Summary: A new device allows researchers to measure how anesthetic affects levels of Alzheimer’s associated proteins.
Source: Mass General.
Mass. General and Harvard researchers use device to measure how anesthetic affects levels of Alzheimer’s-associated proteins.
A team of researchers from Massachusetts General Hospital (MGH) and the Rowland Institute at Harvard University have used a specialized nanoprobe developed by the Harvard/Rowland investigators to directly measure levels of key proteins within living, cultured cells. As described in the journal Nano Letters, the investigators used the device to track levels of the Alzheimer’s-disease-associated proteins amyloid-beta (A-beta) and tau in neurons and other cells exposed to an anesthetic known to produce Alzheimer’s-like changes in the brains of mice. Their results support the view that the generation of A-beta is among the first steps leading to the characteristic neurodegeneration of Alzheimer’s disease.
“To study the dynamics of A-beta and tau, we needed a way to trigger the expression of both proteins and a tool to track dynamic changes of protein expression,” says lead author Feng Liang, PhD, a research fellow at the Rowland Institute.
In 2008, some of the MGH members of the current team showed that the anesthetic isoflurane induced characteristic changes seen in Alzheimer’s disease – including activation of cell-death enzymes and generation of A-beta – in cultured cells and in mouse brains. In 2014, the Harvard/Rowland researchers demonstrated the ability of their nanodevice to detect levels of intracellular proteins in living, cultured cells. The current study merges both of these accomplishments to investigate a key question regarding the mechanism of Alzheimer’s disease – whether generation of A-beta precedes or follows the generation of the abnormal form of tau that characterizes the disease.
The tip of the device developed by the Harvard/Rowland investigators is around 50 nanometers (billionths of a meter) across, about 200 times smaller than a single cell. An integrated gold nanorod serves as the biosensor for what is called surface plasmon resonance – an oscillation of electrons in response to a light signal that can generate an optical readout reflecting protein binding signals. Antibodies targeting specific proteins can be integrated into the probe to give specific measurements of protein levels. The team first demonstrated that it was possible to use the nanoplasmonic fiber tip probe (nFTP) to quantify protein levels in individual cells without affecting their vitality and viability.
Using the nFTP device the investigators then tracked the changing levels of A-beta and the Alzheimer’s-associated form of tau, which is characterized by excess phosphate molecules, in cultured cells that had been treated with isoflurane. The readings indicated that the increase in A-beta expression preceded the rise in phosphorylated tau levels by several hours. The team then showed that, while blocking A-beta expression reduced tau levels, blocking tau did not prevent the initial rise in A-beta. However, without phosphorylated tau expression, A-beta levels eventually began to drop, suggesting a sequence in which A-beta generation stimulates tau phosphorylation, which promotes further generation of A-beta.
“We have brought the traditional immunoassay into living cells with exquisite sensitivity,” says Qimin Quan, PhD, a junior fellow at the Rowland Institute and co-corresponding author of the Nano Letters report. “The device is still limited in its ability to measure a large number of single cells, requiring further improvement. But its high-sensitivity, label-free and single-cell capability make it a unique tool for diagnosing clinically obtained limited samples.”
Zhongcong Xie, MD, PhD, director of the Geriatric Anesthesia Research Unit in the MGH Department of Anesthesia, Critical Care and Pain Medicine and co-corresponding author of the study, adds, “Each year approximately 8.5 million patients with Alzheimer’s disease need anesthesia and surgical care worldwide. Learning how anesthesia affects the mechanisms behind Alzheimer’s will require collaboration among specialists in anesthesia, neurology and engineering. Moreover, this use of both an anesthetic and the nFTP device to measure interactions between A-beta and tau is just a first step.” Xie is a professor of Anesthesia at Harvard Medical School.
Additional co-authors of the Nano Letters study are Yiying Zhang, MD and Yuanlin Dong, MD, MGH Anesthesia; Wooyoung Hong, PhD, Harvard Department of Chemistry and Chemical Biology.
Funding: Support for the study includes a Rowland Junior Fellowship award and National Institutes of Health grants R01 GM088801, R01 AG041274 and HD 086977.
Source: Terri Ogan – Mass General
Image Source: This NeuroscienceNews.com image is credited to Feng Liang, PhD, Rowland Institute, Harvard University.
Original Research: Abstract for “Direct Tracking of Amyloid and Tu Dynamics in Neuroblastoma Cells Using Nanoplasmonic Fiber Tip Probes” by Feng Liang, Yiying Zhang, Wooyoung Hong, Yuanlin Dong, Zhongcong Xie, and Qimin Quan in Nano Letters. Published online June 6 2016 doi:10.1021/acs.nanolett.6b00320
[cbtabs][cbtab title=”MLA”]Mass General. “Nanoprobe Enables Measurement of Protein Dynamics in Living Cells.” NeuroscienceNews. NeuroscienceNews, 14 June 2016.
<https://neurosciencenews.com/protein-dynamics-nanoprobe-4473/>.[/cbtab][cbtab title=”APA”]Mass General. (2016, June 14). Nanoprobe Enables Measurement of Protein Dynamics in Living Cells. NeuroscienceNews. Retrieved June 14, 2016 from https://neurosciencenews.com/protein-dynamics-nanoprobe-4473/[/cbtab][cbtab title=”Chicago”]Mass General. “Nanoprobe Enables Measurement of Protein Dynamics in Living Cells.” https://neurosciencenews.com/protein-dynamics-nanoprobe-4473/ (accessed June 14, 2016).[/cbtab][/cbtabs]
Direct Tracking of Amyloid and Tu Dynamics in Neuroblastoma Cells Using Nanoplasmonic Fiber Tip Probes
Amyloid plaques and neurofibrillary tangles are the pathological hallmarks of Alzheimer’s disease. However, there has been a long-standing discussion on the dynamic relations between Aβ and tau proteins, partially due to the lack of a tool to track protein dynamics in individual live neurons at the early stage of Aβ generation and tau phosphorylation. Here, we developed nanoplasmonic fiber tip probe (nFTP) technology to simultaneously monitor Aβ42 generation and tau phosphorylation (at serine 262) in living, single neuroblastoma cells over 12 h. We observed that Aβ42 generation, under clinically relevant anesthetic treatment, preceded tau phosphorylation, which then facilitated Aβ42 generation. This observation is also supported by measuring proteins in cell lysates using the ultrasensitive label-free photonic crystal nanosensors. nFTP therefore provides an advanced method to investigate protein expression and post-translational modification in live cells and determine outcomes of intervention of Alzheimer’s disease and other neurodegenerative disorders.
“Direct Tracking of Amyloid and Tu Dynamics in Neuroblastoma Cells Using Nanoplasmonic Fiber Tip Probes” by Feng Liang, Yiying Zhang, Wooyoung Hong, Yuanlin Dong, Zhongcong Xie, and Qimin Quan in Nano Letters. Published online June 6 2016 doi:10.1021/acs.nanolett.6b00320