Fasciclin 2 plays multiple roles in promoting cell migration within the developing nervous system of Manduca sexta

被引:0
作者
Knittel, Laura M. [1 ]
Swanson, Tracy L.
Lee, Hun Joo [1 ]
Copenhaver, Philip F. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Cell Dev & Canc Biol, L-215 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Enteric nervous system; Migration; Guidance; Cell adhesion; IgCAM; Alternate isoforms; AMYLOID PRECURSOR PROTEIN; ADHESION MOLECULE NCAM; GROWTH CONE GUIDANCE; LOCKED NUCLEIC-ACID; IN-SITU DETECTION; NEURONAL MIGRATION; GENETIC-ANALYSIS; EMBRYONIC-DEVELOPMENT; DIFFERENT ISOFORMS; IMMUNOGLOBULIN SUPERFAMILY;
D O I
10.1016/j.ydbio.2023.04.009
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The coordination of neuronal and glial migration is essential to the formation of most nervous systems, requiring a complex interplay of cell-intrinsic responses and intercellular guidance cues. During the development of the enteric nervous system (ENS) in Manduca sexta (tobacco hornworm), the IgCAM Fasciclin 2 (Fas2) serves several distinct functions to regulate these processes. As the ENS forms, a population of 300 neurons (EP cells) undergoes sequential phases of migration along well-defined muscle pathways on the visceral mesoderm to form a branching Enteric Plexus, closely followed by a trailing wave of proliferating glial cells that enwrap the neurons. Initially, both the neurons and glial cells express a GPI-linked form of Fas2 (GPI-Fas2), which helps maintain cell-cell contact among the pre-migratory neurons and later promotes glial ensheathment. The neurons then switch isoforms, predominantly expressing a combination of transmembrane isoforms lacking an intracellular PEST domain (TM-Fas2 PEST-), while their muscle band pathways on the midgut transiently express transmembrane isoforms containing this domain (TM-Fas2 PEST+). Using intracellular injection protocols to manipulate Fas2 expression in cultured embryos, we found that TM-Fas2 promotes the directed migration and outgrowth of individual neurons in the developing ENS. Concurrently, TM-Fas2 expression by the underlying muscle bands is also required as a substrate cue to support normal migration, while glial expression of GPI-Fas2 helps support their ensheathment of the migratory neurons. These results demonstrate how a specific IgCAM can play multiple roles that help coordinate neuronal and glial migration in the developing nervous system.
引用
收藏
页码:31 / 46
页数:16
相关论文
共 102 条
[1]   Identification of N-glycosylation sites of the murine neural cell adhesion molecule NCAM by MALDI-TOF and MALDI-FTICR mass spectrometry [J].
Albach, C ;
Damoc, E ;
Denzinger, T ;
Schachner, M ;
Przybylski, M ;
Schmitz, B .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2004, 378 (04) :1129-1135
[2]   Fasciclin II signals new synapse formation through amyloid precursor protein and the scaffolding protein dX11/mint [J].
Ashley, J ;
Packard, M ;
Ataman, B ;
Budnik, V .
JOURNAL OF NEUROSCIENCE, 2005, 25 (25) :5943-5955
[3]  
Baines RA, 2002, J NEUROSCI, V22, P6587
[4]  
Banker G., 1998, CULTURING NERVE CELL
[5]   EXPRESSION OF FASCICLIN-I AND FASCICLIN-II GLYCOPROTEINS ON SUBSETS OF AXON PATHWAYS DURING NEURONAL DEVELOPMENT IN THE GRASSHOPPER [J].
BASTIANI, MJ ;
HARRELSON, AL ;
SNOW, PM ;
GOODMAN, CS .
CELL, 1987, 48 (05) :745-755
[6]   Regulation of Fasciclin II and Synaptic Terminal Development by the Splicing Factor Beag [J].
Beck, Erin S. ;
Gasque, Gabriel ;
Imlach, Wendy L. ;
Jiao, Wei ;
Choi, Ben Jiwon ;
Wu, Pao-Shu ;
Kraushar, Matthew L. ;
McCabe, Brian D. .
JOURNAL OF NEUROSCIENCE, 2012, 32 (20) :7058-7073
[7]  
Bieber A.J., 1991, Seminars in the Neurosciences, V3, P309, DOI 10.1016/1044-5765(91)90048-S
[8]   PSA-NCAM in mammalian structural plasticity and neurogenesis [J].
Bonfanti, Luca .
PROGRESS IN NEUROBIOLOGY, 2006, 80 (03) :129-164
[9]   Binding of the Receptor Tyrosine Kinase TrkB to the Neural Cell Adhesion Molecule (NCAM) Regulates Phosphorylation of NCAM and NCAM-dependent Neurite Outgrowth [J].
Cassens, Claas ;
Kleene, Ralf ;
Xiao, Mei-Fang ;
Friedrich, Claudia ;
Dityateva, Galina ;
Schafer-Nielsen, Claus ;
Schachner, Melitta .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (37) :28959-28967
[10]   Quantitation of TGF-β1 mRNA in porcine mesangial cells by comparative kinetic RT/PCR:: Comparison with ribonuclease protection assay and in situ hybridization [J].
Ceol, M ;
Forino, M ;
Gambaro, G ;
Sauer, U ;
Schleicher, ED ;
D'Angelo, A ;
Anglani, F .
JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2001, 15 (04) :215-222