Moving and Removing Axonal MitochondriaThomas L. Schwarz, PhD
F.M. Kirby Center for Neurobiology
Children’s Hospital, Boston
and Dept. of Neurobiology, Harvard Medical School
Location: Foege Auditorium, GNOM S060
seminar abstract: Mitochondria are dynamic organelles. In every cell they move and undergo fission and fusion. Their distribution and associations with the cytoskeleton change in response to many signals, including the mitotic cell cycle. In addition, because neurons look like no other cell in the organism, with axons of up to a meter in humans, mitochondrial motility is particularly crucial to the survival of the neuron. The neuron also needs to clear away damaged mitochondria efficiently wherever in the cell they may arise. Not surprisingly then, defects in the transport machinery of neurons and in their mechanisms for removing damaged mitochondria have been linked to several neurodegenerative diseases, including ALS and Parkinson’s disease. This talk will present the evidence for a motor/adaptor complex that is responsible for and regulates the movement of mitochondria and will discuss how that movement is regulated by the cell cycle, Ca++, and glucose. We will look at the operation of two proteins PINK1 and Parkin that are mutated in forms of Parkinson’s disease and examine how these proteins operate in axons to clear away damaged mitochondria that might otherwise compromise the health of the cell. Particularly in the case of mitophagy, we will consider the special challenges posed for neurons by their extended geometry and the difficulty of having a PINK1-dependent pathway operating far from the soma.