This shows the outline of a head and neurons.
Right now, though, it’s not clear how big a role the immune system plays in the Parkinson’s brain. Credit: Neuroscience News

Parkinson’s Puzzle: Is the Root in the Gut, Not the Brain?

Summary: For years, Parkinson’s has been labeled a brain disorder. However, intriguing research hints at its origins not in the brain, but the gut.

Researchers suggest a misdirected immune attack in the gut, triggered by a protein, could be the early precursor of the disease. This new perspective raises hopes for early detection, potentially halting Parkinson’s before it reaches the brain.

Key Facts:

  1. Parkinson’s disease, traditionally seen as a brain disorder, may originate in the gut, years before neurological symptoms manifest.
  2. Misfolded alpha-synuclein proteins can appear outside neurons, making them vulnerable to immune system attacks, which might start in the gut, evidenced by constipation symptoms in early Parkinson’s patients.
  3. Researchers believe that stopping the autoimmune response in the gut early on could prevent subsequent damage to brain neurons.

Source: Columbia University

Ask any neurologist: Parkinson’s disease is a brain disorder. The conspicuous symptoms of Parkinson’s disease—uncontrollable tremors, slowed down motions, and the feeling that one’s feet are stuck to the ground—all stem from the loss of neurons in a region of the brain that helps control movement.

But many researchers believe that the neurodegenerative disorder may get started far away from the brain—in the gut—and years before the first neurological signs appear.

New findings by Columbia researchers David Sulzer, PhD, and Dritan Agalliu, PhD, and two of their graduate students are adding to evidence backing this hypothesis—and showing that what triggers initial gastrointestinal changes in Parkinson’s could be a misdirected immune attack.

“If this is the beginning of Parkinson’s in many people, we could potentially identify who has the disease before it ever reaches the brain and hopefully stop it in its tracks,” Sulzer says.

The new findings were published Aug. 18 in Neuron.

Autoimmunity and the gut

The gut-first theory of Parkinson’s, originally proposed 20 years ago, started to intrigue Sulzer after his own research pointed toward the role of an autoimmune response in Parkinson’s.

In Parkinson’s, a protein called alpha-synuclein becomes misfolded, accumulates inside neurons, and slowly poisons the cells. Sulzer’s lab in collaboration with immunologists at the La Jolla Institute of Immunology has shown that small portions of the misfolded alpha-synuclein also can appear on the outside of neurons, which makes the neurons vulnerable to attack from the immune system.

The immune attack could be doing more acute damage to the neurons than the internal deposits of alpha synuclein.

“The blood of Parkinson’s patients often contains immune cells that are primed to attack the neurons,” Sulzer says, “but it’s not clear where or when they are primed.”

The gut was an intriguing possibility because it contains the same neurons and because most Parkinson’s patients experience constipation years before brain symptoms emerge and the disease is diagnosed.

To pursue this hypothesis, Sulzer teamed up with Agalliu, a neuroimmunologist with expertise in mouse models of another neurological disorder (multiple sclerosis) that has autoimmune features.

Immune response to alpha synuclein leads to gut symptoms

To find out if an immune reaction to alpha-synuclein can kick-start the disease and where, Francesca Garretti and Connor Monahan, grad students directed by Agalliu and Sulzer, first created a mouse capable of displaying pieces of misfolded alpha-synuclein on cell surfaces (natural mice do not have this ability). They then injected the mice with alpha-synuclein and monitored what happened in the brain and the gut.

The researchers did not see any signs resembling Parkinson’s disease in the brain, but they did see that an immune attack on neurons in the gut produced constipation and other gastrointestinal effects resembling those seen in most Parkinson’s patients years before they are diagnosed with the disease.

“This shows that an autoimmune reaction can lead to what appears to be the early stages of Parkinson’s and is strong support that Parkinson’s is in part an autoimmune disease,” Sulzer says.

The findings also raise the possibility that early detection—and then interruption—of an immune response in the gut could prevent a later attack on the brain’s neurons and stop Parkinson’s in its tracks.

Wanted: A mouse with Parkinson’s disease

Right now, though, it’s not clear how big a role the immune system plays in the Parkinson’s brain. The answer to that question may become clearer if the researchers find out why the brains of their mice did not develop any signs of Parkinson’s.

The team hypothesizes that the immune cells in their mouse model may not be reaching the brain because the animals are young and age has not yet weakened the blood-brain barrier sufficiently to let immune cells squeeze through. Opening the barrier or accelerating the aging process may lead to mice that develop gastrointestinal and brain symptoms.

“Our ultimate goal is to develop a model of Parkinson’s disease in mice that recreates the human disease process, which doesn’t exist right now,” Sulzer says. “That will be critical in answering questions about the disease that we can’t explore in people and eventually developing better therapies.”

Additional information

All authors: Francesca Garretti (Columbia, now at Icahn School of Medicine at Mount Sinai), Connor Monahan (Columbia), Nicholas Sloan (Columbia), Jamie Bergen (Columbia), Sanjid Shahriar (Columbia), Seon Woo Kim (Weill Cornell Medicine), Alessandro Sette (La Jolla Institute for Immunology), Tyler Cutforth (Columbia), Ellen Kanter (Columbia), Dritan Agalliu (Columbia), and David Sulzer (Columbia).

Funding: This research was funded by Aligning Science Across Parkinson’s through the Michael J. Fox Foundation for Parkinson’s Research, the National Institutes of Health (grants R01NS095435, R01MH112849, and R01EY033994); the JPB Foundation; the National MS Society (RG-1901-33218), and gifts from Newport Equities LLC, the Walz family, and PANDAS Network to the Department of Neurology at Columbia University.

About this Parkinson’s disease research news

Author: Helen Garey
Source: Columbia University
Contact: Helen Garey – Columbia University
Image: The image is credited to Neuroscience News

Original Research: Open access.
Interaction of an α-synuclein epitope with HLA-DRB1∗15:01 triggers enteric features in mice reminiscent of prodromal Parkinson’s disease” by David Sulzer et al. Neuron


Interaction of an α-synuclein epitope with HLA-DRB1∗15:01 triggers enteric features in mice reminiscent of prodromal Parkinson’s disease


  • α-syn32-46 immunization of HLA-DRB115:01 mice triggers weight loss and constipation
  • α-syn32-46 immunizations induce inflammation and neuron loss in the gut
  • Depletion of CD4+, but not CD8+, T cells partially rescues enteric neural loss
  • Both α-syn32-46 and HLA-DRB115:01 are critical for this model of prodromal PD


Enteric symptoms are hallmarks of prodromal Parkinson’s disease (PD) that appear decades before the onset of motor symptoms and diagnosis. PD patients possess circulating T cells that recognize specific α-synuclein (α-syn)-derived epitopes.

One epitope, α-syn32-46, binds with strong affinity to the HLA-DRB115:01 allele implicated in autoimmune diseases.

We report that α-syn32-46 immunization in a mouse expressing human HLA-DRB115:01 triggers intestinal inflammation, leading to loss of enteric neurons, damaged enteric dopaminergic neurons, constipation, and weight loss. α-Syn32-46 immunization activates innate and adaptive immune gene signatures in the gut and induces changes in the CD4+ TH1/TH17 transcriptome that resemble tissue-resident memory (TRM) cells found in mucosal barriers during inflammation.

Depletion of CD4+, but not CD8+, T cells partially rescues enteric neurodegeneration.

Therefore, interaction of α-syn32-46 and HLA-DRB115:0 is critical for gut inflammation and CD4+ T cell-mediated loss of enteric neurons in humanized mice, suggesting mechanisms that may underlie prodromal enteric PD.

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