ARIA is concentrated in the synaptic basal lamina of the developing chick neuromuscular junction.
Open Access
- 15 September 1995
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 130 (6) , 1423-1434
- https://doi.org/10.1083/jcb.130.6.1423
Abstract
ARIA is a member of a family of polypeptide growth and differentiation factors that also includes glial growth factor (GGF), neu differentiation factor, and heregulin. ARIA mRNA is expressed in all cholinergic neurons of the central nervous systems of rats and chicks, including spinal cord motor neurons. In vitro, ARIA elevates the rate of acetylcholine receptor incorporation into the plasma membrane of primary cultures of chick myotubes. To study whether ARIA may regulate the synthesis of junctional synaptic acetylcholine receptors in chick embryos, we have developed riboprobes and polyclonal antibody reagents that recognize isoforms of ARIA that include an amino-terminal immunoglobulin C2 domain and examined the expression and distribution of ARIA in motor neurons and at the neuromuscular junction. We detected significant ARIA mRNA expression in motor neurons as early as embryonic day 5, around the time that motor axons are making initial synaptic contacts with their target muscle cells. In older embryos and postnatal animals, we found ARIA protein concentrated in the synaptic cleft at neuromuscular junctions, consistent with transport down motor axons and release at nerve terminals. At high resolution using immunoelectron microscopy, we detected ARIA immunoreactivity exclusively in the synaptic basal lamina in a pattern consistent with binding to synapse specific components on the presynaptic side of the basal lamina. These results support a role for ARIA as a trophic factor released by motor neuron terminals that may regulate the formation of mature neuromuscular synapses.Keywords
This publication has 47 references indexed in Scilit:
- ARIA can be released from extracellular matrix through cleavage of a heparin-binding domain.The Journal of cell biology, 1995
- Synaptic structure and development: The neuromuscular junctionCell, 1993
- Neu differentiation factor: A transmembrane glycoprotein containing an EGF domain and an immunoglobulin homology unitCell, 1992
- Isolation of the NeuHER-2 stimulatory ligand: A 44 kd glycoprotein that induces differentiation of mammary tumor cellsCell, 1992
- Induction of adult-type nicotinic acetylcholine receptor gene expression in noninnervated regenerating muscleNeuron, 1991
- The Immunoglobulin Superfamily—Domains for Cell Surface RecognitionAnnual Review of Immunology, 1988
- Spatial distribution of acetylcholine receptors at developing chick neuromuscular junctionsJournal of Neurocytology, 1983
- THE PERMEABILITY OF THE BASAL LAMINA AT THE NEUROMUSCULAR JUNCTION. AN ULTRASTRUCTURAL STUDY OF RAT SKELETAL MUSCLE USING PARTICULATE TRACERSNeuropathology and Applied Neurobiology, 1983
- Development of neuromuscular junctions of fast and slow muscles in the chick embryo: a light and electron microscopic studyJournal of Neurocytology, 1977
- Clonal analysis of vertebrate myogenesis: I. Early developmental events in the chick limbDevelopmental Biology, 1974