Understanding 'Disease Mechanisms' of ALS
News Mar 12, 2018 | Original Story by Rob Enslin for Syracuse University.
Researchers in the College of Arts and Sciences (A&S) are making strides in understanding the disease mechanism of amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease.
Carlos A. Castañeda, assistant professor of biology, chemistry and interdisciplinary neuroscience, and Thuy Dao, a postdoctoral researcher in chemistry, have been working with ubiquitin, a tiny molecule that tags obsolete proteins in a cell. They recently found that ubiquitin eliminates droplets of Ubiquilin-2 (UBQLN2) in solution.
The discovery is noteworthy, Castañeda says, because UBQLN2 is a protein-encoding gene, mutations to which cause ALS and various types of dementia, such as frontotemporal dementia (FTD).
“UBQLN2 is found in motor neuron inclusions of patients with ALS,” he says. “We show that UBQLN2 undergoes liquid-liquid phase separation, in which proteins coalesce into protein-rich droplets to form membraneless organelles in cells. Interestingly, dysfunction of membraneless organelle assembly and disassembly is emerging as a common pathogenic mechanism of ALS and other neurodegenerative disorders.”
The ALS Association supports the duo’s research, which in turn is the subject of a major paper in the journal Molecular Cell (Elsevier, 2018).
Other authors include Brian Martyniak G'18, a second-year Ph.D. student in chemistry and biochemistry, who belongs to Castañeda’s lab; members of J. Paul Taylor’s research group from both St. Jude Children’s Research Hospital and the Howard Hughes Medical Institute; and members of Heidi Hehnly’s lab at SUNY Upstate Medical University.
“We want to understand the mechanisms that trigger motor neurons to degenerate in ALS,” says Castañeda, the paper’s lead contact. “It appears that pathological stress granules—membraneless organelles thought to be formed by liquid-liquid phase separation of RNA-binding proteins—trigger ALS and related disorders, leading to cell death.”
Scientists know that when a eukaryotic cell is under stress, it causes certain proteins and RNA to form stress granules (SGs). While this is normal behavior, persistence of SGs or dysregulation of SG dynamics can promote disease states. Castañeda and Dao, in collaboration with Taylor’s group, showed that UBQLN2 was “recruited” to SGs. “This gives our work potential ALS relevance, since mutations in UBQLN2 might lead to defects in either SG assembly, or SG disassembly, or both,” Castañeda says.
There are billions of neurons, or nerve cells, in the nervous system. (The brain alone has more than 100 billion of them.) When ALS attacks neurons, their corresponding muscles weaken and die. People with ALS eventually lose the ability to speak, eat, move or breathe.
Castañeda, who studies proteins associated with neurodegenerative and neuromuscular disease, explains that muscle weakness or stiffness is usually the first sign of ALS: “It is followed by atrophy and paralysis of the muscles of the limbs and trunk, and of the muscles controlling vital functions. The average survival time is three years after diagnosis.”
Ubiquitin and UBQLN2 are part of what of Castañeda calls a “quality-control mechanism,” which maintains proteins at their proper levels during the lifespan of a cell. (Unlike other cells, which live several days or weeks, neurons typically last an entire lifetime.) Any kind of disruption to protein homeostasis usually impairs neuronal development and function.
“We postulated—and eventually confirmed with microscopy and nuclear magnetic resonance spectroscopy—that ubiquitin disrupts UBQLN2 liquid-liquid phase separation,” says Castañeda, who joined Syracuse’s faculty in 2014. “This was significant because ubiquitin tags many proteins, at one point or another.”
Castañeda ultimately hopes to redirect UBQLN2 out the “ubiquinated” substrates in SGs and into protein quality-control pathways. “UBQLN2 is like a shuttle, ferrying misfolded proteins to the cell’s protein-recycling plant,” he continues. “Under normal conditions, SGs dissipate when the stress condition is removed. However, if the condition impairs SG assembly in any way, ALS-linked RNA-binding proteins begin to aggregate.”
While there is no cure for ALS, many people with the disease live longer, thanks to clinical management and two FDA-approved drugs: riluzole and radicava.
Castañeda is optimistic his innovative work with ubiquitin and UBQLN2 will achieve a greater understanding of ALS’ molecular mechanisms and lead to a cure. “UBQLN2 interacts with other RNA-binding proteins, including TDP-43, which is found in 97 percent of inclusions of patients diagnosed with familial or sporadic ALS,” he says. “I look forward to investigating these interactions.”
Studies show that most people who develop ALS are between the ages of 40 and 70, with the disease being 20 percent more common in men. Although scientists struggle to determine the specific genetics or environmental factors that trigger ALS, they find that military veterans, particularly those deployed in the Gulf War from 1990-91, are twice as likely to develop the disease.
“Defects in protein recycling contribute to neurodegeneration,” Castañeda says. “The more we understand UBQLN2’s biological functions—specifically, how its mutations lead to ALS—the better able we can develop new therapies.”
This article has been republished from materials provided by Syracuse University. Note: material may have been edited for length and content. For further information, please contact the cited source.
Thuy P. Dao, Regina-Maria Kolaitis, Hong Joo Kim, Kevin O’Donovan, Brian Martyniak, Erica Colicino, Heidi Hehnly, J. Paul Taylor, Carlos A. Castañeda. Ubiquitin Modulates Liquid-Liquid Phase Separation of UBQLN2 via Disruption of Multivalent Interactions. Molecular Cell, 2018; DOI:10.1016/j.molcel.2018.02.004.
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Comments | 1 ADD COMMENT
Sorice Madina | Apr 03, 2018
My mother was diagnosed with ALS in May 2014. Her doctor put her on riluzole, letting her know there was no cure but the medication might provide her a few more months of delayed symptoms. ALS progresses at different rates and affects different body parts first. My mother, being 80 at the time, fell into a category of what they call "fast progression" (older female). Her arms weakened first, then her hands, her mouth, and throat, and finally her lungs. Throughout her two-and-a-half-year ordeal, she was able to walk with assistance. All the while she continued to take the riluzole. If it bought my mother any time, we will never know. Her neurologist told us that if she couldn't afford it, there was no real need to take it. She lost touch with reality. Suspecting it was the medication I took her off the riluzole (with the doctor’s knowledge) and started her on the ALS natural herbal formula we ordered from GREEN HOUSE HERBAL CLINIC, We spoke to few people who used the treatment here in Canada and they all gave a positive response, her symptoms totally declined over a 7 weeks use of the Green House ALS disease natural herbal formula. She is now almost 84 and doing very well, the disease is totally reversed! (Visit their website ww w . Greenhouseherbalclinic . com) I am thankful to nature, herbs are truly gift from God. I will keep sharing more awareness, Share with friends!!