Differential dynamics of neurofilament-H protein and neurofilament-L protein in neurons

Abstract

Neurofilaments (NFs) are composed of triplet proteins, NF-H, NF-M, and NF- L. To understand the dynamics of NFs in vivo, we studied the dynamics of NF- H and compared them to those of NF-L, using the combination of microinjection technique and fluorescence recovery after photobleaching. In the case of NF- L protein, the bleached zone gradually restored its fluorescence intensity with a recovery half time of ~35 min. On the other hand, recovery of the bleached zone of NF-H was considerably faster, taking place in ~19 min. However, in both cases the bleached zone was stationary. Thus, it was suggested that NF-H is the dynamic component of the NF array and is interchangeable, but that it assembles with the other neurofilament triplet proteins in a more exchangeable way, implying that the location of NF-H is in the periphery of the core NF array mainly composed of NF-L subunits. Immunoelectron microscopy investigations of the incorporation sites of NF-H labeled with biotin compounds also revealed the lateral insertion of NF-H subunits into the preexisting NF array, taking after the pattern seen in the case of NF-L. In summary, our results demonstrate that the dynamics of the L and H subunit proteins in situ are quite different from each other, suggesting different and separated mechanisms or structural specialization underlying the behavior of the two proteins.