| First Author | Hammond VE | Year | 2014 |
| Journal | Cereb Cortex | Volume | 24 |
| Issue | 12 | Pages | 3289-300 |
| PubMed ID | 23897647 | Mgi Jnum | J:226892 |
| Mgi Id | MGI:5698799 | Doi | 10.1093/cercor/bht191 |
| Citation | Hammond VE, et al. (2014) Ndfip1 is required for the development of pyramidal neuron dendrites and spines in the neocortex. Cereb Cortex 24(12):3289-300 |
| abstractText | Ubiquitin ligases of the Nedd4 family are important for axon and dendrite development, but little is known about their adaptor, Nedd4 family-interacting protein 1 (Ndfip1), that is responsible for their enzymatic activation. To study the function of Ndfip1 in cortical development, we generated a conditional knock-out (conditional KO) in neurons. The Ndfip1 conditional KO mice were viable; however, cortical neurons in the adult brain exhibited atrophic characteristics, including stunted dendritic arbors, blebbing of dendrites, and fewer dendritic spines. In electron micrographs, these neurons appeared shrunken with compacted somata and involutions of the nuclear membrane. In culture, Ndfip1 KO neurons exhibited exuberant sprouting suggesting loss of developmental control. Biochemical analysis of postsynaptic density (PSD) fractions from Ndfip1 KO cortical and hippocampal neurons showed that the postsynaptic proteins (Arc and PSD-95) were reduced compared with wild-type controls. In addition, the PI3 kinase/Akt signaling pathway was altered. These results indicate that Ndfip1, through its Nedd4 effectors, is important for the development of dendrites and dendritic spines in the cortex. |
