Molecular Motors May Become Jammed, Playing A Role In The Development Of ALS
The researchers showed how a genetic mutation often associated with inherited ALS caused delays in the transport of these important molecules along the long axons of neurons.
Their findings were published in the online journal PLOS ONE.
Motor neurons are among the longest cells in the human body - some may extend half a person's height, as much as three feet. This poses a problem if all the cellular building blocks are made at one end of the cell, where the nucleus sits, but are needed at the other end of the cell.
Neurons have the molecular equivalents of highways and delivery trucks - nerve fibers and motor proteins - that run along their long axons, ferrying material back and forth. But when shipping is held up, and products aren't getting to where they are needed, the cell can't function optimally. These transport problems can cause neurons to lose contact with other neurons and muscles.
"If the transport process is delayed or slowed, the terminal end of the cell can run out of materials it needs, and can lose its synaptic connection with its neighboring neurons," says Gerardo Morfini, UIC assistant professor of anatomy and cell biology and the co-principal investigator on the study. "Without the connections, the cells die."
"Cell death is the final stage in a long disease process in ALS," said Scott Brady, UIC professor and head of anatomy and cell biology and co-principal investigator. "We wanted to understand the pathological process in neurons leading up to cell death."
Neuroscientists know that mutations in a protein called SOD1 account for many of the 10 percent of ALS cases that are inherited. Ninety percent of ALS cases have no known cause and are termed sporadic.
Brady and colleagues had previously shown, using high-resolution video microscopy of squid axons, that a mutant variant of the protein significantly slowed down the transport of material from one end of the cell to the other.
In the new study, the researchers looked at how the mutated form of SOD1 caused the slowdown in cellular transport. They found that the mutated protein activated molecules called p38 kinases, which in turn modified a major motor protein involved in moving cargo along the nerve axons. These modified motor proteins moved poorly compared to controls that were exposed to unmutated SOD1.
They also showed that transport in in genetically altered mice was also slowed by mutant SOD1, through the same mechanism.
"The pathways between SOD1 and the p38 kinases could provide interesting targets for therapeutic intervention in treating ALS, both for some of the genetic forms and the spontaneous forms, where malfunctioning SOD1 is also a contributing factor," said Brady.
Rodolfo Gatto, Agnieszka Kaminska, Yuyu Song, Natalia Marangoni, Sarah Berth, Gustavo Pigino and Ehsan Tavassolifrom of UIC; Linda Molla and Lisa Baker of the Woods Hole Marine Biological Laboratory; Daryl Bosco, Lawrence Hayward and Robert Brown Jr. of the University of Massachusetts Medical Center; Ashutosh Tiwari of Michigan Technological University; Hannah Brown of the Woods Hole Marine Biological Laboratory and Massachusetts General Hospital; D. Martin Watterson of Northwestern University; Chun-Fang Huang and Gary Banker of Oregon Health & Science University; and Carolina Bagnato of the National University of Rio Negro, Argentina, also contributed to this study.
This research was supported by 2007/2008 MBL summer fellowships and NIH (NS066942A) grants to GM; HHMI-USE Grant #52006287 to Hunter College of CUNY (LM); Muscular Dystrophy Association (MDA) and NIH (R01NS44170) grants to LJH; MDA and NIH (NS23868, NS23320, NS41170) grants to STB; NIH grant MH066179 to GB; NIH grants R01AG031311 and R01NS055951 to DMW; NIH (U01NS05225, R01NS050557, 1RC1NS068391, 1RC2NS070342) grants to RHB; R01NS067206 to DAB; ALSA grants to GM, AT, RHB, and STB; and ALS/CVS Therapy Alliance grants to RHB, GM, AT, LJH, and DAB. RHB and AT received support from the Angel Fund. RHB also received support from the DeBourgknecht Fund for ALS Research, P2ALS and Project ALS.
University of Illinois at Chicago
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