Glial ensheathment of peripheral axons in Drosophila

被引:25
作者
Banerjee, Swati [1 ,2 ]
Bhat, Manzoor A. [1 ,2 ]
机构
[1] Univ N Carolina, Sch Med, Dept Cell & Mol Physiol, Curriculam Neurobiol,Neurodev Disorders Res Ctr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, UNC Neurosci Ctr, Chapel Hill, NC 27599 USA
关键词
peripheral glia; exit glia; glial migration; septate junctions; actin cytoskeleton;
D O I
10.1002/jnr.21574
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The ensheathment of neurons and their axons creates an ion-sensitive microenvironment that allows rapid conduction of nerve impulses. One of the fundamental questions about axonal ensheathment is how insulating glial cells wrap around axons. The mechanisms that underlie insulation of axons in invertebrates and vertebrates are not fully understood. In the present article we address cellular aspects of axonal ensheathment in Drosophila by taking advantage of glial mutants that illustrate a range of phenotypic defects including ensheathment of axons. From the findings of these mutant studies, we summarize that loss of glial cells, defects in glial membrane wrapping, failure of glial migration, and loss of specialized ladderlike septate junctions between ensheathing glial membranes result in axon-glial functional defects. These studies provide a broad perspective on glial ensheathment of axons in Drosophila and key insights into the anatomical and cellular aspects of axonal insulation. Given the powerful genetic approaches available in Drosophila, the axonal ensheathment process can be dissected in great detail to reveal the fundamental principles of ensheathment. These observations will be relevant to understanding the very similar processes in vertebrates, where defects in glial cell functions lead to devastating neurological diseases. (C) 2007 Wiley-Liss, Inc.
引用
收藏
页码:1189 / 1198
页数:10
相关论文
共 104 条
[71]   Key interactions between neurons and glial cells during neural development in insects [J].
Oland, LA ;
Tolbert, LP .
ANNUAL REVIEW OF ENTOMOLOGY, 2003, 48 :89-110
[72]   Signaling in glial development: differentiation migration and axon guidance [J].
Parker, RJ ;
Auld, VJ .
BIOCHEMISTRY AND CELL BIOLOGY, 2004, 82 (06) :694-707
[73]   Cation chloride cotransporters interact with the stress-related kinases Ste20-kelated proline-alanine-rich kinase (SPAK) and oxidative stress response 1 (OSR1) [J].
Piechotta, K ;
Lu, JM ;
Delpire, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (52) :50812-50819
[74]   The local differentiation of myelinated axons at nodes of Ranvier [J].
Poliak, S ;
Peles, E .
NATURE REVIEWS NEUROSCIENCE, 2003, 4 (12) :968-980
[75]   Paranodal interactions regulate expression of sodium channel subtypes and provide a diffusion barrier for the node of Ranvier [J].
Rios, JC ;
Rubin, M ;
Martin, MS ;
Downey, RT ;
Einheber, S ;
Rosenbluth, J ;
Levinson, SR ;
Bhat, M ;
Salzer, JL .
JOURNAL OF NEUROSCIENCE, 2003, 23 (18) :7001-7011
[76]   Polarized domains of myelinated axons [J].
Salzer, JL .
NEURON, 2003, 40 (02) :297-318
[77]   The embryonic central nervous system lineages of Drosophila melanogaster .2. Neuroblast lineages derived from the dorsal part of the neuroectoderm [J].
Schmidt, H ;
Rickert, C ;
Bossing, T ;
Vef, O ;
Urban, J ;
Technau, GM .
DEVELOPMENTAL BIOLOGY, 1997, 189 (02) :186-204
[78]   Rho GTPases:: Signaling, migration, and invasion [J].
Schmitz, AAP ;
Govek, EE ;
Böttner, B ;
Van Aelst, L .
EXPERIMENTAL CELL RESEARCH, 2000, 261 (01) :1-12
[79]   Placental failure in mice lacking the mammalian homolog of glial cells missing, GCMa [J].
Schreiber, J ;
Riethmacher-Sonnenberg, E ;
Riethmacher, D ;
Tuerk, EE ;
Enderich, J ;
Bosl, MR ;
Wegner, M .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (07) :2466-2474
[80]   GPCR signaling is required for blood-brain barrier formation in Drosophila [J].
Schwabe, T ;
Bainton, RJ ;
Fetter, RD ;
Heberlein, U ;
Gaul, U .
CELL, 2005, 123 (01) :133-144