Axonal ensheathment and septate junction formation in the peripheral nervous system of Drosophila

被引:87
作者
Banerjee, S
Pillai, AM
Paik, R
Li, JJ
Bhat, MA
机构
[1] Univ N Carolina, Sch Med, Dept Cell & Mol Physiol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, Curriculum Neurobiol, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Sch Med, Ctr Neurosci, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Sch Med, Neurodev Disorders Res Ctr, Chapel Hill, NC 27599 USA
关键词
peripheral glia; glial septate junctions; chordotonal organs; blood-nerve barrier; neuron-glial interactions; cell adhesion;
D O I
10.1523/JNEUROSCI.5383-05.2006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Axonal insulation is critical for efficient action potential propagation and normal functioning of the nervous system. In Drosophila, the underlying basis of nerve ensheathment is the axonal insulation by glial cells and the establishment of septate junctions (SJs) between glial cell membranes. However, the details of the cellular and molecular mechanisms underlying axonal insulation and SJ formation are still obscure. Here, we report the characterization of axonal insulation in the Drosophila peripheral nervous system (PNS). Targeted expression of tau-green fluorescent protein in the glial cells and ultrastructural analysis of the peripheral nerves allowed us to visualize the glial ensheathment of axons. We show that individual or a group of axons are ensheathed by inner glial processes, which in turn are ensheathed by the outer perineurial glial cells. SJs are formed between the inner and outer glial membranes. We also show that Neurexin IV, Contactin, and Neuroglian are coexpressed in the peripheral glial membranes and that these proteins exist as a complex in the Drosophila nervous system. Mutations in neurexin IV, contactin, and neuroglian result in the disruption of blood - nerve barrier function in the PNS, and ultrastructural analyses of the mutant embryonic peripheral nerves show loss of glial SJs. Interestingly, the murine homologs of Neurexin IV, Contactin, and Neuroglian are expressed at the paranodal SJs and play a key role in axon-glial interactions of myelinated axons. Together, our data suggest that the molecular machinery underlying axonal insulation and axon-glial interactions may be conserved across species.
引用
收藏
页码:3319 / 3329
页数:11
相关论文
共 50 条
[1]   Setting up a selective barrier at the apical junction complex [J].
Anderson, JM ;
Van Itallie, CM ;
Fanning, AS .
CURRENT OPINION IN CELL BIOLOGY, 2004, 16 (02) :140-145
[2]   GLIOTACTIN, A NOVEL TRANSMEMBRANE PROTEIN ON PERIPHERAL GLIA, IS REQUIRED TO FORM THE BLOOD-NERVE BARRIER IN DROSOPHILA [J].
AULD, VJ ;
FETTER, RD ;
BROADIE, K ;
GOODMAN, CS .
CELL, 1995, 81 (05) :757-767
[3]   moody Encodes two GPCRs that regulate cocaine behaviors and blood-brain barrier permeability in Drosophila [J].
Bainton, RJ ;
Tsai, LTY ;
Schwabe, T ;
DeSalvo, M ;
Gaul, U ;
Heberlein, U .
CELL, 2005, 123 (01) :145-156
[4]  
BANERJEE S, 2006, IN PRESS CELL BIOCH
[5]   A Drosophila neurexin is required for septate junction and blood-nerve barrier formation and function [J].
Baumgartner, S ;
Littleton, JT ;
Broadie, K ;
Bhat, MA ;
Harbecke, R ;
Lengyel, JA ;
ChiquetEhrismann, R ;
Prokop, A ;
Bellen, HJ .
CELL, 1996, 87 (06) :1059-1068
[6]   Neurexin IV, caspr and paranodin - novel members of the neurexin family: encounters of axons and glia [J].
Bellen, HJ ;
Lu, Y ;
Beckstead, R ;
Bhat, MA .
TRENDS IN NEUROSCIENCES, 1998, 21 (10) :444-449
[7]   Molecular organization of axo-glial junctions [J].
Bhat, MA .
CURRENT OPINION IN NEUROBIOLOGY, 2003, 13 (05) :552-559
[8]   Discs lost, a novel multi-PDZ domain protein, establishes and maintains epithelial polarity [J].
Bhat, MA ;
Izaddoost, S ;
Lu, Y ;
Cho, KO ;
Choi, KW ;
Bellen, HJ .
CELL, 1999, 96 (06) :833-845
[9]   Axon-glia interactions and the domain organization of myelinated axons requires Neurexin IV/Caspr/Paranodin [J].
Bhat, MA ;
Rios, JC ;
Lu, Y ;
Garcia-Fresco, GP ;
Ching, W ;
St Martin, M ;
Li, JJ ;
Einheber, S ;
Chesler, M ;
Rosenbluth, J ;
Salzer, JL ;
Bellen, HJ .
NEURON, 2001, 30 (02) :369-383
[10]   Chromatid segregation at anaphase requires the barren product, a novel chromosome-associated protein that interacts with topoisomerase II [J].
Bhat, MA ;
Philp, AV ;
Glover, DM ;
Bellen, HJ .
CELL, 1996, 87 (06) :1103-1114