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Volume 271,
Number 17,
Issue of April 26, 1996 pp. 10154-10160
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
Neurotrophin-3
Increases Intracellular Calcium in a Rat Insulin-secreting Cell Line
through Its Action on a Functional TrkC Receptor
(Received for publication, November 28,
1995; and in revised form, January 17, 1996)
Abdelali
Tazi ,
Stephanie
Le Bras,
Hassan Ould
Lamghitnia
,
Jean Didier
Vincent
,
Paul
Czernichow ,
Raphael
Scharfmann
Pancreatic beta cells and neuronal cells show a large number of
similarities. For example, functional receptors for nerve growth factor
are present in beta cells. Here we investigate whether TrkC, a neuronal
high affinity receptor for neurotrophin-3, is expressed in the
insulin-secreting cell line INS-1. We demonstrate the expression in
INS-1 cells of mRNAs coding for TrkC identical in size to those found
in the brain. As in neuronal cells, different alternatively spliced
forms of TrkC mRNA, differing by the insertion of an alternative exon
in their kinase domain, were expressed in INS-1 cells. TrkC protein is
also expressed in INS-1 cells and is functional. Indeed, when INS-1
cells were treated with neurotrophin-3, TrkC became phosphorylated on
tyrosine residues, and the expression of early response genes was
induced. This activation of the receptor was paralleled by a rapid and
transient increase in cytosolic free calcium due to an influx of
extracellular calcium. Functional receptors for NT-3 are thus expressed
in INS-1 cells. This cell line provides a new model for the study of
NT-3 signal transduction and should be useful in the understanding of
the role of neurotrophins in insulin-secreting cells.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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