|
||
J. Cell Biol.,
Volume 143, Number 4, November 16, 1998 1067-1075
7
1 Integrin in Acetylcholine Receptor Clustering

* Department of Cell and Structural Biology, and The clustering of acetylcholine receptors
(AChR) on skeletal muscle fibers is an early event in
the formation of neuromuscular junctions. Recent studies show that laminin as well as agrin can induce AChR
clustering. Since the
Department of Biochemistry, University of Illinois, Urbana, Illinois 61801
7
1 integrin is a major laminin receptor in skeletal muscle, we determined if this integrin participates in laminin and/or agrin-induced AChR
clustering. The alternative cytoplasmic domain variants,
7A and
7B, and the extracellular spliced forms,
7X1 and
7X2, were studied for their ability to engage
in AChR clustering. Immunofluorescence microscopy
of C2C12 myofibers shows that the
7
1 integrin colocalizes with laminin-induced AChR clusters and to a
much lesser extent with agrin-induced AChR clusters.
However, together laminin and agrin promote a synergistic response and all AChR colocalize with the integrin. Laminin also induces the physical association of
the integrin and AChR. High concentrations of anti-
7
antibodies inhibit colocalization of the integrin with
AChR clusters as well as the enhanced response promoted by both laminin and agrin. Engaging the integrin
with low concentrations of anti-
7 antibody initiates
cluster formation in the absence of agrin or laminin.
Whereas both the
7A and
7B cytoplasmic domain
variants cluster with AChR, only those isoforms containing the
7X2 extracellular domain were active.
These results demonstrate that the
7
1 integrin has a
physiologic role in laminin-induced AChR clustering,
that alternative splicing is integral to this function of
the
7 chain, and that laminin, agrin, and the
7
1 integrin interact in a common or convergent pathway in the
formation of neuromuscular junctions.
7
1
This article has been cited by other articles:
|
|