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The Journal of Neuroscience, July 29, 2009, 29(30):9429-9438; doi:10.1523/JNEUROSCI.1472-09.2009

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Cellular/Molecular
Dynein Light Chain LC8 Regulates Syntaphilin-Mediated Mitochondrial Docking in Axons

Yan-Min Chen, Claudia Gerwin, and Zu-Hang Sheng

Synaptic Function Section, The Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke–National Institutes of Health, Bethesda, Maryland 20892-3706

Correspondence should be addressed to Zu-Hang Sheng, Synaptic Function Section, the Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke–National Institutes of Health, Building 35, Room 2B215, 35 Convent Drive, Bethesda, MD 20892-3706. Email: shengz{at}ninds.nih.gov

Mitochondria in the cell bodies of neurons are transported down neuronal processes in response to changes in local energy and metabolic states. Because of their extreme polarity, neurons require specialized mechanisms to regulate mitochondrial transport and retention in axons. Our previous studies using syntaphilin (snph) knock-out mice provided evidence that SNPH targets to axonal mitochondria and controls their mobility through its static interaction with microtubules (MTs). However, the mechanisms regulating SNPH-mediated mitochondrial docking remain elusive. Here, we report an unexpected role for dynein light chain LC8. Using proteomic biochemical and cell biological assays combined with time-lapse imaging in live snph wild-type and mutant neurons, we reveal that LC8 regulates axonal mitochondrial mobility by binding to SNPH, thus enhancing the SNPH-MT docking interaction. Using mutagenesis assays, we mapped a seven-residue LC8-binding motif. Through this specific interaction, SNPH recruits LC8 to axonal mitochondria; such colocalization is abolished when neurons express SNPH mutants lacking the LC8-binding motif. Transient LC8 expression reduces mitochondrial mobility in snph (+/+) but not (–/–) neurons, suggesting that the observed effect of LC8 depends on the SNPH-mediated docking mechanism. In contrast, deleting the LC8-binding motif impairs the ability of SNPH to immobilize axonal mitochondria. Furthermore, circular dichroism spectrum analysis shows that LC8 stabilizes an -helical coiled-coil within the MT-binding domain of SNPH against thermal unfolding. Thus, our study provides new mechanistic insights into controlling mitochondrial mobility through a dynamic interaction between the mitochondrial docking receptor and axonal cytoskeleton.

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Received March 27, 2009; revised June 3, 2009; accepted June 20, 2009.

Correspondence should be addressed to Zu-Hang Sheng, Synaptic Function Section, the Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke–National Institutes of Health, Building 35, Room 2B215, 35 Convent Drive, Bethesda, MD 20892-3706. Email: shengz{at}ninds.nih.gov

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