Axonal Gradient of Arachidonic Acid-containing Phosphatidylcholine and Its Dependence on Actin Dynamics

Phosphatidylcholine (PC) is the most abundant component of lipid bilayers and exists in various molecular forms, through combinations of two acylated fatty acids. Arachidonic acid (AA)-containing PC (AA-PC) can be a source of AA, which is a crucial mediator of synaptic transmission and intracellular...

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Veröffentlicht in:The Journal of biological chemistry 2012-02, Vol.287 (8), p.5290-5300
Hauptverfasser: Yang, Hyun-Jeong, Sugiura, Yuki, Ikegami, Koji, Konishi, Yoshiyuki, Setou, Mitsutoshi
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Sprache:eng
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Zusammenfassung:Phosphatidylcholine (PC) is the most abundant component of lipid bilayers and exists in various molecular forms, through combinations of two acylated fatty acids. Arachidonic acid (AA)-containing PC (AA-PC) can be a source of AA, which is a crucial mediator of synaptic transmission and intracellular signaling. However, the distribution of AA-PC within neurons has not been indicated. In the present study, we used imaging mass spectrometry to characterize the distribution of PC species in cultured neurons of superior cervical ganglia. Intriguingly, PC species exhibited a unique distribution that was dependent on the acyl chains at the sn-2 position. In particular, we found that AA-PC is enriched within the axon and is distributed across a proximal-to-distal gradient. Inhibitors of actin dynamics (cytochalasin D and phallacidin) disrupted this gradient. This is the first report of the gradual distribution of AA-PC along the axon and its association with actin dynamics. The neuronal distribution of arachidonic acid-containing phosphatidylcholine (AA-PC) remains unknown. AA-PC axonal intensity showed a proximal-to-distal gradient, which was disrupted by actin inhibitors. AA-PC occupies a higher portion of PC at distal than at proximal axons and may be associated with actin dynamics. This research provides a better understanding of the neuronal spatial composition of PC.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.M111.316877