Journal article
Non-neural agrin codistributes with acetylcholine receptors during early differentiation of Torpedo electrocytes
Journal of cell science, Vol.109 (7), pp.1837-1846
07/1996
DOI: 10.1242/jcs.109.7.1837
PMID: 8832406
Abstract
Agrin, an extracellular matrix protein synthesized by nerves and muscles is known to promote the clustering of acetylcholine receptors and other synaptic proteins in cultured myotubes. This observation suggests that agrin may provide at least part of the signal for synaptic specialization in vivo. The extracellular matrix components agrin, laminin and merosin bind to alpha-dystroglycan, a heavily glycosylated peripheral protein part of the dystrophin-glycoprotein complex, previously characterized in the sarcolemma of skeletal and cardiac muscles and at the neuromuscular junction. In order to understand further the function of agrin and alpha DG in the genesis of the acetylcholine receptor-rich membrane domain, the settling of components of the dystrophin-glycoprotein complex and agrin was followed by immunofluorescence localization in developing Torpedo marmorata electrocytes. In 40-45 mm Torpedo embryos, a stage of development at which the electrocytes exhibit a definite structural polarity, dystrophin, alpha/beta-dystroglycan and agrin accumulated concomitantly with acetylcholine receptors at the ventral pole of the cells. Among these components, agrin appeared as the most intensely concentrated and sharply localized. The scarcity of the nerve-electrocyte synaptic contacts at this stage of development, monitored by antibodies against synaptic vesicles, further indicates that before innervation, the machinery for acetylcholine receptor clustering is provided by electrocyte-derived agrin rather than by neural agrin. These observations suggest a two-step process of acetylcholine receptor clustering involving: (i) an instructive role of electrocyte-derived agrin in the formation of a dystrophin-based membrane scaffold upon which acetylcholine receptor molecules would accumulate according to a diffusion trap model; and (ii) a maturation and/or stabilization step controlled by neural agrin. In the light of these data, the existence of more than one agrin receptor is postulated to account for the action of agrin variants at different stages of the differentiation of the postsynaptic membrane in Torpedo electrocytes.
Details
- Title: Subtitle
- Non-neural agrin codistributes with acetylcholine receptors during early differentiation of Torpedo electrocytes
- Creators
- A Cartaud - Departement de Biologie Supramoléculaire et Cellulaire, Institut Jacques Monod, CNRS, Université, Paris 7, FranceM A LudoskyM HaasemannD JungK CampbellJ Cartaud
- Resource Type
- Journal article
- Publication Details
- Journal of cell science, Vol.109 (7), pp.1837-1846
- Publisher
- England
- DOI
- 10.1242/jcs.109.7.1837
- PMID
- 8832406
- ISSN
- 0021-9533
- eISSN
- 1477-9137
- Language
- English
- Date published
- 07/1996
- Academic Unit
- Neurology; Molecular Physiology and Biophysics; Iowa Neuroscience Institute
- Record Identifier
- 9984068260202771
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