A new study conducted by The John Hopkins University School of Medicine has found that a pathological protein long associated with Parkinson’s disease triggers cells to increase protein synthesis.
This process eventually kills the subset of brain cells that die off in this neurodegenerative condition.
Researchers from the Johns Hopkins University School of Medicine who conducted the study say the findings, originally published on Nov 29 in Science Translational Medicine, offer potential new targets for treating Parkinson’s disease.
“Parkinson’s disease has major impacts on quality of life for patients, but also for their caretakers and loved ones,” says Ted Dawson, the study leader professor in the Department of Neurology and director of the Institute for Cell Engineering at the unversity. “We hope that research like this will provide mechanistic, molecular-based therapies that can actually slow or halt the progression of Parkinson’s disease.”
Parkinson’s disease symptoms, including a variety of motor and cognitive deficits that worsen over time, result from the death of neurons that produce the chemical messenger dopamine.
Current treatments with drugs such as L-dopa largely focus on replacing the dopamine lost when these dopaminergic neurons die.
Over the past two decades, researchers linked these cells’ death to the presence of a pathological form of alpha-synuclein, a normal protein that is abundant in brain tissue. However, how pathological alpha-synuclein causes dopaminergic neuron death has been unclear.
To pin down its role, Dawson and his colleagues used proximity labeling coupled with mass spectrometry to identify proteins that might interact with pathological alpha-synuclein in both a mouse and a lab cell model of Parkinson’s neurons.
They identified 100 such proteins that overlapped between these two models. When the researchers grouped the proteins by function, they found the majority play roles in ribonucleic acid (RNA) processing and translation initiation; these are key processes used by cells to make new proteins.
Several of the proteins were already known to work with the mammalian target of rapamycin (mTOR), which has a dual role in both regulating protein production and breaking down proteins.
Experiments in mice genetically manipulated to over-express the pathological form of alpha-synuclein showed that it indeed caused cells to increase protein synthesis by activating mTOR.
This process was triggered, the researchers say, when the pathological alpha-synuclein bound to another protein, tuberous sclerosis complex 2 (TSC2), preventing it from connecting with yet another protein TSC1, that keeps mTOR in check.
Treating mice with rapamycin
Treating the genetically engineered mice with rapamycin, a drug that targets mTOR, not only prevented excessive protein production in mice with a condition like Parkinson’s disease, but also eased some of the slow, halting movements and weak grip strength that are hallmarks of Parkinson’s disease in people.
Dawson says it’s still unclear precisely how increased protein production might harm dopaminergic neurons; the proteins might clog up key cellular pathways, or specific proteins produced in excess might be harmful for cells. He and his colleagues plan to investigate that question in future research.
Findings point to new targets
In the meantime, he says, the findings point toward new targets for treating Parkinson’s disease. Researchers may, for example, develop drugs that act like rapamycin. currently used as an anti-rejection and anti-cancer medication — but work specifically in the brain to save dopaminergic neurons, sparing patients unnecessary body-wide side effects. Or, it may be possible to target TSC2 to produce a similar effect.
Other Johns Hopkins researchers who contributed to this study are Mohammed Repon Khan, Xiling Yin, Sung-Ung Kang, Jaba Mitra, Hu Wang, Taekyung Ryu, Saurav Brahmachari, Senthilkumar Karuppagounder, Yasuyoshi Kimura, Aanishaa Jhaldiyal, Hyun Hee Kim, Hao Gu, Rong Chen, Javier Redding-Ochoa, Juan Troncoso, Chan Hyun Na, Taekjip Ha and Valina Dawson.
