Nanoscopic compartmentalization of membrane protein motion at the axon initial segment

被引:81
作者
Albrecht, David [1 ,3 ,4 ]
Winterflood, Christian M. [3 ,4 ]
Sadeghi, Mohsen [2 ]
Tschager, Thomas [4 ]
Noe, Frank [2 ]
Ewers, Helge [1 ,3 ,4 ]
机构
[1] Free Univ Berlin, Inst Chem & Biochem, D-14195 Berlin, Germany
[2] Free Univ Berlin, Dept Math & Comp Sci, D-14195 Berlin, Germany
[3] Kings Coll London, Randall Div Cell & Mol Biophys, London SE1 1UL, England
[4] ETH, Inst Biochem, CH-8093 Zurich, Switzerland
关键词
SUBCORTICAL CYTOSKELETON PERIODICITY; PLASMA-MEMBRANE; ANCHORED PROTEINS; DIFFUSION BARRIER; CORTICAL ACTIN; HOP DIFFUSION; NEURONS; MOLECULE; REVEALS; PHOSPHOLIPIDS;
D O I
10.1083/jcb.201603108
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The axon initial segment (AIS) is enriched in specific adaptor, cytoskeletal, and transmembrane molecules. During AIS establishment, a membrane diffusion barrier is formed between the axonal and somatodendritic domains. Recently, an axonal periodic pattern of actin, spectrin, and ankyrin forming 190-nm-spaced, ring-like structures has been discovered. However, whether this structure is related to the diffusion barrier function is unclear. Here, we performed single particle tracking time-course experiments on hippocampal neurons during AIS development. We analyzed the mobility of lipid-anchored molecules by high-speed single-particle tracking and correlated positions of membrane molecules with the nanoscopic organization of the AIS cytoskeleton. We observe a strong reduction in mobility early in AIS development. Membrane protein motion in the AIS plasma membrane is confined to a repetitive pattern of 190-nm-spaced segments along the AIS axis as early as day in vitro 4, and this pattern alternates with actin rings. Mathematical modeling shows that diffusion barriers between the segments significantly reduce lateral diffusion along the axon.
引用
收藏
页码:37 / 46
页数:10
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