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Am J Physiol Gastrointest Liver Physiol 286: G671-G682, 2004. First published October 30, 2003; doi:10.1152/ajpgi.00283.2003
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NEUROREGULATION AND MOTILITY

Characteristics of intermittent mitochondrial transport in guinea pig enteric nerve fibers

Pieter Vanden Berghe, Grant W. Hennig, and Terence K. Smith

Department of Physiology and Cell Biology/352, University of Nevada, School of Medicine, Reno, Nevada 89557-0046

Submitted 3 July 2003 ; accepted in final form 28 October 2003

Enteric neurons controlling various gut functions are prone to oxidative insults that might damage mitochondria (e.g., intestinal inflammation). To resume local energy supply, mitochondria need to be transported. We used MitoTracker dyes and confocal microscopy to investigate basic characteristics of mitochondrial transport in guinea pig myenteric neurites. During a 10-s observation of 1 mm nerve fiber, on average, three mitochondria were transported at an average speed of 0.41 ± 0.02 µm/s. Movement patterns were clearly erratic, and velocities were independent of mitochondrial size. The velocity oscillated periodically (~6 s) but was not consistently affected by structures such as en route boutons, bifurcations, or stationary mitochondria. Also, mitochondria transported in opposite directions did not necessarily affect each others' mobility. Transport was blocked by microtubule disruption (100 µM colchicine), and destabilization (1 µM cytochalasin-D) or stabilization (10 µM phalloidin) of actin filaments, respectively, decreased (0.22 ± 0.02 µm/s, P < 0.05) or increased (0.53 ± 0.02 µm/s, P < 0.05) transport speed. Transport was inhibited by TTX (1 µM), and removal of extracellular Ca2+ (plus 2 mM EGTA) had no effect. However, depletion of intracellular stores (thapsigargin) reduced (to 33%) and slowed the transport significantly (0.18 ± 0.02 µm/s, P < 0.05), suggesting an important role for stored Ca2+ in mitochondrial transport. Transport was also reduced (to 21%) by the mitochondrial uncoupler FCCP (1 µM) in a time-dependent fashion and slowed by oligomycin (10 µM). We conclude that mitochondrial transport is remarkably independent of structural nerve fiber properties. We also show that mitochondrial transport is TTX sensitive and speeds up by stabilizing actin and that functional Ca2+ stores are required for efficient transport.

myenteric neuron; axonal transport; intracellular calcium stores; MitoTracker



Address for reprint requests and other correspondence: T. K. Smith, Dept. of Physiology and Cell Biology/352, Univ. of Nevada, School of Medicine, Reno, NV 89557-0046 (E-mail: tks{at}physio.unr.edu).




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