain unharmed. Consequently, this process results in selective neurodegeneration within a given neuron type in Alzheimer’s disease, guided by the level of apoE.

Further research could help clarify how apoE and MHC-1 determine which neurons die and which survive in Alzheimer’s disease.

“Additional studies could reveal potential new targets for treatments that may be able to disrupt this destructive process in Alzheimer’s disease and potentially in other neurodegenerative disorders as well,” says Huang.

Other authors on the study include: Ramsey Najm, Alice L. Taubes, Yanxia Hao, Nicole Koutsodendris, Maxine R. Nelson, Antara Rao, and Jason Bant from Gladstone and UC San Francisco (UCSF); Seo Yeon Yoon, Dah-eun J. Amornkul, Qin Xu, Alice An, and Olga Cisne-Thomson from Gladstone; and David A. Bennett from Rush University Medical Center.

Funding: This study was funded in part by the National Institutes of Health (R01AG048017, RF1AG055421, and R01AG055682).

About this Alzheimer’s disease research news

Source: Gladstone Institutes
Contact: Julie Langelier – Gladstone Institutes
Image: The image is in the public domain

Original Research: Closed access.
Neuronal ApoE upregulates MHC-I expression to drive selective neurodegeneration in Alzheimer’s disease” by Kelly A. Zalocusky, Ramsey Najm, Alice L. Taubes, Yanxia Hao, Seo Yeon Yoon, Nicole Koutsodendris, Maxine R. Nelson, Antara Rao, David A. Bennett, Jason Bant, Dah-eun J. Amornkul, Qin Xu, Alice An, Olga Cisne-Thomson & Yadong Huang. Nature Neuroscience


Neuronal ApoE upregulates MHC-I expression to drive selective neurodegeneration in Alzheimer’s disease

Selective neurodegeneration is a critical causal factor in Alzheimer’s disease (AD); however, the mechanisms that lead some neurons to perish, whereas others remain resilient, are unknown.

We sought potential drivers of this selective vulnerability using single-nucleus RNA sequencing and discovered that ApoE expression level is a substantial driver of neuronal variability. Strikingly, neuronal expression of ApoE—which has a robust genetic linkage to AD—correlated strongly, on a cell-by-cell basis, with immune response pathways in neurons in the brains of wild-type mice, human ApoE knock-in mice and humans with or without AD.

Elimination or over-expression of neuronal ApoE revealed a causal relationship among ApoE expression, neuronal MHC-I expression, tau pathology and neurodegeneration. Functional reduction of MHC-I ameliorated tau pathology in ApoE4-expressing primary neurons and in mouse hippocampi expressing pathological tau.

These findings suggest a mechanism linking neuronal ApoE expression to MHC-I expression and, subsequently, to tau pathology and selective neurodegeneration.

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