Fig. 7From: Neuromuscular junction pathology is correlated with differential motor unit vulnerability in spinal and bulbar muscular atrophySoleus NMJs show significant decrease in localization of NFH to the axon terminal. A, C, E, G To evaluate localization of cytoskeletal structural element NFH to the axon terminal, NMJs from tibialis anterior were stained with α-BTX, synaptophysin, and SMI31 (phospho-NFH) or α-BTX, TUJ1 (BIII-tubulin, and SMI32 (unphospho-NFH) and evaluated for colocalization with the synaptophysin or α-BTX, respectively. B Transgenic mice showed no changes in uNFH localization to the terminal; however, knock-in mice showed a significant decrease in uNFH localization with the terminal (D; p < 0.05). D In contrast, pNFH colocalization with the terminal was significantly decreased in transgenic mice (E; p < 0.01) but not in knock-in mice (F). Mann–Whitney Test was used to evaluate statistical significance. uNFH Unphosphorylated neurofilament heavy chain; pNFH Phosphorylated neurofilament heavy chain; NTg Non-transgenic; Tg Transgenic; WT Wild-type; KI Knock-inBack to article page