Background: Neuritic degeneration is an important early pathological step in neurodegeneration.
Aim: The purpose of this study was to explore the mechanisms connecting neuritic degeneration to the functional and morphological remodeling of endoplasmic reticulum (ER) and mitochondria.
Methods: Here, we set up neuritic degeneration models by neurite cutting-induced neural degeneration in human-induced pluripotent stem cell-derived neurons.
Results: We found that neuritic ER becomes fragmented and forms complexes with mitochondria, which induces IP3R-dependent mitochondrial Ca(2+) elevation and dysfunction during neuritic degeneration. Furthermore, mitochondrial membrane potential is required for ER fragmentation and mitochondrial Ca(2+) elevation during neuritic degeneration. Mechanically, tightening of the ER-mitochondria associations by expression of a short "synthetic linker" and ER Ca(2+) releasing together could promote mitochondrial Ca(2+) elevation, dysfunction, and reactive oxygen species generation.
Conclusion: Our study reveals a dynamic remodeling of the ER-mitochondria interface underlying neuritic degeneration.
Keywords: Ca2+; Endoplasmic reticulum-mitochondria coupling; Mitochondrial membrane potential; Neuron degeneration.
© 2016 John Wiley & Sons Ltd.