First author Xiaodong Zhu, principal investigator Jiawei Zhou, and colleagues discovered that neurofilament-L interacts with the pro-inflammatory protein MSC p43 in a yeast two-hybrid screen. Overexpression of neurofilament-L caused the formation of MSC p43-positive aggregates. These data led them to characterize MSC p43’s role in neural development and function.

The protein is expressed in several parts of the CNS, including the ventral horn of the spinal cord and the hippocampus. MSC p43-null mice exhibited a variety of symptoms including lameness of the hind limbs and decreased motor activity on a rotarod test. They also had muscular atrophy and decreased innervation of muscle fibers by two months of age. When the scientists examined the axons in the lumbar ventral roots of two-month-old null mutants, they observed shrunken, collapsed structures. The knockout animals also had fewer myelinated axons than did wild-type mice.

Next, the scientists explored the effects of MSC p43 on neurofilament networks. Overexpression of the protein in SH-SYS5 neuroblastoma cells resulted in punctate aggregates containing neurofilaments, suggesting the network was disassembled. Using electron microscopy, Zhu and colleagues found that neurofilaments were disorganized, with fewer and shorter fibrils than normal, in axons from two-month-old MSC p43-null mice. The animals also showed a two- to threefold increase in neurofilament phosphorylation levels compared to wild-type littermates. Experiments with hippocampal neural cultures bore out the role of MSC p43 as a negative regulator of neurofilament phosphorylation. The altered phosphorylation in the null animals appeared to cause the disruption of the neurofilament network.

The authors suggested that the symptoms of the MSC p43-null mice are similar to those of one type of Charcot-Marie-Tooth disease, which also affects peripheral nerves. Mutations in neurofilament-L have been linked to this type 2D CMT (Mersiyanova et al., 2000). Zhou noted that accumulation of hyperphosphorylated neurofilament has been linked to other diseases, such as ALS (Rouleau et al., 1996) and Parkinson disease (Goldman et al., 1983). “It is likely that the dysfunction of MSC p43 may be relevant to neurological disorders besides CMT,” he wrote in an e-mail to ARF.—Amber Dance.

Reference:
Zhu X, Liu Y, Yin Y, Shao A, Zhang B, Kim S, Zhou J. MSC p43 required for axonal development in motor neurons. PNAS Early Edition. Abstract