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Volume 271,
Number 19,
Issue of May 10, 1996 pp. 11368-11375
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
Evidence That PC2 Is the
Endogenous Pro-neurotensin Convertase in rMTC 6-23 Cells and That PC1-
and PC2-transfected PC12 Cells Differentially Process Pro-neurotensin
(Received for publication, December
29, 1995; and in revised form, February 15, 1996)
Carole
Rovère ,
Pierre
Barbero,
Patrick
Kitabgi
The neuropeptide precursor proneurotensin/neuromedin N
(pro-NT/NN) is mainly expressed and differentially processed in the
brain and in the small intestine. We showed previously that rMTC 6-23
cells process pro-NT/NN with a pattern similar to brain tissue and
increase pro-NT/NN expression in response to dexamethasone, and that
PC12 cells also produce pro-NT/NN but are virtually unable to process
it. In addition, PC12 cells were reported to be devoid of the
prohormone convertases PC1 and PC2. The present study was designed to
identify the proprotein convertase(s) (PC) involved in pro-NT/NN
processing in rMTC 6-23 cells and to compare PC1- and PC2-transfected
PC12 cells for their ability to process pro-NT/NN. rMTC 6-23 cells were
devoid of PC1, PC4, and PC5 but expressed furin and PC2. Stable
expression of antisense PC2 RNA in rMTC 6-23 cells led to a 90%
decrease in PC2 protein levels that correlated with a >80% reduction
of pro-NT/NN processing. PC2 expression was stimulated by dexamethasone
in a time- and concentration-dependent manner. Stable PC12/PC2
transfectants processed pro-NT/NN with a pattern similar to that
observed in the brain and in rMTC 6-23 cells. In contrast, stable
PC12/PC1 transfectants reproduced the pro-NT/NN processing pattern seen
in the gut. We conclude that (i) PC2 is the major pro-NT/NN convertase
in rMTC 6-23 cells; (ii) its expression is coregulated with that of
pro-NT/NN in this cell line; and (iii) PC2 and PC1 differentially
process pro-NT/NN with brain and intestinal phenotype, respectively.

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